The last survivor

This past June I made two trips to the Loess Hills of extreme northwestern Missouri as part of a follow-up survey for Cylindera celeripes (swift tiger beetle).¹ I was hoping to identify additional populations, however small, of this tiny, flightless, enigmatic species to go along with the three that colleague Chris Brown and I discovered last year.  The results were good news, bad news – no new populations were found, but I was able to re-confirm the beetle’s occurrence at two of the sites where we found the beetle last year.

¹ Some of you may recall my excitement at finally finding this long-sought after species in Missouri – apparently limited to the state’s few remaining high quality loess hilltop prairie remnants.

One of the sites that I had hoped might harbor the beetle is Squaw Creek National Wildlife Refuge in Holt Co. – located very near McCormack Loess Mounds Natural Area where the beetle was seen both this year and last.  Squaw Creek features several thousand acres of restored wetland habitat in the Missouri River valley that serve as resting, feeding, and breeding grounds for migratory birds and other wildlife.  Located within the Mississippi Flyway, the refuge is best known for its large concentrations of snow geese and bald eagles.  Wetlands are not good habitat for C. celeripes, but it was not the wetlands I was interested in visiting (well, I am really interested in visiting the wetlands someday – but on these visits I had other goals).  Rather, it was the tiny slivers of loess hilltop prairie that still remain on the fingers of loess bluffs along the eastern boundary of the refuge.  Twice scouring these prairie remnants over a two-week period failed to reveal the presence of the beetle, but on the first visit I did see this lone, rather ragged-looking adult male Cicindela limbalis (common claybank tiger beetle).  Unlike the aforementioned species, C. limbalis is rather common throughout most parts of the state on upland clay exposures. A spring-fall species, adults first emerge in September, have a little fun (which includes feeding but not mating), and then dig back into the ground for the winter before emerging once again in the spring. It is one of the first insects to greet the new season (I’ve seen them as early as late March) – mating and oviposition occur over the next month or two, and by end of May these guys are pretty well spent.  An interesting feature of the populations found in extreme northern Missouri is their higher degree of elytral maculation.  Compare this relatively fully-marked individual with this female that I reared from a larva collected at Knob Noster State Park in west-central Missouri (incidentally, my first ever reared tiger beetle!).

This male is clearly among the last of his generation in this area – not only did I not see any other individuals on the entire trip, but he clearly exhibits signs of wear and tear.  I found him nibbling on this dead millipede (which larger tiger beetles are known to prey upon); however, I don’t think this guy actually killed the millipede.  Rather, I think he found it already dead and was scavenging one of the only meals still available to him.  Closer examination of the face reveals that his left mandible is broken off near the base (best seen in the enlarged photo) – whether a result of battle with over-sized prey or a narrow escape from predation himself is hard to say.  Regardless, with only one “tooth” his ability to capture prey on his own has been severely compromised, and about all he can do is look for already dead prey items on which he can scavenge.  As one of the last survivors of his class, one can only hope that he lived a long and fruitful life, killed much prey, and inseminated many females.

Photo Details: Canon 50D w/ 100mm macro lens (ISO 100, 1/250 sec, f/14-16), Canon MT-24EX flash (1/4 ratio) w/ Sto-Fen diffusers. Typical post-processing (levels, minor cropping, unsharp mask).

Copyright © Ted C. MacRae 2010

…the “better” Eleodes suturalis

As I mentioned in my previous post, I really wasn’t satisfied with the photographs I took of the clown beetle, Eleodes suturalis, that I brought back from Oklahoma. I had placed the beetle in a terrarium of native soil and taken the obligatory whole beetle and head close-up photographs, both showing all the characters needed to identify the species in adequate detail. They were good, scientific photos, but they weren’t very exciting. In fact – they were boring! Now, I know not every subject I photograph is going to be a wower (the giant desert centipede I recently featured probably setting that standard), but it is important to me that the photographs I post here at least be interesting. After taking those first E. suturalis photographs, then being underwhelmed as I brought them up one-by-one on the computer, I started thinking about whether certain insects are just ‘homely’, and no matter how you photograph them they will still be homely. Eleodes suturalis is by no means a homely beetle in real life, but that is due mostly to the impressiveness of its size – a quality not easy to project in photographs.  Beyond that, its somber coloration, lack of unusual morphological modifications, and “beady little eyes” (fide Adrian) don’t offer much else in the way of help.  Combine that with the unflattering salmon coloration of its native soil as a substrate and an exoskeleton just shiny enough to cause annoying specular highlights, and you’ve got a recipe for really boring beetle photographs!

That’s when it occurred to me to try photographing the beetle in a white box.  I’ve only just begun to experiment with this technique and have been impressed with its ability to make somber-colored subjects (e.g., Gromphadorina portentosa) attractive and truly beautiful subjects (e.g. Buprestis rufipes) simply stunning.  The sharp, clean environment of a white box demands a clean beetle, so I gave the beetle (who had done much digging since the previous photo shoot) a good soaking and scrubbing (to the beetle’s great disapproval!).  Yes, I know there is still some dirt on him, but I think a dental pick and wire brush would have been needed to remove every last bit, caked on as it was!  Despite that, I think I achieved the desired effect – specular highlights… gone!  Boring background… gone!  Clean and crisp and ready to impress! The photos also do a much better job of highlighting the 3-dimensionality of the beetle than the original photographs.  Of the many photos I took, my favorite is featured above, and below I present two more that closely approximate the vantage of the two photos I posted from the first shoot in a side-by-side comparison.

For those of you wondering how I managed to secure the beetle’s cooperation for these photos, I used a modification of the “lens cap” technique, covering the beetle with a large glass bowl instead.  The beetle crawled around under the bowl for a bit but eventually would end up settled down against the edge.  By carefully lifting the bowl I was able to avoid disturbing the beetle and fire a few shots before it would start wandering again.  I just repeated the process until I was satisfied I had a few good shots in the sequence.

Does this mean an end to my preference for in situ photographs?  Certainly not.  But some beetles just look better in white!

Photo Details:
White box: Canon 50D w/ 100mm macro lens (ISO 100, 1/250 sec, f/18-20), Canon MT-24EX flash, indirect. Typical post-processing (levels, minor cropping, unsharp mask).
Terrarium: same except f/18, direct flash w/ Sto-Fen diffusers.

Copyright © Ted C. MacRae 2010

The real Eleodes suturalis

I recently posted a photograph of a clown beetle (Eleodes hispilabris) (family Tenebrionidae) that I found last July in the Glass Mountains of northwestern Oklahoma.  I had encountered that individual while stumbling through the mixed-grass prairie in the middle of the night in search of the Great Plains giant tiger beetle (Amblycheila cylindriformis).  Although I eventually found the latter species, it took a few hours, during which time I was forced to examine numerous individuals of another clown beetle, Eleodes suturalis – perhaps the most conspicuously common clown beetle in the Great Plains.  I didn’t bother to take photographs of them, focused as I was on my tiger beetle search and owing to the fact that this was not the first time I’d encountered that species in abundance (the first time being many, many years ago as they crossed the highway en masse just a few miles north of the Glass Mountains in Barber Co. Kansas).  In fact, I was becoming rather annoyed with them due to their great similarity in size and coloration to the object of my desire¹, and only when I found the previously photographed individual doing the defensive “head stand” so characteristic of the group did I relent and break out the camera for a series of shots (not easy in the dark of night).

¹ Wrigley (2008) even suggested a mimetic association for Amblycheila cylindriformis and Eleodes suturalis due to their similarity in size, shape and coloration (black with a reddish-brown sutural stripe).

Of course, that individual turned out not to be E. suturalis, but the closely related species E. hispilabris, a fact that I did not realize until several days later as I was examining the photographs more closely. Fortunately, I happened to bring home with me a live individual of what truly represents E. suturalis, which I show in these photographs.  I’m not sure exactly why I brought a live one home with me – I’ve done more and more of this in recent years, mostly just to observe them and see what they do.²  I think in this case, I was intrigued by the possible mimetic association between this species and A. cylindriformis and wanted an individual for comparison with the several live A. cylindriformis individuals that I also brought back with me.

² The singular focus on collecting “specimens” that I had during my younger years seems to be giving way to a desire to know more about species as living entities and not just their external morphology.

Unlike E. hispilabris (my identification of which I only consider tentative), there can be little doubt that the individual in these photographs represents E. suturalis.  No other clown beetle in the Great Plains exhibits the sharply laterally carinate elytra and broadly explanate (spread outward flatly) pronotum (Bernett 2008).  The reddish-brown sutural stripe of the distinctly flattened elytra is also commonly seen in this species, although occasional individuals of a few other clown beetle species exhibit the stripe as well (including E. hispilabris, which likely was the reason I assumed it represented E. suturalis).  All of the characters mentioned above can be seen in the photographs shown here.  However, I nevertheless find the photos rather unsatisfying.  If you think you know why, feel free to comment, otherwise you can wait for the “better” photos…

Photo Details: Canon 50D w/ 100mm macro lens (ISO 100, 1/250 sec, f/18), Canon MT-24EX flash w/ Sto-Fen diffusers. Typical post-processing (levels, minor cropping, unsharp mask).

REFERENCES:

Bernett, A. 2008. The genus Eleodes Eschscholtz (Coleoptera: Tenebrionidae) of eastern Colorado. Journal of the Kansas Entomological Society 81(4):377–391.

Wrigley, R. A.  2008. Insect collecting in Mid-western USA, July 2007.  The Entomological Society of Manitoba Newsletter 35(2):5–9.

Copyright © Ted C. MacRae 2010

Lens and lighting comparisons

I’ve had my macrophotography rig for one year and a summer now, and while I still hesitate to regard myself a bona fide insect macrophotographer, I’ve learned a lot, feel I’m on the right track, and have had immeasurable fun in the process. I’m a tactile learner – i.e., I do best just trying different things for myself and seeing the results. The photos I show here are some “comparison” shots that I did during my recent giant desert centipede white box photo shoot.

For my photography, I use two macro lenses, both Canon, with almost equal frequency: the 100mm lens (up to 1X), and the MP-E 65mm lens (1X to 5X).  Although the choice is clear if I am much above or below 1X, I find that a large part of my shooting is right around the 1X level.  I’ve often debated which lens I should use in such situations – the longer working distance of the 100mm lens makes it easier to use in the field and less likely to spook the insects I am photographing, but lighting is also more problematic since the flash units are farther away from the subject.  One thing I hadn’t thought about, however, is the possibility of differences in image quality between the two lens (all other things being equal).  The white box session gave me an opportunity to look at this, since the use of indirect flash largely eliminates subject-to-flash distance as a variable.  The two shots below show 1X shots of the centipede – one taken with the 100mm lens and the other with the 65mm lens.  The photos have not been post-processed at all (except size reduction for web posting) to give the truest comparison possible – normally I would do some levels adjustment and unsharp mask (and for these, clone out that annoying blue fiber that ended up on its head!).

Canon 100mm macro lens @ 1X

Canon 65mm macro lens @ 1X

I think one can easily see how much more detail is captured by the 65mm lens (click on each for a larger version, as always), even despite its more limited depth of field (f/14 for the 65mm versus f/22 for the 100mm). This makes me re-think my strategy of using the 100mm when I can and switching to the 65mm only when I have to. In fact, I’ve occasionally opted to add extension tubes to the 100mm when I needed just a bit more magnification, but these photos make me think I should use the 65mm when I can and reserve the 100mm just for sub-1X shooting.

Both photos in the second comparison were shot using the 65mm at f/13, the only difference being the use of indirect flash in one photo and direct flash in the other. I’m not quite sure what to make of this – the direct flash photo is better lit and shows more detail, but this could be an artifact of insufficient flash unit power in the indirect photo. I probably should have done this comparison (or both, for that matter) using E-TTL rather than manual mode on the flash unit (and I may have to do that).

Canon 65mm macro lens, indirect flash

Canon 65mm macro lens, direct flash

Anyway, nothing earth-shattering here, and I may just be figuring out what others have learned long ago. Although I prefer the field for photography, I’m finding the white box – or at least a controlled, indoor environment – valuable for this type of experimentation.

Copyright © Ted C. MacRae 2010

Rearing the Prairie Tiger Beetle (Cicindela obsoleta vulturina)

A Prairie Tiger Beetle larva peers up from its burrow in rocky soil of a dolomite glade in the White River Hills of southwestern Missouri. The head of this 3rd-instar larvae is about the size of a pencil eraser.

I had so looked forward to the long Memorial Day weekend collecting trip – time of season and the weather were perfect, and it had been several years since I’d made a late spring swing through the woodlands, glades, and prairies of western Missouri. But after two fruitless days of searching for nearly non-existent beetles at Ha Ha Tonka State Park, Lichen Glade Natural Area, and Penn-Sylvania Prairie, I was faced with a choice: return home disappointed or try something completely different in an attempt to salvage the weekend.  I chose the latter.

A 3rd-instar Prairie Tiger Beetle larva extracted from its burrow. Total length is ~30mm.

What could be more different than the White River Hills of southwestern Missouri?  The deeply dissected dolomite bedrocks supporting xeric, calcareous glades, dry woodlands and riparian watercourses couldn’t be more different than the gentle, acidic sandstone terrain of those more northerly locations.  Its hilltop glades (“balds”) are the most extensive such system in Missouri, and I’ve already featured several charismatic insects from my travels last summer to this part of Missouri, including Megaphasma denticrus (North America’s longest insect), Microstylus morosum (North America’s largest robber fly), and Plinthocoelium suaveolens (North America’s most beautiful longhorned beetle).  One insect that I also wanted to feature from that area but that eluded me during last fall’s cold and wet collecting trip is the Prairie Tiger Beetle – Cicindela obsoleta vulturina.  This impressive species is highly localized in Missouri, occurring no further north and east than the White River Hills.  Moreover, the populations in this part of the state and across the border in Arkansas are highly disjunct from the species’ main population in the southern Great Plains.  Like a number of other plants and animals, the Missouri/Arkansas disjunct may represent a relict from the hypsithermal maximum of several thousand years ago, finding refuge in these rocky hills after cooling temperatures and increasing moisture caused the grasslands of today’s west to retreat from their former eastern extent.

The ''business end'' - four eyes and two enormous mandibles. The metallic purple pronotum is covered with soil.

Despite its restricted occurrence in Missouri, the species is apparently secure and occurs commonly on the many dolomite glades that are found in the area. I have records from a number of localities in the White River Hills, but the best populations I’ve seen occur at Blackjack Knob in Taney County.  Of course, I would have absolutely no chance of seeing the adults during this Memorial Day weekend – adults don’t come out until late summer rains trigger emergence in late August and early September.  It was not, however, the adults that I was after, for I had seen larvae of what I believed must be this species in their burrows during one of my visits to this location last summer.  Although I have collected several other species of tiger beetles in the area, I reasoned these larvae must represent C. obsoleta vulturina due to their rather large size (this species is one of the largest in the genus in North America) and because they lacked the white bordering of the pronotum typical of species in the genus Tetracha – the only other genus occurring in Missouri with species as large as this.  I had tried to extract some of the larvae for an attempt at rearing, but neither of the two techniques I tried (“fishing” and “jabbing”) had worked.  Fishing involves inserting a thin grass stem into the burrow and yanking out the larva when it bites the stem; however, I found the burrows of this species to angle and turn due to the rocky soil rather than go straight down for a clear shot.  Jabbing involves placing the tip of a knife at a 45° angle about 1″ from the edge of an active burrow, waiting for the larva to return to the top of the burrow, and jabbing the knife into the soil to block the larva’s retreat – a quick flip of the knife exposes the larvae, but in this case jabbing did not work because I always ended up hitting a rock and missing the larva before it ducked back down in the burrow.

Hooks on the abdominal hump of a 3rd-instar Prairie Tiger Beetle larva prevent it from being pulled out of its burrow by struggling prey.

I returned to the site where I had seen larval burrows last year and once again found them.  I tried fishing a few, though I knew this would be futile, then jabbing – again with no success, and then had an idea.  I went to the truck and retrieved a small trowel that I use to dig soil for filling rearing containers, then found an active burrow (larva sitting at the top, though dropping upon my approach) and got in position using the trowel as I would the knife.  I held the trowel firmly with both hands and placed my body behind it so I could use all my weight to force the trowel into the soil and past the rocks when the larva returned to the top of the burrow – worked like a charm!  After taking photographs of the first larva that I successfully extracted, I set to the business of collecting nearly a dozen more over the next couple of hours.  I then filled several containers with soil (using rocks in the larger one to create “compartments” to keep the larvae separated), poked “starter burrows” in the soil, and one at a time placed the extracted larvae in the burrows and sealed them in by pushing/sliding my finger over the hole.  I’ve found this is necessary to prevent the larvae from crawling right back out and digging a new burrow somewhere else – not a problem if there is only one larva in the container (although I prefer they use the starter burrows that I place at the edge of the container so that I can see them in their burrows to help keep track of what they are doing); however, in containers with more than one larva they will often encounter each other and fight, resulting in some mortality.  Larvae sealed in starter burrows eventually dig it open again but generally continue excavating it for their new burrow.  One larva was not placed in a rearing container – it was kept in a vial for the trip home, where it was dispatched and preserved in alcohol as a larval voucher specimen.

This male adult Prairie Tiger Beetle (emerged 10 weeks after collecting the larva) shows the dark olive-green coloration and semi-complete markings typical of the MO/AR disjunct population.

After returning to St. Louis, I placed the rearing containers in a growth chamber and monitored larval activity 2-3 times per week.  Whenever a burrow was opened, I would place a fall armyworm, corn earworm, or tobacco hornworm larva in the burrow and seal it shut.  Some burrows would be re-opened almost immediately and, thus, fed again, while others stayed sealed for longer periods of time.  Tap water was added to the container whenever the soil surface became quite dry – generally once per week, and by late July nearly all of the burrows were sealed and inactive. If these larvae did, indeed, represent C. obsoleta vulturina, then this would be the time they would be pupating.  On August 15 I had my answer, when I checked the containers to find the above male had emerged, and the next day two more adults emerged as well (including the female shown below).

This female adult Prairie Tiger Beetle emerged the same day as the male and shows slightly brighter green coloration.

I put the emerged adults together in the largest rearing container, and within minutes the male and one of the females were coupled. I’ve kept them fed with small caterpillars and rootworm larvae, and numerous oviposition holes were eventually observed on the surface of the soil in the container. In a few weeks, I’ll place this container in a cold incubator for the winter and then watch next spring to see if larvae hatch and begin forming burrows. If so, it will be a chance to see if I can rear the species completely from egg to adult and preserve examples of the younger larval instars.

Photo Details: Canon 50D (ISO 100, 1/250 sec) w/ Canon MT-24EX flash w/ Sto-Fen + GFPuffer diffusers. Typical post-processing (levels, minor cropping, unsharp mask).
Photos 1-2, 5-6: 100mm macro lens (f/14-f/16).
Photos 3-4: 65mm MP-E 1-5X macro lens (f/14).

Edit 9/10/10, 6:30 pm: I checked the terrarium today and discovered 24 brand new 1st-instar larval burrows dotting the soil surface.  They are quite large already, almost as big as 3rd-instar burrows of the diminutive Cylindera celeripes.  I guess I’m surprised to see larvae hatching already, as I expected they would overwinter as eggs and hatch in the spring.  Now that I think about it, however, hatching in the fall makes sense, as this gives them an opportunity to feed some before winter sets in and also allows them to burrow for more protection from freezing temperatures.  I’ve dumped a bunch of 2nd-3rd instar Lygus nymphs into the terrarium for their first meal.

Copyright © Ted C. MacRae 2010

North America’s largest centipede

As I prowled the remote mixed-grass prairie of northwestern Oklahoma in the middle of the night, an enormous, serpentine figure emerged frenetically from a clump of grass and clambered up the banks of the draw I was exploring.  Although I was still hoping for my first glimpse of the Great Plains giant tiger beetle, I was keeping a watchful eye out for anything that moved within the illuminated tunnel of my headlamp due to the potential for encountering prairie rattlesnakes (perhaps the most aggressive of North America’s species).  This was clearly no snake, but at up to 8″, Scolopendra heros (giant desert centipede) easily matches some smaller snakes in length.  Also called the giant Sonoran centipede and the giant North American centipede, it is North America’s largest representative of this class of arthropods (although consider its South American relative, S. gigantea – the Peruvian or Amazonian giant centipede, whose lengths of up to 12″ make it the largest centipede in the world).

Although I had never before seen this species alive, I recognized it instantly for what it was.  Many years ago I was scouting the extreme southwest corner of Missouri for stands of soapberry (Sapindus saponaria), a small tree that just sneaks inside Missouri at the northeasternmost limit of its distribution, in hopes of finding dead branches that might be infested with jewel beetles normally found in Texas.  I had heard that these centipedes also reach their northeastern extent in southwestern Missouri, and just a few miles from the Arkansas and Oklahoma borders I found a road-killed specimen.  I stood there dejected looking at it – too flattened to even try to salvage for the record.

Centipedes, of course, comprise the class Chilopoda, which is divided into four orders.  The giant centipedes (21 species native to North America) are placed in the order Scolopendromorpha, distinguished by having 21 or 23 pairs of legs and (usually) four small, individual ocelli on each side of the head (best seen in bottom photo).  The three other orders of centipedes either lack eyes (Geophilomorpha) or possess compound eyes (Scutigeromorpha and Lithobiomorpha).  These latter two orders also have only 15 pairs of legs (shouldn’t they thus be called “quindecipedes”?).  Among the scolopendromorphs, S. heros is easily distinguished by its very large size and distinctive coloration.  This coloration varies greatly across its range, resulting in the designation of three (likely taxonomically meaningless) subspecies.  This individual would be considered S. h. castaneiceps (red-headed centipede) due to its black trunk with the head and first few trunk segments red and the legs yellow.  As we have noted before, such striking coloration of black and yellow or red nearly always indicates an aposematic or warning function for a species possessing effective antipredatory capabilities – in this case a toxic and very painful bite.

The individual in these photographs is not the first one I saw that night, but the second.  I had no container on hand to hold the first one and not even any forceps with which to handle it – I had to watch in frustration as it clambered up the side of the draw and disappear into the darkness of the night.  Only after I returned to the truck to retrieve a small, plastic terrarium (to fill with dirt for the giant tiger beetles that I now possessed) did I luck into seeing a second individual, which I coaxed carefully into the container.  It almost escaped me yet again – I left the container on the kitchen table when I returned home, only to find the container knocked onto the floor the next morning and the lid askew.  I figured the centipede was long gone and hoped that whichever of our three cats that knocked the container off the table didn’t experience its painful bite.  That evening, I noticed all three cats sitting in a semi-circle, staring at a paper shredder kept up against the wall in the kitchen.  I knew immediately what had so captured their interest and peeked behind the shredder to see the centipede pressed up against the wall. The centipede had lost one of its terminal legs but seemed otherwise none the worse for wear – its terrarium now sits safely in my cat-free office, and every few days it enjoys a nice, fat Manduca larva for lunch.

There are a number of online “fact sheets” on this species, mostly regarding care in captivity for this uncommon but desirable species.  I highly recommend this one by Jeffrey K. Barnes of the University of Arkansas for its comprehensiveness and science-focus.

Photo Details: Canon 50D (ISO 100, 1/250 sec) w/ Canon MT-24EX flash in white box.
Photos 1-2: Canon 100mm macro lens (f22), indirect flash.
Photo 3: Canon MP-E 65mm 1-5X macro lens (f/13), direct flash w/ Sto-Fen + GFPuffer diffusers.
Post-processing: levels, minor cropping, unsharp mask.

Copyright © Ted C. MacRae 2010

Trichodes bibalteatus in Oklahoma

Among checkered beetles (family Cleridae), the genus Trichodes contains among the largest and most strikingly-colored species.  The 11 North American species of this predominantly Holarctic genus are primarily western in distribution, although two species (T. nuttalli and T. apivorus) do occur in the eastern U.S.  The individual in these photos was one of several I encountered feeding on the flowers of a yellow composite in the Gloss Mountains of northwestern Oklahoma during early July.  I take them to represent the species T. bibalteatus based on their close resemblance to the holotype of that species from the LeConte Collection in the Museum of Comparative Zoology at Harvard University.  While these photographs are admittedly far from perfect, they were about the best I could manage at the time considering the gusty post-storm winds that I encountered atop the mesa where these beetles were found (along with my continuing difficulty in achieving proper exposure with subjects on bright yellow flowers).

The striking colors of adult Trichodes and their frequent association with flowers for feeding and mating belies a more treacherous aspect of their life history.  While adults may serve as important pollinators of native plant species (Mawdsley 2004), they also lay their eggs on flowers.  The larvae that hatch from these eggs don’t eat the flower itself, but rather attach themselves to bees and wasps that visit the flower as they gather pollen for provisioning their own nests (Linsley & MacSwain 1943).  The larvae hitch a ride back to the hymenopteran’s nest, where they then prey on the developing brood and usurp pollen provisions for themselves.

Photo Details: Canon 50D w/ MP-E 65mm 1-5X macro lens (ISO 100, 1/250 sec, f/16), Canon MT-24EX flash (1/8 ratio) w/ Sto-Fen + GFPuffer diffusers. Typical post-processing (levels, minor cropping, unsharp mask).

REFERENCE:

Linsley, E. G. & J. W. MacSwain. 1943. Observations on the life history of Trichodes ornatus (Coleoptera, Cleridae), a larval predator in the nests of bees and wasps. Annals of the Entomological Society of America 36:589–601.

Mawdsley, J. R. 2004. Pollen transport by North American Trichodes Herbst (Coleoptera: Cleridae). Proceedings of the Entomological Society of Washington 106(1):199-201.

Copyright © Ted C. MacRae 2010

Clown beetle surprise

As I slowly scanned my flashlight through the darkness across the mixed-grass prairie in the Glass Mountains of northwestern Oklahoma last July, there was one thing that I hoped not to see (prairie rattlesnake, unless from afar) and one thing that I hoped more than anything to see (Great Plains giant tiger beetle, Amblycheila cylindriformis). Fortunately, I encountered none of the former and found several of the latter.  It took awhile before I saw the first one, but in the meantime I saw all too abundantly the clown beetle, Eleodes suturalis.  A member of the family Tenebrionidae, this species is one of the most conspicuous components of the Great Plains beetle fauna.  Adults are commonly encountered walking about the grasslands or crossing roads, especially after summer rains.  I recall my first encounter with this species when I made my first insect collecting trip to the Great Plains in 1986, marveling as I literally watched hundreds of individuals crossing a remote highway in southwestern Kansas.  Now, they were just an annoyance – close enough in size and appearance to the object of my search that I had to pause and look at each one I encountered to verify its identity.¹

¹ In fact, a mimetic association has been suggested for Amblycheila cylindriformis and Eleodes suturalis due to their similarity in size, shape and coloration (black with a reddish-brown sutural stripe) (Wrigley 2008).  This may be true, as Eleodes suturalis is an abundant species capable of defending itself with noxious sprays that contain benzoquinone and other hydrocarbons, while Amblycheila cylindriformis is a much rarer species (as mimics tend to be) that lacks defensive compounds.

After finding a few of the Amblycheila, I encountered this particular individual clinging to a root sticking out of the side of a wash.  My closer look caused it to immediately assume its characteristic defensive headstand pose (from which the name ‘clown beetle’ comes), so I decided to take a few photographs (not an easy task at night).  The photos have been sitting on my hard drive since, but in examining them more closely, I realized that this particular beetle is not E. suturalis.  Rather, it is one of several similar appearing species that co-occur with E. suturalis in the Great Plains and sometimes resemble it due to their large size, sulcate elytra, and occasional presence of a similar reddish-brown sutural stripe.  From these species, E. suturalis is at once distinguished by its broadly explanate (flanged) pronotum and laterally carinate, distinctly flattened elytra.  This individual clearly exhibits more rounded elytra and as best as I can tell keys to E. hispilabris – distinguished from E. acuta and E. obscurus by possessing a normal first tarsal segment (not thickened apically) on the foreleg (Bennett 2008).  Presumably this and the other related species of Eleodes also possess chemical defenses similar to E. suturalis – an example of Müllerian mimicry where multiple species exhibit similar warning coloration or behavior (in this case headstanding) along with genuine anti-predation attributes.

Photo Details: Canon 50D (ISO 100, 1/250 sec, f/14), Canon 100mm macro lens, Canon MT-24EX flash (1/4 ratio) w/ Sto-Fen diffusers. Post-processing: levels, unsharp mask, slight cropping.

REFERENCES:

Bernett, A. 2008. The genus Eleodes Eschscholtz (Coleoptera: Tenebrionidae) of eastern Colorado. Journal of the Kansas Entomological Society 81(4):377–391.

Wrigley, R. A.  2008. Insect collecting in Mid-western USA, July 2007.  The Entomological Society of Manitoba Newsletter 35(2):5–9.

Copyright © Ted C. MacRae 2010