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Spotlight on Cuban Anoles, Part I: Anolis bartschi

A juvenile Anolis bartschi scampers up a limestone boulder.

A juvenile Anolis bartschi scampers up a limestone boulder.

Recently, frequent Anole Annals contributor Martha Muñoz and I had the opportunity to visit Cuba as part of a licensed trip through the Harvard Museum of Natural History. During our two weeks on the island, we visited many localities and had the opportunity to photograph and observe some of Cuba’s most beautiful anoles. In the coming weeks, I’ll be spotlighting some of our favorites. All images presented are © Shea Lambert 2014.

First up: Cuba’s Western cliff anole, Anolis bartschi.

Knight Anole Eating Brown Anole

Photo courtesy Marissa Pierce

Photo courtesy Marissa Pierce

 

New Guide on How to Preserve Material for Genetic Studies

herp book cover

Blurb: “This guide will allow nearly everyone with an interest in amphibians and reptiles to collect and store samples for genetic analyses. It is written at a level appropriate for people with a basic background in biology, including professional scientists moving into a new project as well as wildlife managers, conservation biologists, ecologists, and others working on herpetological projects. The book should also be useful for advanced undergraduates and graduate students just starting their research careers.”

See more at the SSAR book website.

Price: $11

Call for Assistance: Anolis sagrei

Hi Everyone, a quick post to see if anyone out there is interested in contributing to a large ongoing project on Anolis sagrei. We are sampling this species throughout the (mostly) native range, and currently have 77 sampling locations represented. However, we are wondering if anyone would be able to help us fill some remaining gaps.
We are interested in adding additional tissue samples from Central America and the Bahamas. Here is an approximate range map with some desired localities (in blue):

R Graphics Output

Any help is greatly appreciated. I realize that collecting tissues (not to mention all the paperwork) is not a trivial task, so if you are interested in contributing samples please get in touch with me. We will keep AA posted on this project!

Aerial Behavior by Anolis pentaprion

 

Anolis pentaprion taxiing down the runway on a canopy tower at the La Selva Biological Station in Costa Rica. Photo by Vinicio Paniagua.

Anolis pentaprion taxiing down the runway on a canopy tower at the La Selva Biological Station in Costa Rica. Photo by Vinicio Paniagua.

Untitled-1Draco, the flying dragon, has borrowed an anole dewlap, so it’s only proper that anoles return the favor by developing gliding capabilities. It’s been long rumored that Anolis pentaprion, a twig anole from Central America, will launch itself off of perches in canopy and glide away, but now Steve Overbauer, Vinicio Paniagua, Craig Guyer and Mo Donnelly have documented just that in an interesting herpetological natural history note that appeared in the last issue of last year’s volume of Herp Review (Vol. 44, pp. 677-678).  Here’s what they have to say:

“Lizards with gliding or directed aerial descent behaviors are well known from the Old World Tropics (e.g., Draco, Ptychozoon), and snakes and frogs exhibiting these behaviors are found both in the Old and New World Tropics (Dudley et al. 2007. Annu. Rev. Ecol. Evol. Syst. 38:179–201). However, lizards showing directed aerial descent have not been reported from the New World Tropics. Here we report on directed aerial descent capability and behavior in Norops pentaprion, a canopy lizard from eastern Costa Rica, southern Nicaragua, and western Panama (Köhler 2010. Zootaxa 2354:1–18).

The initial discovery of this behavior in N. pentaprion was serendipitous in July 2001 when an individual was captured on a walk-up meteorological tower at canopy level (~ 25 m) at La Selva Biological Station in the Atlantic lowlands of Costa Rica. After identification, the animal was returned to the original location on the tower, but upon release to a horizontal tower brace, it executed a controlled aerial descent to a tree in the distance below. Individuals of N. pentaprion have been occasionally observed on our meteorological towers subsequent to our first observation of directed aerial descent. The lizards are typically at canopy level but are sometimes found well above the canopy on the highest levels of the towers (up to 42 m). While the typical response of N. pentaprion to the presence of personnel on the tower is to race down the tower or hide on the opposite side of vertical supports, the animals will occasionally jump from the tower to escape when approached. Since 2001 we have observed directed aerial descent by N. pentaprion from canopy towers on several occasions. In at least two instances the lizard landed at lower levels on the tower, but in other occurrences they covered substantial distance to adjacent trees including aerial rotations of near 180º. During more than one observation, animals appeared to glide with near-horizontal trajectories towards termination of the descent. Similar to some snakes, frogs, lizards, and ants showing directed aerial descent, N. pentaprion does not have strongly specialized features associated with gliding behavior such as skin flaps, skin extensions, or webbed feet. Norops pentaprion has a relatively flattened head and wide body. During aerial descent this lizard proceeds headfirst, with limbs partially extended and the body strongly flattened, a position that may take advantage of regions of relatively loose skin along the sides of the body (Guyer and Donnelly 2005. Amphibians and Reptiles of La Selva, Costa Rica, and the Caribbean Slope, Univ. California Press, Berkeley, California. 299 pp.).

At La Selva Biological Station this species is uncommon in the understory and is usually found on trees limbs. Norops pentaprion is a member of a closely-related group of anoline lizards subjected to a recent analysis of morphology and morphometrics (Köhler, op. cit.); these related taxa share similar body size characteristics with N. pentaprion and are frequently arboreal. Future observations of some of these species may result in the discovery of similar directed-aerial descent behavior. Canopy pioneer Donald Perry reported lizards with a rose dewlap parachuting between trees in the canopy in Costa Rican forests (Perry 1986. Life Above the Jungle Floor, Simon and Schuster, Inc. New York, New York. 170 pp.), but the species was not identified. In their description of Norops pentaprion, Guyer and Donnelly (op. cit.) indicated that parachuting behavior likely occurs in this species on the basis of our initial observations and those of Perry. Our repeated observations verify directed aerial descent in this species and confirm that the lizard observed by Perry was N. pentaprion, the only lizard in the region with magenta dewlap coloration.”

Anolis stratulus Displaying

Note the arm waving and tongue protrusion!

httpv://www.youtube.com/watch?v=OP3rnPQJT6A

How to Set Up a Lizard Room to House and Breed Anoles

Thinking of setting up a room to maintain and breed lizards for research projects? Back in 2011, the good folks in the Glor Lab–which has done a stupendous job at breeding A. distichus–shared their accumulated knowledge in an 11-part series. Given the fog of memory, it seemed like a good time to remind the world of the existence of this primer, and put the links all together in one place.

So, with no further ado, here are the 11 posts in the “Evolution of a Lizard Room” undecology:

1: Introduction

2: Maintaining humidity

3: The watering wand

4: Crickets

5: The Shopvac

6: Generating food in house

7: Egg-laying

8: Egg inculation

9: Toe clipping

10: Custom cages for breeding experiments

11: Butterfly Cages

For another source of information, check-out the manual put together by the Brodie Lab at the University of Virginia.

Anolis allisoni Featured in Film on Reptile Diversity of Cayos Cochinos, Honduras

httpv://www.youtube.com/watch?v=WyGO_rcVEM0

We’ve had previous posts [1,2] on research on anoles of these islands. Nice footage of ctenosaurs and boas as well.

50% Off Anole Watches for Next 2.5 Hours

What better way to celebrate moving your clock forward than getting that anole watch–available in five ecomorphs–that you’ve been coveting. Pop on over to Zazzle.com now, and don’t delay, because the deal ends at 1 p.m. Eastern Daylight Time. Use code word sundaydeal22.

What Makes Anolis Communities Complete?

One of my favorite graphic representations of a typical anole community is the one where all ecomorphs are hanging out together in a tree and a scrub next to said tree. Each ecomorph has its structural microhabitat place and they are all spaced out evenly across the tree to represent competition. Originally the figure was published by Williams (1983) and then modified later on. Arriving on the Greater Antilles, one thus expects to promptly be able to say hi to all these ecomorphs at the next best tree. Well, from my personal experience, I can tell you that this is unfortunately not the case.

Idealized representation

Localities where all ecomorphs are found together are scarce, and all of them are famous, having served as field sites for the most groundbreaking of anole discoveries. But what about the rest of them? Something must prevent the co-occurrence of ecomorphs in all these other places. This was noted before: Losos (2009) remarked that all utilized structural microhabitats exploited by all ecomorphs are present throughout the islands, so “complete” ecomorph communities should also be able to occur everywhere.

A common explanation for the absence of certain  “functional types” (= Anolis ecomorphs) from local communities is a process that is called “filtering.” Modern community assembly theory distinguishes two such types of filters: 1. Biotic interaction filters and 2. Environmental filters.

 Filters

Biotic filtering involves competitive exclusion: For anoles this phenomenon caused ecological speciation which led to the convergent evolution of the ecomorph communities. But biotic filtering should not be expected to occur at this stage of the radiation: Different ecomorphs are not competing for the same structural microhabitat niche in different localities. This leaves environmental filtering. In our study recently published in Ecology and Evolution, on which I am reporting here, we tested whether environmental filtering could be a possible explanation for the absence of ecomorphs in local communities.

First, we modeled Anolis ecomorph community completeness by constructing environmental niche models for each ecomorph (the sum of species belonging to that ecomorph) on each island. These models were then overlaid for all ecomorphs per island.  ECC map

 The map for ecomorph community completeness shows a very patchy distribution of areas where all ecomorphs are expected to occur. Comparisons of environmental niches among these islands revealed that only Hispaniola and Cuba have their complete Anolis ecomorph communities occurring in a similar bioclimatic parameter space.

This patchiness could be explained by elevation for all islands except Jamaica: the Anolis community completeness map strongly resembles the topographic relief of the Greater Antilles. Looking more closely into the climatic parameters, Jamaica has much lower daily and annual temperature ranges which are also not related to the island’s elevation, whereas in the rest of the Greater Antillean islands, they are. Occurrence probability of ecomorphs seems to be coupled to environmental parameters, which explains why some ecomorphs are “filtered out“ in some locations: they do not encounter a favorable environment there.

Since I mentioned initially that filtering relates to “functional types” (not species), the filtering must be a result of certain functional properties of the Anolis ecomorphs’ phenotype. We wanted to take the study a step further and actually investigate one (among many) possible functional trait: body mass.

Page 124 of 153

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