Aaack!-maeodera

Warning: post contains hardcore, taxonomic, sciencey geekiness!

Just as there is seasonality in the lives of insects, there is seasonality in the work of those who study them.  For the collector/taxonomist, everything revolves around the collecting season — time spent on anything else is time not available for collecting. As a result, I spend a good deal of my time during the summer in the field and on its associated planning and organizing activities, leaving the winter months for processing and identifying collected specimens, incorporating them into the permanent collection, generating reports to fulfill permit requirements, and ultimately preparing manuscripts for publication — the raison d’être.  Winter is also the time when I identify specimens sent to me by other collectors.  I do this not only because I’m such a nice guy (at least I hope I am), but also because such material often contains species I haven’t seen before or that represent new distributions and host plant associations that I can use to augment the results of my own studies.  Such work has occupied much of my time during the past several weeks, and I now find myself close to finishing the last of the nearly dozen batches of beetles sent to me since the end of last winter.

Of the three groups of beetles that I actively study — jewel beetles, longhorned beetles, and tiger beetles — it is the jewel beetles that are taxonomically the most challenging.  Tiger beetles can often be indentified in the field (especially with the publication of Pearson et al. (2006), or “the Bible” among cicindelophiles), and North American longhorned beetles have been reasonably well worked by a strong contingent of both professional and amateur taxonomists over the past several decades.  Jewel beetles on the other hand, despite their dazzling colors and popularity with collectors, continue to befuddle even the most dedicated collectors due to their extreme variability and poorly-defined species limits.  Of the 822 species and subspecies known from North America, fully three-fifths of them belong to one of just three hyperdiverse genera — Acmaeodera, Agrilus, and Chrysobothris.  No recent taxonomic treatments are available for any of these genera, thus, identifying species belonging to them requires access to primary literature, a well-represented and authoritatively-identified reference collection, and extraordinary patience!  This is particularly true of the genus Acmaeodera, the North American members of which were last treated collectively more than a century ago (Fall 1899) (at which time less than half of the current 149 species/subspecies were known to science).  The recent explosion of web-based images has helped matters (a particularly useful site for those interested in North American Acmaeodera is Acmaeoderini Orbis, with its galleries of Harvard type specimens and BugGuide photos); however, images are still lacking for many species, and others are not easily distinguished from the images that do exist.

Acmaeodera robigo Knull (Val Verde Co., Texas)

It is precisely this taxonomic challenge, however, that makes the group so interesting to me.  Opportunities for discovery abound, as basic information is incomplete or totally lacking for many species regarding their geographical ranges and life histories.  One of the species I encountered in a batch of material sent to me by cerambycid-specialist Jeff Huether contained three specimens that I eventually determined to represent Acmaeodera robigo.  Josef Knull (1954) first described this species from specimens collected at Lake Corpus Christi in south Texas, and nothing more was recorded about the species until Nelson et al. (1996) reported a single specimen cut from its pupal cell in the base of Dalea formosa (Fabaceae) at White River Lake in far northern Texas — a range extension of almost 500 miles!  Obviously, I didn’t have this species in my collection, and it was only after a series of eliminations that led me to the original description (and confirmation of my ID by Nearctic Acmaeodera-guru Rick Westcott based on the photos shown here) did I know for sure what it was.  These specimens were collected at Seminole Canyon State Historic Park, thus, extending into west Texas the species’ known range, and they exhibit variability in the elytral markings and punctation that was not noted in the original description.  While only an incremental increase in our knowledge of this species, collectively such increases lead to greater understanding of the genus as a whole, and Jeff’s generosity in allowing me to retain examples of the species increases my U.S. representation of the genus to 130 species/subspecies (87%).

Acmaeodera n. sp. (Santa Cruz Co., Arizona)

The opportunity for discovery is not limited to range extensions and new host records, but includes new species as well.  A few years ago I received a small lot of specimens collected in Arizona by my hymenopterist-friend Mike Arduser (hymenopterists, especially those interested in apoid bees, are excellent “sources” of Acmaeodera, which they encounter frequently on blossoms while collecting bees).  Among the material he gave to me was the single specimen shown here that immediately brought to my mind Acmaeodera rubrovittata, recently described from Mexico (Nelson 1994) and for which I had collected part of the type series.  Comparison of the specimen with my paratypes, however, showed that it was not that species, and after much combing through the literature I decided that the specimen best fit Acmaeodera robigo (despite being collected in Arizona rather than Texas and not matching the original description exactly).  This was before I had true A. robigo with which to compare, so I sent the specimen to Rick Westcott for his opinion.  His reply was “good news, bad news” — the specimen did not represent A. robigo, but it didn’t represent any known species either!  While the prospect of adding a new species to the U.S. fauna is exciting, basing a description on this single specimen would be ill-advised.  Only through study of series of individuals can conclusions be made regarding the extent of the species’ intraspecific variability and its relation to known species.  Until such specimens are forthcoming, the specimen will have to sit in my cabinet bearing the label “Acmaeodera n. sp.”  For all of you collector-types who live in or plan to visit southeastern Arizona, consider this a general call for potential paratypes!  The specimen was collected in early August on flowers of Aloysia sp. near the Atascosa Lookout Trailhead on Ruby Road in Santa Cruz Co.

REFERENCES:

Fall, H. C.  1899.  Synonpsis of the species of Acmaeodera of America, north of Mexico.  Journal of the New York Entomological Society 7(1):1–37.
[scroll to “Journal of the New York Entomological Society”, “v. 7 1899”, “Seq 12”]

Knull, J. N. 1954. Five new North American species of Buprestidae (Coleoptera). Ohio Journal of Science 54:27–30.

Nelson, G. H. 1994. Six new species of Acmaeodera Eschscholtz from Mexico (Coleoptera: Buprestidae). The Coleopterists Bulletin 48:272–282.

Nelson, G. H., R. L. Westcott and T. C. MacRae. 1996. Miscellaneous notes on Buprestidae and Schizopodidae occurring in the United States and Canada, including descriptions of previously unknown sexes of six Agrilus Curtis (Coleoptera). The Coleopterists Bulletin 50(2):183–191.

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 2010

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“Cicindelophilically”

 

My good friends Kent Fothergill and Kelly Tindall passed through St. Louis last week on their way back home from a visit to Columbia.  I was happy for the chance to get together with them – if only for a short visit, as I hadn’t seen them since the summer before last when Kent joined forces with Chris Brown and I to conduct a survey for Cylindera cursitans (ant-like tiger beetle) in southeast Missouri.  (You may recall that I orginally met Kent when he emailed me out of-the-blue after moving to southeast Missouri in 2007 to let me know he liked tiger beetles.  I responded by suggesting that he look for this long sought-after species, which he found the very next day!)  Kent had told me in arranging the visit that they had something they wanted to give me, and since I had some specimens of theirs to return it seemed a convenient way to make the exchange.  I had no idea what it was they wanted to give me, but I knew they’d been to the recent Entomological Society of America meetings in Indianapolis and figured they must have purchased a cool beetle specimen or something for me.

After arriving at my office, they told me that they’d had the chance to meet John Acorn, a rare celebrity in the world of natural history study.  Most people known John as the host and creative force behind Acorn the Nature Nut, an award-winning television series in which John’s inspiring personality and infectious love of nature introduce viewers to various aspects of Alberta’s natural history.  John is also, however, an accomplished entomologist, with one of his special interests being… you guessed it – tiger beetles!  In 2001, John published The Tiger Beetles of Alberta: Killers on the Clay, Stalkers on the Sand, one of the most accessible and highly entertaining treatments of the family (er… supertribe) to date (if I can ever get my act together and write The Tiger Beetles of Missouri, I want to model it after this book).  John was at the ESA meetings selling original artwork of the different tiger beetle species occurring in Alberta, and Kent and Kelly mentioned to him that they had a friend back in Missouri who would love one of his prints – selecting “Cicindela purpurea auduboni black morph”.  Somehow, my name and association with this blog came up, to which John replied, “Oh, I know about Beetles in the Bush” and then signed the print for me as shown below.  Wow!

I hope Kent and Kelly understand my stunned silence upon first seeing the print they had so generously given to me and the inscription it bore.  I felt a little silly afterwards returning their kind gesture by just giving them back specimens that were already theirs.  I’m honored by their friendship and will be reminded of it now everytime I look at the print on my office wall.

REFERENCE:

Acorn, J.  2001.  Tiger Beetles of Alberta: Killers on the Clay, Stalkers on the Sand.  The University of Alberta Press, Edmonton, xix + 120 pp.

Copyright © Ted C. MacRae 2010

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Ants invade Beetles in the Bush!

For months now, your Beetles in the Bush host, Ted, has been nudging me to blog, in the end resorting to offering me a guest blogger gig at BitB. Given this golden opportunity, I’ve decided to utilize my web-logging debut to introduce my favorite insects, the fabulous Formicidae. First, a disclaimer: I have not mastered ant photography, and so will rely on the undisputed king of ant photographers, Alex Wild, through links to his numerous, unexcelled images.

Since about age 5, I can remember being interested in virtually anything living, but especially in small, active creatures. From the beginning, I have had a particular attraction to ants. With some notable exceptions, and aside from the pulchritudinous feature of their svelte waists, ants aren’t what most folks would call pretty, but they are — How else to say it? — just plain “cool”!

First, who are they and where do they come from? Ants constitute a single family, Formicidae, within the insect order Hymenoptera, so their relatives are wasps, bees, sawflies, horntails, gall wasps, and a vast array of small parasitic wasps that are mostly unappreciated except by specialists who study them. Within Hymenoptera, the ants are considered to belong to the superfamily Vespoidea, along with hornets, paper wasps, potter wasps and other solitary relatives.  The evidence at present indicates the first animals we would call ant had diverged from their common ancestry with these other stinging wasps some time in the Cretaceous, 130 million years ago, more or less.  Ants are classified in a varying number of subfamilies, currently at about 20. Fossils in amber up to 100 million years old represent early members of several modern subfamilies, and a few extinct groups. Most of us in the Northern Hemisphere Temperate Zone are familiar only with the big two subfamilies, Formicinae (carpenter ants, weaver ants, honey ants, etc.) and Myrmicinae (fire ants, harvester ants, leaf-cutter ants, etc.). In much of North America, folks may also be familiar with an abundant member of another subfamily, Dolichoderinae, namely odorous house ants, which frequent our gardens, kitchen counters, wall spaces, and even electrical outlets, especially in spring.

Ants are a conspicuous and often dominant presence in the World of the Little (or, what Piotr Nascrecki, in one of my favorite books, calls the “Smaller Majority” ). It is difficult for any observant person to sit still, outdoors in good weather, and not begin to see ants doing what ants do. They scurry about singly, in pairs or threesomes or foursomes, or in long lines, or columns. Our notice may be further piqued by their habit of transporting sundry bits of biomass or mineromass (pebbles, etc.).  Often this is just taking out the inedible food waste, or sawdust or soil excavated while expanding or remodeling their nests.  Less visibly, because more diffusely in space, ants carry a variety of items from foraging to their nests to provide nutrition for their colonies, or to add mass or create functional structure to their nests (to create better drainage, to provide incubation space for developing brood, and in some desert ants, to capture dew). In one of the most spectacular examples of ants transporting things, the so-called “slave-making” ants carry home the mature brood of a related species, these young ants later maturing in the brood-robbers’ nest to become its work force!

Shiny red workers of Polyergus lucidus return with pupae pillaged from a nest of Formica incerta several meters away. Two brown and differently proportioned workers of the latter that matured from raids earlier in the life of this Polyergus colony may be seen at the right of the photo.

Perhaps, not so widely known is that most of what most ants carry home is not some large, heavy particle in their mandibles, but rather is liquid carried in an expansible section of their esophagus called the crop. Because of the fine diameter of their gullets, adult ants cannot eat anything other than the most minute solid particles (e.g., pollen grains, loose cells from their prey).  Solid items may be cut up to feed to the legless, pale larvae, or the larvae may even be placed directly upon the killed prey to bite into it and feed on their own, using their flexible “necks”.  Adult ants get pre-digested food in return, in the form of glandular secretions loosely termed saliva, but which may be either a glandular secretion from the larva itself or simplify pre-liquefied flesh of prey lapped up from the larva’s messy eating.  In some lineages, known as Dracula ants, adults actually “bleed” the larvae through rapidly healing wounds made at particular locations on the larval exoskeleton.

Okay, I need to get back to my regular work, so let’s bring this home (to winter in the United States). Many of us are now in the dead of winter, or so it would seem. But, on sunny days, sap is beginning to flow upward in maple and other trees, and one ant species may actually be seen, creeping slowly through the woods, in search of dead arthropods and earthworms, or perhaps some sweet sap oozing from a sapsucker wound in a tree. This is Prenolepis imparis, sometimes called “winter honeypot ant”. This is a partial misnomer. While foragers may indeed fill their crops to over-full with sweet sap or honeydew, the very bloated “honeypots” in the deep nests of this ant are in fact, fat pots, having converted their food to whitish body fat. This is later converted to a glandular secretion that serves as food for developing larvae.  These ants are likely to be seen anywhere near where oaks of just about any species grow, and the where the soil is moist but well-drained. Look for these shiny little dark brown ants during your walks in the woods, on the sunny days that are sure to increase in number and warmth in the coming months.

Copyright © James C. Trager 2010

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BitB’s Newest Contributor

Those of you who have followed this blog for any length of time have likely noticed fairly regular participation in the comments sections by one James C. Trager.  Occasionally irreverent and always articulate, his informed quips are among those that I have enjoyed the most.  One can surmise from James’ comments that he knows a thing or two about entomology himself, but to say this would be an understatement!  Like me, James is a passionate entomologist whose scientific interests take him deep into many related fields of natural history study.  Unlike me, James is a formally trained insect taxonomist, specializing in ants (family Formicidae).  He has conducted numerous biogeographical and systematic studies on this group, much of it in the southeastern U.S. (list of publications), and is the current project leader for the Missouri Ants and Illinois Ants pages at AntWeb.org (whose ambitious goal is to provide information and high quality color images for each of the ~10,000 known ant species).  James’ deep knowledge of this single taxon, however, does not limit his interest in other insects — singing insects in particular are among his favorites. It is, thus, with great pleasure that I introduce James as the newest BitB contributor.

In fact, James and I have known each other for many years, as we are both based in the St. Louis area.  James is a restoration ecologist at Shaw Nature Reserve, a 2,500-acre ecological preserve located in the Ozark foothills (and just 15 miles from my house).  Originally established by the Missouri Botanical Garden for managed plant collections, its recent focus has shifted to environmental education and ecological research, and James has played a key role in their many ongoing wetland, woodland, prairie and glade (xeric limestone prairie) restoration efforts.  This experience combines with his entomological expertise and extensive travel within the U.S. and abroad (e.g., Ecuador) to give him a breadth of knowledge and perspective achieved by few, and I think you will find his writings most enjoyable.  Look for his first post to appear in the next day or so.

Ted & James in restored woodland at Shaw Nature Reserve. Photo by Madison MacRae.

Copyright © Ted C. MacRae 2010

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Triple Quiz

Photo Details: Canon EOS 50D w/ Canon 100mm macro lens, ISO 100, 1/250 sec, f/20, MT-24EX flash w/ Sto-Fen diffusers.

  1. Entomology Quiz: Name the beetle.
  2. Botany Quiz: Name the plant.
  3. History Quiz: Name the location (yes, attentive readers will be able to deduce this).

While you ponder these questions, please make note of two upcoming blog carnivals:

  • Circus of the Spineless – I’ve waited almost a year to host issue #47 of this venerable blog carnival – look for its appearance early next week.  Send me your submissions by January 31 if you want to be included in this issue – ossified homeotherms need not apply.
  • An Inordinate Fondness – The inaugural issue of this monthly blog carnival devoted to beetles is set to debut in mid-February at the home site.  Post submissions are already starting to come in, so don’t miss this chance to be a founding participant.  Submissions are due by February 15 – either by email or using this handy BlogCarnival submission form.

I’ve discovered a few more interesting blogs since my last blogroll update – the following are definitely worth a visit:

  • Biodiversity in Focus Blog – A new blog by graduate student Morgan Jackson.  Amazing photographs of stilt-legged flies (Diptera: Micropezidae).
  • BunyipCo – David Rentz writes about entomology from Queensland, Australia, with a focus on orthopteroid insects and the rain forest.
  • I Love Insects – Entomology student and insect enthusiast Erika Lenz really loves insects.
  • nbell.dk/BLOG – A relatively new blog by a dragonfly/butterfly enthusiast in Denmark.
  • Forest Fragments – Just a stone’s throw from my backyard, the staff at Washington University’s Tyson Research Center has begun a blog about their 2,000-acre experiment.
  • Exploring the Remnants – A brand new blog from Aaron Brees, who explores Iowa’s natural history.  Drop by and give him a jump start.

For those really interested in exploring entomology-related blogs, Anna Miller has provided nice descriptions of her Top 25 Entomology Blogs.  Yes, I made the list, as did most of the other usual suspects, but you might find one or two that you didn’t know about.

Copyright © Ted C. MacRae 2010

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A matter of diffusion

In my Best of 2009 post, I mentioned four skills that, to me, seemed to be crucial for becoming a successful insect macrophotographer: 1) composition, 2) understanding lighting, 3) knowing how to use a flash, and 4) knowledge of the subject.  Of these, I’m most comfortable with the last – three decades of insect study have given me the chance to observe a tremendous diversity of insects in a variety of situations and habitats.  Many species are located only through understanding of their haunts and habits, and the ability to capture them relies upon successful approach techniques.  Collecting insects has been excellent preparation for photographing them.  I’m also reasonably satisfied with my compositional skills – at least in this early stage of my development as a photographer.  I don’t expect to win any photo competitions (yet), especially since my intent as a photographer is at least as much for scientific documentation as it is for artistic expression, but I’m satisfied that I’m on the right track and developing the eye I’ll need to make good progress.

What I’m not satisfied with yet are the middle two – understanding lighting and knowing how to use a flash.  Let’s face it, I was starting from square one here.  My only prior experience with insect photography were middlin’ attempts in the mid-1980’s using an Olympus OM-10 body, a Zuiko 50mm lens (maximum magnification 1:2), and natural light only.  I quickly lost interest (too distracting for the collecting), picking it back up only for my 1999 trip to South Africa.  Fast forward to May 2009 and my acquisition of a bona fide insect macrophotography setup, complete with Canon’s 100mm f/2.4 and 65mm 1-5X macro lenses and their MT-24EX macro twin flash.  Talk about giving a Ferrari to someone who had just received their learner’s permit!  I like a good challenge, however, and spent the rest of 2009 with camera in hand on several memorable field trips – shooting lots of frames, deleting many on the spot and more when I saw them on the computer, and occasionally stumbling onto a pretty good one.

While I still have much to learn, one thing I did realize is that lighting remains a challenge even with a decent setup such as mine.  The MT-24Ex flash unit, in particular, while seemingly the flash of choice among Canon-using amateur insect macrophotographers, produces a very harsh light.  The capabilities and shortcomings of this flash unit have been reviewed in great detail by several insect macrophotographers much more knowledgeable than I (e.g., Alex Wild, Dalantech, Kurt, etc.), so I simply refer you to their websites if you’re interested rather than try to summarize here.  However, the one thing they all emphasize with this flash unit is the need for diffusers.  Diffusing light is easy; a simple sheet of tracing paper will do.  However, diffusing light in a manner that is equally effective with both the 65mm and 100mm lenses (with their shorter and longer working distances, respectively) and also convenient for field-use is hard.  For most of the 2009 season, I tried using Sto-Fen Omni-Bounce Diffusers, and while they were marginally better than no diffusers at all, the results were still not satisfying.  More recently, I’ve been experimenting with the Gary Fong Puffers, which Dalantech has modified for use with the MT-24EX.  I hadn’t yet committed to constructing the diffusers as described and conducting controlled comparisons between the Puffers and Sto-Fens, but my initial tinkering with the Puffers has me impressed.  Below are two photos of Cicindela splendida (the aptly-named Splendid Tiger Beetle) – the first (which some of you may remember from this post) was taken in the field using the Sto-Fen diffusers and the 65mm lens (1X)…

…while the second was taken recently of this same beetle (in captivity on native soil) using the Puffers attached to the Sto-Fens and the 100mm lens (at slightly less than 1X).

Both photos have been cleaned up a bit with post-processing; however, neither has been altered dramatically.  While not a true one-to-one comparison due to different venues (field versus captivity) and lenses (65mm versus 100mm), the second photo is clearly superior to the first, with softer lighting resulting in richer colors and far fewer specular highlights on the insect body.   I had to bump the lighting up considerably for the second photo, since the Puffer combined with the Sto-Fens cut the light levels quite a bit, yet still the photo lacks any of the harshness and washed appearance of the first photo.  The use of the 100mm lens in the second photo also should have presented a greater challenge for the lighting due to the increased working distance (~8 inches, compared to only 2-3 inches for the 65mm lens).  I’m really quite pleased with the results of this initial experiment – enough to the point that I’ve ordered the necessary materials and am ready to dive into construction of my own set of “Dalantech-Puffers.”

Copyright © Ted C. MacRae 2010

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Friday Flower: Crystallofolia (“Frost Flowers”)

Crystallofolia (frost flowers) on dittany (Cunila origanoides).

While hiking the middle stretch of the Ozark Trail’s Wappapello Section, my friend Rich and I witnessed a bounty of crystallofolia, or “frost flowers”.  These fragile, yet exquisite formations are, of course, not flowers at all, nor are they true frost (which forms directly from water vapor without first condensing), but rather are thin layers of ice that form as water is drawn from cracks in plant stems and freezes upon contact with cold air.  As the water continues to be drawn from the plant by capillary action, newly forming ice pushes older ice further out, creating delicate, folded, curling ribbons of ice that resemble many-layered flower petals.  Air trapped within the ice upon freezing imparts a frothy white appearance.

Frost flowers are not an uncommon phenomenon, and I have seen them on more than a few occasions during my frequent off-season hikes.  However, never before had either Rich or I seen the numbers that we saw during our hike on this, the second day of the New Year.  Frost flowers are normally encountered during the first hard freezes of fall when the ground is not yet frozen.  Water in the stems of certain plants expands as a result of the freezing air temperatures, causing vertical cracks to form along the length of the stem through which the ice ribbons are extruded. The formations are rather ephemeral, usually melting or sublimating away by late morning in fall’s typically mild daytime temperatures.  As fall progresses to winter, water stores in the plant stems become depleted after several freezes or locked up when the ground itself freezes, and as a result frost flowers are rarely seen later than December in Missouri. However, it has been a wet and mild fall and early winter, and after an extended period of moisture during December, Missouri was finally gripped by a severe cold spell with lows in the single digits and daytime highs remaining down in the teens and 20s.  The saturated, yet unfrozen ground provided a good source of moisture for plant stems to draw upon, and continuous subfreezing air temperatures allowed frost flowers to persist throughout the days and attain remarkable size. The photo above was taken in late afternoon as a sinking sun shone brightly on the west-facing slope where this formation was seen, persisting in all its fragile glory.

In Missouri, frost flowers are primarily associated with dittany (Cunila origanoides), species of Verbesina (V. virginica, white crownbeard; and V. alternifolia, yellow ironweed), and camphor weed (Pluchea camphorata).  Frost flowers are rarely seen on any other plant in Missouri, and I don’t know what it is about these plants and not others that make them suitable for frost flower formation.  Dittany is a daintly little member of the Lamiaceae, and as such has square stems – perhaps the angles on the stem are prone to splitting.  However, there are many other lamiaceous plants and non-lamiaceous square-stemmed plant species in Missouri that do not form frost flowers.  Likewise, Verbesina and Pluchea belong to the Asteraceae and do not have square stems.  They are, however, larger, more robust plants with thick, pithy stems that may be capable of holding a large amount of water and mature late in the season after most other plants have already dried up, perhaps allowing them to retain sufficient moisture in the stem late enough in the season to allow frost flower formation when conditions are right.  The majority of the frost flowers we saw were on dittany – dainty, delicate, fragile formations 2-3 inches across. However, at the end of the hike, as we were exploring the area around the parking lot, we found a stand of Verbesina (I suspect V. alternifolia), with which some of the most enormous and robust frost flowers that I have ever seen were associated.  Following are additional views of some of the more impressive formations we saw and the plants they were associated with.

Frost flowers on dittany - shaded, protected areas produced the largest formations.

Partial thawing during ribbon formation causes exquisite twists and turns.

Like snowflakes, each frost flower is one-of-a-kind.

Dittany (Cunila origanoides) dried stem, leaves, and fruits.

Verbesina sp. frost flowers were enormous - this one was approx. 5 inches wide.

Dried fruits of Verbesina sp. (poss. alternifolia).

Copyright © Ted C. MacRae 2009

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Me and my buds!

Those of you who have followed this blog for any length of time have seen repeated references to my friends and colleagues, Chris Brown and Rich Thoma. Rich and I have been collecting insects together for almost 25 years now (since shortly after we bothed first moved to the St. Louis area), and Chris has joined us in the fun for the past ten years as well. It is rare when all three of us can get out in the field together – meshing hectic professional and family lives with the sometimes coincident, sometimes divergent insect collecting goals of three fathers can be challenging. Nevertheless, at least once or twice a year we manage to converge on a date and enjoy each other’s company out in the field. I don’t think I’m ever happier than when I’m in the field (well, except when one of my daughter’s nestles into my lap to watch a movie!), and the chance to share that experience with close friends of like interest is especially gratifying.

Chris is quite an accomplished insect photographer himself, having been at it for much longer than I’ve known him and providing me great coaching as I’ve begun testing the waters myself. Recently, he sent me some photos from our 2009 field trips to the lowlands of southeastern Missouri and the Loess Hills of northwestern Missouri. Those were two exciting trips, revealing new localities for Cicindela scutellaris, the discovery of Cylindera celeripes in Missouri, the rediscovery of Ellipsoptera macra, and even a new state record robber fly.  The sharing kind of guy he is, he’s granted me permission to post them here (plus one taken by Rich Thoma).

Rich (left) and Ted scan 2-track through sandy ground in the southeastern lowlands looking for tiger beetles.

Ted and Chris take a break from looking for tiger beetles in a sand prairie relict. Photo by Rich Thoma.

Ted attempts to extract an adult tiger beetle from its daytime burrow in a sand prairie relict.

Ted scans the open sand in a sand prairie relict for adult tiger beetles.

Ted fishes for a tiger beetle larva in a sand prairie relict.

Ted photographing the robber fly, Ospriocerus abdominalis, at Star School Hill Prairie in the Loess Hills of northwest Missouri.

Distant view of Ted (small spot in center) photographing Ospriocerus abdominalis at Star School Hill Prairie.

Copyright © Ted C. MacRae 2009

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