An elegant Eocene fly

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USA: Colorado, Garfield, Hwy 139, Douglas Pass.

Here is one of the more elegantly preserved specimens among the collection of Green River Formation fossil insects that I am photographing. It is obviously a fly (order Diptera), but I don’t agree with the preliminary identification of “Mosquito?” as indicated on its label. Rather, I think it is one of the fungus gnats—also members of the suborder Nematocera and, thus, closely related to mosquitos (family Culicidae), but with distinctly elongate coxae (bases of the legs) and lacking the elongated proboscis that mosquitos use for sucking blood. It’s hard to decide between Mycetophilidae (fungus gnats sensu stricto) or Sciaridae (dark-winged fungus gnats), which differ in whether the eyes meet above the antennae (Sciaridae) or not (Mycetophilidae). However, Borrer & White (1970) mention that species of the former are generally less than 5 mm in length, while the latter range from 5–10 mm. This specimen measures 4.15 mm from the front of the head to the tip of the abdomen, so  maybe that is evidence supporting Sciaridae (although perhaps there were smaller mycetophilids 50 mya than today).

Here is a view of the whole fossil, measuring approximately 50 mm on each side:

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REFERENCE:

Borrer, D. J. & R. W. White. 1970. A Field Guide to the Insects of America North of Mexico. Houghton Miffton Company, Boston, 404 pp.

Copyright © Ted C. MacRae 2012

Beautiful box of Buprestidae

I’ve been working on identifying Buprestidae accumulated from a variety of sources over the past year—mostly exchanges and gifts, before beginning the processing specimens collected during this past season. Once identified, and combined with specimens gleaned from material submitted by other collectors for identification (I generally only retain examples of species that are poorly represented in my collection or specimens that represent and will serve as vouchers for significant new distributional records), they make for a very pretty box of Buprestidae! It’s kind of nice to keep them collected together like this for a little while, but I’ll soon incorporate them into the main collection where they will more securely protected and to free up the temporary box now containing them for new material as it moves through the process of labeling and identification. (Incidentally, I think I might like to do a series a posts over this winter covering my version of the specimen curation process).

There are some very cool Buprestidae in this box—88 species in all, that originated from a remarkable variety of locations across the U.S., Mexico/Central America, and South America. Do you see any species of particular interest?

236 specimens representing 88 species of Buprestidae

236 specimens representing 88 species of Buprestidae

Copyright © Ted C. MacRae 2012

The gloriously dichromatic Dasymutilla gloriosa

I have a small collection of velvet ants (family Mutillidae) that I’ve accumulated over the years—not through active collection but more as bycatch from my beetle hunting operations. Velvet ants are, of course, not ants at all, but wasps, and as such the females are—like their winged relatives—quite capable of delivering a painful sting if mishandled. They also tend to be seen running rather frenetically across the ground, making them difficult to guide into a collection vial or grab with forceps. You’ve gotta really want ’em if you want to collect them. Still, even though I don’t study them I find them interesting enough to pick up on occasion, and with most groups outside of my area of focus the hope is that eventually they will end up in the hands of somebody who actively studies the group. Such is now the case with my mutillid collection, which will be shipped this week to another collector specializing in the group. In return I will be filling some holes in European representation of my collection of Cerambycidae.

Dasymutilla gloriosa, female | Brewster Co., Texas

Dasymutilla gloriosa, female | Brewster Co., Texas

Without question, the most interesting mutillid species that I’ve encountered is Dasymutilla gloriosa. All mutillids are sexually dimorphic, as only the males are winged, but most also tend to be sexually dichromatic to a greater or lesser degree. No species I am aware of takes this to the same level as D. gloriosa! The males (photo below) are rather typically colored compared to other species in the genus, but the females (photo above) are densely covered with long, strikingly white hairs. While this would seem to make them quite conspicuous, the true effect is the exact opposite as they easily confused with fuzzy plant seed. For this reason they are commonly called thistledown velvet ants. I encountered the female in west Texas in 2003 while walking a mountain trail and at first thought it was the fuzzy seed of a creosote bush (Larrea tridentata) being blown by the wind—except there was no wind! It took me a little while looking closely at it before I could figure out what it actually was. This is the only female of this species that I’ve seen in the wild, and I’ll be a little sad to see it sent to another location.

Dasymutilla gloriosa, male | Riverside Co., California

Dasymutilla gloriosa, male | Riverside Co., California

The male also is the only one I’ve encountered—or at least taken the trouble to collect. I would have never suspected this male, which I collected in southern California in 1991, was the same species as the female that I collected many years later. My thanks to Kevin Williams, who provided the identifications for both of these specimens.

Also called the ''thistledown velvet ant''

Also called the ”thistledown velvet ant”

Copyright © Ted C. MacRae 2012

Dainty, delicate, little fairies

Adela caeruleella | Wayne Co., Missouri

Ever since I saw Chris Grinter’s beautiful photographs, I have wanted to see (and possibly photograph) the tiny little moths known as fairy moths (family Adelidae, formerly considered a subfamily of Incurvariidae). These dainty, delicate, little moths are characterized by their unusually long antennae—especially the males, which can have their antennae up to three times the length of the forewings. This past April I got my wish as my father and I hiked the Shut-ins Trail at Sam A. Baker State Park in Missouri’s southeastern Ozark Highlands.

Females have the antennae ”only” twice as long as the forewings…

Chris was fortunate to see a number of individuals representing at least two species, presumably all males (based on the extraordinary length of their antennae) that were engaged in some rather interesting territorial behaviors. I, on the other hand, saw only this single individual (presumably a female) who seemed content enough to calmly nectar the golden Alexander, Zizia aurea (Apiaceae), flowers on which I found it. This was fine by me, as the dense woodland setting where I saw it wasn’t very conducive to photographing the moth. I wanted a clean, bright background to highlight the moths dark metallic luster, so I snipped the flower (carefully!) on which the moth was nectaring and held it up to the small patch of bright blue sky visible from the trail to take these photos.

…and the basal half distinctly thickened.

I presume this individual represents the species Adela caerueleella based on comparison with online photos. According to Powell (1969) this species is widespread across the eastern U.S. and has been recorded on flowers of American bittersweet, Celastrus scandens (Celastraceae). Microleps.org notes the species is most frequently found along deciduous forest trails and shows a preference for flowers of black snakeroot, Sanicula marilandica (Apiaceae). My late April observation is consistent with the April and May activity period noted by Powell (1969) and late May period for central Illinois noted by Microleps.org.

REFERENCE:

Powell, J. A. 1969. A synopsis of Nearctic adelid moths, with descriptions of new species (Incurvariidae). Journal of the Lepidopterists’ Society 23:211–240.

Copyright © Ted C. MacRae 2012

Book Announcement: Field Guide to the Jewel Beetles (Coleoptera: Buprestidae) of Northeastern North America

It’s not often that I anticipate the release of a book as much as I have with the soon-to-be-released Field Guide to the Jewel Beetles (Coleoptera: Buprestidae) of Northeastern North America. Fortunately, the wait is now almost over—Morgan Jackson, author of Biodiversity in Focus and co-author of the book, has just announced its planned released in early 2013. Even better, he has provided a sneak peak at its contents that is as smartly designed as the book itself.

Obviously, as a serious student of the family Buprestidae, this book would make it into my bookshelf no matter what, and I plan to do a more detailed review of the book once I have a copy permanently in my hands. However, I can tell you that I am already very impressed with the design of the book and the quality of the product. I was fortunate to meet up with Morgan at last month’s Entomological Society of America meetings in Knoxville, Tennessee, and Morgan kindly allowed me to leaf through the carefully guarded copy he had with him (it was difficult handing it back to him). The Prezi preview for the book covers some of the more important features that will set this book apart from other field guides, but worthy of special mention are: 1) the minimum/maximum size silhouette figure in the upper left-hand corner of each species treatment—a tremendously useful feature, 2) inclusion of the both the author and date of the original description of the species (to keep us more taxonomically inclined happy), 3) super high quality dorsal and lateral habitus photographs and of additional key features to aid in identification, 4) geographical range maps coded to show both presumed and recorded ranges, and 5) keys to all treated species, richly augmented with high quality photographs.

There is another reason I am so excited about this book, and that is the authors chose my photograph of Buprestis rufipes (red-legged buprestis), one of North America’s most striking jewel beetle species, to grace the cover of the book. I also provided specimens of a number of uncommonly encountered species which were used for the photographs in their respective species treatments.

Quite remarkably, this book will be available at NO COST—including free shipping anywhere! As a consequence, the book will not be available from commercial book and literature sources. You can request your copy by emailing your mailing address to Morgan at morgandjackson@gmail.com. I don’t know how many copies of the book are being printed, but I have a feeling that supplies will not last long, and in the coming years one will have to beg/borrow/steal from a kindly old colleague to get a copy (you can have my copy when you pry it from my cold, dead fingers!).

Copyright © Ted C. MacRae 2012

Life at 8X: MPMI Cover


The January 2013 issue of Molecular Plant-Microbe Interactions (volume 26, number 1) is now online. Why do I mention this? You may recall the cover photos of the soybean aphid, Aphis glycines, from my post —one of a series of posts I’ve done featuring insects photographed at 8X life-size.

MPMI is a publication of The American Phytopathological Society, and I have Dr. Gustavo MacIntosh at Iowa State University to thank for the appearance of these photos on the cover of this Special Focus Issue. Dr. MacIntosh is Associate Professor of Biochemistry, Biophysics and Molecular Biology and studies hormone-based defense mechanisms in soybeans. In a paper appearing in this special issue, Dr. MacIntosh and co-author Matthew Studham published the results of a study that suggests soybean aphids are able to “short-circuit” soybean defense mechanisms, making it easier for other pests (e.g., soybean cyst nematode) to colonize infested plants as well. Their study revealed large differences in transcription profiles of soybean varieties with and without an endogenous resistance gene (Rag1) in response to aphid infestation and suggested that the aphids are able to circumvent the defense response in susceptible plants by triggering activation of abscissic acid (normally associated with abiotic stress responses) as a “decoy” strategy (Studham & MacIntosh 2013). Plants infested with aphids have been shown to also become more susceptible to soybean cyst nematode—even varieties with genetic resistance to nematodes (McCarville et al. 2012). Dr. MacIntosh saw my photos when I posted them here and asked permission to submit them as candidates for the cover of the MPMI issue in which his paper was to appear.

Dr. Macintosh hopes that his research will enable the development of soybean varieties that will be more resistant to aphids and other pests.

REFERENCE:

McCarville, M. T., M. O’Neal, G. L. Tylka, C. Kanobe & G. C. MacIntosh. 2012. A nematode, fungus, and aphid interact via a shared host plant: implications for soybean management. Entomologia Experimentalis et Applicata 143(1):55–66 [DOI: 10.1111/j.1570-7458.2012.01227.x].

Studham, M. E. & G. C. MacIntosh. 2013. Multiple Phytohormone Signals Control the Transcriptional Response to Soybean Aphid Infestation in Susceptible and Resistant Soybean Plants. Molecular Plant-Microbe Interactions 26(1):116–129 [DOI: 10.1094/MPMI-05-12-0124-FI].

Copyright © Ted C. MacRae 2012

One Bad Beetle

Almost every tiger beetle trip that I take has a mix of gimmes and stretch goals. That’s alright—it’s impossible to find everything every time out, and if I eschewed the common and was happy only when I found something truly rare, then I would probably find myself rather unsatisfied most of the time. For the stretch goals, however, “success” can mean many things—obviously the best case scenario is to find it in good enough numbers to allow responsible collection of an adequate series and photograph enough individuals in situ to ensure that at least a few shots will have the focus, lighting, and composition that I want. Success can also be something less than that—maybe I find only a few and don’t get a very good series, or I have trouble getting field shots and am not happy with the shots I got…or worse I don’t even get field shots! The least successful version of “success” is when I end up with just one single beetle, and the only photographs I get are very ordinary-looking shots of that one beetle in confinement. Like what happened with Cicindela decemnotata (Badlands Tiger Beetle).

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Soda Lake, Wyoming—we searched theses areas of alkaline exposures but never found beetles…

Chris Brown and I knew this species would be a stretch goal when we added “Soda Lake, Wyoming” to the itinerary of our 7th Annual Fall Tiger Beetle Trip™ (location “H” on this map). Cicindela decemnotata is the westernmost representative (Rocky Mountains from the northwestern Great Plains and northern Great Basin north to Yukon) of a group of species that seem to be closely related and resemble each other in their green coloration varying degrees of red on the head, pronotum and elytra and their variably developed white elytral markings (Pearson et al. 2006). Cicindela limbalis, C. splendida and C. denverensis occur as a partially allopatric species complex further east in the Great Plains, while C. sexguttata, C. patruela and C. denikei occupy more forested regions even further to the east. On this trip we were focusing on Great Plains tiger beetles and the dune specialists of the Yampa River Valley of northwestern Colorado. Our drive from northwestern Nebraska to the Yampa Valley would skirt the eastern edge of C. decemnotata‘s distribution, so we decided to stop by Soda Lake where Matt Brust had seen the species in previous years.

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…until we started searching these small ridges of exposed sandy soil.

It took most of the morning to reach the spot, so by the time we arrived we were anxious to get out and start searching the sage brush habitat. For me it was an unfamiliar landscape—at that time my northwesternmost push for tiger beetles yet, and like many western habitats it seemed vast and unending. We were optimistic, however, because it just “looked” like good tiger beetle habitat, with ribbons of alkaline flats weaving through open brush. Of course, as time passes and one starts to recognize that they are again searching ground already covered with no sign of beetles, optimism begins to wane and searches become more deliberate. We were there for almost an hour before I heard Chris call out. He had abandoned the alkaline flats—obvious habitat it would seem—and started looking upon some slightly sandier low ridges a little further to the south. I hustled to where he was standing, and we both looked at the beetle, calmly sitting on the sand, as we deliberated our next move. Should we try to photograph it? It seemed not at all skittish—but what if we failed, it got away, and then we never saw another one? We played it safe, netted it (easily), and placed it in a vial for transfer to a container of native soil should further efforts at finding and photographing the species fail. It was perhaps another 45 minutes before we saw another beetle—I don’t know if it was just a less cooperative individual or the heat of the day had kicked in, but as soon as I started my approach it was gone. We saw another not long after, but same story. Finally we saw one last beetle that seemed to tolerate my approach to the point that I even began looking for it in the view finder—at which point it promptly zipped away. This small prospect of success only served to prolong our vain searching before we eventually we accepted defeat and tried to be happy with the single individual that we had caught and the photographs that we would take of it in its artificial home.

Cicindela decemnotata

Cicindela decemnotata (Badlands Tiger Beetle) | Soda Lake, Wyoming

Part of me really doesn’t like showing photographs of confined tiger beetles—not for any philosophical reasons, but because I just don’t like the way they look. Rarely do they exhibit the elegant stilting and other thermoregulatory behaviors that place them in much more pleasing postures when photographed in situ. Rather, they often have a “hunkered down” look that says “I’m not happy and I don’t want to be here, so I’m not going to smile for the camera!” Since these photos were taken, I have learned a few tricks to deal with confined beetles and achieve more aesthetically pleasing photographs—these include the use of much larger arenas, allowing the beetles more time to accommodate to their environs, and elevating the substrate relative to the camera (maybe a subject for a future post). In the end, however, they are still confined and can’t be passed off as anything but that.

The bold white markings, media band sharply angled and not reaching the edge of the elytra, and ''greasy'' appearance distinguish this species.

The bold white markings, media band sharply angled and not reaching the edge of the elytra, and ”greasy” appearance distinguish this species.

As an aside, tiger beetle pros Barry Knisley, Ryan Woodcock and Mike Kippenhan have recently published the results of an impressive study of this species in which a combination of morphological and molecular evidence support the recognition of four subspecific entities—three described as new (Knisley et al. 2012). The molecular analyses not only support the subspecific distinctions postulated from morphology but also suggest that populations have undergone rapid phylogenetic radiation in the recent geological past. Much of the area occupied by C. decemnotata was covered by an ice shield during the most recent glaciations and, thus, has opened up for colonization only during the past 10,000 years (Pearson and Vogler 2001). The molecular analyses showed a relatively low amount of genetic divergence within C. decemnotata populations, which combined with marked morphological differences suggests recent and rapid radiation—most likely in the wake of glacial recession. A similar situation has been observed with members of the Cicindela maritima species-group, which occupy much the same range as C. decemnotata and, presumably, have experienced similar selection pressures in the recent geological past.

REFERENCES:

Knisley, C. B., M. R. Woodcock & M. G. Kippenhan. 2012. A morphological and mtDNA analysis of the badlands tiger beetle, Cicindela (s. str.) decemnotata Say, 1817 (Coleoptera: Carabidae: Cicindelinae) with the description of three new subspecies. Insecta Mundi 0214:1–49.

Pearson, D. L., C. B. Knisley & C. J. Kazilek. 2006. A Field Guide to the Tiger Beetles of the United States and Canada. Oxford University Press, New York, 227 pp.

Pearson, D. L. and A. P. Vogler.  2001. Tiger Beetles: The Evolution, Ecology, and Diversity of the Cicindelids.  Cornell University Press, Ithaca, New York, 333 pp.

Copyright © Ted C. MacRae  2012

Another autumn oedipodine

Shortgrass/sage brushland habitat in Medicine Bow Natl. Forest, Wyoming

In September 2010, Chris Brown and I explored shortgrass/sage brushland habitat atop the Laramie Mountains in southeastern Wyoming’s Medicine Bow National Forest (location “J” on this map). We were entering the final days of our 7th Annual Fall Tiger Beetle Trip™ and, to that point, had found every tiger beetle species we had set out to look for. This day, however, was the official “skunk” day of the trip, for although we did see one Cicindela limbalis (Common Claybank Tiger Beetle)—collected live to become the subject of one of the crappiest tiger beetle photos I’ve ever taken—we did not see the tiger beetle that we were there to see; Cicindela longilabris (Boreal Long-lipped Tiger Beetle). Of course, I rarely have trouble finding consolation on a skunk day, and during fall this is even easier—the deep blue sky, crisp fall air, and vivid colors of a morphing landscape are enough to make even a bad day of insect collecting better than a good day of just about anything else. And then there are the band-winged grasshoppers (family Acrididae, subfamily Oedipodinae)!  When there are no tiger beetles to be had, there are almost always members of this group around, and other than tiger beetles I don’t think there is another group of insects that I enjoy photographing more.

Arphia pseudonietana (red-winged grasshopper) | Medicine Bow Natl. Forest, Wyoming

As we walked the trails not finding tiger beetles, I noticed these very dark grasshoppers every once in a while. They flew with a particularly noisy crackling sound that exposed bright red hind wings before dropping to the ground and instantaneously becoming almost completely invisible. Once I accepted that tiger beetle photography just wasn’t gonna happen that day, I began paying attention to these grasshoppers and, after working a few individuals, finally found one who was willing to let me get close enough for some photos. I’m not terribly fond of this first photo—the perspective is still too high as I had not yet learned by that time to get down flat on my belly for photographing anything on the ground (remember, this was two years ago). Nevertheless, it is the only one that I have that shows the entire body of the grasshopper. Since this location isn’t too far west of the Nebraska border, I figured an identification should be possible using the Nebraska grasshopper guide (Brust et al. 2008)—based on that work and subsequent examination of photos at BugGuide, I surmise this individual represents Arphia pseudonietana (red-winged grasshopper). There are other species of Arphia in Nebraska, some of which are easily confused with A. pseudonietana; however, most of these are more common further east. The only other species in the genus that occurs west into Wyoming is A. conspersa (speckle-winged grasshopper), and although it is similar in appearance and may have red hind wings (though more commonly orange to yellowish), adults are most common during spring and early summer. Arphia pseudonietana adults, on the other hand, are most active during mid-summer through fall.

The pronotum bears a single notch just in front of the middle.

Grasshoppers, particularly in the western states, tend to be loathed by ranchers who see them as competitors with cattle for meager forage resources, especially in dry years. This species does feed preferentially on a variety of grasses such as western wheatgrass (Pascopyrum smithii), buffalograss (Buchloe dactyloides) and blue grama (Bouteloua gracilis); however, it doesn’t seem to occur at economically important levels except in association with other, more numerous grasshopper species. I’m glad to know this, because for some reason I just don’t want anybody regarding band-winged grasshoppers of any kind as a pest. Other grasshoppers, fine—just not my beloved bandwings!

I presume this 5th instar nymph also represents A. pseudonietana

Later in the day I came across this presumed 5th-instar grasshopper nymph, and although it was quite skittish I eventually managed to get this single photograph before it resumed its frenetic hopping and I gave up in frustration. This is one of the better “one-shots” that I’ve managed to take—my only criticism being that the focus was just a tad too deep to catch the front metafemoral face. I really didn’t have much time to setup for this shot—once I got the critter reasonably in-frame I fired! Anyway, I’m inclined to think this also represents A. pseudonietana, although I’m less confident in that ID than I am for the adult as I wasn’t able to find a real good comparative photograph. Nymphs of A. pseudonietana are apparently most common from mid-spring to mid summer, so the seasonality is a bit off. I would be grateful to any acridophile who stumbles across this post and can provide an ID confirmation or correction (for either the nymph or the adult). Until then, I leave you with a shot that shows why I love fall regardless of whether I’m finding insects!

Quaking aspen glows under the late September sun.

REFERENCE:

Brust, M. L., W. W. Hoback and R. J. Wright.  2008. The Grasshoppers (Orthoptera: Acrididae and Romaleidae) of Nebraska.  University of Nebraksa-Lincoln Extension, 138 pp.

Copyright © Ted C. MacRae 2012