Prey bee mine

Promachus hinei preying upon a small carpenter bee

Promachus hinei preying upon a small carpenter bee

Robber flies of the genus Promachus – the so-called “giant robber flies” – are among the more conspicuous and fearless predators seen in Missouri’s glades. Able to capture almost any flying insect regardless of size, this individual – seen at Long Bald Glade Natural Area in Caney Mountain Conservation Area – was found snacking on what, according to my hymenopterist friend Mike Arduser, appears to be a female individual of the genus Ceratina (the so-called small carpenter bees in the family Apidae). Of the three “tiger-striped” (referring to the yellow and black striping of the abdomen) species of Promachus in the eastern U.S. species, P. hinei is the most common in Missouri. It is distinguished from the more southeastern P. rufipes by its reddish versus black femora and from the more northern P. vertebratus by the larger dark areas dorsally on the abdominal segments and distinctly contrasting two-toned legs. Despite their common name and impressive size, however, they are not the largest robber flies that can be seen in these glades…

Photo details: Canon 100mm macro lens on Canon EOS 50D (manual mode), ISO-100, 1/250 sec, f/13, MT-24EX flash 1/4 power through diffuser caps.

Copyright © Ted C. MacRae 2009

Add to FacebookAdd to NewsvineAdd to DiggAdd to Del.icio.usAdd to StumbleuponAdd to RedditAdd to BlinklistAdd to Ma.gnoliaAdd to TechnoratiAdd to Furl

Revisiting the Swift Tiger Beetle – Part 1

Photo details: Canon 100mm macro lens with 68mm extension on a Canon EOS 50D, ISO 100, 1/250 sec, f/13, MT-24EX flash 1/4 power through diffuser caps

Photo 1 - Cylindera celeripes at Alabaster Caverns State Park in northwestern Oklahoma.

When my hymenopterist friend, Mike Arduser, came back from his first trip to Oklahoma’s Four Canyon Preserve last September, my first thought upon seeing his photos of the area was, “Ooh, that looks like a good place for tiger beetles!” Its rugged red clay and gypsum exposures reminded me of similar country I had seen in the not-too-distant Gypsum Hills of south-central Kansas, where I was fortunate enough to observe a nice population of the fantastically beautiful Cicindela pulchra (beautiful tiger beetle) back in 2005. When I later realized that the area was only 30 miles southwest of a confirmed recent sighting of Cicindela celeripes (swift tiger beetle, now Cylindera celeripes), I thought, “Ooh, I wonder if celeripes might occur there also.”

Photo details: Canon 100mm macro lens with 68mm extension tube on a Canon EOS 50D, ISO 100, 1/250 sec, f/13, MT-24EX flash 1/4 power through diffuser caps

Photo 2 - Cylindera celeripes on lichen-encrusted clay soil at Alabaster Caverns State Park.

Recall that C. celeripes is one of North America’s rarest and least understood tiger beetles. This tiny, flightless, ant-like species has been recorded historically from eastern Nebraska south to north-central Texas, but its range appears to have become highly restricted over the past century. It hasn’t been seen in Nebraska for nearly 100 years now, and most recent records have come from its last known stronghold in the Flint Hills of Kansas. In 2003, however, a photographer by the name of Charles Schurch Lewallen posted on BugGuide a photograph of this species taken at Alabaster Caverns State Park in northwestern Oklahoma, and last year small numbers of adults were seen in the Loess Hills of western Iowa. This last sighting triggered an immediate trip to the site by myself and Chris Brown, who has been co-investigating the tiger beetle fauna of Missouri with me for several years now. The occurrence of this species in Iowa’s Loess Hills had reignited our hopes – faint as they were – that the beetle might yet occur in extreme northwestern Missouri, where the Loess Hills reach their southern terminus. We wanted to see the beetle in the wild to better understand its habitat requirements before resuming our search for this species in northwestern Missouri. We succeeded in finding the beetle – an amazing experience in itself – and brought three adults of this never-before-reared species back to the lab for photographs and an attempt at rearing. We did manage to obtain viable eggs, but we were not successful in rearing the larvae beyond first instar. I wrote about that experience last August in a post entitled, “The hunt for Cicindela celeripes” (that post is now currently in press as an article in the journal CICINDELA).

Photo details: Canon 100mm macro lens with 68mm extension tube on a Canon EOS 50D, ISO 100, 1/250 sec, f/11, MT-24EX flash 1/4 power through diffuser caps

Photo 3 - Cylindera celeripes on gypsum exposure at Alabaster Caverns State Park.

Thus, when my friend Mike asked me earlier this year if I might be interested in joining him on his return trip to Four Canyon Preserve in June, I jumped at the chance. I figured I could look for celeripes at the preserve, and if I failed to find it there then I would go to Alabaster Caverns and see if I could relocate the beetle where it had been photographed in 2003. My goals were modest – I simply wanted to find the beetle and voucher its current presence in northwestern Oklahoma (and if possible photograph it in the field with my new camera!). Before leaving, I wrote to Charles Lewallen, who graciously responded with details regarding the precise location and time of day that he had seen the beetle at Alabaster Caverns, and on the first Friday of June I followed behind Mike and his lovely wife Jane during our ten-hour drive out to Four Canyon Preserve. For three days, I roamed the mixed-grass prairie atop the narrow ridges and dry woodland on the steep, rugged canyon slopes of the preserve – always on the lookout for that telltale “flash” between the clumps of bluestem and grama, ever hopeful that one would prove not to be the ant or spider that it appeared to be (and, indeed, always was). Many tiger beetles would be seen – chiefly the annoyingly ubiquitous Cicindela punctulata (punctured tiger beetle), but celeripes would not be among them. Whether this is due to historical absence from the site or a more recent consequence of the wildfires that swept the area a year earlier is hard to say, but its absence at Four Canyon meant that I would need to make a quick, 1-day detour to Alabaster Caverns before rejoining Mike and Jane at Tallgrass Prairie Preserve in northeastern Oklahoma, where we planned to spend the second half of the week.

Photo details: Canon 65mm 1-5X macro lens on a Canon EOS 50D, ISO 100, 1/250 sec, f/13, MT-24EX flash 1/4 power through diffuser caps

Photo 4 - Cylindera celeripes on gypsum exposure at Alabaster Caverns State Park.

Arriving at Alabaster Caverns I was filled with nervous, excited anticipation. Would I find the species, as Charles Lewallen had, or would I get skunked? I kitted up and started walking towards the area where Charles wrote that he had seen the beetle, noting the annoying “Removal of plants and animals prohibited” sign along the way. I hadn’t taken ten steps off the parking lot when I saw it! I froze at first, hardly believing that I had found it that quickly, then started watching the tiny beetle as it bolted urgently from one grass clump to the next. Recalling my experience with this beetle in Iowa (and fearing I would lose it amongst the vegetation), I captured the specimen and placed it live in a vial – I would talk to the park staff later about taking the beetle, but for now I needed to guarantee I had a backup for the lab in case I was unable to get field photographs of the beetle. I started walking again, and within a few minutes I saw another one – okay, they’re here in numbers. I carefully took off my camera bag and assembled the components, all the while keeping my eye on the beetle, and then I began trying to do what last year had seemed impossible – getting field photographs. It was easier this time – the vegetation was not so dense, so I could keep an eye on the beetle as he darted from one clump to another. I tried to wait until he settled in an open spot, but it soon became apparent that just wasn’t gonna happen without a “helping” hand. I started blocking the path of the beetle as he tried to dart away and then removing my hand to see if he would stay put. There were a few false starts, where the beetle looked like he would sit still and then dart just as I was set to take the shot, but eventually it wore down and started sitting still long enough for me to shoot a few frames. Torn between the need to get as many photographs as possible and the desire to look for more beetles, I decided to look around more to see how common the beetle was. As I walked out into the shortgrass prairie above the canyons, I began to see adults quite commonly. Most often they were seen as they bolted out into the open from a clump of vegetation when disturbed by my approach. The substrate was red clay and gypsum – just as I had seen in Four Canyon Preserve, but unlike that area the clay exposures were heavily colonized by a mottling of green, blue, and gray lichens. It made the beetles almost impossible to see when they were not moving – even at close range! I spent about an hour taking photographs of several individuals, even managing to photograph one that appeared to be parasitized by what I take to be a dryinid hymenopteran.

Photo 5 - Cylindera celeripes with parasite (dryinid hymenopteran?).  Note also the ant head attached to right antenna.

Photo 5: Cylindera celeripes with parasite (dryinid hymenopteran?). Note also the ant head attached to right antenna.

After getting a sufficient series of photographs (is there really such thing?), I went to the park office hoping to convey the significance of this find to the Park Naturalist and to convince him/her to let me take some live individuals with me for another attempt at rearing. The Park Naturalist was out of the office, but the Park Historian was there. I could hardly contain my excitement as I explained to her what I had found, why it was so important, and my hope to try to rear the species with adults collected in the field. She not only responded as positively as I had hoped, but accompanied back out into the field so that I could show her the beetles. She told me it would be no problem to take some live individuals for rearing and to please let them know if there was anything else they could do to help me.  She then provided me with the day’s natural history “dessert” by pointing out a Mexican free-tailed bat (Tadarida brasiliensis) – Oklahoma’s state flying mammal – roosting up in the top of a nearby picnic shelter. Standing atop the picnic table put me within arm’s length of the little chiropteran – close enough to see his tiny little eyes looking quizzically back at me.

Photo 6 - Cylindera celeripes macrohabitat, Alabaster Caverns State Park, Oklahoma.  Note rather widely spaced clumps of vegetation (photo details: Canon 17-85mm zoom lens (17mm) on a Canon EOS 50D, ISO 100, 1/64 sec, f/8).

Photo 6 - Cylindera celeripes macrohabitat at Alabaster Caverns State Park. Note rather widely spaced clumps of vegetation.

It had begun sprinkling rain by then, so with some urgency I got my tools, extracted a couple of chunks of native soil and transferred them to the small “Critter Totes” that I had brought for the purpose, and began searching for live individuals to place within them. The beetles had become scarce as the drizzle turned to light rain, and by the time I had split about a dozen individuals between the two containers the rain was coming down hard enough to start puddling. I continued a last ditch effort to find “just one more,” but a lightning strike within a mile of the park put an end to that – the air now felt electric as I hurriedly walked back to the car (gloating unabashedly inside) and began the three-hour drive towards Tallgrass Prairie Preserve… (to be continued).

IMG_0580_1200x800

Photo 7 - Cylindera celeripes microhabitat at Alabaster Caverns State Park. Note thick encrustation of lichens on clay substrate amidst white gypsum exposures.

Photo details:
#1-3, 5: Canon 100mm macro lens w/ 68mm extension on Canon EOS 50D, ISO 100, 1/250 sec, f/13 (photo 3, f/11), MT-24EX flash 1/4 power through diffuser caps.
#4: Same except Canon 65mm 1-5X macro lens, flash 1/8 power.
#6: Same except Canon 17-85mm zoom lens (17mm), 1/64 sec, f/8, natural light.
#7: Same except Canon 17-85mm zoom lens (35mm), 1/100 sec, f/7, natural light.

Copyright © Ted C. MacRae 2009

Add to FacebookAdd to NewsvineAdd to DiggAdd to Del.icio.usAdd to StumbleuponAdd to RedditAdd to BlinklistAdd to Ma.gnoliaAdd to TechnoratiAdd to Furl

Trilogy of Terror

Last week, Alex at myrmecos tagged me with a fun new meme called These are a few of my favorite stings…. It’s simple – list the things which have stung you (biting doesn’t count), and tag three others for their tales of envenomization. Of course, being the dedicated myrmecologist that he is, Alex leads off with a most impressive list of venomous arthropods, and he selected worthy competition in buzzybeegirl and bugeric.  But me?  I have, for the most part, succeeded in avoiding stings by focusing on a group of insects (beetles) that never evolved such structures.  My domestic list is short and mundane – honey bees, paper wasps, sweat bees, fire ants – and even those not very often.  Alex, however, suspected I might have some tales from exotic lands – thus, I offer the following trilogy and tag Art, Doug, and Kolby.

Tale 1
When I made my first Neotropical collecting excursion some 20 years ago to Ecuador, I was warned by my guide about large, black ants that he called “Congas.” I later learned the species to be what many people call the bullet ant (Paraponera clavata). Now, I’m not an expert on which arthropod truly has the most painful sting, but many people knowledgeable about such matters say it is this species – and I believe them! We were camped out in Sucumbios Province east of Nueva Loja (also called “Lago Agrio”) at an Amazon forest site where recent construction had left rows of month-old slash lining both sides of a 2-km stretch of new road through the forest – can you say woodboring beetles? I roamed up and down that stretch of road, picking a wonderful diversity of longhorned beetles (Cerambycidae) and jewel beetles (Buprestidae) off the slash. At one point, I encountered a whole tree crown laying by the side of the road that required some clambering to get at the beetles crawling on its inner branches. At one point, I braced myself with my arm against a branch and immediately felt an excruciating pain. I looked at my arm and saw one of these large ants clamped onto my arm and quickly slapped it off. I really don’t think words can describe how painful that sting was, and not only did it throb for the rest of the day, but I actually felt sick for the next several days (though I still managed to keep roaming the slash rows). I don’t know if the bullet ant I captured right afterwards was the one that stung me, but I still took great delight in impaling a #2 insect pin through its thorax after I returned home.

Tale 2
Alex mentioned one plant – stinging nettle (Urtica dioica, which also lines one of my favorite mountain bike trails), but I’ve also had a run-in with a much more formidable plant in Mexico. Mala mujer (Cnidoscolus angustidens), which translates as “bad woman” in Spanish, deserves all the respect you can give it. Reported to be one of the most painful stinging nettle-type plants known, it grows commonly from the arid southwest down into the dry, tropical thorn forests of southern Mexico where my colleague Chuck Bellamy and I have made several trips in recent years to search for jewel beetles. One quickly learns to recognize this distinctive euphorbiaceous plant by its green palmate leaves with white veins and thick covering of yellow, stinging trichomes. Unfortunately, in my zeal for beating buprestids from Leucaena diversifolia (netting several of the rare Pelycothorax tylauchenioides and a now paratypical series of what was then an undescribed species of Agrilus), I forgot to maintain my lookout for this common understory plant and got a swipe across the knuckles. Not only did the extreme pain last for hours, but my ring finger began swelling so worrysomely that we stopped in a hospital looking for somebody to cut the ring off. My poor Spanish brought me no sympathy (or service), but fortunately the swelling began subsiding that evening and I didn’t lose my finger. I did, however, live with a rash for the next several days that developed into a hard, purple skin discoloration for the next several weeks.  Bad woman, indeed!

Tale 3
I debated whether to include this experience, but the terror was real so here it is. I wrote about it recently in an article called “Dungers and Chafers – a Trip to South Africa” that appeared in the December 2008 issue of SCARABS Newsletter. Enjoy this excerpt:

After arriving at the park [Borakalalo National Park, North West Province], I could hardly contain myself – I was so anxious to start collecting… We drove through the park for a little bit looking for a good spot to pull over and begin the hunt. After finding such a spot, I grabbed my trusty beating sheet and began doing what I have done so many times before – walking up to a tree, giving a branch a whack with the handle of my net, and hoping to see some prized buprestid laying on the beating sheet. The habitat was ideal for this – dominated by low, spreading acacias such as Acacia tortilis and A. karoo. Buprestids love acacias! I had already learned this in my travels through the American desert southwest and down into Mexico and South America – surely it was the same in South Africa. The first whack yielded nothing – typical. Even when collecting is good, buprestids are never “dripping from the trees,” and often one must literally beat dozens and dozens of trees to really get a good idea of the diversity and abundance of buprestid species that are active in a given area. I whacked a few more trees, with similar results. I then spotted one particularly large acacia tree – something about it said, “beat me!” I walked over to it and gave a branch a whack. All at once, it seemed as though the world was exploding! The air was suddenly abuzz with dozens of large, flying insects, whirring and swirling all around me. My first thought in that initial moment of terror was that I had whacked a hornet’s nest – who knew what kinds of deadly, venomous wasps one might encounter in Africa? Instinctively I ducked and started running, but within a few moments I realized that I was not being chased. Cautiously, I sneaked back towards the tree (after stuffing my heart back down my throat) and realized that they were not hornets after all, but instead beetles. I looked more closely and saw that the tree was literally alive with dozens and dozens of large, green cetoniines resembling our own green June beetle, Cotinis nitida (L.), which seemed to be attracted to the small, white blooms that covered the tree in profusion. I netted a few of the beetles, which I would later determine to represent the common savannah species Dischista cincta (de Geer) (Photo 2). Such was my welcome to Africa, where it seemed the trees literally are ‘dripping’ with beetles!

Disticha cincta (de Geer)

Photo 2. Disticha cincta (de Geer)

Copyright © Ted C. MacRae 2009

Add to FacebookAdd to NewsvineAdd to DiggAdd to Del.icio.usAdd to StumbleuponAdd to RedditAdd to BlinklistAdd to Ma.gnoliaAdd to TechnoratiAdd to Furl

Body Invaders

In keeping with the parasitic theme I established in my last two posts, I happened upon this brief video promotion for a National Geographic special called In the Womb: Extreme Animals which will air this Sunday (May 10). The video features the offspring of a parasitic wasp (Cotesia glomerata) that has injected her eggs into a caterpillar — and now they’re ready to emerge! It’s a fascinating study of parasitoid-host relationships, filmed incredibly from inside the caterpillar! Watch the whole video for the wicked, surprising ending.

Viewing tips: after beginning play, click on “HQ” in the lower right corner to view the video in high quality. Or, click on the video itself to be taken to YouTube, where you have the option to watch the video in HQ and in full screen mode (2nd button from the lower right corner). You will be amazed!

Vodpod videos no longer available.

more about “Body Invaders“, posted with vodpod

Tip of the hat to Adrian, who posted this yesterday (but I really did find it on my own).

Copyright © Ted C. MacRae 2009

Add to FacebookAdd to NewsvineAdd to DiggAdd to Del.icio.usAdd to StumbleuponAdd to RedditAdd to BlinklistAdd to Ma.gnoliaAdd to TechnoratiAdd to Furl

Afrikaans ants

A few for Alex

I photographed these ants in South Africa during my visit to Borakalalo National Park (North West Province) in November 1999.  Dr. Brian Taylor, author of the impressive Ants of Africa website, kindly identified and provided some information about the ants in these photos.  Pachycondyla tarsata - South Africa, North West Province, Borakalalo National Park, 25.xi.1999The first photo shows a worker ant dragging another dead ant.  Dr. Taylor identified the worker as Pachycondyla tarsata, which according to his website is known as the ‘Stink Ant’.  This pan-African species usually forages singly and nests directly in the ground, with the entrance often surrounded by excavated soil and remains of arthropods and other food. He wasn’t sure about the identity of ant being carried but guessed that it could be the queen of Camponotus (Myrmopiromis) fulvopilosus1.  That species is South African and appears to be of the right size for the individual in this photo.  Ants may have taken over the world, but at least they clean up after themselves.

1 Edit 01/17/09: Dr. Taylor sent an email to me saying that, after a second look at the above photo, he now believes the queen being carried by the Pachycondyla tarsata worker probably represents Carebara vidua, discussed below.

These next photos might have been better posted on Wednesday (ahem… “hump” day).  424046-r1-e009_009_mating_ants_21Dr. Taylor identified them as Carebara vidua. According to Lepage and Darlington (1984), colonies of this termitophagous species produce broods of alates ready to fly during the short November rains (as we experienced during our visit), as well as the longer April rains. Male and female alates are usually produced in separate nests, and after the flight the alate males seek out the females. The mating swarm I photographed shows several males attempting to mate with a single female – I counted five males at first, although one dropped off while I continued taking photos trying to get a good shot of the “lucky fellow”. 424046-r1-e010_010_mating_ants_21I am pleased that Dr. Taylor considered these photos informative enough to post on the species page at his Ants of Africa website. Lepage and Darlington (1984) reported nests of this species established in 2-10% of Macrotermes termite mounds  in Kenya, although nests can also occur well away from mounds. In the laboratory, dealate female ants exposed to Macrotermes workers remained passive and elicited no aggression. After 39 days, the mated females were capable of producing broods of about 1,000 workers, able to overpower, kill and eat the much larger Macrotermes workers.

REFERENCES:

Taylor, B. 2008. Ants of Africa. http://www.antbase.org/ants/africa/antcover.htm.

Lepage, M. G. and J. P. E. C. Darlington. 1984. Observations on the ant Carebara vidua F. Smith preying on termites in Kenya. Journal of Natural History 18(2):293-302.

A sand prairie autumn

Splitbeard bluestem seed headsAsk any astronomer when autumn begins, and they will likely tell you it begins at the autumnal equinox – when shortening days and lengthening nights become equal as the sun crosses over the celestial equator. According to them, fall began this year on September 22 – at 11:44:18 A.M. EDT, to be precise. I agree that autumn begins at a precise moment, but it is not at the equinox. Rather, it is that unpredictable moment when a sudden crispness in the air is felt, when the sky somehow seems bluer and shadows seem sharper, and hints of yellow – ever so subtle – start to appear in the landscape. Butterfly pea blossomIn Missouri, with its middle latitudes, this usually happens a few weeks before the equinox, as August is waning into September. It is a moment that goes unnoticed by many, especially those whose lives and livelihoods have lost all connection with the natural world. To plants and animals, however, it is a clear signal – a signal to begin making preparations for the long cold months of winter that lie ahead. Plants that have not yet flowered begin to do so in earnest, while those that have shift energy reserves into developing seeds. Animals take advantage of their final opportunities to feed before enduring the scarcities of winter, digging in to sleep through them, or abandoning altogether and migrating to warmer climes. Insects begin hastily provisioning nests for their broods or laying eggs – tiny capsules of life that survive the harsh winter before hatching in spring and beginning the cycle anew.

Sand prairie in early September.Sand prairie in early October.  Note abundance of splitbeard bluestem seed heads.Across much of Missouri, in the Ozark Highlands and in riparian ribbons dissecting the northern Plains, autumn brings an increasingly intense display of reds, purples, oranges, and yellows, as the leaves of deciduous hardwoods begin breaking down their chlorophyll to unmask underlying anthocyanins and other pigments. Small southern jointweedIn Missouri’s remnant prairies, seas of verdant green morph to muted shades of amber, tawny, and beige. This subtle transformation is even more spectacular in the critically imperiled sand prairies of the Southeast Lowlands, where stands of splitbeard bluestem (Andropogon ternaries – above) turn a rich russet color while fluffy, white seed heads (1st paragraph, 1st photo) appear along the length of each stem, evoking images of shooting fireworks. Small southern jointweed (Polygonella americana – right) finds a home at the northern extent of its distribution in these prairie remnants and in similar habitats in nearby Crowley’s Ridge, blooming in profusion once the cooler nights arrive. Butterfly pea (Clitoria mariana – 1st paragraph, 2nd photo) blooms add a gorgeous splash of soft purple in contrast to the muted colors of the plants around them.

Kent Fothergill, Ted MacRae, and Rich ThomaAfter first becoming acquainted with Missouri’s sand prairies this past summer, I knew a fall trip (or two) would be in order. The extensive deep, dry sand barrens were ideal habitat for sand-loving insects, including certain spring/fall species of tiger beetles that would not be active during the summer months. The cooler nights and crisp air of early fall make insect collecting extraordinarily pleasurable, so it took little effort to convince friends and colleagues Kent and Rich to join me on another excursion to these extraordinary remnant habitats, along with my (then 8 yr-old) daughter Madison (who would likely characterize this as “tallgrass” prairie). Madison MacRae, age 9 (almost)I was, as ever, on the lookout for tiger beetles; however, temperatures were cool, skies were overcast, and the fall season was just beginning, greatly limiting tiger beetle activity during this first fall visit. We did see one Cicindela formosa (big sand tiger beetle), which cooperated fully for a nice series of photographs. We also found single specimens of the annoyingly ubiquitous C. punctulata (punctured tiger beetle) and a curiously out-of-place C. duodecimguttata (12-spotted tiger beetle), which must have flown some distance from the nearest dark, muddy streambank that it surely prefers. Of greatest interest, we found two specimens of C. scutellaris (festive tiger beetle), which in this part of Missouri is represented by a population presenting a curious mix of influences from two different subspecies (more on this in a later post…). Despite the scarcity of tiger beetles, other insects were present in great diversity, some of which I share with you here.

Ululodes macleayanusThis bizarre creature, sitting on the stem of plains snakecotton (Froelichia floridana), is actually a neuropteran insect called an owlfly (family Ascalaphidae). Looking like a cross between a dragonfly and a butterfly due to its overly large eyes and many-veined wings but with long, clubbed antennae, this individual is demonstrating the cryptic resting posture they often assume with the abdomen projecting from the perch and resembling a twig. The divided eyes identify this individual as belonging to the genus Ululodes, and Dr. John D. Oswald (Texas A&M University) has kindly identified the species as U. macleayanus. As is true of many groups of insects, their taxonomy is far from completely understood. Larvae of these basal holometabolans are predaceous, lying on the ground with their large trap-jaws held wide open and often camouflaging themselves with sand and debris while waiting for prey. The slightest contact with the jaws springs them shut, and within a few minutes the prey is paralyzed and can be sucked dry at the larva’s leisure.

Ant lion, possibly in the genus Myrmeleon.Another family of neuropteran insects closely related to owlflies are antlions (family Myrmeleontidae, sometimes misspelled “Myrmeleonidae”). This individual (resting lower down on the very same F. floridana stem) may be in the genus Myrmeleon, but my wanting expertise doesn’t allow a more conclusive identification [edit 4/12/09 – John D. Oswald has identified the species as Myrmeleon immaculatus]. Strictly speaking, the term “antlion” applies to the larval form of the members of this family, all of whom create pits in sandy soils to trap ants and other small insects, thus, it’s occurrence in the sand prairie is not surprising. Larvae lie in wait beneath the sand at the bottom of the pit, flipping sand on the hapless prey to prevent it from escaping until they can impale it with their large, sickle-shaped jaws, inject digestive enzymes that ‘pre-digest’ the prey’s tissues, and suck out the liquifying contents. Finding larvae is not easy – even when pits are located and dug up, the larvae lie motionless and are often covered with a layer of sand that makes them almost impossible to detect. I’ve tried digging up pits several times and have failed as yet to find one. Larvae are also sometimes referred to as “doodlebugs” in reference to the winding, spiralling trails that the larvae leave in the sand while searching for a good trap location – these trails look like someone has doodled in the sand.

Bembix americanaThis digger wasp, Bembix americana (ID confirmed by Matthias Buck), was common on the barren sand exposures, where they dig burrows into the loose sand. Formerly included in the family Sphecidae (containing the better-known “cicada killer”), members of this group are now placed in their own family (Crabronidae). Adult females provision their nest with flies, which they catch and sting to paralyze before dragging it down into the burrow. As is common with the social hymenoptera such as bees and paper wasps, these solitary wasps engage in active parental care by providing greater number of prey as the larva grows. As many as twenty flies might be needed for a single larva. I found the burrows of these wasps at first difficult to distinguish from those created by adults of the tiger beetles I so desired, but eventually learned to distinguish them by their rounder shape and coarser, “pile” rather than “fanned” diggings (see this post for more on this subject).

Stichopogon trifasciatusRobber flies (family Asilidae) are a favorite group of mine (or, at least, as favorite as a non-coleopteran group can be). This small species, Stichopogon trifasciatus (ID confirmed by Herschel Raney), was also common on the barren sandy surface. The specific epithet refers to the three bands of alternating light and dark bands on the abdomen. Many species in this family are broadly distributed but have fairly restrictive ecological requirements, resulting in rather localized occurrences within their distribution. Stichopogon trifasciatus occurs throughout North America and south into the Neotropics wherever barren, sandy or gravely areas near water can be found. Adults are deadly predators, swooping down on spiders, flies and other small insects and “stabbing” them with their stout beak.

Chelinidea vittigerPrickly pear cactus (Opuntia humifusa) grows abundantly in the sandy soil amongst the clumps of bluestem, and on the pads were these nymphs of Chelinidea vittiger (cactus bug, family Coreidae). This wide-ranging species occurs across the U.S. and southward to northern Mexico wherever prickly pear hosts can be found. This species can either be considered a beneficial or a pest, depending upon perspective. On the one hand, it serves as a minor component in a pest complex that prevents prickly pear from aggressively overtaking rangelands in North America; however, prickly pear is used by ranchers as emergency forage, and fruits and spineless pads are also sometimes harvested for produce. In Missouri, O. humifusa is a non-aggressive component of glades, prairies, and sand and gravel washes, making C. vittiger an interesting member of the states natural diversity.

Ammophila sp., possibly A. proceraThis wasp in the genus Ammophila (perhaps A. procera as suggested by Herschel Raney) was found clinging by its jaws to a bluestem stem in the cool morning, where it presumably spent the night. One of the true sphecid (or “thread-waist”) wasps, A. procera is a widespread and common species in eastern North America. One of the largest members of the genus, its distinctive, bold silver dashes on the thorax distinguish it from most other sympatric congeners. Similar to the habits of most other aculeate wasp groups, this species captures and paralyzes sawfly or lepidopteran caterpillars to serve as food for its developing brood. Females dig burrows and lay eggs on the paralyzed hosts with which the nests have been provisioned. Adults are also found commonly on flowers, presumably to feed on nectar and/or pollen.

Dusty hog-nosed snakeRich is a bit of herpatologist, so when he brought this hog-nosed snake to our attention we all had a good time pestering it to try to get it to turn upside down and play dead. I had never seen a hog-nosed snake before but knew of its habit of rolling over and opening its mouth with its tongue hanging out when disturbed, even flopping right back over when turned rightside up or staying limp when picked up. We succeeded in getting it to emit its foul musky smell, but much to our disappointment it never did play dead, instead using its shovel-shaped snout to dig into the sand. Dusty hog-nosed snake - head closeupWe had assumed this was the common and widespread eastern hog-nosed snake (Heterodon platirhinos); however, in our attempts to turn it over I noticed its black and orange checker patterned belly. I later learned this to be characteristic of the dusky hog-nosed snake (H. nasicus gloydi), only recently discovered in the sand prairies of southeast Missouri and regarded as critically imperiled in the state due to the near complete destruction of such habitats. Disjunct from the main population further west, its continued survival in Missouri depends upon the survival of these small sand prairie remnants in the Southeast Lowlands.

Collection Inventory update

The more observant – and taxonomically inclined – among my readers may have noticed the sidebar item entitled, “T. C. MacRae Collection”. The links within that item lead to Google documents detailing the species in those groups of insects that are represented within my collection. I am primarily a beetle guy, and within that vast taxon I focus mostly on the woodboring beetle groups Buprestidae and Cerambycidae and the tiger beetle family Cicindelidae. As you can see, however, I have inventories for several additional groups, including non-beetle families – a testament to my inability to suppress broad interest in insects as a whole. I don’t claim to be an expert in these other groups of insects, but I do enjoy learning about groups outside my chosen field of expertise. It’s a bit of a ‘throwback’ attitude – insect taxonomists of the 19th and early 20th centuries commonly studied multiple families or even orders of insects. This broad approach has largely disappeared in the past 50 years, as taxonomists increasingly have been forced to become narrowly focused on a single insect taxon. I can maintain this broad approach because, while I am a professional entomologist, I am a taxonomist only by avocation. My research is conducted at my own discretion and doesn’t rely on securing grants or fulfilling a departmental mission. Rather, it is directed only by what I find interesting and can reasonably afford in terms of time and expense.

The purpose of this update is twofold – to call attention to two recent additions to the list of inventories, and to explain how the inventories are constructed in the event that some future reader will want to utilize them for reference. In the past two weeks, I’ve received back material accumulated over the years in the families Mutillidae (velvet ants) and Asilidae (robber flies). This material had been sent to experts for identification – doctoral candidate Kevin Williams (Utah State University) graciously provided IDs for the velvet ants, while worldwide asilid expert Dr. Eric Fisher (California Department of Food and Agriculture) kindly identified the robber flies. For each of these groups, an inventory was constructed in which the species represented by my material are listed in the context of the group’s currently accepted higher classification. In each case, higher taxa not represented in my collection are indicated by lighter gray text. A similar approach has been used, to varying degrees, in the other listed inventories. The biggest one, Buprestoidea, represents the bulk of my collection, listing almost 1,500 species from around the world. In this case, not only is the complete higher classification indicated, but all currently recognized world genera are also listed, as well as all known North American species. Again, taxa not represented in my collection are indicated by lighter gray text. Similar inventories have been constructed for Cerambycidae and Cicindelidae, but in these cases the inclusion of taxa missing from my collection is limited to those occurring in North America – their combined worldwide fauna is simply too large for me to concern myself with, given my primary focus on the worldwide buprestoid fauna.

Regarding the Buprestoidea, Cerambycidae, and Cicindelidae – these are my chosen groups of interest in which I am actively building North American representation (worldwide for Buprestoidea). If anyone can provide specimens representing taxa not in my collection, please contact me directly. I am more than happy to exchange for such material. As for the other groups, they are primarily ‘just for fun’ – I collect them when convenient because they are interesting, but more importantly to make them available to others who might have a research interest in them. If anyone working in these groups sees species listed that are of interest to your research, please feel free to contact me for a loan or exchange. I have material in many additional groups not yet listed – inventories will be posted as they become available. If you have interest in a group not listed, please contact me and I’ll let you know what material I have available for loan/exchange.