A festive (tiger beetle) birthday

Last Thursday was my birthday, and as has become my custom, I took the day off and went on my ‘Annual Season Opening Birthday Bug Collecting Trip.’  One or two of you might remember how these plans were scrubbed last year by a last minute business trip, during which I discovered Pipestone National Monument in southwest Minnesota. That experience – and the post that I wrote about it – remain high among my all-time favorites. Despite that, nothing was going to derail my plans to go collecting this year, and at 5:30 in the morning I awoke to begin what would turn out to be as enjoyable and successful a day as I could hope for. I had convinced my colleagues and long-time collecting buddies Rich Thoma and Chris Brown to take the day off as well and accompany me down to the lowlands of southeastern Missouri to search for additional localities of the festive tiger beetle – Cicindela scutellaris.

Records of Cicindela scutellaris in southeast Missouri

Records of Cicindela scutellaris in southeast Missouri

As far as is currently known – C. scutellaris is represented in Missouri by three highly disjuct populations in the extreme northwestern, northeastern, and southeastern corners of the state.  The two northern populations are unambigously assignable to the northern subspecies lecontei, although their absence from areas further south in Missouri along the Missouri and Mississippi Rivers remains a mystery.  The southeastern population apparently represents an intergrade population with influences from both lecontei and the southeastern subspecies unicolor.  While this population was discovered many years ago (I first collected it in the mid-1980s), it remained known only from sand forests in Holly Ridge Conservation Area on Crowley’s Ridge.  A second population was discovered several years ago on sand exposures in the extreme western lowlands near the Ozark Escarpment when Chris Brown and I began our formal survey of tiger beetles in Missouri, and last year I succeeded in locating several populations of the beetle in the critically imperiled sand prairie relicts located along the spine of the Sikeston Sand Ridge.

cicindela_scutellaris_p1020910_2This year, we wanted to determine if intergrade populations also occurred on the Malden Sand Ridge – the southernmost expanse of sand exposures in the southeastern lowlands.  We didn’t know if they did – presettlement sand prairies were less abundant on the Malden Ridge due to its higher soil organic content.  As a result, no sand prairie relicts survived the Malden Ridge’s complete conversion to agriculture.  Undeterred, I got onto Google Maps and scoured satellite imagery of the ridge and located several spots that seemed to have potential – even though they were agricultural fields, they appeared to be of sufficient expanse and with enough sand to possibly support populations of the beetle.

So, on the morning of April 23, my ‘Annual Birthday Season Opening Bug Collecting Trip’ began by meeting up with Rich and Chris and driving the 223 miles from Wildwood to Kennett to explore several locations for a beetle based only on the suggestion of a flickering computer screen.  The first of these locations was a bust – there was a house constructed right in the middle of the site that wasn’t on the Google Map.  cicindela_scutellaris_p1020889_2Maybe the beetle occurred here and maybe it didn’t, but the last thing I wanted to do on a Thursday morning was interrupt a homeowner from their morning routine and ask them if we could collect bugs in their front yard.  Besides, there was another locality just a couple miles up the road that looked equally promising.  We found the spot and drove by slowly – it was an agricultural field that looked like it had been fallow for at least a short time, and although it did not look great (not as much sand as I had hoped) we eventually decided that since we were there we might as well take a look.  It wasn’t long before we saw an individual near the highest part of the field, and through a couple hours of exploring and digging adult burrows we had observed a limited number of adults.  Success!  The landowner happened by while we were there and graciously allowed us to continue our searches.  Through her, we learned that the field had been under soybean cultivation during the previous season.  This was good news to learn that beetles were inhabiting sand exposures on the Malden Ridge despite its complete conversion to agriculture.

Having confirmed the occurrence of C. scutellaris on the Malden Ridge, we then began driving to the next putative locality some miles north along the ridge.  Along the way, Chris spotted a rather large sand expanse in another agricultural field right next to the highway.  cicindela_scutellaris_p1020906_2Even though I hadn’t detected it in my Google Map search, it looked promising enough to explore, and so we did a quick U-turn and found a place to pull over.  This spot can only be described as the ‘festive tiger beetle motherlode’ of southeast Missouri!  Even though the field was obviously under active agricultural use, the beetles were abundant within the fairly large expanse of exposed sand within the field (photo below).  We were quickly able to collect a sufficient series to document the beetle’s range of variation and set about obtaining additional photographs.  I felt fortunate to be able to photograph this mating pair, which nicely illustrates the white labrum of the male (top) versus the dark labrum of the female (bottom) – one character that distinguishes this intergrade population from the similar-appearing six-spotted tiger beetle (C. sexguttata – commonly encountered along woodland trails throughout the eastern U.S., and with both sexes exhibiting a white labrum).  Note also how the male is holding his legs out horizontally (a behavior I’ve seen with other mating pairs) and the more heavily padded tarsi on his front legs. The latter specialization is thought to aid in grasping and holding the female (Pearson et al. 2006), although in this instance it clearly is not serving that function, but I have not yet determined for what purpose the horizontal posturing of the front legs is all about (perhaps it is related to alarm behavior).

cicindela_scutellaris_habitat_p1020899_2We completed the day by documenting the occurrence of this species on the third of only three sizeable sand prairie relicts that remain on the Sikeston Sand Ridge – a private parcel located a few miles south of the other two preserves.  These observations have increased our confidence that C. scutellaris is secure in Missouri’s southeastern lowlands, and that – thankfully – no special conservation measures will be required at this time to assure its continued existence.  We also now have enough material on hand to characterize the range of variation exhibited by individuals across this population.  We hope this will allow a greater understanding of the relative influence of lecontei populations to the north versus unicolor populations to the south in contributing to the makeup of this population.

Since it was my birthday, it was appropriate that I should discover this “gift” next to the rim of my net after I slapped it over a mating pair of beetles.  I haven’t found a large number of Native American artifacts during my time in the field, but this has to be most impressive of those that I have found – it is in almost perfect condition, with only the smallest of chips off of one of the lower corners.  Edit 5/5/09: After a little research, I believe this to be a spear point from the Archaic period (12,000 to 2,500 years ago).

arrowhead_p1020900_2

p.s. – my 100th post!

REFERENCE:

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.

Copyright © Ted C. MacRae 2009

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Bon appétit!

I collected this larva in northwest Nebraska during last year’s Fall Tiger Beetle Trip.  I collected an adult Cicindela lengi (blowout tiger beetle) at the spot – a species that greatly resembles but is much less common than the ubiquitous C. formosa (big sand tiger beetle – see my post Cicindela lengi vs. Cicindela formosa for a comparison of the two species).  Before finally finding that adult, however, I had fished out several larvae from the site in the hopes that they represented that uncommon species (see how I did this in my post Goin’ fishin’).  After collecting the larvae and placing them in a small terrarium with native sandy soil, they burrowed in but then closed up shop – I wasn’t sure whether they had survived or not.  In early December I put the terrarium in a 10°C incubator for the winter and brought it back out earlier this month.  Yesterday, happily, this larva and one other opened up their burrows again, so with any luck I’ll feed them well and they’ll complete their development.  While I do hope they represent C. lengi, other possibilities include C. scutellaris (festive tiger beetle), which would not be exciting, and C. nebraskana (prairie long-lipped tiger beetle), which would be VERY exciting.  One species I do not have to worry about it being is C. formosa, as the larvae of that species make very unique excavations in the sand with the burrow opening directed towards the excavation (I don’t believe I’ve posted photos of that here, yet – I’ll have to do so soon).

In the meantime, here is a closeup of the larva in the video prior to feeding. Those of you who have ever reared or photographed tiger beetle larvae will know just how easily “spooked” these larvae can be – any sudden movement will cause the larva to “drop” into its burrow and sit there for awhile. As a result, it was a real challenge to go through the whole process of taking first the photos and then the video while feeding it without causing it to drop.

cicindela_sp_larva_p1020936

Coming soon – lunchtime for adults!

Copyright © Ted C. MacRae 2009

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I Brake for Dung Beetles!

A few days ago I learned of a new campaign by The WILD Foundation called “Make a Big Impact with Small Change.” Founded in 1974, WILD seeks to protect intact wilderness areas and the wildlife and people who depend upon them. Their new campaign pays homage to dung beetles – usually overlooked by conservationists in favor of the so-called “charismatic megafauna,” but who nevertheless provide an important ecological service by tirelessly processing megafaunal dung. From the WILD website:

Here at The WILD Foundation, we realize that it is not just those large, charismatic animals that inspire conservation – it is often the small, typically unnoticed and vastly under-appreciated ones that inspire us the most….and that are an indispensible part of the ecosystem!

As a way of generating support for their work, WILD is giving away bumper stickers like the one pictured above. I have got to have one of these bumper stickers! It is the best entomology bumper sticker I’ve seen since “I fear no weevil!” The WILD website also features this amusing little video that shows some dung beetles in action:

Vodpod videos no longer available.

more about “I Brake for Dung Beetles!“, posted with vodpod

The website doesn’t provide any clues as to the species of dung beetle or where it was recorded, but judging by its large size I’m guessing that it might have been recorded in Africa, perhaps representing a species of the genus Scarabaeus.  My most memorable dung beetle experiences occurred in Africa, which is blessed with a dizzying diversity of “dungers.”  Following is an excerpt from an article I wrote that appeared in the December 2008 issue of the SCARABS Newsletter, in which I discussed some of these marvelous beetles:

Chafers were not the only scarabs I encountered in abundance at Borakalalo [National Park], and I’ll give you one guess as to what other scarab group I encountered in abundance at this mammal game reserve. That’s right, dung beetles. Never before have I seen such an abundance and diversity of dung beetles in one spot, but then again, never before have I seen such an abundance of dung!  The ground was littered with the stuff – antelope such as gemsbok  and impala, warthogs, giraffes, and a host of other mammals thrive in the protected confines of the park, and the seasonally dry climate allows their dung to dry quickly and accumulate rather than breaking down and disappearing. It did, however, take a few days before I became aware of the area’s dung beetle diversity. Prior to our arrival in the park, the weather had been dry for some time, and so it remained for the first few days we were there. I collected a smattering of different dung beetles during that time, but it seemed like they should be more abundant considering the abundance of available resource. Our third day in the park was interrupted by heavy thundershowers that moved through during the afternoon. The next morning, as we arose and begin wandering away from the camp, the air seemed literally abuzz with dung beetles. They were flying everywhere and crawling all over the ground, frantically rolling and fighting over the reconstituted pieces of dung. Big, black scarabaeines proper such as Kheper clericus (Boheman) and Scarabaeus galenus Westwood (Photo 4), the small metallic

scarabaeus-galenus_1

Photo 4: Scarabaeus galenus (Westwood).

Phalops ardea Klug, the attractive green iridescent species Garetta nitens (Olivier) and Gymnopleurus virens Erichson, their darkened relative Allogymnopleurus thalassinum (Klug) (Photo 5),
Photo 5: Allogymnopleurus thalassinum (Klug) individuals fighting over a mammal dung ball.

Photo 5: Allogymnopleurus thalassinum (Klug) individuals fighting over a mammal dung ball.

and the tiny little Sisyphus costatus (Thunberg),  standing tall on its elongated hind legs while pushing dung with its forward pairs of legs (opposite of what I’ve seen in any other dung beetle), all made their sudden appearance. I spent some time  watching one S. galenus individual excavating a burrow for the prized piece of poop it had snatched (Photo 6).
Photo 6: Scarabaeus galenus (Westwood) excavating a burrow.

Photo 6: Scarabaeus galenus (Westwood) excavating a burrow.

The most impressive dunger that I saw, however, was the enormous, flattened Pachylomera femoralis Kirby (Photo 7).
Photo 7: Pachylomera femorata Kirby.

Photo 7: Pachylomera femorata Kirby.

Looking like flying Tonka trucks and sounding like diesel engines from real trucks, their low-pitched, rumbling buzz filled the air as they searched among the freshly moistened turds. So loud was the noise caused by the beating of their wings that several times I ducked thinking one was about to collide with me. This sudden dunger super-diversity continued into the night, as Anachalcos convexus Boheman, Catharsius sp., Copris elphenor Klug, Metacatharsius sp., Pedaria sp., Scarabaeus goryi (Laporte), three species of Onitis, Caccobius ferrugineus (Fåhraeus), Digitonthophagus gazella (Fabricius), and nearly a dozen species of Onthophagus flew to our ultraviolet light-illuminated sheet.

REFERENCE:

MacRae, T. C. 2008. Dungers and chafers: A trip to South Africa. SCARABS 34:1-9.

Copyright © Ted C. MacRae 2009

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Coral Pink Sand Dunes tiger beetle – range map

Those of you on RSS feed might be interested in revisiting my previous post, Coral Pink Sand Dunes tiger beetle on ARKive.  I’ve added a Google screen shot to the post that shows a visual perspective of the entire range of Cicindela albissima within a tiny inset of the state of Utah.  The image provides a sobering reminder of just how vanishingly small the range of this species is.  If we, as a society, cannot take the steps required to ensure the survival of a beautiful little species such as this one – living on only the tiniest sliver of the lands under our stewardship, it speaks ill of our ability to do so for other species with much greater habitat requirements.

Copyright © Ted C. MacRae 2009

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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

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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

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Magodo – giant twig wilter

petascelis-remipes

In previous posts, I have highlighted some of the insects I observed on a trip to South Africa in November-December 1999.  All of the photos I have shown to this point were taken at Borakalalo National Park in North West Province or at the Geelhoutbos farm of Susan Strauss below the Waterberg Range in the formerly Northern, now Limpopo Province.  Both of these locations are deep inside the bushveld, providing ample opportunity to observe an incredible diversity of insect life.  This is not to say that insects, even spectacular ones, cannot be found in more urban areas.  During the weekend between those two mini-expeditions, I stayed with my friend and colleague, Chuck Bellamy, at his home in Pretoria, a beautiful city with lovely architecture, elegant gardens… and some very impressive bugs!  The bug in this photo was found on a tree in a shrubby enclave, and at well over 35 mm in length it is easily the largest leaf-footed bug (order Hemiptera, family Coreidae) that I have ever seen.  Its chunky build, velvety black coloration with thin yellow lines along the sides and down the center of the thorax, and greatly enlarged hind femora quickly led me to a provisional identification of a male Petascelis remipes, or giant twig wilter.  This ID was confirmed by my friend and colleague Harry Brailovsky, an entomologist at UNAM (Universidad Nacional Autónoma de México) and world expert on Coreidae (and who, incidentally, just recently published a review of this Afrotropical genus – Brailovsky 2008).

According to Picker et al. (2002), these insects are found on plants in the genus Combretum.  Like most species in the family, they have scent (“stink”) glands that provide defensive capabilities. Adults are gregarious and bold, walking towards intruders with antennae vibrating when disturbed, and they are apparently capable of squirting their defensive secretions for some distance.  The nymphs are black as well but futher advertise their noxiousness with warning coloration of red spots on a whitish background. Interestingly, and despite their powerful chemical defenses, this species is considered a delicacy in parts of Mozambique where it is known as Magodo.  In a post called Insects for Dinner (in a blog with the eerily similar title, Beating about the Bush), Bart Wursten of Gorongosa National Park in Mozambique describes how local folk burn small patches of the grassland in which these insects are found to smoke them out and catch them.  The Magodo hunters kill the bugs by breaking off the head and removing the scent glands, which releases a very strong almond-like smell.  In doing this, the locals are able to catch considerable quantities of the bugs, which they eat with supper.

Lest you believe such practices are an anomaly, van Huis (2003) has compiled a list of about 250 insect species used as food in sub-Saharan Africa.  Lepidoptera, Orthoptera and Coleoptera represented the bulk (78%) of species eaten, with Isoptera, Hemiptera, Hymenoptera, Diptera and Odonota making up the rest.  Several examples of toxic insects and the traditional methods used to remove the poisons were given.  It was noted that whether or not insects are eaten depends not only on taste and nutritional value, but also on customs and ethnic preferences or prohibitions.  I’m not one to shy away from the thought of eating insects – after all, shrimp are just bugs that live in water, and insects rank far lower in ‘slime factor’ than many other invertebrates (e.g., oysters) that enjoy great popularity in our culture.  I’ve eaten roasted beet armyworm (Spodoptera exigua) pupae and munched on chocolate covered ants, but that’s kid stuff – the armyworms tasted like the soy sauce in which they were roasted, and the ants tasted like, well… chocolate.  I did once eat a softshelled crab (alive!), and I actually hope to one day taste the enormous grub of the giant metallic ceiba borer, Euchroma gigantea, eaten by indigenous cultures in Central and South America.   Still, I think I’d need a lot of faith in my chef’s scent gland removal prowess before I started scarfing Magodo down like popcorn.

What insects have you eaten?

REFERENCES:

Brailovsky, H.  2008. Notes on the genus Petascelis Signoret and description of one new species (Hemiptera: Heteroptera: Coreidae: Coreinae: Petascelini).  Zootaxa 1749:18–26.

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

van Huis, A. 2003. Insects as food in sub-Saharan Africa. Insect Science and Its Application 23(3):163-185.

Copyright © Ted C. MacRae 2009

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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

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