Magnificently Monstrous Muscomorphs

I suppose tiger beetles have gotten more than their fair share of attention here lately, so for this post I thought I’d highlight insects of a completely different group – flies! Admittedly, as a coleopterist, I tend to view flies with much the same disdain as your average insect non-enthusiast – as pesky, pestiferous vermin worthy of little more attention than a decisive swat. I don’t begrudge them their amazing diversity – at ~100,000 described species worldwide, they are strong contenders with the Lepidoptera and Hymenoptera as the second largest order of insects (of course, you need all three of these orders combined to match the diversity of the Coleoptera). I am also prepared to accept that they may well represent, at least morphologically, the pinnacle of insect evolution (a position that a few hymenopterists I know might argue with) due to their amazing flight capabilities and the morphological adaptations they have developed for such. These include the development of aristate antennae for detecting wind speed, the conversion of the second pair of wings into stabilizing organs (halteres), and the ability to beat the remaining pair of wings at incomprehensible rates – up to 1,000 times per second in some very small midges (even more baffling when one considers that the wing “beat” is actually just a passive result of rhythmic distortions of the thoracic box). I even acknowledge that the vast majority of fly species are not even pests, living their lives innocuously as herbivores, scavenging organic matter that nothing else wants, and preying upon or parasitizing other insects, including important agricultural pests. Still, flies bug me – mosquitoes prevent me from sleeping under the stars without a tent, deer flies drone around my head incessantly while I’m trying to stalk an elusive tiger beetle, stable flies trick me into assuming they are just another house fly (until they bite me!), house flies (the real ones) rudely land on my sandwich with their filthy feet, and eye gnats insist on committing hary kary in my eyes as I walk the trails (I won’t mention their other common name, derived from their habit of clustering around exposed canid genitalia).

There is, however, one group of flies that possess “cool factor” rivaling that of even the most popular insect groups – robber flies and their kin. I’ve always picked them up as an aside, even sending them off for authoritative ID and constructing an inventory of the species in my collection. The brute of a fly pictured here is not a true robber fly, but in the related family Mydidae. Mydus clavatus can be recognized easily in the field by its large size and distinctive black coloration with red/orange on top of the 2nd abdominal segment. Presumably this is an example of Batesian mimicry modeled upon spider wasps (family Pompilidae) in the genus Anoplius. This mimicry allows them to fly rather boldly in the open and is so persuasive that it can not only fool the casual observer, but even the most knowledgable of entomologists might be loathe to handle it despite knowing better. Although common across the eastern U.S., aspects of its life history are poorly understood. Adults have been reported to be predators of other insects, but apparently there are some doubts about the veracity of such reports. Patrick Coin of BugGuide has observed adults (males?) taking nectar from flowers and has suggested that reports of predation by adults might have been an erroneous assumption due to their relation and resemblance to robber flies. Larvae are reported to be predaceous on woodboring beetle larvae, and I have reared adults of this species from a dead sycamore (Platanus occidentalis) stump in southern Missouri that was infested with mature larvae of the large buprestid species, Texania campestris. This habit is similar to robber flies of the genus Laphria, which mimic bumble bees and carpenter bees.

In Greek mythology, Promachos (Προμαχοε) was “the champion” or one “who leads in battle” – an appropriate generic name for the so-called “giant robber flies” of the genus Promachus. These large flies are dominant and fearless predators that will capture just about any flying insect – even adult dragonflies. There are three species of Promachus in the eastern U.S. that exhibit the yellow and black tiger striping of the abdomen seen in this individual, identified as a female Promachus hinei by Herschel Raney at BugGuide due to its reddish femora and occurrence in the central U.S. Promachus rufipes is similar but has black femora with distinctly orangish tibiae and is more common in the southeastern U.S., whereas P. vertebratus has more muted two-toned legs with smaller dark areas dorsally on the abdominal segments and is more common in the northern states. Additional species occur in the region but lack the tiger striping of the abdomen, and even more species occur in the western U.S. Members of this genus generally lay their eggs on the ground near grass roots, and the larvae burrow into soil after hatching and feed on soil insects, roots, and decaying matter before pupating within the soil in an unlined cell.

During my recent trip to Nebraska I encountered this related robber fly genus Proctacanthus, also determined by Herschel provisionally as P. milbertii. These large robber flies with a prominent beard are similar in habit to Promachus species, laying their eggs in crevices in soil and the larvae feeding on soil insects, roots, and decaying plant matter. Proctacanthus milbertii is a late season species that occurs across much of the U.S. and reportedly loves butterflies. However, Joern & Rudd (1982), in studying predation by this species in western Nebraska (where the individual pictured here was photographed) found that grasshoppers made up 94% of the prey captured by this species. Interestingly, nearly all of the remaining prey captures were other P. milbertii, which was carefully verified as such since mating postures can be easily mistaken for prey handling positions. Grasshopper prey species taken by this species were most strongly influenced by availability rather than size, suggesting that even the largest grasshopper species could be captured as easily as smaller species – a testament to the ferocity of this robber fly.

Another family of flies modestly related to robber flies and also ranking high in “cool factor” are the bee flies (family Bombyliidae). The scaly bee fly, Lepidophora lepidocera (ID confirmed by Joel Kits at BugGuide), is a particularly attractive member of the family. The distinctive, hunch-backed shape of this southern U.S. species is shared with the more northern L. lutea, from which it is distinguished by having pale scales only on the 5th abdominal segment and not on the 4th also. Most bee flies are presumbably mimics of – yes – bees; however, the species in this genus might actually be mimics of robber flies instead. Adults are most often seen taking nectar from flowers – this individual was taken on flowers of tall boneset (Eupatorium altissimum). Larvae are characterized by Sivinski et al. (1999) as kleptoparasites on the provisions of solitary wasps in the families Vespidae and Sphecidae – meaning that the larva does not parasitize wasp larvae directly, but instead usurpes the nest provisions on which the wasp larvae were supposed to feed. The little thieves!

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.