Honey Locust Borer

Agrilus difficilis | Beaver Dunes State Park, Beaver Co., Oklahoma

Agrilus difficilis | Beaver Dunes State Park, Beaver Co., Oklahoma

Conditions for collecting didn’t look very promising when I awoke on Day 4 of my early June trip to northwestern Oklahoma. After collecting at Alabaster Caverns State Park the previous day, I had traveled a few hours further west during the evening with plans to collect at Beaver Dunes State Park the following morning. However, heavy rain during the night and lingering sprinkles during the morning had me thinking it might be a lost day. By noon, however, the rain had completely abated, and though the sky still hung low and gray I decided I had nothing to lose by at least trying. I knew quickly that I’d made the right decision, as within minutes of arriving at the park I began seeing jewel beetles (family Buprestidae) landing on my beating sheet. Hackberry (Celtis sp.) was abundant along the roadways and supporting great numbers of individuals in the genera Chrysobothris and Agrilus.

This species is associated almost exclusively with honey locust (Gleditsia triacanthos).

This species is associated almost exclusively with honey locust (Gleditsia triacanthos).

By the time I reached the back end of the campground, I’d collected rather large series of the hackberry associates when I noticed a dying honey locust (Gleditsia triacanthos) tree in one of the campsites. Honey locust (and fabaceous trees, in general) is favored by several species of jewel beetles—at least a dozen species have been recorded in the literature reared from its branches, and another dozen species have been collected on it as adults. As a result, when jewel beetles are active it’s always a good bet that some will be found on honey locust when present, especially if the trees are stressed or dying. I walked up to the tree—a fairly large one—and scanned the lower branches overhead to see if I could notice any activity. I did not, but I nevertheless placed my beating sheet underneath one of the branches, gave the branch a quick “whack” with the handle of my net, and lowered the beating sheet to have a look. To my surprise, I saw at least 50 adults of the jewel beetle species, Agrilus difficilis, sitting on the beating sheet. Because of the cloudy conditions and cool, moist air, the beetles were not very active and did not immediately zip off the beating sheet as they would have had the day been sunnier and warmer, so I was able to rather easily collect a decent series of the beetles without any trouble. I had never seen the beetles so numerous, however, so I continued to beat a few more branches—each yielding just as many adults as the previous. I was astonished by the fact that the beetles were so abundant on the branch, yet I had not seen them even when I specifically looked for the presence of jewel beetles in the branches prior to beating them. Taking another look at the branches, I was able to visually detect just a few individuals, and those only with great difficulty, until I pulled the branch down and was able to look at it up close.

Relatively large size, coppery-purple color without spots on the elytra, and the presence of lateral white patches distinguish this species.

Large size, coppery color, no spots on elytra, and presence of lateral white patches distinguish this species.

Honey locust became a rather popular landscape ornamental tree in the eastern U.S. after the development of thornless cultivars, and while at first the tree seemed to be relatively free of insect pests, A, difficilis has proven to be one of several insects that have adapted to these landscape plants and occasionally cause economic damage. Trees in urban landscapes are often planted in suboptimal sites and suffer from stress to a much greater degree than their native counterparts, and the beetles take advantage of the lowered defensive capabilities of these stressed trees to gain entry. Larvae mine beneath the bark and damage the cambium layer, interfering with movement of water and nutrients. Trees in later stages of attack usually exhibit branch dieback and D-shaped holes in the trunk and main branches where adults have emerged from the tree. In severe cases infestation by this species can result in death of the tree. As mentioned above, there are twelve other species of jewel beetles that have been reared from the wood of honey locust. All of these have been reared only from dead wood rather than living trees, but adults of these species might, nevertheless, be encountered on living trees. They include three species (A. egeniformisA. fallax, and A. pseudofallax) that might be confused with A. difficilis; however, the latter is easily distinguished from these and other congeners by its relatively large size, coppery color with purple luster, absence of any spots or pubescent lines on the elytra, and distinctive patches of white pubescence along the sides. As with most wood boring beetles, chemical control of the adults or larvae is usually not feasible once an infestation has already begun—the best method to avoid infestations in landscape trees is proper site selection and optimal care to prevent stress that reduces the ability of the tree to fend off attack.

Copyright © Ted C. MacRae 2013

INHS Seminar: Tiger Beetles of Missouri

If you are in the Champaign, Illinois area on Tuesday, 29 October 2013, I will be giving a seminar as part of the Illinois Natural History Survey Fall 2013 Seminar Series. I hope to see you there!

My thanks to Dr. Sam Heads for extending to me the invitation and to Jennifer Mui for preparing the very nice poster and attending to travel details.

INHS-Seminar-MacRae_2013-10-29
Copyright © Ted C. MacRae 2013

Quick Guide to Armyworms on Soybean

Throughout the soybean growing areas of the southern U.S. and South America, lepidopteran caterpillars are the most important pest complex affecting the crop. Millions of pounds of insecticides are sprayed on the crop each year in an effort to minimize their impact—a practice that is not always successful and entails significant exposure risks to the environment and farm workers alike. A variety of lepidopteran species occur in soybeans, and proper identification is essential to ensure adequate control and avoiding unnecessary applications. While the most important and commonly encountered species are velvetbean caterpillar (Anticarsia gemmatalis) and soybean looper (Chrysodeixis includens), others include soybean podworms (Helicoverpa zea in the U.S.; H. gelotopoeon and—now—H. armigera in Brazil and Argentina), sunflower looper (Rachiplusia nu), bean shoot moth (Crocidosema aporema), and armyworms of the genus Spodoptera. The last group contains several species that can affect soybean, and while they have traditionally been considered minor pests of the crop a number of species have increased in importance during the past few years.

I have been conducting soybean field trials in both the U.S. and South America for many years now and have had an opportunity to photograph most of the species known to occur on soybean in these regions. Identification of armyworm larvae can be rather difficult due to their similarity of appearance, lack of distinctive morphological differences (e.g. number of prolegs), and intraspecific variability in coloration. Conclusive identification is not always possible, especially with younger larvae; however, the different species do exhibit subtle characters that can usually allow for fairly reliable identification of large larvae. Considering the dearth of direct comparative resources—either in print or online—I offer this quick guide to the six armyworm species that I’ve encountered in soybean.


Spodoptera frugiperda (fall armyworm) | Jerseyville, Illinois

Spodoptera frugiperda (fall armyworm) | Jerseyville, Illinois

Spodoptera frugiperda (fall armyworm). This is not the most important armyworm pest of soybean, in contrast to its great importance in other crops such as corn and cotton. It is, however, the most widely distributed of the species, occurring in both the southern U.S. and throughout soybean growing areas of Brazil and Argentina. When problems do occur on soybean they are usually a result of larvae moving from grassy weeds to small soybean plants in late-planted or double-crop fields. Larvae can damage all stages of soybean, from seedlings (cutting them off at ground level) to later stages by feeding primarily on foliage and even pods. Larvae are somewhat variable in coloration but are distinctive among armyworms by virtue of the pinaculae (sclerotized tubercles) visible over the dorsum, each bearing a single stout seta. Four pinaculae are present on each of the abdominal segments, with those on the eighth abdominal segment forming a square, and larvae also exhibit a pronounced inverted, white, Y-shaped mark on the head.


Spodoptera exigua (beet armyworm) | Stoneville, Mississippi

Spodoptera exigua (beet armyworm) | Stoneville, Mississippi

Spodoptera exigua (beet armyworm). This species is better known as a pest of vegetables but will occasionally damage soybean in the southern U.S. In soybean larvae prefer to feed on foliage of seedling plants but will, if present during reproductive stages, also feed on blossoms and small pods. Late-instar larvae can be rather variable in appearance, but most tend to be green above and pinkish or yellowish below with a white stripe along the side. Larvae can be confused with Spodoptera eridania (southern armyworm) because of a dark spot that might be present on the side, but in southern armyworm the spot is on the first abdominal segment while in beet armyworm (when present) it is on the mesothorax.


Spodoptera ornithogalli (yellowstriped armyworm) | Jerseyville, Illinois

Spodoptera ornithogalli (yellow-striped armyworm) | Jerseyville, Illinois

Spodoptera ornithogalli (yellow-striped armyworm). This species is widely distributed throughout North and South America, but its status as an occasional pest of soybean is limited practically to the southeastern U.S. It is often encountered in soybean in low numbers but can reach pest status in double-crop fields with small plants that have been planted after wheat (similar to fall armyworm). Compared to other species in the genus the larvae are rather uniform in appearance, exhibiting paired, black, triangular spots along the back of each abdominal segment with thin to prominent yellow stripes running lengthwise adjacent to and not interrupted by the spots. Larvae oftentimes have an almost black velvety appearance with distinctly contrasting bright yellow stripes.


Spodoptera eridania (southern armyworm) | Jerseyville, Illinois

Spodoptera eridania (southern armyworm) | Jerseyville, Illinois

Spodoptera eridania (southern armyworm) | Union City, Tennessee

Spodoptera eridania (southern armyworm) | Union City, Tennessee

Spodoptera eridania (southern armyworm). This species is, like fall armyworm, widely distributed from the southern U.S. through Brazil and Argentina. In the U.S. it occurs only sporadically on soybean, usually causing “hot spots” of damage by groups of many larvae hatching from a single egg mass and skeletonizing the nearby foliage before dispersing as they grow larger. In Brazil and Argentina this species has emerged during recent years as one of the most important armyworm pests of soybean, especially in regions where cotton is also grown. Larvae can be somewhat variable in appearance and, in South America, can be easily confused with those of the black armyworm (S. cosmioides), both of which often exhibit prominent black markings on first and eighth abdominal segments and a subspiracular light-colored line along the length of the thorax and abdomen. Southern armyworm, however, rarely exhibits an additional black marking on top of the mesothoracic segment. Additionally, when the subspiracular line is present it is interrupted by the black marking on the first abdominal segment and is less distinct in front of the spot than behind, and if the line is not present then the black spots on top of the first abdominal segment are larger than those on top of the eighth abdominal segment.


Spodoptera cosmioides (black armyworm) | Acevedo (Buenos Aires Prov.), Argentina

Spodoptera cosmioides (black armyworm) | Acevedo (Buenos Aires Prov.), Argentina

Spodoptera cosmioides (black armyworm) | Chaco Prov., Argentina

Spodoptera cosmioides (black armyworm) | Saenz Peña (Chaco Prov.), Argentina

Spodoptera cosmioides (black armyworm) | Acevedo (Buenos Aires Prov.), Argentina

Spodoptera cosmioides (black armyworm) | Acevedo (Buenos Aires Prov.), Argentina

Spodoptera cosmioides (black armyworm). No accepted English common name exists for this strictly South American species that was previously considered a synonym of the North and Central American species Spodoptera latifascia. In Brazil it has been referred to by such names as “lagarta preta” (black caterpillar) and “lagarta da vagem” (pod caterpillar). The latter name has also been applied to other soybean pests, including southern armyworm, so to me “black armyworm” seems the most appropriate English name to adopt. Like southern armyworm, this species is a sometimes pest of cotton and in recent years has become increasingly important in soybean throughout Brazil and northern Argentina. Larvae often resemble and can be easily confused with those of southern armyworm; however, there is almost always a dark spot on top of the mesothoracic segment that is lacking in southern armyworm. Additionally, the light-colored subspiracular line, when present, is not interrupted by the black spot on the first abdominal segment and is equally distinct in front of and behind the spot. When the line is not present the black spots on top of the first abdominal segment are smaller than than those on top of the eighth abdominal segment.


Spodoptera albula

Spodoptera albula (gray-streaked armyworm) | Saenz Peña (Chaco Prov.), Argentina

Spodoptera albula (unbarred or gray-streaked armyworm). While known to occur in extreme southern U.S., this species has been cited as a pest of soybean only in Brazil, although its importance has not matched that of southern or black armyworm. Like most armyworms it is polyphagous, but this species seems to prefer amaranth (Amaranthus spp.). Larvae of this species can be distinguished from other South American armyworms that feed on soybean by the trapezoidal black marking on the mesothorax (usually semicircular to slightly trapezoidal in black armyworm), the black marking on the first abdominal segment not larger than that on the sixth abdominal segment, both of which are smaller than those on the seventh and eight abdominal segments, the white-only rather than white and orange dorsolateral stripe, and the triangular black markings on the abdominal segments each with a small white spot in the middle or at the apex of the marking.

Copyright © Ted C. MacRae 2013

Twig tethered to a twig

Geometrid larva (subfamily Ennominae?) | Plymouth, North Carolina

Geometrid larva (subfamily Ennominae?) | Plymouth, North Carolina

In September I visited soybean field trials across the southeastern U.S. It’s a trip I’ve done every year for the past I don’t know how many years and one that I enjoy immensely due to the opportunities it gives me to see the country, kick the dirt with academic cooperators, sample the local cuisine… and photograph insects. New for me this year was the Carolinas, and in a soybean field in Plymouth, North Carolina I encountered this geometrid larva on the stub of a soybean leaf petiole. Geometrid larvae are known variously as inchworms, cankerworms, spanworms, measuring worms, loopers, etc., depending on the species. Most of the common names refer to the same thing that the family name does—the larval method of locomotion whereby the caterpillar—possessing legs only at the two extremes of its body—”inches” its way along as if measuring the ground it walks on (Geometridae is derived from the Latin geometra, or “earth-measurer”). The resemblance of the larvae of many species to dead twig stumps is nothing short of remarkable, and had it not been for the contrasting coloration I may never have noticed the larva in the first place. I also did not notice until looking at it through the macro lens of my camera the tether attached by the larva to the tip of the twig—invisible to the naked eye but providing energy-saving stabilization for the larva to hold its cryptic position.

I’ve not encountered a geometrid larva in soybeans before, and my impression has been that they are largely deciduous tree feeders (perhaps due to the periodic occurrence in my area of outbreak species such as fall cankerworm). In trying to determine the species, I found no geometrids covered in the Higley & Boethel (1994) handbook on U.S. pests, and when I consulted the Turnipseed & Kogan (1976) and Kogan (1987) global reviews of soybean pests I found reference only to a few minor pests in India and southeast Asia. Hmm, time for BugGuide. Of course, lepidopteran larvae are not nearly as well represented as the adults, but it seemed most similar to species of the subfamily Ennominae, so I turned to Google and searched on “Ennominae soybean.” This turned up Passoa (1983), who reported larvae of Anacamptodes herse as pests of soybean in Honduras (and mentioned references to several other geometrid species associated with soybean in Brazil). Back to BugGuide, where I found the genus Anacamptodes listed as a synonym of Iridopsis, but the species I. herse was not among the list of species represented in the guide. Checking the link provided at the site to a revision of the genus by Rindge (1966) revealed that I. herse is strictly a Central American species. Perhaps another, North American species of the genus also favors soybean, which led me to Wagner (2005) who mentions soybean as a favored food plant for I. humilis. However, the contrasting purple-brown/yellow-green coloration and relatively thickened body of that species are quite unlike this individual. I don’t have Wagner’s book (only his smaller one on caterpillars of eastern forests—no match in there, either), so it may be that my only remaining option is to post the photo at BugGuide and hope that David Wagner encounters it (actually I should get David’s book anyway)¹.

¹ Update 10/5/13 11:30 am CDT—or hope that Brigette Zacharczenko runs into the post via Facebook and offers to pass it along to Dave during their lab meeting on Monday.

REFERENCES:

Higley, L. G. & D. J. Boethel [eds.]. 1994. Handbook of Soybean Insect Pests. The Entomological Society of America, Lanham, Maryland, 136 pp. [sample pages].

Kogan, M. 1987. Ecology and management of soybean arthropods. Annual Review of Entomology 32:507–538 [pdf].

Passoa, S. 1983. Immature stages of Anacamptodes herse (Schaus) (Geometridae) on soybean in Honduras. Journal of The Lepidopterists’ Society 37(3):217–223 [pdf].

Rindge, F. H. 1966. A revision of the moth genus Anacamptodes (Lepidoptera, Geometridae) (1966). Bulletin of the America Museum of Natural History 132(3):174–244 [pdf].

Turnipseed, S. G. & M. Kogan. 1976. Soybean entomology. Annual Review of Entomology 21:247–282 [pdf].

Wagner, D. L. 2005. Caterpillars of Eastern North America: A Guide to Identification and Natural History . Princeton University Press, Princeton, New Jersey, 496 pp. [Google eBook].

Copyright © Ted C. MacRae 2013

GBCT Beetle #3—Crossidius coralinus temprans

On Day 2 of our late August Great Basin Collecting Trip (GBCT), we headed east from Reno towards Fallon (Churchill Co.) and surrounding areas of western Nevada. Our quarry on this day was one of the spectacular Crossidius coralinus subspecies—in this case C. c. temprans. This subspecies was described by Linsley & Chemsak (1961) from large series of specimens collected in Lassen Co., California, but also mentioned were specimens from several locations in west-central Nevada. This material was not included in the type series because of the disjunct distribution but was otherwise not distinguished from the temprans populations, and for us the drive to Churchill Co. was much more feasible logistically than Lassen Co.

Crossidius coralinus temprans (female) | Churchill Co., Nevada

Crossidius coralinus temprans (female) | Churchill Co., Nevada

The female in the photo above is the first individual I encountered at the first stop we made to look for them—a swale about 12 miles west of Fallon in which we noted thick stands of gray rabbitbrush (Chrysothamnus nauseosus) in the early stages of flowering. It was still fairly early in the day, and though we scoured the area thoroughly only a few individuals were seen. The female exhibits some of the main characteristics that set this subspecies apart from the other red/black coralinus subspecies, including the faint bluish overtones, the deep red color, the relatively fine but dense elytral punctation, and its smaller average size. Females in particular exhibit a uniform, broadly expanded black pattern on the elytra that extends along the suture to at least the basal third of the elytra and also possess broadly black humeri connected by a black basal band.

A male from Churchill Co. shows reduction of elytral markings relative to females.

A male, also from Churchill Co., shows reduced elytral markings compared to females.

We had better luck finding individuals in the area 10–15 miles south of Fallon. I’m not sure whether this was due to actual greater abundance or the fact that it was now late morning and temperatures had warmed since our first stop. Nevertheless, we found a mating pair on one of the plants that I had hoped to photograph, but the female got skittish and took flight. Normally when one partner flees the other one does as well, but for some reason the male stayed put—nicely perched on top of the plant—and allowed me to take some photographs. Because I had already disturbed the female, I was pretty sure any attempted handling of the plant to position it with the sky in the background would cause the male to flee as well, so I photographed it as it sat—messy background and all. Still, the male shows the typical characters for males of the subspecies, in particular the faintly bluish dark pattern that is slightly expanded laterally and tapers anteriorly along the suture to the basal one-third of the elytra.

Lateral profile of the male shows a hint of black at the elytral base.

Lateral profile of the male (same individual as above) shows a narrow black band at the base of the elytra.

This lateral shot of the same male was taken, in part, to get an angle that allowed for a cleaner background, but it also more clearly shows the very narrow black band at the base of the elytra that connects the humeri, though the black markings are not as broad as in the female. After photographing this male, we found a spot near Carson Lake where the rabbitbrush was common not just along the road, but in the adjacent rangelands and along dikes adjacent to the wetlands surrounding the lake. There we found pretty good numbers of adults and worked the area for a couple of hours until we had adequate series.

This male from Pershing Co., Nevada has the elytral marking reduced to a narrow sutural stripe.

This male from Pershing Co., Nevada has the elytral markings reduced to a narrow sutural stripe.

Another reason for going east on this day was to take a shot at C. hirtipes bechteli, a subspecies known from only a few localities along the I-80 corridor in north-central Nevada. The westernmost locations were close to Lovelock—a 90-minute drive from where we were, so when we finished up in the area around Fallon we headed towards Lovelock. We knew finding this subspecies was a long shot, since all of the records in Linsley & Chemsak (1961) were from mid- to late September, but since making the effort didn’t impact our ability to arrive at the first planned stop the next day at a decent hour we had nothing to loose by looking for it. We found one of the localities, but the plants at this relatively higher altitude site were still in the earliest stages of bloom, and we didn’t see any adults within about a half-mile stretch of roadside. The effort, however, was not for naught (I love saying that!), as the lateness of the hour and a heavy blanket of smoke from the nearby Rim Fire created a most beautiful blood red sky. Before the day slipped away completely, we stopped at a spot closer to Lovelock to see if we could find a C. coralinus temprans adult to photograph against this unusual backdrop and were immediately rewarded with the fine male shown in the photograph above. Sitting against this marvelous background, the male shows a much reduced black elytral marking that is sometimes the case with males of this subspecies. I hurriedly took as many shots as I could (getting that one photo that I really like is, for me, still a numbers game), but the conditions were fleeting and within a short time it became too dark to take any more.

REFERENCE:

Linsley, E. G. & J. A. Chemsak. 1961. A distributional and taxonomic study of the genus Crossidius (Coleoptera, Cerambycidae). Miscellaneous Publications of the Entomological Society of America 3(2):25–64 + 3 color plates.

Copyright © Ted C. MacRae

Cover Photo—The Coleopterists Bulletin 67(3)

cso67-3co14.inddI hope you’ll all take note of the cover photo on the September 2013 issue of The Coleopterists Bulletin (vol. 67, no. 3), which just arrived in my mailbox. It features the adult jewel beetle, Chrysobothris octocola, that I found in September of last year at Gloss Mountains State Park (Woodward Co., Oklahoma) on a dead branch of mesquite (Prosopis glandulosa). That was a significant find, as it proved to be a new state record for Oklahoma. This is the second straight issue of the journal to feature one of my photos (the  featured the beautiful, metallic green weevil, Eurhinus cf. adonis, which I photographed in Argentina on flowers of Chilean goldenrod (Solidago chilensis).

Ironically, there are no articles in this issue about jewel beetles, but there are two articles covering my other main group of interest, the longhorned beetles, including a generic revision of Prionacalus by Antonio Santos-Silva and colleagues and a preliminary checklist of the Cerambycidae and Disteniidae of Alabama by Brian Holt. The Prionacalus revision appears to be everything we have come to expect from a modern taxonomic revision, complete with detailed taxonomic history and descriptions, key to species, and all species figured by line drawings and high quality photographs (including many of the primary types). Like most taxonomic works, it suffers from a lack of associated natural history information—not a fault of the authors, as such information is almost always lacking for all but the commonest of species in the Neotropics. The situation is a little better for Nearctic species, and the Holt checklist, happily, includes basic host plant associations for most of the species found within the state. I’ll be busily updating my database of distributional and host plant records for North American Cerambycidae from this work over the next week.

If you are not already a member of The Coleopterists Society, consider becoming a member. Not only is The Coleopterists Bulletin included with your membership, but you will also gain online access to archival and recent issues of the journal via JSTOR and BioOne.

REFERENCES:

Holt, B. D. 2013. A preliminary checklist of the Cerambycidae and Disteniidae (Coleoptera) of Alabama. The Coleopterists Bulletin 67(3):241–256 [abstract & references].

Santos-Silva, A., Z. Komiya & E. H. Nearns. 2013. Revision of the genus Prionacalus (Coleoptera: Cerambycidae: Prioninae: Prionini). The Coleopterists Bulletin 67(3):201–240 [abstract & references].

Copyright © Ted C. MacRae 2013

GBCT Beetle #2: Agrilus walsinghami

Late summer and early fall is not normally a very good time to go looking for woodboring beetles, which for the most part are found in their greatest diversity and abundance during spring and early summer. This is especially true in the drier western U.S., although notable exceptions occur in the so called “Sky Islands” of southeast Arizona (where most species have shifted their adult activity periods to coincide with late summer “monsoons”) and the lower Rio Grande Valley of south Texas (where spring and fall rains have resulted in bimodal patterns of adult activity for many species). Across the rest of the U.S. a rather limited assemblage of late-season species is found, mostly longhorned beetles associated with fall-blooming composites such as Megacyllene (e.g., M. decora) on goldenrod (Solidago) and Crossidius (e.g. C. hirtipes immaculatus) on rabbitbrush (Chrysothamnus and Ericameria) and snakeweed (Gutierrezia). Late-season jewel beetles are even less common, but one of the few species that does prefer the latter part of the season is also among North America’s most striking species—Agrilus walsinghami.

Agrilus walsinghami (male) | Davis Creek Park, Washoe Co., Nevada

Agrilus walsinghami (male) | Davis Creek Park, Washoe Co., Nevada

This sexually dimorphic species occurs broadly across the western U.S., from British Columbia (Davies 1991) south to Baja California (Hespenheide et al. 2011) and east to Colorado (Nelson & MacRae 1990). Adults are encountered almost exclusively on gray rabbitbrush, Ericameria nauseosa (formerly Chrysothamnus nauseosus, Asteraceae), which despite the lack of any rearing records is nevertheless presumed to serve as the larval host (Hespenheide et al. 2011).  I was hoping I would encounter this species on my recent Great Basin Collecting Trip (GBCT), as I’ve only seen it once previously (in southeast Arizona). The timing seemed right, as most published dates of collection range from mid-July to mid-September, and in fact I encountered and was able to photograph both male and female on the very first day of the trip (23 August) at the very first locality we visited (Davis Creek Park, Washoe Co., Nevada). As it turned out, I would see this species at perhaps a dozen localities or more during the course of the trip, although never in great numbers at any one locality nor with the sky conditions that allowed for the unusual background colors in these photographs (more on that in a future post).

Agrilus walsinghami (female) | Davis Creek Park, Washoe Co., Nevada

Agrilus walsinghami (female) | Davis Creek Park, Washoe Co., Nevada

The notable feature of this species is, of course, its sexual dimorphism, and it is remarkable that no author even mentioned such until Fisher (1928) discussed it in his revision of the genus in North America. Males have the head and pronotum bronzy brown with faint coppery reflections and the elytra brassy with slight purplish tints, while females are larger and more robust and are uniformly blue to greenish blue above. Both sexes have the underside strongly bronzy green with prominent white densely pubescent patches along the lateral portions of the thorax and abdomen and more or less coppery legs, making them truly one of the more spectacular species of Agrilus.

Pubescence

Males (above) and females both exhibit dense lateral pubescent patches.

All told I probably collected between two and three dozen specimens across the localities we visited in western Nevada and southeastern California. Too bad I don’t have more of a commercial mind, as I later discovered that somebody actually purchased one of these beetles on ebay for $16.38! All I would have needed was ~100 specimens of this “very uncommon!” (not!) species and I could have paid for the entire trip!

REFERENCES:

Davies, A. 1991. Family Buprestidae (metallic wood-boring beetles), pp. 160–168. In: Y. Bousquet [ed.], Checklist of the Beetles of Canada and Alaska. Agriculture Canada Publication 1861/E, Ottawa.

Fisher, W. S. 1928. A revision of the North American species of buprestid beetles belonging to the genus Agrilus. Bulletin of the United States National Museum 145:1–347.

Hespenheide, H. A., R. L. Westcott & C. L. Bellamy. 2011. Agrilus Curtis (Coleoptera: Buprestidae) of the Baja California peninsula, México. Zootaxa 2805:36–56.

Nelson, G. H. & T. C. MacRae.  1990.  Additional notes on the biology and distribution of Buprestidae (Coleoptera) in North America, part III.  The Coleopterists Bulletin, 44(3):349–354.

Copyright © Ted C. MacRae 2013