Female Brown Anole Inspecting Nest Pot

It is not new to most of us that female lizards choose between different nest sites (e.g. Shine & Harlow, 1996; Warner & Andrews, 2002), anoles included (Socci et al., 2005; Reedy et al., 2012 – covered on Anole Annals). But what is new to me is how females assess soil characteristics to decide where to lay their eggs.

Brown anoles in an intimate moment.

Brown anoles in an intimate moment.

For context, I recently started to breed brown anoles in the lab for the first time. I’m using large vertical screen cages in an outdoor set up, which I believe makes them pretty comfortable to keep their daily anole life. There have been lots of  male-male interactions (displaying and serious fights), mating and nesting.

A few days ago I started to notice females head down in the nests pots, breathing heavily from time to time. I wondered if they were inspecting the nest pots before laying and shared a video on Twitter. They take a long time in that position, which made me really curious to know how they assess their chosen nest-site characteristics. Let me know if you know more about it. Posted above is the video I uploaded to youtube.

I feel so lucky to be able to observe all these cool behaviors and I hope to share some more soon!

Are There Seven Species of Anolis distichus?

distichus

The latest work on genetic differentiation and species status within the Anolis distichus group has just been published by MacGuigan, Geneva and Glor in Ecology and Evolution. In line with previous work from the Glor lab, the study finds evidence for seven distinct evolutionary lineages worthy of recognition as species, and further finds that variation in dewlap color in some cases does not correlate with geographic isolation. Finally, geographic isolation seems to play a key role in genetic divergence.

Here’s the abstract, followed by a few comments:

Abstract

Delimiting young species is one of the great challenges of systematic biology, particularly when the species in question exhibit little morphological divergence. Anolis distichus, a trunk anole with more than a dozen subspecies that are defined primarily by dewlap color, may actually represent several independent evolutionary lineages. To test this, we utilized amplified fragment length polymorphisms (AFLP) genome scans and genetic clustering analyses in conjunction with a coalescent-based species delimitation method. We examined a geographically widespread set of samples and two heavily sampled hybrid zones. We find that genetic divergence is associated with a major biogeographic barrier, the Hispaniolan paleo-island boundary, but not with dewlap color. Additionally, we find support for hypotheses regarding colonization of two Hispaniolan satellite islands and the Bahamas from mainland Hispaniola. Our results show that A. distichus is composed of seven distinct evolutionary lineages still experiencing a limited degree of gene flow. We suggest that A. distichus merits taxonomic revision, but that dewlap color cannot be relied upon as the primary diagnostic character.

The authors suggest that there are at least seven species within the distichus complex, but they suggest that it is premature to recognize them officially at this time. Nonetheless, Poe et al. in their recent Systematic Biology paper (hey! who’s going to write a post on this one?) recognize at least some of these taxa as distinct species.

Finally, I do have one tiny bone to pick. The authors state:

“Together these results suggest that dewlap color is not by itself a reliable diagnostic trait in the A. distichus complex, and perhaps in anoles more broadly.”

I take umbrage with the final statement, “and perhaps in anoles more broadly.” The distichus complex has always been recognized as the major exception to the idea that dewlap color variation relates to reproductive isolation. Consequently, demonstrating what has been suggested—with some evidence—for 40 years doesn’t necessarily argue against the role of the dewlap in reproductive isolation more generally. Now, you may quibble with the data underlying this general proposition, and it certainly is worthy of further study, but the results of this study confirm what was already recognized as an exception to this general rule..

 

Effects of Age- and Sex-specific Density on Behaviour and Survival of the Brown Anole

A perching brown anole.

An adult male brown anole.

Greetings anole biologists and enthusiasts! I write to you from Fred Janzen’s 30-year field site along the Mississippi River in northwest Illinois, where I’m collecting data for my dissertation studies. Unfortunately, there aren’t any anoles here, but the painted and common snapping turtle densities are impressive. Fortunately for this post, however, current field work has been paused as a team of inmates are cleaning up debris from recent flooding of the area. Thus, I’ll give a brief update on the last chapter of my master’s research with Dan Warner and the brown anoles* of northeastern Florida.

A good bit of Anolis work has shown that species partition perch height and width to reduce competition. However, less work has focused on habitat partitioning within species of anoles. Thus, my thesis work examined whether similar partitioning exists between age and sex classes of the brown anole, and attempted to identify the drivers and mechanisms of such age-specific habitat use. First, we found that juveniles on Dan’s study islands perch on lower and thinner perches, and use the ground more frequently, than adults (discussed in another Anole Annals post). We then altered the density of adult males in mesh enclosures in the lab, and found that juveniles perch lower in the presence of adult males and have a greater response as adult male density increases (discussed in another Anole Annals post also).

Fig 1

Juvenile Anolis sagrei survival in response to adult male and female density (F4, 164 = 3.67, P = 0.0069).

Quite excited by our findings that adult male density influences juvenile microhabitat choice, we set up two field experiments to assess 1) how adult male and female densities independently affect juvenile microhabitat use and survival, and 2) how juvenile presence affects adult male and female microhabitat use. Interestingly, we found that after just four days of exposure, adult male, but not female, presence reduced juvenile survival (Fig 1). However, we found no evidence that juveniles shifted microhabitat use behaviorally, nor were juveniles selected against in a pattern consistent with the observed age-specific habitat use in the field (e.g., selection favoring low perching juveniles) in response to either adult males or females. One large difference between the lab and field experiments is that the lab experiment used larger juveniles than the field experiment. Perhaps the smaller field juveniles innately perched in safe microhabitats, thus reducing their ability to behaviorally respond to adult threats. In addition, strong past selection favoring low perching hatchlings may have reduced the phenotypic variation needed to detect any selective patterns. The second field experiment revealed that adult microhabitat use is not affected by the presence of juveniles.

This last chapter has recently been published and is freely available through this link until 25 July 2017 (Delaney and Warner. 2017. Animal Behaviour 129:31-41). After that, shoot me an email.

For now, I’ll be studying fitness tradeoffs in maternal investment strategies in turtles. However, once an anologist, always an anologist. So I’ll keep an eye on Anole Annals to get my Anolis fix, until I find my way back south.

Happy noosing!

*Note – I’m certain that “Dan Warner and the Brown Anoles” should be a band name.

 

Phylogeny and Diversity of Monkey Lizards, Anoles’ Closest Relatives

polychrusm

Monkey lizards (Polychrus) are unique among Neotropical arboreal lizards in having strikingly long whip-like tails, as well as long limbs and digits. Interestingly, they resemble Old World chameleons in both morphology and behavior: slow-moving lizards with a laterally compressed body and cone-shaped eyes with partially fused eyelids. Although their phylogenetic position in the iguanid tree of life remains controversial, many authors argue that monkey lizards are the living sister taxon of anoles.

In a study published last week in PlosONE, we present a molecular phylogeny of all eight currently recognized species of Polychrus based on the largest geographic sampling to date. Our species tree places P. acutirostris as sister to all other species of Polychrus. While the phylogenetic position of P. gutturosus and P. peruvianus is poorly resolved, P. marmoratus and P. femoralis are strongly supported as sister to P. liogaster and P. jacquelinae, respectively. Moreover, recognition of the recently described P. auduboni and P. marmoratus sensu stricto as distinct species suggests that the populations of “P. marmoratus” from the Amazon and the Atlantic coast in Brazil represent separate species. Finally, species delimitation analyses suggest, among other things, that the populations of P. femoralis from the Tumbes region (southwestern Ecuador and northwestern Peru) might belong to a cryptic undescribed species.

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Blogging at Evolution 2017: Anole Annals Wants YOU!

With summer just around the corner (any day now, Boston!) that can only mean one thing – the annual ASN/SSE/SSB sponsored Evolution meeting is almost here! This year the anole community is attending in full force with 2 posters, 11 regular talks, and 2 symposium talks.

We regularly cover this meeting here at Anole Annals, and once again we are asking for YOU to help us out. If you will be attending Evolution and are interested in writing a short blog post about one or more of the talks or posters, send me an email (kristin.winchell001@umb.edu) or comment below. I will give you all the information you need to get started and a little help on how to write a blog post for us if you haven’t done so before. We always appreciate the extra help and fresh perspectives.

For those of you not attending the meeting (or maybe still debating attending), here’s the current list of anole talks in the schedule.  Are you particularly excited about a talk at Evolution this year? Did we miss a talk that should be on our list? Let us know in the comments!

Title Lead Author
Are we wrong about territoriality in Anolis lizards? A. Kamath
Evolutionary analysis of viral strains infecting a single anole species S. Prado-Irwin
Deeply conserved genetic constraints influence adaptive radiation of Anolis lizards J. McGlothlin
Macroevolution of the dewlap and diversification of Anolis lizards T. Ingram
Using sexually antagonistic skewers to explore the genetic architecture of sexual dimorphism in Anolis lizards R. Cox
Evaluating the evidence for protein coding convergence in phenotypically convergent anoles R. Corbett-Detig
Variation in dominance traits and body condition in urban Anolis cristatellus D. Briggs
Population trascriptomic analysis of ecologically differentiated, partially reproductively isolated Anolis lizards A. Geneva
Natural selection in behavior? A field experiment with Anolis lizards from the Caribbean O. Lapiedra
Temporal variation of anthropogenic perch use by populations of forest and urban lizards K. Aviles-Rodriguez
The influence of relatedness and size on spatial structure in an urban population of Anolis carolinensis lizards W. Weber
Urban adaptation in Lizards: Connecting phenotypic shifts with performance and survival K. Winchell
Character displacement in evolutionary-novel Anolis lizards J. Stroud
Does competition between the Dominican native Anolis oculatus and the invasive Anolis cristatellus drive changes in ecological, agonistic and reproductive traits? C. Dufour
Population genomics of Anolis carolinensis transposable elements: insertion polymorphisms are abundant but rarely approach fixation R. Ruggiero

Odd-Looking Belizean Anole

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Bill Rainey observed this lizard on a restored portion of one temple at Altun Ha, an ancient Mayan city in modern-day Belize, in an area shaded by trees. Anyone know what it is?

Anolis ruibali: Everything You Need to Know

ruibali

The following is taken from the Society for the Study of Amphibian and Reptile’s website:

Catalogue of American Amphibians and Reptiles

The Catalogue consists of accounts of taxa prepared by specialists, including synonymy, description, diagnosis, phylogenetic relationships, published descriptions, illustrations, distribution map, and comprehensive list of literature for each taxon. Over 900 accounts have been published since the initiation of the series in 1963. The series covers amphibians and reptiles of the entire Western Hemisphere. Previously, accounts were published as loose-leaf separates; beginning in 2013 accounts are published as on-line PDFs.  All accounts are open access and are available for free download at the University of Texas Library Repository.

Just this week, one of the latest catalogue entries is for the little known Anolis ruibali of Cuba, written by Robert Powell, Javier Torres, and Nils Navarro Pacheco.

ruibali2

Teid Lizard Eats an Anole

Poor Anolis, snack box of the jungle. Seems that just about anything will eat an anole. So, it’s not surprise to learn that the teid lizard Kentropyx calcarata joins the lizard of anole consumers. So report Franzini et al. in a recent report in Herpetology Notes. Anolis fuscoauratus was the unfortunate victim, the crime discovered by examination of stomach contents.

How Do Limb, Head and Tail Length Differences Arise during Embryological Development in Lizards?

andrews2

Consider two lizard species that differ in limb length, with one species having relatively longer legs than others. During development, how does this difference arise? Do the limbs start at the same length when they first appear in the embryo, but grow at a greater rate in the longer-legged species? Or is the initial limb bud longer in the embryo of the longer-legged species, and then the rate of growth the same in the two species, preserving the initial difference?

Thom Sanger’s elegant work showed that the latter answer is correct for Anolis: the limb buds of long-legged species start out longer and then grow in parallel with those of shorter-legged species.

But does this finding also hold when comparing across a broader range of lizards? Robin Andrews and Sable Skewes decided to find out, comparing embryos of a chameleon, two geckos, and the brown anole.

The answer: the same pattern as within anoles! And it applies to tail length (but not head length) as well as limbs.

andrews

The Evolution Of Morphological Diversity In Tropidurine Lizards: the Influence Of Habitat

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Uracentron flaviceps (upper photo) and Microlophus thoracicus (lower photo), two tropidurine lizards adapted to rainforests and deserts, respectively.

I was lucky enough to spend some months working at the Museum of Comparative Zoology of Harvard as part of the Losos lab. There I learned a good deal about anoles and got to meet anole-loving people face to face. Even though this atmosphere tempted me to develop a project related to one of the greatest examples of adaptive radiation, I had other plans in mind involving some of their distant cousins: tropidurine lizards! The results of this study are already published (Toyama, 2017) and I will describe a bit of what I found.

Tropidurinae is a group of lizards whose representatives have diversified across South America. They come in different shapes, colors and sizes, as you would expect from any group of organisms spreading in a diverse territory in terms of habitats, climates and altitudes. Rainforests, deserts, mountains and dry forests are just some examples of the different ecosystems where you can find these lizards. Given this scenario, I wondered if the morphological diversity observed in this clade could be linked to the challenges imposed by the different habitats types found in the continent.

Inspired by similar studies that focused on other lizard radiations, I took measurements of functional morphological traits of several species of lizards coming from 10 out of the 12 genera comprising the Tropidurinae. These traits would allow me to look for a possible correspondence between morphology and habitat.

However, as I was not only interested in the link between morphology and habitat use, but also in the morphological diversity itself, I started looking at purely morphological information. The next figure shows the illustrative results of a Principal Component Analysis (PCA), which tries to separate the species as much as possible based on the morphological measurements. In the figure, we can observe how the dots of each color (representing species of the same genus) occupy a particular zone in the graph. This means that, in general, species of the same genus are, as expected, morphologically more similar between them than to species of other genera (exceptions aside, given the overlaps between some genera).

figure2

Scatter plot showing the morphological space defined by PC1 and PC2. Each dot represents the average values for a species, and species are grouped in genera (colors). Abbreviations are shown for some traits as HL (head length), HW (head width), HH (head height), BW (body width), BH (body height), Dist (distance between limbs), Htoe (longest toe of the hind limb), and Ftoe (longest toe of the forelimb).

Going a bit farther in respect to morphological diversity,

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