Ameiva

Ameiva ameiva

Ameiva ameiva Photo from Fagner Delfim’s Flickr page

Here at Anole Annals we like to obsess over our  favorite lizards, anoles of course, but there are a vast array of other reptilian marvels out there,  formidable  Cyclurid iguanas, regally patterned Chilabothrus boas and of course the ever wary ground lizards of the Antilles (and elsewhere), the ameivas. Given the ample opportunity for exploration of these seemingly under appreciated animals  I have taken my best shot at writing a post concerning ameivas,  their morphology, ecology an various other bits and pieces of info I’ve picked up over the years; Enjoy!

The large neotropical genus Ameiva contains roughly thirty-two species largely distributed throughout eastern South America and the Caribbean with a few species  extending into southern Central America. Within this genus are some of the  most ubiquitous lizards of the neotropics, though due to their incredible swiftness and skittish demeanor it is rare that one ever sees one of these charismatic lizards out in the open for any extended period of time and even rarer that the casual observer  may encounter enough of them within a single area to appreciate just how numerous they can be. This rather ambitious  post focuses mainly on the  biogeography of  Ameiva, which in many ways mirrors that of Anolis. Most of the information presented herein comes from a 2012 paper  which , among other things, revises the genus Ameiva, recognizing several monophyletic clades and excluding certain species once thought to belong to the genus. More info on ameivas, as well as some amazing pictures, can be found at Father Alejandro Sanchez’s website.

Four geographically coherent clades or species groups have been identified within Ameiva,  two of which, the ameiva and bifrontata groups, occur in South and Central America as well as in Trinidad and Grenada, while the remaining two, the dorsalis and erythrocephala groups,  are distributed parapatrically throughout the Caribbean. Two additional species, A. parecis and A. concolor remain unassigned to any of these four groups.

The bifrontata group is the smallest of the four clades, consisting of one polytypic  species, A. bifrontata, as well as the closely related A. provitaae.

 This group is almost entirely South American in distribution, occurring in Colombia and Venezuela as well as on the island of Aruba. The clade is thought to share common ancestry with the West Indian  Ameiva species and both groups share several defining morphological characteristics the most obvious of which is the presence of mild to intense red coloration on the tip of the snout of most species, a feature shared by no other teiids.

The Caribbean  Ameiva form a monophyletic clade thought to be of South American origin
with the South American  A. bifrontata  species group thought to be sister  this one.

Jamaica: Caribbean Herpetofauna Island of the Day

Jamaica

If you’re anything like me, the first image you conjure in your mind when you hear the word Jamaica is a phylogenetic tree showing a monophyletic radiation of six Anolis species representing four ecomorph classes and one unique.

What, that’s not what you thought of?

 

Anolis grahami, a beauty!

Anolis grahami, a beauty!

The anoles of Jamaica: Read all about them!
1) Anolis garmani is a crown-giant, although it’s on the small end, if you ask me.
2) Anolis grahami is a trunk-crown and gram for gram one of the prettiest anoles out there.
3) Anolis lineatopus is a trunk-ground anole with a stunningly large cream colored dewlap.
4) Anolis opalinus is a smallish trunk-crown nicely found in a Blue Mountains coffee grove.
5) Anolis reconditus is a unique anole – very little known about it (but see).
6) Anolis valencienni is a twig anole, large and at high population densities for a twig.
7) (And yes, A. sagrei is there, but it’s invaded from Cuba over historical time.)

And as always, check out Caribherp for a full list of the herps of Jamaica and the Caribbean!

Jamaican Twig Anole Observations

Earlier this year ,while conducting crocodile (C. acutus) research in Jamaica, I observed some interesting behavior with the Jamaican Twig Anole (A. valencienni). The croc research is conducted at dusk and into the night, which leaves ample time to watch the anoles (during the day) that share our campsite. All of the Jamaican anole species are present at our camp in the Hellshire Hills except A. garmani. The camp is located just off the beach in a sea grape and buttonwood dominated coastal forest.

While lying in a hammock, I watched a female A. valencienni descend a branch toward a tree hollow. As she approached the hollow, I noticed several other females near the entrance hole. I know that it is documented that this species is a communal nester, but to see it was a real treat. During a quick survey of the immediate area (about 20 meter radius), I observed this same activity at two other tree cavities simultaneously. Up to five females were perched outside the cavities, while one or two inspected the entrance. At one of the tree cavities, the females were very wary and during several hours of observation, I noticed that the gravid females entered and exited (after deposition) freely.

At two other cavities, there seemed to be a backup. Females would enter or partially enter, then quickly exit the hole. It wasn’t hard to deduce that something else was occupying the cavity. Even more interesting was that the females at these cavities were not wary, actually completely aloof to my presence. I was curious as to what was preventing their access, so I peered and blew air into one of the holes. As I did this, the females at the entrance which were looking at my face only inches away shifted their attention into the hole. I still couldn’t see anything, so I utilized a flashlight and after doing so, saw that a Croaking Gecko (Aristelligar praesignis) was “blocking” entry and appeared to defend the cavity from intruders. Additionally, I noticed the walls of the cavity encrusted with eggs. Considering the size and shape of eggs, all appeared to be freshly laid or previously hatched Anolis eggs.

I cannot explain the female anoles’ behavior and complete disregard of my presence; even allowing me to touch them (see video).

I had several hypotheses about this behavior; one is that perhaps females worked cooperatively to intimidate the cavity occupier (gecko) at entrance… even enlisting the observer as an ally?

After egg depsition

After egg depsition

Before egg deposition

Before egg deposition

Gecko in cavity (blurry), eye and eyestripe can be seen.

Gecko in cavity (blurry); eye and eyestripe can be seen.

Could Your Reptile Make You Sick?

Photo from:http://www.panoramio.com/photo/73496249 ?

http://www.panoramio.com/photo/73496240

What do diseases like Ebola, Influenza, SARS, and Rabies have in common? Well, for one, they’re all viruses. Second, and more germane to this discussion, they’re all zoonoses–diseases that are usually harbored in non-human animal hosts but occasionally spill over into humans. Zoonoses are the subject of David Quammen’s excellent and aptly named new book, Spillover.

http://www.realscience.us/2012/07/30/ebola-virus-spreads-across-uganda/

http://www.realscience.us/2012/07/30/ebola-virus-spreads-across-uganda/

Quammen is in peak form with Spillover: he tracks these diseases and the researchers who study them from goat farms in Holland to bat caves in Uganda to wild meat markets on the Chinese mainland near Hong Kong. The book reads like a thriller–where exactly is Ebola lurking?– but doesn’t need fictional plot twists to keep the pages turning. Quammen’s accurate, clear, and exiting descriptions of the epidemiology, ecology, and evolution of zoonotic diseases keeps the pages turning instead.

http://upload.wikimedia.org/wikipedia/commons/5/50/Lesser_short-nosed_fruit_bat_(Cynopterus_brachyotis).jpg

http://upload.wikimedia.org/wikipedia/commons/5/50/Lesser_short-nosed_fruit_bat_(Cynopterus_brachyotis).jpg

A central message of Spillover is that a “successful” zoonosis is the result of opportunity. That is to say,  the life history of many zoonotic agents does not require a pass through human populations; they will survive, reproduce, and spread just fine in their animal hosts. However, if a zoonotic disease happens to find itself in a human body, those viruses (or bacteria, or protozoans, etc.) that can survive will survive, reproduce, and possibly spread to other people. Thus, the story of zoonoses is the story of humans creating the opportunity for spillover by coming into contact with animal hosts. For example, HIV (human immunodeficiency virus) is closely related to SIV (simian immunodeficiency virus) and all evidence suggests that it spilled into human populations through the use of chimpanzees for food. Nipah, a neurological and respiratory disease in Malaysia, Singapore, and Bangladesh, likely spills over into human populations through contact with fruit bat feces, contact that is becoming more common as human cities, towns, and agricultural fields encroach on the tropical rainforests that the bats call home. In sum, close contact with wild animals greatly increases the chance of spillover.

Close contact with wild animals… Close contact… Hmmm, what is it we do again?…

IMG_9314 copy

Photo from: http://www.ahailey.f9.co.uk/appliedherpetology/cariherp.htm

photo from: http://chipojo.webnode.cz/fotogalerie/#! Anolis equestris persparspus

 

 

 

 

 

Photo by Alexis Harrison.

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headless panama anole

 

 

 

 

Oh yeah… Uh oh! 

Reflections on the Joy of Winter Active Anoles

Photo by Janson Jones

Who wouldn’t delight in a passel of festive anoles, frolicking around in mid-December? Janson Jones, a raconteur if there ever was, certainly knows how to live for the moment. Check out his latest saurian musings on Dust Tracks on the Web.

Short Film Featuring P. J. Darlington and Anolis sagrei

In a new film,  Anna Lindemann uses predation by Anolis sagrei  on a group of beetles to explore the evolution of Batesian mimicry. Anna combines her interests in biology, art, and music to produce animations and live productions that explore processes in developmental biology and evolution.

Anna’s newest release, titled “Beetle Bluffs,” is inspired by the observations of biologist P. J. Darlington. Darlington might be most familiar to blog readers as the namesake for the Haitian anole, A. darlingtoni. In 1938, Darlington published a brief series of experiments examining the consumption of beetles with differing color patterns by A. sagrei. He concluded that Batesian mimicry was likely occurring, in which the color patterns of the inedible Thonalmus beetles are mimicked by several other edible beetle species in order to avoid predation. “Beetle Bluffs” combines stop-motion animation and archival material from Harvard University’s Museum of Comparative Zoology to bring life to this story. Enjoy!

Darlington, PJ. 1938. Experiments on mimicry in Cuba, with suggestions for future study. Transactions of the Royal Entomological Society of London 87: 681-695.

Anolis desechensis: Little Known Anole From The Puerto Rican Bank

 

desechensis island conservation FB

 

Anolis desechensis is a member of the A. cristatellus species complex from Puerto Rico. Found only on the tiny island of Desecheo, very little is known about its natural history. In fact, some might question whether it should be a distinct species, but in the absence of any data, it’s hard to say.

This lovely photo comes from the Facebook page of Island Conservation, a wonderful organization devoted–as its name implies–to the conservation of island biota. I just heard a talk yesterday crediting them for eradicating rats from an island in the Galapagos, paving the way for preservation of a unique giant tortoise race. But that’s another story.

Stephen Jay Gould On Replicated Adaptive Radiation In Anoles

image002 copy

“Dear Blair, of course you are right, but the scale is all wrong. Predictability of course within a constrained design and clade of close relatives as in your example. My contingency is at the much higher level of designs themselves.”

Blair Hedges recently sent me the image on the left with the following explanation:

“I was preparing a lecture for my evolution class and came across this reply from Steve Gould to me many years ago (Oct 1986), on a post-it note!

I can’t find my original letter to him but I recall it well.   As a grad student, I heard him give a lecture about the Cambrian Explosion where he claimed that evolution operated differently –contingency instead of adaptation or predictability– at the higher level of animal designs.  I told him I disagreed because I was seeing too much predictability in the adaptive radiations on Caribbean islands to believe that it was not happening throughout life at all levels.

Translation of his reply:  “Dear Blair, of course you are right, but the scale is all wrong. Predictability of course within a constrained design and clade of close relatives as in your example.  My contingency is at the much higher level of designs themselves.”

Not sure how you feel about it, but I still don’t agree with his explanation!  500 mya the Cambrian explosion was just an adaptive radiation like anoles.”

Interestingly, this story jibes very closely with a story of my own. In 1998, a number of colleagues and I published a paper in Science reporting a phylogenetic analysis of Caribbean anoles demonstrating convergent evolution of the anole ecomorphs. A reporter for Science contacted me and in the ensuing discussion, I suggested that an interesting person to contact to get an opinion of the paper would be Stephen Jay Gould. I was quite disappointed when her piece appeared and had no quote from Gould. When I subsequently talked to her, I was astounded to learn that she had, indeed, talked to Gould and he had given a reply pretty much exactly the same as on the post-it above. And…she had decided no one would be interested in what S.J. Gould had to say about replicated, convergent adaptive radiation, and so she didn’t include the quote in her article.

Why Aren’t All Crown Anoles Green? The Case of the Polymorphic Canopy Anole, Anolis cuvieri

Brown/Grey phase Anolis cuvieri, just awakened from a nap. Photo by Alejandro Sanchez.

Brown/Grey phase Anolis cuvieri, just awakened from a nap. Photo by Alejandro Sanchez.

Most arboreal anoles are green, and for a good reason: it’s hard to pick out a green lizard amidst green vegetation. Yet, some species are more subdued in their coloration, with browns or grays–e.g., Anolis luteogularis from Cuba or Anolis microtus from Costa Rica.

An interesting twist is provided by Cuvier’s anole, the crown-giant of Puerto Rico, in which a polymorphism exists in which most lizards are green, but some are brown-grey. We were reminded of this situation by Alejandro Sanchez, who sent the photo displayed above with the comment that it had been a long time since he’d seen one of these morphs. Contrast that with his spectacular photo of the more common green morph below.

Green Anolis cuvieri. Photo by Alejandro Sanchez.

Green Anolis cuvieri. Photo by Alejandro Sanchez.

Rivero in his epic Los Anfibios y Reptiles de Puerto Rico notes the polymorphism, but does not provide any explanation or discussion, and I am unaware of any other literature on this subject. Puerto Rican readers out there: what else do we know? Are they definitely different morphs? Someone once whispered in my ear he had seen brown ones turn green, but the only publication of which I’m aware to discuss this phenomenon, Rand and Andrews (1975), says they don’t. But that was based on a very small sample size. Does the gray/brown morph occur throughout the island? Any idea what it’s all about? Any difference in habitat use? As far as I’m aware, the adaptive significance of this polymorphism has never been studied.

The Role Of Genes And Diet In Determining Dewlap Color

 

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Results of mating trials in Ng et al.’s study. Top two rows are within-population crosses; bottom two are between crosses from different populations that differed in dewlap color. Note that in the top, individuals look like their fathers, whether at the bottom, dewlap colors are intermediate between that of the two populations.

Everybody loves a pretty dewlap, and recent years have seen a lot of interest in studying the factors that determine dewlap color, as well as the role dewlap color may play in species recognition, sexual selection and other processes. Many have suggested that the dewlap is a focus of sexual selection; some have even opined that it is an honest signal of something, maybe good genetic quality, maybe the ability to procure lots of color-inducing dietary items. Unfortunately, we know almost nothing about the genetic basis of dewlap color, nor about the effect of environmental variation.

Anolis distichus exhibits more variation in dewlap color and pattern than any other anole, and thus is the perfect choice for such a study. Julienne Ng just completed her doctoral research at U. Rochester on this species, documenting that variation in dewlap color correlates with environment among populations. Now she and colleagues report on laboratory studies to assess the extent to which variation is determined by genes vs. diet.

Why diet? Because reds and oranges are likely determined by carotenoids, which vertebrates cannot synthesize. Thus, it is plausible that the amount of carotenoids ingested by a lizard may correlate with its color. This hypothesis has only been tested once before, in a study on A. sagrei by Steffen, who failed to find evidence for a diet effect on the red-orange dewlap of this species.

This study had two components. First, to study genetics, lizards from two populations–one with an orange dewlap, the other with a plain whitish dewlap–were crossed in the laboratory. Second, lizards were fed lots of carotenoids.

The results: strong evidence for a genetic basis for variation in dewlap color. Purebred individuals looked like their fathers (top two rows in figure above), but crosses were intermediate in color (bottom two). Pretty strong evidence for a genetic basis for the trait. And the effect of diet? Not so much. No difference in color between lizards in the  carotenoid supplementation treatment vs. the control lizards.

The bottom line is that, at least in this species, genes control variation in dewlap color. Combined with Steffen’s study, there are now two negative results for a role of diet. Of course, work on other species is necessary to confirm the generality of these results, as well as additional investigation into the exact genes responsible for dewlap color.

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