Saturday, October 14, 2017

The Taxonomy Fail Index: a Proposed Modification

In 2010, the ever-prolific ant photographer and notable myrmecologist Alex Wild proposed the Taxonomy Fail Index to quantify error in the identification of organisms. He was inspired by the apparently commonplace idea that cochineal dye is derived from beetles, which, to paraphrase a Krutabulon saying, is total gorgon frass*. Wild proposed the following formula: TFI (Taxonomy Fail Index)=T/H, where T=the period of time since the last common ancestor of organisms A (actual taxon of organism in question) and B (taxon as which the organism in question has been misidentified) lived, and H=period of time since the last common ancestor of humans (Homo sapiens) and chimps (Pan spp.) lived. 

In other words: 
... the Taxonomy Fail Index scales the amount of error in absolute time against the error of misidentifying a human with a chimp. (Wild, 2010)
The periods of time in question are estimated from TimeTree. Of course, these data (compiled from multiple sources) are subject to revision, hence the divergence between Homo and Pan as an anchor: regardless of changes in divergence dating, the error of identifying Sarah Palin as a bonobo (to use Wild's example) will always have a magnitude of 1.0, barring revision to hominid systematics.

The limitation of the TFI, as I see it, is that it provides no means of communicating relative error. The TFI of mistaking a honey bee for a hornet, for example, is 24.4: a number that is uninformative in and of itself. One can contextualize this error's magnitude by saying that it is slightly more stupid than mistaking an opossum for a cat (TFI=23.9), as Alex Wild did, but I would prefer to scale the TFI in some fashion. 

To do so, I calculated the TFI of the most egregious possible Taxonomy Fail: conflating organisms at opposite ends of life's phylogenetic tree. My exemplar was the TFI of identifying Streptococcus sp. as a human being. This comes out to 645.1. The domain Bacteria (Woese et al., 1990) to which Streptococcus belongs is regarded as the sister group of the remaining two domains (Ciccarelli et al., 2006), one of which includes H. sapiens. Theoretically, then, as there is no higher taxonomic rank than that of the domain, 645.1 is the highest possible TFI (barring revision of our notions of life's fundamental phylogeny, which appears improbable at this point). As such, I choose to calibrate the entire Taxonomy Fail Index to the above value. 

Shinkaiya lindsayi (Lecroq et al., 2008), a xenophyophore
One could divide this value by 100, each unit on this Taxonomy Fail Scale being a Wild. Thus, misidentifying any bacterium as any eukaryote or vice versa equals 100 Wilds on the TFS. Therefore, a single Wild equals a TFI magnitude of 645.1/100=6.45. 

With the TFS, we can not only calculate taxonomic error, but provide an inherent comparison between these calculations. To wit: identifying Sarah Palin (or any politician) as a bonobo, or identifying a bonobo as a politician, amounts to 0.155 Wilds on the TFS. For comparison, classifying a xenophyophore (a derived group of gargantuan foraminiferans; Pawlowski et al., 2003) as a sponge (Haeckel, 1889) equals 38.7 Wilds on the the TFS, making this identification one of Ernst Haeckel's more profound mistakes and perhaps the greatest Taxonomy Fail ever to be published under peer review. 

A Megalopyge sp. larva from Peru (Phil Torres), engaging in Muellerian mimicry of Trump's hair
The implications for public discourse are profound: for one thing, misidentifying a megalopygid caterpillar as Donald Trump's hair (18.6 Wilds) is roughly 2 times less erroneous than calling a xenophyophore a sponge.

*A turn of phrase that presupposes gorgons are herbivorous.

Ciccarelli, F. D.; Doerks, T.; von Mering, C.; Creevey, C. J.; Snel, B.; and Bork, P. (2006). Toward Automatic Reconstruction of a Highly Resolved Tree of Life. Science, 311(5765), 1283-1287.

Haeckel, E. (1889). Report on the deep-sea Keratosa. Report on the scientific results of the voyage of H. M. S. Challenger during the years 1873-76. Zoology, 32 (pt. 82), 1-92. 

Lecroq, B.; Gooday, A. J.; Tsuchiya, M.; and Pawlowski, J. (2008). A new genus of xenophyophores (Foraminifera) from Japan Trench: morphological description, molecular
phylogeny and elemental analysis. Zoological Journal of the Linnean Society, 156, 455-464.

Pawlowski, J.; Holzmann, M.; Fahrni, J.; and Richardson, S. L. (2003). Small subunit ribosomal DNA suggests that the xenophyophorean Syringammina corbicula is a foraminiferan. Journal of Eukaryotic Microbiology, 50, 483-487.

Wild, A. (September 9, 2010). The Taxonomy Fail Index. Retrieved 10/13/17 from

Woese, C.; Kandler, O.; and Wheelis, M. L. (1990). Towards a natural system of organisms: proposal for the domains Archaea, Bacteria, and Eucarya. Proceedings of the National Academy of Sciences of the United States of America, 87, 4576-4579. 

Wednesday, September 20, 2017

A "Little Bag of Horror" from the Cretaceous

Of the things that are unlikely to be preserved in the fossil record, the larvae of insects with complete metamorphosis are high on the list. Usually extremely soft-bodied and (it almost goes without saying) small, even their appearance in amber (a medium conducive to the preservation of the small and soft) is rare. An additional taphonomic bias (one that affects the entire fossil record) exists against insect larvae that are not aquatic. So, the description of a fossil larva that is not, say, a Mesozoic fishfly (Corydalidae: Chauliodinae) (of which multiple specimens are known; Liu et al., 2012) is cause for excitement.

Fourth-instar rhopalosomatid larva of unknown genus (Lohrmann & Engel, 2017)
Thus, the news of an indisputable rhopalosomatid larva from Burmese amber (Lohrmann & Engel, 2017) is a cause for excitement. In my case, this is due more to its familial affiliation than its mere identity as an insect larva. You may recall my mention of the Rhopalosomatidae (a small family of aculeate wasps, now one of the two families constituting the Vespoidea sensu stricto;) in the inaugural post of Life, et al.: specifically, I drew attention to the oddity of their ectoparasitoid larvae (which, where known, attack crickets [Gryllidae]), which retain multiple instars' worth of molted exuviae, thus forming a protective snakeskin-like sack (Lohrmann & Engel, 2017). This "little bag of horror", as I termed it, was described in detail by Gurney (1953) in the case of Rhopalosoma nearcticum, the egg of which is characteristically placed behind the host's metacoxa, with the larva being positioned thereupon until pupation (see photographs above and below). The cricket host appears to not give that much of a frass about its terminal situation, as mating is unaffected by the presence of the immature parasite (Alexander and Otte, 1967).

The amber inclusion of an unmistakable fourth-instar rhopalosomatid larva, described in situ behind a cricket's hind leg (Gryllidae; it cannot be identified beyond familial level), is a "confluence of rarities" (Lohrmann & Engel, 2017).  Rhopalosomatids are rare in the fossil record, with only four fossil species having been described; of these, only Eorhopalosoma gorgyra from Burmese amber can be confidently assigned to the family (Engel, 2008). (The other three are compression fossils.) Additionally, hosts of the order to which rhopalosomatids' cricket hosts belong (the Orthoptera) are only rarely preserved in amber (Heads, 2009).

View of rhopalosomatid larva's left side and cricket's underside (Lorhmann & Engel, 2017)
The larva's exquisite preservation reveals that it is in all visible respects indistinguishable from the larva of R. nearcticum, as described by Gurney (1953). Since no other rhopalosomatid larvae have been described (Olixon australiae was reared to adulthood but never described as a larva; Perkins, 1908), however, it would be premature to identify it as a member of this New World species.

Regardless of the specimen's generic identity, it is remarkable that rhopalosomatids' niche, and concomitant morphology, has seemingly changed so little in 98 million years. 


Alexander, R. D. and Otte, D. (1967). Cannibalism during copulation of the brown bush cricket, Hapithus agitator (Gryllidae). Florida Entomologist, 50, 79-87.

Branstetter, M. G.; Danforth, B. N.; Pitts, J. P.; Faircloth, B. C.; Ward, P. S.; Buffington, M. L.; Gates, M. W.; Kula, R. R.; and Brady, S. G. (2017). Phylogenomic Insights into the Evolution of Stinging Wasps and the Origins of Ants and Bees. Current Biology, 27(7), 1019-1025. DOI:

Engel, M. S. (2008). The wasp family Rhopalosomatidae in mid-Cretaceous amber from Myanmar (Hymenoptera: Vespoidea). Journal of the Kansas Entomological Society, 81, 168-164.

Gurney, A. B. (1953). Notes on the biology and immature stages of a cricket parasite of the genus Rhopalosoma. Proceedings of the United States National Museum, 103, 19-34.

Heads, S. W. (2009). A new pygmy mole cricket in Cretaceous amber from Burma (Orthoptera: Tridactylidae). Denisia, 26, 75-82.

Liu, X.; Wang, Y.; Shih, C.; Ren, D.; and Yang, D. (2012). Early Evolution and Historical Biogeography of Fishflies (Megaloptera: Chauliodinae): Implications from a Phylogeny Combining Fossil and Extant Taxa. PLoS One, 7(7), e40345. Retrieved 9/17/17 from

Lorhmann, V. and Engel, M. S. (2017). The wasp larva's last supper: 100 million years of evolutionary stasis in the larval development of rhopalosomatid wasps. Fossil Record, 20, 239-244. Retrieved 9/16/17 from

Perkins, R. C. L. (1908). Some remarkable Australian Hymenoptera. Proceedings of the Hawaiian Entomological Society, 2, 27-35. 

Thursday, July 27, 2017

Three New Orders of Insecta in Burmese Amber: is this Really Necessary?
Prokoenenia wheeleri (Palpigradi: Prokoeneniidae) from Texas; attribution shown
For the past two decades, the amber deposits of the Hukawng Valley in Myanmar's Kachin State have been intensely scrutinized by paleoentomologists. The burmite recovered from this locale dates to the very end of the Cenomanian Stage (98.79 mya; Shi et al., 2012). Containing everything from what is by far the oldest known specimen of the flagrantly obscure arachnid order Palpigradi (largely the same as its modern counterparts; Engel et al., 2016) to uniquely specialized haidomyrmecine ants (weirdly unlike any of their modern counterparts; Perrichot et al., 2016), it is a treasure trove of exquisite Cretaceous microfaunal data.

Just within the past year and a half, three (count 'em, three) new insect orders have been described from Hukawng Valley burmite: namely, the Alienoptera (Bai et al., 2017), Aethiocarenodea (Poinar & Brown, 2017), and Tarachoptera (Mey et al., 2017). (And this is not even to mention the Permopsocida, an order that was established for Permian-Cretaceous insect taxa after the description of a specimen from the Hukawng Valley; Huang et al., 2016). After we pick our collective mandibles up off the floor, we should consider each of these taxa in turn: are their ordinal statuses truly defensible? Or, perhaps, are these better regarded as stem-groups of extant taxa?

Kinitocelis divisinotata, holotype (adult female)
First off, the Tarachoptera. This order consists of two genera, both placed in the Tarachocelidae. This peculiar family is clearly a member of the superorder Amphiesmenoptera, a clade consisting of the extant orders Lepidoptera (moths, and the diurnal moths we call "butterflies") and Trichoptera (caddisflies); of the 14 autapomorphic* amphiesmenopteran characters listed by Kristensen (1984) that are applicable to adult amber inclusions, only 3 are incontrovertibly absent from the Tarachocelidae (for what it's worth, paired setose pronotal warts, setose sclerites below or behind the metathoracic subalare, and rod-like apodemes on the eighth and ninth female abdominal segments; Mey et al., 2017).

Wing scales of Kinitocelis brevicostata (Tarachoptera: Tarachocelidae)
However, the unassuming, mandibulate-moth-like tarachocelids cannot be placed in either extant order of the Amphiesmenoptera. They possess scales on their wings, reminding one of the Lepidoptera; but this resemblance appears to be a superficial convergence, as some trichopterans have developed scale independently of their origin in the Lepidoptera (Huxley & Barnard, 1988)—meaning that it is plausible that scales could emerge independently as well in the Tarachocelidae (Mey et al., 2017). Conversely, the specialized haustellum (proboscis) and single nygma on the forewing characteristic of the Trichoptera are conspicuously lacking in all examined tarachocelid specimens (Mey et al., 2017). 

Head profiles of basal trichopterans and lepidopterans (23-24) and K. brevicostata (Tarachoptera; 25)
In short, not only can the Tarachocelidae not be placed in any extant order, but they also cannot be incontrovertibly judged more closely related to either of the extant amphiesmenopteran orders than to the other. One could say that the Tarachoptera are like what the most primitive Amphiesmenoptera would have been, were it not for some peculiar derived traits of their own: among these are vestigial maxillary palpi (quite unlike the functional examples in the basalmost moths and caddisflies—see above); a single medial wing vein (otherwise known from insects only in the monotypic glossatan moth family Aenigmatineidae, thus far described only from Australia's Kangaroo Island; Kristensen et al., 2014); and the absence of tibial spurs, which with the exception of a few odd lepidopterans are a universal feature of insects with complete metamorphosis. Since tibial spurs are involved in launching adult insects into flight (Burrows & Durosenko, 2015), tarachocelids' lack of them suggests that their flying capability was limited.

While eccentric autapomorphies juxtaposed with basal traits amount to a syndrome typical of stem-groups all across the tree of life, the fact that one cannot argue that Tarachocelidae is more closely akin to either the Trichoptera or Lepidoptera leads me to agree that one could parsimoniously grant the Tarachoptera ordinal rank. However, whether this is necessary is another question.

Type specimen of Aethiocarenus burmanicus
Unlike the Tarachoptera, the Aethiocarenodea were described based on a single species, Aethiocarenus burmanicus. A. burmanicus is known from a single adult female specimen, and is like nothing else on Earth: a small, wingless, flattened insect, with a narrow corpus and a triangular head with its hypotenuse situated opposite to its articulation with the thorax—a condition quite unlike the head of any other insect, extant or otherwise. The head is strongly hypognathous§ (see below), making for a distinctive profile. Adding an additional memorable trait to this already memorable habitus, a pair of apparently secretory glands were situated on the back of the neck (presumably defensive in function) (Poinar & Brown, 2017).

Profile of A. burmanicus holotype head
What do we make of this creature, taxonomically speaking? Very little, judging from Poinar & Brown (2017), who do not speculate on its phylogeny nor even bother to assign it provisionally to any subdivision of the Insecta. The presence of cerci would exclude it from the clade Acercaria (Hemiptera, Psocodea, etc.; Huang et al., 2016) and from those insect superorders that practice complete metamorphosis (e.g., the Amphiesmenoptera), leaving the only possible assignment for the Aethiocarenodea as the Polyneoptera. This assemblage may or may not be monophyletic (Beutel et al., 2013), and there is little basis for direct comparison of the Aethiocarenodea with its fellow members; all fourth tarsomeres extend distally beneath the respective fifth tarsomeres, which Poinar & Brown (2017) note vaguely recalls the tarsal condition of some Dermaptera (earwigs). We thus remain at a loss for valid comparisons to situate the Aethiocarenodea in the insect family tree. However, as argued by Christopher Taylor (rather more eloquently than I could put it), this does not necessarily warrant ordinal status: to place A. burmanicus in its own order is more an admission of ignorance than anything else.

By contrast, the (again monotypic) Alienoptera are clearly akin to mantises (Mantodea). Described from a single male specimen of Alienopterus brachyelytrus (Bai et al., 2016), the taxon is a creature with a triangular head and bristly profemora not unlike those of the most ancient mantids. While most of the features that define the Dictyoptera (cockroaches, termites, and mantises) cannot be falsified on the specimen of A. brachyelytrus, the presence of a profemoral brush (otherwise unique to the Mantodea) and excellently preserved genitalia clinch its classification therein.

Alienopterus brachyelytrus: enlarged arolia, tegmina, and orthognathous head are all visible
The Alienoptera can be distinguished from the Mantodea mainly on the basis of two peculiar characters: greatly shortened, sclerotized forewings analogous to those for which the Dermaptera are named, and utterly unlike anything observed in any Mantodea; and enlarged arolia|| reminiscent of those exhibited by the rockcrawlers (Mantophasmatodea) (Beutel & Gorb, 2008). Mantises, conversely, lack arolia (with the possible exception of the extinct Santanmantis). More conspicuously, the Alienoptera do not have the raptorial forelegs for which all mantises living and extinct are known (Wieland, 2013); the vestiture of the profemora would not have worked in opposition to tibial spines as it would in mantises' case.

Most of these traits are "retained ancestral conditions", since the ancestral dictyopteran presumably also lacked protibial spines and retained arolia; the "array of specialized [alienopteran] features" (autapomorphies, to use phylogenetic jargon) consist only of a saddle-shaped pronotum and earwig-like tegmina. Bai et al. (2016) exclude the species from the Mantodea proper, and reasonably so, but does this justify erecting a new order for the taxon?

In my opinion, no. To begin with, a strict consensus tree using 58 morphological characters firmly placed Al. brachyelytrus as the sister group to the Mantodea (Bai et al., 2016). Even the 30% of this male specimen's genitalia that is visible, a suite of body parts that Bai et al. (2016) duly note have evolutionary plasticity to a degree that they may differ even within the same order (Klass, 1997), "fully conform to the condition within" mantises. Moreover, the characters that exclude Al. brachyelytrus from the Mantodea are mostly "retained ancestral conditions", making this mantodean sister-group not a mantis by dint of lacking derived mantodean traits.  

Al. brachelytrus is as such not excluded from the Mantodea because it has closer kin elsewhere, but because it lacks some (but not all) of the derived traits that define that order: the status of the Alienoptera is thus contingent upon how broadly one wishes to spread the definition of the Mantodea. The bounds of that definitionwhere a basal dictyopteran more closely related to mantises than to any other extant taxon becomes itself a "mantis"are subjective.
Nymph and adult of Cryptocercus punctulatus (Cryptocercidae); photograph by David R. Maddison
For comparison, consider the cockroach family Cryptocercidae. Being subsocial wood-feeders dependent upon oxymonadids and hypermastigids in their hindguts for cellulose digestion, these cockroaches bear an obvious biological and morphological resemblance to termites, and are regarded as the sister-group of the infraorder Isoptera (Engel et al., 2009). With the exception of adult winglessness (an apomorphy), the features that distinguish the Cryptocercidae from termites are basal conditions with respect to the Isoptera: e.g., an ootheca (egg-case; vestigial or absent in termites). One could simply say, therefore, that cryptocercids are stem-group termites: we only call them "cockroaches" due to the convenience of that term. Likewise, one can either refer to Alienoptera as a mantodean stem-group, or as its own order. Arguably, neither position is "false", and so ordinal ranking is a matter of preference: of whether one chooses to lump or to split. And I, personally, would advocate that personal preference does not a new order make.
Bornean Metallyticus splendidus (Metallyticidae); photographed by Paul
On a tangent, given the clear anatomical gulf between cryptocercids and even the most basal known termite (Cratomastotermes wolfschwenningeri, a mid-Cretaceous Brazilian specimen classified in its own family; Engel et al, 2009), one could argue that an analogy between this systematic situation and that of the Alienoptera with respect to the Mantodea is stretching things a bit. However, given that the ancestral ethological condition of the Mantodea was that of prowlers on or under bark (Wieland, 2010; the metallyticid shown retains this basal niche), unlike the clearly foliage-abiding Al. brachyelytrus (Bai et al., 2016), there certainly was an ecological distinction between that insect and contemporary mantises.

In conclusion, I think that of the Alienoptera, Aethiocarenodea, and Tarachoptera, only the latter order is truly deserving of that rank, given the information now available. However, I admit that further data could lend support to the Aethiocarenodea: I think that a comprehensive search of other Cretaceous ambers for kin to this enigmatic little creature is in order. 

*A derived trait unique to a particular taxon.
A sclerite immediately adjacent to the base of the insect wing, providing a place of attachment to the pleural wing muscle.
Ingrowths of the exoskeleton, serving as attachments for muscles.
§With downward-directed mandibles.
||An unsegmented lobe extending from the tip of the insect tarsus, situated between the tarsal claws.
A derived trait (with reference to its ancestral state) in a particular taxon, but not one necessarily unique to that taxon.

Bai, M.; Beutel, R. G.; Klass, K.-D.; Zhang, W.; Yang, X.; and Wipfler, B. (2016). Alienoptera — a new insect order in the roach–mantodean twilight zone. Gondwana Research, 39, 317-326.

Beutel, R. and Gorb, S. N. (2008). Evolutionary scenarios for unusual attachment devices of Phasmatodea and Mantophasmatodea (Insecta). Systematic Entomology, 33(3), 501-510. doi: 10.1111/j.1365-3113.2008.00428.x

Beutel, R. G.; Wipfler, B.; Gottardo, M.; and Dallai, R. (2013). Polyneoptera or "lower Neoptera" - new light on old and difficult phylogenetic problems. Atti Academia Nazionale Italiana di Entomologia, Anno LXI, 2013: 133-142.

Burrows, M. and Dorosenko, M. (2015). Jumping mechanism and strategies in moths (Lepidoptera). Journal of Experimental Biology, 218, 265-266.

Engel, M. S.; Grimaldi, D. A.; and Krishna, K. (2009). Termites (Isoptera): Their Phylogeny, Classification, and Rise to Ecological Dominance. American Museum Novitates, 3650, 1-27. Retrieved 7/26/17 from

Engel, M. S.; Breitkreuz, L. C.; Cai, C.; Alvarado, M.; Azar, D.; and Huang, D. (2016). The first Mesozoic microwhip scorpion (Palpigradi): a new genus and species in mid-Cretaceous amber from Myanmar. Naturwissenschaften, 103(3-4), 19. doi: 10.1007/s00114-016-1345-4. 

Huang, D.-Y.; Bechly, G.; Nel, P.; Engel, M. S.; Prokop, J.; Azar, D.; Cai, C.-Y.; van de Kamp, T.; Staniczek, A. H.; Garrouste, R.; Krogmann, L.; dos Santos Rolo, T.; Baumbach, T.; Ohlhoff, R.; Shmakov, A. S.; Bourgoin, T.; and Nel, A. (2016). New fossil insect order Permopsocida elucidates major radiation and evolution of suction feeding in hemimetabolous insects (Hexapoda: Acercaria). Scientific Reports, 2016(6), 23004. doi:

Huxley, J. and Barnard, P. C. (1988). Wing scales of Pseudoleptocerus chirindensis Kimmins (Trichoptera: Leptoceridae). Zoological Journal of the Linnean Society, 92, 285-312.

Klass, K.-D. (1997). The external male genitalia and the phylogeny of Mantodea and Blattaria. Bonner Zoologische Monographien, 42, 1-341.

Kristensen, N. P. (1984). Studies on the morphology and systematics of primitive Lepidoptera (Insecta). Steenstrupia, 10, 141-191.

Kristensen, N. P.; Hilton, D. J., Kallies, A.; Milla, L.; Rota, J.; Wahlberg, N.; Wilcox, S. A.; Glatz, R. V.; Young, D. A.; Cocking, G.; Edwards, T.; Gibbs, G. W.; and Halsey, M. (2014). A new extant family of primitive moths from Kangaroo Island, Australia, and its significance for understanding early Lepidoptera evolution. Systematic Entomology, 40, 5-16. 

Mey, W.; Wichard, W.; Mueller, P.; and Wang, B. (2017). The blueprint of the Amphiesmenoptera-Tarachoptera, a new order of insects from Burmese amber (Insecta, Amphiesmenoptera). Fossil Record, 20, 129-145. Retrieved 7/16/17 from 

Perrichot, V.; Wang, B.; and Engel, M. S. (2016). Extreme Morphogenesis and Ecological Specialization among Cretaceous Basal Ants. Current Biology, 26, 1468-1472. Retrieved 7/25/17 from

Poinar, G. Jr. and Brown, A. E. (2017). An exotic insect Aethiocarenus burmanicus (Aethiocarenodea ord. nov., Aethiocarenidae fam. nov.) from mid-Creataceous Myanmar amber. Cretaceous Research, 72, 100-104. Retrieved 7/16/17 from

Shi, G.; Grimaldi, D. A.; Harlow, G. E.; Wang, J.; Wang, J.; Yang, M.; Lei, W.; Li, Q.; and Li, X. (2012). Age constraint on Burmese amber based on U-Pb dating of zircons. Cretaceous Research, 37, 155-163. Retrieved 7/25/17 from

Wieland, F. (2010). The Phylogenetic System of the Mantodea (Insecta: Dictyoptera) (unpublished dissertation). Georg-August-Universität, Göttingen.

Wieland, F. (2013). The Phylogenetic System of the Mantodea (Insecta: Dictyoptera). Species, Phylogeny & Evolution; 3, 3-222.

Tuesday, May 2, 2017

A Tropical Monstrosity in Ohio: the Owl Moth

On October 9th of last year, I happened across this beauty in the breezeway of my apartment in Columbus, OH. The specimen was dead, but exceedingly fresh. It had been a chilly night, with a low near 40; she had evidently perished just a few hours beforehand.

Not being a lepidopterist, I really had little idea of what I had found, other than that it was an erebid moth not unlike the Black Witch (Ascalapha odorata). However, further investigation demonstrated that this enormous specimen (wingspan 15 cm., as shown) was in fact a female Owl Moth (Thysania zenobia), along with the Black Witch a member of the Thermesiini. 

Much to my pleasure, the find is unusual. T. zenobia ranges throughout the eastern Americas south to Rio Grande do Sul (Specht et al., 2004),  and occurs in the Greater Antilles and Galapagos Islands (Roque, 1999): according to the Ohio Lepidopterists' Society, it has only been collected in the state on five occasions, none of which occurred in Franklin County (Rings et al., 1992).

Indeed, the animal is a tropical stray. Their caterpillars' cassiine host plants (Specht et al., 2004) do not grow natively in the Lower 48. Early authors even proposed that its appearance in the northern United States was due to human mediation (Felt, 1907). However, given that they have cropped up in good condition in Wisconsin (Ziemer, 1949), New England (Farquhar, 1938) and Ohio (Rings et al., 1992) on occasion, it is now clear that the moths fly northwards under their own power; their native presence in the Galapagos would also indicate excellent dispersal capabilities.

One lepidopterist wrote that he was "unprepared for" collecting a live T. zenobia in Ontario while sugaring for underwings (Catocala spp.): "However, the monster was taken" (Kilman, 1889). I regret that I did not have the same good fortune to see this T. zenobia in life. She would have brought to my mind Albert Giraud's poem cycle "Pierrot Lunaire" (here translated by Cecil Gray):

 And from heaven earthward bound
Downward sink with somber pinions
Unperceived, great hordes of monsters
On the hearts and souls of mankind...
Gloomy, black giant moths.     

Farquhar, D. W. (1938). The Lepidoptera of New England (Doctoral dissertation). Harvard University, Cambridge.

Felt, E. P. (1906). 22nd Report of the State Entomologist on injurious and other insects of the state of New York 1906. New York State Museum Bulletin, 110, 39-44. 

Kilman, A. H. (1889). Correspondence: a rare moth. The Canadian Entomologist, 21(1): 240. 

Rings, R. W.; Metzler, E. H.; Arnold, F. J.; and Harris, D. H. (1992). The Owlet Moths of Ohio: Order Lepidoptera, Family Noctuidae. Bulletin of the Ohio Biological Survey, 9(2), vi+219 pp.

Roque, L. (1999). Two large tropical moths, Thysania zenobia (Noctuidae) and Cocytius antaeus (Sphingidae) colonize the Galapagos Islands. Journal of the Lepidopterists' Society 53(3), 129-130.  

Specht, A.; Silva, E. J. E.; and Link, D. (2004). Noctuídeos (Lepidoptera, Noctuidae) do Museu Entomológico Ceslau Biezanko, Faculdade de Agronomia Eliseu Maciel, Universidade Federal de Pelotas, RS. Revista Brasileira de Agrociência, 10(4), 389-409.

Ziemer, S. E. (1948). Erebus odora and Thysania zenobia in Wisconsin. The Lepidopterist's News, 2(3), 25-36.