Revealing the Diversity in “The Highest Kingdom of Anolis

A view of the Andean scrubland, the main habitat of the lizards of the Anolis heterodermus group.  Rafael Moreno

View of the Andean scrubland, the main habitat of the lizards of the Anolis heterodermus group. Credits: Rafael Moreno.

Several years ago, when I began my biology studies, I was taking a walk in an Andean scrubland near my hometown, Bogotá, and while admiring the twisted shapes of the shrub branches, I noticed a small bright-green elongated spot on a branch, which stood out from the surrounding vegetation. The spot looked like an altered vision produced by entheogenic substances. As I approached the spot, my anxiety increased because it was slowly rotating around the small branch while I was getting closer. But when I was close enough to identify it, my anxiety ceased. It was not a hallucination, but a lizard, an Anolis heterodermus!

Some years later, my anxiety returned when I thought about the future of those lizards due to the advance of a gigantic city hungry for concrete. We decided to investigate it by trying to document the dynamics of populations in scrublands surrounding Bogotá. Even though the city continued its inexorable growth, it seemed that these lizards had several strategies to face the loss and fragmentation of their habitat, but only if the urban development onslaught was not too strong. Thus, my anxiety ceased, but only partially.

To describe the phenotypic variation in heterodermus group

A small sample of the huge phenotypic diversity in A. heterodermus y A. richteri. Credits: Rafael Moreno.

Dewlap Displays Supersede Headbobs, Yet Again

The dewlap is probably the most noticeable thing about anoles. For me, the best way to spot an anole is by the flash of color from the dewlap as a lizard displays. Without that, many anoles would remain cryptic amongst the vegetation. This seems to be the case for the lizards themselves as well. The burst of color and movement as the dewlap is rapidly extended is a wonderful device for attracting the attention of rivals and mates. It’s possible that the dewlap originally evolved as an attention-grabbing flag to augment an existing sequence of elaborate headbob movements in forested environments. These days, the dewlap is a complex signal component in its own right, often with a dizzying array of colours and displayed using a variety of movements.

Anoles aren’t the only ones with a moveable dewlap. The Southeast Asian Draco lizards have a dewlap, and again to back up the headbob movements that make up their main channel of social communication. There are many other parallels between Draco and Anolis lizards, but the similarities in how they communicate is something that particularly fascinates me.

Early on in my fieldwork with Draco, I started discovering species that didn’t seem to use headbobs as part of their social display. It seemed these species had lost the headbob entirely and instead concentrated all of their communication through the dewlap display. These species are a minority, but not by much. It was a puzzle. These Draco had lost a central and complex element of their communication in favour of something that was seemingly more basic. Communication biologists are often fixated on trying to explain how animal communication becomes more elaborate over evolutionary time, but less attentive to why complexity subsequently becomes lost. These Draco lizards were an excellent case study.

Draco melanopogon (photo above) only communicates using the dewlap, whereas Draco sumatranus (opening banner photo) relies on both headbobs and the dewlap, just like anoles.

After nearly a decade of fieldwork on numerous species of Draco throughout Malaysia, Borneo and the Philippines, my trips stalled in 2020, as did the rest of the world. Celebrities had nothing better to do than write biographies, but my lockdown project was to focus on using the data I already had at hand to finally solve the curious case of the missing headbob.

It felt like an endless series of stay-at-home orders in Australia, and well into 2021 too. While the celebrities had gone on to finish their books and were now doing the zoom promotion circuit, my progress was hurdled by home-schooling two young children. We survived home-schooling in the end, and my attempt at figuring out why some Draco have lost the headbob has finally been published.

The evolutionary history of visual displays in agamid lizards

The first discovery is the headbob display is very ancient, evolving something like 130 million years ago or more. That’s before the evolution of Draco, and before the evolution of the anoles, in an evolutionary ancestor to both the iguanid (new world) and agamid (old world) lizard families. This was back in the age of the dinosaurs. Today, virtually all iguanid and agamid lizards use a headbob display or some variant of it in social communication. Which means the absence of the headbob in a handful of Draco species is very unusual.

The loss of the headbob from the social display of Draco is effectively a loss of complexity. A loss of complexity means a loss of “information potential.” Try writing a biography with half the alphabet. You might manage the following or something a little longer: “I was born. I paid taxes.” Thirteen unique letters in total. Obviously not the rich backstory you might hope for. Not because you hadn’t lived a fulfilling existence; rather you don’t have the language complexity to convey it in detail.

There are various reasons animals might lose complexity in their social signals. Perhaps the original need for a complex signal is no longer present. Perhaps the invasion of a new environment puts a brake on the level of complexity that can be accurately perceived. Or perhaps natural selection on other things, like body size, has made performing a complex signal too costly.

The beauty of having spent so much time in the field is the accumulation of a large library of data. By leveraging this information, I was able to test each of the above scenarios. The short of it is, Draco that have lost the headbob are unusually large species. Physically moving the head and body in a headbob display is more energetically expensive than pumping the dewlap in and out. It seems, then, that the physiological cost of performing the headbob became too great for these large species and they shifted to relying only on the dewlap for communication. This implies the communication system of these species is compromised, unless they have made up the loss of information potential somewhere else.

Draco without the headbob have more complex dewlap colour patterns. Each dot is a different species.

In fact, the dewlap itself tends to be more complex in Draco that have lost the headbob. Stealing a method for measuring complexity of anole displays, the dewlap of these Draco are more elaborately coloured than the average Draco. Unfortunately, this is unlikely to have been enough to fully cover the loss of the headbob. This means Draco that no longer use the headbob are relying on a constrained communication system.

The idea that the headbob is likely to be more energetically expensive than the dewlap was originally proposed for the anoles. It was used to explain the physiological basis for why Jamaican anoles might have evolved an innovation that allowed them to move away from a headbob-centred display in favour of one focussed on the dewlap. To be clear, the Jamaican anoles do still rely on headbobs in their social displays. But a rapid series of dewlap pumps features more prominently in their displays compared to the typical anole, like those on Puerto Rico for example.

It seems the dewlap has begun to supersede the headbob in anoles as well.

If you’d rather not slog through the paper itself, you can view a 12 minute video summary instead. If you would like to slog through the paper and can’t access it behind the paywall, drop me an email and I’ll forward you a free copy (t.ord@unsw.edu.au).

English Translation of Special Issue of Lacerta on Anoles Now Available

English translation now available!

 

Robert Hoogveld writes:

This year the Dutch society for Herpetology “Lacerta” celebrates its 80th anniversary. To celebrate, a lot of hard work has been done over the past year on a special edition of our journal, Lacerta, entirely aimed at anoles. We call it the Anolis special. It has become a 256-page book with contributions from Anolis enthusiasts and connoisseurs from the Netherlands, Belgium, Germany, Finland and Canada. It contains articles about, among other things, the study of anoles, behavior and welfare, travel reports with herpetological observations and species descriptions including the experiences of keeping in captivity.

At the moment the book can be ordered for anyone interested.  website: https://nvht-lacerta.nl/.On that website, everybody can order a copy for €20, including shipping world wide.

Parallel Urban Adaptation from Phenotype to Genotype in Anolis Lizards

Anoles are models for studying evolution in the wild. Not only do anoles have a history of repeatedly diversifying to specialize in the same types of microhabitats in the same ways across the Greater Antilles, these lizards also have a tendency to adapt on rapid timescales to environmental change — be it the addition or subtraction of a predator or competitor, a polar vortex, a change to the structural environment, or a hurricane.

Anoles are also models for urban evolution. Why? Anoles are found abundantly across the Caribbean in urban and forest environments where they specialize in divergent microenvironments characterized by shifts in climate and physical structure. Urban habitats tend to be warmer, drier, more open, and dominated by buildings and impervious surfaces instead of vegetation — providing the perfect opportunity for repeated adaptation to a novel combination of environmental conditions. In other words, Caribbean cities provide a replicated natural laboratory to study adaptation as it happens when these lizards colonize and thrive in urbanizing areas. And there is no shortage of urban-tolerant and urbanophilic anole species to choose from!

Species of Anolis lizards are found in urban environments across the Caribbean (photos CC-BY K. Winchell; Earth at night by NASA).

Anatoly Anole Loses His Tail

Greetings Fellow Anole Fans,

I have just published my second anole book, mostly for children with many solid lizard facts most of which I have learned from posts on this website.  Grandmothers, here in mid-Florida where I live, love entertaining their young visitors with facts and stories about these curious little creatures. Also, right on the title page of the book, Anatoly announces that he is NOT A GECKO!   Ardi Schneider, Vero Beach, FL

 

My Research Trip to Florida to gather Info for The Lizard Scientists

I thought you anole lovers might like to read the post I wrote about my research trip to Florida for my book “The Lizard Scientists” for my colleague Caroline Arnold’s blog “The Intrepid Tourist.

A student at the school found this anole egg and showed it to me–great find!

I was hardly a tourist, but rather a lizard-loving author sweating in the Florida sun while observing James Stroud and Kamau Walker capture, measure, take notes, etc. about the anoles living on Jame’s research island in the Fairchild Gardens. There’s a chapter in the book devoted to James’ research.

I also joined photographer/anole researcher Neil Losin to photograph some different anoles near Parkland and visited a school where students gathered population info on anoles on their school ground.

The whole trip was great, and I went home impressed by the hard work and the cheerful enthusiasm of everyone for these lovable lizards.

Naturalized Lizards Collide on Kauai: Nocturnal Brown Anole-on-Gecko Predation

While hunting sagrei for fun this evening with my 3-year-old, we spotted a large male Anolis sagrei eating what I think is a mourning gecko (Lepidodactylus lugubris). This happened at 7:18 pm in the presence of minimal artificial light from lamps (albeit strong artificial light from my headlamp). Plenty of sagrei were already asleep on leaves. Surprising to find a diurnal lizard preying on a nocturnal/metaturnal gecko.

 

Exploring the Drivers of Sexual Dimorphism in the Green Anole

Our brains are fast to picture differences between males and females, probably because these differences are everywhere in nature. Popular examples might include the manes and antlers of lions and deer, which are specific to males, or maybe the striking sexual differences in coloration in many birds (think of the classic peacock example). Besides these illustrative cases, size differences between the sexes might be even easier for us to accept as a common pattern in nature. Males are, on average, larger than females in elephants, pheasants, iguanas, and in our own species. Females, however, take the role of the larger sex in other animals like spiders, snakes, and many bird species. In any case, I think one could conclude that we are familiar with the idea of males and females being phenotypically different, and that we are especially aware of sexual differences in size.

Going a step further, I think we even have a general idea of why these differences exist, at least in the case of size differences between sexes (which I will now refer to as sexual size dimorphism, or SSD) and especially in the case where males are larger than females. “Males are larger because they need to be stronger” might be a stereotyped idea, but it is ultimately true in many cases as males usually need to physically compete with other males to get access to reproduction.

Island Colonization, Drought, and Competition in Panama

You open your eyes, blinking away water, you’re on a beach you don’t recognise, and never set out to visit. You look up and along the coast, it’s an island, the flora is alien to you, the climate hotter, and you’re already sweating. An eldritch cry emanates from the forest near you, new wildlife, things you have never seen before skulk around beyond the vines that lay before you.

Lifting yourself up, you decide to escape the blazing sun. You leave the beach and push through the wall of vegetation that veils the forest from the beach. You expect it to be cooler, but it isn’t. The forest is completely new to you, as you move through the undergrowth, unfamiliar insects dart away, flying past plants you’ve never seen before. As you press on through the undergrowth you wonder how long you will have to spend here? How much more time do you have here?

New Book for Young Readers on Anoles and the Scientists Who Study Them

Dorothy Patent, an author who specializes in writing books for young readers about science and nature, has turned her attention to our favorite lizards. Lavishly illustrated with beautiful photos by the Day’s Edge team of Nate Dappen and Neil Losin, the book is a fabulous introduction to studying  evolution as it occurs.

Scientists featured will be familiar to AA readers: Shane Campbell-Staton, Jason Kolbe, Rob Pringle, James Stroud, Kristin Winchell and me.

A perfect stocking stuffer for kids of all ages (though 8-12 years old (3rd – 7th grade) is the target audience!

Here’s the description from Amazon:

In this groundbreaking, exceptionally researched installment of the award-winning Scientists in the Field series, discover how lizards rapidly adapt to life in the Caribbean islands, allowing scientists to study Charles Darwin’s theory of evolution by natural selection in real time. 

Award-winning author Dorothy Hinshaw Patent joins forces with scientists/filmmakers Neil Losin and Nate Dappen, whose work is detailed in the Smithsonian Channel documentary “Laws of the Lizard,” to explore how the small but mighty lizards we call “anoles” are used by scientists to study basic principles of evolution and ecology.

Travel with the team to Florida and the Caribbean as they research how anoles followed similar but independent evolutionary paths on the four major islands of the Greater Antilles (Puerto Rico, Hispaniola, Jamaica, and Cuba). So while anoles on different islands may look like close relatives, they often are not! This is Darwin’s principle of natural selection at work.

And it makes anoles the perfect subjects for experiments that study how animals adapt to new challenges—such as climate change—in this exciting and timely addition to a celebrated series.

 

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