Eye to eye with a copperhead

I don’t know what it is about Osage copperheads (Agkistrodon contortrix phaeogaster) that makes every encounter with one so special. They are perhaps the most common of Missouri’s five venomous snake species, and I’ve seen them more often than I can count. Still, every time I see one I simply must stop and marvel. This particular individual was seen a few weeks ago at Sam A. Baker State Park in Missouri’s southeastern Ozark Highlands. You might say it was “sloppy seconds”—I had actually gone to the park to look for timber rattlesnakes (Crotalus horridus), a juvenile of which I had seen during last year’s Annual-Birthday-First-Bug-Collecting-Trip-of-the-Season™ trip. I did not see any rattlesnakes this time, as access to the rockpilish cliffs along Big Creek where I saw the juvenile last year was blocked by high water, but I was quite pleased to find this copperhead underneath a log while we were there.

Copperheads are marvelous photographic subjects. Beautiful, rarely seen by those who don’t know how to look for them, and with an air of “danger” about them. Yet they are among the most docile of all snakes, venomous or otherwise. They don’t use aggression or warning sounds when threatened like cottonmouths (Agkistrodon piscivorus) or rattlesnakes, nor do they dash for cover like most non-venomous species. Instead, they rely on their cryptic, dead-leaf coloration to make them invisible. It works—even I, my eyes tuned to see just about anything after a half-century of clambering through the brush, didn’t immediately notice this individual when I first rolled over the log under which it had taken cover (although I did immediately notice the little red-backed salamander, Plethodon cinereus, at the other end of the area covered by the log). I suspect I’ve walked right by many more copperheads than I have seen, completely unaware of their presence.

Their docile nature also invites extreme close-ups that I wouldn’t dare attempt with a rattlesnake or cottonmouth—at least not without a much longer lens than my 100mm. These photos make it seem that I was right on top of the snake, although at a maximum magnification of around 1:2 there was still a reasonable amount of working distance (I did, however, keep my hands well back of the front of the lens—just for good measure). Still, in all my copperhead experiences, I have never seen a copperhead actually try to strike unless I touched it (not what you think!).

Eventually it’d had enough of our gawking and began to look for new cover.  As it uncoiled, I could see it’s still greenish but not too yellowish tail, indicating that it was still a youngster, though perhaps a little older than the first copperhead I tried to photograph.  We watched it as it crawled into the loose, dry leaves… and disappeared.


Copyright © Ted C. MacRae 2011

Pardalophora phoenicoptera – Orange-winged grasshopper

For some reason, I’ve found myself increasingly fascinated with certain grasshoppers—not just any grasshoppers, but band-winged grasshoppers (family Acrididae, subfamily Oedepodinae).  And not just band-winged grasshoppers, but band-winged grasshopper nymphs.  It began last year when I found adults and nymphs of Trimerotropis latifasciata in the Glass Mountains of northwestern Oklahoma.  I believe it has something to do with the combination of their frequent association with the same habitats where I look for my beloved tiger beetles and their marvelously cryptic coloration.  Adults themselves are cryptic enough—that is, until they flash their brightly colored hind wings, but the nymphs are positively invisible until they move.  Moreover, many species show a wonderful range of intraspecific diversity in their crypsis—Ronald Reagan may have thought every redwood tree looked the same, but when you’ve seen one band-winged grasshopper nymph, you most certainly have not seen them all.


These two band-winged nymphs were seen at St. Joe State Park (St. Francois Co., Missouri) in the vast central “sand flats” of the park (actually waste areas of crushed limestone tailings left from lead mining operations during the previous century).  At first I assumed they each represented a different species, but based on comments at BugGuide I take both of them to represent Pardalophora phoenicoptera (orange-winged grasshopper)—distinguished from Xanthippus by having only one notch in the pronotal crest and unusual amongst most grasshoppers in that the winter is passed as a nymph rather than egg.  This leads to well-developed nymphs at the beginning of spring and adults much earlier in the season than many other grasshoppers.  These photos were taken on April 28, and the size of the wing pads suggests they are not quite full-grown yet, maybe 3rd or 4th instars.  Acridoid aficionado David J. Ferguson has found this species in the Ozarks on rocky/gravelly hilltops (e.g., “cedar glades”) and on gravelly or stable sandy slopes in sunny openings in Oklahoma. He places the species (particularly the green ones) high on his favorite hopper list, and I’d have to say I agree with him (so far).

One of these days, I’m going to find and photograph the king of all green oedepodines—Trimerotropis saxatilis!

Update 6/8/11: Dave Ferguson has kindly confirmed the ID, writing:

…yes these are identified correctly.  Assuming 5 instars, they look like 4th (where there are 6 instars, numbers 4 and 5 look a lot alike).

Copyright © Ted C. MacRae 2011

Litaneutria minor – agile ground mantid

Litaneutria minor - agile ground mantid

Have you ever seen a mantid that lives exclusively on the ground?  Most mantids are ambush predators, hiding amongst the bushes while patiently waiting for unsuspecting prey to happen within striking range.  However, a few small groups of mantids have adopted a different strategy – running down their prey!  One such group is the ground mantids, represented in the U.S. by two genera – Litaneutria and Yersiniops.  These small mantids, cryptically colored brown or gray, occur in desert and grassland habitats across the western U.S.  This particular individual was seen in the expansive shortgrass prairie atop the Pine Ridge in northwestern Nebraska.  The rounded eyes and brown coloration identify it as as a member of the genus Litaneutria (the tops of the eyes are pointed in Yersiniops, giving them a “horned” appearance, and they tend to be more gray).  Two species of Litaneutria are found in the U.S. – this one, L. minor, occurring broadly throughout the Great Plains and western U.S. into southwestern Canada (it is Canada’s only native mantid), while a second species, L. obscura, is restricted to the desert southwest.¹  Several common names have been applied to L. minor, including lesser ground mantid, minor ground mantid, and agile ground mantid.  While the first two represent more precise literal translations of the scientific name, I like the latter which well describes the ability of these mantids to hop over rocks and dart swiftly through sparse prairie vegetation in pursuit of prey or to evade predators (and inexperienced collectors!).  Despite its small size (total length less than 1.5″), the presence of wings – albeit small – indicate this is an adult. All females of this species are brachypterous (short-winged), but most males are as well.  However, males apparently have a small spot at the base of the forewings, which seems lacking in this individual, and a smoother pronotum – also not readily apparent in this individual, so I’m guessing that this is an adult female. 

¹ BugGuide and many other web sources list five additional U.S. species in the genus (including L. borealis, described from northwestern Nebraska).  However, Vickery and Kevan (1983) note that these were all synonymized under L. minor by Hebard in 1935 (sorry – I couldn’t find that reference).

“Mantid” vs. “mantis” vs. “praying mantis.”  It has become common to use the terms “mantid” and “mantis” (or even “praying mantis”) interchangeably.  However, in its strictest sense the term “mantis” is most properly applied to species of the genus Mantis – of which Mantis religiosa – the European mantid or praying mantis, introduced to the U.S. in the late 19th century (either accidentally on a shipment of nursery plants or deliberately for pest control – depending on the source) is the most widely recognized.  The term “mantid” refers to any species in the suborder Mantodea as a whole.

Carnivorous cockroaches!  When I was in college back in the late 1970s, mantids and most other “orthopteroid” insects had long been considered suborders of a single order, the Orthoptera.  Around that time began a great dismantling of the Orthoptera, pared down to only the grasshoppers, crickets, and katydids while the other former suborders (mantids, walkingsticks, cockroaches, etc.) were raised to full order status.  The walkingsticks (Phasmida), grylloblattids (Grylloblattodea), and gladiators (Mantophasmatodea) all continue to enjoy their elevated status (Tree of Life Web Project 2003); however, a close relationship has been established between the mantids, cockroaches, and termites² (Kristensen 1991), resulting in the sinking of all three former orders into a single order, the Dictyoptera (Tree of Life Web Project 2002) (and not to be confused with the lycid beetle genus Dictyoptera).  Mantids, thus, can be considered derived cockroaches with morphological specializations for predation!

² Long accorded an order of their own – the Isoptera, recent molecular phylogenetic studies have placed termites not only with the cockroaches, but within them (Ware et al. 2008).  Just as mantids can be considered cockroaches that evolved as predators, termites can be considered cockroaches that evolved to eat wood (with the help of cellulose-digesting gut symbionts)!

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

REFERENCES:

Kristensen, N. P. 1991. Phylogeny of extant hexapods. Pp. 125–140 in Insects of Australia: A Textbook for Students and Research Workers. Volume I and II. Second Edition. I. D. Naumann, P. B. Carne, J. F. Lawrence, E. S. Nielsen, J. P. Spradberry, R. W. Taylor, M. J. Whitten and M. J. Littlejohn eds. Carlton, Victoria, Melbourne University Press.

Tree of Life Web Project. 2002. Dictyoptera. Version 01 January 2002 (temporary). http://tolweb.org/Dictyoptera/8253/2002.01.01 in The Tree of Life Web Project, http://tolweb.org/

Tree of Life Web Project. 2003. Neoptera. Version 01 January 2003 (under construction). http://tolweb.org/Neoptera/8267/2003.01.01 in The Tree of Life Web Project, http://tolweb.org/

Vickery, V. R. and D. K. M. Kevan. 1983. A monograph of the orthopteroid insects of Canada and adjacent regions. Lyman Entomological Museum and Research Laboratory Memoir 13:216–237.

Ware, J. L., J. Litman, K.-D. Klass, and L. A. Spearman. 2008. Relationships among the major lineages of Dictyoptera: the effect of outgroup selection on dictyopteran tree topology. Systematic Entomology 33(3):429–450.

Copyright © Ted C. MacRae 2010

What’s more difficult to see…

…than a Trimerotropis latifasciata (broad-banded grasshopper) adult on lichen-encrusted clay exposures?


Answer: A T. latifasciata nymph on lichen-encrusted clay exposures.


My thanks to David J. Ferguson for confirming my initial ID as a species of Trimerotropis and provisionally placing these individuals as T. latifasciata.  Of course, I’m not at all an expert in grasshopper identification, but I recognized these individuals, found atop the red, flat-topped mesa of Gloss Mountain State Park in northwestern Oklahoma, for their great similarity to T. saxatilis (lichen grasshopper), a striking, more greenish species (at least here in Missouri) that I had hoped to but did not see during my visit to Lichen Glade Natural Area back in late May (it may have been too early in the season for them).  At first I thought these individuals might represent that species, considering the abundance of lichens that encrusted the clay exposures atop the mesa.  However, according to David the red hind tibia (seen in the photo below of a different adult – sans left front leg), longer wings, occurrence on clay (rather than rock or sand), and location in the Great Plains make T. latifasciata the most tenable choice.

Like T. saxatilis and other species of the genus, T. latifasciata provides a marvelous example of the use of camouflage (i.e., blending in with surroundings) – a form of crypsis – to avoid detection by predators.  Finding this species only strengthens my desire to find (and photograph) T. saxatilis – speckled green, white and black – amidst the green lichens that encrust the red igneous outcroppings of the St. Francois Mountains some 100 miles south of St. Louis.

Photo Details: Canon 50D w/ 100mm macro lens, (ISO 100, 1/250 sec, f/18-20, Canon MT-24EX flash (1/4 ratio) w/ Sto-Fen diffusers, and typical post-processing (levels, minor cropping, unsharp mask).

Copyright © Ted C. MacRae 2010

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An irresistible sight!

One of the few highlights of my Memorial Day weekend collecting trip came in the earliest moments of my visit to Ha Ha Tonka State Park.  My destination was Ha Ha Tonka Savanna Natural Area, and a short walk through fire-restored woodland led me to the open glade where just a few years earlier a UMC student had collected the rare and little-known Agrilus impexus.  Entering the glade, I was all set to begin sweeping the vegetation along the woodland/glade interface, paying special attention to any honey locust (Gleditsia triacanthos) that I might happen to find in the area as a potential host for the beetle.  What I saw instead as the glade opened up in front of me was a sight that any collector of wood-boring beetles will find almost irresistable – a recent wind-throw!  In this case, it was a black oak (Quercus velutina) laying in full sun – its bright brown leaves suggesting that it had fallen within the past few weeks (and would thus still be emitting the volatiles that wood-boring beetles find so attractive).  I wanted to begin looking for A. impexus, but I knew there would be beetles actively crawling on the trunk and branches of that tree.  I couldn’t resist it – I dropped my sweep net and beating sheet and made my way to the tree (in the end it didn’t matter, since no other beetles – including A. impexus – would be seen that day).

I already had an idea what I might find.  Recent wind-throws are the domain of Chrysobothris, and if the tree is a deciduous species then this means members of the Chrysobothris femorata species-group.  I recently featured one of six newly described members (C. caddo) of this taxonomically challenging group (Wellso and Manley 2007), providing a synopsis of the now twelve species in the group and their primarily host preferences.  Fully half of these are associated primarily or exclusively with oaks four occurring in Missouri (quadriimpressarugosiceps, shawnee, and viridiceps).  Of these, C. quadriimpressa is the most commonly encountered (although the others are by no means uncommon), and all of the nearly dozen or so beetles I found on this particular tree in fact represented that species. Confirmation of my ID would require microscopic examination of the female pygidium (which is shallowly impressed on each side of the middle) and male genitalia, but in general this species can be distinguished in the field by its smallish size (~10-12 mm in length – rugosiceps and shawnee tend to be larger) and the post-median pair of foveae (circular impressions) on the elytra being joined (they are distinctly separated in viridiceps).

As we’ve seen with other species of jewel beetles (e.g., C. caddo, Dicerca lurida, D. obscura), adults of C. quadriimpressa are incredibly cryptic and nearly impossible to see on the bark of their hosts – at least until they move.  They are notoriously difficult to approach – their large eyes and penchant for rapid escape flights suggesting excellent vision.  This is a useful capability for insects that must expose themselves to would-be predators (and beetle collectors) during daylight hours while actively searching dead trees for mates and oviposition sites.  One thing I can’t figure out, however, is the role of the intensely blue feet in this and other cryptically colored Chrysobothris species (see also C. caddo).  Any ideas?

Photo Details (insect): Canon 50D (ISO 100, 1/250 sec, f/16), Canon 100mm macro lens w/ Kenco extension tubes (68mm), Canon MT-24EX flash (1/4 ratio) w/ Sto-Fen diffusers.  Post-processing: levels, unsharp mask, minimal cropping.

REFERENCES:

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

Copyright © Ted C. MacRae 2010

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The Marvelously Cryptic Dicerca lurida

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

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

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

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

REFERENCE:

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

Copyright © Ted C. MacRae 2010

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The Moth and Me #11

The Moth and MeWelcome to issue #11 of The Moth and Me, the monthly carnival devoted to the “forgotten” lepidopterans. Most people – even entomologists – regard these as the lesser leps, denizens of the night, as if to hide their somber-colored drabness from the flashy brilliance of their rhopaloceran relatives. Of course, this simply isn’t true, as the contributions to this month’s issue well demonstrate. Butterflies may be among the largest insects on earth, but the largest lepidopteran in the world is a moth. They may also be as gaudily colored as the rainbow itself, but what butterfly is more colorful than the Urania day-flying moths (the genus name literally means, “The heavenly one”).   And, they may be almost universally accepted by a largely insect-indifferent public, but who among us does not think back to that first sight of a luna moth as the most stunning insect we had ever seen to that point.  Yes, moths are all that butterflies are, and for this month’s issue of TMaM, 15 contributions by nine writer’s show us why.

Family Saturniidae – Giant Silkworm & Royal Moths

Tales from the Butterfly Garden: LepcuriousLuna moths belong to the royal moths of the family Saturniidae, and as the name implies they are not the only stunningly beautiful member of the group. Kristen at Tales from the Butterfly Garden: Lepcurious writes about an encounter with the Sweetbay Silkmoth (Callosamia securifera).  Like other members of the family, larvae of this species are rather particular about the type of tree that they utilize for food, which in the case of this moth is sweetbay (Magnolia virginiana).  I’m a little too far north here in Missouri for this tree, so I have never seen this moth.  However, I have seen (and reared) some of its close relatives, the Promethia Silkmoth (Callosamia promethea) which hosts on several plant species and the Tulip-tree Silkmoth (Callosamia angulifera) which hosts on Tulip Tree (Liliodendron tulipifera).

Family Zygaenidae – Leaf Skeletonizer Moths

xenogereJason Hogle at xenogere is fond of the unusual and has a gift for finding it. In his post The Unmoth, Jason shows us a male grapeleaf skeletonizer (Harrisina americana) – not your typical moth!, The uniformly black color and bright red neck collar just screams “Don’t eat me – I’m poisonous”, and indeed species in this family are among the few insects capable of producing hydrogen cyanide!  As the name suggests, larvae skeletonize the leaves of both wild and cultivated grapes (Vitis spp.), as well as the related Virginia creeper (Parthenocissus quinquefolia).

Family Noctuidae – Noctuid Moths & Tiger Moths

Tales from the Butterfly Garden: LepcuriousRoyal moths are not the only stunningly colored moths that Kristen at Tales from the Butterfly Garden: Lepcurious has found in Florida, as she shows in this post on Oleander Moths (Syntomeida epilais) and a companion piece on its Oleander host plant.  This striking day-active moth, also called Uncle Sam Moth (for its red, white, and blue colors) and Polka-Dot Wasp Moth (for obvious reasons), may seem like an easy-to-spot target for would be predators, but its gaudiness is actually warning of the toxic chemicals it has sequestered in its body from the Oleander on which it fed as a larva.  Oleander contains the toxins oleandrin, a cardiac glycoside, and neandrin and is toxic if ingested.  Although oleander is an Old World exotic, oleander moths may also be found feeding on devil’s potato vine (Echites umbellata), which may have been their native Florida host before the introduction of oleander to the United States.

See TrailAside from the underwings (genus Catacola) and the recently incorporated tiger moths, Noctuids are typically thought of as the “basic brown moths” – relying on just the aforementioned groups to add a splash of color to the family’s otherwise drearyness.  Nothing could be further from the truth – check out the stunning Eight-spotted Forester (Alypia octomaculata) in this post by Matthew York at See Trail. Larvae of this beautiful little moth feed on ampelopsis, Virginia creeper, and other plants in the grape family (similar to the grape leaf skeletonizer above). “A great moth; brilliant color, diurnal…… and yes… Noctuid. Some moths, like people, don’t go with the trends.”

See TrailFor the most part, tiger moths shun the daytime in preference for the safety of the night. That does not mean, however, that they are any less colorful, as Matthew York at See Trail shows in his post Poor Grammia. Notarctia proxima, the Mexican Tiger Moth, and its relatives have had a bit of name shuffling over the years at the hands of taxonomists – formerly placed in the genera Grammia and Apantesis. Whatever name you call it, the striking white and black striped forewings give a clue about their common name of tiger moths, and the red, black-tipped abdomen not only add to its beauty, but belies the defensive compounds it surely contains.

Speaking of tiger moths and defensive compounds, watch the video that Chris Grinter at The Skeptical Moth included in his post Moth Perfume. In it, Chetone angulosa gives a striking display of a common defensive mechanism for the group – excreting hemolymph (sweating blood, so to speak!). So spectacularly does the moth do this that you can actually hear the hissing sound of the fluid being pumped from the body. Moreover, there seem to be at least a couple of active ingredients in the froth – one that smells like peppermint, and another that causes numbing of the tongue (as Chris can testify firsthand – he is a truly dedicated experimental naturalist!).

Karthik's JournalIn similar fashion to our North American species of underwing moths (Catocola spp.), the related Eudocima materna, one of the fruit-sucking moths of south India, uses its drab-colored forewings to hide its brilliantly colored hindwings, as Karthik at Karthik’s Journal shows us in his post Startling Displays.  This forms a double line of defense against would-be predators – the forewings blend marvelously into the color of the tree trunks upon which it rests during the day, camouflaging the insect and making it nearly invisible.  If this doesn’t work, a sudden flash of the hindwings may startle the predator just enough to allow the moth to take flight to another tree – where it instantly “disappears” as soon as it closes its wings.

Snails Eye ViewAustralia also has some very colorful fruit-piercing moths, and Bronwen Scott at Snails Eye View presents some beautiful photos of the particularly strikingly-colored Othreis iridescens. Like other members of the group, this Far North Queensland endemic feeds on fruit (Pycnarrhena novoguineensis and Hypserpa laurina, both Menispermaceae, in the case of this species), but as it is apparently the rarest of the primary fruitpiercing moth species in Australia it is not considered to be a pest (and Bronwen would cut it some slack even if it was!).

EntophileAdults are but only one of four life stages that all moths go through. If moths are the “forgotten” leps, then caterpillars are the “forgotten” moths. In many cases, the caterpillar stage cannot be recognized until it becomes a moth (and in some cases the caterpillars are completely unknown). Fortunately, Navy entomologist corycampora at Entophile recognized the caterpillar he found on his croton bush, which he features in the post Croton caterpillar, Achaea janata (Linnaeus), (Lepidoptera: Noctuidae). These “eating machines” can be just as fascinating to observe as their scaled adult counterparts, and while croton seems to be a preferred host in Hawaii, it apparently also feeds on castor beans (judging by its other common name, Castor Oil Semi-looper).

Family Notodontidae – Prominent Moths

the Marvelous in NatureOften dismissed as noctuids, the prominent moths tend to be fuzzier, more thickly-bodied moths that rest with their wings curled around their abdomen or tented over their back (rather than flat like noctuids and most other moths). TMaM organizer Seabrooke Leckie at the Marvelous in Nature has a love affair with prominents, and in her post Georgian Prominent, she features the nicely thick-bodied and fuzzy Georgian Prominent, Hyperaeschra georgica. The caterpillars of this widespread species feed on oak (Quercus spp.), thus, unless you live in the Pacific Northwest you stand a good chance of encountering this species – if you’re you’re willing to make the effort.

Family Psychidae – Bagworm Moths

xenogereMany of us are probably familiar with the evergreen bagworm moth (Thyridopteryx ephemeraeformis), whose large, cone-shaped bags almost look like fruit hanging from the evergreen bushes on which the caterpillars feed. But did you know there are other species of bagworms as well? Jason Hogle at xenogere does, and he compares and contrasts two of them in this duo of posts, Rainy day on the patio and The Other Bagworm. One huge and prominent, the other (Dahlica triquetrella) very small and oft unseen. One with all manner of plant matter stuck to its bag, the other usually mistaken for small bits of dirt or wood. Jason is so good, he can even determine the sex of the caterpillar inside the bag!

Family Sphingidae – Hawk Moths

Roundtop RumingsCarolyn at Roundtop Rumings is hoping that somebody can Name this moth, which she found on the door of her cabin in the forests of Pennsylvania. Don’t let her inability to name this moth fool you, however, for her post contains loads of information on exactly the kinds of characters one should take note of when trying to identify hawk moths. Large size and membership in a popularly studied group aren’t enough – what do the hindwings look like? Are there any spots on the abdomen? As a coleopterist, I hesitate to offer my relatively uninformed opinion on the exact genus and species for this moth, but I’m going to go out on a limb here and suggest maybe something in the genus Ceratomia, perhaps the waved sphinx (C. undulosa)?


I hope you have enjoyed this issue of The Moth and Me, and my sincere thanks go out to all of those who contributed!  The hosting slot for next month’s issue of TMaM is still open, but you can submit your contributions anyway to Seabrooke Leckie at the home site for inclusion in the June 2010 issue once a host is selected.  The submission deadline is June 13, with the issue appearing a few days later.  Perhaps you might like to host the June issue – hosting is not only fun, but also a great way to introduce readers to your site and generate a little traffic.  Contact Seabrooke at the home site if you’re interested – I’m sure she would love to hear from you.

Copyright © Ted C. MacRae 2010

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BitB Best of 2009

In my first post of 2009, I looked back at the photographs I had posted during 2008 and picked some of my personal favorites. I hesitated then to call myself a photographer (and still do), but I at least now have suitable equipment to aid in my progress toward that eventual goal. I have learned much over the past six months in my first attempt at serious insect macrophotography (prioritizing in situ field photographs of unmanipulated subjects as a matter of personal choice).  Through this, I’ve come to realize the following skills to be the most important for success:  

  1. Composition
  2. Understanding lighting
  3. Knowing how to use a flash
  4. Knowledge of the subject

I’ll give myself a “A” in the last of these, but in the other areas I still have much to learn. With this caveat, and for the last post of 2009, I offer the following twelve photographs as my final choices for the 2nd Annual “Best of BitB”:  

Best beetle

Cylindera celeripes (swift tiger beetle), Woodward Co., Oklahoma

From Revisiting the Swift Tiger Beetle – Part 1 (June 30).  A decent enough photograph, especially considering that I’d had my camera for about a month when I took it.  However, the discovery of robust populations of this formerly rare and enigmatic species throughout northwestern Oklahoma (and later also in northwestern Missouri) was the most significant find of the 2009 field season, and this photograph is the best capture of that moment.

Best fly

Stylogaster neglecta, a species of thickheaded fly

From Overlooked, needle-bellied, thick-headed fly (Aug 14).  One of my first good “black background” shots.  The white tip of the abdomen compliments the white flower stamens against the background.

Best “true” bug

Beameria venosa, a prairie obligate cicada

From North America’s smallest cicada (Aug 4).  So many different shades of green with white frosting on the bug’s body.  I tried taking this shot in portrait and it just didn’t work—I liked this landscape shot much better.

Best predator

Promachus hinei (Hines giant robber fly) & Ceratina sp. (small carpenter bee) prey

From Prey bee mine (Sept 14).  Robber flies are immensely photogenic, especially those in the genus Promachus due to their prominent “beards.”

Best camoflauge

Dicerca obscura on bark of dead persimmon

From The “obscure” Dicerca (June 19).  Sparkling and gaudy as specimens in a cabinet, the coloration of many jewel beetles actually helps them blend almost perfectly with the bark of their preferred tree hosts.

Best immature insect

Tetracha floridana (Florida metallic tiger beetle) 3rd-instar larva

From Anatomy of a Tiger Beetle Larva (Oct 22).  “Otherwordly” is invariably the first word that comes to mind when someone sees a tiger beetle larva for the first time.  I was lucky enough to get this one in profile with a nice view of its abdominal hump and its curious hooks.

Best arachnid

Centruroides vittatus (striped bark scorpion)

From A face only a mother could love (Oct 6).  Despite some minor depth-of-field problems with this photograph, I’m fascinated by its “smile.”

Best reptile

Eastern collared lizard (Crotaphytus collaris collaris) adult male

From North America’s most beautiful lizard (July 10).  A simply spectacular lizard—all I had to do was frame it well and get the flash right.

Best wildflower

Spiranthes magnicamporum (Great Plains ladies

From Great Plains Ladies’-tresses (Dec 7).  Few flowers are as photogenic as orchids, even native terrestrials with minute flowers such as this one.  I like the frosty texture of the lip and the starkness of the white flower on the black background.

Best natural history moment

Thermoregulatory behavior by Ellipsoptera hirtilabris (moustached tiger beetle)

From Tiger Beetles Agree—It’s Hot in Florida! (Dec 18). I chose this photo for the classic “stilting” and “sun-facing” thermoregulatory behaviors exhibited by this tiger beetle on a blistering hot day in Florida.

Best closeup

Megaphasma denticrus (giant walkingstick)

From North America’s longest insect (Aug 21).  I haven’t tried a whole lot of super close-up photographs yet.  I liked the combination of blue and brown colors on the black background.

Best Landscape

Sand Harbor Overlook, Lake Tahoe, Nevada

From Sand Harbor Overlook, Nevada (March 23).   My choice for “best landscape” again comes from Lake Tahoe.  This is not a great photo technically—I was still using a point-and-shoot and had to deal with foreground sun.  However, none of the other photos I took during my March visit to the area captivate me like this one.  I like the mix of colors with the silhouetted appearance of the trees on the point.

Copyright © Ted C. MacRae 2009

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