Colorado’s Great Sand Dunes Tiger Beetle

Great Sand Dunes National Park | Saguache and Alamosa Counties, Colorado (click for 1680 x 887 version)

Last year’s Annual Fall Tiger Beetle Trip entered its last day as an unqualified success. Travel partner Jeff Huether and I were doing the “Great Western Sand Dune Tour” on a quest to find and photograph some of North America’s most geographically restricted tiger beetles. The first four days featured successful visits to northwestern Colorado’s Maybell Sand Dunes for Cicindela scutellaris yampae and Cicindela formosa gibsoni, southeastern Idaho’s St. Anthony Sand Dunes for Cicindela arenicola, and southwestern Utah’s Coral Pink Sand Dunes for the prize of the trip—Cicindela albissima. The only endemic that we had failed to find was Cicindela waynei at southwestern Idaho’s Bruneau Sand Dunes (hopefully this was a result of poor fall emergence conditions rather than an indication of further decline of this perilously endangered species).

Small sand dune west of GSDNP in the Nature Conservancy's Medano-Zapata Ranch.

Day 5 featured a visit to southwestern Colorado’s Great Sand Dunes to look for the endemic Cicindela theatina. As on every day previous of the trip, the morning drive saw cool but rising temperatures under bright, sunny skies, so we were optimistic about our chances. Between Great Sand Dunes National Park (type locality of the beetle) and The Nature Conservancy’s Medano-Zapata Ranch west of the park, the entire 290 km² range of C. theatina is on protected land. Not knowing whether the beetle would be out and, if so, how extensively it would occur, our plan was to approach the Park from the west through Zapata Ranch and stop at any sand dunes we sighted along the way until we found the beetle.  It didn’t take long—as soon as we entered the Ranch we began to see small sand dunes in the distance, and within minutes after making the 1-km hike towards one particularly promising looking dune we saw the beetles. Even though this was the fifth western sand dune endemic I had seen in as many days, the first moment I laid eyes upon it was no less exciting—flashing red and green on coppery, white marked elytra, it seemed all hair and teeth!

Great Sand Dunes tiger beetle (Cicindela theatina) | Medano-Zapata Ranch

Despite this being my first sighting of the species, there was no doubt about it’s identity. The only other tiger beetle that occurs with and could possibly be mistaken for C. theatina is the blowout tiger beetle, C. lengi; however, the broad marginal band that runs completely around the elytra and the green/brown dorsal coloration of C. theatina are enough to distinguish it from that species. Temperatures were still a bit on the cool side, but the beetles were already remarkably active and skittish. Like the other sand dune species we had already seen, they were enormously difficult to approach—numerous failed attempts were necessary before I encountered the slightly more cooperative female shown in these photos (although she still required several minutes of stalking to get her sufficiently accustomed to my presence to allow these shots).

Like most sand dune tiger beetles, adults are densely hairy on the lateral and ventral surfaces.

Adults ''hug'' the sand for warmth during the cooler morning hours.

The dense covering of white hairs on the lateral and ventral surfaces of the adults belies their adaptation to the abrading sands of their wind-swept habitat. Scouring sands, however, are not the only hardships that the adults must contend with. Temperatures on the dunes can range from as low as 40° F on a chilly morning to nearly 140° F during the heat of the day. Accordingly, much of the adult beetle’s activities revolve around thermoregulation to maintain optimal body temperatures for activity (Pineda and Kondratieff 2003). These include not only stilting, shade-seeking, and mid-day burrowing to avoid excessive warming (see my post  for examples of these behaviors), but basking to gain warmth when temperatures are still a bit too cool for effective foraging (photo above).

Fabulous metallic red and green highlights on the head and pronotum contrast with the reddish brown elytra and their white lateral markings.

Despite the fact that the entire range of this species is encompassed by protected land, WildEarth Guardians filed a petition for federal listing as an endangered species in 2007 (Tweit 2010). Whether protection will be granted remains to be seen—Coral Pink’s C. albissima has a global range only 1.3% the size of C. theatina‘s range (only slightly more than half of which is on protected land), yet that species has been awaiting listing for nearly three decades now! (Too bad C. theatina doesn’t have real fur, feathers, or those endearing mammalian eyes that would surely allow it to jump to the front of the line.)

For the first time in BitB Challenge history, we have a 4-way tie for the win. Dorian Patkus, Mr. Phidippus, Mike Baker, and David Winter all share the honors for . Mr. Phidippus is the big winner, however, as he strengthens his grip on the overall lead with a lead of 13 or more points over his nearest rivals (Roy, Tim Eisele, Mike Baker, and Dennis Haines). The competition is far from over though—a single misstep is all it would take to see the emergence of a new leader before this session is over.

REFERENCES:

Pineda P. M. and B. C. Kondratieff. 2003. Natural history of the Colorado Great Sand Dunes tiger beetle, Cicindela theatina Rotger. Transactions of the American Entomological Society 129(3/4):333–360.

Tweit, S. J. 2010. Beetle Mania. National Parks 84(4):24–25.

Copyright © Ted C. MacRae 2012

ID Challenge #15

Who am I, and where do I live?

It’s been almost a month since the last challenge, and since Alex got back to his roots I think I’ll do likewise. This is a straight up identification—the order and family are obvious (or should be), so I’m going to limit ID points to genus and species. However, to make up for this loss of higher taxa points I’ll be awarding points for correctly guessing/deducing/intuiting where this little beastie lives or providing any unique comments on its natural history. As always, standard challenge rules apply, including moderated comments to give everyone a chance to submit their answers.  Bonus points will be awarded to for answering first in the case of multiple correct answers, and discretionary bonus points are also up for grabs. Good luck!

Copyright © Ted C. MacRae 2012

I am an Entomologist

In my last post (Best of BitB 2011), I showed my favorite 13 insect (mostly) macrophotographs from 2011. Such “Best of …” posts have become an annual tradition here at BitB, and I like them because they give me a chance to review my photographs for the year and assess my progress as an insect macrophotographer. Others seem to like them also, as previous editions remain among this blog’s most popular posts despite the passage of time. Hopefully this latest edition will achieve similar popularity, and if it does I will be truly grateful.

Despite this, however, I find that I still have trouble considering myself a true “insect macrophotographer” rather than an “entomologist with a camera.” It’s not that I don’t want or hope to achieve such a moniker, and I’ve been thinking lately about why this should the case. I’ve realized that it really has less to do with self-opinion and more to do with the importance I still place on and satisfaction I get out of my other entomological pursuits. Not only have I been fortunate to find stable employment conducting entomology research, but I’ve also managed to find satisfying outlets for my avocational entomological interests. I am an Entomologist (with a capital ‘E’), and although I’ve enjoyed immensely my recent growth as an insect macrophotographer, I did have other other, purely entomological accomplishments in 2011 that I think also deserve mention:

  • Managing Editor of The Pan-Pacific Entomologist. It has been my life-long goal to become editor of a major entomology journal, and this past April I was presented with just such an opportunity with The Pan-Pacific EntomologistMy seven prior years as the journal’s Coleoptera Subject Editor prepared me well for the role (and further confirmed for me that the chief role was something I wanted to do), and in the seven months since I took over, the Editorial Board and I have processed 50 manuscripts, are about to submit files for our 4th issue, and have shaved more than two months off of the deficit that separates us from our eventual goal of on-schedule publishing.
  • Five papers published. With co-authors Chris Brown and Kent Fothergill, 2011 saw the publication of our series of papers assessing the conservation status of the tiger beetles Habroscelimorpha circumpicta johnsonii, Dromochorus pruinina, Tetracha carolina, and Cylindera cursitans in Missouri and Cylindera celeripes in the eastern Great Plains. Survey work for these species dominated my field activities during the past decade and formed the basis for these papers, and it was immensely satisfying to finally see the results of all that work finally appear in print. The real impact of this work, however, will be seen in the coming years as I work with conservation stakeholders who will utilize the information that we have gathered.
  • First seminar presented fully in Spanish. I don’t talk much about my professional activities—part of being an industry entomologist is the necessity to maintain company confidentiality. I have mentioned, however, my role in soybean entomology research and my recent travels to Argentina as part of this work. In November I finally realized one of my professional goals of giving a seminar fully in Spanish. It was a long time coming—I took Spanish lessons for a short time in the late 1990s but have otherwise had only one or two trips per year to Argentina and Mexico with which to improve my skills. It was during my trip to Argentina this past March that something finally ‘clicked’ and I found myself for the first time able to engage fully in conversation. My colleagues in Argentina must have noticed this as well, as it was they who requested that I not only give a seminar during my November visit, but that I do so in Spanish. The presentation went well, and I now find myself more motivated than ever to pursue what before seemed only a pipe dream—full fluency.
  • Senior Research Entomologist. After three decades of working as an entomologist—the last two in industry, I now can add “Senior” to my title. What this means in practice I’m not quite sure—I’m still doing largely what I have been doing for the past few years, and in this environment compensation is linked more to accomplishments than title. Maybe it’s just recognition of dogged persistence. Still, it sounds cool and looks good in the email signature line!
  • 32 species/subspecies of tiger beetles! This is the fun stuff! Nothing is more enjoyable for me than locating, observing, and photographing tiger beetles in their native habitats. It’s even better when they are uncommonly observed or rare endemic species. In 2011 I looked for tiger beetles in seven states (Arkansas, Colorado, Florida, Idaho, Missouri, Oklahoma and Utah), and of the 32 total species and subspecies that I found (listed below) the highlights must include three of North America’s rarest tiger beetle species: Cicindela albissima (Coral Pink Sand Dune Tiger Beetle), Cicindela arenicola (St. Anthony Dune Tiger Beetle), and the recently rediscovered Cicindelidia floridana (Miami Tiger Beetle).  Another eight endemic or highly restricted species and subspecies were also found, and I was able to obtain in situ photographs of all eleven in their native habitat (as well as most of the non-endemics that I had not already photographed). In the list that follows, bold text indicates endemics, and links to any photographs I posted are provided when available:
    • Genus Cicindela
      • Cicindela albissima Rumpp, 1962 [photos]
      • Cicindela arenicola Rumpp, 1967 [photos]
      • Cicindela formosa formosa Say, 1817
      • Cicindela formosa generosa Dejean, 1831 [photos]
      • Cicindela formosa gibsoni Brown, 1940 [photos]
      • Cicindela lengi lengi W. Horn, 1908
      • Cicindela purpurea audubonii LeConte, 1845
      • Cicindela scutellaris scutellaris Say, 1823
      • Cicindela scutellaris yampae Rumpp, 1986 [photos]
      • Cicindela sexguttata Fabricius, 1775
      • Cicindela splendida Hentz, 1830
      • Cicindela theatina Rotger, 1944 [photos pending]
      • Cicindela tranquebarica borealis E. D. Harris, 1911
      • Cicindela tranquebarica kirbyi LeConte, 1866
      • Cicindela tranquebarica tranquebarica Herbst, 1806 [photos]
    • Genus Cicindelidia
      • Cicindelidia floridana (Cartwright, 1939) [photos]
      • Cicindelidia haemorrhagica haemorrhagica (LeConte, 1851)
      • Cicindelidia obsoleta vulturina (LeConte, 1853) [photos pending]
      • Cicindelidia punctulata punctulata (Olivier, 1790)
      • Cicindelidia rufiventris rufiventris (Dejean, 1825)
      • Cicindelidia scabrosa (Schaupp, 1884) [photos]
    • Genus Cylindera
      • Cylindera (Cylindera) curistans (LeConte, 1860) [photos]
      • Cylindera (Cylindera) unipunctata (Fabricius, 1775) [photos]
    • Genus Ellipsoptera
      • Ellipsoptera hamata lacerata (Chaudoir, 1854) [photos, photos, photos, photos]
      • Ellipsoptera hirtilabris (LeConte, 1875)
      • Ellipsoptera marginata (Fabricius, 1775)
    • Genus Habroscelimorpha
      • Habroscelimorpha dorsalis saulcyi (Guérin-Méneville, 1840)
      • Habroscelimorpha severa severa (LaFerté-Sénectère, 1841)
      • Habroscelimorpha striga (LeConte, 1875) [photos]
    • Genus Tetracha
      • Tetracha (Tetrachacarolina carolina (Linnaeus, 1767) [photos]
      • Tetracha (Tetrachafloridana Leng & Mutchler, 1916 [photos, photos]
      • Tetracha (Tetrachavirginica (Linnaeus, 1767)

Copyright © Ted C. MacRae 2012

Best of BitB 2011

Welcome to the 4th Annual BitB Top 10, where I get to pick my 10 (more or less) favorite photographs of the year. As an insect macrophotographer I still feel like a relative newcomer, although with three seasons under my belt fewer and fewer people seem to be buying it anymore. Granted I’ve learned a lot during that time, but the learning curve is still looking rather steep. I don’t mind—that’s the fun part! With that said, I present a baker’s dozen of my favorite photographs featured here during 2011. I hope they reflect the learnings I’ve had the past year and maybe show some progress over previous years (2009, 2008 and 2010).

One more thing—I’m including a special bonus for the first time in this year’s edition. Each of the photos shown below is linked to a 1680×1120 version that may be freely downloaded for use as wallpaper, printing in calendars, or any other use (as long as it’s personal and non-profit). It’s my way of saying thanks for your readership and support.


From  (posted 8 Jan). I’ve done limited photography with prepared rather than live specimens. However, the recreated aggressive-defensive posture of this greater arid-land katydid (Neobarrettia spinosa)—or “red-eyed devil”—was too striking to pass up. A clean background allows every spine and tooth to be seen with terrifying clarity.


From  (posted 6 Feb). I had never seen a cactus fly until I encountered this Nerius sp. I’m especially fond of the bizzarely-shaped head and un-fly-like spines on the front legs.


From  (posted 17 Feb). This photo of a fungus weevil, Phaenithon semigriseus, is one of the first where I nailed the focus right on the eye at such a magnitude of closeup (~3X) and also got the composition I was looking for. I didn’t notice at the time, but the beetle seems to be “smiling.”


From  (posted 28 Mar). One of the field techniques I’ve been practicing this year is actually holding the plant with the subject in one hand, resting the camera on my wrist and controlling it with the other hand, and manipulating the position of the plant to achieve a desired composition. It’s a difficult technique to master, but the results are worth it. The jumping spider, Euophrys sutrix, represents one of my earliest successful attempts with this technique.


From  (posted 30 Mar). This South American tree fruit weevil looks like it is sitting quite calmly on a branch. In reality, it never stopped crawling while I attempted to photograph it. Crawling subjects are not only difficult to focus on but also almost always have a “bum” leg. I achieved this photo by tracking the beetle through the lens and firing shots as soon as the center focus point flashed, playing a numbers game to ensure that I got at least one with all the legs nicely positioned. I’d have been even happier with this photo if I had not clipped the antennal tip.


From  (posted 4 May). Face shots of predatory insects are hard to resist, and in this one of the fiery searcher beetle, Calosoma scrutator, the angle of the subject to the lighting was perfect for showing off every ridge and tooth in its impressive mandibles.


From  (posted 10 May). I’ve taken plenty of lateral profile shots of tiger beetles, but I like this slightly panned out one especially because of the sense of scale and landscape created by the inclusion of the plantlets and the view over the small rise.


From  (posted 18 May). I found these Edessa meditabunda stink bug eggs on the underside of a soybean leaf in Argentina almost ready to hatch. The developing eye spots in each egg gives the photo a “cute” factor rarely seen in such super close-ups.


From  (posted 15 July). Some of my favorite insect photos are not only those that show the bug in all its glory, but also tell a story about its natural history. This nymphal lichen grasshopper, Trimerotropis saxatilis, is almost invisible when sitting on the lichens that cover the sandstone exposures in its preferred glade habitat. 


From  (posted 23 Aug). I know this is the second beetle face shot I’ve included in the final selections, but it was while photographing this rare Florida metallic tiger beetle, Tetracha floridana, in the middle of the night that I discovered the use of extension tubes to improve the quality of flash lighting (decreased lens to subject distance results in greater apparent light size). This is perhaps one of the best illuminated direct flash photographs that I’ve taken, and I also like the symmetry of the composition.


From  (posted 17 Sep). The three-cornered alfalfa hopper (Spissistilus festinus) is a common pest of alfalfa and soybean in the U.S. However, despite its abundance, I’ve never noticed the bizarre zig-zag pattern of the eyes until I took this photo. Even though both the insect and the background are green, there is sufficient value contrast to create a pleasing composition. Bumping up the ISO and a lower FEC setting prevented overblowing the light greens—easy to do with full flash macrophotography.


From  (posted 4 Oct). This longhorned beetle had settled in for the night on its Ericamera nauseosa host plant, allowing me to use higher ISO and lower shutter speed settings with a hand-held camera to achieve this very pleasing blue sky background, while retaining the sharpness of detail of the subject that comes from full-flash illumination. The blue sky background provides a more pleasing contrast with the colors of this particular beetle and flowers than the black background that is more typically seen with full-flash macrophotography.


From  (19 Dec). An uncommon underside view of these purple tree fungus (Trichaptum biforme) caps and use of flash illumination allows the colors to literally glow against the bright green lichens also growing on the tree. Keeping aperture at a moderate setting allows blurring of the caps further back, adding three-dimensionality to the photo and preventing it from looking ‘flat.’


Well, there you have it, and I hope you’ve enjoyed my selections. Please do tell me if you have a favorite among theses (and if there were other photos posted during 2011 that you think deserved making the final selections).

Copyright © Ted C. MacRae 2011

Swift Tiger Beetle: Species on the Brink

ResearchBlogging.orgIn July 2008, Chris Brown and I made a spur-of-the-moment trip to Hitchcock Preserve near Council Bluffs, Iowa, where only a week earlier Cylindera celeripes (Swift Tiger Beetle), one of North America’s most enigmatic tiger beetles, had just been discovered. Reportedly once common in the blufftop prairies of western Iowa and further west in eastern Nebraska and Kansas, this tiny (6–8 mm in length), flightless beetle has suffered severe population declines over the past 100 years. Only small numbers of individuals have been encountered outside of the type locality (Fort Riley, Kansas) in recent years, and in Nebraska the species is now considered extirpated (Spomer et al. 2008). Our reasons for going to Iowa had to do with our as yet unsuccessful effort to find the species in northwestern Missouri as part of our broader studies of the state’s tiger beetle fauna. Although it had never been recorded from Missouri, we felt there was some chance it might be found in the tiny loess hilltop prairie remnants still remaining in the state at the southern terminus of the Loess Hills landform. We reasoned our failure to find the species might be related to its very small size and rapid running capabilities (giving them more the appearance of small ants or spiders than tiger beetles), limited temporal occurrence, and tendency to hide amongst the bases of grass clumps (Pearson et al. 2006). If we could find the species at a locality where they were known to occur, perhaps an improved search image and better understanding of their precise microhabitat preferences would help us locate the species in Missouri.

Fig. 1. Cylindera celeripes (LeConte) adults at: a) Hitchcock Nature Center, Pottawattamie Co., Iowa (13.vii.2008); b) Alabaster Caverns State Park, Woodward Co., Oklahoma (10.vi.2009); c) same locality as “b”, note parasite (possibly Hymenoptera: Dryinidae) protruding from abdomen and ant head attached to right antenna; d) Brickyard Hill Natural Area, Atchison Co., Missouri (27.vi.2009). Photos by C.R.Brown (a) and T.C.MacRae (b-d).

We didn’t realize it at the time, but that trip marked the beginning of a two-year study that would not only see us succeed in finding C. celeripes in Iowa, but also discover new populations in Missouri and northwestern Oklahoma (Figs. 1a–d). With so much new information about the species and the long-standing concerns by many contemporary cicindelid workers about its status, it seemed appropriate to conduct a comprehensive review of the historical occurrence of this species to establish context for its contemporary occurrence and clarify implications for its long term protection and conservation. This was accomplished through compilation of label data from nearly 1,000 specimens residing in the collections of contemporary tiger beetle workers, all of the major public insect museums in the states of Iowa, Kansas, Missouri, Nebraska, Oklahoma, and Texas, and the collections at the U.S. National Museum and Florida State Collection of Arthropods. Collectively, this material is presumed to represent the bulk of material that exists for the species, representing nearly all localities recorded for the species and time periods in which it has been collected.

Label data confirmed the historical abundance of this species, especially in the vicinity of Manhattan and Fort Riley, Kansas; Lincoln and Omaha, Nebraska; and Council Bluffs, Iowa. Hundreds of specimens were routinely collected in the native grassland habitats around these areas during the late 1800s and early 1900s, their abundance documented by entomologists in both journal articles and private letters. One of the most interesting examples of the latter was by Nebraska collector F. H. Shoemaker, who wrote the following in a 1905 letter to R. H. Wolcott:

There is another trip, down the river to the big spring by the railroad track near Albright, then across the river (the heronry route) where we collect hirticollis, repanda, vulgaris [= tranquebarica], cuprascens, and – vat you call ‘im? – celeripes! I took 147 of the latter in an hour and a half Sunday, and the supply was undiminished.

Fig. 8. Historical and currently known geographical occurrence of Cylindera celeripes by county. Red = last record prior to 1920; orange = last record 1941–1960 (“?” = questionable record); green = last record 1991–1996; blue = last record 2005–2011.

Although the recent collections of C. celeripes from near Council Bluffs and through the years near Fort Riley show that the species has managed to persist in these areas, there is little question that it is far less abundant and widespread now than it was in the early 20th century (Fig. 8).  Not only are the areas in which present day populations are known to occur limited, but the numbers of individuals seen in them are very low. In Missouri, the species was listed immediately after its discovery in the state as a species of conservation concern with a status of S1 (= “critically imperiled”) due to the highly restricted occurrence of suitable habitat (loess hill prairie) in the state and small populations observed within them. The situation is even worse in Nebraska, where the species has not been seen for nearly 100 years despite dedicated searches by expert contemporary tiger beetle workers such as Matt Brust and Steve Spomer. Considering the near-complete elimination of suitable native grassland habitats by conversion to agriculture and degradation of the few existing remnants due to encroachment by woody vegetation and invasive exotics, the likelihood of finding extant populations of C. celeripes in Nebraska seems remote. Only in the Red Hills of northwestern Oklahoma does the species appear to be secure due to the extensiveness of suitable areas of habitat and robust numbers of individuals observed within them at the present time. An enigmatic record exists from Arkansas, based on a single individual collected near Calico Rock in 1996. This individual represents a significant extension of the known geographical range of the species, but repeated attempts to find the species at that locality during the past year were not successful.

The persistence of populations, albeit small, in multiple areas, along with the occurrence of robust populations in northwestern Oklahoma, makes it unlikely that C. celeripesqualifies for listing as a threatened or endangered species at the federal level. Nevertheless, the limited availability of suitable habitat in many areas and low population numbers found within them clearly suggest that conservation measures are warranted at the state level, especially in Iowa, Kansas and Missouri, to prevent its extirpation from these states. In these states, land management practices should be implemented at sites known to support populations of the beetle in an effort to maintain and expand the native grassland habitats upon which they rely. These include various disturbance factors such as mechanical removal of woody vegetation, judicious use of prescribed burning, and selective grazing (taking care to do so in a manner that minimizes impacts to beetle populations).

REFERENCES:

MacRae, T. C. and C. R. Brown. 2011. Historical and contemporary occurrence of Cylindera (s. str.) celeripes (LeConte) (Coleoptera: Carabidae: Cicindelinae) and implications for its conservation. The Coleopterists Bulletin 65(3):230–241 DOI: 10.1649/072.065.0304

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

Spomer, S. M., M. L. Brust, D. C. Backlund and S. Weins.  2008. Tiger Beetles of South Dakota & Nebraska. University of Nebraska, Department of Entomology, Lincoln, 60 pp.

Copyright © Ted C. MacRae 2011

Arriving now in a mailbox near you…


The latest issue of Cicindela (A quarterly journal devoted to Cicindelidae) has just been issued. My copy arrived yesterday and features on the cover a photograph that I took of Tetracha carolina in Florida this past August (original photo and more can be seen in my post ).

I’m also happy to report that I was lead author and co-author on the two papers included this issue. I’ll provide a more detailed summary of those papers in another post—look for it in the near future, or better yet contact Managing Editor Ron Huber to begin receiving your own copies of this fine journal (subscription and contact information here).

Copyright © Ted C. MacRae 2011

Cicindela albissima—The Coral Pink Sand Dunes Tiger Beetle

Coral Pink Sand Dunes State Park, Utah

The week had started off good, with three species of western sand dune endemic tiger beetles (Cicindela formosa gibsoni, C. scutellaris yampae, and C. arenicola) and a variety of sometimes spectacular Crossidius longhorned beeltes having been encountered.  Mid-week, however, had brought a lull in our success—the long drive to southwestern Idaho was not rewarded with finding C. waynei, endemic only to Bruneau Sand Dunes State Park, and an even longer drive was required to backtrack and then drop down to the southwestern corner of Utah in hopes of finding the equally rare and restricted C. albissima.  Had it not been for our continued success with different species and subspecies of Crossidius longhorns the drive might have felt like a lesson in futility.  Still, on a collecting trip a new day and new locality brings new hope, and anticipation grew as we passed through lodgepole pine forests on stunning black lava fields and wind-carved red sandstones on the final approach to Coral Pink Sand Dunes State Park.

Colored pink by iron oxide minerals, the dunes are estimated at 10,000 to 15,000 years old.

Words cannot describe the stunningly spectacular landscape that unfolded before us as we entered the park.  The scenery alone makes Coral Pink Sand Dunes worthy, in my humble opinion, of National Park status, but it is C. albissima—occurring only on the park’s vivid pink dunes and nowhere else in the world—that makes this place truly special.  Precisely where in the park the beetle lives is a matter of public record, as Chris Wirth (author of the intermittent but highly focused blog Cicindela) and Randolph-Macon College Professor Emeritus Barry Knisley have produced a wonderfully detailed and well illustrated brochure about the beetle and its life history, population trends, and limiting factors.  What remained to be determined was whether the beetles would be active during the brief window of time available to look for it.  Cicindela albissima is a so-called “spring-fall” species in reference to the bimodal adult activity period, but activity in the fall is much less predictable than in the spring depending on moisture availability.  The day was perfect—temperatures in the 70s by mid-morning, only a light breeze, and a sharp, blue, cloudless sky.  All we could do was look.

Adult beetles were found on the northern edge of this dune. A majority were seen amongst sparse vegetation rather than barren areas.

It didn’t take long really to find them, as the adults were already out in encouragingly strong numbers. Of the several dozen adults we saw, all but one were seen atop the northern edge of one particular sparsely vegetated dune.  I suspect the larval burrows were at the bottom of the steep northern dune escarpment in the more stable wind-scoured sandstone clays that lay between individual dunes.  Vivid white and floating across the sand on long delicate legs, the elegance of their beauty was a stark contrast to the harshness of the surrounding landscape.  With a miniscule range of only 400 hectares, C. albissima is one of North America’s rarest tiger beetles, and I felt truly priviledged to join the small ranks of those who have seen this beetle alive in its native habitat and could appreciate the significance of the event.  Of course, the sense of accomplishment would not be complete unless I also succeeded in photographing the species in the field, and although the adults were quite wary and active, I was happy with several of the photos that I ended up with.  Similar to what I observed with C. arenicola, adults amongst the vegetation seemed slightly less skittish than those out in the open, so it was in the vegetated areas that I concentrated my efforts.  My only regret was not adding extension tubes to allow some real closeup portraiture, but the beetles seemed far too wary to have put up with the decrease in working distance that would have entailed.  At any rate, here are some of my favorites:




What the future holds for C. albissima remains unclear.  Designation of the beetle’s home range as a preserve (albeit tiny) would seem to offer long term protection, but a  large portion of this area is open to off-road vehicular traffic (although not a single one was seen during the time that we were there).  An even greater threat exists in the potential for extended drought affecting the entire population, and as greenhouse gases continue to accumulate in the atmosphere the chance of impacts from unusual weather events only grows. I feel lucky to be among the few that have witnessed this beautiful species in nature, but I sincerely hope I am not among the last.

ORV tracks can be seen just outside the conservation area boundary

Copyright © Ted C. MacRae 2011

Isn’t she splendid?!

Cicindela splendida | Bald Hill Glade Natural Area, Ripley Co., Missouri

This gorgeous female Cicindela splendida emerged recently from one of my rearing containers.  She was one of several 3rd instar larvae that I collected this past June from their burrows in a dolomite glade in southeastern Missouri.  I had suspected they might represent this species because of the bright, metallic sheen on their heads and decided to rear them out to find out for sure.  Rearing tiger beetles is fun and easy—all you have to do is fill a container with native soil, make a “starter” burrow¹ and drop them in. In this case, I also partially sunk a native rock into the soil in the center of the container, something I have started doing recently as it gives the emerged adult an elevated and more visually appealing surface on which to perch than the soil should I desire to take photographs.

¹ Larvae will dig new burrows on their own, but starter burrows allow you to place the burrow where you want it.  They are essential if more than one larva is introduced to the container, as wandering larvae will fight when they encounter each other. I like to start the burrow in a corner of the container (a pencil works great for this) and push down to the bottom of the container so I can see into the burrow from outside to monitor the larva as it develops.  After introducing the larva to its burrow, I push the soil around the entrance to seal it lightly to keep the larva from immediately crawling back out.  The larva will eventually reopen the burrow but generally accepts it, digging it out further to its liking and shaping the entrance to precisely fit the size and shape of its head.

Reared from 3rd instar larva, burrow in sparsely vegetated clay exposure of dolomite glade.

With tiger beetle rearing, feeding time is fun time! Our lab rears insects for testing in abundance, and there are always leftovers. Really just about any insect that can be pulled into the burrow will be acceptable as prey, but lepidopteran caterpillars are my favorite. I use mostly early instar tobacco hornworm larvae, choosing the size as appropriate for the size of the tiger beetle larva—the big ones (e.g. 3rd instar Tetracha) can handle caterpillars 35-40 mm in length and 6-8 mm in diameter, while neonates must be used for the smallest ones (e.g. 1st instar Cylindera celeripes and C. cursitans). I find it endlessly entertaining to sneak up on the larva sitting at the entrance of its burrow, slowly position a caterpillar above the burrow entrance with forceps, and dangle it to entice the tiger beetle larva to lurch out, grab the caterpillar, and drag it down into its burrow—all in a split second! If the larva drops down from the burrow entrance during my approach I just drop the caterpillar into the burrow (though this isn’t nearly as much fun).

Copyright © Ted C. MacRae 2011