Tuesday Teaser


A recent post by Art Evans at What’s Bugging You reminded me about this photograph that I took some 10 years ago.  This will likely be a difficult challenge, but I’m willing to entertain guesses about its identity and where I found it.  For location, let’s just say I’ve featured quite a few insects from this place in past months – it might take a little digging to figure it out, so first correct answer is worth 4 points.  Knowing this will be key to figuring out its identity.  In that regard, order will be a gimme, so the first person who stumbles upon this will likely earn the measely 2 points available for correctly answering that question.  Family will be more difficult – 4 points if you score first on this one (hint – beware of recent taxonomic changes).  Genus will be a real, though not impossible challenge (in fact, necessary resources to determine this are available online) – a whopping 6 points await the first person to correctly identify that taxon.  Sadly, a definite species name won’t be possible (another clue?), but there is a short list of species that have been described from the general area, so bonus points are available for anyone willing to take on that challenge.  I have no additional pictures of this beast, so look for the answer as a comment to this post in a couple days or so.

Copyright © Ted C. MacRae 2010

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Gromphadorina portentosa

I found myself with a few spare moments this weekend, so I decided to finally put together a white box and see what I could do with it.  And what better subject for a white box maiden voyage than Gromphadorina portentosa, the Madagascan hissing cockroach.  Grotesquely beautiful, it also presents a challenging subject for flash-based macrophotography because of its hard, shiny exoskeleton that produces strong specular highlights with all but the most highly diffuse of light sources.  It was also the only live subject I had on hand at the moment, other than a few larval noctuids – not nearly as impressive as these behemoths!  There were some early glitches – the enormous size of these insects made for long working distances, with the result that my box was almost too small!  However, placing the subjects at the back of the box allowed the camera lens and flash units to sneak just inside the front drape, and the closer shots went more smoothly.  I’m quite happy with the results – at least as a first attempt, and I think the method shows even more promise for some preserved specimen photographs that I am planning.

The males, of course, have “horns” on the pronotum, but one thing I had never noticed before is the well-developed lip at its anterior edge.  This is certainly an adaptation to the “shoving” matches that males engage in with each other frequently.  This face-on shot shows him for the formidible opponent that he is!

Sexual dimorphism is fairly evident in this species, as least compared to your average cockroach.  Like most insects, females tend to be a little larger, especially when they are gravid as the one below appears to be.  In my colony I note that they also tend to be more uniformly dark in color than the males, although that is not quite so evident with this particular female.

The big difference is, of course, the weakly developed pronotal protuberances.  Females don’t engage in the shoving matches that males do, so there is no need for the heavily armed pronotum.  Nevertheless, small pronotal humps are still found in the adult females.  Note also the lack of a well-developed lip on the anterior edge of the female pronotum.

Photo Details: Canon 100mm macro lens on Canon 50D, ISO 100, 1/200 sec, f/8-11, indirect MT-24EX flash in white box.

Copyright © Ted C. MacRae 2010

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Lampetis drummondi larva?

Back in February, I learned that Mark Volkovitsh (Zoological Institute, Russian Academy of Science, St. Petersburg) would be visiting Chuck Bellamy (California Department of Food and Agriculture) in Sacramento the very week that I was planning to be in Lake Tahoe. Chuck and Mark are two of the worlds leading specialists in Buprestidae, or jewel beetles, and have worked together on a number of projects dealing with the taxonomy and systematics of buprestid beetles. Mark, in particular, has focused on describing the larval forms of buprestids (“white wormy things,” as my wife calls them) and using larval morphology to supplement adult morphology in phylogenetic analyses. I’m not anywhere near being in their league in terms of authority in the family – a comparative dabbler, really – but for some reason they’ve both seen fit to accept me into the fraternity. I’ve been fortunate to spend time in the field with each of them, as well as visit them at their respective institutions.  When I learned of Mark’s coincident visit, I couldn’t resist the chance to make the 2-hour drive from Lake Tahoe to Sacramento and spend the day with Mark and Chuck at the CDFA and discuss things buprestological.  The wife and kids were fine with that, since her brother also lives in Sacramento, and it would be a chance for them to do some sight-seeing before we all got together for dinner.  Upon arriving at CDFA, I also met Andy Cline, a nitidulid specialist at the CDFA (re-met actually, turns out we’d met some years back), and the four of us went out for an animated lunch at a nearby restaurant over some of the most delicious barbeque that I’ve ever tasted.

L-R: Mark Volkovitsh (Russia), Chuck Bellamy (CDFA), me, Andy Cline (CDFA)

After lunch, I was most interested in discussing with Mark some buprestid larvae that I had collected in Big Bend, Texas in 2004. My colleague Chris Brown and I were hiking a low desert trail west of Rio Grande Village when we encountered a large, uprooted Goodding willow (Salix gooddingii) tree laying on the river bank. Wilting leaves were present on some of its branches, suggesting that the half-dead had been washed to its current location by the river during a recent flood. At the base of the trunk where the main roots projected, I noticed what appeared to be frass (the sawdust that wood boring beetle larvae eject after eating it – that’s right, grub poop!) under the edge of the bark at the live/dead wood interface. I used my knife to cut away some of the bark and immediately encountered a huge buprestid larvae. Its enormous size is matched only by a few desert southwest species: Polycesta deserticola, which breeds commonly in oak and is known from willow, but breeds only in dead, dry branches; and Gyascutus planicosta, whose larvae are restricted to the living roots of Atriplex and a few other asteraceous shrubs.  Clearly, it could not be either of these species.  The only other desert southwest buprestids large enough to produce a larva this large (~50 mm) are Lampetis drummondii and L. webbii. However, the larvae of both of these species are unknown, as is basic information regarding what hosts they utilize for larval development. Lampetis webbii is quite rare, but L. drummondii is, in fact, one of the most conspicuous and commonly encountered buprestid species in the desert southwest – that fact that its larva has remained unknown suggests that it utilizes living wood, probably feeding below the soil line.  Thus, I immediately began to suspect that the larva might represent this species – a truly exciting development. 

As I continued digging into the wood, I encountered a second, somewhat smaller larva in a neaby gallery, and further digging revealed another clue about its identity in the form of fragments of a dead adult beetle – all brilliant blue/green in color (identical to the color of L. drummondi), and the largest (the base of an elytron, or wing cover) showing the same pattern of punctation exhibited by L. drummondi adults. I placed the two larvae individually in vials with pieces of the host wood; however, I knew there was little chance that either larva, requiring living tissue upon which to feed, would complete its development once removed from its host gallery.  They did survive for a time after my return to St. Louis, but when the largest larva became lethargic, I decided to go ahead and preserve them.  I sent the photograph below (taken by Chris) of the living larvae to Mark, who confirmed that it did indeed appear to be a species of Lampetis, based on its large size and the narrowly V-shaped furcus on the pronotal shield (typical for members of the tribe to which Lampetis belongs). 

Buprestid larva (prob. Lampetis drummondi) under bark of Salix gooddingii at trunk base - Big Bend National Park, Texas. Photo by Christopher R. Brown.

Considering the complete lack of published information on the larval biology of Lampetis drummondi and the several lines of evidence that these larvae, in fact, represent that species, it would be worthwhile to publish a description of the larva.  However, formal description requires dissection, and I did not know how to do this.  Mark, on the other hand, has dissected literally hundreds of buprestid larvae, including representatives of nearly every genus for which larvae are known.  He is the buprestid larva expert, and what a thrill it was for me to learn how to do this from the Master himself, using the larger of these two probable Lampetis larvae as the subject.  While we were dissecting the larva, we compared its features to those published for the European species Lampetis argentata (Danilevsky 1980) – the only member of the genus for which the larva is known – and confirmed their similarity and the larva’s likely close relationship to that species.  Coincidentally, the larva of L. argentata develops in living roots of saxaul (Haloxylon) – a genus of large shrubs/small trees (family Amaranthaceae) that grows in the deserts of Central Asia.  It thus appears that Lampetis species may, as a general rule, utilize living wood below the soil line for larval development, explaining why the larva of only one (now two) of the nearly 300 species in the genus worldwide has been found.

REFERENCES:

Danilevsky, M. L. 1980. Opisanie zlatki Lapmetis [sic] argentata (Coleoptera, Buprestidae) – vreditelya saksaula [Description of the larva of Lapmetis [sic] argentata (Coleoptera, Buprestidae) – the pest of HaloxylonZoologicheskii Zhurnal 59:791–793.

Copyright © Ted C. MacRae 2010

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Pismire Puzzle

I returned home from a much-needed vacation late last night, and even though it was a family trip I have much to share from the past 10 days. However, I must remain coy about where I was for the time being so that I may present this little quiz:

Who am I?

I had planned to post this yesterday, but the best title I could come up with – “Monday Myrmecine Mystery” – was just too similar to a Monday tradition on another blog that we’ve all grown to love.  (Also, I just couldn’t get to it.)  No longer constrained by an M-themed title, I came up with this alternative¹ that I hope will make the 12-year old boy in each of us giggle aloud.

¹ Pismire (from pissemire) is an archaic name of Scandinavian origin for ant. Derived from pisse urine (referring to the smell of formic acid) + mire ant.

What am I doing?

I expect members of the Formicine Guild will jump all over this, so I should probably make this quiz about more than just the name of the ant (which I don’t know, so does that make this an illegal quiz?).  Maybe I should offer double points to non-myrmecologists for a proper ID (but then, I would need the consensus of the myrmecologists – perhaps a conflict of interest?).

Why do I do this?

I could also offer points for correctly guessing what the ant is carrying – which again I wasn’t able to figure out, so I guess points will have to be awarded for the most plausible explanation.  What I do know is the ant carried this carcass while meandering aimlessly over the same patch of ground – occasionally stopping very briefly to dig its jaws into it before resuming its wanderings.  I followed the ant for about 10 minutes, and it never left an area of about 1 square foot – no nest nearby that I could see, no direction to its travels, no apparent purpose to its labors.

This is where I live.

I most definitely know where I was, so firm points are on offer for correctly guessing the answer to that question – either on the basis of the ant ID or the above photograph of its habitat.  Yes, that is snow on the ground – lots of it!

Copyright © Ted C. MacRae 2010

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The Inexorable March of Spring!

Granted, the progress of spring seems to advance in halting baby steps with occasional falls onto its muddy bottom, rather than as a determined forward march, but spring is welcome, no matter how it arrives. When little green tips start poking up and there’s a bit of that “spring smell” in the air, I simply must get out and catch up on the status of Nature — the old-fashioned way (she doesn’t have a Facebook account). Over the last week, I’ve gone forth in search of signs that everything else living is about as tired of winter as I am, and wants to get this spring show on the road! There is already so much happening, I can’t recount it all here — A partial list of unphotographed notables: owls breeding; hawks nesting; woodcocks doing their silly, repetitive and almost invisible (because it’s nearly dark) courtship displays; wood ducks on forest ponds; year-round resident songbirds reestablishing territories; spring peepers, chorus frogs, wood frogs and southern leopard frogs singing, especially in the fishless ponds; winter crane flies and midges swarming in sun flecks in the woods; wild filberts, silver and red maples flowering, etc…

Formica pallidefulva sniffs the spring air


Of course, I look for the first ants out at this time of year, though with the exception of 10 March, when the temperature exceeded 70F, they haven’t been notably active. However, that afternoon I encountered, among others, a worker of Formica pallidefulva poking its head out cautiously to sniff the spring air. This is one of my favorite local ants — largish (5-6mm), abundant, active in daylight even when it’s hot, usually shiny bronzy red to red-brown, usually with a darker gaster (the apparent abdomen of ants) around here, but ranging from a beautiful reddish gold (in the deep South) to almost pure black-coffee brown (New England and southern Canada) across its wide geographic occurrence (Rocky Mountain foothills of Wyoming to New Mexico, all the way east to Québec and Florida). It has the added charm of being the host species to a wide range of social-parasitic and dulotic (“slave-making”) ants both in its own and in another closely related genus, with which it lives in temporary or permanent mixed colonies (as with the Polyergus illustrated in my last post). The image below of these ants bringing home a charred earthworm was taken almost one year ago, as one of Shaw Nature Reserve’s prairie areas was beginning to resprout after a prescribed burn a few weeks earlier. Ants will take their food raw or cooked!

Formica pallidefulva with charred earthworm


Prenolepis imparis alate in the clutches of a gerrid

Another ant I mentioned last time I was with you, Prenolepis imparis, has the distinction of being the only ant in our fauna that has mating flights while there is still a good chance of frost in the forecast for the next few weeks. In this picture of a mating pair at  BugGuide, note the size difference that inspires their name “imparis”, Latin for disparate. Any time after mid-February when it is sunny and not too windy, and the temperature rises above 65F, the winged males and females reared the preceeding fall, fly out to partake of a grand insectan orgy. Typically, they have big flights on the first couple of appropriately warm days, then some smaller ones (i.e., fewer individuals participating) over the next few weeks. The flying males look like gnats, bobbing up and down in drifting swarms, a few feet off the ground over a shrub, near a woodland edge or in a sunny opening. (One of my co-workers got into the midst of a group of such swarms once when we were conducting a prescribed burn in a wooded area, and I recall her commenting she “felt like Pigpen with all the little bugs flying around”!) The much larger, golden-brown females lift slowly off the ground, fly ploddingly (or is it seductively?) through the male swarms, are there mobbed by the tiny fellows, and then glide away and slightly downward, mating in flight with the winner of the males’ tussling. Rather clumsy fliers, the females do not always land in a good spot, as occurred to this hapless one that ended up as a feast for a water strider. Those that survive break off their wings, dig a burrow, seal themselves in, and raise a small brood of workers on food produced in their own bodies (like say, milk in mammals or “cropmilk” in doves and some other birds.)

But lest you to think I only have eyes for ants, I feel indeed fortunate to have encountered a tarantula this week, of the same species as Ted recently posted and I didn’t even have to go to Oklahoma for it. This bedraggled individual was at the mouth of its completely flooded burrow in what is most often a very dry habitat — a dolomite glade. Stunned and muddy at the time, my guess is this creature, belonging to a resilient and ancient lineage, will dry off, clean up, and saunter away as soon as she warms up.

Aphonopelma hentzi in flooded burrow


And speaking of emerging from flooded burrows, how about this handsome fellow, a male three-toed box turtle, his sex revealed by his bright orange and red markings, coming up for a breather? In truth, it was perhaps only just warm enough to make him need air, but not really enough so for him to be up and about, so he just sat there, nearly immobile, looking pretty, notwithstanding mud and leaves glued onto his shell.

Male box turtle emerges


Copyright © James C. Trager 2010

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North America’s largest jewel beetle

Euchroma gigantea in Jamaica. Photo © Steve Meyer


In recent weeks I’ve featured a few jewel beetles that I have encountered amongst specimens sent to me for identification (see “Aaack!-maeodera” and “Acmaeodera carlota in northern Arizona“).  While the new distributions and even unknown species that they represent are fascinating from a scientific perspective, their diminutive size (~6 mm in length) probably makes them less than spectacular to the non-specialist.  The family Buprestidae does, however, contain some very large species, including a few that qualify as bona fide giants.  One such species, Euchroma gigantea (Giant Metallic Ceiba Borer Beetle), occurs from Mexico through Central America, the West Indies, and most of South America.  At a maximum of 65mm in length, it is not only North America’s largest jewel beetle, but also the largest jewel beetle in the entire Western Hemisphere.

My colleague Steve Meyer encountered and photographed this individual in Negril, Jamaica.  Although its scientific name translates to “colorful giant”, the beetle in the photo is especially so due to the delicate, waxy bloom covering its elytra. This bloom is secreted by the adult after transforming from the pupa and prior to emerging from its larval host, giving it a bright yellow-green appearance.  After the beetle emerges and becomes active, the bloom is quickly rubbed off and the beetle takes on the shiny, iridescent purple-green color by which it is more familiar.  The presence of bloom on this individual suggests that it had just emerged from the trunk of the kapok tree (Ceiba pentandra) on which it was sitting.  Kapok and other large trees in the family Bombacaceae serve as hosts for larval development for this species (Hespenheide 1983).

Indigenous peoples in Central and South America have long utilized the dazzlingly colored elytra of these beetles to create beautiful natural jewelry and adorn their clothes and textiles.  The species is also eaten in both the larval and adult stages – Tzeltal-Mayans in southern Mexico (Chiapas) roast the adults when available, and the Tukanoans (northwestern Amazon) also eat the larvae (Dufour 1987). I have eaten a few insects in my day, but none as thick and massively juicy as the grub of this species must be. Holometabolous larvae typically contain a rather high percentage of fat (up to 66% dry weight) to meet the demands of pupal development and adult reproduction, and I suspect this makes the larvae quite tasty (especially when roasted). If there is any insect in the world that I really, really, really want to eat – it is the larva of this one!

REFERENCES:

Dufour, D. L.  1987.  Insects as food:  A case study from the northwest Amazon.  American Anthropologist 89(2):383–397.

Hespenheide, H. A.  1983.  Euchroma gigantea (Eucroma, giant metallic ceiba borer), p. 719.  In: D. H. Janzen [ed.], Costa Rican Natural History, University of Chicago Press, Chicago.

Copyright © Ted C. MacRae 2010

Tuesday Tarantula


One of my destinations on my annual fall tiger beetle collecting trip last October was The Glass Mountains in northwestern Oklahoma. Rising from the red Permian beds of the central Great Plains, the Glass Mountains are a series of mesas and buttes capped by thick layers of the sparkling, glass-like crystal selenite. It is still common to see them referred to as the “Gloss” Mountains, the result of a transcription error by a mapmaker back in the late 1800s, and although the soils that comprise the formations are very old (laid down as sedimentary deposits during the Permian Era some 250 million years ago), the landscape itself is relatively young – a result of erosion by glacial outwash from the Rocky Mountains during the past 1 million years.

Of course, I was not here to study crystals or geology, but to look for tiger beetles! It was at this spot that earlier in the year (June) I had discovered a new population of Cylindera celeripes (Swift Tiger Beetle), a rarely-collected flightless species that has declined worrisomely during the past century, and another seldom-collected flightless species, Dromochorus pruinina (Frosted Dromo Tiger Beetle), was also a good find. Neither of these species were my reason for being here in October, however, since by then adults of both have long disappeared. Instead, I was hoping that the large, unidentified larvae that I had seen in their burrows at this site back in June would be out as adults. Their great size suggested two possibilities – Cicindela obsoleta (Large Grassland Tiger Beetle) or C. pulchra (Beautiful Tiger Beetle), either of which would be a great find. Alas, overcast skies and a cold, biting wind made whatever tiger beetles were there – lovers of sun and warmth that they are – remain secreted within their protected haunts. I still have a shot at finding out what they are – I successfully extracted two larvae from their burrows and fed them well in the laboratory with fat fall armyworm larvae before putting them to sleep for the winter in a 10°C (50°F) incubator.  If all goes well, I’ll wake them up this spring and finish them out to adulthood this year.

There were a few consolation prizes on the day, one of which was this large, lumbering male tarantula seen slowly making its way down the red clay slopes. For all their charisma and noteriety, it’s interesting to note that the taxonomy of U.S. tarantulas (almost all of which belong to the genus Aphonopelma) is rather poorly known – some 50 species have been described, but many of the descriptions are inadequately based on limited material (or even single specimens) and often rely upon variable, highly artificial characters (Prentice 1997). Brown or black species with no distinctive coloration (such as this one) seem to present the greatest challenge; however, the internet seems to have concluded that the only tarantula present in Oklahoma is Aphonopelma hentzi.


This spider can be distinguished as a mature male by way of the tibial hooks that can be seen on the undersides of the front pair of walking legs in the first photo.  Female and immature tarantulas normally stay in their burrows during the day and come out at night to hunt, but wanderlust strikes the adult males during late summer and fall, during which time they’ve been documented traveling as far as 1.3 km over a period of 2-3 weeks (Janowski-Bell and Horner 1999) – presumably in search of females with which to mate.  It is only after the male’s final molt that wanderlust sets in and the tibial hooks appear, which are said to function in holding the female (and her fangs!) at a safe distance during copulation.


It may seem hard to believe, given its large size and slow movement, but I found this spider exceedinly difficult to photograph compared to the tiger beetles that I have spent much more time with. I’m not used to photographing subjects with a 4-5 inch leg spread, which made it difficult for me to judge working distance and get a handle on proper settings and positions for the flash units. Once I did get that under control, I found the tarantula’s incessant desire to keep moving maddeningly frustrating. Tiger beetles, as active and flighty as they are, nevertheless eventually sit still long enough to allow at least a shot or two before bolting, but this tarantula… just… never… stopped… moving! I can’t tell you how many shots I discarded because it’s legs were splayed awkwardly in multiple directions. Eventually, however, I got enough shots that I felt there should be at least a few good ones among them, and those are the ones I share here.


Most male tarantulas will die within a few weeks or months of their final molt. Still, that doesn’t deter me from scooping them up whenever I find them and bringing them home to enjoy as pets for whatever time they have left. My daughters probably like tarantulas best of any of the critters that I bring home – I never have to ask “Has anybody fed ‘Hairy’?” (and props to awesome wife for enduring something most ‘normal’ wives couldn’t even begin to contemplate).

REFERENCE:

Janowski-Bell, M. E. and N. V. Horner.  1999.  Movement of the male brown tarantula, Aphonopelma Hentzi (Araneae, Theraphosidae), using radio telemetry.  The Journal of Arachnology 27:503–512.

Prentice, T. R. 1997. Theraphosidae of the Mojave Desert west and north of the Colorado River (Araneae, Mygalomorphae, Theraphosidae). The Journal of Arachnology 25:137–176.

Copyright © Ted C. MacRae 2010

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Acmaeodera carlota in northern Arizona

Acmaeodera carlota Fall – Coconino Co., Arizona

This is another of the interesting species that I encountered during my examination of material submitted for identification this past winter.  Acmaeodera carlota is one of 149 species/subspecies in North America belonging to this very difficult genus (recall my recent post, Aaack!-maeodera), and as with so many of its congeners it wasn’t described until after the last revision of the genus more than a century ago (Fall 1899).  Obviously, the genus badly needs another revision – or at least a revised key – so that the known species can be identified with some degree of confidence without having to send specimens to a specialist. There have been a handful of buprestid workers in recent decades who may have been able to accomplish this daunting task, but to date none have been willing to embrace this considerable challenge.

As far as is known, A. carlota occurs only in Arizona.  Fall (1932) described this species from a few specimens collected from cactus blossoms near Globe, Arizona (~90 miles east of Phoenix).  Since then, the only specific information recorded about this species was by Westcott et al. (1979), who reported adults cut from wood of Quercus dumosa near Sunflower (~60 miles northwest of the type locality) and collected from flowers in west-central Arizona near Wikieup.  Fall’s original description leaves much to be desired (as is the case for nearly all original descriptions prior to the last 50 years or so), and to this point no images have been published in the literature or appeared on the web.  This particular specimen was found in a batch of material sent to me by cerambycid-enthusiast Jeff Huether (the same batch containing the previously discussed Acmaeodera robigo), and the only reason I was able to identify it was by comparing it to a specimen given to me by the late Gayle Nelson, who collected the species near Wikieup after its occurrence was reported there by Westcott and colleagues.  The interesting thing about this specimen is that it was collected near Page, Arizona – nearly 200 miles north of any of the previous known localities and just south of the Utah border.  In suspect this species occurs even more broadly and is not, as the limited records suggest, restricted to Arizona.

Acmaeodera carlota belongs to a group of species that I loosely refer to as the A. tubulus-species group.  It is not clear that all of the species are actually closely related, but they do all resemble each other in their small size (<8 mm), general appearance (i.e., black with confused yellow maculations on the elytra), and inclusion in the so-called ‘Truncatae’ group (a subdivision of the genus established by 19th Century coleopterist George Horn to include those species having the prosternal margin nearly straight and not retracted from the sides). Within the Truncatae, the species in the tubulus-species group are distinguished by lacking a subapical crest on the last ventral segment and general appearance.  Only three species were known at the time of Fall’s revision (conoidea, neglecta, and tubulus); however, an additional eight species have been described since (carlota, ligulata, neoneglecta, opuntiae, parkeri, sabinae, starrae, and thoracata).  I have collected many of these species in my travels across the southwestern U.S. and lack only starrae and thoracta in my collection (the latter is known only from the type).  In the case of A. carlota, note the rather flattened dorsal surface that is densely clothed with long, stiff, dark, suberect hairs; the coarsely, contiguously punctate pronotum; and the subrugose, slightly irregular elytral intervals, which serve to distinguish this species from others in the group.

The group’s namesake, Acmaeodera tubulus, is widespread and common across the eastern U.S., making it relatively easy to identify. However, the remaining species of the tubulus-species group are limited to the south-central and southwestern U.S., and the lack of available identification keys and suitable descriptions makes them nearly impossible to identify except by comparison with determined specimens. As a result, I have built a key to the species in the Acmaeodera tubulus-species group that I use to assist in my own identifications.  The key is based on distinguishing characters given in the original descriptions (if any) and augmented by my examination of the material at my disposal.  I invite users to test the key with their own material and let me how well it works.

My sincere appreciation to Jeff Huether for allowing me to retain this specimen in my collection as a voucher for the range extension that it represents.

REFERENCES:

Fall, H. C.  1899.  Synonpsis of the species of Acmaeodera of America, north of Mexico.  Journal of the New York Entomological Society 7(1):1–37 [scroll to “Journal of the New York Entomological Society”, “v. 7 1899”, “Seq 12”].

Fall, H. C.  1932.  Four new Buprestidae from Arizona.  The Pan-Pacific Entomologist, 8(2) (1931):81-84.

Westcott, R. L., W. F. Barr, G. H. Nelson, and D. S. Verity.  1979.  Distributional and biological notes notes on North and Central American species of Acmaeodera (Coleoptera: Buprestidae).  The Coleopterists Bulletin, 33(2):169-181.

Copyright © Ted C. MacRae 2010

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