Many editors have recently come to acknowledge that an anole on a book or journal cover generates much enthusiasm from the community (here, here, here, here, here, here and here– I hope that I didn’t miss any). The trend continues in the February issue of Proceedings of the Royal Society. In this issue Sanger et al. describe the developmental bases of limb length convergence among trunk-ground and trunk-crown habitat specialists (previously described on Anole Annals). It should be noted that the only thing that can possibly trump the beauty and eloquence of an anole in its native environment are developmental series of anole embryos (see here for further proof)
Year: 2012 Page 46 of 47
George Gorman, who pioneered the use of molecular tools to study anole phylogenetics from the late 1960’s to the early 1980’s, asks:
“Why not examine karyotypes of Dactyloa?”
He says:
“In the 1960’s and ‘70’s, before the DNA revolution, the systematic examination of karyotypes of reptilian taxa mushroomed, and, to some extent helped orient our thinking about relationships among various clades. This was certainly the case within Anolis at various hierarchical levels, from species determination to definition of distinct species groups. To my knowledge, there has been very little added to our knowledge about karyotypes of mainland Anolis that Etheridge placed in the latifrons series of Alpha Anolis, now frequently referred to as the Dactyloa clade. (if these are long-lost terms, Etheridge’s Beta anoles are the Norops section; all other lineages are within his “Alpha” section).
Background
There is a very pervasive, either primitive or convergently arrived at, karyotype among the Sauria…consisting of 12 metacentric macrochromosomes, and 24 microchromosomes. This karyotype may be found in many families and in all species of many genera within families. This was also the known published karyotype of A. carolinensis….the only anole that had been examined until about 1965.
Here’s a brief summary of what followed:

Braving the elements in Charleson.
We all think of anoles as warm weather, tropical beasties, but of course, that’s not entirely the case. Many live at quite high elevations and are active at cool temperatures. For example, this past summer we saw A. orcesi active (as active as it gets) when temperatures were 20 C and below.
In addition, anoles get relatively far north into temperate areas of the United States. One might think that they’d just go to sleep in the winter and not come back out til the spring warmth, but that’s not the case. Faithful contributor Marc Tollis discusses one recent observation over on his own blog, Anolis Tollis.

Lineage accumulation curves (Fig. 2, Rabosky and Glor 2010) showing that Hispaniola (blue), Jamaica (purple), and Puerto Rico (orange) have reached speciation-extinction equilibrium. Cuba (red) is still gaining species.
Losos, J.B., and D. Schluter. 2000. Analysis of an evolutionary species-area relationship. Nature 408: 847-850.
Losos and Schluter (2000) return to Caribbean anoles to test three hypotheses about the species-area relationship: (1) that there is an area threshold above which speciation surpasses immigration as a source of new species; (2) above the threshold size, speciation events per unit time should increase with island area; and (3) the slope of the species-area relationship should become steeper above the area threshold. Qualitatively similar to Losos (1996), this paper was novel in that a newly available, nearly complete, mt-DNA phylogeny allowed Losos and Schluter to reconstruct immigration and speciation events and to model whether species number has reached speciation-extinction equilibrium.
Read all about it here.
Frigid temperatures in Boston are making me long for the warm waters of Vieques, PR and the time I was there in October. Truth be told, I work for Jonathan Losos in a mostly administrative role, but even that has turned me into an avid lizard hunter when on vacation in the tropics. I even set a goal for myself – to find and photograph all three species of anoles on the island – except for the one no one has seen in almost 100 years. I trusted that if several professionals have not been able to find A. roosevelti, than my chances were slim (although, I did keep my eyes out for large lizards falling out of trees, just in case). To my absolute delight, the other three species, A. cristatellus, A. pulchellus, and A. stratulus could all be seen running around the manicured garden that surrounded the house I was staying in. We named one “King” and watched him move from palm tree to palm tree, displaying to the other anoles in the vicinity. (I’ve observed many anoles in Ecuador, but had never seen an anole move its tail back and forth before as a display – adorable!)
I watched a spirited courtship between a male and female A. pulchellus in ferns, and spent far too much time trying to get a shot of A. stratulus – particularly one that could always be seen on the wall of the pool house, but would promptly run through the door when I pulled out my camera.
There was even an A. stratulus running around without a front hand. He seemed to move about just fine, though, both through the house and around the vegetation outside. I was proud of my non-biologist friend that worried about him missing “so many sticky toes”. Also entertaining was a fight between two juveniles – unfortunately shot with my cheap telephoto lens, so the quality is poor, but it’s still entertaining: video
Looking forward to a week in the Bahamas in May – another vacation, but I’m sure it too will be filled with anoles.
Losos, J.B. 1996. Ecological and evolutionary determinants of the species-area relation in Caribbean anoline lizards. Philosophical Transactions of the Royal Society of London B 351: 847-854.
As alluded to previously, MacArthur and Wilson (1967) did consider evolutionary processes when they developed their Theory of Island Biogeography. Specifically, in situ evolutionary diversification (i.e. speciation) may contribute substantially to the species diversity of an island and should be considered in any general attempt to model species-area relationships on islands. Building on Rand’s 1969 paper studying the ecological determinants of species richness in Caribbean anoles, Losos (1996) incorporates an evolutionary perspective into the Caribbean Anolis species-area story.
Hello again from North Charleston!
We started off strong: this morning’s “Sexual Selection in Herps” session was dominated by anole talks. Bieke Vanhooydonck, from the University of Antwerp, discussed sexual dimorphism and dewlap growth in Anolis baracoae. By repeatedly measuring individuals over the course of their development into adulthood, Vanhooydonck observed a number of morphological changes. All the observed morphological characteristics showed no significant difference between males and females, with only the key exception of dewlap size. Male dewlaps were found to be larger. The development of dewlaps in the genders diverges, and the male dewlaps subsequently outgrow the female dewlaps, when lizards reach sexual maturity. An interesting and unexpected discovery made by this study was the significant decrease in male dewlap size that occurs with old age. Vanhooydonck proposed that this might be caused by loss of elasticity in skin.
Following her was Michele Johnson of Trinity University, who discussed the interplay of natural and sexual selection in Anolis sagrei and Anolis maynardi. She hypothesized that the difference in head shapes for male and female Anolis lizards may be driven by diet, male-male competition, or female choice. Looking to the particularly elongated head of A. maynardi, Michele explored the potential function implications of extreme head shape. Actively foraging A. maynardi lizards appeared to move more than “sit-and-wait strategists” A. sagrei. In A. maynardi dominance trials, Michele found that the winner of male-male territorial competitions is most commonly the male with the shorter snout (and therefore increased bite force). However, in female choice trials it was observed that females most frequently chose the male with the longer snout. Although she noted her findings are still preliminary, this leaves us with an intriguing question: if the selective forces from male competition and female choice are counteracting one another, what will ultimately determine snout length in A. maynardi populations?
A bit later, Martha Muñoz (ñote: with regard to the ñame-tag failure, it is really ñot that hard to type ñ. C’mon SICB) presented her research on behavioral and physiological adaptations to the thermal environment in the Hispaniolan cybotes group. The diverse species of lizard in this group occupy a broad range of elevation, habitat composition, and thermal environment. If Anolis lizards are not using behavior to mitigate extreme temperatures in their habitat, we might anticipate changes in physiology. No differences were observed between the study species preferred or mean field body temperatures, which implies that they are actively and purposefully thermoregulating. However, she explained that there are limits to behavioral control. What if there was no access to shade for reprieve from the heat? Or what if it was too cold to bask? From her data, Martha suggests that the cybotoids are able to evade extreme heat, but an inability to avoid extreme cold in some environments has made it advantageous to adapt a physiological tolerance to the cold.
The poster session was dotted with Anolis research as well, including such topics as A. carolinensis satellite cells and tissue regeneration. Ellie Cook, who I met while she was working with Michele Johnson in the Dominican Republic this summer, had a great poster displaying her analysis of the affect of parasitism on dewlap coloration in Anolis brevirostris. Her data show that whiter, duller dewlaps are correlated with greater ectoparasite loads. She suggests this may the result of cartenoids being diverted during parasite-instigated immune response.
This has been a fantastic first conference experience for me! I am really sorry to be leaving so soon. I have been super impressed by the Anole community’s contributions to SICB – please keep updating, guys!
There’s more than just anole biologists congregating at the SICB 2012 meeting.
To say it’s been cold here in Charleston, SC would be an understatement. Tuesday night, after the conference tipped off, it was 25 degrees Fahrenheit. But today, the temperature picked up a bit and moved into the 50s. Since we know they don’t hibernate in the winter months, I thought it might be possible that the local anoles may take advantage of the sunny afternoon to do a little basking. Just as the poster session was underway at about 3pm, I decided to give it a shot and take a look around what would be prime Anolis carolinensis habitat in the spring and summer: the bushes and a brick wall around the pool.
Sure enough, I spotted one male and two females right away! I texted Bryan Falk immediately, and we set to flexing our off-season collecting muscles. Doing a quick tour around the conference center, we managed to observe 6 and catch 3. No anoles were injured during this brief collecting trip – perhaps only mildly perturbed 🙂