Beetle Love

An Inordinate FondnessIt seems like it has been a long time coming, but the Inaugural Issue of An Inordinate Fondness, the monthly blog carnival for the world’s most diverse group of animals (um… beetles), has finally made its debut! I can’t tell you how much pondering, pleading, fretting, and tweaking went into bringing this newest of blog carnivals to fruition, but it was all worth it. My sincerest thanks to everyone who helped me along the way (especially Seabrooke, Amber, Jason, and Mike) and to all who contributed for this first issue. I hope you’ll take a moment to stop by and check out the many fine contributions. If you love beetles, you’ll love this issue. If beetles haven’t exactly turned you on before, maybe you’ll find a new appreciation for them after experiencing the collective passion of the contributors. If you’ve written a post about beetles, perhaps you’ll consider participating in AIF #2 to be hosted by Amber at Birder’s Lounge. I recommend this handy submission form, or contact Amber directly if you prefer. The submission deadline for issue #2 is March 15, 2010.

House of HerpsAlso, Jason over at xenogere has just released House of Herps #3- The Time Machine. Jason has shown himself to be a natural talent at blog carnival hosting, and this edition is no exception. In his unique, singular style, Jason guides you on a trip through time to visit reptiles and amphibians of the past, present, and future.

In celebration of the debut of An Inordinate Fondness, I close with this preview of a feature that CBS did on Christopher Marley for the program “Sunday Morning.” Here is a man who not only shows the same passion for these fascinating animals that many of us feel (though I’m not sure I would characterize Titanus giganteus as “dangerous”), but also has the talent to channel his passion into exquisite works of art (sorry about the commercials!).

Vodpod videos no longer available.
More about “Sunday Morning – Preview: Beetle Art“, posted with vodpod

Okay, after hosting three blog carnivals in the past 4 weeks, I think I’ll go hibernate for awhile!

Copyright © Ted C. MacRae 2010

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Alkali Tiger Beetle

Eunota togata globicollis - Salt Plains NWR, Oklahoma

I haven’t written much about my early October trip to Oklahoma, where I had hoped to confirm a hunch that the gorgeous Cicindela pulchra (Beautiful Tiger Beetle) would be found in the red clay/gypsum hill habitats of Woodward and Major Counties (the same place where I had found the much rarer Cylindera celeripes the previous June).  Unfortunately, a sudden cold snap and overcast skies conspired against me for the duration of that short, 5-day trip, reducing tiger beetle activity to near zero and sending me back to Missouri with little to show for my efforts — save a scorpion, a torpid Cicindela splendida, and some very beautiful ladie’s-tresses orchids in peak bloom.  I did have one moderately successful day, however, when I returned to Salt Plains National Wildlife Refuge in north-central Oklahoma, a place where I observed seven species of tiger beetles during my June trip.  An eighth species that I did not see on that trip, but which I had observed in previous years, was my goal this time, and despite the cold temperatures and cloudy skies I was fortunate to find several individuals of Eunota togata globicollis.  Occurring primarily on saline flats in the central and southern Great Plain, this subspecies was called the Alkali Tiger Beetle¹ by Erwin and Pearson (2008), who reserved for the nominate form (found in salt marshes and tidal flats along the Gulf Coast) the more descriptive name White-cloaked Tiger Beetle².  A third subspecies, E. togata fascinans (Salt Flat Tiger Beetle) is restricted to salt flats in central New Mexico and west Texas (Pearson et al. 2006) (you may remember this subspecies from my habitat partitioning post last month).

¹ In reality, I have come to consider the term ‘alkali’ as a bit of a misnomer, as it is saline soils specifically — not just those with high pH (alkaline) — that the species is fond of. Moreover, there are many species of tiger beetles in addition to this one that are associated with saline soils.

² Okay, I might as well just get all this off my chest. Pearson et al. (2006) gave common names to each species of tiger beetle in the U.S., but not subspecies. I think most non-taxonomists probably consider this a good thing, although it is not without its problems (some species already had multiple common names applied to them, forcing choices that are sure not to please everyone). Erwin and Pearson (2008) took this further and came up with common names for all of the subspecies as well, and like any good taxonomist they steadfastly applied existing common names only to nominate forms. Eunota togata, however, is an example where the original common name would have been better applied to one of the non-nominate subspecies. The species epithet togata means “cloaked” (being derived from the Latin word toga — a reference to the broad white band running along the elytral margins). Each of the two non-nominate forms are distinguished by the white band being more broadly expanded (indeed, almost entirely covering the elytra in subspecies fascinans), yet it is the nominate subspecies — the least “cloaked” of the three — that retains the original common name. A silly argument I suppose, but if we start applying the “prinicple of priority” to common names in the same manner as scientific names, then what have we gained? Of course, I am of the opinion that most insect groups are too diverse and their taxonomy still too unstable to warrant a rigid system of “official” common names. Is it really any easier to learn White-cloaked Tiger Beetle than Eunota togata? How about Mount Ashland Night-stalking Tiger Beetle instead of Omus cazieri? And this is not even considering what happens when category-level shifts occur. For example, the genus Tetracha was formerly called the Big-headed Tiger Beetles; however, its former subgenera were recently elevated to genus level. Erwin and Pearson, accordingly, applied the common name to the entire subtribe containing Tetracha and its relatives and applied a new common name, Metallic Tiger Beetles, to the new, more limited concept of Tetracha. Thus, in an ironic case of common name instability despite no change in scientific name, the Virginia Big-headed Tiger beetle (Tetracha virginica) became the Virginia Metallic Tiger Beetle. Are your eyes bugging yet? Common names may be appropriate for higher vertebrates, but can they really be used effectively for beetles and other insect groups where the increasing use of molecular tools is sure to result in additional, perhaps radical, shifts in taxonomy? There — I said it, and I feel a lot better!

This species is restricted to saline flats in the central/southern Great Plains.

Of the eight tiger beetle species that I’ve now observed at Salt Plains NWR, half of them (Cicindela fulgida, C. nevadica knausii, E. togata globicollis, and Habroscelimorpha circumpicta johnsonii) are true saline habitat specialists.  One of the other four species (Cicindela tranquebarica kirbyi) is also fond of saline habitats but also occurs commonly on dry, sandy soils as well, and two show a high affiinity for nearly any moist (Cicindela repanda) or moist to dry (Cicindela punctulata) soils with little regard for salinity.  Only Cicindela formosa, a denizen of dry, deep sands seems a little out of its element on the moist, salty mud at Salt Plains NWR — perhaps the few individuals I’ve observed here are incidental visitors, mistaking the white, barren expanses of salt-encrusted soil for the dry sand the species prefers during disperal searches.  This again brings up the question of habitat partitioning for competition avoidance among tiger beetle species sharing the same habitat.  Eunota togata globicollis is active during the spring and fall and, thus, temporally isolated from C. nevadica knausii and H. circumpicta johnsonii (both summer-active species).  The other saline specialist at Salt Plains NWR (C. fulgida) is active during the same seasons as E. togata globicollis; however, in my observations that species prefers the sparsely-vegetated zone at the edge of the saline flats, while E. togata globicollis prefers to stay out in the more open areas.  These observations mirror those of Melius (2010) for E. togata fascinans and the other seven species he noted in the Laguna del Perro area of New Mexico, and of Willis (1967), who recorded as many as 11 sympatric tiger beetle species in saline habitats in the central U.S.

Saline flats at Salt Plains NWR are home to eight species of tiger beetles.

Microhabitat selection and seasonal occurrence are not the only isolating mechanisms that can minimize interspecific competition among the different tiger beetle species at Salt Plains NWR.  Cicindela tranquebarica kirbyi is also a spring/fall species and doesn’t appear to display a preference for open versus vegetated areas, potentially allowing it to compete directly with both E. togata globicollis and C. fulgida.  However, C. tranquebarica kirbyi is a decidely larger species, while the other two are smaller, and correlated with such differences in overall size is the size of their mandibles.  Mandibular size directly correlated to prey size in a number of tiger beetle species (Pearson and Mury 1979), thus providing another mechanism for avoiding competition between these three co-occurring species. 

Photo details:
Beetles: Canon 100mm macro lens w/ 68mm Kenco extension tubes on Canon EOS 50D (manual mode), ISO 100, 1/250 sec, f/18-20, MT-24EX flash 1/4 power w/ Sto-Fen diffusers.
Landscapes: Canon 17-85mm zoom lens (22mm) on Canon EOS 50D (landscape mode), ISO 100, 1/100 sec, f/10, natural light.

REFERENCES:

Erwin, T. L. and D. L. Pearson. 2008. A Treatise on the Western Hemisphere Caraboidea (Coleoptera). Their classification, distributions, and ways of life. Volume II (Carabidae-Nebriiformes 2-Cicindelitae). Pensoft Series Faunistica 84. Pensoft Publishers, Sofia, 400 pp.

Melius, D. A. 2009. Post-monsoonal Cicindela of the Laguna del Perro region of New Mexico. CICINDELA 41(4):81-89.

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.

Pearson, D. L. and E. J. Mury. 1979. Character divergence and convergence among tiger beetles (Coleoptera: Cicindelidae). Ecology 60:557–566.

Willis, H. L.  1967.  Bionomics and zoogeography of tiger beetles of saline habitats in the central United States (Coleoptera: Cicindelidae).  The University of Kansas Science Bulletin 47(5):145-313.

Copyright © Ted C. MacRae 2010

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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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