The ever-increasing diversity of Oklahoma beetles

My idea to return to Oklahoma’s Gloss Mountains this spring actually began taking shape during last year’s fall visit to the area, when I found a single Chrysobothris octocola adult on a dead mesquite (Prosopis glandulosa) branch. While common across the southwestern U.S. in association with this plant, its occurrence in the Gloss Mountains represented a northeastern range extension and new state record for Oklahoma! On that same trip I also collected an interesting beetle in the family Rhipiphoridae representing the species Toposcopus wrightii—also not previously recorded in the literature from Oklahoma. Combined with finding Acmaeodera macra here the previous year, it was becoming clear to me that area held good potential for other more typically southwestern species of wood boring beetles. Although I had by then visited the area several times, most of these visits were more focused on tiger beetles rather than wood boring beetles. If I could find such interesting species of wood boring beetles when I wasn’t focused on them, imagine what I might find if I timed a visit in late spring when such species should be at their peak of adult activity.

Chrysobothris quadrilineata | Gloss Mountains State Park, Major Co., Oklahoma

Chrysobothris quadrilineata | Gloss Mountains State Park, Major Co., Oklahoma (new state record).

Of course, success came quickly during this early June visit. I immediately found C. octocola common on the mesquite and would collect a nice series of voucher specimens before the day was over, and the second species I encountered, also on mesquite, was the longhorned beetle Plionoma suturalis—another new state record! I spent a bit of time working the mesquite, and when I had collected a sufficient series of both species, I turned my attention to the eastern red-cedars (Juniperus virginiana) in the area. Actually, I had had my eye on the red-cedars since last fall, when I noticed that nearly every tree had dead branches mixed in amongst the living branches. Closer examination revealed the workings of jewel beetle larvae in all of these dead branches, and a few larvae typical of the genus Chrysobothris were cut from one of the branches. A common species in the Great Plains associated with Juniperus is C. ignicollis, but these larvae looked rather big to represent that species, so I bundled up some dead branches and brought them back home for rearing but forgot to check on them before I left on this trip. At any rate, I walked up to one of the red-cedars, placed my beating sheet under a dead branch, gave the branch a whack with the handle of my net, and onto the sheet fell a rather robust Chrysobothris that I didn’t immediately recognize. I knew it wasn’t C. ignicollis, a much smaller species that I have collected on numerous occasions, so I thought maybe it could be C. texana, another western Juniperus-associate that I’ve collected less commonly. Still, the robust body and broad, distinct elytral and pronotal ridges had me second guessing that identification (especially after I found some individuals that looked more like what I remembered C. texana looking like). Over the next two days I beat hundreds (literally!) of dead juniper branches, finding many C. ignicollis but every now and then getting also one of these big, robust individuals.

Chrysobothris quadrilineata

Adults were beaten from dead branches on live Juniperus virginiana (new adult host).

After returning home, I checked my heavily annotated copy of Fisher (1942) and quickly determined the robust specimens as representing C. quadrilineata—a rather uncommon species and one that I’d never collected before. Described by LeConte in 1860 from New Mexico and recorded early in the 20th century from Arizona, Nevada and California, it has in more recent years been found to occupy a rather wide distribution across the western U.S., including Texas (Barr & Westcott 1976), Colorado, Oregon, South Dakota (Nelson et al. 1982), and Utah (Nelson 1987). Notice one state that is not in that list—Oklahoma! That’s right, another new state record! I later found photographs of this species on BugGuide taken in the very same area a year earlier (7 June 2012).

Chrysobothris quadrilineata

Adults also emerged from dead J. virginiana branches collected Sept. 2012 (first reported larval host).

When I returned home, I also checked the rearing cans and found several adults had emerged from the branches I collected last September. The only host associations that have been recorded for this species are adults collected on Juniperus californica (Linsley & Ross 1940) and J. pachyphloea [= J. deppeana] (Barr & Westcott 1976). Thus, J. virginiana not only represents a new host record for the species but is also the first known larval host. Considering how broadly distributed across the western U.S. this species is, it seems likely that it utilizes a number of Juniperus spp. throughout its range.

REFERENCES:

Barr, W. F. & R. L. Westcott. 1976. Taxonomic, biological and distributional notes of North American Chrysobothris, with description of a new species from California (Coleoptera: Buprestidae).  The Pan-Pacific Entomologist 52(2):138–153.

Fisher, W. S. 1942. A revision of North American species of buprestid beetles belonging to the tribe Chrysobothrini. U. S. Department of Agriculture, Miscellaneous Publication 470, 1–275.

Linsley, E. G. & E. S. Ross. 1940. Records of some Coleoptera from the San Jacinto Mountains, California.  The Pan-Pacific Entomologist 16(2):75–76.

Nelson, G. H. 1987. Additional notes on the biology and distribution of Buprestidae (Coleoptera) in North America, II.   The Coleopterists Bulletin 41(1):57–65.

Nelson, G. H., D. S. Verity & R. L. Westcott. 1982. Additional notes on the biology and distribution of Buprestidae (Coleoptera) of North America.  The Coleopterists Bulletin 35(2) [1981]:129–152.

Copyright © Ted C. MacRae 2013

“Rare jewel beetles discovered in Mexico by team of scientists!”

I hope you’ll excuse the hyperbolic title, but such has been my impression with some of the headlines I’ve seen recently in the popular media regarding newly described insect taxa in various parts of the world. The “discovery” of new species in far away, tropical lands sounds exciting and ground-breaking to many people, who envision teams of scientists wearing pith helmets and cargo shorts machete-slashing their way through miles of virgin forest before stumbling into a secret biodiversity hot-spot, their weeks of toil and sweat finally paying off by becoming the first white men to lay eyes upon a bounty of strange, exotic, never-before-seen creatures. In reality, new species of insects are not at all hard to find—in fact, depending on where you go it can be downright easy. Admittedly the chances are greater in the tropics, where many areas remain little explored, but even in well-studied North America new species turn up regularly. This includes popularly collected beetles in the very well-studied eastern U.S., where I’ve already described one new jewel beetle (family Buprestidae) and one new longhorned beetle (family Cerambycidae) from right here in my home state of Missouri (MacRae 2000, 2003) and am in the process of describing another new jewel beetle. No, finding new species is easy—recognizing them as such is the hard part. That’s not to say that new species cannot be recognized when first encountered, but I suspect that a majority of new insect species aren’t actually “discovered” until they’ve been brought back from the field, curated, and sat in a cabinet for years or decades—unrecognized for what they really are due to resemblance to known species until somebody comes along and examines them more critically.

Such is the case with two jewel beetle species that Chuck Bellamy and I describe in a paper just published in The Pan-Pacific Entomologist (MacRae & Bellamy 2013). I joined Chuck on several trips to Mexico in 1992 and again from 2004–2006 to explore the tropical thorn woodlands in the southern states of Oaxaca, Puebla, Guerrero and Michoacán. Jewel beetle diversity is high in these still relatively intact woodlands, with a number of new species already having been described from the area in recent years, and all-told we collected well over 100 species. At least a dozen or more of these look to be new, and considering that the Mexican jewel beetle fauna as a whole includes more than 800 known species the actual number could greatly exceed 1,000. The two described in this most recent paper resemble the common, widespread species Actenodes calcaratus. This big, beautiful jewel occurs from the southwestern U.S. through Mexico and Central America to northern South America, developing as larvae in dead wood of a variety of fabaceous hosts. We collected several of what we thought was this species during our trips, but a number of subtle but consistent differences in punctation and surface sculpturing emerged as we began comparing them more critically against A. calcaratus from other locations. The coup de grâce, however, was the coloration of the male face—normal bronze in A. calcaratus (Fig. 5) and similar to the female (Fig. 6), but flash-green in male A. scabrosus (Fig. 2) and green-violaceous in male A. michoacanus (Fig. 8). It’s quite remarkable that both of these species differ from their more widespread relative by subtle morphological characters but such striking sexually dimorphic facial coloration, and we subsequently found a similar situation with another species in the genus (A. undulatus) that otherwise bears little resemblance to A. calcaratus.

Figs. 1–9. Actenodes spp. 1–3. Actenodes scabrosus. 1–2. Male holotype. 1. Dorsal habitus. 2. Frontal view. 3. Female paratype (Guerrero). 4–6. A. calcaratus. 4–5. Male (MEXICO, Guerrero, Hwy 95, 5 km S Milpillas, 7.vii.1992, "big dead tree", G. H. Nelson [FSCA]). 4. Dorsal habitus. 5. Frontal view. 6. Female (MEXICO, Hwy 95, 2 km S Milpillas, 6.vii.1992, on Acacia farnesiana, G. H. Nelson [FSCA]), frontal view. 7–9. A. michoacanus. 7–8. Male holotype. 7. Dorsal view. 8. Frontal view. 9. Female paratype, frontal view. All scale bars = 5 mm.

Figs. 1–9. Actenodes spp. 1–3. Actenodes scabrosus. 1–2. Male holotype. 1. Dorsal habitus. 2. Frontal view. 3. Female paratype (Guerrero). 4–6. A. calcaratus. 4–5. Male (MEXICO, Guerrero, Hwy 95, 5 km S Milpillas, 7.vii.1992, “big dead tree”, G. H. Nelson [FSCA]). 4. Dorsal habitus. 5. Frontal view. 6. Female (MEXICO, Hwy 95, 2 km S Milpillas, 6.vii.1992, on Acacia farnesiana, G. H. Nelson [FSCA]), frontal view. 7–9. A. michoacanus. 7–8. Male holotype. 7. Dorsal view. 8. Frontal view. 9. Female paratype, frontal view. All scale bars = 5 mm.

In the case of both of these new species, the first specimens were actually collected more than 40 years ago but remained “hidden” among specimens of A. calcaratus until we examined the collections containing them more closely. While it might seem that the striking male facial coloration both of these species exhibit should have resulted in their quick recognition as undescribed species, even seemingly obvious characters such as this can be overlooked when an otherwise great resemblance to a common, widespread species prevents their critical examination.

REFERENCES:

MacRae, T. C. 2000. Review of the genus Purpuricenus Dejean (Coleoptera: Cerambycidae) in North America. The Pan-Pacific Entomologist 76(3):137–169.

MacRae, T. C. 2003. Agrilus (s. str.) betulanigrae MacRae (Coleoptera: Buprestidae: Agrilini), a new species from North America, with comments on subgeneric placement and a key to the otiosus species-group in North America. Zootaxa 380:1–9.

MacRae, T. C. & C. L. Bellamy. 2013. Two new species of Actenodes Dejean (Coleoptera: Buprestidae) from southern Mexico, with distributional and biological notes on Buprestidae from Mexico and Central America. The Pan-Pacific Entomologist 89(2):102–119.

Copyright © Ted C. MacRae 2013

Observation and Bias in Biology

The following is a guest post by my friend Kent Fothergill. Read more of Kent’s musings at his blog, biologistsoup.


Observation is a key activity in scientific inquiry. People who work with insects can make many interesting observations from collected insects: distribution, phenology, etc. Observations can be documented and analyzed later from photographs. A collection of photographs can also yield information about: associations with other species, behavior, while providing the same information as collected specimens – as such photography is a new tool changing entomology. Of course, most observations are made using only human senses without photographic or specimen documentation, but all observations can be subject to biases.

Observer biases are our evolutionary legacy. Our brains evolved to process and interpret data based on patterns observed in previously processed data. Because of the vast amount of data flowing in from our five senses and our limited ability to focus on data, our brains let most data be background. Even the subset of data that we focus our attention on is filtered, who hasn’t taken a photograph and found something much more interesting in the photograph than the original subject (e.g., these mites on harvestmen)? All data, even the data subset we are focused on can be misinterpreted. When teaching scientific methods, my students always enjoyed the optical illusion exercises to demonstrate why objective analyses and accurate measurement are important.

Remember, that the brain also compares incoming data to previous data. This allows pattern recognition. Recently, Ted and I were blacklighting along the Mississippi River in Southeast Missouri. We found a pair of Elaphidion mucronatum (spiny oak borer) a very common insect in Southeast Missouri. So common that many would move on to other more interesting subjects at that point. The insects were in a mate guarding situation.  Because I had a name for the behavior, my brain put my observation in the mate guarding category. At this point I would have moved on, except Ted wished to document the subject with his camera rig, which meant I would do what any friend should: watch the insects while Ted ran to vehicle to get his camera so he would be able to photograph them. While Ted was gone things got interesting. The male was positioned above the female, who was more or less caged between his legs. The pair was moving in unison on the tree trunk with very little actual contact between the pair. This was interesting, but when the female E. mucronatum suddenly shot out from under the male ending up 10’ vertical below him on the side of the tree trunk I was stunned. The male covered this distance with amazing speed and recaptured the female. After a couple minutes the female again shot out from under went down a few feet and doubled back ending out of sight above the male. At this point the male remained motionless for a brief period. When Ted came back with his camera, I took my eyes off of the male to tell him about what I had seen, and the male had vacated the area. Later, on the very same tree, we saw a mate guarding pair (presumably the same individuals) coming down towards us.

I have viewed many mate guarding insects. Mate guarding is a male insect using its body to prevent other males from mating with this female. Evolutionary biologists will explain mate guarding behavior in terms of enhanced male reproductive success, and that is why mate guarding persists. I never questioned this explanation, but should have. The E. mucronatum observation caused me to see mate guarding in a new way and realize that mate guarding involves a male and female component – I know this seems obvious, but I had my own cultural bias to overcome in this regard. I had never considered that mate guarding could involve non-willing females.

Based on a 10 minute observation of a very common insect my new understanding of mate guarding now recognizes that mate guarding influences female fitness also. Mate guarding persists when it creates a change in fitness in the male and female such that there is a positive net change in fitness for reproductive output for all individuals involved. In the case I witnessed, there may actually be a reproductive cost for the female and that is why she tried to avoid/escape the mate guarding. I have much more to learn about mate guarding.

Science is a way of objectively seeing the world and testing what you have seen to approach truth. This observation of E. mucronatum was also a mirror that showed my cultural bias and how that bias influenced my interpretation of my observations. For me, this observation could be a watershed event.

The moral(s) of this story:

  1. Life is short: enjoy time in the field with friends.
  2. Pay attention. There are new and wonderful things to observe even in the common and mundane.
  3. Be aware of the biases that can keep you from the truth.
  4. Have fun out there!

Copyright © Kent Fothergill 2013

Cover photo for the June 2013 issue of The Coleopterists Bulletin

Eurhinus cf. adonis on Solidago chilensis | Chaco Province, Argentina

Did anybody think that weevil photograph on the cover of the June 2013 issue of The Coleopterists Bulletin (vol. 67, no. 2) looked familiar? If so, it’s  because you saw it first in my April 28, 2013 post,  This is Eurhinus cf. adonis (ID courtesy of Charles O’Brien), which I photographed near La Escondida in Chaco Province, Argentina on flowers of Solidago chilensis. This photo reminds me that I need to pay more attention to portrait-style photographs, as landscape oriented photos don’t often fit very well on magazine and journal covers.

Beyond being my first cover for The Coleopterists Bulletin (and I hope not the last), the issue contains a number of papers that I will be studying with interest. These include a paper describing new species of Chrysobothris (Buprestidae) from the West Indies with notes on others, a checklist of longhorned beetles (Cerambycidae) from Montana, and the synonymization of Megacyllene comanchei under M. angulifera—all by Mike Ivie and colleagues (I did have the privilege of reviewing the Chrysobothris paper, and my Megacyllene comanchei“—now M. angulifera—specimens were among those examined). Also of interest to me is a paper about wood-boring beetle emergence (including Buprestidae and Cerambycidae) from ponderosa pines killed by mountain pine beetle and fire in the Black Hills of South Dakota. Finally, Brett Ratcliffe has included a primer on best writing and curatorial practices for describing a new species of beetle—as a somewhat but not highly practiced alpha taxonomist, this should be an interesting read for me that will hopefully give me a chance to correct any nascent bad habits that I may be developing. Scarabaeologists and weevil specialists should be equally pleased with this issue, with a half-dozen or more papers in each group filling most of the remaining pages.

Copyright © Ted C. MacRae

Plionoma suturalis in Oklahoma—a new state record!

When I returned from my vacation/insect collecting trip to western Oklahoma two weeks ago, most people upon learning where I went responded with a funny look that said, “Why would you want to go to Oklahoma?” Even entomologists familiar with my inclination for beetles merely assumed I went there to collect tiger beetles and were surprised to learn that, for this trip, I was actually targeting jewel beetles (family Buprestidae) and longhorned beetles (family Cerambycidae). Jewel beetles and longhorned beetles, of course, are largely associated with dead wood, and western Oklahoma is smack dab in the middle of the Great Plains. However, this does not mean that there are no trees in the area, or that whatever trees do exist are merely western examples of pedestrian eastern species with a depauperate beetle fauna. In fact, I came to this area precisely because previous visits had seemed to indicate high potential for interesting species of woodboring beetles. On my September 2011 visit, passing through on my way back from Colorado, I found several individuals of the unusual fall-active Acmaeodera macra (representing a northern range extension), and during last year’s fall visit I found a single Chrysobothris octocola adult on a dead mesquite (Prosopis glandulosa) branch—a northeastern range extension and new state record for Oklahoma! Interesting records for other species of beetles over the past few years also supported the idea that western Oklahoma was understudied and held the promise of more interesting new records for anyone willing to spend time in the area.

Plionoma suturalis (male) | Gloss Mountains, Major Co., Oklahoma

Plionoma suturalis (male) on mesquite (Prosopis glandulosa) | Gloss Mountains, Major Co., Oklahoma

Nearly all of these interesting records have been found in the Gloss Mountains, a fascinating system of gypsum capped, red clay mesas in Major Co. I now regard the Gloss Mountains State Park as my “portal” to northwestern Oklahoma and can’t imagine traveling to or through the area without stopping and spending time knocking around this fascinating, brick-red landscape. Such was the case during this year’s trip, and while I had decided to spend at least the first field day in and around the State Park, the collecting was so good that I stayed for a second day and returned for a third later in the week. The beetle shown in these photos is part (and only part) of the reason why. Arriving in the morning of the first day in the field, I headed straight for the mesquite tree on which I had found the C. octocola adult last fall. It’s a common species in the southwestern U.S. that normally wouldn’t warrant any special attention, but since the Oklahoma record was based on a single specimen I wanted to see if I could find additional individuals to confirm that the species was actually established in the area and that last year’s record wasn’t just a one-off. I whacked a dead branch, and onto my beating sheet fell a C. octocola adult! I whacked another dead branch, and off fell another adult! As it was, I would find the species as abundantly here, in strict association with mesquite, as I have seen it at other locations further to the southwest. Soon after collecting the first few C. octocola adults, however, I whacked a live branch on the same mesquite tree, and off fell two large, colorful longhorned beetles that I recognized instantly as representing the species Plionoma suturalis.

Plionoma suturalis (female) | Gloss Mountains, Major Co., Oklahoma

Plionoma suturalis (female) on mesquite flowers | Gloss Mountains, Major Co., Oklahoma

Plionoma suturalis belongs to the great tribe Trachyderini. Beetles in this tribe are known for the bright colors, attraction to flowers, and diurnal (day-active) tendencies, and while we have a few species in the eastern U.S. they are far more diverse in the southwestern states. Plionoma suturalis and another U.S. species (P. rubens) are known to occur from Texas west to California and south into northern Mexico, but I immediately had the feeling that finding this species in Oklahoma was a significant record. The beetles were abundant on the mesquite trees that lined the parking lot and dotted to landscape below the main mesa, with many observed feeding on the flowers (the trees were in full bloom) and numerous mating pairs also observed. Considering its abundance at the site and possible significance of the record, I collected several dozen specimens to serve as vouchers (not to mention I had only collected a handful of specimens in all of my previous years of collecting). Checking my database later that evening (I never leave home without my computer!) confirmed my suspicions—Oklahoma was not only a new state record, but a significant northeastern range extension. In fact, the closest previous record was by Lingafelter & Horner (1993), who recorded eight specimens from Wichita Co., Texas—just over 200 miles to the south! Further, the Wichita Co. specimens were all collected in 1956, and subsequent collecting had yielded no additional specimens, leading the authors to consider the status of this species in north-central Texas as doubtful.

The female feeds on flowers of mesquite (Prosopis glandulosa)

Large number of individuals were seen feeding on mesquite flowers.

Plionoma suturalis is one of only a handful of North American longhorned beetle species in which the adults exhibit bimodal seasonal activity, with adults appearing during the spring months, disappearing during the summer, and reappearing in the fall (see  for a previous example from Missouri) (Linsley 1962). In the Lower Rio Grande Valley of south Texas (where the activity of many species of longhorned beetles and other insects is distinctly bimodal to coincide with moderate temperatures and increased precipitation during spring and fall), this species has been found on fresh-cut mesquite and huisache (Acacia farnesiana) in the fall months and on the blossoms of fabaceous trees during spring and early summer (Hovore et al. 1987).

REFERENCES:

Hovore, F. T., R. L. Penrose & R. W. Neck. 1987. The Cerambycidae or longhorned beetles of Southern Texas: a faunal survey. Proceedings of the California Academy of Science 44(13):283–334, 20 figs.

Lingafelter, S. W. & N. V. Horner. 1993. The Cerambycidae of north-central Texas. The Coleopterists Bulletin 47(2):159–191, 7 figs.

Linsley, E. G. 1962. The Cerambycidae of North America. Part III. Taxonomy and classification of the subfamily Cerambycinae, tribes Opsimini through Megaderini. University of California Publicatons in Entomology 20:1–188, 56 figs.

Copyright © Ted C. MacRae 2013

Agrilus fuscipennis on Persimmon

Agrilus fuscipennis

Agrilus fuscipennis may not be the largest or the prettiest member of the genus occurring in Missouri (that honor is reserved for Agrilus concinnus, or “hibiscus jewel beetle”—MacRae 2004). Nevertheless,  it comes pretty darned close! Add to that the fact that it is among our most seldom encountered jewel beetles, and you can understand how excited I was to see this species on my sheet after beating a small persimmon (Diospyros virginiana) tree last weekend at Hercules Glades Wilderness in the White River Hills of extreme southwestern Missouri. In fact, I have only collected this species three times previously—all single specimens beaten from persimmon, and all back in the 1980s!

Agrilus fuscipennis

Jewel beetles are unquestionably popular among insect collectors, due no doubt in large part to their vivid, metallic colors. I think the family, however, would be even more popular were it not for the genus Agrilus. Fully one in five species of jewel beetles belongs to this genus, which at nearly 3,000 described species and counting (Bellamy 2008) is perhaps the largest genus in the entire animal kingdom. As might be expected, such hyperdiversity has resulted in taxonomic quagmire, with species limits difficult to define and many hardly distinguishable except by examination of male genitalia (MacRae 2003). Additionally, in contrast to the rest of the family which is generally recognized as containing some of the most spectacularly beautiful beetles in the world, the most species of Agrilus are small, usually less than 8 mm in length and often as small as only 4–5 mm, and also lack the vivid colors (at least, to the naked eye) for which the rest of the family is so noted.

Agrilus fuscipennis

Agrilus fuscipennis is one of several species that buck this general Agrilus theme. While not forming a discrete taxonomic group within the genus, they are all unified by the following characteristics: 1) relatively large for the genus (A. fuscipennis measures 12–14 mm length), 2) vivid red pronotum and black elytra, and 3) mine the lower trunks, crown and main roots of living rather than dead host plants. For A. fuscipennis the larval host is persimmon, and other similar species include A. vittaticollis on serviceberry (Amelanchier) and A. concinnus on wild hibiscus (Hibiscus). These other species also are not very commonly encountered, at least in my experience, perhaps partly because they are not as easily reared from their hosts as species that develop as larvae in dead wood (the latter can be easily reared by retrieving infested wood from the field and placing in containers to trap emerging adults).

Agrilus fuscipennis

In the interest of full disclosure, these photos were taken in the studio after returning home. Although the persimmon branch is real, the “blue sky” is actually just a colored index card. I prefer to photograph insects in the field, especially with insects such as tiger beetles where it is desirable to include elements of the insect’s natural habitat in the photograph. However, I don’t have a problem with studio photography if field photographs prove too difficult or time-consuming or present too high a risk of escape by a prize specimen. My normal protocol for the latter is to place the first individual in a vial and continue to search for another that I will then try to photograph in the field. If that doesn’t work then I still have the first individual as a backup for studio photographs. In the case of this beetle, I found it on the very first clump of persimmon that I beat but never saw another despite beating persimmon for the rest of the afternoon (just like the three I found separately back in the 80s)! I have plans to photograph A. concinnus later this summer on its Hibiscus host plant in southeastern Missouri—hopefully I will succeed in getting true field photographs of that species.

Agrilus fuscipennis

REFERENCES:

Bellamy, C. L. 2008. World catalogue and bibliography of the jewel beetles (Coleoptera: Buprestoidea), Volume 4: Agrilinae: Agrilina through Trachyini. Pensoft Series Faunistica 79:1–722.

MacRae, T. C. 1991. The Buprestidae (Coleoptera) of Missouri.  Insecta Mundi 5(2):101–126.

MacRae, T. C. 2004. Beetle bits: Hunting the elusive “hibiscus jewel beetle”. Nature Notes, Journal of the Webster Groves Nature Study Society 76(5):4–5.

Copyright © Ted C. MacRae 2013

Flatfaced longhorn: Leptostylus transversus

Leptostylus transversus | Holly Ridge Conservation Area, Stoddard Co., Missouri

Leptostylus transversus | Holly Ridge Conservation Area, Stoddard Co., Missouri

The longhorned beetle subfamily Lamiinae is one of the few subfamilies in the beetle world to have its own common name—flatfaced longhorns. This photo of one of its members, Leptostylus transversus, doesn’t show the character very well, but as with all members of the subfamily the face is completely vertical, a condition called “orthognathous” (mouthparts directed downwards), while all other longhorned beetles exhibit a more prognathous (mouthparts directed forward) condition. (A third possible condition, opisthognathous, refers to mouthparts directed backwards, a condition not occurring in longhorned beetles but common in leafmining species of jewel beetles and leaf beetles.)

I beat this individual this past May from dead branches at Holly Ridge Conservation Area in Stoddard Co., Missouri. Leptostylus transversus belongs to the tribe Acanthocinini, one of the largest tribes in the family and incredibly diverse in the tropics. Most members of this tribe are colored like mottled bark, as is this one, with many also exhibiting tubercles, erect setae or tufts of setae that combine to give the beetles a rather warty appearance. I presume the combination of coloration and irregular outline contributes to their overall cryptic appearance.

When I studied the longhorned beetle fauna of Missouri (MacRae 1994), this was one of the most common species that I encountered (268 specimens from throughout Missouri were examined). Despite its abundance, two interesting features were noted for this species. Firstly, it exhibits a distinctly bimodal temporal occurrence, with most of the specimens I examined being captured either during March through June or September through October and almost none during July or August. I am not aware or many (any?) other species, at least in Missouri, that exhibit such a strongly bimodal occurrence. There are several possible explanations, such as the occurrence of two generations per year or an adult “aestivation” (summer hibernation) period, but I think it more likely that adults emerge primarily during late summer and fall, overwinter as adults, and then become active again the following spring. This latter suggestion seems to be supported by reared specimens in my collection, the great majority of which have emerged from their hosts after mid-August.

The second interesting feature of this species is its extreme polyphagy. Many longhorned beetles are quite polyphagous, but most still utilize primarily angiosperms or gymnosperms and not both. Leptostylus transversus, on the other hand, shows no preference for either group—specimens in my collection have been reared from the angiosperms Amelanchier arborea (serviceberry), Carya ovata (shagbark hickory) and Diospyros virginiana (persimmon) and the gymnosperms Juniperus virginiana (eastern red-cedar), Pinus echinata (shortleaf pine), and P. sylvestris (Scots pine). In fact, even most species that prefer gymnosperms tend to utilize either pine or juniper but not both.

REFERENCE:

MacRae, T. C. 1994. Annotated checklist of the longhorned beetles (Coleoptera: Cerambycidae and Disteniidae) known to occur in Missouri. Insecta Mundi 7(4) (1993):223–252.

Copyright © Ted C. MacRae 2013

2013 Oklahoma Collecting Trip iReport

I’m back home after my week-long collecting trip to western Oklahoma, and at the risk of sounding hyperbolous I can only describe it as one of the most successful collecting trips I’ve ever had. Seriously! These kinds of trips don’t happen all that often for a variety of reasons—timing is off, rains didn’t happen, weather was uncooperative, etc. etc. Once in a while, though, everything comes together, and this was one of those times. The trip was also a return to my roots so to speak—I’ve been rather distracted in recent years with tiger beetles, but jewel beetles (family Buprestidae) and, to a lesser extent longhorned beetles (family Cerambycidae), are really the primary focus of my taxonomic studies. It had been several years since I’d had a good “jewel beetle trip,” so that was the focus of this trip. In planning the trip, I recalled seeing jewel beetle workings in several woody plant species in the same area during last September’s trip, and the occurrence of May rains seemed to bode well for my early June timing.

Gloss Mountains State Park, Major Co., Oklahoma

Gloss Mountains State Park, Major Co., Oklahoma

My instincts proved to be justified—in seven days in the field I collected an estimated 1000–1500 specimens representing at least two dozen species of Buprestidae and a dozen or more Cerambycidae. More important than the numbers, I collected a number of species in good series that I have either not or only rarely collected before, and in fact the second beetle that I collected turned out to be a new state record! Of course, I also brought along my full-sized camera and associated gear and photographed many of the species that I collected. I will feature these photos in future posts, but for this post I thought it might be fun to give a high level view of the trip illustrated only with photos taken with my iPhone (which I also carry religiously in the field with me). The iPhone is great for quick snaps of scenery and miscellaneous plants and animals for which I don’t feel like breaking out the big camera, or as a prelude to the big camera for something I’d like to share right away on Facebook. Moreover, there are some types of photos (landscapes and wide-angles) that iPhones actually do quite well (as long as there is sufficient light!).

Gloss Mountains State Park, Major Co., Oklahoma

Atop the main mesa at Gloss Mountains State Park, Major Co., Oklahoma

My first destination was Gloss Mountains State Park (Major Co.), a stunning system of gypsum-capped, red-clay mesas. I’ve already found a number of rare tiger beetles here such as Cylindera celeripes (Swift Tiger Beetle), Amblycheila cylindriformis (Great Plains Giant Tiger Beetle) and Dromochorus pruinina (Frosted Dromo Tiger Beetle), and in the past two falls I’ve found two interesting jewel beetle records: Chrysobothris octocola as a new state record, and Acmaeodera macra as a northern range extension. On this trip, I started out beating the mesquite  (Prosopis glandulosa) and immediately got the longhorned beetle Plionoma suturalis—a new state record! They were super abundant on the mesquite, and I collected several dozen specimens along with numerous C. octocola as well. I then moved over to the red-cedar (Juniperus virginiana), which was showing a high incidence of branch dieback, and collected nice series of several buprestids, including what I believe to be Chrysobothis ignicollis and C. texanus. Up on top of the mesa there are small stands of hackberry (Celtis laevigata) and soapberry (Sapindus saponaria), both of which are very good hosts for Buprestidae. Not much was on the soapberry, but I beat large series of several Buprestidae from the hackberry, including what I believe to be Chrysobothris caddo and—the real prize—Paratyndaris prosopis! My old friend C. celeripes was also out in abundance, so I collected a series to add to my previous vouchers from this site. Back down below, I marveled at a juvenile western diamondback rattlesnake (Crotalus atrox) in the area where I found some more A. cylindriformis larval burrows. Daylight ran out before I could dig them up, and after 11 hours in the field I was exhausted, so I returned the next morning and got one 1st- and two 3rd-instar larvae and went back up on top of the mesa and beat several more P. prosopis from the hackberry.

Bullsnake (Pituophis catenifer sayi) | Alabaster Cavern State Park, Woodward Co., Oklahoma

Bullsnake (Pituophis catenifer sayi) | Alabaster Cavern State Park, Woodward Co., Oklahoma

My second stop was at Alabaster Cavern State Park (Woodward Co.), where C. celeripes was again abundant on the gypsum-clay exposures surrounding an impressive gorge thought to be a collapsed cave complex. I focused on beating hackberry because of the success with buprestids on this plant at Gloss Mountains SP, and although they were not quite as abundant here as at Gloss Mountains I still managed to end up with good series of C. caddo and several species of Agrilus. Because I had spent the morning at Gloss Mountains, I had only a partial day to explore Alabaster Caverns and, still getting used to the weight of the camera bag on my back, decided to leave the big camera in the car. This was a mistake, as I encountered my first ever bullsnake (Pituophis catenifer sayi) and had to settle for iPhone photos of this species—the photo above being the best of the bunch. An approaching storm put an end to my second day after another 10 hours in the field, and I drove an hour to Woodward.

Moneilema sp. on Opuntia phaecantha | Alabaster Cavern State Park, Woodward Co., Oklahoma

Moneilema sp. on Opuntia macrorhiza | Alabaster Cavern State Park, Woodward Co., Oklahoma

My third day started out at nearby Boiling Springs State Park, a riparian oasis on sandy alluvium alongside the nearby Cimarron River. The woodlands are dominated by hackberry and American elm, and although a few buprestids were beaten from hackberry and honey locust (Gleditisia triacanthos), the numbers and diversity were not enough to hold my interest in the spot. After lunch, I decided to return to Alabaster Caverns SP and explore some other areas I had not had a chance to explore during the previous partial day. It’s a good thing that I did, as I ended up finding a nice population of longhorned cactus beetles in the genus Moneilema associated with prickly pear cactus (Opuntia macrorhiza). I collected a nice series of adults and also learned a few lessons in how to photograph these beetles on their viciously protective host plants. The photo above gives a taste of what will come in the photos that I took with the big camera. After eight hours in the field and darkness falling, I drove two hours to Forgan in Beaver Co.

Beaver Dunes State Park, Beaver Co., Oklahoma

Beaver Dunes State Park, Beaver Co., Oklahoma

Day 4 in the field started out cold and ominous, having stormed heavily during the previous night and with thick clouds still hanging in the sky. I feared the day might be a wash but decided to venture to Beaver Dunes State Park anyway and take my chances (beating can still be productive even in cold weather as long as the foliage is not wet). It’s a good thing that I did, as the buprestids were as numerous as I’ve ever seen them. The park’s central feature is a system of barren sand dunes that are frequented by ORV enthusiasts and surrounded by hackberry woodlands. The park also has a reservoir and campground, around which are growing a number of cottonwoods (Populus deltoides).

Hackberry Bend Campground, Beaver Dunes State Park, Beaver Co., Oklahoma

Hackberry Bend Campground, Beaver Dunes State Park, Beaver Co., Oklahoma

These hackberrys and cottonwoods proved to be extraordinarily productive. On the former I collected large series of several species of Chrysobothris and Agrilus, and while I collected fewer Buprestidae on the latter, these included Agrilus quadriguttatus and Poecilonota cyanipes! The latter species I had never collected until last year (from Cerceris fumipennis wasps), and beating the lower branches of the declining cottonwoods produced a series of about a dozen specimens. I also got one specimen on black willow (Salix nigra), along with a few Chrysobothris sp. and what I take to be Agrilus politus. Also in a low branch of one of the cottonwoods was a bird’s nest with a single egg that, according to Facebook comments, either represents the American Robin or a Gray Catbird. (I returned the next day and saw two eggs in the same nest.)

American Robin or Gray Catbird nest w/ egg | Beaver Dunes State Park, Beaver Co., Oklahoma

American Robin or Gray Catbird nest w/ egg | Beaver Dunes State Park, Beaver Co., Oklahoma

As the day drew to a close, I found two interesting longhorned beetle species at the edge of the dunes: one large, powdery gray Tetraopes sp. on milkweed (Asclepias sp.), and huge numbers of Batyle ignicollis evidently perched on the yellow spiked inflorescence of an as yet undetermined plant. I have seen this species on many occasions, but always in low numbers, yet here were literally hundreds of individuals on the plants, all having assumed a characteristic pose on the inflorescence suggesting that they had bedded down for the night. I only spent eight hours in the field on this day because of the late start, and as darkness approached I began the two-hour drive to Boise City.

Black Mesa landscape

Sculpted sandstone landscape in the vicinity of Black Mesa State Park, Cimarron Co., Oklahoma

The final two days in the field were supposed to be spent exploring the area around Black Mesa in the extreme northwest corner of Oklahoma, and another hour of driving was needed to get to the area from Boise City. I first went to Black Mesa State Park, and while the landscape was stunning (see above) the area was extremely dry. I feared the collecting would not be at all productive in this area but wanted to give the area a good effort before making a call. As I approached the entrance to the park, I saw a jeep parked by the side of the road with a license plate that read “Schinia,” which I recognized as a genus of noctuid moths that are very popular with collectors. I pulled over and talked to the driver, who was indeed a lepidopterist from Denver and had just arrived himself. We talked and exchanged contact information, and learning of my interest in beetles he directed me to a small stand of Gambel oak (Quercus gambelii) and one-seed juniper (Juniperus monosperma) on a sculpted sandstone escarpment not far from the park. I found the spot, and although I beat three Chrysobothris sp. from the first juniper tree that I whacked, another hour of beating produced only one more beetle from the juniper and nothing from the oak. I returned to the spot where we had met and encountered him again on his way out! We stopped and chatted again and found a few specimens of what I take to be Typocerus confluens on the yellow asters, but by then I was having my doubts about staying in the area. I told him I was going to check out a ravine in the park and then decide.

Petrified forest | Black Mesa State Park, Cimarron Co., Oklahoma

Petrified forest | Black Mesa State Park, Cimarron Co., Oklahoma

The petrified forest ended up being the only interesting thing I found in the ravine—the area was so dry that I think even the real trees were almost petrified! At any rate, it was clear that I was not going to have much success in this area. I looked at my watch, knowing that it would take three hours to drive back to Beaver Dunes, and estimated that if I left now I could get in about three hours of collecting at Beaver Dunes where I’d had so much success the previous day. Thus, I did what I rarely do on a collecting trip—drive during the afternoon!

Beaver Dune

The main dune at Beaver Dunes State Park, Beaver Co., Oklahoma.

A chunky grasshopper nymph inhabiting the dune

A chunky grasshopper nymph inhabiting the main dune.

I arrived back at Beaver Dunes with several hours of daylight still remaining, so I decided to take a look around the main dunes before heading towards the woody plants. I’ve actually visited Beaver Dunes previously, on the tail end of a fall tiger beetle trip in 2011. At that time I had seen only the rather common and widespread species Cicindela formosa (Big Sand Tiger Beetle) and C. scutellaris (Festive Tiger Beetle), but I thought there could still be a chance to see the much less common C. lengi (Blowout Tiger Beetle). Early June, however, is a little late to see the spring tigers, and in fact I saw only a single C. formosa. Nevertheless, I find dune habitats irresistible—alien habitats occupied by strange plants and animals, and I spent a bit of time exploring the main dune before heading back towards where I had collected so many Buprestidae the previous day.

Low water levels in the reservoir at Beaver Dunes are a result of three years of drought.

Low water levels in the reservoir at Beaver Dunes are a result of three years of drought.

Western Oklahoma, like many parts of the central U.S., has suffered rather severe drought conditions for the past several years. This was evident not only in the large amount of branch dieback seen in the woody vegetation of the area (and probably a contributor to my success at collecting Buprestidae) but also the very low water level in the park reservoir. In the photo above the small cottonwood saplings in the foreground and large cottonwood trees in the left background indicate the normal water level. Cottonwoods, of course, like to keep their feet wet, and the trees around this reservoir—left high and dry by the drought—have responded with major branch dieback and lots of subsequent adventitious sprouting at the bases of the main branches. It was from this adventitious growth that I had beaten most of the Poecilonota cyanipes that I collected the previous day, so I repeated the cottonwood circuit in the hopes of collecting more. Not only did I collect more, but I collected twice as many as the previous day, so I ended up with a very nice series of more than two dozen individuals of the species from the two days collecting. I also did a little more beating of the hackberry trees which had produced well the previous day and collected several more Chrysobothris caddoC. purpureovittata, and Agrilus spp. such as A. leconteiA. paracelti, and perhaps others. When I arrived I was unsure whether I would stay here the following day, but eventually I decided I had sampled the area about as well as I could and that I would go back to the Gloss Mountains for my last day in Oklahoma. Thus, as the day began to wane I began hiking back to the car and spent the next two hours driving back to Woodward to spend the night.

Steep slope below the main mesa | Gloss Mountains State Park, Major Co., Oklahoma

Steep slope below the main mesa | Gloss Mountains State Park, Major Co., Oklahoma

Echinocereus sp. | Gloss Mountains State Park, Major Co., Oklahoma

Echinocereus sp. | Gloss Mountains State Park, Major Co., Oklahoma

Arriving at the Gloss Mountains the next morning was like coming home! I’ve spent so much time at this place and found so many great insects, yet every time I come here I find something new. Today, however, my goals were more modest—I wanted to improve on my series of Paratyndaris prosopis and Chrysobothris texanus, so I focused most of my time beating the hackberry and juniper on top of the mesa and continued beating the juniper down below as well. Success! I collected four more Paratyndaris off of the hackberry, but the C. texanus were far more abundant on this day than they were earlier in the week—I probably got another two dozen individuals of this species. Of course, I also got distracted taking photographs of a number of things, so the day went far more quickly than I realized. I wanted to leave around 6 pm and get in about three hours of driving so that I would have time to make it into Missouri the next morning and have a nice chunk of time to collect before finishing the drive and arriving home on Saturday night. It was actually closer to 7:30 pm before I hit the road, the reason for the delay being the subject of a future post (I will say that BioQuip’s extendable net handle comes in handy for much more than collecting tiger beetles!).

Dolomite glades | Hercules Glades Wilderness, Taney Co., Missouri

Dolomite glades | Hercules Glades Wilderness, Taney Co., Missouri

Long Creek | Hercules Glades Wilderness, Taney Co., Missouri

Long Creek | Hercules Glades Wilderness, Taney Co., Missouri

For my last day of collecting, I decided to stop by at one of my favorite spots in the White River Hills of extreme southwestern Missouri—Hercules Glades Wilderness in the Mark Twain National Forest. I’ve been to this place a number of times over the years, but in recent years my visits have usually been late in the season to look for the always thrilling to see Cicindelidia obsoleta vulturina (Prairie Tiger Beetle). It had actually been about 25 years since I’d visited these glades during the spring, and because of the success I’d had collecting in Oklahoma I was really optimistic that I would find the same here. Sadly (and inexplicably), insect activity was very low, and it didn’t take long for this to become apparent as branch after branch that I beat along the trail through the dry-mesic forest down to Long Creek yielded nothing. By the time I got to the creek I still had not collected a single beetle. A consolation prize was found along the creek, as beating the ninebark (Physocarpos opulifolius) produced a few specimens of the pretty little Dicerca pugionata, and a couple more consolation prizes were found further up the trail approaching the main glade when I saw a Cylindera unipunctata (One-spotted Tiger Beetle) run across the trail and then beat a single Agrilus fuscipennis from a small persimmon (Diospyros virginiana) tree at the edge of the glades. It had been about 25 years since I last collected the latter species, so I was very happy to see it, but no more were seen despite beating every persimmon tree that I saw during the rest of the day. At the end of the day, I had hiked seven miles and collected only six beetles—a rather inauspicious ending to what was otherwise a wonderfully successful trip.

A rare ''selfie''

The author takes a rare ”selfie” at Gloss Mountains State Park.

Arriving back at the car at the end of the day on the last day of an extended collecting trip is always a little depressing—despite the vagaries of travel, cheap hotel beds, meals on the go, and general exhaustion, I’m never happier than I am when I am in the field. Still, the success that I’d had during this trip did much to ease my depression, and arriving home late that night and seeing my girls again (who waited up for me!) finished off any remaining depression.

© Ted C. MacRae 2013