6 Oct 2025—Fall continues to advance in the St. Louis area, and despite very dry conditions during the past two months the fall bloomers continue to make their appearance. One of the area’s most reliable and interesting places to see fall blooms is Victoria Glades south of Hillsboro, where orchids, gentians, and asters anchor a unique suite of fall-blooming plants that are rarely seen elsewhere in our mostly forested environs.
The group chose the Nature Conservancy portion of the complex to explore, as it was in the mesic forest along the riparian corridor below the glade on this side that the first of two orchids—the charmingly diminutive and seldom-seen Spiranthes ovalis (lesser ladies’ tresses)—was expected to be seen in bloom. Despite having recently taken GPS coordinates for the plants, it took several minutes of the group scouring the area around the coordinates before the tiny plants were finally found. Its delicate blooms, fall flowering season, small size, presence of basal and cauline leaves at anthesis, and preference for mesic habitats all serve to identify this species. Missouri’s populations are considered var. erostella, which lack certain essential flowering organs and are, thus, self-pollinated (cleistogamous).
Spiranthes ovalis var. erostellata (lesser ladies’ tresses—family Orchidaceae).
Clambering up and out of the creek bed and onto the open glade, the group found, again with some difficulty, the second orchid we were looking for—Spiranthes magnicamporum (Great Plains ladies’ tresses). Unlike S. ovalis, however, this species is much more commonly seen on dolomitic glades throughout the state, and there have been fall seasons at Victoria Glades featuring spectacular displays of it. Sadly, it does not appear that this will be one of those falls, almost surely because of the near absence of rain in recent months. The first two plants were found under and next to a cut eastern red-cedar, whose cadaver perhaps provided just enough protection to prevent a complete drying of the soil underneath and allowed the two plants to proceed to flowering. Of the nine species of Spiranthes presently known to occur in Missouri, S. magnicamporum is among the showiest due to its robust, often doubly helical inflorescences and relatively large flowers with spreading and arching lateral sepals. It is also among the most fragrant, with a sweetish fragrance of coumarin, which some people liken to vanilla.
I’ve been visiting Victoria Glades for more than 40 years, yet I continue to see things I haven’t previously notified. This time it was Trichostema coeruleum (pennyroyal bluecurls), a member of the mint family (Lamiaceae). [Note: Trichostema coeruleum was known until recently as Trichostema brachiatum—now a synonym of Trichostema dichotomum.] Unlike Trichostema dichotomum (bluecurls), which prefers glades and other dry habitats with acidic substrates (e.g., sandstone), T. coeruleum prefers such habitats with calcareous substrates (e.g., dolomite). A third species of the genus, Trichostema setaceum (narrow-leaf bluecurls), also occurs in Missouri but is restricted to sand prairies in extreme southeastern Missouri.
Dolomite glades are also the preferred habitat for many species of plants in the family Orobanchaceae, a bizarre family of mostly hemiparasitic plants that derive at least some of their nutrition not from the sun, but by tapping into the roots of nearby plants. Castilleja coccinea (scarlet paintbrush) is perhaps the best known of these, in most years joining the cacophony of wildflowers that form colorful displays across Victoria Glades during spring and early summer. There are, however, several less conspicuous but equally beautiful wildflowers in the family that are restricted in the area almost exclusively to the dolomite glades of Jefferson Co. One of these is Agalinis skinneriana (Skinner’s or pale gerardia/false foxglove), which the group found sporadically still in bloom across the open glade. There are several species of Agalinis in Missouri, some of which are quite common. However, A. skinneriana can usually be recognized by the characteristic habitat and generally upward-facing flowers with spreading to reflexed upper corolla lobes. The plants are also relatively slender and fewer-branched than the more common A. tenuifolia (common gerardia/false foxglove) and A. gattingeri (rough-stemmed gerardia/false foxglove).
Agalinis skinneriana (Skinner’s or pale gerardia/false foxglove—family Orobanchaceae).
Another plant in the family Orobanchaceae that the group saw was Buchnera americana (American bluehearts), represented by a single plant still bearing two worn blossoms. Normally blooming from June through September, plants in full bloom have no look-alikes and are not likely to be confused with anything else. Despite this, the vervain-like fruit-bearing structure of this late straggler fooled the group into at first thinking it was a species of Verbena until its true identity was realized.
Buchnera americana (American bluehearts—family Orobanchaceae).
No group of plants more iconically represents fall than goldenrods (genus Solidago) and true asters (genus Symphyotrichum), and no place allows as many uncommonly seen species to be seen together as the dolomite glades. Three species of goldenrods were seen during the day—the super common Solidago nemoralis (old field goldenrod), the less common but more showy Solidago rigida (stiff goldenrod), and the highly restricted Solidago gattingeri (Gattinger’s goldenrod) (we were not able to locate a fourth species—Solidago radula [rough goldenrod], which we have observed during previous visits on the MDC portion of Victoria Glades). It was the true asters, however, that truly tested our plant identification abilities. Relatively easier are the purple asters, of which we found three species. The first and most abundant was Symphyotrichum oblongifolium (aromatic aster), recognized by its recurved phyllaries and branched habit with narrow, linear leaves that become more numerous and smaller in the upper plant. If one is still in doubt as to its identity, however, one needs only to crush the leaves between the fingers and enjoy its distinct aroma.
Along the intermittent creek and near the interface with the dry post oak woodland on the north of the glade, we encountered a second species—Symphyotrichum oolentangiense (azure aster). Identification of this species came only near the end of the outing, as a key identifying characteristic of this species—the presence of distinctly petiolate cordate basal leaves that are rough to the touch—was not seen on any of the plants examined before then. At that point, we suspected Symphyotrichum turbinellum (prairie aster) due to the vase-shaped involucres. While that species has been found at Victoria Glades, it is usually a much more highly branched plant associated with more wooded habitats (despite the common name). Finally, we found a plant with such leaves present, albeit dried up, and then another with the leaves present and still fresh to confirm the identification.
Symphyotrichum oolentangiense (sky blue aster—family Asteraceae).
In a small area at the northernmost point of the glade, we found Symphyotrichum sericeum (silky aster). This species is immediately recognizable from afar by the silvery cast to the foliage—this, combined with its highly preferred habitat of glades or dry prairies are usually enough to identify the species, although it is said that the flowers are often more purple and less bluish than other “purple asters.”
As we walked the margins of the glade, the group kept their collective eyes out for Gentiana puberulenta (downy gentian), a striking and rarely seen fall flowering species that has been found on several occasions at Victoria Glades. The species has been seen at Victoria Glades on a few occasions in past years, and the locations of these sightings were scoured thoroughly but without success. Unexpectedly, near the end of the outing, a single plant in flower was located—its perfectly fresh blossom initially hidden from view underneath fallen leaves. One of three members of the genus Gentiana in Missouri, this species is easily differentiated by having the corolla spread open at maturity. Missouriplants.com notes “The rich, deep blue color of the corollas is a striking and uncommon hue among our flora.” A strikingly beautiful final find of the day indeed, and a perfect note on which to gather for lunch at historic Russell House in nearby Hillsboro.
For me, no botany outing is strictly about plants (just as no entomology outing is strictly about insects), so there were a few interesting insect observations on the day. On our way to look for Spiranthes ovalis (lesser ladies’ tresses), June noticed a caterpillar on the Ulmus rubra (slippery elm) that we decided must represent Halysidotus tessellaris banded tussock moth).
Later, after lunch with the group, I returned with the goal of more closely inspecting Physocarpus intermedius (Midwest ninebark) along the glade toeslopes and intermittent creek to see if Dicerca pugionata was out. It has been many years since I’ve seen this species in the fall (but it has also been many years since I’ve really tried to look for it during the fall). I started first with the plants along the moist toeslopes along the west side of the glade, checking several of the now very scraggly-looking plants without success. Along the way, I encountered an especially beautiful Spiranthes magnicamporum, so I paused to take photos. While doing so, I noticed a cryptically-colored crab spider on its blossoms—Mecaphesa asperata (northern crab spider)—the first time I’ve ever seen a spider hunting on the flowers of an orchid.
Mecaphesa asperata (northern crab spider—family Thomisidae) on flowers of Spiranthes magnicamporum (Great Plains ladies’ tresses).
Towards the end of the toeslopes, finally, two D. pugionata plopped onto my sheet. The plant they were on was near the far end of the toeslopes, and if I hadn’t seen any beetles by the time I reached the far end I would have given up the search. Finding them, however, motivated me to hike over to and continue looking along the intermittent creek, where I saw three more beetles in three different spots, the last one—satisfyingly—on the very last plant I checked before the creek disappears into denser woodland.
Dicerca pugionata (ninebark borer—family Buprestidae) beaten from living Physocarpus intermedius (Midwest ninebark).
Mission accomplished, I enjoyed one more leisurely stroll across the glade before calling it another (successful) day in the field.
This—the 18th “Collecting Trip iReport”—covers the second of two insect collecting trips to the southwestern U.S. this season—this first one occurring from June 4–13, during which I placed “bottle traps” and “jug traps” at several locations, and this one from September 3–14 to retrieve the traps and take advantage of any late-season collecting opportunities. I was fortunate on this trip to have longtime collecting buddy and melittologist Mike Arduser joining me, during which we visited the same 15 localities that I visited on my precious trip back in June (one in northwestern Oklahoma, six in northern Arizona, six in southern Utah, and two in southern Nevada) plus two additional localities (one each in northwestern Oklahoma and northeastern New Mexico).
I’m on my way out west with fellow collector Mike—today being only a travel day but with a quick stop in Texas Co., Oklahoma to retrieve bottle traps set back in June and then a night of camping at Black Mesa State Park before continuing the drive west tomorrow. After 7 hours, we needed to stretch our legs and stopped at Salt Plain National Wildlife Refuge’s Sandpiper Trail—a spot we both have visited several times and know well. Recent rains had the alkaline flats filled with more water than I’ve seen during any previous visit, …
Salt Plain National Wildlife Refuge, Alfalfa Co., Oklahoma.
… and only a few Ellipsoptera nevadica knausi (Knaus’ tiger beetle) and Eunota circumpicta johnsoni (Johnson’s tiger beetle) were seen on the drier margins of the alkaline flats. Several Epicauta conferta (red-cornered blister beetle) were seen lumbering across the path, and a Diogmites angustipennis (prairie robber fly) posed nicely on the trail for pictures as well.
Showy Eustoma russellianum (prairie gentian)—a plant I’ve never seen before—were blooming spectacularly and prolifically in the vegetated areas bordering the alkaline flats.
It was a quick but interesting stop that rejuvenated the legs before we continued our journey westward.
The first “real” stop of the trip was ~5 miles north of Goodwell in Texas Co., Oklahoma where I placed three white bottle traps in early June hoping to capture the very rare Acmaeodera robigo, which had been photographed here on flowers of Melampodium leucanthemum (blackfoot daisy) and the photos posted on BugGuide. I was never able to contact the photographer, but since bottle traps are so effective at sampling species of Acmaeodera I reasoned placing three traps here (one at the precise spot and two more several hundred yards to the north and to the south) would give me the best chance of collecting it. It had already been dark for an hour before we reached the spot, but despite the darkness and late hour I had no trouble finding each of three traps. I was happy to see all three traps still in place, undisturbed, and filled to the brim with insects. I tried to pick out the larger insects (mostly crickets and grasshoppers) and stir through the remaining contents of each trap a bit to see if I could detect any Acmaeodera, but the majority of insects appeared to be small blister beetles, followed by bees. The darkness made further sorting impossible, so I bagged the contents of each trap and saved for later sorting. [Edit: later sorting found only a couple of Acmaeodera mixta? in just one of the traps and no A. robigo.]
We arrived at our first overnight spot—Black Mesa State Park—quite late (~11:30 pm) and quickly setup camp before retiring for the evening. In the middle of the night I got up, came out of the tent, and was greeted by an incredible amazing starscape that is normally only seen during winter. Taurus was already high in the sky, and Orion was well above the horizon with a brightly shining Jupiter not too far to its left.
Night sky at Black Mesa State Park. Orion has risen, with Taurus above and Jupiter just rising in the lower left.
Day 2
In the morning, a canyon towhee (Melozone fusca) kept us company as we prepared breakfast and then broke camp for another mostly travel day
Canyon towhee (Melozone fusca).
Our destination this evening is Devils Canyon Campground near Monticello, Utah, to which we will travel by way of northeastern New Mexico and then southwestern Colorado.
Abandoned homestead outside of Clayton, New Mexico.
Shortly after crossing into Colorado we made a pit stop for ice and I began searching the pavement around the gas station looking for beetles that may have come into the previous night’s lights. I didn’t find any cerambycids but I did find a small tenebrionid beetle that didn’t look like familiar to me.
Crossing the Sangre de Cristo and then the San Juan ranges were as spectacular a mountain crossings as any that Colorado has to offer, and a coffee stop in Pagosa Springs (at Faire Society Cafe and Patisserie) provided not only good coffee and pastries to fuel me for the rest of the drive to Devils Canyon Campground near Monticello, Utah, but interesting and creatively framed art work to treat the eyes while waiting for our orders.
“Art wall” in Faire Society Cafe and Patisserie, Pagosa Springs, Colorado.
“Butterflies”—Faire Society Cafe and Patisserie, Pagosa Springs, Colorado.
“Gentleman Frog”—Faire Society Cafe and Patisserie, Pagosa Springs, Colorado.
“Cow”—Faire Society Cafe and Patisserie, Pagosa Springs, Colorado.
Weather during the drive had been good all day, but on the final approach to Devils Canyon Campground the skies began looking worryingly threatening. The last time I came here (early June) I had intended to camp here but got rained out and took a motel in town. I did not want a repeat of that, so we kept our fingers crossed and made the final drive to the campground. Although still threatening, it was not actually raining when we arrived (unlike last time), so we took our chances and set up camp. No sooner than that did the rain start! Fortunately, the tent was already up, so it just meant that instead of cooking dinner at the site, we would instead go to town and have dinner (Dave’s BBQ). When we got back to camp, the rain had stopped (although we could tell that it had rained hard), so I decided to walk the roads looking for night-active beetles. I knew this was probably a fruitless exercise—by then the post-rain temps at this 7000’ site were already down to the mid-50s, but it would give me a chance to stretch my legs after two straight days of driving, and I could also take that opportunity to retrieve the bottle and jug traps that I had set back in June. The bottle trap was disappointing, especially after seeing the ones I’d set near Goodwell, Oklahoma filled to the brim with insects—just a handful of bees (for Mike) and no beetles of any kind. This was surprising given the many Acmaeodera I have collected in alpine habitats just like this (Ponderosa pine and Gambel oak). The SRW-baited jug trap, on the other hand, was nicely (if not overwhelmingly) productive (Tragosoma sp., Enaphalodes sp., small elaphidiines, small acanthocine with very long antennae, Xestoleptura?)—enough to make it worth the effort. I was also pleased to see that the jug trap was in still place and intact with the catch in good shape despite three months in the field. The bait bottle was still about half full of red wine, but since the propylene glycol had dried the trap was no longer trapping insects. As I’d expected, no night-active insects were seen in the way to the traps or on the way back.
Day 3
It was a chilly morning, and though it had not rained since our arrival last night the skies remained overcast. The day’s plan was to continue west to the Ponderosa Grove Campground in southwestern Utah (north of Kanab), but with only five hours of driving required to get there we would have time to make a few stops along the way. Before leaving I started checking the Ericameria nauseosa (rubber rabbitbrush), several of which had begun blooming in the campground, and found a few Crossidius coralinus and Acmaeodera amabilis on the flowers. I was tempted to suggest staying put—at least for a short time—and exploring the area a little more fully, but my real objectives were further west and I elected to stick with the plan.
Crossidius coralinus (family Cerambycidae) on flowers of Ericameria nauseosa (rubber rabbitbrush).
Acmaeodera amabilis (family Buprestidae) on flowers of Ericameria nauseosa (rubber rabbitbrush).
One of the stops I’d made along this way last June was 4 miles east of Bluff in San Juan Co., Utah, where the famous Mont Cazier had collected what would later be described as Agrilus utahensis. I did not find it in June (nor did I fully expect to, since the record was from late July), and I was equally skeptical about my chances this time given how much later it was in the season. On the way here, we got caught behind an oversized load on the highway that was so big it required three highway patrol chaperone vehicles to clear the road ahead. Going at about half the speed limit, I worried we might have to follow it the entire way to our turnoff, which would nearly double our travel time to the first spot. Fortunately, the caravan pulled over at one point to let the long train of trsffic that had accumulated behind it pass, and we were on our way (the convoy would later pass us at the very spot where we had stopped to collect).
Oversized convoy!
The location was disappointing dry and crispy, although Gutierrezia sarothroides (broom snakeweed) was coming into bloom. Sweeping it eventually produced about a dozen Crossidius pulchellus and two other beetles (a clytrine leaf beetle and a weevil), and Mike collected a handsome series and diversity of bees off of flowering Eriogonum sp. (buckwheat).
Crossidius pulchellus (family Cerambycidae) on flowers of Gutierrezia sarothrae (broom snakeweed).
Our drive afterwards through southeastern Utah and northeastern Arizona took us through some of the most amazing scenery that the American West has to offer—red sand/siltstones sculpted through the eons by wind and rain have created a landscape that can only be described as “planetary.”
Monument Valley, southeastern Utah.
Eventually, the dramatic landscape gave way to a more monotonous series of desert plateaus periodically interrupted by dramatic descents and canyons as we got deeper into north-central Arizona. Though pleasing to the eye, there were few signs of greenery of flowers to tempt the passing entomologist except occasional stands of Ericameria nauseosa (rubber rabbitbrush) beginning to bloom in higher elevation spots. We kept our nose to the grindstone, hoping to see better things once we passed through Page and crossed back into south-central Utah, but the landscape became even crispier, with a stop about 20 miles northwest of Page to look for Nanularia brunnea on Eriogonum inflatum (which I had found two years ago in late June) being a total bust. We expected/hoped that the higher elevations around Ponderosa Grove Campground (~6000’) would provide better collecting and continued there without haste. Our expectations/hopes proved well-founded, as blooming rabbitbrush was seen with greater frequency as we traveled north of Kanab and even more so along Hancock Rd approaching the campground. We took a few moments to scout out a good campsite and setup camp before spending the rest of the available daylight hours exploring. For me the rabbitbrush was most tempting, and scouting plants in the campground and the vicinity east produced small but nice series of Crossidius coralinus and Typocerus balteatus. As I was doing so, a sinking sun and virga to the east produced an impressive rainbow that became irresistible for photography—not only as a subject itself but as a backdrop for the beetles I was finding.
Rainbow at Ponderosa Grove Campground.
Crossidius coralinus (family Cerambycidae) on flowers of Ericameria nauseosa (rubber rabbitbrush).
Typocerus balteatus (family Cerambycidae) on flowers of Ericameria nauseosa (rubber rabbitbrush).
After some downtime back at camp (and grilled sirloin steaks for dinner), I did my customary nighttime patrol to check for night-active insects. This campground was especially productive when I did this back in June and found several Zopherus utahensis and other tenebrionids on the trunks of the massive Ponderosa pines that are the namesake of this campground.
A near-full moon rises over our campsite at Ponderosa Grove Campground.
This time was no different—while I found only a single Z. utahensis, I did also find a few specimens of Coelocnemis sulcata, including a mating pair, on the trunks of the trees …
Coelocnemis sulcata (family Tenebrionidae) mating pair on trunk of Pinus ponderosa (Ponderosa pine) at night.
… and a single Embaphion sp. on the ground at the base of another. There are several massively-trunked Juniperus osteosperma (Utah juniper) in the campground as well, on which another C. sulcata was found. Despite this success and the relatively early hour, I was exhausted and called it quits for the night and retire. We will spend the entirety of the day here tomorrow, so I’ll have another chance to check the tree trunks again tomorrow night.
Day 4
After a relaxing morning at the campsite (during which time I caught up on my field notes while enjoying double-pour-through coffee), I walked over to the sand dune-adjacent woodlands to retrieve the traps that I’d set there back in June and brought them back to the campsite for sorting. I was happy to see Ericameria nauseosa (rubber rabbitbrush) and many other plants in bloom and looked forward to checking them more closely after servicing the trap catches.
Ericameria nauseosa (rubber rabbitbrush) blooming in sand dune habitat at Moquith Mountain Wilderness Study Area.
The yellow bottle trap had ~15-20 beetles, including several Acmaeodera spp., a lepturine cerambycid, and a tiny Dichelonyx-like scarab (a relief after getting skunked with the bottle trap I’d set in Devils Canyon). There were also a fair number of bees in the trap, which I gave to Mike. The SRW-baited jug trap also did well, containing Tragosoma sp., Enaphalodes sp., several Psyrassa sp., and another colorful little lepturine along with several Euphoria inda, several small clerids, a mantispid, and numerous small beetles I take to be oedemerids. After processing the trap catch, I went back over to the woodlands and dunes, spending more than three hours collecting off the flowers of E. nauseosa and other flowers.
Typocerus balteatus was found not uncommonly on the flowers in most of the areas that I covered, while Crossidius coralinus and C. suturalis were found a bit more sparingly.
Crossidius coralinus (family Cerambycidae) on flowers of Ericameria nauseosa (rubber rabbitbrush).
Crossidius suturalis (family Cerambycidae) on flowers of Ericameria nauseosa (rubber rabbitbrush).
I also found Acmaeodera rubronotata on the flowers of Grindelia squarrosa (curlycup gumweed), Dieteria canescens (hoary tansyaster), and E. nauseosa, but they were limited to the woodlands and not seen in the dunes.
Acmaeodera rubronotata (family Buprestidae) on flowers of Dieteria canescens (hoary tansyaster).
I also found several individuals of an interesting little weevil on the rabbitbrush flowers, its gray/black longitudinally striped body making a good subject for photography (for which I also brought back a live A. rubronotata and a mating pair of ambush bugs), and spent a bit of time photographing some of the other blooming plants in the area.
By the time I feel like I’d gotten a good enough look at the area, nearly four hours had gone by and I was famished. Sardines and Triscuits did the trick, after which we did a quick ice run into town and back—the highlights being an authentic Sinclair dinosaur (he’s smiling!) and an real (though non-functioning) pay phone.
The famous “Sinclair dinosaur.”
He’s smiling!
An authentic (though non-functional) pay phone.
Returning to the campground, I walked with Mike back into the dunes to retrieve his bowl traps. I had hoped that some of them would pick up Acmaeodera (as is often the case with bowl traps and why I have started utilizing them on my own collecting trips), but the only species that would be out in this area at this time of season would be A. rubronotata, which I had already collected earlier in the day (there were none).
Mike services a “bowl trap.”
After a period relaxing (with a cold beer and burgers hot off the grill), I began my customary night walk. I have yet to find a cerambycid on tree trunks at night here, but still I enjoy night walks here as much as anywhere due to the consistent presence of ironclad beetles and other tenebrionoids on the trunks of the massive Ponderosa pine trees that give the campground its name.
Another near-full moon rises over the campsite.
Tonight would be no different—I found Zopherus uteanus on just the second tree that I examined (right in our campsite), and I would also find two species of tenebrionids in the vicinity on the trunks of ponderosas (Coelocnemis sulcata and Eleodes obscura sulcipennis) and a third species (ID unknown) on the ground at the base of one of them.
Zopherus uteanus (family Zopheridae) on trunk of Pinus ponderosa (Ponderosa pine) at night.
Coelocnemus sulcata (family Tenebrionidae) on trunk of Pinus ponderosa (Ponderosa pine) at night.
Eleodes obscura sulcipennis (family Tenebrionidae) on trunk of Pinus ponderosa (Ponderosa pine) at night.
At that point, I decided to go outside of the loop towards a couple of large P. ponderosa at the entrance, and on the way I found another E. obscura sulcipennis on the trunk of a massively old Juniperus osteosperma (Utah juniper). There was nothing on the P. ponderosa trees that I had targeted, but nearby was another large one, and high up on the trunk (as far as my fully extended net could reach) was another Z. uteanus, and several C. sulcata—including a mating pair—were found on the ground at its base.
At that point I decided to limit my tenebrionoid collecting to only Zopherus unless I saw species that I hadn’t seen before, so I passed by some additional tenebrionids of the same species as the previous on a large P. ponderosa in the RV loop, then saw a large, multi-branched Pinus edulis (Colorado pinyon pine) that I thought might be interesting to check. I did not find any beetles on it, but I did locate at eye level—with considerable difficulty!—a male Oecanthus californicus (western tree cricket). I was not only able to take a photograph of it with its wings fanned but also record an audio track up close (posted on iNaturalist).
Oecanthus californicus (western tree cricket—family Oecanthidae) male singing on trunk of Pinus edulis (Colorado pinyon pine) at night (song).
Returning to the tent loop, I checked all of the large P. ponderosa trees and junipers that had—during the past visit and last night—been so productive, but the only beetles I found was a very small tenebrionid that, fortunately, was yet another species I had not previously seen here (ID unknown). After two hours of searching tree trunks, I called an end to the night, which also meant a close to the collecting at this spot—tomorrow we will drive to Kyle Canyon in southern Nevada!
Day 5
Our exit from Ponderosa Grove took us through more of the spectacular canyonland that southern Utah is famous for and past the incredible Coral Pink Sand Dunes State Park (so spectacular it is that I think it could—despite its small size—be a national park). A dramatic descent down into the Virgin River valley and the town of Hurricane was only the first such descent—the second one being even more dramatic as I-15 dropped off the edge of the Colorado Plateau along the Virgin River Gorge. The remainder of the drive to Kyle Canyon northwest of Las Vegas was mindnumbing in its contrast—an endless stretch of interstate highway through a vast expanse of low, hot, featureless desert punctuated at regular intervals by palm tree dotted oases, each with a gaudy, glittering casino at its center. Driving up Kyle Canyon Rd put an end to this, however, as each thousand foot gain in elevation brought with it an increasingly interesting landscape. At about 4500’ elevation, I had set a couple of bottle traps—one yellow, one blue—hoping to catch the recently described Acmaeodera raschkoi (whose namesake—Mike Raschko—I had happened to meet at Ponderosa Grove Campground last June a few days before I set the traps!). Mike R. had also placed a bottle trap (white) at the site and was kind enough to reset it for me so I would have three colors sampling the area. Both of my traps were still in place, intact, and filled with numerous Acmaeodera that I take to be A. quadrivittata (along with many bees for Mike A.) and the yellow also containing a larger species that I didn’t immediately recognize (not unusual since I have never collected this area). Unfortunately, I did not see any specimens that appeared to be A. raschkoi, and even more unfortunately the white bottle trap had been pulled from the ground (although I was able to recover a few A. quadrivittata that were still inside the trap). Not much else was going on at the site—only a few things in sparse bloom but no beetles visiting the flowers, nor was there any rabbitbrush around on which to look for Crossidius.
We got a scare when we arrived at the campground and saw a sign at the entrance saying “Campground Full.” This was bad—if this campground was full, then surely the much more heavily used one down below was also full, and I didn’t look forward to spending the rest of the afternoon scrambling for a campsite somewhere in the Spring Mountains. We drove through the campground anyway, and, in fact, there were many campsites available! Looks like somebody forgot to do their job!
“Campground Full” sign at a not-full Hilltop Campground above Kyle Canyon, Nevada.
Crisis averted, we selected a nice spot overlooking the desert below and set up camp. Cool evening temps come early at this high elevation (~8300’), so with the remaining afternoon hours I retrieved and sorted my SRW-baited jug trap, finding several Tragosoma sp. but, curiously, not a single other longhorned beetle (or any beetle for that matter). Searching around the area afterwards, I extracted a dead Dicerca tenebrosa partial carcass in its emergence hole in a stump of Pinus monophylla (single-leaf pinyon pine), then went back down to the area I had collected last time, focusing especially on the two large half-dead Juniperus osteosperma (Utah juniper) trees on which I had seen damage from the rarely collected Semanotus juniperi (on one of which I collected three adults later that night). There was nothing on the first (the one on which I found the beetles), but at the second one I saw a large wind-thrown branch that I had not noticed last time. It exhibited S. juniperi damage and emergence holes on the lower part, and chopping into it I quickly recovered a dead but intact carcass of yet another S. juniperi adult. Further chopping turned up nothing, and I was about to walk away when I thought maybe I should cut into the upper part of the branch as well to look for evidence smaller woodboring species. Doing so, I quickly encountered a Chrysobothris sp. larva, and with that I decided to bring the entire upper part of the branch back for rearing. There wasn’t much else going on—few plants were in flower and nothing was seen on the trunks of trees or various pieces of downed wood that were laying about, so I went back to camp.
Alpine pinyon/juniper woodland at Hilltop Campground above Kyle Canyon, Nevada.
An elevation of 8300’ affords spectacular views into the desert below.
Later in the evening, we watched a spectacular moonrise, then enjoyed “surf ‘n’ turf” (grilled sirloin steak and salmon) before I started up my customary night walk to check tree trunks for night-active beetles.
Angel Peak Radar Station at sunset.
“Corn Moon” rising.
Peeking through the trees.
Last time here when I did this, I found not only S. juniperi but also a few Zopherus uteanus, so I was hopeful for my chance tonight despite the lateness of the season. It started out well—on the first P. monophylla tree that I checked (right at our campsite), I found Oeme costata and a weevil.
Oeme costata (family Cerambycidae) on trunk of P. monophylla (single-leaf pinyon pine) at night.
Those would be the last live beetles I would see (other than an occasional tenebrionid beetle, none of which I collected). However, I would still find success—back at the J. osteosperma on which I had found three S. juniperi back in June, I found three more. They were not alive, however, but dead carcasses at the base of the tree—two nearly completely intact and the other partially so.
Western deer mouse (Peromyscus sonoriensis) at night.
Day 6
We had planned to visit few localities at middle and lower elevations but stopped to check out the profusely-blooming Ericameria nauseosa (rubber rabbitbrush) right outside the campground entrance for bees and beetles. Curiously, hardly anything was seen on the flowers despite the by then late-morning hour, sunny skies, and temps above 70°F. It seemed odd to me that there were no Crossidius beetles on the blooms, and the thought occurred to me that maybe the occurrence of E. nauseosa in the area itself could be a relatively recent phenomenon since it is only seen—albeit profusely—along the roads and highways in the area but nowhere further within the native habitats. With nothing going on, we pushed down to the lowest elevation point that caught our eye on the way in yesterday—the Step Ladder Trailhead at ~6700’.
Again, E. nauseosa was blooming profusely around the parking lot, but a quick perusal made it clear the situation would be similar here as well. Mike, on the other hand, was having good success collecting bees off of E. nauseosa and especially Gutierrezia sarothrae (broom snakeweed), so I was content to stay and refocus by searching for infested wood. I noticed a lot of Quercus gambelii (Gambel oak) and quickly found one with a dead but still attached, fully-barked branch. I broke the branch off the tree, and there in the broken butt of the branch was a large chrysobothroid larvae! This quickly prompted a decision to collect the infested branch and put it up for rearing. A second larvae was found in a small dead (but still fully-barked) tree nearby, which was added to the bundle. While this was going on, Mike found what seemed to be Agrilus blandus? in his net while sweeping bees from the flowers of G. sarothrae. I recall collecting this species in southern California in flowers of Eriogonum (wild buckwheat), so finding it on other flowers—particularly if Eriogonum is in the area (but not seen because it was not blooming) did not seem out of the question. My much more thorough sweeping of the plants around the area where he found it, however, produced no additional specimens. I was also interrupted in my sweeping attempts by a couple of curious bystanders—one a woman from Ukraine who wondered what the plant was that I was sweeping (I told her “broom snakeweed”) and what it was good for (“brooms” I wryly replied and then quickly clarified its role in the ecosystem), and then offered me a beetle collecting tip by telling me about large beetles they call “bombers” and that bite people sitting in spas in Southern California (I presume these are diving beetles in the family Dytiscidae); and the other a young man who was pleased to hear I was from St. Louis because he used to live there when he was married to his ex-wife. This all happened while I was in the middle of my sweeps, so I held the net bag firmly to keep insects from escaping my net until I could resume my sweeping. Eventually, I gave up the ghost and resumed my search for dead, infested wood, eventually finding a Cercocarpus ledifolius (curl-leaf mountain mahogany) tree with one recently-dead and one older dead branch, the former buprestid-infested (verified by cutting into the wood and finding young buprestid larvae) and which I collected for rearing.
View of Fletcher Peak from Step Ladder Trailhead.
After lunch back at the campground and some time spent processing specimens (as well as enjoying the antics of our resident golden-mantled ground squirrel [Callospermophilus lateralis certus]), …
Mount Charleston golden-mantled ground squirrel (Callospermophilus lateralis certus).
… I wanted to check out the nearby Deer Creek Picnic Area where I’d seen a lot of iNaturalist observations (suggesting it might be an interesting place). At first all I saw was the massive parking lot below an equally massive road-cut slope—the only thing that looked like a trail was a steep drop down to the creek below. I checked it out, only to find it dead-ending at the creek and clambered back up.
A massive Ponderosa pine looms above.
Then I saw a gravel trail behind the guardrail on the opposite side of the highway and found it leading to a paved path up the creek. Much of the trail was covered with a deep layer of gravel from flooding (and indeed some of the picnic tables were also nearly completely buried). I hiked the trail as it ascended alongside the creek under massive ponderosa pines until it dead-ended at a gravel road and turned around. The only plants in flower was Ericameria nauseosa (rubber rabbitbrush), and it was only near the highway, and while I saw no insects that I wished to collect, I did see a large Adejeania vexatrix (orange bristle fly) that frustrated my attempts to photograph it until I finally “pre-set” the focus, exposure, and zoom and quickly fired off a few shots at the distance I’d set it for as soon as the fly landed. The virtual lack of insect activity here confirmed what we’ve been seeing in the area as a whole, so I’ll be anxious to leave tomorrow and head for (hopefully) greener pastures at Leeds Canyon back in southwest Utah.
Adejeania vexatrix (orange bristle fly—family Tachinidae) on flowers of Ericameria nauseosa (rubber rabbitbrush).
Day 7
The drive from Kyle Canyon to Leeds Canyon was essentially a straight shot on I-15—normally a recipe for extreme boredom; however, coming back up through the Virgin River Gorge was a different, even more awe inspiring experience than the descent two days earlier. Ascending such a steep narrow canyon has the breathtakingly tall canyon bluffs looming high overhead, dwarfing the traffic, even the largest semi tractor trailers, snaking up below, whereas descending into a seemingly bottomless chasm feels a little more “dangerous.” We arrived at Leeds Canyon relatively early thanks to the “only” 3-hours drive. The area looked very dry, but a variety of blooming plants kept us optimistic as we made our way up the canyon road towards Oak Grove Campground at the top.
Leeds Canyon in southwestern Utah.
Sadly, optimism turned to dismay in an instant when we encountered a “Road Closed” sign about halfway up—a result of the ongoing fire risk that has bplagued the area this season. We checked to see if the campground on the other side of the mountain range was available, only to learn that it was closed due to fire damage. At that point, our decision was made for us—we would need to continue another two hours to the Kaibab Plateau where I had my last sets of traps to retrieve and where we could camp at Jacob Lake. While we were here, however, we took the opportunity to stop at a spot along Leeds Creek and see what we could find.
Oak Grove Rd crosses Leeds Creek in the lower part of Leeds Canyon.
Several different plants were in bloom, on which I’d hoped to find either Acmaeodera or longhorned beetles, the first that I looked at being Dieteria canescens (hoary tansyaster), but I only saw small dasytines (a few of which I collected). Nothing was seen on Solidago velutinus (velvety goldenrod) or Sphaeralcea grossulariifolia (gooseberry leaf globemallow) flowers, but then Mike came up with a Crossidius discoideus on flowers of Gutierrezia sarothrae (broom snakeweed).
Crossidius discoideus (family Cerambycidae) on flowers of Gutierrezia sarothrae (broom snakeweed).
Careful searching of the plants in the surrounding area atop a small hill turned up an additional half-dozen individuals, but none were seen on any of the plants further up or down along the road. By this time, we’d spent about an hour and decided to finish the additional 2-hours drive needed to get to Jacob Lake.
Megaphorus sp. (family Asilidae).
Historic home in nearby Harrisburg, Utah.
Some of the western U.S.’s worst fires this season occurred on Arizona’s Kaibab Plateau. The Dragon Bravo Fire destroyed over 100 structures on the Grand Canyon’s North Rim—including the historic Grand Canyon Lodge and the North Rim Visitor Center, while the White Sage Fire simultaneously burned significant areas of Kaibab National Forest north and east of Jacob Lake. It was the latter that, unfortunately, swept across both of the sites where I had placed traps a month earlier in June, so I was not optimistic about the likelihood that they had survived. Fortunately, the fires did not reach the immediate vicinity of Jacob Lake, so the campground was unaffected and—unusual in my experience—nearly devoid of people. After setting up camp, I went back north into the burn zone to see if my traps 1) had survived and 2) could be retrieved. The area around the site was almost completely destroyed, with charred black skeletons of trees dotting blackened soils devoid of any vegetation.
Aftermath of the White Sage Fire in the Kaibab National Forest.
I had low expectations for the traps at this site even before the fires, as the area had already burned several years early and was in the early stages of recovery (I had decided to place traps here anyway because I wanted to see what the woodboring beetle fauna in a recovering area might look like).
Blackened trunks punctuate a stark landscape.
I continued walking the 2-track toward the trap location surveying the damage, came around a bend, and saw it—a lone, still-green pinyon pine with my jug trap hanging from a branch and a bottle trap, its yellow funnel only slightly heat deformed, still planted in the soil beneath the tree!
A lone green tree amongst the destruction—with my traps in the tree and below it both intact!
At first I was elated, but then I saw the jug trap reservoir was dry and almost completely empty save for a few dried beetle carcasses—the trap had survived the fires, but the associated winds had blown the trap and dumped the contents (none of which could be detected on the ground beneath). The bottle trap, on the other had, looked to be full of insects with plenty of liquid still in the reservoir, so I was hopeful that I would retrieve some good specimens from it. This proved to be the case (sort of!) as I pulled a few Anthaxia sp., a meloid, and lots of bees (for Mike) from the trap. The dried carcasses in the SRW-baited jug trap turned out to be an elaphidiine & several silphids.
After leaving the first trap site and driving towards the second (a few miles east of Jacob Lake), I saw little to no fire impacts as I continued east of Jacob Lake. However, as I got closer to the site I began to see impacts—first along the ridge above, then down the slope and engulfing the area where I had placed my traps. Fortunately, the fire did not seem to have been as severe in the immediate area, so I remained hopeful.
Intact jug trap in burned woodland east of Jacob Lake, Arizona.
The bottle trap was found first and was in much the same condition as the bottle trap at the previous location—it’s blue funnel slightly heat-deformed, but the reservoir was filled with liquid and insects. Later sorting yielded an Acmaeodera diffusa?, a Melanophila sp., a couple of Anthaxia sp., a clerid, and lots of bees (for Mike). The Melanophila sp. was especially welcome—known collectively as “fire beetles” for their attraction to active fires, its presence in the trap may have been been a direct result of the fire. The SRW-baited jug trap was quickly found next, and much to my relief the trap was not only intact and undamaged but also filled with insects (in fact, the propylene glycol had not even completely dried). Later sorting would yield only a single longhorned beetle (plus a silphid and a Euphoria inda), but that longhorned beetle would prove to be the catch of the trip—Calloides nobilis mormonus! I have reared a single individual of the nominate subspecies from fire-damaged oak collected in Missouri, so I suspect the presence of this beetle is also a direct result of the fires that swept through the area—a satisfying irony.
Calloides nobilis mormonus (family Cerambycidae) attracted to sweet red wine-baited jug trap.
Back at camp and after another “surf & turf” dinner of sirloin steak and salmon, I did my customary nighttime walk to look for night-active beetles on the ground and in tree trunks. I had good luck with this here back in June, finding a Zopherus uteanus and several other beetles, but tonight’s catch consisted of just a single Temnochila sp. (family Trogosittidae) and a single weevil (superfamily Curculionoidea) crawling on the large trunks of Pinus ponderosa.
Unidentified weevil (superfamily Curculionoidea) on trunk of Pinus ponderosa (Ponderosa pine) at night.
Day 8
I’d seen a fair amount of Ericameria nauseosa (rubber rabbitbrush) in bloom at the second site the previous day when I retrieved my traps but didn’t see any insects (or, at least, beetles or bees) on them. I figured this was due to the early evening hour, so we decided to come back during the day to try again. The E. nauseosa flowers were still, puzzlingly, devoid of insects (save for honey bees and enormous numbers of a large, black, bristly tachinine fly—possibly Archytas metallicus or Juriniopsis adusta).
Tachinine fly (possibly Archytas metallicus or Juriniopsis adusta—family Tachindae) on flowers of Ericameria nauseosa (rubber rabbitbrush).
Like at Kyle Canyon, the absence of Crossidius spp. on E. nauseosa flowers was surprising, as I have seen them on this plant at almost every other location I have ever checked. You can’t make things appear no matter how hard you look, however, so we continued into some openings farther up the slop and encountered a few other plants in bloom. One was Dieteria canescens (hoary tansyaster), on the flowers of which I found a few small beetles of an unknown family. Nearby I saw several dead main branches in a clump of Quercus gambelli (Gambel oak)—cutting into them revealed a very small woodboring beetle larvae, so I collected several of the stems for rearing. Coming back down the slope I found a single cryptocephaline on the flower of Eriogonum racemosa (redroot buckwheat) and a single Acmaeidera rubronotata on flowers of Gutierrezia sarothrae (broom snakeweed)—the latter on which Mike had also found a single Crossidius discoideus. (This seems to be the first record of any species of Crossidius from the Kaibab Plateau! Maybe the other species are here as well but are not quite out yet at this relatively early date in fall.)
Crossidius discoideus (family Cerambycidae) collected on flowers of Gutierrezia sarothrae (broom snakeweed).
We were getting ready to leave when I spotted a large, fallen Pinus ponderosa (Ponderosa pine) with the twigs brown but still attached (indicating it might be the right “amount” of dead to host woodboring beetles. Damage by such could be seen on the smaller branches, and cutting into them confirmed the presence of larvae and led to a second wood-cutting/bundling session to bring the beetle-infested twigs and branches back for rearing.
Chasing more floriferous pastures, we went back up to higher elevations and stopped at a spot close to the campground where we 1) saw a great diversity of plants in bloom and 2) could safely pull off the highway. A huge diversity of blooming plants were seen (from which Mike collected ~20 species of bees), but the only beetles of interest that I saw and collected were numerous small black/red cryptocephalines on the flowers of Eriogonum racemosum (redroot buckwheat). After Mike was satisfied he’d sufficiently sampled the diversity of bees at the site, we looked for another place to collect.
We drove south towards DeMotte Campground on Hwy 67, but much of the landscape was complete devastation due to the fires and no access was allowed beyond Kaibab Lodge. It was depressing to see the immense scale of destruction and loss of natural resources, but as one forest worker that Mike talked to put it, “It’s just trees, and he didn’t have to call anybody’s family [i.e., there was no loss of life].” We then drove back down past my second trap location where we had collected earlier in the day to see if we could find better stands of Gutierrezia sarothrae (broom snakeweed) on which to look for more Crossidius discoideus (still represented in the area by the single individual Mike had collected earlier). We drove through even more complete and utter destruction but eventually found undamaged areas at about 6600’ elevation. Not only was there G. sarothrae in bloom, but also Chrysothamnus visicidiorus (green rabbitbrush) and Ericameria nauseosa (rubber rabbitbrush)—all three species serving as hosts for various Crossidius and providing a perfect scenario for comparing and contrasting the sometimes-tricky-to-identify plants! The promise of Crossidius, however, would not be realized, and after an hour of searching—finding only a lone weevil on the flowers of E. nauseosa—did I finally admit defeat and concede that Crossidius from this after would have to come some other time.
Inflorescences of Gutierrezia sarothrae (left), Chrysothamnus viscidiflorus (middle), and Ericameria nauseosa (right). Note the distinct ray florets of G. sarothrae and blue-green leaves of E. nauseosa.
I hadn’t planned to do my customary nighttime walk this evening—my motivation waning after the less than meager success of the previous night, continuing relative absence of beetle life I’d seen during the day, and temps now dropping towards the 50s. A cute but shy Uinta chipmunk in our campsite captured my photographic interest as we relaxed, and the setting sun turned the clouds a stunning pink!
An Uinta chipmunk (Neotamias umbrinus) climbs a Ponderosa pine to stay as far from my camera as possible!
However, as night fell the siren song of the nighttime walk began singing its tune and I was unable to resist.
The setting sun turns the clouds an exceptional pink.
It turned out to be a more successful night than I’d expected—I found a small species of tenebrionid [Edit 10/1/25: Eleodes pimelioides] on the rocks surrounding the campsite, and there turned out to be dozens of the little buggers crawling though the pine duff in the campground.
Eleodes pimelioides (family Tenebrionidae) in alpine coniferous forest at night.
Nothing else was seen, however, and since tomorrow would be a long travel day I called it an early night.
Day 9
On a mostly travel day, we tried to take a big bite out of the many miles that still separate us from St. Louis, where we planned to be in three days time. We got another look at the devastation east of Jacob Lake before reaching the dramatic drop off the Kaibab Plateau and down into the Vermilion Cliffs National Monument—their massive red bluffs accompanying us all the way to Mojave Canyon. Just south of there as the highway climbed up and out of the valley, we made a quick stop to remove excess clothing (having gone from high elevation to low), and alongside the road I spotted a Crossidius pulchellus on the flowers of Gutierrezia sarothrae (broom snakeweed). This is the furthest southwest I have collected this species, and I was tempted to continue looking to see if I could find the other G. sarothrae associate—C. discoideus—as well. We still had a long drive ahead of us, however (destination Mills Rim Campground in northeastern New Mexico), so I resisted temptation and we continued the drive.
The Vermilion Cliffs, stunning as they were, still weren’t the highlight of the drive. That honor would come from the moonscape formations along Hwy 89 as it followed the Echo Cliffs and then turned east onto Hwy 160 towards Tuba City. We then passed through a series of stunning plateaus and drops on Hwy 264 as it passed through the Navajo and Hopi Reservations. One abandoned house as we dropped down off the Ganado Mesa was especially picture-worthy.
Abandoned home on the Ganado Plateau near Kykotsmovi Village, Arizona.
Eventually we crossed the state line at Picture Rocks into New Mexico, and, suddenly, the landscape seemed more “tame” and less hostile. I don’t normally like interstates, and the stretch of I-40 to Albuquerque did nothing to change my opinion of them, but I must admit that I-25 north towards Santa Fe was among the most picturesque I have ever seen. Eventually, we left the mountains and found ourselves once again on the western edge of the Great Plains—its vast featureless expanse a true contrast to the landscape we had witnessed throughout most of the day. This apparent homogeneity, however, is misleading—tucked away in places unknown to most are some remarkable natural areas, and Mills Rim is one such place. We arrived after dark, so the explorations of its hidden charms would have to wait until the next day, but after getting camp set up I did a short nighttime walk to see what was out and about.
Night sky at Mills Rim Campground, Harding Co., northeastern New Mexico.
Only one beetle, Stenomorpha sp. (family Tenebrionidae) ambling across the ground, was seen.
Many plants in bloom were also seen however, so I went to bed optimistic about my prospects for finding beetles the next day.
Day 10
Mosquitoes were bad during the previous night, and they were bad again the following morning, prompting liberal use of repellent to a much greater degree than I am used to. At the same time, the presence of mosquitoes indicates abundant moisture in an area, and it was with that optimism that I set about searching for jewel beetles, longhorned beetles, tiger beetles, and whatever other insects could catch my eye in this hidden jewel of a place. Surrounded by treeless grasslands (and preserved as the Kiowa National Grasslands), Mills Rim Campground sits at the edge of Mills Canyon—a chasm in the landscape at the edge of a plateau bordering the foothills of the Rocky Mountains. Firmly embedded in the Great Plains, the juniper/pine/oak woodland at the edge of and down in the canyon features plants and animals at their easternmost extent—residents of the Rocky Mountains that have found an isolated home in the middle of the grasslands. Pinus edulis (Colorado pinyon pine), Pinus ponderosa (Ponderosa pine), Juniperus monosperma (one-seed juniper), Juniperus scopulorum (Rocky Mountain juniper), Quercus grisea (gray oak), and Quercus × undulata (wavy leaf oak) all make their homes here, hosting innumerable insect species that are normally more at home in the Rocky Mountains.
View into Mills Canyon from Mills Rim Campground.
I’ve collected here several times and recorded many different western species of beetles, but the height of the season seems to be in June and July. Mid-September, in contrast, seems to be near the tail end of the season, the numbers and diversity of beetles and other insects dropping from their highs earlier in the season. The flowers of Gutierrezia sarothrae, however, were hosting lots of insects. In addition to Crossidius pulchellus, Chauliognathus basalis, Bothrotes canalicularis, and Collops sp., Mike found numerous bee species, mostly females, collecting pollen from the flowers.
Crossidius pulchellus (family Cerambycidae) on flowers of Gutierrezia sarothrae (broom snakeweed).
Chauliognathus basalis (family Cantharidae) on flowers of Gutierrezia sarothrae (broom snakeweed).
Bothrotes canalicularis (family Tenebrionidae) on flowers of Gutierrezia sarothrae (broom snakeweed).
A couple of species of robber flies—Ospricerus sp. and Efferia sp.—were also taken in flight, presumably patrolling the flowers of G. sarothrae for bee prey.
Ospricerus sp. (family Asilidae) patrolling flowers of Gutierrezia sarothrae (broom snakeweed) for bee prey.
Nysius sp. (false chinch bugs—family Lygaeidae) on flower of Erigeron divergens (spreading fleabane).
Mirabilis linearis (narrowleaf four o’clock—family Nyctaginaceae).
After a rest and rehydration break, I followed the road down Mills Canyon as it approaches the Canadian River to see if I could find Ericameria nauseosa—should I be able to, it would surely be at or near the easternmost limit of occurrence for the species in this part of New Mexico.
Mills Canyon above the Canadian River.
A bit further down Mills Canyon Road.
About half a mile down the road I began seeing Acmaeodera rubronotata on the flowers of G. sarothrae, and I eventually secured a series of about a half dozen specimens. This is a nice record, as I found a single specimen a couple of years ago at Black Mesa in northwestern Oklahoma—a new state record and northeastern range extension, and this record helps bridge the gap between that record and the species’ more normal range of distribution across New Mexico and Arizona. Finally, nearly a mile into the canyon, I found one large blooming E. nauseosa and a smaller pre-bloom plant, but there were no Crossidius beetles on them, nor were any additional plants were seen a hundred yards or so further down the road, so I turned around.
Ericameria nauseosa (rubber rabbitbrush—family Asteraceae) along Mills Canyon Road.
On the way back out of the canyon, I collected a Calopteron sp. (family Lycidae) on senescing Melilotus alba (white clover) and photographed a female Stagmomantis limbata (Arizona mantis—family Mantidae).
Stagmomantis limbata (Arizona mantis—family Mantidae) on flowers of Gutierrezia sarothrae (broom snakeweed).
Back at camp, a couple of scarabaeoid beetles flew to the light of the lamp while we were relaxing with refreshments in hand and waiting for the coals to be ready. This suggested that maybe conditions were favorable for setting up the ultraviolet lights to attract other insects.
A final night of relaxing at camp with refreshments in hand.
After finishing dinner, we did exactly that and saw a few interesting insects show up, but shortly after setting up the lights the wind began to kick up, the temps began to drop, and increasingly frequent gusts making further lighting impossible!
Stagmomantis limbata (Arizona mantis—family Mantidae) male attracted to ultraviolet lights.
Schistocerca nitens (gray bird grasshopper—family Acrididae) attracted to ultraviolet lights.
Ophion sp. (short-tailed ichneumon wasp—family Ichneumoidae) attracted to ultraviolet lights.
Day 11
It was a rather sleepless final night in the tent—winds whipped as we turned in for the night, and shortly afterwards we awoke to rain splattering our faces through the fly-less tent roof. We quick got up and put on the rain fly, then listened to light but steady rain for most of the rest of the night. By the time we got up it had mostly stopped, but cool conditions with low-hanging, fast-moving clouds caused us to quickly break camp and save coffee and breakfast for Mocks Coffee Shop in Clayton, New Mexico near the Oklahoma state line (let me tell you how difficult it was for me to drive two hours first thing in the morning without coffee!). We had wanted to make our final collecting stop at a a lot near Kenton in the Black Mesa area of extreme northwestern Oklahoma, but the forecast for the area showed only slightly warmer temperatures and very gusty winds. This would make collecting there pointless, so we instead traveled four more hours east to get in front of the cold front at another of our favorite collecting spots, Gloss Mountain State Park in Major Co.
Gloss Mountain State Park features gypsum-capped mesas atop Permian red siltstones.
I was hoping to see an attractive late-season jewel beetle—Acmaeodera macra, which I had collected here and at nearby Alabaster Caverns State Park in previous years during late September. Temps were good (well over 80°F) when we arrived but the hour was already late (near 4:00 p.m.), so we had limited time for collecting before insects would start bedding down for the evening (usually around 5:00 to 6:00 p.m. at this point in the season). Megatibicen dorsata (bush cicada) and Neotibicen aurífera (prairie cicada) males were still singing abundantly, filling the air with their distinctive songs (video of M. dorsata male singing here).
Megatibicen dorsata (bush cicada—family Cicadidae) male singing on my hand after being taken from the stem of Helianthus annuus (annual sunflower).
Helianthus annuus (annual sunflower) and Grindelia ciliata (wax goldenweed) were blooming prolifically, off the flowers of which Mike collected a fair diversity of bees. I’d hoped to find beetles on the flowers as well, but they were limited almost exclusively to Chauliognathus limbicollis.
Chauliognathus limbicollis (family Cantharidae) on flower of Grindelia ciliata (wax goldenweed).
I did collect a male/female pair of Tetraopes femoratus (red-femured milkweed borer) on the seed pod of Asclepias engelmanniana (Engelmann’s milkweed) and photographed the striking and beautiful caterpillar of Schinia gaurae (clouded crimson moth) on the stem of Oenethera glaucifolia (false gaura).
Tetraopes femoratus (red-femured milkweed borer—family Cerambycidae) on seed pod of Asclepias engelmanniana (Engelmann’s milkweed).
Schinia gaurae (clouded crimson moth—family Noctuidae) on the stem of Oenethera glaucifolia (false gaura).
After that, I went up on top of the main mesa where I expected A. macra to occur. Heterotheca stenophylla (stiffleaf false goldenaster), on the flowers of which I collected A. macra in previous years, was blooming abundantly, but intense searching their flowers produced no beetles. I also noticed that Gutierrezia sarothrae (broom snakeweed), abundant in the area as well, was in only the earliest stages of bloom, suggesting to me that it might still be a bit too early for the jewel beetles to be out. By the time the 6:00 hour arrived, insect activity was noticeably diminished, and we wrapped up this, our final, collecting stop of the trip.
No camping is available at Gloss Mountain State Park, so we knocked out another hour and a half of travel by driving to Ponca City in north-central Oklahoma and taking a hotel there. For the first time since we left, we enjoyed dinner at a restaurant (fried catfish for me!), a hot shower, and a real bed!
Day 12
The following morning, we were surprised to learn that the only coffee shops in town were Starbuck’s and drive-throughs. This just wasn’t going to cut it for us on our final travel day, so we drove 15 minutes north to the small town of Newkirk and enjoyed great coffee, breakfast sandwiches, and scones at “Savvy Cactus” (Newkirk Mercantile Boutique & Espresso Bar). (The coffee was good enough that I bought a bag of their coffee!)
“Savvy Cactus” Newkirk Mercantile Boutique & Espresso Bar in Newkirk, Oklahoma.
The rest of the drive back to St. Louis was spent reflecting on the many experiences we’d just had and synthesizing the new knowledge while enjoying the landscape as it skirted the southern edge of the Flint Hills of Kansas and traversed the familiar hills and dales of our beloved Missouri Ozarks—the end of a 3,931-mile trip!
Fr. James Sullivan (left) and Ted MacRae (right) stand under a banyan tree in Key Largo, Florida, 9 May 1986 (photographer unknown).
In Spring 1986, the Rev. James Sullivan (Fr. Sullivan to those who knew him) and I made a two-week trip to Florida with the objective to explore as much of the state as we could—from the Panhandle to the Keys! My goal, of course, was to collect beetles2, especially woodboring beetles in the families Buprestidae and Cerambycidae (it was only my third trip outside of Missouri for such purpose), while Fr. Sullivan’s was to identify and document as many plant species as possible. This apparent dichotomy in interests was not as clean as it may seem—as an entomologist interested in host plant relationships, the chance to spend time in the field with as accomplished a botanist as Fr. Sullivan was too good to pass up, and Fr. Sullivan’s passion for studying insect associates of the plants he studied greatly aligned our interests. My memories of that trip have faced in the nearly 40 years since, jogged only by the specimens I collected now residing in my cabinet and two trays of 35 mm slides taken with an Olympus OM10 SLR film camera. Fortunately, Fr. Sullivan was more diligent than I in journaling his observations during that trip, a copy of which he gave to me. This report is an attempt to summarize our observations using these materials. In his journal, Fr. Sullivan made the following disclaimer: “Plant determinations in these notes must be regarded as tentative: We have not had the use of a complete flora for any portion of the State of Florida. We have been as precise as possible with the use of several less complete sources. ★This star symbol indicates plant determinations that were later confirmed by the use of the Flora of Tropical Florida or by other adequate keys.”
[Note: names for most of the plants included in this report were confirmed by Fr. Sullivan, the primary exceptions being those indicated with question marks (?). As a result, I have omitted use of the star symbol in this report. Also note that plant taxonomy has likely changed immensely during the past 39 years. Scientific names, common names, and plant families given are those we used at the time, and only in a few cases have they been harmonized with current nomenclature (my notes in [square brackets]). An asterisk (*) denotes plants and insects that were also photographed.]
We left St. Louis on the morning of April 28 with the goal of spending the night in Montgomery, Alabama. The next morning, true to form, Fr. Sullivan got up early to explore the area around the hotel before continuing the drive south. He noted two plants: Cirsium horridulum and Sapium sebiferum (Euphorbiaceae), the latter a fast-growing deciduous tree known as Chinese tallow and native to eastern Asia. All parts of the tree emit a milky white sap when damaged, which is toxic and can cause gastrointestinal upset if ingested. As we continued south, we noted the first Spanish moss (Tilandsia usneoides) draping the trees along Hwy 281. The growth was very well-developed, leading Fr. Sullivan to speculate that it also probably occurred north of Montgomery along I-65 but that we missed it due to our nighttime arrival.
Later in the day we arrived at our first destination, Torreya State Park in the Florida Panhandle, home of the extremely rare Florida nutmeg (Torreya taxifolia*) tree that grows only on the bluffs along the Apalachicola River. We explored the heavily forested hills and ravines of the area and found examples of this plant alongside the road near the entrance to the campground. However, we documented a diverse list of other plants including Acer barbatum [= A. saccharum ssp. floridanum] (Florida maple), Actaea pachypoda, Amorpha fruticosa, Aralia spinosa, Ascyrum sp., Callicarpa americana, Calycanthus floridus, Calycarpon lyoni, Cnidoscolus stimulosus*, Conopholis americana, Conradina canescens*(Lamiaceae), Croomia pauciflora* (Stemonaceae), Decumaria barbara, Dirca palustris, Erigeron strigosus, Erythrina herbacea*, Euonymus americanus*, Lonicera sempervirens*, Halesia sp., Hydrangea quercifolia*, Ilex opaca, Itea virginica*, Lygodium japonicum, Mitchella repens, Myrica serifera, Onoclea sensibilis*, Opuntia humifusa*, Rhaphidophyllum hystrix (needle palm), Ruellia carolinensis*, Sebastiana fruticosa* (Sebastianbush, Euphorbiaceae), Spiranthes praecox*, Viburnum sp., and Wahlenbergia marginata. Insect collecting consisted primarily of an assortment of longhorned beetles attracted to ultraviolet (UV) lights at night.
After two nights at Torreya State Park, we traveled further down the peninsula along the central spine to Highlands Hammock State Park, one of the oldest state parks in Florida protecting 9,000 acres of old-growth cypress swamp and oak hammock. We first explored the Wild Orange Grove Trail (noting wild orange trees as well as our first alligator!) but moved to other areas of the park over the next two days. We noted the occurrence of three species of palms here: Rhaphidophyllum hystrix (needle palm), which lacks the leaf midrib of and has fewer leaf divisions than Sabal palmetto (cabbage palm), the most common palm and distinguished by a strong leaf midrib, and Serenoa repens (saw palmetto) with its saw-toothed petiole edges. We repeatedly saw the tortoise beetle Hemisphaerota cyanea on the leaves of S. palmetto. A nice variety of longhorned beetles was also collected here, including the Florida endemic Typocerus flavocinctus and several lamiines at UV lights at night. A blister beetle (family Meloidae) similar to our Nemognatha nemorensis was common on the flowers of Aster reticulatus* and Pterocaulon pycnostachyum* (both Asteraceae), and on flowers of Cirsium horridulum we saw the leaf-footed bug Acanthocephala terminalis* (Coreidae). Other plants that Fr. Sullivan noted include Abrus precatorius*, Ardisia crenulata* (crenate berry bush, Myrsinaceae), Asimina pygmaea* (?), Bacopa sp.*, Bidens pilosa*, Callicarpa americana*, Cuthbertia graminea (?), Emilia sonchilfolius, Eriocaulon sp.*, Erythrina herbacea, Hypericum sp.*, Ilex cassine, Ilex glabra, Lachnocaulon anceps, Lygodesmia aphylla*, Lyonia lucida*, Mikania scandens, Oxalis violacea* (?), Persea borbonia, Polygala lutea*, Schrankia microphylla*, Tephrosia chrysophylla, Urena lobata, Utricularia sp.*, and Xyris sp.* Fr. Sullivan also noted in his journal a list of a dozen “rare” birds such (e.g., cardinal, catbird, crow, etc.!).
Our next destination was outside the northwestern limits of Everglades National Park at Collier-Seminole State Park, which lies partly within the great mangrove swamp of South Florida (one of the largest mangrove swamps in the world) and covering one of three original stands of royal palm (Roystonea elata [= Roystonea regia]) in Florida (the park was previously called Royal Palm Hammock). We primarily explored the Royal Palm Hammock Nature Trail and along the water’s edge around the boat basin, where Rhizophora mangle* (red mangrove) lined the edges of the salt marsh. Two species of Solanum were observed, primarily S. erianthum (potato tree) but also S. donianum*, and we noted the pleasant fragrance of a Eugenia sp. that escaped identification. Bursera simaruba (“tourist tree”), with its distinctive peeling bark, was also common here. We noted Baccharis halimifolia heavily infested with the leaf beetle Trirhabda bacharidus*, saw Heliconius charitonius butterflies on the wing, and observed a cluster of young seed bug nymphs* (Lygaeidae), likely one of the milkweed-associated species, on a vining species of milkweed. Deer flies (family Tabanidae) were a real problem for both of us, and we had to use head nets (Fr. Sullivan even resorted to wearing his London Fog jacket!). Other plants documented included Acrostichum sp., Alternanthera sp. poss. philoxeroides (Amaranthaceae), Batis maritima, Bidens pilosa var. radiata, Blechum brownei, Borrichia frutescens*(sea daisy), Commelina diffusa, Dicliptera assurgens*, Dicromena sp.* (white-bracted sedge, Cyperaceae), Eugenia sp.*, Ipomoea alba (moon flower), Ipomoea sagittata*, Passiflora pallens, Pithecellobium unguis-cati (cat claw), Pluchia odorata (camphor weed), Polygala grandiflora var. angustifolia, Psychotria undata*, Solidago sp.*, Triodanus sp., Urena lobata*, and Zanthoxylum fagara (lime prickly ash). Similar to previous localities, a diversity of longhorned beetles were attracted to UV lights at night.
After two days at Collier-Seminole, we drove east along the Tamiami Trail, noting the magnificent stands of bald cypress (Taxodium distichum) in the Big Cypress Swamp Preserve and seeing the first water hyacinths (Eichhornia crassipes) in bloom. We also saw Australian pines (several species in the genus Casuarina)—angiosperms rather than gymnosperms. Its needles are much longer than true pine (genus Pinus), and the trees appeared very dark green as seen from a distance. Eventually we landed at John Pennekamp Coral Reef State Park on Key Largo. Most people visit this park to dive and explore the spectacular living reefs of the Florida Keys; however, we had more terrestrial objectives. We began by exploring the coral limestone woodland along the Wild Tamarind Trail, where Metopium toxiferum*was common along the woodland border (and we took care not to touch!). A large ichneumonid wasp* (Ichneumonidae) was seen perched in the understory, and we noted the impressively oversized female of the spider Nephilia clavipes* being courted by an equally strikingly diminutive male. Lysiloma latisiliqua* was abundant in the woodland, as was Bursera simaruba* its bark red and peeling like a sunburned tourist! Coccoloba uvifera was also abundantly fruiting, and other plants seen include Alternanthera sp., Conocarpus erecta var. sericea, Schinus terebinthifolius*, and an unidentified composite (either Eupatorium villosum or Garberia sp.). Along the Mangrove Trail we saw (of course) not only red mangrove Rhizophora mangle*) but also black mangrove (Avicennia germinans*, Avicenniaceae) and white mangrove (Languncularia racemosa, Combretaceae). These three plants are placed in three unrelated families, yet all show a high degree of fidelity to mangrove ecosystems. At a Persea americana* orchard in the adjunct Shaw Property, we saw Hamelia patens* in bloom and Lysiloma latisiliqua growing around the orchard’s edge. Other plants seen in the area include Abutilon sp., Batis sp.*, Eupatorium villosum* (?), Gaillardia pulchella*, Heliotropium angiospermum, Heliotropium curassavicum, Hibiscus tiliaceus, Melanthera sp., and Rivina humilis*.
Our plan the following day was to continue down the length of the Keys, making stops at a few selected places along the way before spending the night in Key West. At our first stop on LowerMatecumbe Key, we noted Avicennia germinans, Eustoma exaltatum*, and Polygala baldwini (as well as a Great Blue Heron) and then continued southwestward to Long Key State Recreation Area [now Long Key State Park]. Most people visit Long Key for its beaches and fishing, but we came to the preserve to explore the endangered coastal dune ecosystem that it protects. Few insects were seen, but a number of interesting, mostly highly salt-tolerant, plant species were seen. These include Abutilon sp., Argemone mexicana*, Cassasia clusiifolia*, Chrysobalanus icaco, Ipomoea pes-caprae, Lantana involucrate, Manilkara bahamensis* (wild dilly, Sapotaceae), Scaevola plumieri* (inkberry, Goodeniaceae), Solanum diphyllum, and Suriana maritima* (bay cedar). We finished the day at Key Deer Preserve on Big Pine Key, a sanctuary for the smallest subspecies of white-tailed deer in North America. We did not see any deer, but we did see some interesting plants. Byrsonima cuneata* (Malphigiaceae) was common here, as was Croton linearis. Along the Nature Trail we saw the orchid Bletia purpurea* (pale pink) and also recorded Aletris sp., Chrysophyllum oliviforme (Sapotaceae), Dichromena sp., Ernodia littoralis*, Metopium toxiferum, Pithecellobium sp., Polygala verticillate (?), and “thatch palms” (plus a hissing alligator!).
The next two days were spent at Everglades National Park, where we began our visit by exploring the Long Pine Key Nature Trail, where Cladium jamaicensis* (sawgrass) and Taxodium distichum* dominated the landscape. We noted that it was easy to pass one’s fingers over the sawgrass blade edge in one direction, but not so easy in the other! It was here that I found what I considered a real prize—my first ever bumelia borer (Plinthocoelium suavelons)! I also collected the very colorful Trichodes apivorus on the flowers of Sabal palmetto. Fr. Sullivan had even more success with the plants—so much, in fact, that we were only able to explore the east end of the trail. Several plants belonging to largely tropical plant familys were seen, including Dodonaea viscosa (varnish leaf, Sapindaceae), Tatrazygia bicolor* (Melastomataceae), and Dipholis salicifolia (willow bustic, Sapotaceae). Polygala balduinii (or a similar species) and an unidentified Buchnera sp. were common. The recorded list of other plant species seen was diverse: Asclepias lanceolata*, Baccharis sp., Byrsonima cuneata, Calopogon sp.* [likely C. tuberosus var. simpsonii], Croton linearis, Dichromena sp., Heliotropium polyphyllum var, polyphyllum (H. leavenworthii ) (Boraginaceae), Jacquemontia jamaicensis, Lobelia glandulosa*, Melanthera angustifolia (Asteraceae), Myrica cerifera, Myrsine guianensis, Passiflora sp.*, Persea bordonia, Piriqueta caroliniana, Psychotria nervosa, Rhus sp., Sabatia sp. poss. brevifolia*, and Stillingia sylvatica ssp. tenuis (Euphorbiaceae). We returned again to Long Pine Key Nature Trail the following day to explore the west end near Pine Glades Lake, finding many of the same plants recorded the previous day but also Ageratum littorale (?), Bletia purpurea, Justicia ovata var. lanceolata*, Lippia stoechadifolia, and Morinda royoc. From there we moved on to the P.K. Nature Trail, where Cynanchum blodgettii was seen twining over much of the vegetation—including other plants of its own species!. Fr. Sullivan spent a good deal of time studying a plant found growing at the edge of Pine Glades Lake, which he presumed to be a species of Lippia that exhibited pleated leaves with matching teeth (leading him to call it “corduroy lippia” or “pleated lippia”). Eventually he settled (and later confirmed) the species as Lippia stoechadifolia, a Neotropical species limited in the U.S. to south Florida and the Keys. Other plants observed included Angadenia berterii, Urechites lutea, and (my favorite) Zamia floridana* [likely Z. integrifolia var. silvicola].
Back at Key Largo near Tarpon Bay (below our motel), Fr. Sullivan continued exploring the plants, especially the mangroves. He noted that Avicennia has “dewdrops” but that the other mangroves do not. This relates to the processes used by the plant to eliminate excess salt, which in Avicennia involves salt water “perspiration” that dries in the heat of the day (indeed, the residue of salt flecks is useful in distinguishing Avicennia from the other mangroves) but in Rhizophora is done by accumulating salt in the oldest leaves before they turn yellow and drop. He also noted that Avicennia and Rhizophora can be distinguished by color; Avicennia, which normally grow a little farther from the water, are closer to gray-green, while Rhizophora are closer to yellow-green. Tridax procumbens was a common roadside weed around the motel—its flowers and fluffy seedheads rise on long scapes, as if leafless, but are actually attached to the sprawling, hairy stems, which bear many deeply cleft leaves with opposite arrangement. He also noted Morinda royoc growing not only in the woods but also hedgerows. It is like Psychotria [both species are in the Rubiaceae], but without the large, nervy leaves. The fruits aggregate to look like large, yellowish mulberries. Hamelia patens grows right along the highway here, and several large Solanum shrubs with stellate trichomes on the leaves and white flowers were seen that may be a complex of species including S. donianum, S. verbascifolium, S. erianthum, or yet another species.
On May 10, the field visits were over, and it would take two days of driving to return to St. Louis. Even beginning the drive home, however, did not stop Fr. Sullivan from botanizing. During a stop at the drawbridge on Hwy 1 between Key Largo and the mainland, Fr. Sullivan collected Stachytarpheta jamaicensis, its flower tubes emerging from upward pointing, elongate triangular bracts, and its leaves being coarsely dentate. Also, from the highway in northern Florida, we saw what appeared to be the frequent occurrence of blooming Asimina. These were low plants with white flowers and leaves present. Spending several days in south Florida also gave Fr. Sullivan a chance to contemplate the different hammock habitats that we had visited, and he noted the following: “A hammock is basically a hardwood forest. A hammock in Florida has a significance parallel to that of a glade in Missouri: it is a relief from the ordinary situation. In the Everglades hammocks take the form of “hillocks”: The forest seems to build itself above the level of the sawgrass wetlands. In Highlands County, on the other hand, the hammocks occupy depressions in the topography. It is natural for the pinelands to burn with some degree of regularity, but the wet depressions are protected from most fires. Fire actually helps Pinus to have a competitive edge (since the needles make good tinder and the resin burns so hot, the pines contribute to their own survival situation), but in the wet depressions the broadleaf hardwoods are able to take over. The State Parks often feature the hammocks. As we go farther south, the hardwood species become more tropical. We have seen a lot of Bursera simaruba, a hammock feature, but have yet to see Ceratiola ericoides, which is more a representative of the norm for this state. Visiting Mahogany Hammock in the Everglades we learn that it is protected from sawgrass fires by a natural moat surrounding it. The moat results as limestone strata are eaten away by the hardwood-produced acids.”
1 Deceased April 15, 2025.
2 Permits for collecting beetles were obtained from the Florida Department of Agriculture and the National Park Service.
Welcome to the 17th “Collecting Trip iReport” covering the first of two planned insect collecting trips to the southwestern U.S. this season—this first one occurring during June 4–13. This was another solo trip, and while it was not as long as I’d hoped, I still managed to visit 15 different localities—one in northwestern Oklahoma, six in northern Arizona, six in southern Utah, and two in southern Nevada.
I left Kansas City in the morning with two goals: 1) look for Acmaeodera robigo (family Buprestidae) in Texas Co., Oklahoma (based on a 2011 observation posted to BugGuide), and 2) make it to Black Mesa State Park in the far northwestern corner of the Oklahoma panhandle before sunset (to avoid having to set up camp in the dark). It was a long day of driving (mostly through heavy rain), but by the time I arrived at the A. robigo locality, skies were clear and the area was dry. Texas Co. is the largest (and seemingly flattest!) of the three Oklahoma panhandle counties, but I have not collected in the county previously because most of it has been converted to cultivated wheat. This particular location, however, lies within the Beaver River drainage and, thus, features native shortgrass prairie vegetation.
Beaver River drainage where Acmaeodera robigo was observed in 2011.
The host plant mentioned in the A. robigo observation, Melampodium lecanthemum (blackfoot daisy—family Asteraceae), was blooming abundantly along the roadsides, so I checked the flowers carefully up one side of the highway and down the other side.
Melampodium lecanthemum (blackfoot daisy).
Nothing was seen on the flowers, but given the lateness of the hour and cool temps I did not expect to see anything. Still, I set three white bottle traps in the area within patches of M. leucanthemum and will plan on retrieving them up later this season. With luck, the traps will have attracted adults if the species as they visit the nearby flowers.
Bottle trap, antifreeze, and a spade are all that is needed to trap flower-visiting insects.
Moving west I quickly entered Cimarron Co.—I always enjoy seeing this double-line of utility poles stretching to a seemingly endless horizon at the border between Texas and Cimmaron Counties. The latter is not only the westernmost county in the state, it is also the only county in the U.S. that borders four other states (Texas, New Mexico, Colorado, and Kansas).
Entering Cimmaron Co., the westernmost county in Oklahoma.
I made it to Black Mesa State Park with plenty of daylight left to set up camp. Per usual, after getting camp setup I enjoyed “refreshments” and waited for nightfall to walk the roads looking for nocturnal beetles (or any other critters that might be out and about). I did see an Eleodes sp. (darkling beetle—family Tenebrionidae) early in, but the night was chilly, and the onset of light drizzle put an end to the walk.
Ready for bed!
This would not be the end of my nighttime hiking, however—at 3am I was awakened by the drone of a motor, and it was loud enough that sleep would be impossible. Thinking it was an inconsiderate camper down at the RV campground, I decided to investigate and discovered it was a water pump within the campground. I decided if I couldn’t sleep, then somebody else would also have to be awakened, namely the campground host. It took the elderly woman a few minutes to come to the door after I rapped a few times on her RV, and I apologized for waking her before explaining the situation. She said she wouldn’t know anything about how to turn it off, to which I replied that I didn’t expect her to know that but I’ll bet somebody does and maybe she could make a call and figure out who that is or this wouldn’t be the last time somebody wakes her at 3am. I figured that would be the last of it, that I’d be awake until morning, and that I would have another nine hours of driving the next day on only three hours of sleep. But, to my relief, about a half hour later a park maintenance vehicle pulled up to the pump house, and a young man turned the motor off (I thanked him profusely). I did eventually get back to sleep and awoke to birdsong and clearing skies.
Day 2
There is a low water bridge at the south entrance to the park that crosses a normally dry creek. However, this time the creek was filled with water with lush growth of sedges and grasses along the water’s edge. This is a perfect situation for Taphrocerus species (family Buprestidae), and at this literal transition point from the eastern to the western fauna I’m not sure what species I might encounter there. Unfortunately, thorough sweeping of the sedges produced no beetles, so the question will for now remain unanswered.
Creek at south entrance to Black Mesa State Park, Oklahoma.
Heading south and then west from the park takes you shortly into the northeastern reaches of New Mexico and the town of Clayton. Whenever I pass through Clayton I like to stop at Mock’s Crossroads Coffee Mill for a bag of freshly ground coffee.
Mock’s Crossroads Coffee Mill, Clayton, New Mexico.
Skimming across the northern reaches of New Mexico for the next several hours was uneventful with no indication of a repeat of the heavy rain that pounded me for much of my drive yesterday across Kansas and Oklahoma. The situation changed, however, as I crossed the Continental Divide on the approach to Farmington.
I think I’m going to get wet.
I’m sure I’m going to get wet.
Sure enough, I once again had the pleasure of driving through driving rain. In addition, I arrived at my next planned spot just north of town (Brown Springs Campground) to find the entrance and main road under several inches of water. No point in trying to collect there, so I continued on towards the next stop (Devils Canyon Campground) in southeast Utah (San Juan Co.) in hopes of arriving early enough to set up camp before dark. Things looked promising as I crossed through the southwestern corner of Colorado towards Monticello, Utah, as patchy clouds filled a sun-filled sky.
Near Dove Creek, Colorado.
The presence of large oval emergence holes in the lower part of the limb confirmed that this tree was, indeed, under attack by such, and stripping the bark around the holes revealed fresh workings from the larvae indicating that some of them may still be inside the tree.
By the time I reached the campground, however, the rain had returned—not hard, but steady. I didn’t relish the thought of setting up camp in the rain and did something I almost never do—heading back into town and spending the night in a motel! At least I was able to enjoy a burger cooked by someone else for a change.
Day 3
Day 3 started off gray and overcast with the threat of more rain, but looking at radar and the areas I was going further west had me optimistic that I would get out of the rain once and for all. My ultimate stop for the day would be Jacob Lake Campground in north-central Arizona (Cocconino Co.), and my plan was to stop at a number of places along the way. Devils Canyon Campground itself, however, was still under clouds, meaning that collecting there would likely not be very productive. Nevertheless, despite last night’s rainout and the continuing cool, wet conditions, I decided to place some traps that I could pick up later in the season and, thus, get at least a sample of the area’s beetle fauna.
Devils Canyon Campground, Utah.
The campground lies at ~7000 ft, and I found a ridge with ponderosa pine/gamble oak forest on the slope to one side and pinyon/juniper/oak woodland on the crest of the ridge to the other. On the ponderosa side I set a white bottle trap, and on the pinyon/juniper side I set a sweet red wine-baited jug trap. There wasn’t much in bloom at the time other than a few yellow composites and the occasional Oenothera cespitosa (tufted evening primrose—family Onagraceae) with blossoms still wide open despite the daylight hour due to the overcast, cool conditions.
Oenothera cespitosa (tufted evening primrose).
Coming down off the plateau towards Bluff, Utah, thick low clouds gave way to higher broken clouds with warmer temps (mid-60s). I stopped a few miles west of town at a location where Mont Cazier once collected what was later described as Agrilus utahensis (family Buprestidae) and began sweeping roadside vegetation. While I was sweeping, I encountered three Amannus vittiger (family Cerambycidae) on the flowers of Sphaeralcea coccinea (scarlet globemallow—family Malvaceae) (along with a few meloids and bees for others). The record of A. utahensis was from quite a bit later in the season (late July), so I didn’t really expect to find it (although I was hopeful). However, I did sweep what appears to be Agrilus malvastri.
Amannus vittiger collected on flowers of Sphaeralcea coccinea (scarlet globemallow).
Sphaeralcea coccinea (scarlet globemallow).
A short distance west of the stop had me entering northeastern Arizona, and traveling west of Dennehotso on Hwy 160 I encountered patchy, low lying clouds though which beams of bright sunlight lit up the red rocks below and cast a reddish hue on the bottoms of the clouds.
West of Dennehotso, Arizona on Hwy 160.
A bit further west on Hwy 160 is a formation apparently known as “Baby Rocks.”
Baby Rocks, west of Dennehotso, Arizona,
As I drove, I kept my eye out for areas along the highway with stands of plants in bloom, and I found just such at a roadcut on Hwy 98 near mm 325 as I approached Page, Arizona (Cocconino Co.). There was a fair amount of Sphaeralcea coccinea in bloom, off which I collected a handful of Acmaeodera pubiventris lanata and one Amannus vittiger from the flowers. I swept the grasses and other roadside vegetation thoroughly, but that produced nothing. I returned my attention to the Sphaeralcea and swept it thoroughly as well to be sure I didn’t miss anything. Good thin I did, as that turned up one more each of A. p. lanata and A. vittiger as well as a few Agrilus sp. prob. malvastri.
Acmaeodera pubiventris lanata on flower of Sphaeralcea coccinea (scarlet globemallow).
After passing through Page, Arizona, rather than continuing straight west to Jacob Lake Campground, I veered north into Kane Co., Utah to revisit a locality I’d visited a couple of years ago about 23 mi northwest of Page on Hwy 89. The last time I stopped here (late June 2023), I found a few Nanularia brunneata (family Buprestidae) on the stems of Eriogonum inflatum (desert trumpet—family Polygonaceae). That visit was about three weeks later in the season than this time, and not only was the area dry (despite all the rain east of here), but there was very little new growth on any of the E. inflatum plants—just the dried stalks of last year’s growth. Still, there was fresh growth present at the spot, in the form of Ericameria nauseosa (gray rabbitbrush—family Asteraceae), on which I collected a single cryptocephaline leaf beetle, and along the roadside rain shadow in the form of Sphaeralcea parvifolia (small-leaved globemallow), on the flowers of which I collected several more Agrilus sp. prob. malvastri. Eventually, I did find a single E. inflatum plant with small sprouts of new growth on which I found several clytrine leaf beetles. Sweeping the S. parvifolia produced one more Agrilus sp. prob. malvastri, a single Acmaeodera navajoi—a species I collected here abundantly two years earlier, and a series of a very small chrysomelid leaf beetle species that I observed feeding on the foliage.
Once I got a bit further west, the landscape turned green again, indicating recent rains, so I checked iNaturalist for nearby records of E. inflatum that I could check for N. brunnea. There was one a few miles east of Kanab (Kane Co.) and on the way to Jacob Lake Campground, so I stopped by to see if I could find the plants. Unfortunately, the record turned out to be on private property, so I couldn’t go to the precise location. I looked around the area outside the property but didn’t see any plants; however, S. parviflora was blooming abundantly along the roadsides, and sweeping it produced a few more Agrilus sp. prob. malvastri and a couple of small bees (for Mike).
11 mi E of Kanab, Utah.
There were also several blooming Opuntia polyacantha var. erinacea (Mojave pricklypear—family Cactaceae), which I checked for Acmaeodera, but I found only one large bee (again, for Mike). With the sun by then dropping close to the horizon, I called it a day and headed for the campground.
Opuntia polyacantha var. erinacea (Mojave pricklypear)—pink-flowered form.
I arrived at Jacob Lake Campground (Cocconino Co., Arizona) and got camp setup before dark, which settled in as I was cooking dinner. It was chilly at this relatively high elevation (7900 ft)—temps were already in the mid-50s and were forecast to drop down into the 40s by morning. Despite the chill, I found a Zopherus uteanus (family Zopheridae) and a smaller tenebrionid on a cut stump of Pinus ponderosa (ponderosa pine).
Zopherus uteanus on cut stump of Pinus ponderosa (ponderosa pine) at night.
Later, I walked the site—not really expecting to see much because of the chill, but I did find three Iphthiminus lewisii (family Tenebrionidae) on the trunk of a recently fallen P. ponderosa and saw two more on a pine stump.
Iphthiminus lewisii on trunk of recently fallen Pinus ponderosa (ponderosa pine) at night.
With three days of travel—the first two mostly rainy and today dry but still quite cool, I’m hoping the forecasted warmer, sunnier conditions for tomorrow and onward come true and I can get this collecting trip in high gear.
A waxing gibbous moon illuminates my camp at 7900’ in Jacob Lake Campground, Kaibab National Forest, Arizona.
Day 4
After morning coffee (and moving to a different campsite—long story!), I went back north a bit to the area near Lefevre Overlook that had been only lightly impacted by the widespread burns that occurred here a few years ago and is showing signs of recovery. It felt “early season” with patchy clouds, moderate temps in the low of mid 70s, and plenty of moisture in the soil with lots of plants in bloom. Insects were not abundant, but with continued beating I collected a couple of Anthaxia sp. (family Buprestidae) and a variety of small clytrines, cryptocepahlines, and curculionids off of Purshia standsburyana (Standsbury’s cliffrose—family Rosaceae) in flower.
Purshia standsburyana (Standsbury’s cliffrose).
As the morning warmed, insects seemed to become a bit more active, although the day continued to feel “early season.” Persistent visual searches and beating of a variety of plants turned up a few small black/yellow Pidonia? (family Cerambycidae), one Acmaeodera diffusa?, and one Anthaxia sp. on flowers of Hymenopappus filifolius (fine-leaved hymenopappus—family Asteraceae); one Agrilus sp. prob. malvastri, another Pidonia?, and one A. diffusa? on flowers of Sphaeralcea ambigua (desert globemallow); several small clytrine and cryptocephaline leaf beetles and curculionid weevils on Quercus gambelii (Gambel oak—family Fagaceae); and several A. diffusa? and a few Anthaxia sp. on flowers of Tetraneuris acaulis (four-nerve daisy—family Asteraceae). Sweeping through the area where the T. acaulis was growing produced nothing further of interest, so I placed a sweet red wine-baited jug trap and a yellow bottle trap in the area—hopefully they will each attract a variety of interesting beetles over the next few months.
Sweet red wine-baited jug trap hanging in a tree and a yellow bottle trap sunk into the ground below.
A bit further down, the mountain escaped the fire that ravaged many other parts of the mountain. I expected to see much more insect activity, but the opposite instead was the case. This may be related to the lower incidence and diversity of flowering plants, which were likely triggered at the previous spot by the fire. I did find a small area where Sphaeralcea ambigua was blooming abundantly and sweeping through them produced a fine series of Agrilus sp. prob. malvastri along with a few bees (for Mike). I walked up the slope a ways, but there was virtually nothing in bloom—unlike what I had seen at the previous spot. Eventually, I did find a few Hymenopappus filifolia and Tetraneuris acaulis, but the only I beetle I saw on any of them was a single Acmaeodera diffusa? on the latter.
Escobaria vivipara (viviparous foxtail cactus).
Without anything luring me further up the slope, I worked my way back down towards the car and was about ready to call it a day when I decided to take a gander a bit down the slope—just in case I might see something of interest. Nothing captured my attention, however, so I worked my way over a bit to take a different route back. That’s when I saw it! All day long I had been keeping my eye out for large Utah junipers (Juniperus osteosperma—family Cupressaceae) with thigh-sized main limbs—one of which was dying (not dead), possibly a result of woodboring beetles, and before me was just such a tree!
Juniperus osteosperma (Utah juniper) with dying main limb.
The presence of large oval emergence holes in the lower part of the limb confirmed that this tree was, indeed, under attack by such, and stripping the bark around the holes revealed fresh workings from the larvae indicating that some of them may still be inside the tree.
Large oval emergence hole caused by a species of longhorned beetle.
Fresh frass packed in the galleries by longhorned beetle larvae.
I hiked back to the car to get my chainsaw—brought along on the trip just for such an eventuality—and cut a portion of the infested limb out of the tree so I could bring it home and attempt to rear out the adults. My hope is that the species infesting the tree is Semanotus juniperi (family Cerambycidae), a very uncommonly encountered longhorned beetle that breeds in the large limbs of juniper in this area, so I’ll be keeping my fingers crossed. Hauling out the infested bolt along with the chainsaw was a struggle, but eventually I made it back to the car and celebrated a successful last act to what had up to that point been a not too spectacular first full day in the field.
Bolt of Juniperus osteosperma (Utah juniper) infested with longhorned beetles.
I needed a break after working the chainsaw and hauling out the wood, so I went back to the campsite to enjoy an end-of-the-day “beverage” and eventually dinner. However, part of me was thinking Inshould have collected more of that infested juniper to increase my odds of successfully rearing whatever was infesting it, so I resolved to do exactly that in the morning.
Dinner on the grill at Jacob Lake Campground.
Before dinner as I was gathering kindling, I had noticed a large, fallen ponderosa pine behind the campsite and returned after dark to see if there might be any nocturnal beetles attracted to it. It seemed recently dead, but as I inspected the upper branches more closely I saw that it had been dead long enough that whatever would have been attracted to it had already come and gone. I thought maybe I could find beetles under the bark and began peeling the bark in the trunk. The bark was still intact but was just loose enough that I could peel it off in large sheets. Doing so, however, revealed only a couple of click beetles (family Elateridae). I didn’t see any other fallen or dead trees in the area, but on the trunks of large living ponderosa pines I found a tenebrionoid and several individuals of a Lecontia discicollis (burnt conifer bark beetle (family Boridae). [Edit: thanks to Alex Harmen for the identification on this one!] Nearby was a cut stump of a very large ponderosa pine, and peeling back the thick bark at the base of the stump revealed yet another elaterid species and two darkling beetles. I was hoping to find more Zopherus uteanus, but no such luck!
Lecontia discicollis (burnt conifer bark beetle) on trunk of Pinus ponderosa (ponderosa pine) at night.
Day 5
After a morning of the coffee ritual and observing campsite wildlife, I made an ice run at the nearby service station.
I was having second thoughts about taking only a single bolt of wood from cerambycid-infested Utah juniper that I found at the end of yesterday’s collecting and decided to go back to get more of the infested wood to improve the likelihood of successfully rearing adults from the wood. It would not be an easy job—I’d have to haul the chainsaw down the the tree, cut off the two remaining infested bolts, cut the bolts down to cartable pieces, and then haul the chainsaw and wood bolts back to the car, likely requiring several trips. It was worth it, however, because as I was stripping bark to see where I needed to make the initial cut, I encountered an intact cadaver of one of the beetles that had died while trying to emerge from the wood. I carefully extracted the abdomen from the tree and found the head and pronotum in the bark and placed them in a vial, and they without a doubt represent the species I was hoping they were—Semanotus juniperi, a super rare species that very few people have ever collected [tip of the hat to Ron Alten for sharing his knowledge about this beetle with me and enabling me to find this beetle for myself!]. I’ll be able to put the beetle back together when I get home, and I’m hopeful I’ll rear at least a small series of beetles from the wood I’ve collected.
I love the smell of chainsaw in the morning!
Having carted the additional bolts of wood back to the car and confident in my ability to recognize the work of this species, I looked for—and found—a few more trees that the beetle had infested. However, in each case the workings were old and no beetles were encountered chopping into the wood. I also spent some time looking for much smaller emergence holes in the thick trunk bark of several junipers and carefully shaving the bark to see if I could find another rare longhorned beetle species, Atimia vandykei. I found several galleries that might have been this species, but no beetles or larvae were encountered, leading me to think I might have been a bit late and the adults have mostly emerged. A large, recently dead Pinus edulis (Colorado pinyon pine) also caught my attention, as it looked fresh enough to still contain wood boring beetles that might have infested it. The wood was very hard and difficult to chop into, but I didn’t encounter any larvae of any kind and elected not to collect a bolt or two for rearing. Lastly, I spent some time looking for dead Gambel oaks, which in this area could host Xylotrechus rainei (family Cerambycidae), a recently described species that few have collected. I found several dead stems of the shrubby oak species that contained workings consistent with those of Xylotrechus, but in each case the workings were old and no beetles or larvae were present. This string of “failures” might have seemed like the makings of a bad day, but the success with S. juniperi overshadowed those failures and I left the site happy (though exhausted!).
The author sports his new field hat (an early Fathers Day gift!).
I returned to the first stop of yesterday to see if I could find junipers in this area infested with S. juniperi, reasoning that since the area had burned a few years ago some of the still-living trees might be stressed, thus making them more vulnerable to infestation. I also wanted to see if the bottle and jug traps I placed yesterday had caught anything of interest (even though it had only been one day). Along the way I picked up a single Anthaxia sp. on the flower of Tetraneuris acaulis and a few Acmaeodera diffusa? on flowers of Sphaeralcea ambigua. There wasn’t anything of interest in either trap, so I set about looking for infested junipers. I found only one, but again the workings were old and no larvae or adults were encountered. I also examined a few dead stems of Gambel oak, but none showed signs of infestation. (I suspect they had been killed by the fire and the damage to the wood by the fire made the stems unsuitable for infestation.) I did, however, find a small more recently dead Colorado pinyon pine that showed signs of recent infestation all along the trunk and collected it for rearing. By then, the day had warmed considerably and I was already exhausted from the morning’s chainsaw session, leading to a loss of motivation to keep looking. I needed a change of pace and decided to head higher up the mountain back into the ponderosa pine forest for some more “traditional” woodboring beetle collecting.
Callophrys gryneus (juniper hairstreak) on flowers of Hymenopappus filifolia (fine-leaved hymenopappus).
The forest at this site is dominated by ponderosa pine, and the strategy here was straightforward—look for large, dead or dying trees, either standing or recently wind-thrown, and inspect the examine the trunks for woodboring beetles. I came to this spot two years ago in early July, so this time was about four weeks earlier in the season. I had two specific targets (beyond woodboring beetles in general)—Chalcophora (family Buprestidae) and Monochamus (family Cerambycidae). Both of these genera are the subject of molecular studies being conducted by other researchers that I know, and I’ve been promising to send them fresh specimens killed and preserved in ethanol. The first wind-thrown tree I encountered was still green-needled, and I expected to find buprestid beetles all over it. Instead, all I saw were a few small Enoclerus sp. (family Cleridae). Large dead standing trees dotted the open forest, and I carefully approached and circled each one looking for beetles, paying special attention to those in full sunlight. Time after time, however, I was frustrated. Each time, I chopped into the wood a bit to examine what was going on underneath the bark, and while workings were plentiful I never encountered any larvae.
4.2 mi N Jacob Lake on Hwy 89A, Kaibab National Forest, Arizona.
Finally, I approached a large standing dead tree, and perched on its trunk in the sunlight was Chalcophora angulicollis (western sculptured pine borer). I’m happy to give this specimen up for DNA sequencing, especially since I already collected a specimen at this same spot two years ago (before the molecular study began).
Chalcophora angulicollis (western sculptured pine borer) on trunk of dead Pinus ponderosa (ponderosa pine).
I peeled a good portion of bark of the tree it was perched on but found nothing except a large elaterid larva (I wonder if it was Alaus melanops [western eyed elater], a predator or woodboring beetle larvae).
Alaus melanops (western eyed elater) collected from under bark of dead Pinus ponderosa (ponderosa pine).
For a long time afterwards that would remain the only beetle I encountered until I found a large standing tree in the early stages of death (needles pale green but not brown) with a female Dicerca tenebrosa (family Buprestidae) searching the trunk, occasionally stopping to probe a crack or crevice with her ovipositor. Patiently waiting at the trunk rewarded me with a second individual within a short period of time.
Dicerca tenebrosa on trunk of dead Pinus ponderosa (ponderosa pine).
Another long period of nothingness ensued as I zigzagged from dead tree to dead tree, eventually retracing my steps to the only two trees on which I had found buprestids. Even that failed to produce additional beetles, but as I was standing at one of them I heard a woodpecker persistently pecking and searching and pecking on a nearby tree. The tree looked perfectly healthy at first glance, but I figured the woodpecker had to know something that I didn’t (I’m always willing to learn from locals!) and walked over to the tree. It was immense, and a closer look at the crown revealed a few browning needles scattered throughout the crown. Then a closer look at the trunk revealed several of the same small Enoclerus sp. I saw earlier crawling on it. Woodpeckers and checkered beetles don’t lie, and this tree was clearly under stress and under attack by woodboring beetles. An initial circling of the trunk revealed no other beetles, but then I noticed the gangly antennae and legs of a male/female pair of Monochamus clamator, the male apparently mate-guarding the female. I’ll be happy to contribute one of these specimens to my colleague for DNA sequencing and keep the other for my collection.
Monochamus clamator on trunk of stressed Pinus ponderosa (ponderosa pine).
By that time, the sun was starting to get rather low in the horizon and I was utterly exhausted after a full day of walking, chopping, chainsawing, and hauling. I passed by the two previously successful trees on the way back to the car, to no avail, and headed back to camp (stopping at the nearby market for a celebratory milkshake before going into the campground).
Caenochrysis sp. (family Chrysididae) on trunk of dead Pinus ponderosa (ponderosa pine).
Day 6
The day’s plan was to head north to the area around Coral Pink Sand Dunes system in southern Utah, but before I left I decided to go down the east slope of the Kaibab Plateau a bit to see it I could find a good transition zone (one that hadn’t burned) from the higher elevation ponderosa pine forest to the juniper/pinyon woodland just below. A few miles east of Jacob Lake, right as I hit 7000’ (there was even a sign to that effect) while descending into the canyon, I saw a small pulloff with ponderosa pine forest (and even some fir) on the east-facing slope to the right and juniper/pinyon/oak woodland on the west-facing slope to the left—perfect! It struck me as a good-looking spot to set some traps, so I set a blue bottle trap in an open area on the juniper/pinyon/oak side of the highway and hid a sweet red wine-baited jug trap in the woodland right above it. I then started beating the patches of Gamble oak hoping for Brachys (family Buprestidae) but finding only a single Anthaxia sp. and several species of clytrine leaf beetles and curculionid weevils. There was a patch of Sphaeralcea ambigua in flower near the pulloff, off which I collected several Acmaeodera diffusa? plus another of those small black /yellow lepturines (Pidonia? sp.) that I found yesterday, and I swept some chunky black dermestids and a couple of bees (for Mike) from the flowers of Hymenopappus filifolia. Next came a long period of nothingness! I found another Utah juniper with damage on the main trunk by Semanotus juniperi, but once again it was old with no larvae or adults encountered after another exhausting chopping session. At this point, I turned my attention to the ponderosa pine forest across the highway, as I’d noticed some large dying/dead trees here and there that I wanted to check for buprestids. Despite checking every dead or declining pine within eyeshot, I didn’t find a single beetle! This, combined with the earlier fruitless chopping session, sapped my motivation, and I started heading back towards the car. Only a few A. diffusa? on the flowers of Opuntia polyacantha var. erinacea and Heterotheca hirsutissima (harsh false goldenaster—family Asteraceae) momentarily captured my attention on the way back.
Opuntia polyacantha var. erinacea (Mojave pricklypear)—yellow-flowered form.
As I neared the car, I saw a nicely blooming Purshia stansburyana and beat a nice series of Anthaxia (Haplanthaxia) caseyi from it. I’m not sure if the population in this area is assignable to any of the currently recognized subspecies, so I’ll be interested to study them closer and compare them to other unassignable populations I’ve found in other parts of Utah and Arizona. Right before I reached the car, I saw another juniper that begged “chop me.” I complied and then hated myself for it, as the result was the same as all the other junipers I’ve chopped into since finding that first one with Semanotus juniperi in it. With that, I said goodbye to the Kaibab Plateau and headed north towards Ponderosa Grove Campground near Coral Pink Sand Dunes north of Kanab, Utah.
Clytrine leaf beetle on flower of Purshia stansburyana (Stansbury’s cliffrose).
I reached the area around Coral Pink Sand Dunes (Kane Co., Utah) by mid-afternoon. My favorite campground in that area is Ponderosa Grove Campground—it’s large, spacious campsites are not only well shaded by the namesake, unique-for-the-area grove of massive ponderosa pines, but it is also located right across the road from Moquith Mountain Wilderness Study Area, a BLM-managed area with easy access to the northern portion of the Coral Pink Sand Dunes system (for those who may be asking, this portion of the dune system lies outside the boundaries of Coral Pink Sand Dunes State Park, which protects the only known habitat of the highly vulnerable Coral Pink Sand Dunes tiger beetle, Cicindela albissima).
After picking a campsite (I was glad to see only a few sites occupied) and unloading my gear, I hightailed it to the dunes with one objective—find Chrysobothris nelsoni (family Buprestidae). I collected this species before on my previous trip here back in late June of 2023, but I spent a day and a half looking for it and managed to only a small handful of specimens. I thought the earlier timing might be better, but Norm Woodley was here a couple of weeks before and did not see the species, giving me reason to be also skeptical.
Looking across the dunes at Moquith Mountain Wilderness Study Area.
On the way to the dunes, I set out a yellow bottle trap and sweet red wine-baited jug trap in the sandy juniper/pine woodland bordering the dune. Upon entering the dunes, I immediately started seeing the host plant, Eriogonum alatum (winged buckwheat—family Polygonaceae), a distinctive plant with a basal rosette of linear leaves and, on some plants, a tall stem bearing the inflorescence. One plant in particular, right at the dune entrance, spoke to me saying “look at me.” I don’t know why, but I went over to it, tapped the basal rosette over my net, and off fell a nice large female C. nelsoni! Well, that was fast. I looked at a couple more plants and saw on a second adult (this one a smaller male) sitting head down at the base of the inflorescence stem—two specimens on the first three plants I looked at!
Chrysobothris nelsoni on basal rosette of Eriogonum alatum (winged buckwheat).
Chrysobothris nelsoni on basal rosette of Eriogonum alatum (winged buckwheat).
Chrysobothris nelsoni on stem base of Eriogonum alatum (winged buckwheat).
I found quite a few more (although not quite at that same frequency) over the next hour or so before they seemingly just disappeared. I noted the lateness of the hour and wondered if they have a ‘bedtime’—perhaps they burrow into the sand around the base of the plants for the night—and started back towards camp, picking up a few Eleodes caudifera lumbering across the surface of the sand along the way. I decided at that point, now that I had a nice series of the beetle, to bring the “big camera” over the next morning and try to get much nicer photos of the beetles on their host plant that what I can achieve with this iPhone.
Eleodes caudifera lumbers across the sand.
It had been a long day by that point—I was both famished and exhausted and needed a bit of time to rest and refuel. I had brought two salmon filets along with me, which should have been enough for two meals, but I was so ravenously hungry that I cooked and ate both.
Chill time at Ponderosa Grove Campground.
The rest and food gave me a bit of a spark, and as sunset approached I was inspired to set up the blacklights. Conditions were not close to ideal—a waxing gibbous, nearly full moon along with cool(ish) temperatures are usually enough to kill blacklighting. However, it was warmer than the past several nights at Jacob Lake (1300 ft higher elevation), so I compromised by setting up only the two ultraviolet lights (which I can run right off the car batter) but not the mercury-vapor lamp (which would have required hauling out and running the generator).
Not long after I turned the lights on, I noticed the bright, unmistakable glow of a mercury-vapor lamp at the far other end of the campground. I was like “That has to be an entomologist!” so hiked on down to introduce myself. As I entered the campsite, a man approached me and said “Hello, Ted.” Now I’m thinking okay we’ve met before, but I’m a dummy with poor social skills because I don’t recognize him. He said “My name is Mike.” The omission of his last name had me doubly thinking that I was an idiot because the mention of his name still wasn’t enough to trigger my memory of his last name or who he even was. When I asked him his last name, he said Rashko. I recognized that name instantly—he is the person who discovered Acmaeodera rashkoi, recently described by Rick Westcott and one of the species I had targeted on this trip. I told him of my plan and asked him how he knew who I was. It turns out he is a longtime follower of this blog and had seen my license plate (MOBUGS) earlier in the day. He was traveling from his home in Oregon to Flagstaff to meet his family and stopped here to spend the night and see what he could collect. We had a wonderful time chatting about the art of collecting and about colleagues we know (especially Rick, whose ears were burning I’m sure). I showed him the nice series of C. nelsoni that I’d gotten earlier in the day and told him we could go back in the morning before he left so that he could get some. We got so involved talking that we forgot to even look at his sheet to see what insects had come in until a Polyphylla uteanus (Coral Pink Dunes June beetle—family Scarabaeidae) smacked into his head and bumbled its way over to the sheet (Mike let me keep it). A large female Monochamus clamator also landed on the sheet (which Mike kept).
Eventually we said our goodbyes, and I wandered back to my campsite where I was mildly optimistic that my ultraviolet lights had brought in something. Sadly, there were no beetles of interest, but there was a stunning Hyalophora gloveri (Glover’s silk moth—family Saturniidae) and eventually two small white sphingid moths—all of which I kept for Rich Thoma back home. Success for me that night, however, was not yet out of sight. I made a round to inspect the massive trunks of the ponderosa pines dotting the campground and was rewarded with a nice little series of Zopherus uteanus.
Zopherus uteanus on trunk of Pinus ponderosa (ponderosa pine) at night.
I also found a few of the weirdly explanate Embaphion glabrum (family Tenebrionidae) crawling on the ground beneath the trees. A second round to look at the trees yielded no additional beetles, however, so I turned the lights off and turned in.
The “Big Dipper” prominently graces the western sky during the wee morning hours.
Day 8
Just as I had promised the night before, I wandered down to Mike’s campsite in the morning to see if he wanted to look for Chrysobothris nelsoni. He was already out looking for “beetles in the bush” around his campsite, and together we worked our way over to the dunes. It didn’t take long for me to see one of the beetles in its host plant, which I pointed out to Mike so he could see it and try to catch it himself. That beetle got away, but almost immediately he saw another one on a neighboring plant and succeeded in capturing it. We saw several more, but unlike the previous evening they were faster and more difficult to catch with the rising late-morning temps. Mike caught a couple more (and I one for the record) but had to leave, so we exchanged contact info and said our goodbyes.
Morning on the dunes.
The author (left) with Mike Raschko (right).
Back at the campsite, I looked around a bit to see what else I might collect. There was a nice diversity of plants in bloom, many which could be expected to be visited by buprestid beetles—Sphaeralcea parviflora (small-leaf globemallow), Opuntia aurea (golden pricklypear cactus), Hymenopappus filifolia, etc., but no beetles were seen. There were clumps of Gamble oak and Amelanchier utahensis (Utah serviceberry—family Rosaceae), but beating them produced nothing. The only thing I found was a recently windthrown branch of Utah juniper, which, when I stripped back some of the bark, proved to be in the early stages of infestation by longhorned beetles, probably a Callidium sp. The lack of insect activity (except for C. nelsoni) presented a quandary—should I stay another night (as planned), or should I pack up and head to my next destination (either Leeds Canyon, Utah or Kyle Canyon, Nevada)? I decided it was already too late in the day to head somewhere else—by the time I got there it would be late in the day, and I didn’t relish the idea of searching for an available campsite late with no reservation at such a late hour. I decided I might as well stay put and make the best of it—which I could do by going back over to the dunes and look for more C. nelsoni. The day’s heat, however, was not only making the beetles very difficult to catch but also starting to get to me. Fortunately, distant thunderclouds came closer and closer until they were directly overhead. Rather than rain, however, it was virga, so I got the best of both worlds—an immediate cooling off that was not only comfortable for me but also settled the beetles down without the rain that would have sent me scurrying back to camp.
Virga brings relief from the heat to the dunes.
In the end, I succeeded in collecting another nice series of specimens.
Chrysobothris nelsoni on basal rosette of Eriogonum alatum (winged buckwheat).
By then it was mid-afternoon and I was famished, so I headed back to camp to refresh, refuel, rehydrate, and catch up on my field notes. Comically, as I was writing my notes, I happened to be watching one of the common sagebrush lizards (Sceloporusgraciosus) that had been hanging around the campsite as it bit at and then rejected some type of insect that was crawling on the logpile next to the firepit. I got up to see what it had rejected, and it turned out to be Danosoma brevicorne (family Elateridae), which I am happy to add to the collection.
Common sagebrush lizard (Sceloporusgraciosus).
Danosoma brevicorne on woodpile.
After some chill time at the campsite [it was actually very busy—I wrote my field notes from earlier, charged all my devices using an inverter hooked up to the car battery, and downloaded photos from my “big camera” memory card to the computer], I went back to the dunes to see if I could get “big camera” photo of the beetles. It was touch-and-go at the start—shortly after reaching the dunes it started sprinkling and the wind started picking up. All I could do was wait it out, hope conditions improved, and be ready to bolt if the skies opened up. Just as quickly as it started up, however, it blew over, and I was able to start looking for beetles. As with every other time during this visit, it didn’t take long. The first beetle I found was a bit hidden within the crown of the plant, but I was able to carefully move the leaves out of the way without disturbing the beetle and got a nice series of shots. I was happy with the photos, but I wanted photos that were a little less “cluttered.” The perfect opportunity for such arose when I saw a beetle sitting out near the tip of a leaf. It was not in the best position—other leaves were partially blocking it from view, so I carefully grabbed the leaf at the base and gently pulled until it detached from the plant. Fortunately, the beetle wasn’t phased by the tugging and continued to sit calmly on the leaf. I wanted a blurred pink sand background, which I thought would look spectacular behind the brilliant green color of the beetle, so I stuck the base of the leaf in the sand to prop it up and adjusted the angle and distance in concert with my camera and flash settings until I achieved the desired effect. I’m super happy with how some of these photographs turned out, so look for them to appear in a future post. I’m probably lucky that the mini-storm moved through when it did, as the cool conditions likely calmed the beetles down and made them more willing subjects. By the time I finished photographing the second beetle, the sinking sun signaled a dinner bell, and I walked back to the campground super satisfied with how this visit had turned out.
After dinner, I turned the ultraviolet lights on despite the just-shy-of-full moon and customary coolish temperatures. I didn’t expect anything to show up, but you don’t know if you don’t try (nothing ever showed up!).
Mustard makes everything fancy in the field.
While waiting for nothing to come to the lights, I made several rounds of the large ponderosa pines, expanding the circuit to include some further toward the west end of the campground. As with the night before, I found a half dozen Zopherus uteanus crawling on the trunks (one was up too high to reach, though, and when I knocked it down with a stick it disappeared into the thick vegetation below the tree). I’d really like to know what these guys are up to during the day (hiding in the leaf litter at the base of the trees?) and what the larvae are doing (no idea!), but they certainly seem to be associated with pines (I’ve also collected Zopherus concolor at night on the trunks of Colorado pinyon pine). I also found a few more tenebrionid darkling beetles, including another Embaphion glabrum, crawling on the sandy ground beneath the trees. I expanded my search to include the trunks of some of the large Utah junipers, finding a few more tenebrionids on them.
Embaphion glabrum in ponderosa pine grove at night.
With midnight approaching, I soaked in my last bit of experience at the place before retiring for the night and leaving the next morning.
A waxing gibbous, almost full moon rises high above the campground.
Day 9
I left Ponderosa Grove Campground about 9:30 am with the plan to spend the next couple of days in Kyle Canyon and Lee Canyon northwest of Las Vegas. The drop down from the Colorado Plateau via the Virgin River Canyon was long the most spectacular stretches of freeway I’ve ever seen, but the sad reward waiting at the bottom was searing +100°F heat (the highest I saw registered on my car’s thermometer was 108°F!). Fortunately, turning off I-11 and heading west on Kyle Canyon Road gradually gained elevation. Before reaching the canyon proper, however, I had one of the trip’s top goals to take care of—setting a bottle trap for the recently described Acmaeodera raschkoi (recall that I encountered the namesake of this species, Mike Raschko, just two days prior at Ponderosa Grove Campground). I found the type locality no problem (where the modest gain in elevation had reduced the temperature to only 100°F!) and also found the trap that Mike had just set the day before we met.
Lower Kyle Canyon Rd—type locality of Acmaeodera raschkoi.
I placed yellow bottle trap about 59 m to the west from Mike’s trap and a blue bottle trap about 45 m to the east. There was no reason to stay at the locality and try to collect, as things were super dry, the only green vegetation seen besides the Yucca jaegeriana (eastern Joshua tree—family Asparagaceae) dotting the landscape was a small Cylindropuntia ramosissima (branched pencil colla—family Cactaceae).
I had originally planned to camp lower down in the canyon at Kyle Canyon Campground, but by the time I got there it was already nearly filled to capacity. There were a couple of campsites still available, but the campground as a whole had a noisy, crowded vibe that wasn’t my cup of tea. I decided to take a chance and head further up the mountain to Hilltop Campground to see if I could find something more to my liking. It was a short drive up the mountain, and this campground also was nearly filled to capacity. However, it was a much quieter vibe, and among the three campsites still available was one that was isolated from all the others on the side of the mountain with spectacular views across the canyon and down into the desert below. Also, the 8300 ft of elevation offered much cooler conditions—a welcome change from the searing temperatures I had endured earlier in the day. It was perfect!
View from Hilltop Campground, Spring Mountains, Nevada.
I quickly set up camp and began looking around. Not far from the campsite I found a wind-thrown branch Utah juniper, and slicing into the bark I found a dead adult Semanotus sp. prob. caseyi amplus (not as exciting as S. juniperi, but still a nice find) and a small scolytid bark beetle boring an oviposition gallery. I did a bit of chopping into the bark and found small new cerambycid galleries (probably either Callidium or Semanotus) and some very large frass-filled galleries at the larger end that may be Semanotus juniperi. I found the frass-plugged entrance hole to the sapwood —a sign that the beetle had not yet emerged—and chipped away on either side of the gallery into the sapwood until I saw the large cerambycid larvae sitting it it. This confirms that the wood is actively infested, and I’ll cut it up and bring it home for rearing. At the empty campsite next to mine, I found a small, recently dead Abies concolor (white fir—family Pinaceae), and closer inspection of the trunk revealed an adult Dicerca tenebrosa tenebrosa, and on a return trip to the tree I saw another one (but too high up to capture ☹️). I also hung a red wine-baited jug trap just south of the campsite. There wasn’t much else going on in the area and it was getting late, so I got dinner started.
Sunset at Hilltop Campground.
I didn’t even consider setting up lights—the combination of a full moon and the cool, windy conditions that typify sites at this high of an elevation made the chance of success highly unlikely (in fact, it got so cool that I needed to pull on a fleece pullover). That did not, however, mean I could not do any night collecting—examining tree trunks has become a favorite strategy of mine that can be done on almost any night regardless of temperatures or wind. Trees under stress or recently dead (as well as recent wind throws or woodpiles) are especially good to look at, and I had noticed several during my earlier foray that I made a point to check. At the same time, I have also learned not to ignore living, seemingly healthy trees, as these can also harbor interesting beetles. Of course, the very first tree I headed for was the recently dead white fir on which I had collected Dicerca tenebrosa a few hours earlier, and I was rewarded right off the bat with an unusually small Zopherus uteanus. I wondered if this might be an interesting locality for the species, but I saw the species was recorded from Kyle Canyon in a review of the genus by Triplehorn (1972) (at which time it was still placed in the family Tenebrionidae). I quickly found another individual, this time on the trunk of a large Utah juniper—interestingly, the first non-pinaceous host on which I’ve found the species (although still a gymnosperm).
Zopherus uteanus on trunk of large Juniperus osteosperma (Utah juniper) at night.
What I was most anxious to check, however, was a large Pinus monophylla (single-leaf pinyon pine) that I had seen nearby with a long, twisting scar from a lightning strike gashing down the trunk—surely there would be something on that (there wasn’t despite checking it repeatedly for the next couple of hours). What did produce beetles, though, was a large, recently wind-thrown branch from that very tree laying on the ground nearby—two species and multiple specimens of each, one (Oeme? sp.) searching frenetically back and forth along the branch, and the other (Haplidus? sp.) in the form of a mating pair. I found it interesting that my inspection of the branch earlier during the day produced nothing.
Oeme? sp. on fallen branch of Pinus monophylla (single-leaf pinyon pine) at night.
Haplidus? sp. mating pair on fallen branch of Pinus monophylla (single-leaf pinyon pine) at night.
At this point, the night was already a reasonable success, but the greatest success lay just ahead. I had noticed a few large Utah junipers that showed evidence of infestation by Semanotus juniperi—or at least that what I presumed based on what I had learned about that species in the Kaibab Plateau a few days earlier. Not that I thought I would see adults of that species, but I figured the trees would have to be under some stress and might attract other beetles (I had already collected Z. uteanus off of one a few minutes prior). The first one I checked had nothing on it, but when I checked the second one I noticed a large black longhorned beetle on the trunk underneath some shredded bark. I carefully removed the overlying bark to get a better look at it and quickly realized that it was, indeed, S. juniperi! As I prepared to take a photograph, I noticed movement a bit higher on the trunk, and there sat a second individual! In the fraction of a second that followed, the memory of all the chainsaw work I had done a few days earlier in an effort to rear proper specimens flashed through my mind, yet here before me now were two live adults on their host in the wild. I presume the tree is attracting the adults and that there are already numerous individuals inside of it, as I found large swaths of larval galleries under the bark but no obvious adult emergence holes. The tree itself looks healthy and shows no outward sign of stress, and were it not for the evidence of larval galleries I wouldn’t have even suspected it was infested. As with Z. uteanus, this species also has been recorded from Kyle Canyon (Hammond & Williams 2013).
Semanotus juniperi on trunk of large Juniperus osteosperma (Utah juniper) at night.
Over the next hour, I continued inspecting trees in the area, but especially those on which I’d found beetles, and eventually that effort was rewarded with a third S. juniperi on the same tree I collected the previous two. The final collection of the night occurred just after that, when I found not one but two more Z. uteanus, this time on the trunk of P. monophylla. I made one more quick round of the trees, but as it was now midnight I accepted the bounty of the night and turned in.
Days 10 & 11
Unfortunately, I had to end the trip rather abruptly due to a confluence of circumstances at home. The final straw was the rapid decline of Berlioz—our 20-year-old cat (only lifelong cat lovers will understand the bond between a man and his cat). It was not a surprise, and in the morning as soon as I was able to break camp, I left Kyle Canyon and spent the next two days blasting north on I-15 and west on I-70. Sadly, I wasn’t able to make it home before he passed. I’ve had many cats over the course of my life, but King Berlioz was the best!
Buprestidae (plus one Elateridae) selected from specimens in the insect collection at the Illinois Natural History Survey sent for identification.
I’ve been working hard the past couple of weeks on one of three batches of Buprestidae in the insect collection at the Illinois Natural History Survey sent to me for identification. I’ve already completed one of these batches, which included all specimens strictly from Illinois. This second batch includes specimens from the not only the rest of North America (sensu lato), but South America and the West Indies as well. Out of ~450 total specimens, in this batch, I identified 167 species, with eight new state and two new country records.
Why do I do it? While I’d like to say it’s because I’m just a nice guy, and I do genuinely enjoy helping to improve the level to which public insect collections are curated, my motives aren’t completely unselfish. First, it is a chance for me to glean the specimens for new data in the form of unknown distributional and host plant records. This is a main area of interest for me, and the data provide fuel for my publications on the subject. Second, and perhaps, it is a chance to encounter species that are absent or poorly represented in my cabinets. Most public collections allow specialists to retain a certain number of duplicates of the species they identify. This allows me to increase the representation of species in my collection, which in turn increases its usefulness as a resource for even further identifications. (In this particular case, the INHS collection manager graciously allowed me even to retain a handful of singletons in exchange for some other species that helped to improved the representation in their collection.) Finally (and perhaps most importantly), regularly examining new material helps to continually refine my understanding of species concepts. Sometimes this causes me to reassess a previous identification in light of an improved understanding (a reference collection is only useful if its representatives are correctly identified).
For those wondering, here is what 165 species of Buprestidae looks like:
I’ve been spending time lately identifying beetles sent to me from the collection of the Illinois Natural History Survey in Champaign-Urbana. There are a lot of old specimens in the batch, which means I not only have to identify the beetles themselves, but also interpret their often cryptic, handwritten labels (a common feature of insects collected before the advent of computers and word processing programs). This particular specimen (and its label) had me confounded for quite a while before I finally figured it out.
I recognized the species instantly as Euchroma giganteum, perhaps the largest jewel beetle in the world (interestingly, there is a related but slightly smaller species called Euchroma goliath), and the obviously very old locality label on it stated simply “Peru”. That wasn’t the problem—the species is known to occur there, but the unusually dark coloration and near absence of any pubescence (hairs) on the underside are atypical for the species. There are, however, several described subspecies, including two occurring in Peru, and I suspected it might represent one of them. Unfortunately, I had no identified specimens of any of the subspecies with which I could compare the specimen, nor was I able to find images of any of the subspecies online. All I had was the literature, and most of it was written in German and French and published more than 100 years ago! However, as fortune would have it, a fellow jewel beetle enthusiast (Joshua Basham) had recently sent me translated summaries of the key papers, and after considerable study comparing the characters of the specimen with the descriptions in the literature, I decided that the specimen must represent the subspecies Euchroma giganteum harperi. There was a problem, however—that subspecies doesn’t occur anywhere near Peru. Instead, it is found in the West Indies and extreme northeastern South America (Guyana). This meant that either my identification was wrong, or the specimen is mislabeled. The latter is not an uncommon occurrence with old specimens in old collections and of uncertain provenance. Still, I could not be sure either way. Perhaps the second, much more cryptic label on the specimen could provide clues to help confirm my identification.
The first two lines clearly state the species name, but the rest of the label was simply too illegible to decipher. I studied the label with a magnifying glass, but that didn’t help, nor did putting it under a dissecting scope. As a last resort, I took a photograph of the label to post online and ask for help in deciphering it. As I was preparing the post, I noticed the “har-“ at the end of the third line, and it dawned on me that this was the first part of the subspecies name that I had determined the specimen to represent. The rest of the label then quickly fell into place— the full subspecies name with authors (Euchroma giganteum L. [= “Linnaeus”] ss. [= “subspecies”] harperi Sharp). (Now that I know this, I cannot look at the label and not see it.) With this, I felt much more confident with my identification, so much so that I took the final step and placed my own (much more legible) identification label on the specimen (along with an annotation noting the locality error). In all, I probably spent an entire hour on this specimen, but the benefit (besides the satisfaction of finally succeeding) is that I gained a much firmer understanding of the species and subspecies distinctions, which allowed me to revise the identifications of a few specimens in my own collection (though I still lack the other subspecies).
Welcome to the 16th “Collecting Trip iReport” covering this season’s third—and final—insect collecting trip to eastern and southern New Mexico. This trip occurred during September 9–18, following “Act 2” on June 17–28 and “Act 1” on May 14–25, and had the objective of retrieving 18 “jug traps” and six “bottle” traps placed on the first trip. Unlike the previous two trips, I traveled solo this time, but I still managed to visit 16 different localities—14 in New Mexico, one in Oklahoma, and one in Kansas.
3.2 mi SSW of Piqua Woodson County,Kansas On my way to Black Mesa State Park (in the northwestern corner of Oklahoma) where I will be spending the night, I stopped at this abandoned quarry at the suggestion of Dan Heffern, who grew up in the area and collected his first Megacyllene decora (amorpha borer) here as a teenager on the Amorpha fruticosa that grows commonly on the steep banks surrounding the now water-filled reservoir.
Abandoned quarry lined with Amorpha fruticosa.
The timing seemed right, as patches of goldenrod (Solidago sp.) surrounding the reservoir were also just coming into bloom, but no adults were seen on either the stems of amorpha or the flowers of goldenrod. I did get to see a garter snake try (and fail) to catch a leopard frog. The snake had hold of the frog by one of its hind legs, but the frog used its other hind leg to eventually free himself while peeping desperately. I was kind of rooting for the frog, even though it would have been interesting to watch the snake as it ingested its prey.
A common garter snake (Thamnophis sirtalis) captures—momentarily—a leopard frog (Lithobates sp.).
I was hoping to make it to Black Mesa State Park (at the far western end of the Oklahoma panhandle) before dark, but the sun setting on a lonely stretch of highway well beforehand told me that wouldn’t be possible.
The sun sets in a lonely stretch of highway in far southwestern Kansas.
Black Mesa State Park West Canyon Campground Cimarron County, Oklahoma I arrived at the park well after sunset, but the tent went up quickly and I found a Cicindelidia punctulata (punctured tiger beetle) on the exposed clay after I finished.
Cicindelidia punctulata (punctured tiger beetle—family Cicindelidae) on clay exposure in juniper chaparral. The greenish cast suggests the population in this area represents an integrade between the nominotypical eastern subspecies and the western C. p. chihuahuae.
This prompted me to put the headlamp on and walk the roads to look for beetles. Amblycheila cylindriformis (Great Plains giant tiger beetle) has been taken in the park, though in July (September is likely a bit too late). Nevertheless, I walked to the spot where it had been found about a mile up the road, scanning the road with my headlamp as I walked.
Phoetaliotes nebrascensis (large-headed grasshopper—family Acrididae) in juniper chaparral at night.
A few big black Eleodes darkling beetles gave me the occasional false start, but in the end I did not find the tiger beetle. I did, however, get to see a beautiful 1st-quarter moonset amidst light high clouds and a starry starry night.
A waxing crescent moon glows feebly in the western sky.
Day 2
0.1 mi S Hwy 325 on D0035 Rd Cimarron County, Oklahoma There is an iNat record of an Amblycheila cylindriformis (Great Plains giant tiger beetle) larval burrow at this spot. Even though the record is a couple of years old, I thought I’d stop by and see if I could find one for myself. I did, fairly quickly I might add, right along the top edge of the steeply-sloped clay embankment alongside the road.
Amblycheila cylindriformis (Great Plains giant tiger beetle—family Cicindelidae) larval burrow at top edge of sloped clay embankment in mesquite chaparral.
A bit more searching nearby revealed the carcass of an adult embedded in the clay slope—I dug it out (in pieces) and saw the abdomen covered with a bit of spider webbing. I’m still not sure how it came to be embedded within the clay with only the head and probotum exposed.
Amblycheila cylindriformis (Great Plains giant tiger beetle—family Cicindelidae) cadaver embedded in sloped clay embankment in mesquite chaparral.
Amblycheila cylindriformis (Great Plains giant tiger beetle—family Cicindelidae) cadaver excavated from sloped clay embankment in mesquite chaparral.
Mills Rim Campground Kiowa National Grassland Harding County, New Mexico It took a couple of hours of driving to get to this, the first of six trap locations I have in New Mexico. I was happy to see all three jug traps still hanging, intact, and full of catch. All three had lots of Euphoria (mostly fulgida) and a fair number of elaterids, but other than a single Tragosoma sp. (I haven’t collected one of these in many years!) in the SRW trap the cerambycids seemed limited to just a few elaphidiines. The bottle trap had lots of bees (for Mike) and Euphoria kerni, but I did see a few Acmaeodera spp. and—remarkably—another Tragosoma sp. (an unusual catch for a bottle trap!).
Rim above Mills Canyon.
While I was checking the traps, I kept an eye out for tiger beetles and flower-visiting longhorns and buprestids. I did see one Acmaeodera rubronotata on flowers of Gutierrezia sarothroides (broom snakeweed), but this was the only one despite looking at many flowers and I chose not to linger.
“San Jon Hill” 9.3 mi S of San Jon Quay County, New Mexico Another two-hour drive brought me to “San Jon Hill”—a sandstone escarpment at the edge of a plateau featuring juniper/oak/pinyon woodland. Again, all three of my jug traps were still hanging and intact, and the SRW and SRW/EtOH traps were full of beetles! The EtOH trap, on the other hand, was bone-dry with far fewer specimens. Like Mills Rim, Euphoria (again, mostly fulgida) were dominant, but I was elated to see multiple Enaphalodeshispicornis (a species I’ve never collected) along with a few E. atomarius in all the traps. The SRW/EtOH and EtOH traps also had several Aethecerinus wilsonii—a great find that I first got near Kenton last year. There was also a Stenaspis solitaria in the EtOH trap along with the expected smattering of elaphidiines and elaterids in all three traps. The bottle trap also was overwhelmed, primarily with bees (for Mike), but I did see a fair number of Acmaeodera spp. (I’m hoping this includes A. robigo, one of which was in this trap last time).
Aethecerinus wilsonii (family Cerambycidae) taken in EtOH-baited “jug” trap in juniper/oak/pinyon woodland on sandstone escarpment.
Stenaspis solitaria (family Cerambycidae) taken in EtOH-baited “jug” trap in juniper/oak/pinyon woodland on sandstone escarpment.
Enaphalodeshispicornis (family Cerambycidae) taken in EtOH-baited “jug” trap in juniper/oak/pinyon woodland on sandstone escarpment.
Otherwise, I saw little insect activity despite the abundance of plants in flower—a Eusattus reticulatus (sand darkling beetle) crawling on the ground being my only other capture.
Eusattus reticulatus (sand darkling beetle—family Tenebrionidae) in juniper/oak/pinyon woodland on sandstone escarpment.
Continuing further south towards Oasis State Park, there is a field of wind turbines that, on my previous passing, provided a picturesque scene. This time again provided such opportunity.
Bovines bunch beneath a wind turbine.
Oasis State Park Roosevelt County, New Mexico The drive from my last stop was supposed to be only 1½ hours, but having to reroute after sitting a while for a motionless train and an unexpected but welcome FaceTime call with my grandson conspired to delay my arrival at the park until well after darkness had settled. No problem—I’ve set up many a tent in the dark, and the burger cooked on the grill afterwards was no less tasty. (I also had sufficient reception to relish watching Kamala Harris clean TFG’s clock, which was followed “Swiftly” by a major endorsement and only served to further buoy my mood.) After the evening’s entertainment, I set out to check a couple of light sources in the park to see if they’d attracted any beetles—a small utility building near the RV campground, and a mercury-vapor streetlight closer to the tent campground. Tenebrionids abounded in number and diversity under both light sources, and I took from each several examples of the weirdly-explanate Embaphion muricatum.
Embaphion muricatum (family Tenebrionidae) under mercury mercury-vapor light in sand dune habitat.
Scarabs were limited mostly to small melolonthine, but I did pick up nice series of at least two species of bolboceratine geotrupids.
Eucanthus sp. (family Geotrupidae) under mercury mercury-vapor light in sand dune habitat.
I had hoped to encounter the sand dune endemic longhorned beetle, Prionus spinipennis (I don’t know if it actually occurs here), but on my last visit in June I encountered its early-season counterpart P. arenarius. None were seen, however, so I am hopeful that I find it further south at Mescalero Sands, where it is known to occur and where I plan to go in the next couple of days.
Day 3
Passing through Portales in the morning, I did a double-take as I passed this “low rider.” I circled around the block so I could get another look, and for the rest of the day I had the eponymous song from Cheech & Chong’s Up In Smoke as a brain-worm.
“All my friends know the low rider (yeah)”
Portales Recreation Complex Roosevelt County, New Mexico My first stop for the day turned out to feature little-disturbed (i.e., ungrazed) dry grassland surrounding the ballfields. There are some iNat records of a couple of fall-occurring longhorned beetles (Megacyllene angulifera, Tragidion coquus) from here, so I thought I’d try my luck as I head south towards Mescalero Sands. The season felt a little early, as even though there were plenty of Helianthus annuus (annual sunflower) in bloom, the Gutierrezia sarothrae (broom snakeweed) was not. Still, I checked the sunflowers but saw only Chauliognathus basalis (Colorado soldier beetles) in abundance. The visit was “not for naught,” however—walking the sandy loam 2-track through the lower west side I encountered three species of tiger beetles: Jundlandia lemniscata rebaptisata (rouged tiger beetle), Cicindelidia punctulata chihuahuae (Chihuahua punctured tiger beetle), and—my favorite—Cicindelidia obsoleta obsoleta (large grassland tiger beetle).
Jundlandia lemniscata rebaptisata (rouged tiger beetle—family Cicindelidae) on sandy-loam 2-track through dry grassland.
Cicindelidia punctulata chihuahuae (Chihuahua tiger beetle—family Cicindelidae) on sandy-loam 2-track through dry grassland.
Cicindelidia obsoleta obsoleta (large grassland tiger beetle—family Cicindelidae) on sandy-loam 2-track through dry grassland.
“Mydas Alley” 6.6–6.9 mi S of Floyd Roosevelt County, New Mexico There are some iNat records of several interesting tiger beetles at this spot—an endless dry grassland with a sandy/red clay 2-track cutting through it. These include Cicindela formosa rutilovirescens (Mescalero Sands tiger beetle)—a main target for the trip, Cicindelidia obsoletaobsoleta (large grassland tiger beetle), and Cicindelidia nigrocoerulea (black sky tiger beetle).
Sandy-loam 2-track at “Mydas Alley.”
I didn’t have much expectation for the latter, since the record is based on a single, dead individual, and I’d just found C. o. obsoleta at the previous site closer to Portales, but I was really hoping to find C. f. rutilovirescens. Almost immediately I caught what I thought could be C. nigrocoerulea on the sandy/red clay 2-track near where I parked; however, it turned out to be the similar Cicindelidia punctulata chihuahuae (Chihuahua punctured tiger beetle), distinguishable by the single seta on the basal antennomere instead of two (an eyeglass on a lanyard around the neck at all times can really come in handy), its subparallel elytra that are slight wider posteriorly rather than subarcuate, and the generally shinier rather than opaque surface of its elytra.
Cicindelidia punctulata chihuahuae (Chihuahua tiger beetle—family Cicindelidae) on sandy-loam 2-track through dry grassland.
I found more C. punctulata further down the 2-track (although they looked more like the nominotypical subspecies due to their dark brown rather than greenish coloration), and I found myself paying attention to almost every C. punctulata that I encountered hoping one might be C. nigrocoerulea. Sadly, none would prove to be the latter (at least based on my examination in the field—subsequent closer examination at home may prove otherwise). I did, however, encounter a single Cicindela scutellaris scutellaris (festive tiger beetle) to add another tiger beetle species to the trip list.
Cicindela scutellaris scutellaris (festive tiger beetle—family Cicindelidae) on sandy-loam 2-track through dry grassland.
At the far end of the 2-track, I noticed something sitting on the stem of Eriogonum annuus (annual buckwheat) and was delighted to see it was Crossideus discoideus—one of the genera of fall-active longhorned beetles that I was hoping to encounter on the trip.
Crossidius discoideus (family Cerambycidae) on stem of Eriogonum annuum (annual buckwheat) in dry grassland.
A bit of careful searching in the immediate vicinity revealed more individuals on the stems and flowers of the plants growing in the area, and on the way back I found another C. discoideus on the spent flower of Heterotheca subaxillaris (camphorweed) near the front part of the 2-track. I had not, however, seen my main objective—C. f. rutilovirescens—and was beginning to resign myself to getting skunked on the species. As I reached the car and turned to go briefly down the 2-track to the east, however, I saw one on the more wide open section of the 2-track, then quickly saw another! Those would be the only two I would see until I turned back and approached the car again, seeing the third and final individual of the stop.
Cicindela formosa rutilovirescens (Mescalero Sands tiger beetle—family Cicindelidae) on sandy-loam 2-track through dry grassland.
I was hoping to get field photos with the “big” camera, but their scarcity made me decide to wait for my next chance at Mescalero Sands, where I hope to find them as well. The number of tiger beetle species seen on the trip now stands at six (if I include the Amblycheila cylindriformis carcass seen yesterday in the Oklahoma panhandle).
Presler Lake Chaves County, New Mexico Over the past couple of years, I have begun to rely ever more heavily on the natural history platform iNaturalist as a source for finding promising localities for interesting species. The first two localities I visited today were both found prior to my departure on this trip while searching for localities where species of Buprestidae, Cerambycidae, and Cicindelidae have been recorded. This locality was not found before I left, but rather after I left the last spot and saw that several species of beetles, including Eunota togata globicollis (alkali tiger beetle), had been reported from the area around this alkaline lake.
Alkaline flats around Presler Lake.
As I walked toward the lake, I noticed lots of Isocoma pluriflora (southern goldenbush), normally a good host for Crossidius longhorned beetles, that was already past bloom and wondered if any Crossidius would still be found on them. As I reached the lake margin, I saw a Crossidius suturalis male, but it was instead perched on Atriplex canescens (four-winged saltbush). No sooner than after I had photographed the beetle, marked its location, and made an entry in my notes, I noticed another—this one a big female perched on the spent bloom of I. pluriflora.
Crossidius suturalis suturalis (family Cerambycidae) on flowers of Isocoma pluriflora (southern goldenbush) along margin of alkaline lake.
The locality where E. t. globicollis had been recorded was on the far west side of the lake, so I walked the lake margin in that direction while checking the saltbush and goldenbush along the way. It was quite a while before I found another C. suturalis on I. pluriflora, and on another plant very nearby I found a nice little cetoniine scarab: Euphoria pilipennis—a species I’ve never collected before.
Euphoria pilipennis (family Scarabaeidae) on flowers of Isocoma pluriflora (southern goldenbush) along margin of alkaline lake.
The walking and checking was eating up time, however, and I noticed that the sun was beginning to dip rather low in the western sky. I needed to focus on finding E. t. globicollis if I wanted to get back to the car before it got dark (I would still have another hour’s drive to get to my campground near Roswell). I’d walked towards the lake margin earlier, going as far as I could go toward the water before my shoes started sinking into the thick, alkaline-encrusted mud, and didn’t see any tiger beetles, so I was not really expecting to see the species (it had been recorded there during the height of the summer). Remarkably, right as I made my closest approach to the spot, I saw one—E. t. globicollis running on the wet mud near the water’s edge of the alkaline lake.
Eunota togata globicollis (alkali tiger beetle—family Cicindelidae) along wet margin of alkaline lake.
I walked the margin all the way back to where I needed to divert back to the car and saw several more individual, but I was unsuccessful in capturing any beyond the first one!
Bedtime for tiger beetles approaches.
As I neared the car and the sun sank behind the horizon, I assumed the day’s collecting was done. Just then, I noticed a Gyascutus sp. sitting on Atriplex canescens (based on location, I suspect it is G. planicosta obliteratus), and within a few steps from there I saw another C. suturalis on I. pluriflora. This prompted some additional looking in the area around the car, but eventually the light became too dim to allow effective searching. It was an impromptu stop at an unlikely location and ended up being a successful stop for the trip.
Day 4
Palmer Lake Campground Bottomless Lakes State Park Chaves County, New Mexico I arrived at my favorite campsite in this campground well after dark last night, so I was pleased to see the area as green as could ever be imagined when I awoke this morning. Copious blooms of Allionia incarnata (trailing four o’clock) and Kallstroemia parviflora (small-flowered carpetweed) were blanketing the adjacent gypsum/red siltstone slopes.
Allionia incarnata (trailing four o’clock—family Nyctaginaceae) on slope below gypsum/red siltstone escarpment.
Not much of note was seen on the blooms, but I did find the fascinatingly-inflated Cysteodemus wislizeni (black bladder-bodied blister beetle) crawling on the ground amongst them.
A quick walk up into the draw behind the campsite also revealed little besides a variety of darkling beetles (family Tenebrionidae)—some of them monstrously-sized. However, once back at the campsite I found a rather beat up right elytron of what I believe to be Amblycheila picolominii (plateau giant tiger beetle). Since I included A. cylindriformis (Great Plains giant tiger beetle) to my running list of tiger beetle species seen on the trip, I’ll add this one as well as #8.
Amblycheila picolominii (plateau giant tiger beetle—family Cicindelidae) right elytron on slope below gypsum/red siltstone escarpment.
Bitter Lake National Wildlife Refuge Chaves County, New Mexico I found another iNaturalist record of Cicindelidia nigrocoerulea (black sky tiger beetle) at this refuge, which is located just north of Bottomless Lakes. I didn’t find this species at the previous spot where I looked for it (as far as I know), and since the refuge is managed by the U.S. Fish & Wildlife Service, I can only “look but don’t touch” (no collecting permit). Because of this, I decided to make today a “big camera” day instead of an “insect net” day.
Alkaline flats at Bitter Lake National Wildlife Refuge.
Tiger beetles were scarce on the dry alkaline flats where the record was taken (albeit, many years ago and in July) and limited to the über-common Eunota circumpicta johnsonii (Johnson’s tiger beetle) and Eunota togata globicollis (alkali tiger beetle). I’ve photographed both of these species already but attempted a few shots of each anyway to get some practice (photographing tiger beetles is challenging at best, requiring patience, persistence, and a willingness to get down on the ground no matter how dirty you will get). I found it difficult to approach either species (but especially the latter) in what was by then the heat-of-the-day, and the only shots I managed were of two individuals (one of each species)—engaged in shade-seeking behavior. I did find the mostly complete skeleton of what I take to be a common snapping turtle (Chelydra serpentina).
Common snapping turtle (Chelydra serpentina) skull along alkaline lake margin.
The margins of the oxbow lake on the other side of the parking lot were much wetter, and accordingly the tiger beetles were much more abundant there as well. In addition to the aforementioned E. c. johnsonii, which here also was by far the most abundant species, I observed Cicindelidia ocellata ocellata (ocellated tiger beetle)—common throughout the southwest, and Cicindelidia tenuisignata (thin-lined tiger beetle)—much less commonly encountered and a species I’d first seen during my previous trip to Bottomless Lakes in June. I managed to photograph a mating pair of E. c. johnsonii, but try as I might I was unable to photograph C. o. ocellata or C. tenuisignata—a rather deflating failure for someone who prides himself in his tiger beetle photography skills. For now, the iPhone photos that I took last time of individuals of the latter species attracted to ultraviolet light at night will have to do. There was a good amount of Isocoma pluriflora (southern goldenbush) still in good bloom around the parking lot, and I managed to photograph a fine male Crossidius suturalis suturalis on the flowers.
Palmer Lake Campground Bottomless Lakes State Park Chaves County, New Mexico The day’s high heat not only made futile any further attempts to photograph tiger beetles at Bitter Lake, but gave me pause about going out for more collecting as soon as I returned to my campsite—I needed a bit of time to chill. Eventually, however, I worked up the motivation to strap on the pack and grab the net. I had earlier noticed a nice stand of Isocoma pluriflora (southern goldenweed)—a good host for Crossidius longhorned beetles—at the end of the campground road, and that became my first destination. It took a bit of time before I found C. s. suturalis on the flowers, but after working the stand for about an hour I had a nice handful.
Crossidius suturalis suturalis (family Cerambycidae) on flowers of Isocoma pluriflora (southern goldenbush) in saltbush chaparral.
Many other insects were also visiting the flowers, most visibly a large Pepsis tarantula hawk (prob. P. grossa)—which I could not photograph—and numerous colorful blister beetles that I take to be Pyrota concinna—which I did photograph.
Pyrota concinna (a blister beetle—family Meloidae) on flowers of Isocoma pluriflora (southern goldenbush) in saltbush chaparral.
I next visited the small, slightly elevated picnic area next to the campground, where last time I had collected a small series of a nice, large buprestid, Gyascutus planicosta obliteratus, on Atriplex canescens (four-winged saltbush). I saw one yesterday at Presler Lake, and I hoped they might be still hanging around here as well, but no dice. I did, however, notice a small beetle clinging onto the foliage of Neltuma glandulosa (honey mesquite, formerly Prosopis glandulosa), which turned out to be a very late-occurring Acmaeodera mixta. I noticed that the temps were suddenly getting milder, signaling the onset of evening and reminding me to head back to camp since I wanted to drive to Mescalero Sands (about 40 miles away) for some evening/night collecting.
Mescalero Sands Recreation Area Chaves County, New Mexico There are two species of Prionus longhorned beetles endemic to the sand dunes of southeastern New Mexico and western Texas—P. arenarius, which occurs during spring and early summer, and P. spinipennis, which occurs during late summer and fall. I’ve collected the former twice—once several years ago here at this very spot, and again this year at Oasis State Park back in June. I’ve never collected P. spinipennis, however, and figured they should be out by now. I had brought with me a few prionic acid lures, to which the males are attracted (prionic acid is a main component of the pheromones that females of all Prionus species release to call mates), and I also hoped to find and photograph the sand dune subspecies of Cicindela formosa—i.e., C. f. rutilovirescens (which I found yesterday near Portales but did not photograph). Unfortunately, my arrival just 20 minutes before sunset precluded the latter possibility, so instead I hiked into the dunes a short distance to place the pheromone lures and enjoyed a spectacular sunset and moonrise, with the sky morphing from blue to orange before finally turning black.
Mescalero Sands at sunset.
A first-quarter moon rises above a flock of roosting vultures.
The sky morphs from blue to orange.
Sunset impression.
As soon as darkness fell, I began scanning the sand for anything crawling. Darkling beetles (family Tenebrionidae) appeared in numbers and diversity—my favorites, as always, being the weirdly-explanate Embaphion muricatum, which were as common as I’ve ever seen them.
Embaphion muricatum (family Tenebrionidae) in sand dunes at night.
A sand dune endemic Jerusalem cricket, Ammopelmatus mescaleroensis (Mescalero Jerusalem cricket), some of them being quite large, was also quite common.
Ammopelmatus mescaleroensis (Mescalero Jerusalem cricket—family Stenopelmatidae) in sand dune habitat at night.
About an hour after sunset, I finally saw one—a male P. spinipennis walking urgently across the sand in the general direction of the pheromone lure. I was glad my hunch had paid off and waited to see when the next male would arrive.
Prionus spinipennis (family Cerambycidae) attracted to prionic acid lure in sand dune habitat at night.
Sadly, I waited and waited—expectantly walking the dunes in the area around the vicinity of the lure looking for the next one, but it never came. Perhaps I am a bit on the early side of their adult activity period. Nevertheless, one is better than none, and it gives me a reason to look forward to returning to the dunes some other time during the heart of the fall season. After an hour had passed with no other individuals seen, I called it a night and drove back to my camp at Bottomless Lakes, where the pre-dawn sky was a star-studded as I’ve ever seen!
Orion rises in the moonless, early morning sky.
Day 5
7 mi E of Queen, X Bar Rd Eddy County, New Mexico My original plan was to leave today and spend the next two days at Dog Canyon Campground in Guadalupe Mountains National Park just across the Texas state line. That would serve as a base from where I could service the traps that I have on the New Mexico side of the line and also afford me an opportunity to take a day off of collecting and hike the park’s spectacular system of trails. Unfortunately, when I went online a few days earlier to reserve my campsite, I learned that the campground was closed until December due to a water line break! This was a major disruption to my plans, because the only other campgrounds between Bottomless Lakes and Dog Canyon are private KOA-types (ugh!) and the dreadfully ugly Brantley Lake State Park! I decided then to keep my campsite at Bottomless Lakes and just drive to the Guadalupes to service my traps. Afterwards I would drive back and spend an extra night in the far roomier and more beautiful campground at Bottomless Lakes. Again, I was pleased to see the SRW trap hanging and intact, although the reservoir had developed a slow leak and was nearly drained. The catch, however, was still moist, suggesting that the leak had developed only recently and, thus, had no negative impact on data collection. The catch was similar to “San Jon Hill” in that there were numerous Enaphalodes hispicornis and smaller numbers of E. atomarius, Eburiahaldemani, and a variety of smaller elaphidiines. Sadly, the SRW/EtOH trap had self-destructed—the bottom half of the trap was found lying on the ground not far from its still-hanging upper half (w/ bait even in the still-hanging bait bottle). The EtOH trap was also hanging and intact, though the bait bottle was dry (I’m seeing this pattern repeatedly—SRW and SRW/EtOH bait bottles still have some bait after 10 weeks in the field, but EtOH bait bottles are dry); however, there were only a few small elaphidiines representing the cerambycids. The white bottle trap had a decent catch of Acmaeodera spp. and bees (for Mike). However, there wasn’t much else going on insect-wise (the chunky, remarkably rock-like nymph of Leprus sp.—either L. intermedius [Saussure’s bluewinged grasshopper] or L. wheelerii [Wheeler’s bluewinged grasshopper]—notwithstanding).
Leprus sp. (bluewinged grasshopper—family Acrididae) in juniper/oak/pinyon woodland.
The lack of insect activity had me ready to leave as soon as I finished retrieving the traps. However, as I was emptying the last jug trap, I noticed that Dasylirion leiophyllum (smooth sotol) was growing in the area and decided I should check them for Thrincopyge buprestids—colorful species that breed in the newly senesced flowering stalks of the plants. I checked a few without success and suspected it was probably too late in the season to find the adults, then broke an old flowering stalk off of one of the plants and saw the characteristic adult emergence holes of the beetles in the lower part of the stalk. This at least confirmed their presence in the area. Then I saw a plant with a newly senescing flowering stalk. Cutting into the lower portion of the stalk revealed a fresh, frass-packed larval gallery, suggesting larvae are currently working inside the stalk, so I broke the stalk from the plant, carried it back to the car, and cut/bundled it up for transport back home and placement in a rearing box. With luck, the larvae will complete their development to adulthood and emerge next spring.
5.6 mi E of Queen Eddy County, New Mexico On my last visit to the area, I found Cicindelidia laetipennis (polished-winged tiger beetle, formerly C. politula petrophila) just over the Texas state line at high elevations in Guadalupe Mountains National Park. I was hoping to see (and properly photograph) it again this time, but the closure of Dog Canyon Campground nixed those plans. Fortunately, I found an iNat record for the species on the New Mexico side of the line (in fact, less than two miles from my previous trapping spot) and made plans to see if I not only could find it but photograph it with the “big camera.” As it turned out, the habitat was perfect—a wash of exposed limestone on a short 2-track above 5000’ elevation.
Exposed limestone habitat for Cicindelidia laetipennis (polished-winged tiger beetle) in juniper/oak/pinyon woodland.
Portulaca pilosa (shaggy portulaca—family Portulacaceae) in exposed limestone juniper/oak/pinyon woodland.
For the majority of the time I was there, however, I didn’t see any individuals. I did find the occasional Acmaeodera rubronotata on flowers of Eriogonum hieraciifolium (hawkweed buckwheat) and a lumbering Tenebrionidae that I take to be Philolithus aeger crawling on the clay portion of the 2-track.
Eriogonum hieraciifolium (hawkweed buckwheat—family Polygonaceae) in limestone/clay juniper/oak/pinyon woodland.
Philolithus aeger (family Tenebrionidae) on limestone/clay 2-track in juniper/oak/pinyon woodland.
On the way back, however, I saw the first individual, and not too long afterwards I saw the second. These would be the only individuals I would see—not nearly enough to get my camera gear and hike back in an effort to get proper field photos. Once again, my previous iPhone photos will have to do for now.
Back at the car I was about to pack up and move on to my next trap location when I noticed Grindelia nuda (curlycup gumweed) in bloom around the parking area. Since I’d collected a small handful of A. rubronotata on buckwheat flowers, I thought I might check out the gumweed flowers as well. Not only did I find several more individuals of that species, I also found one individual of A. opacula (formerly A. disjuncta).
Acmaeodera rubronotata (family Buprestidae) on flowers of Grindelia nuda (curlytop gumweed) along roadside in limestone/clay juniper/oak/pinyon woodland.
Acmaeodera opacula (family Buprestidae) on flowers of Grindelia nuda (curlytop gumweed) along roadside in limestone/clay juniper/oak/pinyon woodland.
Klondike Gap Rd, Hamm Vista Lincoln National Forest Eddy County, New Mexico As with the season’s previous two visits to this spot, the area looked dry and flowerless. Such conditions rarely warrant making the effort to take a closer look at things, and I wanted to get back to Bottomless Lakes with enough daylight left to search for tiger beetles at an area in the park that I not checked before—Lea Lake Recreation Area. With this in mind, I set about retrieving the traps and was happy to see the SRW trap hanging and intact (this trap was down last time due to rope failure). Also, even after nearly three months, the reservoir was moist and the bait bottle still had bait. There were lots of cerambycids in the catch, including several Enaphalodes hispicornis, E. atomarius, Tragidion coquus, Eburia haldemani, and smaller elaphidiines. The SRW/EtOH trap also, thankfully, was still hanging and in much the same condition as the SRW trap, but I did note far fewer cerambycids. This also seems to be the trend that I have noticed over the last two seasons of comparing these baits (although I must await stats analysis to see how real this is). The EtOH trap was also hanging and intact with plenty of liquid in the reservoir, but the bait bottle was dry (same as other locations), and there were hardly any cerambycids (same as some, but not all, other locations). Sadly, the white bottle trap was completely missing—I even managed to find the exact hole where it was pulled from, but the trap itself was nowhere in sight. This was frustrating, because it was by far the best-performing bottle trap on my last visit. I hate to think that someone deliberately stole it, but the thought is hard to resist—animals (primarily raccoons) often pull traps to eat the catch, but they don’t take the trap with them.
Lea Lake Recreation Area Bottomless Lakes State Park Chaves County, New Mexico I’d been wanting to look for tiger beetles around Lea Lake since I arrived and was planning on today being the day. Unfortunately, the extra time I spent at the previous spots beyond retrieving the traps (i.e., for cutting up the sotol stalk and looking for Cicindelidia laetipennis)—along with an unplanned but needed stop for supplies—resulted in me arriving only 20 minutes before sundown. There was a particular tiger beetle species I was looking for—Cicindelidia haemorrhagica woodgatei (Woodgate’s tiger beetle), of which several observations from here had been posted on iNat. The alkaline flats right alongside the lake looked perfect for tiger beetles, and I immediately began finding and collecting a variety of tiger beetle species.
Lea Lake.
Most were expected—Eunota circumpicta johnsonii (Johnson’s tiger beetle), E. togata globicollis (alkali tiger beetle), and Cicindelidia ocellata ocellata (ocellated tiger beetle). One individual, however, gave me pause—both when I first saw it and then when I pulled it from the net. At first glance it looked like the über-common and widespread Cicindelidia punctulata (punctured tiger beetle), but it didn’t seem quite right for the species, and its dark coloration contrasted with the greenish color exhibited by most individuals in this area (representing the western subspecies, C. p. chihuahuas, or Chihuahua tiger beetle). Then I noticed the rather rounded elytral sides and the generally dull elytral surface and immediately suspected that I had just collected my first Cicindelidia nigrocoerulea (black sky tiger beetle)—a goal for the trip and one that I had not succeeded in finding at three locations I had gleaned from iNaturalist and visited earlier! Closer examination of the photo and the specimen convinced me I was correct, so even though I did not find the species I was looking for, I still found another one that was a priority for the trip. [Edit: after some discussion, the consensus on iNaturalist is that this individual represents C. punctulata. Alex Harmon noted the elytra sides aren’t round enough for C. nigrocoerulea and that the texture is better for C. punctulata. He also noted that, for what it is worth, that C. nigrocoerulea are either blue, green, or black rather than brown as in this individual. After looking at my field guide upon my return back home, I am inclined to agree with him.]
Cicindelidia punctulata (punctured tiger beetle—family Cicindelidae) on alkaline flats along lake margin.
With the sun setting rapidly and so many tiger beetles still around, I decided that I would delay my departure from the area in the morning and come back to Lea Lake—perhaps I will still find C. h. woodgatei after all!
Dusk on the alkaline flats adjacent to the lake.
Pasture Lake Campground Bottomless Lakes State Park Chaves County, New Mexico Back at camp after cooking dinner (salmon—more on this), I decided to “night walk.” I hadn’t had a chance to do this the previous two nights because of reasons, and I wanted to take advantage of one last opportunity to look for Amblycheila picolominii (plateau giant tiger beetle), which I found on both of my previous visits here this year. The closest and easiest place to get to where I had found one was at the bottom of the steep, narrow ravine coming off the gypsum/red siltstone slopes just behind my campsite, so I headed there first. Within minutes after clambering down into the bottom of the ravine, I found one!
Amblycheila picolominii (plateau giant tiger beetle—family Cicindelidae) in bottom of gypsum/red siltstone ravine at night.
Filled with optimism about finding more, I searched the remainder of the ravine bottom, but no more were seen. After emerging from the ravine back at the campsite, I sat at the table briefly to update my field notes before continuing to other areas. At one point I looked up, and there was another one right at my feet! I looked away briefly to grab a vial, and when I looked back it was gone—nowhere to be seen! I searched the entire campsite in a gradually enlarging spiral, but to no avail. I started questioning whether I had actually seen what I was sure I had seen—there are few places to hide anywhere in this very large campsite, and I could not understand how such a large and conspicuous beetle could completely evade me like that. That would ultimately prove to be the last individual “seen” during the entire evening. Nevertheless, during my spiral search I encountered an interesting situation at the “salmon oil pit” (I had rinsed the accumulated oils from the salmon before cooking it and dumped the wash into a small pit that I dug in the soil). There were two tiger beetles inside the pit—Tetracha carolina carolina (Carolina metallic tiger beetle) and Eunota circumpicta johnsonii (Johnson’s tiger beetle)—presumably scavenging on the tasty oils saturating the soil (tiger beetles are well known scavengers when the opportunity arises).
Tetracha carolina carolina (Carolina metallic tiger beetle—family Cicindelidae) attracted to salmon oil on ground at base of gypsum/red siltstone slope at night.
Eunota circumpicta johnsonii (Johnson’s tiger beetle—family Cicindelidae) attracted to salmon oil on ground at base of gypsum/red siltstone slope at night.
Also during my spiral search, I found several Cysteodemus wislizini (black bladder-bodied blister beetle), each perched on the foliage of Tribulus terrestris (puncture vine). I didn’t know if there was any significance to the association, but I found them on no other plant (the significance would be revealed the next morning). Lastly, I encountered several individuals of a tank-like species of Stenomorpha darkling beetle in the mesquite/saltbush chaparral next to the campsite. I am unsure of the species (the genus is super diverse), but I collected a few specimens and will eventually update their identity in the iNat observation that I posted.
Stenomorpha sp. (family Tenebrionidae) in gypsum/red siltstone mesquite chaparral at night.
I spent a fair bit of time walking the roads afterwards and even went to the picnic area on the other side of Pasture Lake Campground to see if I could find more A. picolominii, but as alluded to earlier that effort would prove futile. At the end of the fifth collecting episode for the day (interspersed with five hours of driving), I collapsed exhausted onto my cot with a few minutes to spare before midnight!
Day 6
As I was drinking my morning coffee and working on yesterday’s field notes, I noticed another Cysteodemus wislizini (black bladder-bodied blister beetle) on Tribulus terrestris (puncture vine) where I had collected a few on the same plants the night before. This one, however, was not only perched on the plant, but also consuming its flowers. I would see two more on the same plants during the course of the morning, so it seems there is at least an adult floral host association between the beetle and this plant.
Cysteodemus wislizeni (black bladder-bodied blister beetle—family Meloidae) feeding on flower of Tribulus terrestris (puncture vine) in mesquite/saltbush chaparral below gypsum/red siltstone slopes.
Lea Lake Recreation Area Bottomless Lakes State Park Chaves County, New Mexico Before leaving the park, I wanted to spend some time looking for tiger beetles at Lea Lake. I’d gotten only a quick taste of the fauna there with yesterday’s 20-minutes-before-sunset visit, during which time I’d collected four species, including the new-for-me Cicindelidia nigrocoerulea (black sky tiger beetle), and I was hoping today to add a fifth—Cicindelidia haemorrhagica woodgatei (Woodgate’s tiger beetle) which has been reported here several times already. This time I started at the east end of the alkaline flats, seeing and collecting another C. nigrocoerulea as well as a few individuals each of the other three species I’d seen yesterday—Cicindelidia ocellata ocellata (ocellated tiger beetle), Eunota circumpicta johnsonii (Johnson’s tiger beetle), and Eunota togata globicollis (alkali tiger beetle)—on the alkaline flats along the lake margin. I noticed Isocoma pluriflora (southern goldenbush) at the far end of the flats and checked them for Crossidius suturalis, finding a handful of individuals on the flowers, before turning my attention back to tiger beetles and working my way towards the west side of the lake. I wanted to get proper field photographs of the species I had not yet done so (at least, with the “big camera”), which at that point were only C. nigrocoerulea and C. o. ocellata. I never did see another of the former, but the latter were common enough that I was able to “work” a few individuals before finding a (relatively) cooperative one. I hadn’t planned on collecting any more individuals of E. c. johnsonii, but then I encountered two beautifully sumptuous green individuals and couldn’t resist.
Eunota circumpicta johnsonii (Johnson’s tiger beetle—family Cicindelidae) green form on alkaline flats along lake margin.
Shortly afterwards, I noticed several individuals of a species I’d not yet seen at that location—Cicindelidia tenuisignata (thin-lined tiger beetle)—in an area of the alkaline flats that was wet from lake water lapping over the edge. I was able to not only collect a handful of specimens, but also get decent photographs of one of them—making moot my inability yesterday to photograph this species and C. o. ocellata.
Cicindelidia tenuisignata (thin-lined tiger beetle—family Cicindelidae) on alkaline flats along lake margin.
In the same area, I thought I’d collected a third C. nigrocoerulea, but it turned out to be the common Cicindelidia punctulata (punctured tiger beetle) with which it can be confused. Interestingly, it was dark-colored (as in the eastern subspecies—C. p. punctulata), not green (as in the western subspecies—C. p. chihuahuae). In the end, the number of species seen around the lake increased to six, but—unfortunately for me—C. h. woodgatei was not one of them. By then I’d been at it for two hours, and the heat of the day (99°F) was upon me. Such temps are no good for trying to photograph tiger beetles, so I found some shelter to eat a bit of lunch and then started west towards my next set of traps at a high elevation site near Cloudcroft.
Escaping the heat during lunch.
Switchback Trailhead Lincoln National Forest Otero County, New Mexico I always enjoy the drive from Roswell to Cloudcroft—searing desert heat yields to cool mountain air, and the landscape morphs from a flat, featureless, heavily-populated (and, thus, littered) plain, to sweeping, undulating hills of juniper chaparral, to foothills of oak woodland, and finally to bonafide mountains with dense forests of stately pines and firs.
Prime property south of Roswell.
Poetically, I was greeted at the higher elevations by not only cool air, but rain (I think it has done this on every trip I’ve made in this direction). The rain was nothing more than sprinkles, though with a brief 1–2-minute windshield-cleaning episode. By the time I reached my trap locality, clouds remained, but the rain had moved on. I picked this locality because of its ease of access to the precise habitat I wanted to sample—Gamble’s oak forest. When I first encountered the location in May (and again when I returned to service the traps in June), the area was deserted—just what I want in a trapping locality to minimize the chance of vandals finding and disturbing the traps. This time, however, I was horrified to find the area choked with vehicles and tents—the place was literally teeming with people. I got a bad feeling in the pit of my stomach about whether I would find my traps still hanging and intact, and these fears were confirmed when I approached the location of the SRW trap and found it was completely missing—not a shred of evidence that the trap had ever been there! This was really disappointing for obvious reasons, but, additionally, this was the trap that produced the most interesting catch of all traps at all locations on the previous visit. Fortunately, the SRW/EtOH trap was still hanging and intact with liquid in the reservoir and bait in the bottle. The catch was voluminous and appeared to consist largely of flies, yellowjackets, and butterflies; however, fingering through it I did find some interesting longhorned beetles: Tragidion coquus, Stictoleptura canadensis (a new addition to the list of species trapped), and the previously captured Stenocorus copei. This lifted my spirits a bit knowing that at least one trap had survived the human onslaught. The lift, however, was short lived when I approached the EtOH trap and found it lying on the ground—completely disassembled! I found most of the parts, but the nylon rope and carabiner used to hang the trap were gone—someone actually had to untie the rope at one end and unclip the carabiner at the other to take them. I really don’t understand the depravity of people that mess with other people’s stuff with no regard or remorse. Vandalizing traps not only wastes my time, effort, and expense, but in this case it also negatively impacts the integrity of the study I am conducting. It’s hard enough trying to anticipate and mitigate against weather, animals, equipment failure, and errors in deployment without also having to outfox the criminal element. I’ll have to consult with a statistician on the best way to analyze the trapping results while taking into account the loss of some trap events (i.e., unique trap/date combinations). On a positive note, the white bottle trap that I reset last time was still in place and had captured a nice quantity of both Acmaeodera and Anthaxia.
Hwy 70 at “Point of Sands” Otero County, New Mexico After checking the traps near Cloudcroft, my original plan was to camp at Upper Karr Canyon, a high elevation national forest campground south of Cloudcroft. However, seeing the zoo of campers at the trapping site, along with the throngs of people and cars I’d seen in town, suggested to me that any campground in the area was probably already filled to capacity on what I realized was a Saturday night of a holiday weekend (Monday is Mexican Independence Day). I noted that my next trapping location at Aguirre Springs Campground in the Organ Mountains-Desert Peaks National Monument was another 2-hour drive, but that I had plenty of time to make it there before dark—even if I stopped and collected along the way. Heading straight there wouldn’t solve the problem of finding an open campsite on a Saturday night, but at least the location was further removed from a town teeming with visitors. As for collecting along the way, I could think of no better spot than “Point of Sands”—a spot along U.S. Hwy 70 where the dunes of White Sands National Monument breach the fenceline and continuously spill out onto the highway. It’s a chance to get a quick taste of the dune flora and fauna without the need for permits, entry fees, etc. I stopped here also on both trips earlier this season, and while I didn’t find much out of the ordinary either time, I keep returning for two reasons—Acmaeodera recticollis and Sphaerobothris ulkei, two rather uncommon and desirable buprestid species that breed in Ephedra (jointfir). I collected a small series of the former here a couple of years ago, but my only evidence that the latter occurs here is a carcass I found lying on the ground a few years earlier. Someday, I will come to this spot at the right time and find adults of that species active on the Ephedra. Once again, however, that time would not be this time—despite the much more comfortable conditions than last time (when temps were 108°F), the only insect I saw worth putting into a bottle was the tank-like darkling beetle, Philolithusaeger, crawling on the white sand.
Philolithus aeger (family Tenebrionidae) on white sand at sand dune/saltbush chaparral interface.
I also had hopes of finding Crossidius longhorned beetles when I noted stands of Isocoma pluriflora (southern goldenbush) and Gutierrezia sarothrae (broom snakeweed) in bloom—both of which are favored hosts for beetles in this genus. None were found, however—just blister beetles, so after completing the circuit up one side of the road and down the other, I continued the drive to Aguirre Springs.
Lytta biguttata (two-spotted blister beetle—family Meloidae) on flowers of Gutierrezia sarothrae (broom snakeweed) in saltbush shrubland.
Aguirre Springs Campground Organ Mountains-Desert Peaks National Monument Doña Ana County, New Mexico My fears about the campground being filled seemed realized as I entered the loop and saw site after site already occupied. Fortunately, on the backside of the loop I found a few unoccupied sites, one of which was quite nice—buffered from the view of the road and nearby sites by trees and shrubbery and with a nice level area for the tent. It felt good to be back in one of my favorite places, and another “dirty burger” dinner tasted quite good!
“Dirty burger” on the grill.
Afterward, I walked the loop to see if I could find any beetles (hoping for Amblycheila, of course), but the only thing I saw were the occasional Eleodes darkling beetle and the glowing eyes of spiders, including the always charismatic Geolycosa sp. (burrowing wolf spider).
Geolycosa sp. (burrowing wolf spider—family Lycodidae) in juniper/oak/pinyon woodland at night.
Day 7
In the morning, I decided to relax a bit and work on my field notes while enjoying coffee and the views, then headed out to retrieve my traps.
The spectacularly jagged peaks of the Organ Mountains loom over oak woodlands below.
Yesterday’s poor trap fortune turned around completely when all three traps were found in place, intact, … and loaded with beetles! These included several species of elaphidiine longhorned beetles and a diversity of cetoniine scarabs. Two species of the latter group were Cotinis mutabilis (figeater beetle) and Gymnetina cretaceasunbbergi—both new for me! I don’t think the former is all that uncommon, but the latter apparently represents a recently-described subspecies that is endemic to the Organ Mountains.
Cotinis mutabilis (figeater beetle—family Scarabaeidae) in sweet red wine (SRW)-baited “jug trap” in juniper/oak/pinyon woodland.
Gymnetina cretacea sundbergi (family Scarabaeidae) in sweet red wine (SRW)-baited “jug trap” in juniper/oak/pinyon woodland.
The same pattern of fewer beetles in the EtOH trap was found here, although all three traps displayed greater total mass than their respective counterparts at other locations. After retrieved the EtOH trap, it hit me that I had just taken down the last trap at the last location in the final season of the 3-year study! There is still much work still to do—specimens to sort, prep, mount, and identify… data to assemble, crunch, and ponder… manuscripts to write, polish, submit, and revise… co-authors to correspond with and coordinate. However, with all that said, finishing the field work still feels like a major victory! At this point, I have no other place where I must go, so I am content to spend the rest of the trip exploring this beautiful area (this makes up for me not getting to spend a day hiking in Guadalupe Mountains National Park).
Ferocactus wislizeni (fishhook barrel cactus—family Cactaceae) flowers in juniper/oak/pinyon woodland.
As I was retrieving the traps, I scanned the nice variety of plants in bloom for beetles and quickly encountered not only Crossidius pulchellus on flowers of Gutierrezia sarothrae (broom snakeweed), but also Acmaeodera opacula, A. amplicollis, and A. rubronotata on the same as well. These are all late-season, mid- to high-altitude species, and surely the floral associations are well known. However, i did find two potential new ones—A. amplicollis (observed) and A. rubronotata (collected) on flowers of Pectis papposa (chinchweed). I don’t recall encountering this plant in my review of literature on host associations of North American Buprestidae and will have to look into this when I return from the field.
Crossidius pulchellus (family Cerambycidae) on flowers of Gutierrezia sarothrae (broom snakeweed) in juniper/oak/pinyon woodland.
Acmaeodera amplicollis (family Buprestidae) on flowers of Gutierrezia sarothrae (broom snakeweed) in juniper/oak/pinyon woodland.
Acmaeodera rubronotata (family Buprestidae) on flowers of Pectis papposa (chinchweed) in juniper/oak/pinyon woodland.
On the way back to camp to drop off the traps and refuel, I saw a Euphoria verticalis crawling on the broken granite substrate.
Euphoria verticalis (family Scarabaeidae) crawling on ground in juniper/oak/pinyon chaparral.
I’d gotten iPhone images of three of the Gutierrezia-associates, but since I have some flex time I decided to grab the big camera and see what kind of real photos I could get. I walked to an area with blooming Gutierrezia much closer to my camp on the south side. I found several C. pulchellus, photographing a mating pair, but persistent searching beyond the area never turned up any of the buprestids. So I looped back through the campground and walked back to the ravine I’d visited earlier. There, back up and down the ravine, I photographed C. pulchellus, A. rubronotata, and A. amplicollis (I never saw another A. opacula beyond the first). I then tuned my attention to other subjects: a snout butterfly, a scoliid wasp, a few plants, and something for a future quiz. I was content with the day and strolled back to camp to rest and cook dinner (steak!).
Dusk settles over Aguirre Springs Campground.
After dinner (and a thrilling football game between my beloved Chiefs and rival Bengals!), I did my “night walk,” this time leaving the campground loop and walking along Aguirre Springs Rd a short distance before turning back. Again, I encountered Eleodes darkling beetles—this time congregating on the trunk of a very large juniper cadaver—and the siren call of a wolf spider’s glowing eyes luring me in for images. I managed a dorsal shot, but she skedaddled before I could fire off a frontal portrait. [Edit: discussion on iNaturalist suggests this is an undescribed species currently known as the “big-eyed” Hogna with its pale, ghost-like markings. It seems to be common in New Mexico.]
Hogna n. sp. (“big-eyed” wolf spider—family Lycosidae) wanders about the juniper/oak/pinyon woodland at night.
The waxing gibbous moon threw enough light on the majestic peaks above to make for one the most beautiful night skies you’ll ever see!
A waxing gibbous moons throws light on the nighttime mountain landscape.
A tiny lantern lights up a lone campsite.
Day 8
I didn’t sleep well—my stomach began rumbling in the middle of the night, and by the time I got up I had full-blown GI problems. I had wanted to go down to lower elevations before the temperatures got too high in hopes of finding late-season “hangers on” of larger southwestern buprestids in the genera Gyascutus and Lampetis, but it seemed prudent instead to take it easy during the morning and give myself a chance to feel better. This did seem to happen… eventually… or perhaps it was just the product of wishful thinking!
Morning at Aguirre Springs Campground.
Bar Canyon Trail Organ Mountains-Desert Peaks National Monument Doña Ana County, New Mexico I went to a spot where late-season occurrences of Gyascutus, Lampetis, and Acmaeodera had been recorded on iNat.
Bar Canyon Trail ascends from Soledad Canyon Rd on the west slope of the Organ Mountains.
I got an early indication of good luck when I found Acmaeodera rubronotata and A. opacula on the flowers of Picradeniopsis absinthifolia (hairyseed bahia). I also found another Cotinis mutabilis (figeater beetle), this one on flowers of Gutierrezia sarothrae right around the parking lot.
Cotinis mutabilis (figeater beetle—family Scarabaeidae) on flowers of Gutierrezia sarothrae (broom snakeweed) in mesquite/acacia thornscrub.
A bit further up the trail, I found two additional species—A. amplicollis and A. maculifera—also on P. absinthifolia, and further still along the trail I found more of the former.
Acmaeodera maculifera (family Buprestidae) on flower of Picradeniopsis absinthifolia (hairyseed bahia) in mesquite/acacia thornscrub.
Alongside the trail was a wash, where Fallugia paradoxa (Apache plum) was growing—checking the flowers was, for the most part, fruitless; however, I did find on them singletons of A. opacula and A. rubronotata. There were other plants in flower as well that seemed like they should be good beetle hosts—notably Gymnosperma glutinosum (gumhead), from which I collected a single A. rubronotata. Otherwise, however, there was little to be seen (except the occasional monstrous lubber grasshopper).
Brachystola magna (plains lubber grasshopper—family Romaleidae) in mesquite/acacia thornscrub.
I was happy to see the variety of Acmaeodera on P. absinthifolia flowers—especially A. maculifera, a species I had not seen for two decades(!), but my GI problems seemed to worsen as I felt increasingly weak and overheated. Less than one mile up the trail, I simply couldn’t continue further and turned back towards the car for—what I thought—was an end to the day’s activities.
North Fork Las Cruces Arroyo Doña Ana County, New Mexico After a quick stop in town to purchase symptom relief, I intended to go straight back to the campground and rest for the remainder of the day. Apparently unable to stick to a good plan, however, I decided to scan iNat one last time to see if there were interesting records of Buprestidae from nearby areas and saw that A. maculifera had been taken in a wash just a few miles away. I couldn’t resist the temptation to take one more look at one more spot before heading back up the mountain. Walking down into the wash felt like descending into a furnace! It was by then mid-afternoon, and even though I had rehydrated I still felt weak on the feet. The promise of beetles, however, continued singing its siren song, and I quickly found what proved to be Heterotheca zionensis (Zion false goldenaster) abundantly in bloom and looking like a perfect host for Acmaeodera.
Heterotheca zionensis (Zion false goldenaster—family Asteraceae) in xeric wash.
At first I found nothing, but with continued searching I found a spot where several Crossidius pulchellus and a single Acmaeodera scalaris were seen clinging to its flowers—the latter being another buprestid species for the trip (though, admittedly, a rather common species). I managed to finally find several A. maculifera on the flowers after additional searching (along with A. opacula), but I was declining rapidly and decided best to turn around. Passing near the spot where I had first found beetles, I found more A. maculifera (along with A. rubronotata) and lingered to better my series. This last little delay, however, proved to be too much for me, and for the first time ever I experienced “being sick” in the field! My body was sending me a message, and it was loud and clear (not that it wasn’t loud and clear before then!). I went back up the mountain and spent the rest of the day sleeping and resting in the cool mountain air back at camp.
The view from my campsite is simply breathtaking!
Day 9
My original plan for the day (depending on how I was feeling) was to break camp and start heading back to the northeast. With luck, I would make it to the Oklahoma panhandle with enough daylight to explore a few localities in Texas Co. that I hadn’t visited before. I did get a much better night’s sleep; however, I still felt weak and had to take my time breaking camp. This delayed my planned early morning departure a bit, and the need for frequent stops made a pre-evening arrival even less likely. In the end, it didn’t matter as rain moved through the area, bringing abruptly cool, cloudy conditions and wiping out any hope of any insect activity in the waning hours of the day. I did, however, get to see an oversized Texan as I sliced through the uppermost tip of that oversized state and was greeted by an ironically hypocritical welcome sign as I entered adjacent Oklahoma.
An oversized Texan!
An “unwelcoming” welcome sign. Do they even see the irony?
Day 10
3.2 mi SSW of Piqua Woodson County, Kansas I got another text yesterday from Dan Heffern, who told me that his brother had found several Megacyllene decora (amorpha borer) on Amorpha fruticosa near his home in eastern Kansas. I had already checked the nearby locality near Piqua (where he had seen this species many years ago) without success, but I reasoned that it may have been too early and that another look (now that the species is known to be out) was warranted. I was feeling better, but not great, and was, thus, glad to encounter relatively mild conditions when I arrived. On the very first clump of Amorpha that I checked, I found a big Megatibicen dorsatus (bush cicada) female sitting on its stem, …
Megatibicen dorsatus (bush cicada—family Cicadidae) female on stem of Amorpha fruticosa along margin of quarry.
…and shortly afterwards I found the left elytron of M. decora on the ground amidst Amorpha and flowering Solidago sp.
Megacyllene decora left elytron on ground amidst Amorpha fruticosa and flowering Solidago sp. along margin of quarry.
“What luck!”, I thought, and proceeded to inspect each Amorpha clump and flowering Solidago that I could find. Remarkably, my search for adults would prove fruitless, and for the second time on the trip I would have to walk away from the spot empty-handed. I was also starting to feel weak and overheated again after an hour of searching, suggesting that I was still not recovered and that perhaps I should focus on finishing the drive to St. Louis so I could recover in the comfort of my home—a rather inauspicious ending to what was, by all other measures, as fun and successful a collecting trip as I could ever hope for!
Alternate title: “The importance of authoritative identification and voucher specimen information when documenting a new occurrence of an exotic species.”
For many years now (indeed, decades!), I have been assembling a “Catalogue of Buprestoidea of North America, Mexico, Central America, and the West Indies.” Still a work in progress, it serves as a personal database of literature citations for all species of Buprestoidea occurring in that region—both native and introduced, along with full synonymies, information on type specimens and repositories, distributions, host plants (larval, adult, and flower), natural enemies, and attractants, and comments on erroneous reports and taxonomic issues. The relatively recent appearance of two other catalogues for this superfamily—one by Nelson et al. (2008) for North America north of Mexico, the other by Bellamy (2008–2009) and worldwide in scope—might seem to render this effort duplicative. Nevertheless, both catalogues contain errors and omissions that should be corrected, and numerous additional papers on the taxonomy, nomenclature, and biology of species of Buprestoidea have been published in the years since the appearance of these catalogues. Additionally, my vision of the eventual published version of my catalogue includes full synonymies and more detail in the aforementioned sections. Don’t look for it to be published anytime soon, as it is nowhere close to ready—perhaps it will prove to be my final magnus opus, much as the Nelson et al. and Bellamy catalogues capped the careers of their respective authors.
Last December, whilecomparing provincial records in my database with the second edition of Checklist of Beetles (Coleoptera) of Canada and Alaska (Bousquet et al. 2013), I encountered in the latter an entry for the Palearctic (Europe and Asia) species Buprestis haemorrhoidalis in British Columbia. This was news to me, and I quickly checked the Nelson et al. and Bellamy catalogues, neither of which included North America in the reported distribution of this species (the Bellamy catalogue did report an introduction of the species to South America). The Bousquet et al. checklist post-dates the Nelson et al. and Bellamy catalogues by five years, so I assumed the supporting record would be found within one of the papers from within that time period that I had not yet databased; however, no such paper was found.
I then turned to my old friend Google and searched “Buprestis haemorrhoidalis British Columbia”, and the very first result was a placeholder page for the species at the popular insect website BugGuide (Belov 2017–2023). No North American observations had yet been posted to the page, but two references were cited—the aforementioned Bousquet et al. checklist, and a paper by Humble & Allen (2006). The link to the paper was nonfunctional, but I found a PDF at the Purdue University website (see link in citation below). In the paper, B. haemorrhoidalis was included in a list of invasive species reported to be “established” in Canada, giving 1992 as the date of introduction. No information regarding the source of the record or the existence of voucher specimen(s) was given, but the authors’ affiliation with the Pacific Forestry Centre in Victoria, British Columbia hinted at this being the basis of the listing in the Bousquet et al. catalogue. Neither the Nelson et al. nor Bellamy catalogues cited this reference, but its publication date (2006) is close enough to the two catalogues (2008) and the venue obscure enough (not an entomology journal) that the omission is not unexpected. A more exhaustive literature search turned up nothing but a single more recent summary listing of the record by Ruzzier et al. (2023), citing Humble & Allen (2006).
Unable to find anything online, I emailed the corresponding author (Leland Humble), but the message bounced back as undeliverable. This prompted me to reach out to several current buprestid workers, all of whom concurred with my presumption that this must—in the absence of any supporting evidence to the contrary—represent a non-established interception or a misidentification of a native species. One of them, Eduard “Edo” Jendek (Bratislava, Slovakia), an expert in invasive Buprestidae, contacted Jon Sweeney (Canadian Forest Service, Atlantic Forestry Centre), who informed him that Humble was deceased and suggested sending an inquiry to Meghan Noseworthy, currently research manager at the Pacific Forestry Centre arthropod reference collection (PFCARC). In response to my inquiry, Meghan informed me that a specimen under the name B. haemorrhoidalis was, indeed, listed in their collection database. She was able to locate the specimen and graciously arranged to have it sent to me on loan so I could examine it and confirm or correct its identity. When the shipment arrived, I opened the box and saw this:
Unit tray from the Pacific Forestry Centre arthropod reference collection containing putative voucher specimen of “Buprestis haemorrhoidalis.”
Comparison of the specimen to a series of B. haemorrhoidalis in my collection quickly revealed it is not that species. This was no longer an ID confirmation, but an ID correction—almost surely a native North American species. Remarkably, the first clue to its true identity was found on the labels attached to the specimen itself—the initial identification label by “A.Davies” (undated) as “Buprestis haemorrhoidalis” had been repositioned upside-down on the pin, and a second identification label by “R.L.Westcott ‘07” as “Buprestis subornata (LeC.” [closing parenthesis missing] was placed beneath it. As expected, the specimen agrees in all respects with a series of B. subornata in my collection. While B. haemorrhoidalis superficially resembles B. subornata, it differs in its well-defined, serially punctate elytral intervals (B. subornata has poorly-defined, impunctate intervals) and its smoother, shinier elytral surface compared to the latter species. Indeed, the two are placed in separate subgenera—B. haemorrhoidalis in Ancylocheira, and B. subornata in Buprestis s. str.
Putativevoucher specimen of “Buprestishaemorrhoidalis.” In reality, the specimen represents the North American native species Buprestis subornata (LeConte, 1860).
Examination of the specimen labels leaves little doubt that this specimen is the basis of the Humble & Allen (2006) report of B. haemorrhoidalis in Canada—the specimen resides in the PFCARC (the institute with which L. Humble and E. Allen were affiliated), and the reported date of introduction (1992) matches the specimen date of collection. There also can be little doubt that this specimen is the basis of the Bousquet et al. (2013) report of B. haemorrhoidalis in British Columbia—the label indicates collection in “Kelowna B.C.”, and the initial identifier (A. Davies) is the author of the Buprestidae chapter in the first edition of the Canada checklist (Davies 1991) and a coauthor of the second edition.
Labels that had been placed on the voucher specimen show that its identity was corrected shortly after the record was published (the Davies label was repositioned upside-down on the pin). 
This examination refutes any notion that B. haemorrhoidalis has ever been introduced to or established within North America. However, it also highlights the problems that allowed a misidentification to not only be reported in the literature, but also accepted and propagated. The initial erroneous identification by Davies is puzzling—not so much because it happened (erroneous identifications happen all the time), but because it was identified as an exotic species with no known prior occurrence in North America. The identification of any exotic species for the first time is a significant finding that should raise alarms and be immediately confirmed by a recognized specialist with taxonomic expertise in the group to which it belongs. While this did eventually happen with Westcott’s corrected identification in 2007, it was not before the erroneous identification had already been introduced to the literature by Humble & Allen (2006).
The fact that the erroneous identification was even published at all is itself problematic—there was no prior, peer-reviewed publication to support its summary listing in a review article published in a non-entomology journal, nor was there any citation of specimen data or voucher location to address the absence of such. The use of the word “established” to characterize the presence of the species in Canada is also curious, although I note that the authors were mycologists, not entomologists, and may not have appreciated the significance of that term in the context of invasive exotic insects. (The more appropriate term, erroneous ID notwithstanding, would have been “apparently introduced or mislabeled”.)
The acceptance of the erroneous report by Bousquet et al. (2013) is yet another puzzle, as the identification had been corrected by Westcott—a recognized expert of Buprestidae—six years earlier. Obviously, the PFCARC neglected to correct the listing of the specimen under B. haemorrhoidalis—both in their collection database and in the collection itself—despite this correction (now 17 years ago!). I also note that the Canadian National Collection website lists a specimen (record #CNCCOLEO00091957) with identical label data, but again only the initial identification as B. haemorrhoidalis is mentioned—the corrected identification as B. subornata is not. Since Davies (a coauthor of the second edition) made the initial identification, perhaps the remaining authors had no reason to doubt it. Nonetheless, the reported occurrence of an exotic, apparently invasive species with no supporting reference documenting the circumstances of its collection should have triggered confirmatory follow-up before its inclusion in the updated version of the checklist.
Had any of the above circumstances been avoided, the erroneous report of an exotic invasive species established in North America would not have been propagated in subsequent literature (i.e., Ruzzier et al. 2023) or on a popular insect website (i.e. BugGuide). Let this serve as a cautionary tale to current and future entomologists, especially those with an interest in invasive species and cataloguing efforts. I have a (much shorter) corrective note about this in a soon-to-be-published paper that will likely set the record straight among most North American buprestid workers. However, the erroneous record could still be propagated by those not interested explicitly in Buprestidae (e.g., invasive species specialists) and, thus, may be unlikely to encounter my corrective note. As they say, it’s hard to unring the bell.
Literature Cited
Bellamy, C. L. 2008–2009.A World Catalogue and Bibliography of the Jewel Beetles (Coleoptera: Buprestoidea). Vols. 1–4 (2008), Vol. 5 (2009). Pensoft Series Faunistica No. 76. Pensoft Publishers, Sofia, Moscow, 3264 pp. [Description]
Bousquet Y., P. Bouchard, A. E. Davies & D. S. Sikes. 2013. Checklist of beetles (Coleoptera) of Canada and Alaska. Second edition. ZooKeys 360:1–402. [PDF of original work no longer available; see Introduction and Data Paper]
Davies, A. 1991. Family Buprestidae: metallic wood-boring beetles, pp. 160–168. In: Y. Bousquet (Ed.), Checklist of beetles of Canada and Alaska. Research Branch, Agriculture Canada, Publication 1861/E, 440 pp. [PDF]
Humble, L. M. & E. A. Allen. 2006. Forest biosecurity: alien invasive species and vectored organisms. Canadian Journal of Plant Pathology 28:S256–S269. [PDF]
Nelson, G. H., G. C. Walters, Jr., R. D. Haines & C. L. Bellamy. 2008.A Catalog and Bibliography of the Buprestoidea of America North of Mexico. The Coleopterists Society, Special Publication No. 4, iv + 274 pp. [PDF]
Ruzzier, E., R. A. Haack, G. Curletti, A. Roques, M. G. Volkovitsh & A. Battisti. 2023. Jewels on the go: exotic buprestids around the world (Coleoptera, Buprestidae). NeoBiota 84:107‒135. [Full text, PDF]
Beetles In The Bush 