And the winner is…

Okay, time to fess up on which of my photos was selected for the 2013 ESA World of Insects Calendar, but before I do let me say that getting readers’ comments on which one they thought was selected proved to be a very interesting exercise. The final tally is as follows (I gave ½ a vote for mentions of a photo as a second choice):

1. Trimerotropis saxatilis nymph – 4½ votes
2. Crossidius coralinus fulgidus – 3½ votes
3. Tetracha floridana – 3 votes
4. Buprestis rufipes – 2 votes
4. Edessa meditabunda eggs – 2 votes
6. Megaphasma denticrus – 1 vote

My personal favorites were Buprestis rufipes, Crossidius coralinus fulgidus and Tetracha floridana, with the second having what I thought was the best “calendar appeal.” I also thought the Trimerotropis saxatilis was strong for its natural history back story. It thus comes as no surprise that these were the top four vote-getters among those who commented.

The two photos that did not receive any votes are interesting—Spissistilus festinus, because the post containing that photo is one of the Top 5 posts on this blog (based on page views); and Cicindela formosa generosa, because that was the photo selected by ESA for their 2013 Calendar! I went back and forth on whether to include the photo in the final selections, but it won out over some others I was considering because of its composition—not many tiger beetle closeups contain as much scale and depth. I guess that’s what ESA like about it as well, but whatever the reason it seems I need to develop a better sense of what photo judges are looking for.

Since nobody guessed the correct photo, I’m going to give all who commented 5 “participation” points, and those of you who used italics with scientific names will get an additional 2 bonus points. Brady Richards maintains his spot atop the overalls in BitB Challenge Session #6 with 66 points, but Mr. Phidippus‘ 58 points moves him into second place over Sam Heads with 54 points.

For those who did not vote for this photo (or, everybody!), maybe access to this 1680×1120 version of the photo (click to enlarge) will help change your minds.

Cicindela formosa generosa (Coleoptera: Carabidae: Cicindelinae) – eastern big sand tiger beetle

Copyright © Ted C. MacRae 2012

2013 ESA World of Insects Calendar Selection

Today I received word from Richard Levine at the Entomological Society of America that one of my photos had been selected for the 2013 version of their famed World of Insects Calendar!

Excuse me for a moment please… (pumps fist, stirs the pot, does a very bad moon walk…)

Okay, I’m back. Honestly, this is an honor that I did not expect—at least not yet. Historically dominated by such giants in the world of insect macrophotography as Piotr Naskrecki,  Thomas Myers, and others, competition for ESA’s World of Insects Calendar is fierce. Last year more than 500 photographs were submitted for 13 slots (12 months and an introductory page) by 98 photographers from around the world. I was one of those photographers, though not selected (no surprise as I was a first-time submitter). However, I took great pleasure in seeing fellow bug blogger Adrian Thysse nab two of the 2012 slots, and I increased my resolve to try again for next year with a selection of eight mostly newer photographs.

At the suggestion of Dave Stone, I present each of those photos below along with a short description of why I submitted it. However, I’m not going to tell you which photo ultimately was selected—I thought it might be fun to see which photo you think was selected and why. As added incentive for guessing, I’m going to award 10 BitB Challenge points to each person who correctly picks the selected photograph. BitB Challenge Session #6 is coming down to the wire, so this could have a big impact on the overall standings.

The 2013 Calendar will become available for sale later this year (probably October) at the ESA website—last year’s version cost only $12 (discounted to $8 for ESA members, and free for those attending the annual meeting [which I will be attending this year]).


Megaphasma denticrus (Phasmida: Diapheromeridae) – giant walkingstick

From North America’s longest insect (21 Aug 2009).  This is one of my earlier super-closeup attempts. I liked the combination of blue and brown colors on the black background.


Buprestis rufipes (Coleoptera: Buprestidae) – redbellied Buprestis

From Special Delivery (13 July 2010).  The use of a white box shows off the brilliant (and difficult-to-photograph) metallic colors well, and I like the animated look of the slightly cocked head.


Edessa meditabunda (Hemiptera: Pentatomidae) – alquiche chico

From  (18 May 2011). I found these Edessa meditabunda stink bug eggs on the underside of a soybean leaf in Argentina almost ready to hatch. The developing eye spots in each egg gives the photo a “cute” factor rarely seen in such super close-ups.


Cicindela formosa generosa (Coleoptera: Carabidae: Cicindelinae) – eastern big sand tiger beetle

From  (10 May 2011). I like this slightly panned out view because of the sense of scale and landscape created by the inclusion of the plantlets and the view over the small rise.


Trimerotropis saxatilis (Orthoptera: Acrididae) – lichen grasshopper

From  (15 July 2011). Some of my favorite insect photos are not only those that show the bug in all its glory, but also tell a story about its natural history. This nymph is almost invisible when sitting on the lichens that cover the sandstone exposures in its preferred glade habitat. 


Tetracha floridana (Coleoptera: Carabidae: Cicindelinae) – Florida metallic tiger beetle

From  (23 August 2011). I used extension tubes to improve the quality of flash lighting (decreased lens to subject distance results in greater apparent light size), and I like the symmetry of the composition.


Spissistilus festinus (Hemiptera: Membracidae) – threecornered alfalfa hopper

From  (17 September 2011). Even though both the insect and the background are green, there is sufficient value contrast to create a pleasing composition, punctuated by the bizarre zig-zag pattern of the eyes.


Crossidius coralinus fulgidus (Coleoptera: Cerambycidae) – a rabbitbrush longhorned beetle

From  (4 October 2011). The blue sky background provides a pleasing contrast with the colors of this particular beetle and flowers.

Copyright © Ted C. MacRae 2012

Even a 12-year old can discover the larva of a rare, endemic species!

Since discovering the larva of the rare, endemic Florida metallic tiger beetle (Tetracha floridana) in the small, intertidal mangrove marsh behind my sister-in-law’s condominium in Seminole, Florida three years ago, I’ve looked forward to subsequent visits to see the adults (they’re nocturnal) and gather additional material needed to write the larval description. I had to wait a few days on this year’s trip due to rain (it is Florida, after all), but eventually a dry evening came along and I began “suiting up” for my nighttime foray. Much to my delight, my 12-year old nephew Jack wanted to come with me. Jack had never been in the field with me before, but according to his mom he has become quite interested of late in science and biology. My daughter Maddie, also 12 years old (and a veteran of many trips to the field with me), also wanted to go, so together the three of us slathered on the insect repellent and headed into the dark towards the marsh.

Larva of Micronaspis floridana (Florida intertidal firefly) | Pinellas Co., Florida

We had only my headlamp as a light source, so the kids trailed behind me as I picked a line through the brush, across a small creek, and onto a ridge that snakes through the marsh that marked one of the areas where I had seen good numbers of the beetles last year. We collected a small number to keep alive and place in a terrarium of native soil, the hope being that they would lay eggs so I could obtain some 1st-instar larvae for the formal description, but what I was really looking for were larval burrows. As we (well, I) searched the ground in front of me with the lamp and the kids trailed behind me in the dark, Jack suddenly stopped and said, “What’s that?” I shone my light to where he was pointing but didn’t see anything and so resumed my search. Right away he said, “There it is again.” I asked if it was a rabbit (we’d seen them at the edge of the marsh during the day), and he said, “No, it’s like a light or something.” I turned off the lamp, and gradually the faint, green glow reappeared. I recognized the source of the light instantly as that of a larval firefly, although truthfully I have never actually seen an actual firefly larva. Seeing a great teaching moment for the kids, we walked to the light, knelt down, and shone the lamp directly on the ground from where the light was coming to find the small (~10 mm long) larva moving slowly through the moist, algae-covered rocks. It had the classic, retractable firefly head and curiously quadruply-spined tergites. I congratulated Jack on finding the larva, emphasizing that I would have never seen it myself had he not been there and been so observant despite not having a lamp.

Larvae of this species exhibit the retractable head characteristic of firefly larvae.

I went back a few nights later by myself so I could concentrate on photographing some of the things we saw in the marsh the previous night, including the firefly larva. I had no problem relocating one in the same place we found it before (I just turned off my headlamp and waited for the green glow). I’m generally not keen on posting photographs of unidentified insects (just me, but I find photos much more interesting when accompanied by the natural history back story), and I was sure this larva would remain unidentified (I have little knowledge of adult fireflies, much less their larvae). This seemed even more likely after perusing the few identified and many unidentified firefly larvae photographs on BugGuide and finding nothing even remotely similar. I was about to give up when I decided to try the search term “Lampyridae Florida Pinellas” (“Pinellas” being the county where we found the larvae—my thinking being that maybe there was a Florida firefly checklist that could narrow down to the county level the possible species), and high in the results was a page titled Florida intertidal firefly (fiddler crab firefly). On that page was a photo of the larva, although not nearly large and detailed enough to be sure it was the same, but still in my mind almost surely this species because of the stated restricted habitat—intertidal zone of Florida coastal salt marshes! I sent these photographs to lampyroid aficionado Joe Cicero, who kindly confirmed my identification. 

Restricted to intertidal marshes in coastal Florida.

Because it occurs only at the edges of salt water marshes around the peninsular coast of Florida, M. floridana is a classic example of shoestring geographic isolation and, thus, serves as a good model for studies of genetic isolation and its impact on speciation (Lloyd 2001). Along with T. floridana, it now makes at least two rare, Florida-endemics occurring in the small private, preserve behind my sister-in-law’s condominium (both of which were first found as larvae rather than adults). Although the larva of M. floridana is already known—albeit by a rough black and white photograph (McDermott 1954)—it’s rarity and restricted habitat nonetheless make it an exciting find well deserving of the more detailed color photographs shown here. However, as I told Jack after receiving confirmation of its identity, he gets full credit for the discovery. I took him into the field with me with the intention of showing him some new things, and he turned the tables on me! Yes, even a 12-year old can discover the larva of a rare, endemic species!

REFERENCES:

Lloyd, J. E. 2001. On research and entomological education V: a species concept for fireflyers, at the bench and in old fields, and back to the Wisconsian Glacier. Florida Entomologist 84(4):587–601.

McDermott, F. A. 1954. The larva of Micronaspis floridana Green. The Coleopterists Bulletin 8(3/4):59–62.

Copyright © Ted C. MacRae 2012

Planet’s Coolest Critters – Tiger Beetles

Cicindela scutellaris rugifrons – photo by Harry Zirlin.

Readers of this blog know well (and hopefully share) my affection for tiger beetles (family Cicindelidae). That should come as no surprise, as tiger beetles rank among the most popular of all beetle groups. The reasons for this are many—for me it is their extreme polytopism (geographically based variation in coloration and markings), affinity for extreme habitats, and charismatic behavior (both adults and larvae), while for others it may be from a more basic research perspective (e.g., thermoregulatory behaviors, molecular phylogeny, and visual physiology) or as models for conservation research. I think most, however, will simply declare that tiger beetles are just… well, cool! That is the perspective of Harry Zirlin, who wrote this charming little article entitled, Planet’s Coolest Critters – Tiger Beetles at PetsLady. After introducing the group and its diversity, lifestyles, and behaviors, Harry notes the increasing popularity of tiger beetles with birders, butterfly watchers and nature photography buffs and the recent proliferation of field guides that have enabled their elevation to the ranks of “watchable wildlife.” Maintaining tiger beetles in terraria allows an even closer look at their beauty and behaviors, and Harry gives some useful tips on how best to accomplish this. It’s a pleasant little read, and I recommend you check it out!

Copyright © Ted C. MacRae 2012

Working with Cerceris fumipennis—Epilogue

Cerceris fumipennis nest littered with Neochlamisus sp. beetles

In Working with Cerceris fumipennis Part 1 and Part 2, I talked about the use of this species as a biosurveillance tool for Buprestidae. These wasps are specialist predators of jewel beetles, which they capture almost exclusively and paralyze with their sting to use as food provisions for their offspring in underground nests. I also mentioned that there are other species of Cerceris, each specializing in its own distinct prey group, and at my site in east-central Missouri I found C. bicornis, a weevil specialist, almost as common as C. fumipennis. Thus, when I came upon this particular Cerceris wasp nest, I wondered it I had encountered yet another species in the genus, for littered around it were case-bearing leaf beetles in the genus Neochlamisus.

The bright coppery coloration suggests Neochlamisus platani

I counted 11 beetles lying on the diggings surrounding this nest, and as is typical with buprestids around C. fumipennis nests these beetles all appeared to represent the same species (I’ve done a little collecting of Neochlamisus beetles in Missouri—the especially bright coppery coloration suggests to me N. platani, a species found on eastern sycamore, Platanus occidentalis). I’ve also noted that C. fumipennis nests littered with beetles on the surface also have beetles—usually of the same species—freshly cached underground, so I decided to dig up the nest to see what might be in it. As I inserted the grass stem and started digging, I heard the distinctive buzzing indicating the wasp was still inside the nest, and when it appeared I noted the distinctive three yellow facial markings that identify it as a female C. fumipennis. As suspected, the nest contained another seven beetles of the same species, and I would later learn that C. fumipennis, while specializing on jewel beetles, does occasionally take other prey. Philip Careless and colleagues recorded two leaf beetles, including Neochlamisus bebbiana, and one weevil as hosts for this wasp at their Working with Cerceris fumipennis website. If my species ID of these beetles is confirmed, this should represent yet another non-buprestid host record for C. fumipennis, although I should also mention that out of several hundred observations this was the only non-buprestid prey I observed around or in a C. fumipennis nest.

Copyright © Ted C. MacRae 2012

Palmetto Tortoise Beetle, Hemisphaerota cyanea

Hemisphaerota cyanea (palmetto tortoise beetle) on saw palmetto (Serenoa repens)| Levy Co., Florida

While most leaf beetles (family Chrysomelidae) are found associated with herbaceous plant species, many members of the subfamily Hispinae—which includes leaf mining beetles and tortoise beetles—are found on the foliage of woody plants. In North America the most distinctive of tortoise beetles found on trees is the palmetto tortoise beetle, Hemisphaerota cyanea. These distinctive dark blue, hemispherical-shaped (hence, the genus name) beetles with yellow antennae are found in the deep southeastern U.S. on the fronds of saw palmetto, Serenoa repens, and other native and introduced palms. I found the beetles in these photographs near Cedar Key Scrub State Preserve in Levy Co., Florida while searching white sand 2-tracks through sand scrub habitat for the Florida-endemic Cicindelidia scabrosa (Scabrous Tiger Beetle).

Beetles scarify the leaf epidermis, leaving trough-like feeding marks.

I first saw this species during my first insect collecting trip to Florida back in 1986. I didn’t know much then (other than that I really, really enjoyed traveling to different parts of the county to collect insects!). I was in Everglades National Park (with a permit) when I first noticed them dotting saw palmetto fronds. I think I had actually noticed them for some time but thought they were some type of scale insect before eventually realizing it was actually not only a beetle, but a tortoise beetle (one of the many groups of insects in which I was interested during those early, formative days).

Specially modified tarsi and a hemispherical shape allow the beetle to clamp itself tightly against the leaf to repel attack by ants and other insect predators.

I also remember being struck by how difficult it was to pry the adults off of the leaves on which they were sitting. It turns out that these leaf beetles have specially modified tarsi with thousands of bristles tipped with adhesive pads on the undersides. Normally only a few of the pads contact the leaf surface, but when the beetle is threatened it clamps all of them against the leaf and secretes an oil that strengthens the adhesive capabilities of the pads. Thus secured, the beetle clamps its hemispherical-shaped body down tightly against the leaf and is able to resist the efforts of ants and other predators to pry it from the leaf.

Copyright © Ted C. MacRae 2012

One-Shot Wednesday—Proctacanthus fulviventris ovipositing

Proctacanthus fulviventris | Dixie Co., Florida

Today I spent the day just south of Florida’s “arm pit” to look for the state’s near-endemic tiger beetle Cicindelidia scabrosa (Scabrous Tiger Beetle). I first found this species last August on a white-sand 2-track through sand pine scrub habitat near Cedar Key Scrub State Preserve (Levy Co.). Although I was happy enough with the photographs that I got that day, the small spot of habitat that I found them in had yielded only a few specimens. My goal this time was to find the species in additional localities  to get a better idea of its precise habitat preferences and obtain a better series of specimens that more fully represents the range of variability exhibited by the species in its pubescence, color and elytral markings. By day’s end I would meet this goal, having found the species at four locations in Levy Co. and further north in Dixie Co. My first stop was actually in Dixie Co. near Lower Suwannee National Wildlife Refuge, where I found good numbers of individuals on a white-sand 2-track through pine scrub. A variety of robber flies (family Asilidae) were also seen along the 2-track, but I resisted the urge to photograph them because of the task at hand. Eventually, however, I came upon a female of this rather large species with her abdomen deeply inserted into the loose sand, surely in the act of oviposition. This was too much to pass up, so I set down the net, took off the backpack, and put the camera together. Unfortunately, in the time it took to do this, the fly had already withdrawn her abdomen and was rapidly “sweeping” the tip of the abdomen back and forth over the hole—I presume to cover and hide it. I snapped this first frame (the little bit of motion blur can be seen at the tip of the abdomen), but then I moved carelessly (not my usual habit) when scooting in for a closer shot. This spooked the fly and caused it to fly off, and I was left with this single image.

As much as I like robber flies, I can’t say that I’m well versed in their taxonomy. However, the large size (25–30 mm in length) and overall gestalt suggested to me that it belonged to the nominate subfamily, and cruising through online photographs eventually led me to Proctacanthus fulviventris. The individual seems to agree well with the description of this species provided by Hine (1911), including the bright yellow beard, black femora and red tibiae, and reddish abdominal terga. If my identification is correct, this species—like C. scabrosa—is also a Florida near-endemic whose distribution extends barely into southern Georgia. It’s dark coloration and light brown wings, combined with its large size, surely make it one of the more impressive-looking robber flies, and I’m sorry that I did not attempt to get more photographs of this species while I had the chance, as I did not see it at any of the other locations that I visited on the day.

Incidentally, by my interpretation the scientific name of this species translates to “yellow-bellied spiny-butt”!

REFERENCE:

Hine, J. S. 1911. Robberflies of the genera Promachus and Proctacanthus. Annals of the Entomological Society of America 4(2):153–172.

Copyright © Ted C. MacRae

Working with Cerceris fumipennis—Part 2

During the 6-week period from late May to early July this year, I collected ~400 jewel beetle specimens representing at least 20 species (see Working with Cerceris fumipennis—Part 1). A final accounting of the species represented won’t be done until this winter, but the genera represented include Acmaeodera, Actenodes, Agrilus, Anthaxia (Haplanthaxia), Buprestis (Knulliobuprestis), Chrysobothris, Dicerca, Poecilonota, and Spectralia. Perhaps two-thirds of the specimens were “ground-picked”¹, while most of the remaining third were “stolen” directly from wasps by netting wasps in flight as they returned to their nest carrying prey.

¹ It’s not clear to me why I found so many abandoned buprestids at nest entrances. The wasps are known to drop prey when threatened and, rather than search for and relocate the prey, fly off to look for a new beetle(Careless et al. 2009). I observed this myself in several cases when I missed netting the wasp but swiped the net close enough to scare it, at which time it dropped the beetle and flew off (and I popped the beetle in a vial). However, the bulk of the beetles I found on the ground were not only at the nest entrance, but even mixed within the diggings surrounding the nest. My first act when checking each field was to check each nest, pick up any adults lying on top of the burrow diggings, and then carefully spread out the diggings with a knife or trowel to collect the beetles hidden within them. One nest contained as many as 13 Agrlus obsoletoguttatus inside the diggings. I wondered at one point if the wasps were leaving the beetles at the burrow entrance and then digging out the burrow before coming back to retrieve them, but I never actually witnessed this. On the other hand, I observed numerous wasps approaching their burrows while carrying prey, and every time the wasp dropped directly into the burrow. In fact, I could even predict what beetle species I was likely to find inside the nest based on the species I found around the entrance (more on that below).

This ball field with contains several dozen Cerceris fumipennis nests.

There is a third method that I used to collect beetles that I haven’t yet discussed, and that is digging them out of nests. In the latter part of the survey period (late June and early July), beetle numbers dropped rapidly, as did apparent wasp activity. As mentioned in the previous post, this drop off in activity came precisely at the time of season when I have observed buprestid beetle activity to decline in Missouri. As the drop off in activity was taking place, I began wondering what I would find if I tried digging up some of the burrows. Of course, digging up a nest takes much more effort than netting wasps or picking beetles up off of the ground, so it becomes important not only to identify whether a nest actually belongs to C. fumipennis and if it is active and likely to contain freshly captured beetles.  In addition, I observed the burrows of a variety of other insects in these fields as well, some of which are shown here and which might be confused with burrow entrances of C. fumipennis.

Cerceris fumipennis nest with Chrysobothris sp. adult left on diggings.

Cerceris fumipennis burrows exhibit perfectly circular, pencil-sized entrances surrounded by a symmetrical mound of diggings with a fine rather than granular texture. There are other Cerceris species that make nearly identical burrows, but they prey on other insects rather than buprestid beetles. At my site I found C. bicornis, a weevil specialist, almost as common as C. fumipennis. Their burrow entrances on the whole seemed slightly larger, but I could not use this as consistent distinguishing character. What I could use, however, was the presence of weevils rather than buprestids lying on the ground near the nest entrance. (I also observed this species returning to its nest and noted a rather faster, more powerful flight that made them even more difficult to capture than C. fumipennis). In contrast, there can be no doubt that the burrow above, with a buprestid beetle lying on the ground near the entrance, belongs to C. fumipennis

² The white plastic tag marks the burrow to facilitate locating nests on subsequent visits. It is secured with a golf tee and also can be rotated so that the hole covers the entrance. The hole is large enough to allow the wasp to leave but too small for a returning wasp to enter while carrying a beetle. The idea was to rotate the tags when I first entered a field to cover all the burrow entrances, watch for wasps returning with prey, and then net the wasps as they tried (in vain) to enter the burrow. However, I never actually observed a wasp trying to enter a covered burrow, even after leaving a field and returning 20–30 minutes later.

I presume this nest to be that of Bembix americana (sand wasp).

For the first few weeks, I thought the burrows such as that shown in the above photo also belonged to C. fumipennis. However, I never found beetles lying on the ground near the entrance, nor did I ever observe a wasp to enter or leave the burrow. I eventually noticed several distinct differences in burrow architecture—the burrow entered the ground at an angle rather than straight down, the diggings were distributed asymmetrically to one side of the entrance, and the latter seemed consistently a little larger than those of C. fumipennis. In addition, these burrows always seemed to be in the sandier portions of the fields. While I never associated any insect directly with these burrows, I did observe sand wasps (perhaps Bembix americana) in the vicinity and have seen similar-looking burrows dug by these wasps at Sand Prairie Conservation Area.

Larval burrows of Cicindelidia punctulata and other tiger beetles lack diggings around the entrance.

Tiger beetle larval burrows might also be confused with C. fumipennis burrows, especially after rain or high winds which can wash/blow away the diggings from around the entrance. I found adults of the punctured tiger beetle, Cicindelidia punctulata, fairly commonly at the site and presume the numerous tiger beetle larval burrows that were also present belong to that species. Larval tiger beetles burrows also enter the ground straight down and are, at first appearance, also perfectly round, but they are usually a little too small for C. fumipennis (those of Tetracha spp. being an exception)—the presumed C. punctulata burrow in the above photo measures about 5 mm in diameter. In addition, closer examination reveals a slight “D” shape to the burrow entrance (upper right in the above photo—the tiger beetle larva rests its jaws against the flat side) and, more distinctively, beveling of the ground around the rim of the burrow entrance. Cerceris fumipennis nests lack the slight D-shape and distinctive beveling.

Use a grass stem as a guide while carefully digging away the surrounding soil.

Years of practice digging up tiger beetle burrows prepared me well for my first attempts at digging up C. fumipennis burrows. While it might seem an easy task to follow a hole into the ground while digging soil away from it, in practice the burrow can be quickly lost after even a few inches due to falling soil covering the hole and making it impossible to relocate. I use a thin, flexible but sturdy grass stem to preserve the burrow path, inserting the stem into the burrow and down as far as it will go and then removing the soil carefully from around the hole with a knife or trowel. I try to avoid letting soil fall over the hole by prying the soil away from the hole, but if the hole does get covered the grass stem allows it to be easily relocated.

This nest contained a single Buprestis rufipes

Cerceris fumipennis burrows are not very deep—only 10–15 cm, and angle to one side a few cm below the surface before leveling out near the bottom. I noticed the nest in the above photo because I saw a wasp fly into it. When I went over to look at it I found a Buprestis rufipes lying on the ground near the entrance and so decided to dig it up. As I expected, I found another B. rufipes at the bottom of the burrow (two above photos courtesy of Madison MacRae).

…while this one contained a cache of seven Agrilus quadriguttatus.

The above photo shows a cache of seven Agrilus quadriguttatus that I found at the bottom of another burrow. In this case, the prey is rather small compared to large prey such as Buprestis and Dicerca. While nests provisioned with species in these latter genera often contained only a single beetle in them, I nearly always found multiple beetles in nests provisioned with the smaller Agrilus species. One nest contained as many as 13 Agrilus obsoletoguttatus, among the smallest of the species I found utilized by C. fumipennis at this site.

Buprestidae taken from five different Cerceris fumipennis nests.

Some of the nests I dug up contained multiple species of beetles, but far more commonly I found only a single species in a given nest. The photo above shows the diversity and number of beetles found on one date after digging up five different nests. From top left the beetles are: 1) 1 Buprestis rufipes; 2) 2 Agrilus quadriguttatus and 1 A. obsoletoguttatus; 3) 2 A. quadriguttatus and 1 A. obsoletoguttatus; 4) 8 A. obsoletoguttatus; and 5) 2 Poecilonota cyanipes, 2 A. quadriguttatus, and 1 A. pseudofallax. It would make sense for wasps to provision nests with greater numbers of smaller beetles to ensure adequate food for their larvae to complete development. How the wasps actually locate their prey, and why this species has specialized almost exclusively on buprestid beetles, is a mystery (at least to me); however (and here comes the speculation du jour), I suspect the wasps may have keyed in on volatiles used by the beetles—either those released by suitable hosts or by each other to facilitate mate location. Use of buprestid pheromones or freshly dead host volatiles would allow wasps to more efficiently locate buprestid prey and, once locating a source (a tree harboring a particular beetle species), could return repeatedly to provision their nest fully. It seems less likely that wasps rely exclusively on visual location of prey, as this would involve a large amount of random searching through trees and passing up numerous, seemingly equally suitable prey.

REFERENCE:

Careless, P. D., S. A. Marshal, B. D. Gill, E. Appleton, R, Favrin & T. Kimoto. 2009. Cerceris fumipennis—a biosurveillance tool for emerald ash borer. Canadian Food Inspection Agency, 16 pp.

Copyright © Ted C. MacRae 2012