“My favorite bettle”

Today’s essay is by guest blogger (and perhaps future entomologist), Madison MacRae. Currently a 3rd grade student at Pond Elementary School, Madison’s interests include ice skating, tetherball, basketball, piano, dancing, singing, and hiking/bug collecting with her dad. Next year they will be something else. Madison would like to be a grade school teacher when she grows up. She would also like to be a nurse… and a fire fighter… and a football player. This is Madison’s second guest contribution to Beetles In The Bush, the first appearing on February 6, 2008 where she discussed the job responsibilities of a professional entomologist. For today’s contribution, Madison will be discussing one of the insects she saw on a visit to Missouri’s sand prairies back in early September [Ed. note: the insect in question appears to be an intergrade population of Cicindela scutellaris, characterized by their green coloration (unicolor influence) with variable maculation (lecontei influence)]. The original article was submitted as school work (with no prompting or prior knowledge by her dad!) and is reprinted here by the kind permission of its author.

MacRae, M. I.  2008.  My favorite bettle.  Privately published, 1 p., 1 color pl.

“Dungers and Chafers – a Trip to South Africa”

Those of you who enjoy field trip accounts should check out the December 2008 issue of SCARABS. The lead article – authored by your’s truly – is a scarabcentric travelogue of an insect collecting trip I took to South Africa several years ago. Scarabs?!, you say? Well, even though I focus on bups, ‘bycids, and tigers (some would argue that actually demonstrates lack of focus), I never pass on the opportunity to collect “cool” insects of all types when traveling somewhere as “exotic” as Africa – and scarabs are definitely cool! Still, I did manage to sneak past the editors a few words and pictures about buprestids, one of the more impressive of which I offer here as further enticement. You can also read about heart attacks, flying Tonka trucks, and evil minions.

Photos: (above) me standing next to a termite mound near the Waterberg, Northern Province (photo by Chuck Bellamy); (left) Evides pubiventris (family Buprestidae, tribe Evidiini) suns itself on high terminal foliage of Lannea discolor (family Anacardiaceae), Waterberg, Northern Province.

Two new species of Agrilus from Mexico

ResearchBlogging.orgThe enormous, cosmopolitan genus Agrilus (family Buprestidae – commonly called jewel beetles or metallic woodboring beetles) contains nearly 4,000 described species (Bellamy 2008). With many more still awaiting description, it is perhaps the largest genus in the entire animal kingdom (Bellamy 2003). Agrilus species are primarily twig and branch borers, utilizing recently dead wood for larval development – although there are notable exceptions, e.g. Agrilus anxius (bronze birch borer), A. bilineatus (twolined chestnut borer), and A. planipennis (emerald ash borer), which attack the trunks of living trees and, thus, are of significant economic importance in forest and ornamental landscapes. Host specificity among Agrilus species ranges from highly monophagous – associated exclusively with a single plant species – to rather oliphagous – utilizing several, usually related, plant genera. Adults of Agrilus species are most often found on the foliage of their larval hosts and do not generally visit flowers, as is common in some other genera (e.g., Acmaeodera and Anthaxia). Interestingly, despite the diversity and worldwide distribution of the genus, no species of Agrilus are known to be associated with coniferous plants – a fact that has limited their expansion into the vast northern boreal forests.

Texas, Bexar Co., San Antonio, nr. Fort Sam Houston, em. 25.iv-14.v.1997 ex Phoradendron tomentosum coll. ii.1997, D. Heffern & D. W. SundbergAs can be imagined by its enormity, a comprehensive understanding of the genus will remain a distant goal for many years. Progress will come incrementally, as formal descriptions of new species gradually improve our knowledge of the fauna that exists in each of the world’s main biogeographic provinces. In a recent issue of the online journal Zootaxa, Dr. Henry Hespenheide (UCLA) describes two new species of Agrilus from Mexico. These two species are interesting because of their association with ‘mistletoe’ plants in the genus Phoradendron (family Viscaceae1), obligate hemiparasites that attach to branches and stems of various woody trees and shrubs in tropical and warm temperate regions of the New World. Plants in this genus are known to support a variety of host-restricted insect herbivores, principally in the orders Hemiptera, Coleoptera and Lepidoptera. A single buprestid species has been associated with Phoradendron to this point – Agrilus turnbowi, recently described from specimens reared from dead stems of Phoradendron tomentosum attached to mesquite (Prosopis glandulosa) in southern Texas (Nelson 1990) and pictured here from a specimen in my collection that was reared from dead mistletoe collected at the type locality. At the time of its description, this species was not relatable to any of the other known species in the genus.

1 The Angiosperm Phylogeny Group (2003) includes the Viscaceae in a broader circumscription of the family Santalaceae. However, recent molecular studies suggest the Santalaceae are polyphyletic, with strong support for Viscaceae as a distinct, monophyletic clade (Der & Nickrent 2008).

The two new Mexican species – A. andersoni from Guerrero and Puebla (Figs. 1-3), and A. howdenorum from Oaxaca (Figs. 4-6) – are apparently related to A. turnbowi, which they resemble by their purplish-red coloration and complex pattern of golden setae on the elytra. They are also superficially very similar to each other but differ most notably in size and the overall color and pattern of setae on the elytra.

Figures 1–3. Agrilus andersoni Hespenheide: 1. dorsal habitus; 2. lateral habitus (scale bar indicates 2.0 mm); 3. genitalia of male (scale bar indicates 0.5 mm) (from Hespenheide 2008).

Figures 4–6. Agrilus howdenorum Hespenheide: 4. dorsal habitus; 5. lateral habitus (scale bar indicates 2.0 mm); 6. genitalia of male (scale bar indicates 0.5 mm) (from Hespenheide 2008).

Hespenheide speculates that the color and pattern of the golden setae on the elytra may serve to make the beetles less conspicuous by disruptive coloration, noting the similar coloration of the setae to the leaves of Phoradendron as seen in the photograph of Agrilus howdenorum on its host plant (Fig. 7). This form of crypsis may also be enhanced by the purplish-red ground coloration of the adult, which resembles that of the small, darkened blemishes often observed on the foliage of these plants.

Figure 7. Agrilus howdenorum adult on mistletoe host plant near Diaz Ordaz, Oaxaca, México. The golden setae on the elytra are similar in color to the leaves of the mistletoe and may function as a disruptive color pattern. Photograph by C.L. Bellamy (from Hespenheide 2008).

REFERENCES

Angiosperm Phylogeny Group. 2003. An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG II. Botanical Journal of the Linnean Society, 141: 399-436.

Bellamy, C. L. 2003. The stunning world of jewel beetles. Wings, Essays on Invertebrate Conservation, 26(2): 13-17.

Bellamy, C. L. 2008. A World Catalogue and Bibliography of the Jewel Beetles (Coleoptera: Buprestoidea), Volume 4: Agrilinae: Agrilina through Trachyini. Pensoft Series Faunistica No. 79, 722 pp.

Der, J. P. & D. L. Nickrent. 2008. A Molecular Phylogeny of Santalaceae (Santalales). Systematic Botany, 33(1):107-116.

Hespenheide, H. A. (2008). New Agrilus Curtis species from mistletoe in México (Coleoptera: Buprestidae) Zootaxa, 1879, 52-56

Nelson, G. H. 1990. A new species of Agrilus reared from mistletoe in Texas (Coleoptera: Buprestidae). The Coleopterists Bulletin, 44(3):374-376.

A new species of Xenorhipus from Baja California

ResearchBlogging.orgA few months ago I discussed Trichinorhipis knulli of the tribe Xenorhipidini (family Buprestidae). Members of this tribe exhibit highly sexually dimorphic antennae, with the distal segments of the male antennae highly modified into a very extended flabellate or lamellate condition. The surfaces of the flabellae/lamellae are covered with numerous, presumably olfactory sensillae that are lacking on female antennae (which retain the unmodified serrate condition), strongly suggesting a function involving detection of female sex pheromones. Although chemosensory structures are present on the antennae of nearly all buprestids, the extreme modification exhibited by the males of species in this tribe is not a common occurrence. Nevertheless, similar modifications have evolved independently in a few other genera within the family, including Knowltonia (four species in western North America), Mendizabalia and Australorhipis (monotypic genera in South America and Australia, respectively), and two species of the enormous Australian genus Castiarina. Indeed, males of Knowltonia and the two Castiarina species possess what might be termed ‘bipectinate’ or ‘biflabellate’ antennae due to dual projections from the terminal antennomeres (see Bellamy & Nylander 2007 for a more complete discussion of male antennal modifications in Buprestidae). The tribe Xenorhipidini is the most diverse group in which these modifications have arisen, comprised of the monotypic Trichinorhipis from California and the closely related Hesperorhipis (four species in Arizona and California) and Xenorhipis (until now, 14 species from North and South America and the West Indies).

Xenorhipis bajacalifornica Westcott, 2008 – holotype ♂ (1) & allotype ♀ (2).
Photos by Steve Valley (Oregon Department of Agriculture).

In a recent issue of the online journal Zootaxa, Rick Westcott (Oregon Department of Agriculture) describes a new species of Xenorhipis from the Cape Region of Baja California Sur, Mexico. Although assigned to the genus Xenorhipis, the new species – X. bajacalifornica – seems to bridge the gap between the genera Xenorhipis and Hesperorhipis. As currently recognized, Xenorhipis is distinguished from Hesperorhipis by the shape of the posterior coxal plates, which are scarcely narrowed laterally in the former genus, while in the latter genus they are triangular and with the hind margin strongly oblique. In X. bajacalifornica the posterior coxal plates are somewhat triangular but not as acute laterally as in some species of Hesperorhipis. Xenorhipis bajacalifornica also differs from other described Xenorhipis in its strongly abbreviated elytra, which in males barely reach the second ventrite – similar to species of Hesperorhipis. Other described Xenorhipis exhibit less abbreviated elytra, which cover at least the first three ventrites and in some species almost the entire abdomen. Despite these similarities to Hesperorhipis, a consistent distinguishing character between the two genera was found in the male antenna – in Xenorhipis the flabellar processes begin with the second antennomere, while in Hesperorhipis they begin with the third. It was on this basis that the new species was assigned to the genus Xenorhipis. (The genus Trichinorhipis differs from both Xenorhipis and Hesperorhipis by its rounded rather than quadrate pronotum and its unabbreviated elytra that cover the entire abdomen and has, as a result, been placed in its own subtribe.)

Xenorhipis brendeli ♂Xenorhipis brendeli ♀The photos left show the male (L) and female (R) of Xenorhipis brendeli, the only species in the tribe occurring in eastern North America (west to Minnesota and eastern Texas). Adults of this species are not commonly encountered and have been collected on a variety of deciduous hardwoods but reared almost exclusively from species of hickory (genus Carya). These individuals were reared from dead branches collected in southeastern Missouri – the male from pecan (Carya illinoensis) and the female from shellbark hickory (Carya laciniosa). The male exhibits the scarcely abbreviated elytra that cover almost the entire abdomen (as discussed above). Stan Wellso reported large numbers of males attracted to caged live females in Texas, apparently responding to sex pheromones released by the females.

Xenorhipis osborni ♀Xenorhipis osborni ♂This is another species in the genus – Xenorhipis osborni – known from west Texas. Joseph Knull described the species in 1936 from specimens collected in the Davis Mountains on whitethorn acacia (Acacia constricta), but larval hosts remained unknown until I reared a series of these specimens from dead branches of black acacia (Acacia rigidula) collected above the Pecos River in Val Verde County. I’ve also reared a few specimens from dead branches of catclaw acacia (Acacia greggii) collected in Big Bend National Park, and I wouldn’t be surprised if it breeds in other species of acacia. Again, in this speices the elytra are only slightly abbreviated, though more so than in Xenorhipis brendeli above and also more so in the male (L) than in the female (R). The male of this species is one of the prettiest I’ve encountered in the tribe.

Hesperorhipis albofasciatus ♂Hesperorhipis albofasciatus ♀The genus Hesperorhipis is illustrated here by these photos of H. albofasciatus. These specimens were reared by Rick Westcott from dead branches of walnut (Juglans sp.) – its only known host – collected in Tulare County, California. The elytra in this species are much more abbreviated than in Xenorhipis brendeli and X. osborni but similar to those of X. bajacalifornica – again with the male (L) exhiting greater abbreviation than the female (R). The three remaining species of Hesperorhipis exhibit even more highly abbreviated elytra than H. albofasciatus.

Dr. Charles Bellamy (California Department of Food and Agriculture) is currently revising the tribe. It will be interesting to see how, ulimately, he treats Xenorhipis and Hesperorhipis, given the blended characters exhibited by some species.

REFERENCE

Westcott, R. L. (2008). A new species of Xenorhipis LeConte and of Mastogenius Solier from Mexico, with a discussion of Chrysobothris ichthyomorpha Thomson and its allies and notes on other Mexican and Central American Buprestidae (Coleoptera) Zootaxa, 1929, 47-68

Cicindela scutellaris lecontei x scutellaris unicolor intergrades in southeast Missouri

An individual from Sand Prairie Conservation Area.  Note the uniform blue-gray coloration and complete lack of maculations, making this individual indistinguishable from true unicolor.Cicindela scutellaris (festive tiger beetle) is widely distributed in the U.S., having been recorded from most areas east of the Rocky Mountains except Appalachia, the lower Mississippi River delta, and south Florida. Within this range, the species occupies deep, dry sand habitats without standing water. It is often found in the company of Cicindela formosa (big sand tiger beetle), whose range largely coincides with that of C. scutellaris (except the southeastern Coastal Plain). More than any other North American Cicindela, populations of this species show extraordinary variability in color across its range of distribution. Seven geographically recognizable subspecies are generally accepted, with considerable variation evident within some of these and along zones of contact between them.

An individual from further south on the Sikeston Ridge (~20 mi S of Sand Prairie Conservation Area).  Note the generally blue-green coloration as in unicolor, but it also exhibits fairly well developed maculations and a suffusion of maroon color on the elytra - distinct influences from subspecies lecontei.The greatest portion of the species’ range is occupied by nominotypical populations in the Great Plains and subspecies lecontei in the Midwest and northeast. Similar to what I’ve noted in previous posts for other species, a broad zone of intergradation between these two subspecies occurs along the upper Missouri River. Other subspecies occupy more limited ranges along the upper Atlantic Coast (rugifrons), southeastern Coastal Plain (unicolor), eastern Texas and adjacent areas of northwestern Louisiana and southwestern Arkansas (rugata), and north-central Texas (flavoviridis), and the highly restricted and disjunct yampae is found only in a small area of northwestern Colorado. Populations in the upper Midwest and Canadian prairie are sometimes regarded as distinct from lecontei (designated as subspecies criddlei) due to their broadly coalesced marginal elyral maculations, and an apparently disjunct population of small, blue individuals in south Texas may also be regarded as subspecifically distinct.

Another individual from Sand Prairie Conservation Area.  It is similar to the unicolor-type individual in Photo 1 but also exhibits small maculations derived from its lecontei influence.Although Missouri lies well within the boundaries of its range, this species has been found in only three widely-separated parts of the state – near the Missouri River in the northwest part of the state, near the Mississippi River in the extreme northeast corner, and in the southeastern lowlands (formally known as the Mississippi River Alluvial Basin). The two northern Missouri populations are assignable to and typical of lecontei, with their uniform dull maroon to olive green coloration and continuous to near-continuous ivory-colored border around the outer edge of the elytra. Additional dry sand habitats occur along the lower Missouri River in central and east-central Missouri and along some of the larger rivers that drain the Ozark Highlands; however, this species has not been located in these habitats despite their apparent suitability and occurrence of C. formosa with which it frequently co-occurs. The reasons for this distributional gap between the northern and southern populations – some 400 miles in width – remain a mystery. The southeastern Missouri population is not clearly assignable to any subspecies, apparently representing an intergrade between lecontei to the north and unicolor to the south. Accordingly, individuals from this area are known by the unwieldy appellative “Cicindela scutellaris lecontei x scutellaris unicolor intergrade.” Pearson et al. (2005) states that intergrades between lecontei and unicolor are evident only in northern “Missouri” (an obvious error for Mississippi) and Tennessee. Thus, the existence of intergrades in southeastern Missouri suggests that the zone of intergradation extends further north than previously realized.

A second individual from ~20 mi S of Sand Prairie Conservation Area.  Similar to the individual in Photo 2 except with smaller maculations.  Note the gorgeous suffusion of maroon, especially on head and pronotum - a spectacular individual.Prior to this season, I had located two main population centers in the southeastern lowlands – one at Holly Ridge Conservation Area in Stoddard County, and another at Sand Pond Conservation Area in Ripley County. Holly Ridge is located on Crowley’s Ridge – an erosional remnant of Tertiary sand and aggregate sediments left behind by the late Pleistocene glacial meltwaters whose scouring action formed the surrounding lowlands, while the sandy sediments at Sand Pond were deposited west of Crowley’s Ridge along the southeastern escarpment of the Ozark Highlands during that same period. These erosional and depositional events created the deep, dry sand habitats that Cicindela scutellaris requires. I had known also about the Sikeston Sand Ridge further to the east – another erosional remnant of Tertiary sands deposited by the ancient Ohio River – but had not explored it closely until this season when I initiated my surveys at Sand Prairie Conservation Area. I expected Cicindela scutellaris might occur here, and in my first fall visit in early September I found two individuals in the sand barrens (alongside Cicindela formosa). Another individual was seen here in early October, but more robust populations were observed at a small, high-quality sand prairie remnant (last photo) further to the south along the Sikeston Ridge, and around eroded sand barrens behind private residences still further to the south. Clearly, the species is well-established in the southeastern lowlands wherever open dry sand habitats can be found.

Sand prairie habitat for Cicindela scutellaris in southeast Missouri.  Note the well-spaced clumps of grass, in this case splitbeard bluestem.The individuals shown here exemplify the range of variation exhibited by Cicindela scutellaris populations in southeast Missouri. They greatly resemble subspecies unicolor by their uniform shiny blue-green coloration. Indeed, the individual in the first photo might well be classified as such due to the complete absence of white maculations along the elytral border. Most individuals, however, show varying development of such maculations, ranging from small disconneted spots to the more developed apical “C”-shaped mark – clearly an influence from subspecies lecontei. Another apparent lecontei influence is the suffusion of wine-red or maroon coloration that can be seen on the head, pronotum, and elytra of the individuals in photos 2 and 4. These characters make this population divergent from the typically monochromic unicolor (as its name suggests). Because of their bright green coloration and white maculations, individuals in this population greatly resemble subspecies rugifrons, but that subspecies is limited to the northern Atlantic seaboard. They also resemble the common and widespread Cicindela sexguttata (six-spotted tiger beetle) but can be distinguished from that species by the more noticeably domed profile of the elytra, rounded rather than tapered elytral apex, and dark labrum of the female (both sexes of C. sexguttata have a white labrum).

There is one additional sand ridge in Missouri’s southeastern lowlands – the Malden Ridge. This sand ridge occurs south of Crowley’s Ridge and is much smaller than the Sikeston Ridge. No significant remnant habitats remain on the Malden Ridge, but it is possible that sufficient areas of open sand remain that might support populations of C. scutellaris. Determining whether this is true will require some time studying Google Earth and even more time on the ground to search them out. If they do exist, however, it will be interesting to see what level of influence by lecontei is exhibited in this most southerly of Missouri populations. Only spring will tell!

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.

New species and a review of the genus Tragidion

ResearchBlogging.orgSpecies of Tragidion are among the larger and more attractive cerambycids in North America, making them popular among collectors. Their bright orange and black coloration clearly functions in mimicking spider wasps (family Pompilidae) in the genera Pepsis and Hemipepsis – the so-called “tarantula hawks.” Unfortunately, species of Tragidion have been difficult to identify due to a high degree of morphological similarity between species, wide range of variation across geographic areas within species, unusually high sexual dimorphism and dichromatism, and apparent potential for hybridization in areas of geographic overlap. This has confounded efforts to delimit species boundaries, resulting in a confusing assortment of names whose proper application has eluded even the most esteemed of North America’s cerambycid taxonomists. Recently, some much needed clarity was provided by Ian Swift and Ann M. Ray in the journal Zootaxa. Their taxonomic review of Tragidion – the first systematic treatment of the entire genus – recognizes seven species in North America and another four restricted to Mexico. Two species – T. agave from California and Baja California and T. deceptum from montane areas of the southwestern U.S. and northern Mexico (both pictured) – are described as new, and a third – T. densiventre from desert areas of the southwestern U.S. and northern Mexico – is raised from synonymy under T. auripenne. Four new synonymies are also proposed, and dorsal habitus photographs and a key to all species are provided. Life history information is limited for most species of Tragidion. One species – T. coquus – occurs broadly across the eastern and central U.S., where it breeds in a variety of dead hardwoods, especially oak. Several species occur in the southwestern U.S. and northern Mexico – some are found in xeric lowland desert habitats, where they breed in dead branches of Prosopis glandulosa and Acacia greggii (T. densiventre) or dead flower stalks of Yucca and Agave (T. agave and T. armatum), while a fourth (T. deceptum) is found in more montane habitats mining the heartwood of recently dead branches of Quercus. Adults of another species in California and Baja California, T. annulatum, are strongly attracted to brushfires and burning vegetation, and individuals have been observed landing on still-burning and smoldering shrubs, causing their legs and abdomens to melt to the surface of the branches. At several post-burn sites, the melted bodies of this species were common on the charred branches of their hosts, and females have been observed ovipositing on woody shrubs that have been burned. This species likely plays an important role in the decomposition of burned woody material in coastal areas of California. The remaining U.S. species – T. auripenne – is known from only a handful of specimens collected in xeric habitats in the Four Corners region of the southwestern U.S. It’s life history, as well as those of the four strictly Mexican species, remains essentially unknown.

Tragidion agaveTragidion agave Swift & Ray 2008, ♂ & ♀ – California & Baja California. Tragidion deceptumTragidion deceptum Swift & Ray 2008, ♂ & ♀ – southwestern U.S. and northern Mexico.

REFERENCE: Swift, I., Ray, A. M. (2008). A review of the genus Tragidion Audinet-Serville, 1834 (Coleoptera: Cerambycidae: Cerambycinae: Trachyderini) Zootaxa, 1892, 1-25

It’s a girl!

I’ve been interested in collecting insects since I was 10 years old, and my current collection dates back to spring semester 1978 when, after finally declaring a major, I kicked off my life as an entomologist with Entomology 101. I did my graduate work on the now-defunct Homoptera (I just can’t call them hemipterans), using laboratory rearing to figure out life history details of several species of leafhoppers. Although my allegiance would soon switch to beetles (where it has remained ever since), my interest in rearing insects would persist. It wasn’t long before I began rearing wood boring beetles as a way of studying their distributions and host plant associations. I’ve reared beetles from literally hundreds of batches of wood – buprestids, cerambycids, bostrichids, clerids, ostomids, you name it – if it breeds in wood, I’ve reared it. Not to mention the parasitic hymenopterans and even predaceous asilids associated with them. Rearing has been part of my professional life as well. In the early part of my career in industry, I supervised an insectary that maintained laboratory colonies of nearly two dozen arthropod species to support research. We reared moths, beetles, flies, roaches, aphids – even mites and nematodes. However, despite having reared hundreds of species of insects, I had never reared a tiger beetle – until now!

This little gal – a gorgeous individual representing Cicindela limbalis (common claybank tiger beetle) – was waiting for me when I returned from my recent trip to western Nebraska and South Dakota. I had collected her as a 3rd instar larva from her burrow atop a steep clay bank in western Missouri, where my colleague and I were conducting our survey for Cicindela pruinina (now Dromochorus pruininus). I had entertained the hope that it might prove to be that species, but the abundance of larval burrows within this patch of habitat – where C. pruinina had not been seen – and the fact that they contained mostly 3rd instars suggested it would prove to be one of the spring-fall clay associated species. After fishing her from her burrow, I filled an empty Starbuck’s Frappucinno bottle (there is, apparently, only one place in the Ozarks where availability of good coffee obviates the need to resort to a cold, sugary, “coffee-flavored” drink in the morning) with native clay and dropped her in, where she immediately proceeded to dig a new burrow. She was thoughtful enough to dig her burrow right down along the glass so that I could keep an eye on her over the next several weeks, occasionally dropping in a fat fall armyworm larva and watching it meet its gruesome yet mercifully quick death. A few weeks before my trip, she sealed up her burrow and disappeared from view. Curious (and impatient), I emptied the soil from the bottle and found her down at the bottom, quiescent but apparently healthy. I put the soil back into the bottle and dropped her in, and she immediately dug a new burrow, sealed it up, and disappeared from view once again. My curiosity satisfied, I had an easier time leaving her alone after that, and when I returned from my trip, there she was.

Cicindela limbalis occurs throughout Missouri on eroded or sparsely vegetated clay soils, although it is less common in the southern Ozark Highlands – being largely replaced by Cicindela splendida (splendid tiger beetle). I’ve most often encountered C. limbalis on roadside embankments, along 2-tracks through open forest and woodland, and in glade habitats. This individual shows the greatly reduced elytral maculations that are typical of populations found throughout most of Missouri – only in the extreme northern tier of counties is the full pattern of maculation expressed (as exemplified by this individual from central Nebraska). At one time, this reduced maculation was the basis for recognition as a separate subspecies (C. limbalis transversa); however, no distinct geographical forms are currently recognized for this species (unusual in cicindelid taxonomy). Regardless of her taxonomic identity, I’m enjoying watching my new pet – she now occupies a larger, roomier terrarium filled with native clay, into which she has dug a burrow and spends most of her time sitting at its entrance. As she did when she was a 3rd instar, she enjoys a fat fall armyworm larva for lunch every few days. She will eventually take up permanent residence in a neat row inside a wooden, glass-topped box, but for now I’m going to do everything I can to delay that fate. Of all the many thousands of insects that I’ve reared over the years, she is my favorite.