Coral Pink Sand Dunes tiger beetle on ARKive

I’ve been meaning to write about ARKive for awhile now. ARKive is a unique collection of videos, images and fact-files assembled from among the world’s very best wildlife videographers and photographers in an attempt to create a centralized digital library of life on Earth. Their short to mid-term priority is the completion of audio-visual profiles for the 16,300-plus species on The IUCN Red List of Threatened Species, before moving on to profiling all species that have ever been filmed or photographed. With backing from many of the world’s leading conservation organizations, ARKive hopes to “promote public understanding and appreciation of the world’s biodiversity and the need for its conservation, through the power of wildlife imagery.”

With tiger beetle season almost now upon us, it seems appropriate to highlight the media collection that ARKive has assembled for one of North America’s most spectacularly beautiful and critically imperiled tiger beetles, Cicindela albissima (Coral Pink Sand Dune tiger beetle). This amazing species is not only stunning in appearance, with its nearly pure white elytra, but has perhaps the most restricted habitat of any tiger beetle species in North America – the entire population being restricted to 400 hectares within coral-pink-sand-dunes_3Utah’s Coral Pink Sand Dunes State Park and the adjacent Bureau of Land Management (BLM) dune management area (Pearson et al. 2006). The Google screen shot at right shows the entire range of this species as a light pink swath (inset shown on larger map of the state of Utah).  Regarded initially as a subspecies of the widespread C. limbata (sandy tiger beetle), recent molecular studies showed this beetle to be only distantly related to that species and, thus, deserving of full species status (Morgan et al. 2000).

Unfortunately, the beetle’s highly restricted habitat continues to be adversely affected by ongoing, recreational off-road vehicle use, especially in the interdunal swales used by the larvae. Impacts occur not only by direct run-over mortality, but also through disruption of normal adult and larval activity, damage to vegetation, reduction of arthropod prey of C. albissima, and mixing of the upper soil layer which increases desiccation of the larval microhabitat (Knisley and Hill 2001). The species was nominated for federal protection under the Endangered Species Act in 1996 (when it was still considered a subspecies of C. limbata), and two years later a Conservation Agreement between BLM, U.S. Fish and Wildlife Service, Utah Department of Parks and Recreation and Kane County was established in an effort to protect the critically sensitive habitats in which this species lives. Despite these conservation measures, ongoing monitoring and research within the protected areas has documented a continuing decline in the population, suggesting that these areas may not be of sufficient size to enable the population to increase, and off-road vehicle use continues outside of the protected areas (U.S. Department of Interior, Fish and Wildlife Service (FWS) 2008). While still only a candidate for federal listing as an endangered or threatened species, the FWS now considers the magnitude of the threat from off-road vehicles, in view of these recent findings, to be high and imminent. As a result, the FWS has increased the priority of the species’ candidacy from 8 to 2 (1 being the highest priority a candidate species can receive).

While I would dearly have loved to embed one of ARKive’s extraordinary videos or photographs of C. albissima within this post, copyright considerations do not allow that.  What I can do is provide hyperlinks directly to the site, and I encourage everyone to visit ARKive and see their images of this gorgeous species.

Photos by Christine Breton: adult beetle, dorsal view, adult beetle, adults mating, habitat

Videos by Ganglion Films: overview, adults mating, adult burrowing in sand, OHVs threatening protected habit.

In addition to the ARKive images, Chris Wirth, author of the blog Cicindela, has taken photographs of this species and presents stunning examples of both the larva and the adult in his post Cicindela albissima (Re-post). I myself am making plans to visit Coral Pink Sand Dunes – perhaps this season – to find and photograph this species for myself. When I succeed, rest assured those photographs will appear on this site.

REFERENCES:

Knisley, C. B., and J. M. Hill. 2001. Biology and conservation of the Coral Pink Sand Dunes tiger beetle, Cicindela limbata albissima Rumpp. Unpublished report.

Morgan, M., C. B. Knisley and A. Vogler. 2000. New taxonomic status of the endangered tiger beetle Cicindela limbata albissima (Coleoptera: Cicindelidae): evidence from mtDNA. Annals of the Entomological Society of America 93(5):1108-1115.

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

U.S. Department of Interior, Fish and Wildlife Service. 2008. 50 CFR Part 17. Endangered and threatened wildlife and plants; review of native species that are candidates for listing as endangered or threatened; annual notice of findings on resubmitted petitions; annual description of progress on listing actions; proposed rule. Federal Register 73(238) (December 10, 2008):75176-75244.

Copyright © Ted C. MacRae 2009

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

Tiger Beetle Safari

In looking back at my posts over the past few weeks, I realized that it has been far too long since I’ve actually talked about beetles.  Perhaps “Petals In The Bush” would be a better name for this blog!  I still have some botanical thoughts to get off my chest before the insect season starts in earnest, but until then, and in anticipation of the upcoming summer’s hunts, I offer this fun, light-hearted introduction to collecting and keeping tiger beetles by Peter Schriemer.  Pay particular attention to the method he uses to capture these elusive little creatures:

Tiger Beetles are my favorite type of beetle! Entomologist John Acorn got me hooked on these little guys. They live across the country in various habitats, so you may not need to travel far to go on a Tiger Beetle Safari of your own!

Vodpod videos no longer available.

more about “Tiger Beetle Safari“, posted with vodpod

Capturing tiger beetle adults can a little (lot) more difficult than implied by this video. Adults have excellent eyesight, and many species are extremely wary. It takes practice, patience, and lots of second chances. The collecting method shown in the video is what I refer to as the “stalk and slap” method – the beetle is slowly stalked until within net reach, and the net bag is slapped over the beetle.  This method works well enough, but it has its limitations.  If there are any gaps between the ground and the net rim, the beetle will quickly dart through them and fly away.  This is easy to prevent on sandy and soft clay substrates, as the net rim can be sealed against the ground by kneeling quickly on each side of the rim to embed it slightly and using the hands to hold up the net bag and locate the beetle.  Still, there are a few things I don’t like about this method – the beetle may hide against the inside of the rim and be difficult to locate, and once found it may be difficult to grab the beetle through the net if it is against the ground (don’t even try lifting the rim and reaching under – the beetle will zip out and be gone).  This method can also be taxing on the legs, as each attempted capture involves kneeling and standing back up (getting harder and harder for these 50+ year old knees to do).

The major limitation of the slap method, however, is that it doesn’t really work on hard, uneven surfaces. Many species are found in glades and other habitats with exposed rock substrates. In these types of habitats, the net rim simply cannot be clamped tightly enough to eliminate the gaps (not to mention the added difficulties in kneeling on these surfaces).  Because of this, I have adopted a technique that I call the “tap and swipe” method.  Here again, the beetle is stalked until within net reach (made easier with a longer handle), but rather than slapping the net bag over the beetle, the rim of the net is tapped against the ground next to the beetle and then assertively swiped sideways to catch the beetle just as it starts flying.  A quick 180° flip of the net rim closes the opening to prevent the beetle from escaping, and it is easily seen in the hanging net bag, where it can be grabbed from outside the net bag with one hand to secure it before reaching into the net bag with the other hand.  With a little practice, one eventually learns to reach down into the open net bag and grab the beetle while preventing it from flying up and out.  All of this can be done while standing, so it’s easier on the knees.

The tap method does require more knowledge about the beetle’s escape behavior in order to anticipate how quickly and in which direction the beetle will fly – some species delay take off just slightly, thus requiring a slight “pause” between the tap and the swipe. However, once their behavior is learned I have found this method to be more consistently successful than the slap method – even on soft substrates.  For species that I haven’t encountered in the field before, I use the slap method at first (if I can) until I have a feel for their escape behavior. If I can’t, I use the tap method and hope for the best!

Copyright © Ted C. MacRae 2009

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

Ship-timber beetle

Atractocerus brevicornis

One of the more unusual, and enigmatic, beetles that I encountered in South Africa was this beetle in the pantropical genus Atractocerus.  Placed in the family Lymexylidae (ship-timber beetles), species in this genus look less like beetles than they do large flying ants or strange damselflies due to their highly reduced elytra that expose their greatly elongated abdomen and leave the hind wings uncovered.  The hind wings also are unusual in that they are held fan-like in repose rather than folded as in most other beetles.  Atractocerus brevicornis is the only species in the genus found in Africa (Scholtz & Holm 1985).

Adults are attracted to light at night, as was this individual that came to our ultraviolet light at Geelhoutbos farm below the Waterberg Range in Limpopo Province. Nothing is known about the biology of Atractocerus, but larvae of other genera are reported to bore into hardwoods and palm stems (Picker et al. 2002). Larvae of the genera Lymexylon and Melittomma are believed to form symbiotic associations with ambrosia fungi that grow on the walls of their galleries (Young, 2002).  Adult females deposit fungal spores in a sticky matrix when they lay their eggs, and the hatching larvae carry the spores into wood on their bodies.  The large eyes of Atractocerus, however, suggest a predatory lifestyle. The common name of the family originates from a northern European species that has in the past been a destructive pest of ship timbers.

Atractocerus species are rarely encountered and therefore, not well studied. Their evolutionary history is still unknown; however, the oldest known lymexylid fossil is a very primitive member of the genus Atractocerus preserved in 100 myo Burmese amber (Grimwold & Engel 2005). Thus, the lineage containing these beetles had already appeared by the mid-Cretaceous and may have originated as early as the Jurassic, a fact that has earned them the moniker “living fossils.” These beetles were once thought to be among the most primitive of all Coleoptera – their simple wing venation, almost undifferentiated antennae and tarsi, and naked abdomen being likened to a supposed neuropteran common ancestor. Most authors now consider the family to be most closely related to the cucujiform groups Cleroidea and Cucujoidea (Wheeler 1986, Young 2002), although some have placed it in the Elateriformia near the Lampyridae based on wing venation. Scholtz and Holm (1985) accepted a cucujiform placement but related the group to the Styopidae (twisted-winged parasites), apparently due to the similarity of their highly reduced forwings.  At the same time, they acknowledged the many morphological and behavioral differences between the two groups, the latter itself being the subject of much evolutionary debate due to disagreement about whether the reduced forwings of male stylopids are truly homologous to the elytra of Coleoptera (some have even suggested homology with the halteres of Diptera that were switched from the metathorax to the mesothorax as a result of homeotic mutation). Most authors now place this latter group in the separate order Strepsiptera.

REFERENCES:

Grimaldi, D. and M. S. Engel. 2005. Evolution of the Insects. Cambridge University Press, New York, xv + 755 pp.

Picker, M., C. Griffiths and A. Weaving. 2002. Field Guide to Insects of South Africa. Struik Publishers, Cape Town, 444 pp.

Scholtz, C. H. and E. Holm (eds.). 1985. Insects of Southern Africa. Butterworths, Durbin, South Africa, 502 pp.

Wheeler, Q. D. 1986. Revision of the genera of Lymexylidae (Coleoptera: Cucujiformia). Bulletin of the American Museum of Natural History 183:113-210.

Young, D. K.  2002. 71. Lymexylidae Fleming 1821, pp. 261-262.  In: R. H. Arnett and M. C. Thomas [eds.], American Beetles, Volume 2, Polyphaga: Scarabaeoidea Through Curculionoidea, CRC Press, Boca Raton,880 pp.

Copyright © Ted C. MacRae 2009

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

Sanctuary for the Betulaceae

Nestled on the eastern side of the St. Francois Mountains, where the craggy exposures of the Ozarks most ancient rocks begin to subside underneath the Cambrian sandstones laid down over them, lies Hawn State Park – considered by many to be the loveliest of Missouri’s state parks. I have written previously about Hawn – in fact, it was the subject of my very first post on this blog. I have long treasured Hawn for its excellent insect collecting, diversity of plants and habitats, and unbridled beauty. I have hiked the incomparable Pickle Creek and Whispering Pine Trails many times – far more than any other trail in the state, and each time I fall more deeply in love with what, to me, represents the essence of the Missouri Ozarks in their most pristine state.

Lamotte sandstone cutThe charm of Hawn results from a unique combination of geological features. The Lamotte sandstone outcrops that dominate Hawn’s landscape are the oldest sedimentary rocks in the state, formed from coarse sand deposits that were laid down over the Precambrian rhyolites and granites that form the core of the St. Francois Mountains. These sand deposits were themselves buried under limestone and dolomite layers formed at the bottom of vast seas that later covered much of the interior of the continent. Subsequent periods of uplift and erosion once again exposed these sandstones, whose unique ability to hold groundwater has resulted in the formation of spring-fed streams that have cut deep into their soft layers to create canyon-rimmed valleys with tall vertical cliffs. rhyolite shut-ins One of these streams is Pickle Creek, which is fed throughout the year by Pickle Spring and has in some places cut all the way down to the underlying igneous rock to form “shut-ins.” In contrast to the slow, sandy bottomed stretches where Pickle Creek is still cutting through sandstones, the water in these igneous shut-ins rushes through narrow openings in the highly resistant rock. The igneous and sandstone exposures found in Hawn are spectacularly beautiful and support a unique flora due to the acid soils they produce. One group of plants that have taken sanctuary in these moist, acid soils is the Betulaceae, or birch family. Missouri is home to five native species of Betulaceae¹, and while none of them are extraordinarily uncommon they are limited in their occurrence to natural communities with sufficient moisture and exhibit a clear preference for acidic soils. This confluence of conditions occurs perfectly along Pickle Creek, allowing all five native species to grow here side-by-side – a betulaceous “hot spot” that represents not only the full diversity of the family in Missouri, but also the total generic diversity of the family in North America. In fact, only one other genus (Ostryopsis, shrubs related to Corylus and restricted to China) is assigned to the family on a global basis (Furlow 2004).

¹ Dr. George Yatskievych, in his recently published Steyermark’s Flora of Missouri (2006), regarded the presence of Corylus cornuta in Missouri as unlikely despite earlier reports of such. Dr. Yatskievych also recorded a single escape of the European species Alnus glutinosa from Springfield, Missouri.

The Betulaceae are deciduous trees and shrubs that occur primarily in the boreal and cool temperate zones of the Northern Hemisphere, although outposts are also known from high elevations in the Neotropics and, as mentioned above, China. Fossils of this ancient lineage of flowering plants are traceable to the late Mesozoic (upper Cretaceous), and the family appears to form a clade with hamamelidaceous plants. As would be expected from a group with boreal affinities, most species exhibit adaptations for survival in cold climates, such as small stature, shrubby growth habits, and small leaves. Several of Missouri’s species have performed well and gained acceptance as ornamental trees and shrubs, while others are important as sources of hazelnuts (genus Corylus) or ecologically for their ability to fix nitrogen (genus Alnus). My interest in these plants has nothing to do with their economic importance, but rather in their role as host plants for several rarely encountered species of woodboring beetles. Often, insects in this group may be collected on foliage of their hosts during the summer, making host identification fairly easy due to the presence of leaves. This is not always possible, however, due to limited periods of adult activity or low population densities. Rearing these insects from their hosts provides additional opportunity to document their occurrence, and winter is often the best time to collect the dead branches in which they breed, since by that time they have nearly completed their development and will be ready to emerge as soon as temperatures rise during spring. Identifying woody plants without foliage can be a challenge, but the ability to distinguish host plants by non-foliage characters such as bark, growth habit, bud shape, etc. greatly facilitates studies of wood boring beetles through rearing. In the past I have relied heavily on Cliburn and Klomps’ (1980), A Key to Missouri Trees in Winter, which utilizes mostly details of the twigs and buds to discriminate among Missouri’s 160+ species of trees. However, after a certain level of familiarity is gained, one eventually learns to recognize winter trees and even downed logs or fallen branches simply by their “look”.

Betula nigra - habit

Betula nigra - habit

Betula nigra - old bark

Betula nigra - old bark

Betula nigra - sapling

Betula nigra - sapling

Betula nigra (river birch) is the only member of this largely boreal genus found in the middle and southern latitudes of the U.S. and, thus, cannot be confused with any of Missouri’s other betulaceous species². It is the largest of the five and, along with the following species, is the most demanding in terms of keeping its “feet” wet. Trees are usually encountered right at the water’s edge, with tall, slender, often twisted or leaning trunks. Young trees and large branches on older trees exhibit gorgeous reddish brown bark peeling in thin, papery sheets, becoming thick and scaly on the main trunks of older trees. Small branches are dark, purplish brown in color with smooth bark and distinctly horizontal lenticels.  I have reared a small jewel beetle from fallen, dead branches of this tree collected at several locations in Missouri – this beetle turned out to be new to science, which I described and named Agrilus betulanigrae in reference to its (then) only known host (MacRae 2003).  I have also reared tremendous series of another jewel beetle, Anthaxia cyanella, which at the time was not known to utilize this host and was considered uncommon.  As it turns out, Betula nigra is its preferred host, and the rearing of large series from many locations resulted in improved knowledge about color forms and variability in this species (MacRae & Nelson 2003).

² The widely planted but dreadfully non-adapted Betula pendula (European white birch) and B. papyrifera (paper birch) can be recognized by their distinctly white bark. These species are limited to urban landscapes where they rarely achieve significant stature before declining and eventually succumbing to insect pests such as Agrilus anxius (bronze birch borer). River birch provides an equally attractive and much more durable choice!

Alnus serrulata - habit

Alnus serrulata - habit

Alnus serrulata - sapling

Alnus serrulata - sapling

Alnus serrulata - old cones

Alnus serrulata - old cones

Alnus serrulata (common alder, hazel alder, smooth alder, tag alder…) also demands to be next to (or even in) the water.  Unlike B. nigra, however, this species rarely reaches true tree status, instead usually forming shrubby thickets along the water’s edge.  Saplings can resemble those of B. nigra due to their smooth brownish bark, but the latter is usually more purplish, and the lenticels of A. serrulata are not distinctly horizontal as in B. nigra. The large purple-red buds also differ from the small brown buds of B. nigra, and during winter A. serrulata is adorned with numerous staminate catkins.  The persistent woody cones also cannot be mistaken for those of any other species of Betulaceae in Missouri. Associated with this plant is the longhorned beetle, Saperda obliqua, which reaches its southwesternmost distributional limit in Missouri on the basis of a single specimen collected some 25 years ago right here along Pickle Creek and given to me by lepidopterist George Balogh. Numerous attempts to find this species here since then have not (yet!) been successful.

Carpinus caroliniana - habit

Carpinus caroliniana - habit

Carpinus caroliniana (blue beech, hornbeam, musclewood) is one of my favorite betulaceous species. The beautifully fluted trunks and smooth, light gray bark are remniscent of the limbs of a sinewy, muscular person – every time I see this tree I cannot resist the temptation to grab and stroke the hard limbs (should I be admitting this?). This character begins to show even in very young trees, making its identification during winter quite easy. These trees also like to be near water, but they are not so demanding to be right at the water’s edge as are the previous two species. They usually form small trees, often in clumps with multiple trunks.  There are some notable insect associations that I’ve found with this plant.  One is a small jewel beetle, Agrilus ohioensis, which I reared from dead branches of this plant collected along Pickle Creek (Nelson & MacRae 1990), and which after more than 20 years still remain the only known Missouri specimens of this species.  Another is the longhorned beetle, Trachysida mutabilis, a single adult of which I reared from a dead (almost rotting) branch of this plant collected not too far from Pickle Creek in Iron Co.  This beetle also is the only representative of its species known from Missouri (MacRae & Rice 2007).

Ostrya virginiana - habit

Ostrya virginiana - habit

Ostrya virginiana - trunk

Ostrya virginiana - trunk

Ostrya virginiana (hop hornbean, American hornbeam) has a form and growth habit very similar to C. caroliniana, but its leaves that persist through the winter make it instantly recognizable from afar.  In Missouri, this habit is most often seen with the oaks (Quercus spp.).  This species can be found even further away from the water than the previous species, and its small stature combines with the orangish, persistent leaves to form a distinctive understory layer during winter.  Also, in contrast to the smooth gray bark of Carpinus, this species exhibits scaly, light reddish brown to brownish gray bark.  I have succeeded in rearing one of the two known Missouri specimens of another jewel beetle, Agrilus champlaini, from O. virginiana collected along Pickle Creek (the other specimen was reared from wood collected at Graham Cave State Park, another site where sandstone bedrocks favor an O. virginiana understory).  Unlike most other jewel beetles, A. champlaini forms galls in small living branches of its host.  I have collected the distinctive swellings during winter on many occasions but managed to rear only these two individuals (plus one ichneumonid parasitoid).  I have also noted similar swellings on Carpinus but have not yet managed to definitely associated them with this beetle.

Corylus americana (hazelnut, American hazelnut) is the smallest of Missouri’s five betulaceous species, always forming shrubs, sometimes in thickets, and never assuming the form of a tree. Its staminate catkins present during winter immediately identify plants of this species as Betulaceae, but the small, globe-shaped buds are unlike the more pointed buds of Ostrya and the elongated, reddish buds of Alnus. This species is the least demanding in terms of being near water and can be found even in upland prairies and glades. I haven’t yet associated any woodboring beetles with this plant in Missouri, but there are several jewel beetles known from the eastern U.S. that utilize Corylus (Agrilus corylicola, A. fulgens, and A. pseudocoryli) and could occur in Missouri.

pine savanna - fire managementThe upland habitats at Hawn are of interest as well. Lamotte sandstones are the dominant bedrock, creating acid soils that support a canopy dominated by Missouri’s only native species of pine, Pinus echinata (shortleaf pine), several species of oak, and a diversity of acid-loving shrubs primarily in the family Ericaceae (including the stunningly beautiful Rhododendron prinophyllum, or wild azalea). Historically, so-called “pine savanna” was prevalent in this area, a natural community in which periodic fires maintained an open structure amongst the fire-adapted pines and allowed a diverse herbaceous layer beneath the open canopy. Much of Hawn has closed up after decades of fire suppression; trail through pine savannahowever, the Department of Natural Resources has implemented a rotational burn management regime to recreate pine savanna habitat within Hawn’s Whispering Pines Wild Area. Evidence of what appeared to be very recent burns could be seen at several places as I hiked along the Whispering Pines Trail, and while many visitors might have been alarmed at the apparent “damage” they were observing, my heart sang with the prospect of seeing mature pine savanna communities taking hold throughout my beloved Hawn. As I stood atop this ridge and looked back down from where I had come, I could almost see Henry Schoolcraft and Levi Pettibone in the distance on horseback, perhaps pausing to gaze at an elk.

REFERENCES:

Cliburn, J. and G. Klomps. 1980. A Key to Missouri Trees in Winter, 2nd edition. Missouri Department of Conservation, Jefferson City, 43 pp. (subsequently revised)

Furlow, J. J.  2004. Betulaceae in Flora of North America @ efloras.org. http://www.efloras.org/florataxon.aspx?flora_id=1&taxon_id=10101.

MacRae, T. C. 2003. Agrilus (s. str.) betulanigrae MacRae (Coleoptera: Buprestidae: Agrilini), a new species from North America, with comments on subgeneric placement and a key to the otiosus species-group in North America. Zootaxa 380:1–9.

MacRae, T. C., and G. H. Nelson. 2003. Distributional and biological notes on Buprestidae (Coleoptera) in North and Central America and the West Indies, with validation of one species. The Coleopterists Bulletin 57(1):57–70.

MacRae, T. C. and M. E. Rice. 2007. Distributional and biological observations on North American Cerambycidae (Coleoptera). The Coleopterists Bulletin 61(2):227–263.

Nelson, G. H. and T. C. MacRae. 1990. Additional notes on the biology and distribution of Buprestidae (Coleoptera) in North America, III. The Coleopterists Bulletin 44(3):349–354.

Yatskievych, G. 2006. Steyermark’s Flora of Missouri, Volume 2. The Missouri Botanical Garden Press, St. Louis, 1181 pp.

Copyright © Ted C. MacRae 2009

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

“Armoured tank beetle”

anomalipus-elaphus1

Photo details: Panasonic DMC-FX3 (macro setting w/ auto exposure, aperature, and focus), illumination by two 23w compact fluorescent light bulbs. Post processing details: Adobe PhotoShop Elements 6.0 to crop, adjust brightness and contrast, remove pinhead, erase background, and sharpen.

In my last post, I briefly mentioned a beast of a beetle that we had given the nickname “armoured tank beetle.” Using (Picker et al. 2002), I determined this beetle to represent the species, Anomalipus elephas (family Tenebrionidae) – whose actual common name of “large armoured darkling beetle” was amazingly close to our made-up common name (not to mention the appropriateness of its specific epithet) – and linked to an online photograph of the species. As it turns out, the genus Anomalipus is quite large, with 51 species distributed throughout eastern and southern Africa – 34 of which have been recorded from South Africa proper (Iwan 2002). I’ve learned better than to ascribe species names to specimens in diverse groups of which I am not an expert based on a photograph of a common species, so for now this specimen will have to be called Anomalipus sp. Endrödy-Younga and Tschinkel (1993) report that all species in this genus are heavily built with strong legs, with most species being restricted within their geographical range to dense bush-covered patches of woody savanna.

After I wrote that post, I got to looking at the larger of my two specimens and thought, “Gee, I bet I could get a nice shot of that thing.” After all, it measures an impressive 32 mm in length (that’s 1¼ inches, folks!). Here is the result, and I have to admit I’m quite pleased given my equipment limitations (I only wish I’d thought to brush him off a little bit). This really has to be the most beautiful “big, black, ugly beetle” I’ve ever seen. I recall when I was pinning these two specimens that the exoskeleton was so hard I literally had to use my scissors to hammer the pin to get it going into the specimens. I like “armoured tank beetle” better.

In unrelated news, there are a couple of Carnivals everyone should be aware of – I’m doing my part to get the word out:

Circle of the Spineless – Ed Baker over at Invertebrate Diaries is set to host the next issue on March 2, 2009. There’s your deadline!

Linneaus Legacy – The January issue, hosted at Greg Laden’s Blog, was a good one.  Seeds Aside is hosting the February edition and is hoping to post it later this week if he gets enough submissions!  Go to this post for details on where to submit your post (or those from other blogs you enjoy).  EDIT: Too late – edition #16 is now posted.

REFERENCES:

Endrödy-Younga, S. and W. Tschinkel. 1993. Estimation of population size and dispersal in Anomalipus mastodon Fåhraeus, 1870 (Coleoptera: Tenebrionidae: Platynotini). Annals of the Transvaal Museum 36(4):21-30.

Iwan, D. 2002. Catalogue of the World Platynotini (Coleoptera: Tenebrionidae). Genus 13(2):219-323.

Picker, M., C. Griffiths and A. Weaving. 2002. Field Guide to Insects of South Africa. Struik Publishers, Cape Town, 444 pp.

Copyright © Ted C. MacRae 2009

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

Tempting tok-tokkies

In the 19th and early 20th centuries, some of the America’s greatest entomologists were coleopterists.  Army surgeons John L. LeConte and his protégé George W. Horn, California’s Henry C. Fall, Col. Thomas L. Casey (much maligned for his mihi itch¹ affliction, although in recent years regaining due respect for his insight on generic relationships), and “the Professor” Josef N. Knull, just to name a few.  What did these fine men have in common?  They studied beetles – not just tiger beetles or jewel beetles, but the entire order!  The world was much smaller then, and new information was generated at a much more leisurely pace.  Today such an approach is impossible.  With 300,000 described species in the order (conservatively) and growing, today’s students of Coleoptera must narrow their focus in one way or another – either by concentrating on one family or ecological guild, or by restricting their studies to a small geographic region.  I’ve tried, more or less successfully, to follow suite – jewel beetles are my primary focus, and I restrict my work with the ecologically similar longhorned beetles only to North American species.  Well, and I’m also working on tiger beetles, but only in Missouri… although I have begun taking fall tiger beetle trips to neighboring states.  Hmm, on second thought, I guess I haven’t been that successful at focusing (sigh! – and a likely explanation for my perpetual backlog of specimens unprocessed and papers unwritten).

¹In taxonomy, a term usually cast towards those who have a combination of disregard for quality over quantity when describing new taxa and a demonstrably high ego (Evenhuis 2008).

Whatever focus I do manage, it all goes out the window when I have the chance to collect in another country – especially someplace as exotic as Africa.  This is not a huge problem, as I can at least stay pretty much focused on just beetles.  Moths and butterflies are pretty, but it just takes too much effort to keep each specimen in good shape.  Bees and wasps also capture my interest, but I never know for sure whether I’ll get stung, and the extra precautions required to avoid such possibility are enough to make me pass on them.  Orthopterans don’t generally excite me unless they’re big and gaudy – in which case just one or two for the collection is fine.   And flies? Well, they’re flies! About the only non-coleopterans that regularly distract me are treehoppers – running into a mess of them, with their bizarre, fantastical shapes will always stop me in my tracks.  Fortunately, they’re not so abundant that they are constantly grabbing my attention.

Beetles, though – that’s a different story.  While I can resist the temptation to collect many of the groups outside of my sphere of interest, there are others that are consistently too tempting for me to pass up.  One of these is the Tenebrionidae, or darkling beetles.  With some 20,000 described species worldwide, it is among the most speciose of beetle families (larger than my beloved Buprestidae), and this diversity combines with difficult taxonomy to make them truly challenging for even the most serious students of the family.  For hacks like me, they’re impossible.  Moreover, they’re not even especialy pretty – usually just black.  Why do I collect them? Mostly because of their (in many cases) large size, comically awkward shuffling gait, and often exaggerated surface sculpturing.  Especialy diverse in more xeric habitats, I’ve collected quite a few in my frequent trips through the southwestern U.S. and even managed to get many of them identified by tenebrionid icon Charles A. Triplehorn.  Southern Africa is a true center of diversity for this group, with some 3,500 species recorded from the area – nearly 20% of the global diversity!  A number of particularly large species that go by the common name “tok-tokkies” make their homes in the dry Namib desert and surrounding bushveld.  Along with dungers and chafers and tyrant ground beetles, tok-tokkies would prove to be one more distraction in my nevertheless successful quest for African jewel beetles.

Psammodes hirtipes

Psammodes hirtipes

“Tok-tokkie” refers not to a particular genus or tribe of tenebrionids, but rather a number of flightless species that have developed a unique “tapping” method of communication between males and females.  The name “tok-tokkie” is onomatopoeic, referring to the sound these beetles make when they tap their abdomen on the ground.  In the same way that fireflies have species-specific patterns of flashes, different species of tok-tokkies tap with differing frequencies.  The beetle makes the noise by raising its abdomen and then bringing it down on the surface of the ground several times in quick succession.  Males initiate the tapping and await a response from a receptive female.  Signals are exchanged back and forth until, eventually, the two locate each other and mate.  Females lay eggs in shallow excavations in the dry, sandy soil, and the larvae that hatch feed within the soil on the roots of small plants. The dry Namib Desert has some of the most astounding species of tok-tokkies. Some – called “fog tok-tokkies” – have developed specially modified grooves to trap moisture from fog banks rolling onto the Atlantic coast. Others drink by doing a “head-stand” to allow condensed dew to trickle down to their mouths. Heat avoidance is another challenge in the Namib. Some species extrude dots of white wax from small pores on their elytra in response to increasing sunlight intensity, eventually appearing white-spotted or striped. The wax reflects the sun’s rays and helps keep the beetle cool. Other species beats the heat by running – in fact, the fastest running beetle in the world is one of the Namib tok-tokkies (and not, as I would have suspected, a tiger beetle). Unlike its mostly clumsy brethren around the rest of the world, this beetle blasts across the scorching sand at lighting speeds. A related species boasts the longest relative leg length of any beetle in the world.

Psammodes virago

Psammodes virago

I knew none of this in 1999 when I was in South Africa’s Northern (now Limpopo) Province, and while the tok-tokkies we encountered in the bushveld habitat below the Waterberg Range were not quite as marvelous as those of the nearby Namib Desert, they were still irresistible to this indefatigable beetle collector. Not knowing their names, we came up with our own names for them based on their appearance. Psammodes hirtipes was “wrinkle butt” due to the numerous prominent tubercles at the sides and rear of its otherwise smooth elytra. Psammodes virago, was “helmet beetle” because of its smoothly domed “army helmet” shape. Our designation of “armoured tank beetle” for Anomalipus elephas (photo credit) was amazingly close to its actual common name of “large armoured darkling beetle” (Picker et al. (2002), as was “white legs” for Dichtha incantatoris (photo credit), which Picker et al. (2002) call the “white-legged tok-tokkie”. In all, I collected some dozen species of tenebrionids during my stay at Geelhoutbos farm. Most of the smaller ones are still unidentified, but hopefully someday they will prove useful to some tenebrionid specialist.

The online magazine Travel Africa offers an informative article about the Namib tok-tokkies and this humerous video from National Geographic:

Vodpod videos no longer available.

more about “Namib beetles – Travel Africa Magazine“, posted with vodpod

REFERENCES:

Evenhuis, N. L. 2008. The “Mihi itch”—a brief history. Zootaxa, 1890:59-68.

Picker, M., C. Griffiths and A. Weaving. 2002. Field Guide to Insects of South Africa. Struik Publishers, Cape Town, 444 pp.

Copyright © Ted C. MacRae 2009

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

Tragidion confusion

Back in October, I discussed a recent review of the cerambycid genus Tragidion, authored by Ian Swift and Ann Ray and published in the online journal Zootaxa.  These gorgeous beetles mimic the so-called “tarantula hawks” (a group of large, predatory wasps in the family Pompilidae) and have been difficult to identify due to poorly-defined species limits, wide range of geographic variation, unusually high sexual dimorphism, and apparent potential for hybridization in areas of geographic overlap. Swift and Ray (2008) recognized seven North American and four Mexican species, including two newly described species and another raised from synonymy. It was an excellent work that provided much needed clarity based on examination of types and included detailed descriptions and dorsal habitus photographs of all species and separate keys to males and females to facilitate their identification. Unfortunately, my summary caused some confusion regarding species that occur in the deserts of southern Arizona, southern New Mexico and western Texas. In this post, I’ll clarify that confusion and provide details for distinguishing these species.

Formerly, it was thought that two species of Tragidion inhabited this region, with populations exhibiting smooth elytra and breeding in dead stalks of Agave and Yucca (Agavaceae) representing T. armatum and those exhibiting ribbed elytra and breeding in dead branches of a variety of woody plants representing T. annulatum. This concept dates back to the landmark monograph of the Cerambycidae of North America by Linsley (1962). Swift and Ray (2008) noted that Linsley’s concept of T. annulatum was based on an erroneously labeled type specimen, and that true T. annulatum referred to populations in California and Baja California (for which other names – now suppressed – were being used). This left the AZ/NM/TX populations attributed to T. annulatum without a name. The previously suppressed name T. densiventre was found to refer to populations inhabiting lowland habitats and breeding in Prosopis and Acacia (Fabaceae), but those occurring in montane habitats and breeding in Quercus (Fagaceae) represented an as yet undescribed species, for which the name T. deceptum was given. I included Swift and Ray’s figure of T. deceptum in my post – but mistakenly included the male of T. densiventre alongside the female of T. deceptum!

This error may never had been noticed, had it not been for the discriminating eyes of BugGuide contributor, Margarethe Brummermann. Margarethe is currently collecting photographs for a field guide to Arizona beetles and had photographed a male and female of a “ribbed” species in Montosa Canyon. Using the illustration of T. deceptum” in my post, Margarethe concluded her specimens represented T. deceptum and asked me to confirm her ID. When I told her the specimens represented T. densiventre, her confusion was understandable (given that her male appeared identical to the T. deceptum” male in my post). Further query on her part prompted me to do a little digging, and I discovered my error. The figure in my post has since been corrected – both that figure and a figure from Swift and Ray (2008) showing the male and female of T. densiventre are included below, along with additional information to allow their identification.

tragidion_densiventre

Tragidion densiventre Casey, 1912

Tragidion densiventre was formerly synonymized under T. auripenne (a rare species known from the four corners region of northern Arizona, southern Utah, southwestern Colorado, and northwestern New Mexico). Males of T. densiventre can be distinguished by their longer antennae, tawny-tan elytra and distinctly red-brown head, legs, and scape, while females have shorter antennae and the elytra red-orange. Both males and females of this species are distinguished from T. deceptum by their five elytral costae that curve inward toward the suture and extend to near the elytral apices, as well as their relatively narrower basal black band. Females of this species may be further distinguished from T. deceptum by their all black (or nearly so) antennae. Tragidion densiventre is found predominantly in xeric lowland desert habitats in Arizona, New Mexico, and west Texas (as well as northern Mexico). Larvae have been recorded developing in dead Prosopis glandulosa and Acacia greggii, and adults have been observed aggregating on sap oozing from stems of Baccharis sarothroides (Asteraceae) and flowers of larval host plants. Although the biology of this species has not been described in detail, it is likely that the observations of Cope (1984) for T. auripenne refer to this species. This is the classic T.annulatum” commonly observed in the desert southwest.

Tragidion deceptum

Tragidion deceptum Swift & Ray, 2008

Tragidion deceptum superficially resembles T. densiventre due to its ribbed elytra; however, it is actually more closely related to the Mexican species T. carinatum. Like T. densiventre, the males exhibit longer antennae and tawny-tan elytra, while females have shorter antennae and orange-red elytra. However, the head, legs and scape of males are black, as in females of the species, rather than red-brown as in males of T. densiventre. Females exhibit distinctly annulated antennae, in contrast to the all black antennae of T. densiventre. Both males and females are distinguished from T. densiventre by the elytral costae – only four rather than five, not incurved towards the suture and extending only to the apical one-third of the elytra. In addition, the basal black band is very broad – exceeding the scutellum by 2 × its length. This species is similarly distributed across the desert southwest as T. densiventre but occurs in more montane habitats, where it breeds in recently dead branches of several species of Quercus. Like T. densiventre, adults are often found feeding and aggregating on Baccharis sarothroides, and in a few lower canyons bordering desert habitats in the Huachuca Mountains of southeastern Arizona this species and T. densiventre have been collected feeding alongside each other on the same Baccharis plants. Tragidion deceptum is one of several species in the genus (along with T. coquus in eastern North America) that have been collected using fermenting molasses traps (more on this in a future post).

REFERENCES:

Cope, J. 1986. Notes on the ecology of western Cerambycidae. The Coleopterists Bulletin, 38:27–36.

Linsley, E. G. 1962. The Cerambycidae of North America. Part III. Taxonomy and classification of the subfamily Cerambycinae, tribes Opsimini through Megaderini. University of California Publicatons in Entomology, 20:1-188, 56 figs.

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

Copyright © Ted C. MacRae 2009

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

Done with dung, meat please!

ResearchBlogging.orgNo feces for this species.” “Carnivorous dung beetle shuns dung and decapitates millipede.” “Little dung beetle is big chopper.” “Dung beetle mistakes millipede for dung.” These were some of the clever headlines that I had to compete with in coming up with my own opener for a remarkable beetle that titillated the science blogosphere last week. At the risk of being redundant, I’d like to revisit that beetle and offer a few (hopefully novel) thoughts of my own. I can say that I have a unique and special treat for those willing to read further.

First the background. Deltochilum valgum is a so-called “dung beetle” in the family Scarabaeidae that lives in the lowland rain forests of Peru. As suggested by its common name, it belongs to a group of beetles that are well known for their dung feeding habits. Over 5,000 species of dung beetles are known throughout the world, all of which carve out balls of dung and bury them as provisions for larval development – or so it was thought.  As reported by Trond Larsen of Princeton University and colleagues in Biology Letters, D. valgum has apparently abandoned its ancestral dung ball-rolling behavior in favor of a predatory lifestyle. Its prey – millipedes! Moreover, the species exhibits several distinct morphological traits that appear to have evolved as a direct result of their predatory behavior. Adult beetles were repeatedly observed killing and eating millipedes, and their disdain for dung was rather conclusively demonstrated by an exhaustive, year-long trapping program in which pit-traps were baited with a variety of bait types known to attract dung beetles (e.g., various kinds of dung, carrion, fungus and fruit) – and millipedes.  In all, over 100,000 dung beetles representing 132 species were trapped (what a nice collection!), 35 of which were found to scavenge on dead millipedes, but only five of these dared tackle live millipedes.  Of these, only D. valgum ignored all other foods – it only came to traps baited with live millipedes.

Larsen et al. determined that adults of D. valgum are opportunistic hunters and were much more likely to attack injured millipedes than healthy ones, even those weighing 14 times as much as the beetle.  Ball rolling behavior was never observed by D. valgum.  Most dung beetles have wide, shovel-shaped heads used to scoop and mold dung balls, but D. valgum has a much narrower head with sharp “teeth” on its clypeus (Fig. 1A vs. 1B).  The teeth apparently aid in killing the millipede by piercing the ventral surface behind the head and prying upwards (decapitating it), and the narrow, elongate head facilitates insertion into the millipede body for feeding.  Further, the hind tibia are elongate and curved, which are used to “grip” millipedes by holding them up against the dorsally reflexed pygidium (Fig. 1C vs. 1D).  This allows the beetle to drag its coiled up victim with one hind leg while walking forward on the other five (Fig. 1E).  Once killed, the beetles proceeded to break their prey into pieces and consume their meaty innards, leaving the disarticulated millipede exoskeletons licked clean (Fig. 1F).  One of these “attack” episodes was filmed (using infrared lighting so as not to affect their nocturnal behavior) and can be seen in this BBC News video.

Deltochilum valgum

Figure 1. (a) Dorsal view of D. valgum head. Sharp clypeal teeth and angled clypeus act as a lever to disarticulate millipede. Narrow, elongate head permits feeding inside millipede; (b) dorsal view of Deltochilum peruanum head, lacking characters described in (a), head used to mould dung balls; (c) lateral view of D. valgum pygidium and hind tibia. Dorsally reflexed pygidial lip is used to support millipede during transport. Elongate, strongly curved hind tibia is used to grip millipede. (d ) Lateral view of D. peruanum pygidium and hind tibia, lacking characters described in (c), hind tibia used for rolling dung balls. (e, f ). Predation strategy by D. valgum. (e) Dragging live, coiled millipede with one hind leg, walking forwards; ( f ) feeding on killed millipede with head inside
segments; disarticulated empty millipede pieces nearby.
Credit: Larsen et al. (2009).

Much has been made about this remarkable shift from coprophagy to predation, which Larsen et al. speculate was driven by competition for limited resources with the many other dung beetle species that occur in the Peruvian rainforests. In fact, adult dung beetles are known to feed on a variety of resources besides dung, as exemplified by the range of baits used in their survey. Thus, my first thought after reading the coverage was actually a question: “Has this species abandoned dung provisioning completely as a reproductive strategy?” Everything I had read focused exclusively (quite understandably) on the bizarre feeding habits of the adults, but there was no mention of what the species’ larval provisioning strategies were. Wanting more information about this, I contacted Trond Larsen, who graciously sent me a PDF of the paper. Unfortunately (though not a criticism of the paper), no further insight about this was found in the paper either. Indeed, in all of the observations recorded by Larsen et al., millipedes killed by D. valgum were consumed entirely by the adults, and no mention was made of how or whether millipedes were utilized for larval provisioning. I wondered if D. valgum had truly abandoned dung provisioning for larval development (a remarkable adaptive switch), or if in fact the species might still utilize the strategy for reproduction (perhaps having specialized on a dung type not included in their survey), while also exploiting millipede predation as adults for a nutritional advantage. I asked Trond about this, to which he replied with this juicy tidbit (I told you I had a special treat!):

Yes, I would very much like to know what the reproductive/nesting behavior of D. valgum is. My best guess is that they also use millipedes as a larval food source, but as you say, we haven’t observed that behavior yet. I have observed other generalist dung beetle species rolling balls out of dead millipedes, presumably to bury for the larvae, so I certainly think it would be an adequate food source. Many dung beetle species use carrion for their larvae.

I am quite confident that D. valgum does not use any kind of dung. I have sampled these dung beetle communities very thoroughly, with many dung types and other bait types, and also with passive flight intercept traps that catch all beetles. Every dung beetle species that feeds on dung is at least sometimes attracted to human dung (this is not the case in African savannahs though, but is in neotropical forests – that is a whole different story). There are still a small handful of species we catch in flight intercept traps that we don’t know what they eat, although some of these mysteries have recently been solved – many of them live in leaf-cutter ant nests for example.

While predation of millipedes by a dung beetle is itself a fascinating observation, demonstrating the abandonment of dung provisioning in favor of captured prey for larval development would be a truly remarkable example of an ecological transition to exploit a dramatically atypical niche. I hope Trond (or anybody for that matter) actually succeeds in observing millipede/prey utilization for larval provisioning by this species.

Many thanks to Trond Larsen for his delightful correspondence.

SOURCE:
Larsen, T. H., A. Lopera, A. Forsyth and F. Génier. 2009. From coprophagy to predation: a dung beetle that kills millipedes. Biology Letters DOI: 10.1098/rsbl.2008.0654.

Copyright © Ted C. MacRae 2009

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