AA readers may remember from previous AA blog posts (here and here) that we have been tackling the field of anole palaeontology; the wonderful world of Amber Encased Anoles. This month, the first paper has been published in the Zoological Journal of the Linnean Society, on the Mexican amber fossil Anolis electrum (from the collection of UC Museum of Paleontology, Berkeley). And what a fossil!
Kevin Chovanec of East Tennessee Sate University presented one of the most surprising and important posters at the JMIH conference this summer. In his poster, Kevin provides solid fossil evidence for the oldest crown group anole. Working with samples discovered along the Gulf Coast of Florida, Kevin found abundant and well-preserved fossil remnants from anoles. Apparently this material has been around for a while, but has been neglected as attention at these localities focused on identification of mammalian fossils. Kevin has identified the remains of what appear to be at least two species of anoles in deposits that are dated as 26-28 Ma and at least one species in deposits that are 19 Ma. None of this material possesses the traits that are diagnostic for members of the carolinensis series (the only group of extant anoles that was endemic to the United States prior to a wave of recent introductions). His work suggests the existence of a multi-species anole fauna dating back to the Oligocene. A phylogenetic analysis suggests that Kevin’s fossils are members of the anole crown group, but it is not possible to place them with any more phylogenetic precision. He did note, however, that they also lack the transverse vertebral processes that are diagnostic for the β anoles (a.k.a. Norops). The work Kevin presented was part of his masters project at East Tennessee State. I can’t wait to see what other insights emerge from Kevin’s work!
Anole jeans! Now marked down to $25. Get ’em while they last!
Extensive googling reveals that the jeans are made by Nice Work Textile Jeans, Inc.
Long time AA readers will know that anoles frequently pop up in haute couture, perhaps most recently when Tommy Bahama created an anole-colored T-shirt.
Four years ago, we reported on the distribution of the Puerto Rican crested anole all along the Caribbean coast of Costa Rica. We also found the species inland, as far west as Turrialba and Siquerres, but not Guapiles (see map to right). A year later, we returned for a quick follow-up as part of a herpetology course spring break trip to Costa Rica. The weather wasn’t great and we failed to find cresteds in any place not previously reported; however, observations of brown basilisks, another sun-loving species, suggested that the weather was suitable enough, and that perhaps the absence of the anoles was real.
Two years later, this past March, another herpetology class trip ensued, and so another expedition was launched to Guapiles and environs. The team included AA correspondent Katie Boronow, an award-winning senior with expertise on A. cristatellus, and a sophomore in training for Miami field work this summer (more on them in posts to come).
And the results???
As mentioned in the previous post, the journal Herpetological Review is an excellent resource for anole natural history information. A frequent contribution is range extensions, often by county, for both native and introduced species. Range extensions are important pieces of information for biologists, as accurate county-level distributional data is crucial in many important exercises, such as mapping species richness in a region or identifying range boundaries (and then asking why the range ends in certain areas). This quarter’s issue has the following two range extensions.
Christopher Thawley and Fern Graves report a new county record for Anolis carolinensis in Bullock Co., Alabama, just south of Auburn. This apparently fills a hole in the confirmed range of the species in that part of Alabama.
Cory Adams and friends report an extension of Anolis sagrei range in Angelina Co., Texas. Interestingly, this specimen, as well as a specimen from Nacogdoches, Texas, were found in potted plants in Home Depot and Lowe’s garden departments. The authors posit that these animals turning up in East Texas are not range extensions, as in owing to the expansion of individuals from established ranges, but instead are the result of novel introductions facilitated by interstate transport of goods such as potted plants. If this is the case, these animals could have come from anywhere, not just the invasion front along the Gulf states. In other words, if the potted plants are coming from, say, Florida, then these animals would be leapfrogging their established conspecifics to potentially start new colonies and expand the range.
Adams, CK, D. Saenz, and JD Childress. 2014. Anolis sagrei (Brown Anole). Distribution. Herpetological Review 45: 282.
Thawley, CJ and F. Graves. 2014. Anolis carolinensis (Green Anole). Distribution. Herpteological Review 45: 282.
The journal Herpetological Review, published by the society for the Study of Amphibians and Reptiles, frequently has interesting anecdotal reports of natural history observations of anoles. This quarter’s edition has two: nocturnal activity in Anolis cristatellus and prey stealing behavior in Anolis sagrei. Here is a synopsis:
Dean and Jennifer Metcalfe report on nocturnal behavior of A. cristatellus wileyae observed (while perhaps on vacation) at the Nanny Cay Resort and Marina on Tortola, British Virgin Islands. The authors observed that the subject anole had navigated the interior of their hotel room in near darkness after dusk, selecting a nocturnal perching site on a lampshade. They suggest that this is similar behavior to that of an anole selecting an arboreal perch site at dusk. Two questions come to mind though. First, whether the room was completely dark- as the authors acknowledge that some light might have been entering the room- and whether the animal came from the outside into the room to perch or was residing in the room. Second, the author mentioned that this was the only anole seen on Tortola during her brief stay, which is also a bit unusual as the species should be abundant there. This might not add much to our understanding of anoles, but it certainly raises some questions about the co-habitation of humans and anoles.
The second note comes from David Delaney, a master’s student in Dan Warner’s lab at UAB, and friends, who report on an opportunistic A. sagrei in Ormond Beach, Florida. The anole had apparently been observing a predation attempt of a spider-wasp on a funnel-web spider. To summarize, the wasp attacked and envenomed the spider, captured it, and began dragging it across the ground. At this point the anole jumped to the ground, grabbed the spider, and took it up the tree to eat it. The wasp, likely disappointed, fled the area to hunt again.
Metcalfe, DC and JE Metcalfe. 2014. Anolis cristatellus wileyae (Vrigin islands Crested Anole). Nocturnal Activity. Herpetological Review 45: 323-324.
Delaney, DM et al. 2014. Anolis sagrei (Brown Anole). Prey stealing behavior. Herpetological Review 45: 324-325.
Hanna Wegener, a student with Jason Kolbe at the University of Rhode Island (and an Anole Annals contributor), presented a poster at JMIH on her efforts to identify the factors that drive morphological differentiation among Anolis sagrei populations found on 16 Bahamian islands near Staniel Cay. Hanna investigated morphometric, ecological, genetic, and demographic variation among these populations and, unlike many previous studies, considered variation in both males and females. Although Hanna did find significant morphometric variation among islands and between sexes, she did not find the significant correlation between morphometric variation and habitat use reported in prior work. She also did not find a significant relationship between morphometric and genetic variation. She did, however, find that population density influences morphometric variation, with lizards living at higher population densities having significantly longer heads than those found on lower density islands. Because these lizards on densely populated islands are also more likely to exhibit evidence of injury from other anoles (e.g., loss of limbs, digits, or claws), it is possible that their longer heads may indicate a response to intra-specific competitive interactions. However, interpretation of these results remains complicated because there is not a direct connection between injury and intra-specific competition, and the lizards on densely populated islands had longer heads, but not the wider heads that would have been expected if the goal of their morphometric shift was to increase bite force. Hanna undoubtedly has many more exciting questions to investigate with her ongoing research.
Where do anoles poop? Will they chase laser points? Find out on Casey Gilman’s new blog on her Florida field research, Adventures Down South. Meanwhile, Chipojolab keeps the world abreast of goings-on in the Leal Lab. Most recently–Leal back in the Bahamas and multiple lab members cavorting in Puerto Rico! And Ambika Kamath’s afoot with her field crew in Gainesville, dodging frisbees and fire ants in quest of the wily festive anole. Finally, at Lizard and Friends, Michele Johnson talks about Puerto Rican anoles that are biting off more than they can chew. Or are they?
Do you have a blog on your research? If so, let us know!
Andrew Battles from the Kolbe Lab gave a talk at JMIH presenting data on performance-habitat relationships comparing lizard performance on rough and smooth surfaces. The data were collected on Guana Island in the British Virgin Islands using Anolis cristatellus and A. stratulus as study species. Andrew and his advisor, Jason Kolbe, were interested in whether lizards perform differently on artificial and natural surfaces.
They used three different running tracks (37°-incline rough track, 90°-incline rough track, 90°-incline smooth track), assuming that artificial surfaces are smoother than natural ones. The rough tracks consisted of a board covered in window screen and the smooth track was a plain 2-by-4 board. They used a high-speed camera to measure maximum velocity, how often a lizard paused during the run and how often it slipped. While both species ran significantly slower, paused and slipped more often on the smooth surface, A. cristatellus performed even worse than A. stratulus. Andrew and Jason then conduced a field survey to test whether lizards in a human-modified habitat use both artificial and natural perches. In addition, they rated roughness of natural and artificial perches. When both types of perches were available, lizards used artificial perches more often than natural ones.
This is surprising, because artificial perches are significantly smoother than natural ones and lizards perform worse on smooth surfaces. Possible explanations are that other factors such as food availability and/ or predation may drive habitat selection on artificial substrates.