Brazil Bugs #2

A few more photographs from this past week in Campinas, Brazil.  It rained during the afternoon but stopped by the time I arrived back at the hotel, allowing me to stroll the lavishly landscaped grounds during the mild evening hours.  There is a pink-flowered shrub forming a hedge row in back of the hotel that is highly attractive to many types of insects.  The identity of the shrub remains a mystery to me, and most of the insects I’m finding on it I can recognize only to family – I’m hoping the hotel staff will be able to name the former and that the readers of this blog might be able to provide IDs for the latter.

Calycopis sp. poss. origo (Lepidoptera: Lycaenidae). ID by Dave Hubble and Chris Grinter.

It took a bit of effort to find an unobstructed view of this hairstreak butterfly (family Lycaenidae) as it visited the flowers within the shrub.  Every time I tried to move foliage out of the way to get a good view, the butterfly became alarmed and flew to another part of the hedge row.  My antics drew the attention of a hotel worker, who was apparently interested enough in what I was doing to act as a spotter whenever the butterfly flew to help me relocate it.  Eventually I got a few shots that I was happy with, including the above.

A flesh fly (Diptera: Sarcophagidae).

I presume this to be a type of flesh fly (family Sarcophagidae) based on the stout bristles and color pattern that seems typical for the family.  I like the striking contrast in coloration between the fly and the flower.  There are a few fly bloggers who I’m hoping might be able to give a better identification.

A potter/mason wasp? (Hymenoptera: Vespidae).

This appears to me to be some kind of potter or mason wasp (family Vespidae, subfamily Eumeninae) – it was a bit smallish at only about 12mm in length.  I hope one of the knowledgeable wasp bloggers out there (ahem… Eric?) can at least confirm this level of identification and perhaps the tribe or genus as well. 

Azya orbigera (Coleoptera: Coccinellidae). ID by Tucker Lancaster.

Every ladybird beetle (family Coccinellidae) I’ve ever seen is some variation of black and red/orange/yellow and has a smooth, glabrous appearance.  This beetle is cobalt blue with a dense pubescence over the dorsal surface, but it still seems to me to be some type of ladybird beetle.  It was a tiny little thing, so I suppose it could be one of the multitude of small beetle families with which I am unfamiliar.

Quedas sp.? (Hemiptera: Cicadidae).

This cast cicada exuvium was not on the shrub, but on a nearby tree at about eye level.  I really wish I could have seen the cicada that emerged from it, because this is certainly the biggest cicada exuvium I have ever seen.  I was about to simply label it “family Cicadidae” but seem to recall that cicada higher classification is in a bit of flux these days.  At any rate, given its great size I wonder if it might represent one of the giant cicadas in the genus Quesada.

I still have many more insect photographs from the past week and will certainly increase that number over the next week as well.  Stay tuned!

Copyright © Ted C. MacRae 2011

Rush skeletonplant pea gall wasp

Lygodesmia juncea with galls of Antistrophus lygodesmiaepisum (Hymenoptera: Cynipidae) on stem.

The Loess Hills landform along the western edge of Iowa and extreme northwestern Missouri is home to a unique assemblage of plants and animals.  The majority of these are associated with loess hilltop prairies – grassland remnants that have their origins in the hypsithermal maximum of several thousand years ago and that persist as small relicts on the landform’s steep, dry, south- and west-facing slopes.  Many of the plants and animals found in these grassland remnants are more typically found further west in the Great Plains, but hang on in the Loess Hills as hypsithermal relicts.

Antistrophus lygodesmiaepisum galls on stem of Lygodesmia juncea.

One such hypsithermal relict is rush skeletonplant, Lygodesmia juncea, a wirey, leafless-looking plant in the family Asteraceae¹.  More common in the Great Plains, this plant occurs in Missouri only on these loess hilltop prairie remnants.  The first time one encounters this plant, they are left with the impression that the plant bears small, pea-like fruiting structures along the length of its stem.  These are not fruiting structures, however, but galls made by the cynipid wasp Antistrophus lygodesmiaepisum.  Although this insect does not have a common name, it is associated exclusively with L. juncea, as suggested by its specific epithet (which also alludes to the pea-like galls with the suffix -pisum), so I see no reason why this wasp cannot be called the “rush skeletonplant pea gall wasp.”  Some sources variably misspell the genus as Anistrophus (without the first “t”) or the species name as simply pisum, a synonym first introduced by Ashmead in the late 19th century a few years after the species was described (I made both mistakes [and also erroneously referred to L. juncea as skeletonweed] in one of my earliest posts: The Loess Hills in Missouri).  It would seem that Antistrophus lygodesmiaepisum is the correct name, according to Pickering (2009).

¹ Not to be confused with rush skeletonweed, Chondrilla juncea – also in the Asteraceae, which despite the similarity of common names, specific epithet, and general appearance (except with yellow flowers) is an altogether different plant that was introduced from the Mediterranean Region and is now considered an invasive weed in much of the Great Plains.

Antistrophus lygodesmiaepisum larva in gall on stem of Lygodesmia juncea.

Rush skeletonplant exudes a latex-like sap when damaged, making it unpalatable to most grazers – this latex-like sap can be seen when the galls made by the wasps are cut open.  Cynipid wasps are the second most diverse group of gall-making insects behind the gall midges, and many species are mono- or oligophagous (Ronquist and Liljeblad 2001), meaning that they are associated exclusively with a single plant species or group of closely related species.  Antistrophus lygodesmiaepisum is one such monophagous species, thus its occurrence in Missouri, like that of L. juncea, is restricted to the tiny loess hilltop prairie remnants in extreme northwestern Missouri.  In recent years, these prairie relicts have suffered heavily from conversion to agriculture, abusive grazing, and suppression of fire that has led to invasion by woody and exotic plants.  In Missouri, only about 50 acres of loess hilltop prairie remain, and only half of these are in conservation ownership, making it among the most critically imperiled of natural communities in Missouri.  While lacking the conservation charisma of L. juncea and the dozen or so other plants and vertebrates that are restricted in Missouri to these prairie remnants, A. lygodesmiaepisum nevertheless deserves equal consideration as a Missouri species of conservation concern.

I knew this would be a difficult ID Challenge and am quite impressed that at least a few people figured out at least the correct genus.  Tim Eisele scored 8 points in this challenge to not only take the win but also move way up into a 3-way tie for 4th place in the overalls.  Ben Coulter continues to be Mr. Consistency, earning 4 points for 2nd place and retaining his overall lead by an almost insurmountable margin (see what happens when you play every game!).  JasonC beat out the other contenders for the final podium spot on the basis of a bonus point, but the hot contest continues to be the battle for 2nd place overall.  Janet Creamer still holds it at 14 pts, but there is a veritable gaggle of contenders nipping at her heals – the next few challenges could be interesting.

Photo 1: Canon 100mm macro lens (ISO 100, 1/250 sec, f/2.8).
Photos 2-3: Canon MP-E 65mm 1-5X macro lens (ISO 100, 1/250 sec, f/14).
All photos: Canon 50D , Canon MT-24EX flash w/ Sto-Fen + GFPuffer diffusers. Typical post-processing (levels, minor cropping, unsharp mask).

REFERENCES:

Pickering, J.  2009.  Database of Hymenoptera in America north of Mexico. http://www.discoverlife.org/proceedings/0000/6/html/Cynipidae (accessed 20 Jan 2011).

Ronquist, F. and J. Liljeblad.  2001.  Evolution of the gall wasp-host plant association.  Evolution 55(12):2503–2522.

Copyright © Ted C. MacRae 2011

Guest Blogger: Dogbane for Dinner

Our guest blogger for today is Anne McCormack. I have known Anne (or known of her) for more than 25 years now, first as a long-time editor of Nature Notes, the journal of the Webster Groves Nature Study Society, and more recently on a personal basis as I, myself, have followed in her editorial footsteps. Anne is an astute naturalist whose breadth of knowledge spans not only botany but also entomology and ornithology, all of which she write about in her own blog at Gardening with Binoculars.


I planted Common Dogbane (Apocynum cannibinum) because some of my butterfly-watching friends reported numbers of juniper hairstreak butterflies on the patch of dogbane at Powder Valley Nature Center in Kirkwood. I assumed incorrectly that dogbane was a host plant for hairstreaks, and believing it to be little more than caterpillar food, I placed it in a hot, dry, narrow strip along the driveway. Ragged, caterpillar-chewed leaves wouldn’t be noticed there, and I forgot about it. After a few seasons, it was still a modest-sized clump, but the leaves were in great shape. In fact, it had grown into an attractive bush of airy, elegant lime-green foliage, wine-red stems, and tiny white flowers. It’s quite a contrast to its relative, Common Milkweed, growing next to it, which looks as if it were designed by Dr. Seuss—even before it gets chewed to bits. At this point I decided it was time to look it up and see why it had failed to support hordes of munching caterpillars. As you have already guessed, gentle reader, the Juniper Hairstreak’s host plant is juniper, not dogbane, but good old Common Dogbane is a great nectar plant. Now that Dogbane and I understand each other better, I can appreciate the amount of traffic its tiny white blooms bring in, like this Peck’s Skipper butterfly. Ants, butterflies, tiny native bees, honeybees, and this mason wasp are busy there all day long.

Along with several species of moth, it is the host plant for the Dogbane Beetle, which spends its larval stage devouring the roots and its adulthood dining on the leaves of Dogbane, and nothing but Dogbane. Dogbane Beetle can be confused with Japanese Beetle by beginners like myself, but unlike its fellow Coleopteran, Dogbane Beetle is harmless. That makes its iridescence all the more gorgeous, as shown in this wonderful photo by Courtnay Janiak. It’s a native insect that has shared a long evolutionary history with this under-appreciated native plant. American Indians valued it for its bark, which is tough but peels off in long strips. They plaited it for bowstrings and anything that called for twine; hence, its other common name, Indian Hemp. Don and Lillian Stokes, in their 2002 PBS show about bird watching, demonstrated how birds seek out the dry stems of this perennial, pulling off strips for nests in early spring. Nesting material can be hard to come by for birds in the tidy suburbs, so I don’t clean up the stems after frost. “Bane” in the name refers to the toxin cymarin in the plant’s leaves, though the plant would have to be covered in braunschweiger before my dog would be interested. Edgar Denison, in Missouri Wildflowers, translates the genus name Apocynum as “away dog.” The species name cannibinum refers to hemp. Its seedpods remind me of French green beans. These split at the end of the season, and the seeds fly away on fibers similar to milkweed seeds. Collect some and try this plant in your butterfly or native plant garden. Give it a spot where it’s easy to watch the colorful visitors.

Dogbane beetle (Chrysochus auratus) - Copyright © Courtnay Janiak

Copyright © Anne McCormack 2010

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Pseudomethoca simillima – a model for Enoclerus ichneumoneus?

Pseudomethoca simillima (family Mutillidae) - the model?

Enoclerus ichneumoneus (family Cleridae) - the mimic?

Last week, I posted the above photograph of Enoclerus ichneumoneus (orange-banded checkered beetle) and mentioned its possibly mimetic appearance to velvet ants in the family Mutillidae (order Hymenoptera).  By some stroke of serendipity, I encountered a species of Mutillidae the very next day in Missouri’s southeastern lowlands that seems to be a good candidate for one of, if not the, model species that E. ichneumoneus might have evolved to resemble.  Several individuals were encountered as they zigzagged urgently on dry sand deposits along the Mississippi River (where I had hoped, unsuccessfully, to find another locality for our intergrade population of Cicindela scutellaris).  Comparison of the individual in the photo with specimens in my collection (all identified by mutillid expert Kevin Williams, Utah State University) suggests this is Pseudomethoca simillima, and the photo is also a good match with other photographs of the species at BugGuide.  One thing that bothers me with the idea of this being a model for E. ichneumoneus is that I have not seen P. methoca commonly in Missouri (I have only three specimens in my collection), while E. ichneumoneus is one of our most common clerids.  There is another mutillid species in Missouri – Dasymutilla quadriquttata – that also seems to have potential as a model for E. ichneumoneus and that I have encountered much more commonly in the state.  However, D. quadriguttata is somewhat larger than E. ichneumoneus.  At any rate, other than the statement by Mawdsley (1994) that E. ichneumoneus seems to mimic mutillids, I can’t find that any more specific information has been recorded about the possible model(s) for that species.

As a caveat, I shall add that this mutillid was the… most… uncooperative… insect… that I have ever tried to photograph!  They really never stop moving, so you have to track the moving insect through the lens and fire shots when you think you’ve got it centered and focused.  Most of the time you don’t!  Using the Canon 1-5X macro lens for this did not make things any easier.  I tracked this female for quite a while and fired off a number of shots, only to get this one that I thought was fairly decent (and still just missed the focus on the near side of the pronotum).

Speaking of mutillids, I simply must photograph my specimen of Dasymutilla gloriosa (sometimes called the thistledown velvet ant) – you will not believe it!

Photo Details:
Pseudomethoca simillima: Canon MP-E 65 mm 1-5X macro lens on Canon 50D, ISO 100, 1/250 sec, f/14, MT-24EX flash 1/8 power w/ Sto-Fen diffusers. Minimal cropping and post-processing.
Enoclerus ichneumoneus: Canon 100mm macro lens on Canon 50D, ISO 100, 1/250 sec, f/14, MT-24EX flash 1/4 power w/ Sto-Fen diffusers. Minimal cropping and post-processing.

REFERENCE:

Mawdsley, J. R. 1994. Mimicry in Cleridae (Coleoptera).  The Coleopterists Bulletin 48(2):115-125.

Copyright © Ted C. MacRae

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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

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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.