The Alluring Anoles of Alto Velo

Alto Velo Island. Photo by R. Graham Reynolds.

Although I have not been a prolific poster on AA, I have enjoyed contributing articles about the obscure and rarely seen anoles of the Greater Antilles and Lucayan archipelagos, such as Anolis ernestwilliamsi, Anolis fairchildi (1,2,3), and Anolis scripts (1,2,3,4,5).

Here is another post in that series, focused on Anolis altavelensis, the Alto Velo anole. First, a bit of background. I am currently collaborating with Joe Burgess of the National Park Service (USA), Brad Keitt of the American Bird Conservancy (USA), and Jorge Brocca of SOH Conservación (Dominican Republic) on a multi-year project focused on the ecological restoration of Alto Velo Island. This project includes detailed surveys of terrestrial fauna, followed by the removal of invasive species and recovery monitoring.

Alto Velo Island is located about 30 km off the coast of southern Hispaniola, south of the town of Pedernales, Dominican Republic. Part of Jaragua National Park, the island is separated from Isla Beata, and the mainland of Hispaniola, by a deep-water channel. This means that the island contains some endemic reptile species, including A. altavelensis, as well as endemic Leiocephalus and Sphaerodactylus. It also means that not many scientists have visited, as the island is very challenging to reach without either a large boat or a very skilled panga captain. The crossing is dangerous at the best of times, with winds regularly reaching 15–25 kts and waves 1.5–2 m, conditions that are challenging, if not reckless, for open vessels. There are no landing beaches, and a rocky coast surrounded by reefs await those who cross the Beata Channel. As I can now personally attest, this island is not for the faint of heart.

But what awaits is spectacular! Alto Velo Island is very tall, much taller than you might perceive from a satellite view, with a peak of 150 m and a series of dramatic hills that fall precipitously down to the blue sea. A wide, flat plain graces the north end, although a mixture of invasive grasses and African milkweed mars the landscape. The island has historically been heavily impacted by guano mining, an extractive industry that has left numerous islands and islets in the Caribbean in ecologically degraded states, as well as probably contributed to the extinction of some reptile species (such as on Navassa Island). Nevertheless, some endemic reptiles remain on Alto Velo, including the anole.

Anolis altavelensis. Photo by Joseph Burgess.

And what an anole is found there! Anolis altavelensis is dramatically beautiful, even among a superlative group of the bark anoles (distichus series) that are renowned for their variety and beauty. This species is electric orange, meaning that a sweep of a flashlight over a bush at night resembles a Christmas tree with small orange jeweled ornaments dotting the green leaves. Spectacular!

Happily, the species is relatively common on the island, despite an extremely damaging history of guano mining, burning for goat grazing, and infestation with cats, rats, and many invasive plants. Some native vegetation remains, particularly on the steep slopes, but a goal of the restoration project is to restore the native vegetation as well. Stay tuned for updates on this project as we hope to see Alto Velo restored to its ecological vibrancy and remote beauty.

Non-native Herps Still Increasing in the Most Heavily Invaded Herp Community in the World.

A large green lizard in the foreground perched on a tree, with an open grassy area behind and a natural area in the distance.

Anolis equestris during one of our Miami surveys

There truly is never a dull moment in South Florida, especially for those of us who love herps. South Florida is a herper’s paradise with at least 63 exotic herps recorded in the state in addition to some unique and endemic native species. In fact, South Florida is the global hotspot for non-native herps, and the world’s most invaded continental ecoregion. While almost all the herps we see while walking around Miami are non-native, we are also almost always in heavily human-modified habitat. This led us to wonder if we would see more native species if we were at sites where native habitat was preserved. Back in 2017, we set out to answer this question, comparing herp communities between 15 parks with natural habitats and 15 parks with primarily anthropogenic features (think playgrounds, baseball fields, and dog parks). Spoiler alert: Non-native species dominated the herp communities in all of the parks, natural and anthropogenic alike. Non-natives made up a whopping 90.6% of all individuals we identified. Perhaps unsurprisingly for those who have grown accustomed to the small lizards scurrying along their sidewalks and fences, 86% of everything we saw was from the genus Anolis.

Fast forward to 5 years later. It’s 2022 and all of us herpetologists in Miami are constantly being asked by anyone who learns of our lizard expertise, “What’s this big new lizard I keep seeing?! It’s got an orange head and tail and a blue body,” or “I keep seeing these lizards with curly tails hanging out around my house – what are they?” These two large predatory lizards, agamas and curlytails, are clearly spreading around the county, to the point where even non-lizard-people are taking note. As we look around, we can’t help but wonder if there could be a change in the composition of our already very exotic herp community in Miami in just the 5 years that have passed since our former study. So, we set out to answer that question.

Several months later we’d completed the same surveys at the same 30 parks, with a fantastic team of researchers, exactly five years after our first study. What did we find? Well, despite both the incredibly short time span and South Florida already being the most invaded herpetofauna community in the world, we found that non-native herps were still increasing in both richness and abundance, in amounts that were measurable in just a 5-year period! Non-native herp abundance increased significantly by 32.7%, while native abundance did not change significantly (only a 6% increase). This time around, 92.3% of our observations were non-native herps. Once again, most of our observed individuals were anoles (82%), and brown anoles and green anoles were our most commonly observed species, both being found at 97% of all sites surveyed. It is worth mentioning, however, that even the 7.7% of observations that were classified as “native” have a caveat: Most of these observations were Anolis carolinensis. As readers of Anole Annals likely know, there is now evidence that most Anolis carolinensis in Miami are hybrids with the non-native Anolis porcatus. If these are reclassified as non-native, our native count is down to just ~1%.

Figure caption: Bar graphs showing the difference in mean (a) abundance and (b) richness (±95% Confidence intervals) by year. Total abundance (p = 0.043) and richness (p = 0.001), as well as non-native abundance (p = 0.032) and richness (p = 0.0012), increased significantly from 2017 to 2022, whereas native abundance and richness did not (p > 0.4).

While Anolis spp. make up most of our observations, it was really the agamas and curlytails that stole the show this time around.

How I built a 6 foot long stainless steel anole lizard sculpture: the Movie

Screenshot from https://www.instagram.com/reel/DCnjCxhJmVS/

Read about Steve Nielsen, the artist, here.

Dewlap Drama in the Slender Anole: a Tale of Two Throats

Figure 1.

Distribution of sampling localities for individuals included in our breeding experiment. A Male slender anole dewlaps come in two morphs: solid and bicolor (photographs taken by John David Curlis). B Sampling localities in the Canal Zone of central Panama and associated morph frequencies of males in those populations (circle size corresponds to relative sample size from each site). The frequency of solid morph individuals generally declined from the Pacific to the Caribbean versant of Panama. C Sampling localities for individuals included in our Poolseq experiment. All these individuals were collected along a central trail that bisects Soberanía National Park, near the town of Gamboa.

Color us intrigued! In the world of Anolis lizards, the dewlap—a colorful throat fan used for communication—is one of the most iconic features. It’s been flaunted, flashed, and filmed in countless studies of behavior and adaptive radiation. But for all the attention it gets, we still know surprisingly little about how this flashy ornament is inherited at the genetic level.

Enter the slender anole (Anolis apletophallus), a small but charismatic lizard that ups the dewlap drama with a striking polymorphism. Males come in two distinct throat flavors: the “solid” morph, sporting a fully orange dewlap, and the “bicolor” morph, featuring a mostly white dewlap with a splash of orange at the base. What’s behind this variation?

To find out, we set up 99 crosses (yes, 99!) using individuals from populations that were either monomorphic (fixed for one morph) or polymorphic (home to both morphs). The results? A classic Mendelian plot twist. The dewlap polymorphism in this species is likely controlled by a single autosomal locus, with the solid orange morph dominant over the bicolor version. Simpler than we expected—but the story doesn’t end there.

Pooled sequencing revealed a strong candidate locus (single-minded 1, SIM1) that may underly the slender anole dewlap polymorphism. A Manhattan plot illustrating genomic differentiation between the dewlap morphs using pairwise FST values, and B Fisher exact tests. The red lines in B and C represent the Bonferroni correction (p value= 8.9), with points above the line indicating significantly differentiated SNPs across the slender anole genome. C One locus on scaffold 3, the transcription factor SIM1, contained a peak of many highly differentiated SNPs between morphs. The vertical green bars in the inset represent exons and the arrow represents the direction of genome annotation. D Nucleotide diversity (π) of SIM1 for the bicolor (green) and solid (brown) dewlap morphs. Note that nucleotide diversity was often higher in the dominant solid morph. E SNP panel showing segregating alleles in all significant SNPs (n = 175) in the candidate region of SIM1 for each morph plotted as a heatmap. We denote ref/ref in green representing that solid morph individuals were fixed for one allele and alt/alt in purple indicates that bicolor individuals were fixed for an alternative allele. Ref/alt in blue represents more than two alleles segregating at that position for either the solid or bicolor population. F Male slender anole dewlaps come in two morphs: solid and bicolor.

We also dove into the genome using pooled sequencing (Pool-seq) to search for regions associated with the trait. Our outlier analysis spotlighted a single genomic region with a strong signal—and within it, a prime suspect emerged: single-minded 1 (SIM1), a transcription factor with a flair for phenotypic control. Could this be the mastermind behind dewlap color in slender anoles?

The plot thickens, and we’re excited to keep unraveling the genetic threads behind one of the most iconic signals in lizard evolution. Stay tuned!

Link to the paper just published in Heredity.

A Three-Legged Lizard Mystery

Photograph by April Brown

Anole Annals has featured a series of posts on three-legged lizards over the years (e.g., here and here). Now we need help. Some time around 2017, April Brown contributed a photo of a brown anole missing both of its forelegs. The photo was taken in Winter Park, FL. We’d like to contact April, but can’t locate her. Can anyone solve the mystery?

Inter-island hostilities

A clip of a much longer video:

Two anoles, the ubiquitous Jamaican (Graham’s, Anolis grahami), which adorns every wall in Bermuda, and the seldom seen Barbados (A. extremus), just an occasional shadow in the shade, somehow finding themselves on the desirable territory of my bedroom window. They never came to blows, but the latter was definitely the winner, the Jamaican eventually retreating with his tail between his legs (metaphorically) after 8 minutes of posturing.

For more on the introduced anoles of Bermuda, see previous AA posts (here and here).

Anolis cannibalis

 

Photo by Wendy Frith

I live in Bermuda.

Many years ago, my daughter and I witnessed a large male Graham’s anole devour a small female, same species. We were horrified as we had watched these particular individuals so often we’d named them…the male was Pat Rafter as he spent much of his time up by the porch ceiling light catching bugs there; the victim was Porsche, because she was always on the porch wall railing. 

One day, I heard a scream from the porch…not from the lizard, but from my daughter: “Pat is eating Porsche!” and I arrived in time to see him sitting in her favorite spot with her back-half still protruding from his mouth. After the final gulp, he sat basking in the sun for a long time, then waddled off leaving an extra-long turd behind. My daughter and I went over and addressed it, with many apologies. We hadn’t known he was not just merely blue (and turquoise and purple) but was a reptilian Bluebeard…in fact, even worse: a Cannibal Bluebeard!

On the other side of the house there was a male I named Brown (because a friend of mine had a brown dog he’d named Purple). I taught him to accept food from my finger, and to come to the bathroom window when I whistled Bach’s Brandenburg Concerto #3 in G. He’s the one pictured at the top and bottom of this post.

Drawing by Wendy Frith.

Understanding Animal Behaviour, a Non-Fiction Graphic Novel

I dislike textbooks. I still remember the dismay as an undergraduate student of spending all that money to buy hugely expensive textbooks. And if there was any sense of excitement on cracking the cover of a textbook for a new course, it was soon scuttled by pages and pages of dense, dry text.

Now, as an educator, the cost of textbooks is still concerning but it’s their dubious pedagogical value that has led me to ditch them entirely from the courses I teach. Textbooks are great reference sources, but poor learning aids. They cover far too much material, often lack real-world context, and rarely illustrate the scientific process that led to a discovery.

There’s quite a bit of research in education showing that textbooks are not only considered boring by students, but students often struggle to recall and synthesize information obtained from them. Today’s students don’t read compulsory textbooks because the information they are more used to accessing is visually-based, focussed pieces of content online. So it isn’t really surprising that students have an aversion to reading course texts. This aversion is considered by many educators as one of the most critical issues plaguing higher education today.

Maybe you couldn’t care less about what undergraduates get up to (or not get up to). Maybe you’re just interested in learning cool things about animals, like anoles (obviously, and fair enough!). In any case, check out the soft release of the free graphic novel, Understanding Animal Behaviour.

What is the Proper Scientific Name of a Lizard when the Original Latin Is Incorrect?

Anolis winstoni from https://commons.wikimedia.org/wiki/File:Anolis_oculatus_at_Coulibistrie-b01.jpg

Peter Mudde writes:

I am chairman  of Lacerta, the Dutch Herpetological society. I also am a regular contributor to the magazine Lacerta. Lacerta  recently made an “Anolis special.” We are preparing a printed English version and we have an internal discussion about the matter below. 

In 1962 the late Skip Lazell, a regular contributor to Anole Annals described Anolis oculatus winstoni, stating: “This subspecies is named for Charles A. Winston, Manager of Woodford Hill Estate, and his family.” In recent years, the epithet “winstoni” has been changed to “winstonorum” as that would be he proper grammatical form if the subspecies was indeed named after Winston and his family (Michels and Bauer, 2004). This was critisized by Dubois (2007).

Now I am not familiar with the latest in zoological taxonomy, but I was under the impression that a name once given could not be corrected afterwards. That’s why the American alligator still misses a character in it’s scientific name.

Indeed, the combination Anolis occulatus winstonorum has emerged several times, mainly in non-scientific literature. Now my question is: how do those working with anole taxonomy refer to this subspecies?  Your verdicts please.

Anything New on Time Budgets in Anoles?

Anolis trinitatis (https://reptile-database.reptarium.cz/species?genus=Anolis&species=trinitatis)

A couple of my REU students from 2008 “rediscovered” their field notes and want to finish what they didn’t get done that summer. We were on St. Vincent and their project involved time allotment throughout the day by the anoles (Anolis trinitatis and A. griseus) at their study site on the grounds of the botanical gardens in Kingstown. They had done a solid literature review but now need to update it. We have had a hard time finding anything on time budgets published since then. We have found a number of papers on how activity is affected in urban environments but our study site really wasn’t urban (despite the location). So, in brief, I’m wondering if anyone is aware of any studies published since 2009 that examined time budgets in anoles?

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