Are we loving our prairies/glades/woodlands to death?

I had such high hopes for last weekend’s collecting trip – late May is boom time for insects across Missouri, we have had good moisture this spring, and I would be visiting some high-quality natural communities that I had not visited for a long time.  My stated goals (the jewel beetles, Agrilus impexus and A. frosti) were long shots – I knew that and would have been fine coming home without those species (which I did) had the the collecting been otherwise productive (which it was not).  Still, I’ve been doing this for a long time now, and I’ve learned to draw on my accumulated experience when things don’t go as planned to give myself the best shot at turning a bad collecting trip into a decent one when things don’t go as planned.  The itinerary with which I start is rarely the one that I actually follow, and this past weekend was a good example of such.

My first stop was Ha Ha Tonka State Park, one of Missouri’s premier parks, boasting high-quality chert, dolomite, and sandstone savanna interspersed with dolomite glades.  It is on these glades and savannas that I hoped to find Agrilus impexus, or failing that at least collect a nice diversity of other jewel beetles on the oaks and hickories of the savannas and surrounding woodlands.  However, it was with some reservation that I even came here after being told by my colleague at the Department of Natural Resources just 2 days before my trip that 75% of the park’s grasslands and woodlands had been burned within the past two years.  For an insect collector, this is never good news – in all my years of collecting insects, my experience in relatively recently-burned habitats has been consistent: collecting sucks!  I decided, however, to visit Ha Ha Tonka anyway because of the quality of the natural communities it contains, thinking perhaps I might be able to find pockets of unburned habitat supporting good insect populations.  This was not to be. I beat oak after oak in the savannas and woodlands – nothing!  I swept little bluestem and Indian grass in the glades – nothing!  The foliage was lush and green and the savanna and glade landscapes highly diverse – given the time of season the place should have been teeming with insect life, yet it almost seemed sterile. Were it not for a few Chrysobothris quadriimpressa jewel beetle adults that I found attracted to a recently wind-thrown black oak tree, I would not have seen any insects here at all.  It appeared my fears about park-wide depression of insect populations had been realized.  However, not one to waste a visit I decided to explore some of Ha Ha Tonka’s fascinating geological features.  Ha Ha Tonka contains one of Missouri’s best examples of karst geology, with complex structures formed from the collapse of a major cave system.  The Devil’s Promenade is one of the more spectacular examples of such, its horseshoe-shaped cliff representing the former interior walls of a now-collapsed cave.  As dusk approached, the day’s poor insect collecting caused me to abandon my plans to stay here and blacklight for nocturnal beetles.  Instead, I decided to break from the itinerary, drive further west and explore Lichen Glade Natural Area in the morning before heading to the Penn-Sylvania Prairie BioBlitz later that afternoon.

Devils Promenade, Ha Ha Tonka State Park

Lichen Glade Natural Area is a small area owned by The Nature Conservancy that boasts a high-quality sandstone glade surrounded by post oak/black jack oak forest.  My first visit to the area more than 20 years ago was during May, and it was one of the most productive collecting trips I’ve had with a number of Agrilus spp. (including A. frosti) beaten from post oak (Quercus stellata) along the woodland edge.  I didn’t visit again until fall of 2002, when Chris Brown, Rich Thoma and I found claybank tiger beetles (Cicindela limbalis) sunning on the exposed sandstone outcrops, and I made one more visit the following May to beat more insects off of post oak.  The Lichen Glade that I returned to this past weekend was a very different place from when I last visited – the surrounding woodlands had been extensively opened (I would guess within the past few years based on the size of the post oak resprouts), and fire had been used throughout the area.  Anticipation turned to frustration when no amount of beating of the woodland vegetation and sweeping of the glade vegetation turned up beetles in any appreciable numbers (or any insects for that matter) and two hours worth of effort yielded not a single buprestid beetle!

Sandstone glade community, Lichen Glade Natural Area

With resignation, I headed on over to Penn-Sylvania Prairie, where during the introduction to the BioBlitz I learned that nearly half of the 160-acre prairie was burned last December and all of it had been burned within the past few years.  I knew what I was going to find – nothing!  Okay, I shouldn’t say nothing, as there actually were some beetles present.  However, the numbers and diversity were low, with all of the species encountered representing common, widespread species.  Moreover, it was not just beetles – all of the invertebrate group leaders (which included experts on snails, ants, butterflies, and bees) reported low overall abundance and diversity in their groups of interest.  Only the vascular plants – the metric by which the value of prescribed burning is always assessed – showed high diversity, with 300 species of mostly native prairie plants recorded for the site.  It was a fun event, with probably ~75 attendees and a delicious pot luck dinner that evening; however, it would have been more enjoyable had there actually been a nice diversity of insects present to document for the preserve.

My comments may make it seem that I am against the use of prescribed burning.  This is not true – I understand the critical role that fire as a management technique plays in restoring and maintaining examples of Missouri’s historically fire-mediated landscape. Without fire and other processes to mimic natural disturbance factors, most of Missouri’s historical grasslands and woodlands suffer relentless encroachment by woody vegetation. However, the modern landscape is very different from the historical landscape, where fires of unpredictable scale, intensity, and frequency operated within a vastly larger scale to create a shifting mosaic of natural communities in various stages of ecological succession. Such processes cannot be recreated on today’s severely fragmented landscape, where the precious few remaining tracts of native habitat are relatively to extremely small and more often than not separated from each other by vast expanses of homogeneous and “inhospitable” habitat (e.g., agricultural, urbanized, or severely degraded lands).  It is in that context that I have great concerns about how aggressively fire has been used in recent years on our state’s natural areas and the impact this is having on insect populations – specialist and generalist alike.  Fire proponents will point to published studies that show little to no effect by the use of fire for managing small, isolated remnants on specialist insects (see review in Henderson 2010).  However, there are an equal number of studies that suggest such concerns are well-founded (see review in Panzer 2002). A consistent limitation in all of the studies that have been conducted is the lack of very large and long un-burned remnants.  Prescribed burning has been adopted so rapidly and pervasively that there just aren’t any significant un-burned remnants left to properly include as controls in such studies.  As a result, the insect fauna present at a given site at the start of such a study is already skewed towards those species that successfully recolonized the area post-burn.  At a minimum, the data to this point are inconclusive, and certainly the potential for impacts has not been given the consideration it warrants in designing fire-management plans for our own state’s prairies and glades. Furthermore, as rapidly and aggressively as fire has been adopted on our few, small, widely disjuct remnants, the opportunity for proper investigation of those potential effects may be gone.  A particularly egregious example of the lack of consideration being given to prairie invertebrates in designing fire management plans is shown in these photos of Iowa’s Sylvan Runkel State Preserve before and after a late May burn and the impact of that burn on a resident population of Nevada buck moths (Hemileuca nevadensis).

Here in Missouri, as in Iowa, it’s a problem of scale – the landscape is too fragmented and remnants too disjunct to manage based strictly on floristic response.   Populations of generalist insect species will recover, and even specialist species may be able to overcome such management practices if they are widely distributed and sufficiently mobile. But what about conservative species with low vagility, such as the swift tiger beetle (Cylindera celeripes) and our disjunct population of the frosted dromo tiger beetle (Dromochorus pruinina), flightless species restricted in Missouri to the few tiny remnants of loess hilltop prairie in northwestern Missouri and a single 2.5-mile stretch of roadside habitat in west-central Missouri?  Until directly relevant data, gathered here in Missouri, are forthcoming to suggest otherwise, I believe the most judicious use of fire possible should be practiced in restoring and maintaining our grasslands and woodlands.  In-season burns may have been a part of the historical landscape, but their use today has great potential to result in local extirpations and should be used only after the most careful consideration.  Leaving un-burned refugia within remnant habitats to accelerate recovery would also be prudent – yet many land managers disregard this practice because of its logistical difficulties. This is especially true in small parcels, yet it is precisely these remnants that have the most to gain from their use (or lose from not doing so!).  In the historical landscape, every burn was a patch burn – no matter what its size, there were always adjacent or proximal unburned habitat from which recolonization could occur.  Elk and bison, too, were integral components of the presettlement prairie landscape – their roamings caused intermittent, localized disturbances that were likely not only crucial to the tiger beetles that I study but may also have contributed to vegetational diversity through patch succession.  Techniques that mimic these natural disturbance factors include mowing, haying, and managed grazing.  They can be utilized to mimic those disturbances as well as delay woody encroachment, and their use in land management should be considered for their ecological value rather than deprioritized because of their relatively greater complexity and cost to implement. Mechanical removal and selective use of herbicides offer additional tools for addressing woody encroachment while minimizing potential impacts to insect populations. An effective management program that considers all of the flora and fauna of a remnant may not be possible unless all of these management tools are utilized, or at least properly considered. As my good friend James Trager said in a recent email (quoting Andrew Williams), habitat restoration “cannot rest on any single management practice, nor practicing it too extensively.”

REFERENCES:

Henderson, R. A.  2010. Influence of Patch Size, Isolation, and Fire History on Hopper (Homoptera: Auchenorrhyncha) Communities of Eight Wisconsin Prairie Remnants.  Wisconsin Department of Natural Resources, Research Report 189, 22 pp.

Panzer, R. 2002. Compatibility of prescribed burning with the conservation of insects in small, isolated prairie reserves. Conservation Biology, 16(5):1296-1307.

Copyright © Ted C. MacRae 2010

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Critters, and berries, and trees! (Oh, my!)

Several of my favorite blog carnivals have posted new issues this week – should make for some good reading over the weekend. If you’ve not yet had the chance to explore these carnivals, they are a nice way to find blogs of interest that you may not otherwise encounter. If you have, then you know the quality and diversity of their contributions make them an easy way to catch up on the latest thinking in their respective subjects. Head on over and explore the links – and as always, don’t forget to tip the waiter!

Circus of the Spineless #51 is up at Deep-Sea News.  Against the backdrop of the sickening and ongoing debacle in the Gulf Coast, Kevin Zelnio reminds us that it is not just fish, birds, and dolphins that are/will be suffering for a long time to come, but the unsung invertebrates as well. (Personal opinion – somebody better go to prison over this!). It is in this context that 19 contributions are presented, spanning 4 phyla and 3 arthropod classes. Insects, as always, are well represented (for my part, I temporarily set aside my beetle-myopia to promote a new ant paradigm).

Berry Go Round #28, titled “The best of the best in plant biology, conservation, photography, and evolution”, can be found at Greg Laden’s Blog. It’s nice to see heavy-hitter Greg giving some much needed support to this delightful blog carnival – not just by providing a well-organized collection of links to recent blog posts about plants, but also in discussing the value of blog carnivals – regardless of their size – and ways to make them more useful. I especially like this suggestion:

And, if you are engaged in social networking in any way (Facebook, Twitter, Whatever) please send this carnival out on that network, and at least a selection of the blogs linked herein.

I haven’t featured this blog carnival in awhile, but Casey has posted a fine Festival of the Trees #48 at Wandering Owl Outside. Liberally sprinkled with his own tree photographs, Casey presents an issue focused on the uses of trees – both by wildlife and, most interestingly, by the indigenous cultures of North America.  Another intriguing post shows the current state of worldwide deforestation – “the numbers are UGLY!”

Copyright © Ted C. MacRae

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“Trying” to photograph whirligig beetles

Nobody figured out exactly what I was doing in the photograph shown in the previous post (does anybody now see the whirligig beetles in the lower left corner of the photo?), but I sure enjoyed the guesses.  Several people alluded to dropping the camera or falling into the water, while others mentioned my heretofore unrevealed contortionist abilities.  However, Morgan Jackson‘s tale of trying to photograph Platypsyllus castoris has it all – rarely photographed species and the inordinate lengths we go through to get the shot.

Of course, whirligig beetles (family Gyrinidae) are much more commonly encountered than Platypsyllus castoris, but they can’t be any easier to photograph.  I spotted them as Rich and I balanced our way across a massive sycamore tree trunk while crossing the Black River during our early April hike of the lower Wappapello Section of the Ozark Trail.  I don’t know much more about whirligig beetles (or aquatic insects in general) than your average land-lubbin’ entomologist (in fact, I don’t think I’ve collected any since college systematics – yes, that long ago!), but for some reason I felt the need to try to photograph them.  Sure, the fallen tree provided a rare opportunity to get reasonably close to these very skittish insects without having to wade, but I think it was actually just the challenge of trying to photograph something in constant zigzagging motion that appealed to me.  Rich’s warnings that I would drop my camera were not enough to dissuade me, and after reaching the other side I ditched the backpack and tiptoed out with just my camera.

It seems like I’ve said this often in recent months, but these are my new hardest insect to photograph.  Not only are there the usual difficulties of framing and focusing a subject that is always in motion, but that motion is fast, erratic, and unpredictable, making tracking through the lens an extraordinary challenge.  Moreover, balancing precariously on a debris pile in the middle of the river strains the body and adds an element of danger (yes, I would be in deep doodoo if I dropped that camera).  I kept my eye on one particular individual that was swimming nearest to me, and after watching for a bit I saw that it was making a relatively predictable circuit that passed fairly close to me each time around.  I started trying to follow it through the lens and snap shots as it passed by – most of them turned out like this (actually, most of them turned out worse than this):

However, with each pass I got better, and I started getting shots with at least part of the beetle in focus.  So intent I was on what I was doing that I didn’t even know Rich had taken the photograph of me in the previous post until he showed it to me afterwards (he said he wanted to document the camera drop!).  Eventually I got this shot:

It’s far from a perfect photo – I had to adjust the levels because I hadn’t figured out the best lighting to use for something on the water’s surface, and the specular highlights from the flash on the forward elytron are rather extreme.  But the entire beetle is in focus, and we can make a reasonable guess as to its identity.  There are only two genera of whirligig beetles in Missouri – Dineutus and Gyrinus – and the large size (~12 mm in length) and hidden scutellum clearly identify this individual as something in the former genus.  Moreover, the rounded elytral apices (seen on other individuals as well) narrow it down even further to just a few possible species.  Unfortunately, they are distinguished primarily by ventral coloration; however, the bad first photo clearly does show dark legs, suggesting this may be D. ciliatus and not the orange-legged D. emarginatus.  I don’t even really care what species it is (did you ever think you’d hear me say that?), I’m just happy to have gotten a reasonably good photograph of an insect that surely few people have photographed well.

Copyright © Ted C. MacRae 2010

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Long Weekend Bug Collecting Trip!

On Saturday, I’ll be joining a number of other Missouri biologists as a Group Leader for a BioBlitz at Penn-Sylvania Prairie (“C” on the map above).  Penn-Sylvania Prairie is a 160-acre tract of native tallgrass prairie in southwestern Missouri owned by the Missouri Prairie Foundation. I’ll be leading the “Beetles” group (of course), and as far as I can tell there has been little to no work done to survey beetles in this prairie.  Late May is an awesome time to look for beetles in southwestern Missouri, and with the forecast calling for sunny skies with highs in the mid-80’s, what better opportunity to add an extra day to an already long holiday weekend and do a…

Long Weekend Bug Collecting Trip!

The BioBlitz is not until Saturday afternoon, so I’ve padded the itinerary with a few nearby southwestern Missouri spots that I’ve wanted to visit for some time now.  The first stop will be Ha Ha Tonka State Park (“B”) and its mosaic of dolomite glades and post oak savanna.  My interest in this area stems from two jewel beetle specimens collected there by a student at the University of Missouri, who gave them to me for identification.  These two specimens caused a stir when I first saw them, as I could not definitely ID them – they resembled Agrilus impexus, a common inhabitant of the desert southwest and Mexico, but they were much larger and, of course, were found in Missouri.  These specimens played a key role in clearing up a case of taxonomic confusion on the identity of Agrilus impexus when I sent them to U.S. Agrilus-guru Henry Hespenheide.  Through comparison with type specimens, he determined that these were among a smattering of specimens collected across the Great Plains that represent the true A. impexus, while the common southwestern U.S. species to which the name had long been applied was actually an undescribed species.  He described the latter as Agrilus paraimpexus (Hespenheide 2007), and the true A. impexus remains rare and little known.  Obviously, my two specimens are the only ones known from Missouri, and indeed only one other specimen of this species has been collected in the past 60 years!  I know that makes finding it a long shot, but the student who collected them told me he swept them from woody vegetation along the edge of a glade at Ha Ha Tonka Savanna Natural Area.  I suspect they may be associated with honey locust (Gleditsia triacanthos), thus, I will have my beating sheet and will be beating lots of honey locust on Friday – wish me luck!

On Sunday, I’ll work my way slightly northeast to some of the sandstone glades that are found in St. Clair Co. where the Osage Plains to the west transition into the Ozark Highlands to the east.  The two most interesting of these are Lichen Glade Natural Area (“D”) and Dave Rock Natural Area (“E”).  Here, sandstone glades and bluffs are surrounded by dry and dry mesic sandstone woodlands dominated by post oak (Quercus stellata) and blackjack oak (Quercus marilandica).  Many years ago, I beat a single specimen of Agrilus frosti off of post oak at Lichen Glade.  I have not collected the species since, and I know of only one other Missouri specimen collected by state agriculture personnel in a malaise trap in central Missouri.  I also hope to photograph the lichen grasshopper (Trimerotropis saxatilis), which I have seen commonly at both of these sites.  This Great Plains species is at its eastern limit of distribution in Missouri, occurring exclusively on sandstone and igneous glades where its cryptic coloration makes it nearly invisible against the acidic, lichen-covered rocks that dominate these habitats.

Otherwise, I have no specific goals for the trip, but as late May is prime time in this area for jewel beetles, I’ll be doing lots of general beating on the oaks and hickories that many species in this family favor as hosts for larval development.

REFERENCE:

Hespenheide, H. A.  2007. The identity of Agrilus impexus Horn, a new species, and taxonomic notes and records for other Agrilus Curtis species (Coleoptera: Buprestidae).  Zootaxa 1617:57–66.

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Cylindera celeripes Larva Revealed

In a recent post, I provided the first ever glimpse of the previously unknown larva of Cylindera celeripes, or swift tiger beetle.  This little-known flightless species is among the tiniest in North America (adults measure only 8 or 9 mm in length), and so far nobody has succeeded in rearing the species in the lab, or even finding its larva.  As the photographs in that post showed, I am reasonably close to accomplishing that first goal, having successfully obtained a number of eggs from field-collected adults placed in a terrarium of native soil. I fed the subsequent larvae a diet of small rootworm larvae and Lygus nymphs before putting them to sleep for the winter in a cold incubator, and the larvae resumed activity when I pulled them out of the incubator 2 months ago. Since then, they have feasted heavily on small noctuid larvae that we rear in our lab, and now most of the dozen or so larvae have sealed their burrows – I presume for pupation before (hopefully) emerging as adults in the next few weeks.

Cylindera celeripes 3rd instar larva - USA: Oklahoma, Woodward Co.

There is more to the story, however.  I had brought the adults back home in June 2009 from a population I found at Alabaster Caverns State Park in northwestern Oklahoma.  This was a reasonably robust population – news enough for a species that has not been seen in good numbers for many years now, and my discovery of equally healthy populations at several other locations in the general area gives new hope for the long-term prospects of a species that some regard as a potential candidate for listing as an endangered species. It also gave me hope that I might be able to find the larva were I to return to the area in the fall.  I also had a hunch that Cicindela pulchra (beautiful tiger beetle) could be found in the area, based on some very large larvae I found during that June trip, so in early October I made a quick return to northwestern Oklahoma to search for these two species.  While it was too cold and wet to have any hope of finding Cicindela pulchra adults (I still think the species is there), it did not prevent me from realizing my other goal.  May I present one of the first ever field-collected larvae of Cylindera celeripes!

Cylindera celeripes 3rd instar larva - closeup of hump on 5th abdominal segment with hooks to aid in securing the larva in its burrow

I found the larvae at Alabaster Caverns where I had found the adults earlier in June, and although the larval burrows were very small (only 2 to 3 mm in diameter), I knew what they were immediately when I saw them.  As I had observed for the adults, burrows tended to be near the edges of barren patches of soil in proximity to vegetation and not out in the middle of the barren areas.  This makes sense, considering where it would be more likely for prey to be encountered.  Because the weather was cold and gray, I didn’t see (or expect to see) larvae actively sitting at the tops of their burrows, so I began “fishing” to see if I could yank a few from their burrows.  I fished quite a few burrows for the first half hour or so, but none of my attempts were successful.  I began wondering if the larvae were even active at all or if they had already entered hibernation for the upcoming winter.  While I was fishing, I noticed that the burrows all seemed rather shallow – only about 6” or so (most tiger beetles, having larger larvae, dig burrows that are much deeper). This gave me an idea.  I went back to the truck and retrieved a small spade that I carry in case… well, I’d never actually used it before.  Anyway, I inserted a grass stem into a burrow and sunk the spade into the ground right next to it, making sure I got the spade at least as deep as the grass blade.  I then removed the spade and sunk it into the ground on the other side of the burrow, then pried until the entire chunk of soil came up intact.  With the bottom of the soil chunk exposed, I used my knife to carefully remove slivers of soil until I found the end of the grass stem that I had inserted into the burrow.  Carefully removing the soil in this area revealed the larva in a side chamber at the bottom of the burrow.  Success!  I took many photos of that larva right then and there, and over the next hour or so collected several more larvae, all but one of which I presumed were 3rd instars.  I packed each larva in its own small vial of native soil for the trip home, and although I have been attempting to rear them out for confirmation of their identity, there is little doubt that they do indeed represent this species.

Cylindera celeripes 3rd instar larva - that grotesquely beautiful head!

The photographs I’m showing here are not those first field photographs that I took when I first discovered the larvae.  Looking at those photographs after I returned home, I was dissatisfied with the amount of soil and debris that covered the larvae – especially their grotesquely unique head and pronotum.  Instead, I removed one of the larvae from its rearing tube and gave it a “bath” – brushing it with a fine camel-hair brush in a shallow dish of water – to clean it up for the photographs shown here.  After the photo shoot, I sacrificed this larva for the collection – it will be the basis for a formal description of the larva of this species (along with examples of the 1st and 2nd instars that I had sacrificed from my rearing, not yet confident that I would succeed in getting any of the others to 3rd instar).  The only thing I am waiting on before preparing that description is to see whether I actually succeed in rearing this species from egg to adult – stay tuned!

Photo Details: Canon 50D (ISO 100, 1/250 sec, f/13-16). Canon MP-E 65mm 1-5X macro lens, MT-24EX flash (1/8 power) w/ Sto-Fen diffusers. Typical post-processing (levels, unsharp mask).

Copyright © Ted C. MacRae 2010

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Introducing Chrysobothris caddo

This set of photographs comes from my June 2009 trip to northwestern Oklahoma, which I found at Boiling Springs State Park in Woodward County. They represent only the second buprestid species that I attempted to photograph with my (then) new camera and macro lens setup, the first being Chrysobothris ignicollis which I found at nearby Four Canyon Preserve. The latter species is commonly associated with Juniperus throughout much of western North America – indeed, the individuals I photographed were found on freshly cut J. virginiana (eastern redcedar), and I have reared the beetle from dead branches of this and other Juniperus species. The individual in these photographs represents another species in the same genus – Chrysobothris caddo. It was also found on cut redcedar; however, it is not normally associated with that plant. In fact, it is not very well-known at all, as it was only just described in 2007 (and these may well be the first ever identified photographs of the species).

Chrysobothris caddo is one of a number of new species that were described by Wellso and Manley (2007) in their revision of the Chrysobothris femorata species-group from North America. I’ve previously mentioned the taxonomic difficulties associated with this group, last revised by Fisher (1942), and it had been known for some time that several species – including some unnamed – were masquerading under the “catch-all” taxon of Chrysobothris femorata. Normally, the only people who care about such situations are taxonomists and those who enjoy placing ID labels on specimens (me on both counts – I just hated those “Chrysobothris femorata species-group” labels).  However, there was farther reaching impact in this case since C. femorata is a widespread and important economic pest of shade and fruit trees (eggs are laid on the trunks of the trees, which are then damaged by the boring actions of the larvae that hatch from them). The Wellso/Manley revision has brought some degree of clarity to species limits within the group (doubling its number of described species), but they remain difficult to identify since their recognition relies upon “suites” of characters rather than single “key” characters. For example, we know this individual (a female, based on the form of the pygidium, or upper surface of the tip of the abdomen) represents C. caddo because (see if you can find the characters in the photos as we go here):

  • the antennae are narrowed to the apex (eliminating C. rugosiceps, which has the last antennal segment strongly quadrate)
  • the post-median (back of middle) foveae (circular impressions) of the elytra (wing covers) are joined (eliminating C. viridiceps, which has the foveae distinctly separated)
  • the pygidium is deeply impressed on each side of the middle (eliminating C. quadriimpressa, which has the pygidium shallowly impressed)
  • the pygidium lacks a hyaline (membranous) lateral margin (eliminating C. adelpha, which is unique in possessing this character)
  • the elytra have the posteriolateral margins arcuate and the tips bronze (eliminating C. femorata, in which the margins are straight and the tips reddish)
  • the elytral costae (longitudinal ridges) are connected by cross-veins and interrupted by the foveae (eliminating C. comanche, which lacks cross veins and has indistinct foveae)
  • the frons (face) has the callosities (elevated patches) transverse and bronze (eliminating C. shawnee, which has larger, bronze-black callosities)

Are you cross-eyed yet?! If not, there are four additional species in the group that are distinguished by similarly subtle character suites but whose geographical occurrence outside of Oklahoma (see checklist below) automatically eliminates them from consideration.

Chrysobothris caddo is primarily associated with Celtis (hackberry), and my finding it on redcedar is simply an incidental association. There was a large tree dump in the back area of the park with freshly cut wood from a variety of plant species – such tree dumps are famous collecting grounds for woodboring beetles in the families Buprestidae and Cerambycidae. However, little importance can be given to beetle-plant associations observed in such situations, with multiple potential host plant species in such close proximity to each other. The third photograph shows another female probing cracks in the bark of cut Ulmus rubra (slippery elm) with her ovipositor – perhaps she will have laid an egg or perhaps not, and if she did it is unknown whether the larva that hatched would be able to feed and develop successfully to adulthood on this non-preferred host.

For those with an interest in this group, following is a checklist of the species with their geographical distribution and preferred hosts:

  1. Chrysobothris adelpha Harold – eastern US and southern Canada west to Texas.  Primarily associated with Carya, also reared from Amelanchier and Prosopis.
  2. Chrysobothris caddo Wellso and Manley – Florida west to Arizona and north to Missouri, abundant in Texas.  Primarily associated with Celtis, reared also from Cercis and Ebanopsis [= Pithecellobium].
  3. Chrysobothris comanche Wellso and Manley – New Mexico, Texas, and Utah.  Associated exclusively with Juglans.
  4. Chrysobothris femorata (Olivier) – all continental states and Canada.  Associated with a wide variety of woody plant species, especially those in landscape and orchard settings.
  5. Chrysobothris mescalero Wellso and Manley – New Mexico and Texas.  Associated exclusively with Quercus.
  6. Chrysobothris quadriimpressa Gory and Laporte – eastern US west to Continental Divide.  Primarily associated with Quercus, reared also from Juglans, Liquidamber, and Sapindus.
  7. Chrysobothris rugosiceps Melsheimer – eastern US and southern Canada west to Texas.  Primarily associated with Quercus, reared also from Castanea.
  8. Chrysobothris seminole Wellso and Manley – Georgia and Florida.  Associated exclusively with root crowns of Chrysoma, making it the only species associated with a non-woody host.
  9. Chrysobothris shawnee Wellso and Manley – eastern US west to Colorado.  Primarily associated with Quercus, reared also from Salix and Prunus.
  10. Chrysobothris sloicola Manley and Wellso – Known only from Michigan in association with Prunus.
  11. Chrysobothris viridiceps Melsheimer – eastern US and southern Canada west to Continental Divide.  Associated primarily with Quercus, reared also from Carya, Prosopis, and Ulmus.
  12. Chrysobothris wintu Wellso and Manley – Arizona and California.  Primarily associated with Quercus, reared also from Salix and Prunus.

I have, over the years, collected numerous specimens of most of the species in this group (lacking only mescalero, seminole, and sloicola in my collection), with specimens now assignable to caddo, comanche, shawnee, and wintu included in the original type series as paratypes.

Photo Details: Canon 50D (ISO 100, 1/250 sec, f/14-16), Canon 100mm macro lens, Canon MT-24EX flash (1/4 ratio) w/ Sto-Fen diffusers. Typical post-processing (levels, unsharp mask, minimal cropping).

REFERENCES:

Fisher, W. S.  1942. A revision of North American species of buprestid beetles belonging to the tribe Chrysobothrini.  U. S. Department of Agriculture, Miscellaneous Publication 470, 275 pp.

Wellso, S. G. and G. V. Manley. 2007. A revision of the Chrysobothris femorata (Olivier, 1790) species group from North America, north of Mexico (Coleoptera: Buprestidae). Zootaxa 1652:1–26 (first page only).

Copyright © Ted C. MacRae 2010

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The Marvelously Cryptic Dicerca lurida

Dicerca lurida on trunk of wind-thrown mockernut hickory (Carya alba).

This is Dicerca lurida (family Buprestidae), another of several woodboring beetle species that I found on the trunk of a large, wind-thrown mockernut hikcory (Carya alba) tree during my early April hike of the lower Wappapello Section of the Ozark Trail.  Actually, I had already spent some amount of time at the tree photographing a checkered beetle (Enoclerus ichneumoneus) and a longhorned beetle (Stenosphenus notatus) giving a ride to a phoretic pseudoscorpion before I even noticed not one, but several of these cryptically colored jewel beetles on the trunk of the tree.

Like other species in the genus, the brilliant metallic gaudiness of Dicerca lurida as a pinned insect specimen in a cabinet belies its near invisibility when sitting on the bark of its host trees.  Several different trees have been reported as hosts (Nelson 1975), but hickories of the genus Carya seem to be the most preferred.  The beetles rapidly colonize wind-thrown or cut trees and branches while the wood is still hard and strong, and I have collected it from a number of hickories and reared it from dead pignut hickory (Cary glabra) and shellbark hickory (Carya laciniosa), as well as sandbar willow (Salix exigua).  Most jewel beetles are active as adults only during a limited time during the season – typically late spring and early summer in eastern North America, but species of Dicerca occur as adults throughout the year – even during winter hibernating under loose bark.  This individual probably represents one of those hibernating adults that resumed activity in the first warm days of spring, searching for freshly killed host trees on which to mate and lay their eggs.  Widespread across eastern North America, it is perhaps the commonest species of the genus and one of the commonest jewel beetles in North America.  Yet, despite its abundance, year-round occurrence, relatively large size, and attractive coloration, its cryptic habits keep it seldom seen by those who don’t look for it.

Photo Details: Canon 50D (ISO 100, 1/250 sec, f/18), Canon 100mm macro lens, Canon MT-24EX flash (1/4 ratio) w/ Sto-Fen diffusers. Typical post-processing (levels, unsharp mask, minimal cropping).

REFERENCE:

Nelson, G. H. 1975. A revision of the genus Dicerca in North America (Coleoptera: Buprestidae). Entomologische Arbeiten aus dem Museum G. Frey 26:87–180.

Copyright © Ted C. MacRae 2010

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