Year: 2015 Page 2 of 25

Another Anole-Themed Wedding

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Two years ago, we reported on a lovely wedding cake with green anole atop, from the nuptial festivities of Alex Gunderson and his wife Katie. Now word comes to us of another anole wedding. AA correspondent Kristin Winchell, who doubles as a grad student in Liam Revell’s lab, was married to Jonathan Zschau this past September on Nantucket Island. As the photo above attests, the wedding cake was tastefully adorned with a bride, a groom, and an anole.

Actually, it was a double wedding. A photo of the second bride, Ms. Ann Ole, is pictured below (made by the groom’s aunt).

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SICB 2016: What Do You Want to Read About?

Screen Shot 2015-12-04 at 12.27.29 PMIt’s that time of year again: The weather is getting colder, lights and trees are going up, and mulled wine and eggnog are on the menu. I’m obviously referring to the annual meeting of the Society for Integrative and Comparative BIology (SICB). If you’re new to our blog, you’ll learn that SICB is a big deal here at Anole Annals. We like to keep our readers abreast of new and emerging trends in Anolis research. The upcoming SICB, which will be held from January 3rd to 7th in Portland, Oregon, will be no different from previous years. In between trying craft beers and local coffees, we’ll be busy blogging away about new studies in anole ecology, physiology, biomechanics, and evolution.

As you probably also know, anole research is on the rise. The program for the 2016 SICB meeting suggests that this trend is continuing. By my count, there will be 26 anole-related talks and posters at the upcoming meeting, so anoles will certainly have a strong presence. You can see a table with the talks and posters listed here. One of the downfalls of so many talks, however, is that it’s logistically challenging to cover everything on this blog. So, if you’re interested in reading posts from the upcoming meeting, do fill out the poll below. I recognize that there is overlap between topics, but I just want to get an idea of what priorities I should set at at the meeting. On another note, if you will be attending the meeting and you are interesting in blogging, please email me at martha.munoz@gmail.com. We are always looking for bloggers and I can help get you set up to make things easy.

Calotes (Brachysaura) minor: A Uniquely Adapted Agamid from the Arid Zones of South Asia

Brachysaura minor is a medium-sized (60 mm SVL) agamid lizard from South Asia. It is one of very few agamids to vocalize (Vitt and Caldwell, 2014). Some individuals from this species produce a loud squeak when captured, probably as a defense.  But this species also has some unique morphological characters,  probably due to its terrestrial habit, including a stout body, short tail, short fifth toe, broad head with spines and large labial scales (Figure 1). Since its description (in 1827) this species has been placed in a variety of genera in the subfamily Agaminae based on external appearance.

Figure 1: An adult male Calotes (Brachysaura) minor from Wardhwan, Gujarat state, India.

Figure 1: An adult male Calotes (Brachysaura) minor from Wardhwan, Gujarat state, India.

In the recently published paper (Deepak et al, 2015), we used multiple lines of evidence (osteology, hemipenis and external morphology, and molecular phylogeny) to determine the systematic position of this species. These three lines of evidence suggest that Brachysaura minor is a Calotes and genetic data suggest that it is nested well within the widespread Asian genus Calotes which belongs to the sub family Draconinae (Figure 2).  Calotes is one of the most common agamid genera in the Indian subcontinent. Most species in this genus perch on vegetation, with some species like Calotes grandisquamis and Calotes nemoricola living higher up in the rainforest trees in the Western Ghats. Calotes minor on the other hand is a completely terrestrial species, found in open grasslands perched on small rocks.

Figure 2: Bayesian tree inferred from mtDNA data in MrBayes 3.2. The values assigned on the internodes indicate maximum likelihood bootstrap values, dark circles indicate posterior probability support above 95% and light circles indicate less than 95% probability. From Deepak et al. 2015.

Figure 2: Bayesian tree inferred from mtDNA data in MrBayes 3.2. The values assigned on the internodes indicate maximum likelihood bootstrap values, dark circles indicate posterior probability support above 95% and light circles indicate less than 95% probability. From Deepak et al. 2015.

A general trend in agamid lizards is that “the length of the tail does not correlate with the number of caudal vertebrae” (Moody, 1980). Interestingly, there are some outliers in this trend: the short-tailed, terrestrial Calotes minor and its very distantly related cousin from southern parts of Africa, Agama hispida, both have fewer caudal vertebrae than their sister species. The ground dwelling Moloch horridus from Australia and Xenagama batillifera from the horn of Africa also have the same range of caudal vertebrae (Moody, 1980).  Relative to body length, Calotes minor has the shortest tail length compared to many other Calotes (Figure 3A). On the other extreme, the arboreal Calotes calotes has the longest tail among Calotes (Figure 4). They live on trees in southern India and Sri Lanka.

Figure 3: Plot of body measurements of Calotes minor (blue circles (males), red circles (females)) compared to other known Calotes spp. (Blue triangles (males), red triangles (females)). Black circle sub-adult male. A) SVL versus tail length of 17 out of the 25 described species of Calotes. B) SVL versus fifth toe length of 9 out of the 25 described species of Calotes.

Figure 3: Plot of body measurements of Calotes minor (blue circles (males), red circles (females)) compared to other known Calotes spp. (Blue triangles (males), red triangles (females)). Black circle sub-adult male. A) SVL versus tail length of 17 out of the 25 described species of Calotes. B) SVL versus fifth toe length of 9 out of the 25 described species of Calotes.

While the above pattern may suggest that short tails have evolved repeatedly in terrestrial agamids, both Sitana ponticeriana and Otocryptis wiegmanni, which are terrestrial, have very long tails. However, another trait is shared by the terrestrial Sitana and Otocryptis, namely the extreme reduction (Otocryptis) or loss (Sitana) of the fifth toe. Therefore, we decided to look at the fifth toe length in relation to SVL in Calotes minor as well. The completely terrestrial Calotes minor has the shortest fifth toe compared to many of its arboreal sisters (Figure 3B). In western India and parts of central India, there are vast expanses of open grasslands with only few rocks embedded in it and Calotes minor may have evolved to occupy these niches.

Figure 4: Calotes calotes from Rameshwaram Island, Tamil Nadu state, India.

Figure 4: Calotes calotes from Rameshwaram Island, Tamil Nadu state, India.

Citations:

Moody, S.M.(1980): Phylogenetic and historical biogeographical relationship of the genera in the family Agamidae (Reptilia: Lacertilia)  – Thesis, The  University  of  Michigan,  Michigan, 373 pp.

Vitt, L.J.  and J.P. Caldwell. (2013). Herpetology, Fourth Edition: An Introductory Biology of Amphibians and Reptiles 4th Edition. Academic Press, San Diego.

Russell A.P. and Rewcastle S.C. (1979): Digital reduction in Sitana (Reptilia: Agamidae) and the dual roles of the fifth metatarsal in lizards. Canadian Journal of Zoology 57: 1129-1135.

 

Last Chance – Vote for the Best Photos of 2015!

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Don’t forget to submit your votes for the Anole Annals Photo Contest 2015! The poll will close THIS THURSDAY, December 3, so make sure you get your votes in before then. Anole Annals 2016 calendars with the winning 12 photos  will be available for purchase soon after!

Third Specimen of Anolis toldo Discovered

Anolis toldo. Photo by Luis Diaz.

Anolis toldo. Photo by Luis Diaz.

Luis Diaz reported on Facebook the discovery of the lizard shown above. He reports: “Anolis toldo, adult female; third individual of the species known and first specimen in the National Museum of Natural History of Cuba. The discovery of this specimen was a result of the joint expedition by the National Museum of Natural History of Cuba and the American Museum of Natural History. It was found on October 19, 2015, at night, on a tree fern in a new location (outside the only known: the plateau of El Toldo ). This is one of the few photos of the species.” The photo was tagged aat Alejandro de Humboldt National Park.

Anole Annals Photo Contest 2015 – Time to Vote!

Thank you to everyone who submitted photos for the AA 2015 contest, we received so many amazing shots! We’ve narrowed it down to the top 40, and now it’s time to vote! Choose your 5 favorites in the poll below.

Anoles in Texas!

It’s just come to AA‘s attention that the University of Texas School of Journalism posted an article on invasive anoles in Texas, featuring Yoel Stuart. Check out the article online, and the nifty, albeit chameleon-tainted, poster below.

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Don’t Mess with a Green Lizard

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I’m sure there’s a story behind this photo circulating on Facebook, but I don’t know what it is. Anyone care to speculate?

New Research: Geographical Variation in Morphology and its Environmental Correlates in a Widespread North American Lizard, Anolis carolinensis

An online preview version of this paper was published Nov. 4 in the Biological Journal of the Linnean Society.

I began this project in late 2012 as a research assistant to Shane Campbell-Staton, now a Postdoctoral Fellow at the University of Illinois Urbana-Champaign. As part of his dissertation on Anolis carolinensis, Shane saw an opportunity for an interesting side project regarding its morphological variation. The lizard’s geographic range is massive – ranging from Florida to Texas in the east, and north to Tennessee – but surprisingly few studies had examined the way limb and body traits vary between populations, let alone over its broad distribution. Given evidence for Caribbean relatives adapting to variable environmental conditions even over short distances, we were curious whether the same would hold true for the green anole.

Using a set of samples Shane had collected from 14 locations around the southeast (Figure 1), I set out to answer a few questions about geographic variation in the green anole: which traits vary most in this species? How is this variation distributed, and does it correlate with environment? We were also interested in the degree to which this species conformed (or didn’t) to Bergmann’s and Allen’s rule, two eco-geographic principles well studied in reptiles.

Density and distribution of sampling in the study.

Figure 1: Density and distribution of sampling in this study.

The process started, as always, with data collection – in this case, taking X-rays of over a hundred specimens, extracting a set of 26 morphological traits, and pairing them with environmental and genetic data for each site in our study. The resulting dataset was large and multidimensional, and required several iterations of analysis to find a clear and logical approach to test our hypothesis (as an undergraduate, this process of analysis and re-analysis taught me a valuable lesson in troubleshooting, data management, and experimental design).

Looking at our results, we did end up finding a high degree of morphological variation in this species, mostly driven by head width and length. These features marked out several highly distinct populations and generated some striking visual comparisons (Figure 2). Previous studies by Herrel, Lailvaux, Corbin, and McBrayer suggest that this kind of variation may be driven by the role of bite force and head shape in prey capture and combat, and future work on A. carolinensis should follow up on this possibility. We also recovered some morphological clustering among non-proximal populations, which opened the door for examination of possible convergence as a result of environmental similarity over the species’ range.

Head shape variation between an anole from Cedar Creek, OK (left) and one from Punta Gorda, FL (right).

Figure 2: Head shape variation between an anole from Cedar Creek, OK (left) and one from Punta Gorda, FL (right).

We found that, in general, anoles in more seasonal and colder climates of the north tend to have to have relatively longer limbs and wider and shorter heads than those from less seasonal/warmer locations in the south. With regard to limbs, this pattern may be related to an observed “reversed” Allen’s rule – that appendage length would actually increase in colder climates as a way to more rapidly uptake heat. This explanation is similar to that of the “reversed” Bergmann’s rule previously proposed for some lizards, but for which our data were inconclusive.

In the end, I believe the patterns of variation and environmental correlation that we found in the study will help to establish A. carolinensis as a strong candidate for further studies of morphological variation over a large range, especially with the recent publication of the species’ genome. As an undergraduate, I felt lucky to make a contribution to the literature and to have the opportunity to see through a project from start to finish.

Are you planning to get recertified as an environmental expert? Then click on NREP Recertification Terms and Conditions to get all the information you need in one place.

Finally, please reach out to me with any questions or comments about the study! My code and data are archived on my github page.

Anolis sagrei Survey Continued: Eleuthera, The Bahamas

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I just got back from a short trip down to Eleuthera in The Bahamas where I was assisting Anthony Geneva (Harvard post-doc) in sampling lizards. Also along for the trip were Sofia Prado-Irwin (Harvard Ph.D. student) and Rich Glor (University of Kansas). We went with the main goal of sampling Anolis sagrei from four habitat types found commonly in the Bahamas as an extension of an ongoing project in the Losos lab (previous posts from: Rum CayConcepcion IslandRagged IslandBiminiMangrove habitat, and Great Isaac Cay). Specifically, we were looking to sample Anolis sagrei in mangrove, secondary coppice forest, closed coppice forest, and beach scrub habitats. These habitats differ in the height of the canopy, density of the understory, and composition of plants.

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We focused entirely on the southern half of the island near Rock Sound and Cape Eleuthera. We were successful in sampling two beach scrub habitats, two mature coppice forest, one secondary coppice forest, and one mangrove habitat. We were able to catch all four of the anole species found on Eleuthera: Anolis angusticeps, Anolis distichus, Anolis sagrei, and Anolis smaragdinus. We also encountered a number of other native herp species: the Bahamian boa (Chilobothrus striatus), Ameiva auberi, Eleutherodactylus rogersi, curly tailed lizards (Leiocephalus carinatus), and the Bahamian racer (Alsophis voodoo), as well as a couple of non-native species: Cuban tree frog (Osteopilus septentrionalis), and Hemidactylus mabouia.

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In my own research I work with Anolis cristatellus, the Puerto Rican crested anole. I am always surprised when I catch A. sagrei by how much smaller they are than A. cristatellus, although very similar in appearance otherwise. On this trip, I was also surprised that the A. sagrei, as well as the A. angusticeps and the A. smaragdinus, appeared to be much smaller than those I had encountered on Bimini last spring.

We also found that the density of lizards was quite low compared to what we expected and what I had experienced in Bimini, both during the day and at night. In all four of the habitat types, we saw an abundance of hatchlings, juveniles, females, and small males, but relatively few full adult male A. sagrei. For A. angusticeps and A. smaragdinus, we encountered only a few individuals total during the week of sampling. This reminded me of an odd experience I had last fall in Puerto Rico with A. cristatellus. It was the same time of year and I had an extremely difficult time locating mature animals in sites where I had previously sampled large numbers during the spring and summer months. Instead, I observed a large number of very young animals and females. I’m curious if this is a coincidence or if perhaps there is a strong seasonal effect on either male behavior (i.e., reduced visibility outside of the mating season) or male abundance (i.e., reduced numbers because of mortality during the mating season). In other words, are the males still there, but hiding, or are they really lower in abundance in the late fall? Or maybe I was coincidentally unlucky on both trips… I am very curious to hear thoughts on this!

Anolis sagrei using coral ground habitat.

Anolis sagrei using coral ground habitat.

Finally, I want to end with a short natural history note on the habitat use of the A. sagrei in the mangrove habitat. In this habitat we observed A. sagrei using perches at drastically different heights: some were 6 feet up, others were on the ground. Interestingly, the ones on the ground did not appear to be in transit, but seemed to be using the pockmarked karst as perches, running into one of the many holes when approached. Has any one else observed this behavior before? It seems so different from the typical trunk-ground anole perch and behavior to me.

That’s all for now. Currently Anthony is sampling additional islands in the Bahamas along with Melissa Kemp (Harvard post-doc) and Colin Donihue (Yale Ph.D. candidate / Harvard visiting student). Best of luck to them, I can’t wait to hear how the rest of the trip went!

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