Colors And Shapes Of The Horned Anole

 

Ecuador's most wanted! This lizard was thought to be extinct for nearly fifty years, and still after its "rediscovery" in 2005, it remains hard to locate.

Ecuador’s most wanted! This lizard was thought to be extinct for nearly fifty years, and still after its “rediscovery” in 2005, it remains hard to locate.

Most records of Horned Anole are in disturbed areas, including near roads vegetation, botanical gardens and bamboo trees.

Most records of Horned Anole are in disturbed areas, including near roads vegetation, botanical gardens and bamboo trees.

It took me more than two years of constant visits to Mindo, a cloud forest-town in the Western Ecuadorian Foothills, to meet with the Horned Anole (Anolis proboscis)! I always felt it was a mythological reptile, not only for Ecuadorian herps but throughout the world. Has anyone seen a lizard with a long appendix on the tip of his nose, a wide color throughout the body, prehensile tail and even spines on the back? It is difficult not to speak mystically when we refer to Horned Anole.

For over 50 years it was listed as “Possibly extinct,” until 2005, when a group of Ecuadorian scientists “rediscovered” it. But it was not until two years ago when the global and local Anole experts, led by Jonathan Losos, Steven Poe and Fernando Ayala, started several expeditions to investigate everything about its morphology, phylogeny and natural history.

Its tail is prehensile and is possibly used to embrace the branches when it sleeps.

Its tail is prehensile and is possibly used to embrace the branches when it sleeps.

The Horned Anole is a diurnal and slow-moving lizard that usually is found perched between 4-8 meters above the ground. Although most records are in vegetation on roadsides, highways and near open areas can be very difficult to find due to their excellent camouflage that blends perfectly with twigs full of mosses, lichens and epiphytes, perfectly rhyming its colorful skin.

But what use their proboscis? Sexual selection and defense of territory are the first hypotheses that leap to the mind. Science will tell us soon! But even that, we are left to enjoy its beauty and unparalleled mystique.

 

 

Definitely its silhouette is unmistakable. His sharp proboscis distinguishes it from all Ecuadorian lizards.

Definitely its silhouette is unmistakable. His sharp proboscis distinguishes it from all Ecuadorian lizards.

It can be difficult to find. Not only because they are commonly perched on high branches, but also for their camouflage, forming an ideal combination with branches and colorful leaves.

It can be difficult to find. Not only because they are commonly perched on high branches, but also for their camouflage, forming an ideal combination with branches and colorful leaves.

It is slow-moving and spends most of its time 450–800 cm from ground and feeds on a variety of arboreal arthropods.

It is slow-moving and spends most of its time 450–800 cm from ground and feeds on a variety of arboreal arthropods.

 

Anolis proboscis sleeps on horizontal twigs and leaves (juveniles seem to prefer lower perches).

Anolis proboscis sleeps on horizontal twigs and leaves (juveniles seem to prefer lower perches).

Some Cool Anole Photos

Not sure how I came across these on the web, but I found Robert Hoogveld’s flickr page and he kindly allowed me to post these fabulous photos. Some may recall the post on Robert’s article on A. proboscis two years ago. Apparently, he has some more good stuff up his sleeves, or so he tells me.

Photo by Robert Hoogveld

Anolis marmoratus. Photo by Robert Hoogveld

 

Photo by Robert Hoogveld.

 

Anolis (Chamaelinorops) barbouri. Photo by Robert Hoogveld.

 

 

 

 

Photo by Robert Hoogveld

Anolis oculatus. Photo by Robert Hoogveld

Marine Subsidies, Washed-up Seaweed, and Insect Damage To Plants: What’s the Role Of Lizards?

Seaweed washed ashore on a Bahamian island. Photo by Dave Spiller.

Ecologists are increasingly recognizing the myriad connections not only among species within an ecosystem, but between species in different ecosystems. Case in point: seaweed often washes ashore, and it affects leaves on the plants found near the shoreline. How’s that, you might ask? Well, the seaweed decays and releases nutrients that act as fertilizer, increasing the growth of land plants. That’s good for the plants, but it also makes their leaves more tasty, and hence plant-eating insects are attracted and cause more damage to the leaves.

That seems straightforward enough, but then it gets more complicated. As the seaweed decays, it attracts lots of insects. And the insects, in turn, attract lizards. And, in fact, if you happen to be studying this process on small islands in the Bahamas, as Jonah Piovia-Scott and a team from UC-Davis were, then those lizards are our favorites, brown anoles. And if there are more brown anoles around, then they’ll eat more of the herbivorous insects that plague the land plants, and so the washed-up seaweed actually decrease the damage to land plant leaves, thanks to the helpful consumption of the anoles.

Except…maybe the lizards will be so delighted by the seaweed that they’ll spend all of their time there, eating the insects on the seaweed, and thus neglecting the insects on the landplants, so now the effect of seaweed on the land plants becomes negative again.

path diagramSo which is it? That’s what Piovia-Scott et al. set out to discover, and they’ve just reported the results in a paper in Oecologia. And the diagram to the left explains it succinctly. Seaweed increases nitrogen in the leaves, which increases herbivory. Seaweed also increases lizard density, which decreases herbivory, though the negative effect isn’t as great as the positive effect of the nitrogen. Moreover, seaweed also causes lizards to shift their diet, which has a small (and statistically non-significant) positive effect on herbivory because the lizards aren’t eating as many of the land plant herbivores. Bottom line: seaweed increases leaf damage; lizards can’t prevent it, in part because their effects are schizophrenic: more lizards, but eating fewer herbivores.

Interestingly, these results are opposite of what the same team of authors found in a study we discussed two years ago. The difference was that in that study, a big pile of seaweed was laid out at one time and the results were followed over a short period, whereas this study followed natural seaweed deposition and compared sites differing in the amount of seaweed washed ashore, following their sites for a lengthier period of time.

One last point: how did the researchers document that the lizards were switching diet? Not from sitting around and watching the lizards, but by measuring the carbon isotope ratios in their tails. Marine vegetation tends to have higher ratios of Carbon-13 than terrestrial sources, and so insects feeding on plants from different areas will, in turn, have different ratios, which means that, in turn, one can look at the Carbon-13 ratios in lizard tissue and get a sense of from which ecosystem they’re deriving their carbon. And in this case, the more seaweed, the higher the ratio. Pretty nifty!

Attempted Predation Of A “Yelping” Cuban Treefrog By A Knight Anolis

httpv://youtu.be/Du9oQr8PQC4

This occurred at 10:20 AM April 12, 2004 in South Miami Florida. I was working in my kitchen at my home in South Miami Florida with my back porch door open, when my attention was captured by a loud “yelp-yelp” sound in repetition. I also noticed that I heard the “distress” call of a cardinal – similar to what I would hear if there was a cat or snake in my backyard. I grabbed my Sony cybershot 3.2MP and ran out my back door. On an adjacent pony tail palm (Nolina recurvate) just below the crown, about 8’ off the ground I saw a large knight anole (Anolis equestris) in a head down position. The anole had in its mouth, the back legs (below the knees) of a Cuban treefrog (Osteopilus sepentrionalis). The frog was making a very loud repetitive “yelp-yelp” sound while trying to climb out/away from the lizard’s mouth using its front legs. There were a pair of cardinals and mockingbirds, and a blue jay that were attracted to the sound. The cardinal was calling, and the mockingbird was approaching and slowly opening and moving its wings in a “swimming fashion,” making it obvious as it walked across the ground. The birds’ focus seemed due to the frog’s call. I have never experienced any reaction of a bird to the many resident Knight anoles in my property or elsewhere. I managed to get a short clip (meaning to take an image) and a captured still is what you see attached. After a few more cycles of yelping, the frog managed to break free from the Anolis’ mouth and hopped away behind my AC unit. Having had some firsthand past experience with Osteopilus’s antipredatory compounds, I wondered if they had the same effect on lizard’s bucccal cavity as they did on this (at the time intoxicated) human. I had heard a very similar call from an unidentified tree frog in Costa Rica 1998. It had been captured by a parrot snake (Leptophis sp.) that fell to the ground in front of a friends horse while we were jungle riding in Guanacaste. To humans, the call does sound very much like a baby, or toddler’s wail. I would be interested in knowing if it serves to attract other predators giving the “crier” a possible distracting means of escape.

Glitter Anole

Woo-hoo! Check out these anole beauties. And the green one actually has a red dewlap and looks passably like Anolis carolinensis. Google “plush anole” or “glitter anole” and you can have your own–for as little as eight buckaroos.

But there’s a backstory. Over the years, two undergraduates who worked in my lab each gave me a plush anole as a thank you present when they graduated. One day I was talking on the phone and idly picked up one of the stuffed fellows. Still attached to it was the information tag. And as I opened the tag, which contained natural history information, reasonably accurate, on A. carolinensis, I was amazed to see this:

No doubt, you can see one cause of my amazement. That’s no Carolina green anole, but rather its ecomorphic döppelgánger from Hispaniola, A. chlorocyanus. And, moreover, that’s not just any photo of a Hispaniolan green–that’s my photo! And, as you might have guessed, used without permission.

Incensed, I looked to the bottom of the tag for the company that makes the toy, Fiesta Toys. I looked them up online and went to their contact page. I filled in the little box on the page, noting that they had used my intellectual property without my permission. I pushed “send,” figuring I’d never get any response, much less satisfaction.

How Often Do Lizards Capture Enormous Prey? And How Often Are They Unable To Consume It?

The photograph above from Daffodil’s Photo Blog shows a brown anole that has just caught a roach almost as big as itself. The lizard was actually able to run away with its prey, so we don’t know if it was consumed.

This, in turn, reminds us of a previous post of DFB in which a green anole again caught a really large prey item, in that case a moth, but again the outcome was unknown.

Imagine eating a Big Mac 80% of your body weight. Think how long you could run on that, and you’re warm-blooded–lizards have a much lower metabolic rate. How often do anoles get this bonanza? Certainly, most of their prey items are quite tiny in relative terms. And how often do they catch prey that they ultimately can’t ingest? There  is a lot of data on anole diets in the literature, but no one has every synthesized it to see what general messages can be extracted, what broader questions–such as this one–can be addressed. Would make for an interesting project.

Review Of The Giant Dactyloa Anoles Of Panama With Description Of A New Species

 

Anolis ginaelisae

Anolis ginaelisae

Six large anoles of the Dactyloa clade occur in western Panama. In their explorations, Lotzkat and colleagues have collected all of them, and have just published a paper in Zootaxa reviewing these species. Their phylogenetic analyses based both on DNA and morphological characters confirm the existence of the six taxa, but also find geographically-oriented genetic differentiation in two species. In combination with morphological data, the authors split A. microtus into two species, the new one under the name A. ginaelisae.

The paper includes a nice review of all the species including spiffy color plates (see A. ibanezi below as an example) and natural history notes (short take: they’re all arboreal and almost all individuals have been caught at night). A key is also included.

Anolis ibanezi

Anolis ibanezi

One last note. The derivation of the new specific epithet gianaelisae is touching: “Sebastian Lotzkat dedicates this exceptionally beautiful new species to his even more enchanting fiancée Gina Elisa Moog, who has made more than a third of his life worthwhile by now, in deepest gratitude for that wonderful time and pleasant anticipation of a mutual future.”

Abstract: “Six species of giant alpha anoles of the genus Dactyloa are known to occur in western Panama: Dactyloa casildae, D. frenata, D. ibanezi, D. insignis, D. kunayalae, and D. microtus. Based on own material collected along the highlands in Bocas del Toro, Chiriquí, and Veraguas provinces and the Comarca Ngöbe-Buglé of western Panama, we review their variation in morphological characters and the 16S rRNA mitochondrial gene. Our results support all six nominal taxa, but reveal considerable genetic differentiation between populations of the two highland species, D. casildae and D. microtus, respectively, from different localities. Correlated morphological differences confirm the existence of a cryptic species among populations currently assigned to D. microtus, which we describe as Dactyloa ginaelisae sp. nov. We provide point distribution maps, morphology and color descriptions, photographs in life, conservation status assessments, and an identification key for all seven species.”

Brown Anole – Green Anole Interactions

Periodically, we’ve discussed how green and brown anoles interact now that they’ve been thrown into  sympatry in the southeastern U.S. and elsewhere–do they fight, do they mate, do they just ignore each other? Perhaps, it seems, a little bit of each. In any case, the latest report comes from Janson Jones over at Dust tracks on the web, who presents a nice tryptich of observations and photos on a one-side green-brown interaction in southern Georgia. As always, the photos are sumptuous and the text entertaining.

Frog Eats Anole

Brown anole being eaten by a Cuban Treefrog. Photo by jwood10016.

Surely you remember the heart-warming story–the best post AA has ever had–about Gordon, the green anole that was almost eaten by a Cuban tree frog, but somehow escaped and lived to see many more days (if you haven’t, check it out now!). Well, apparently the story doesn’t always end so happily for anole-kind. Above is a photo from Orlando, Fl, of a brown anole going down the hatch, and there’s no reason to believe that it came back up. There’s a whole series of photos on planetisuzoo.

Research Projects Of Anolis lizards In Cuba

Anolis homolechis

From 2009, we have investigated the evolution and ecology of Anolis lizards in Cuba, collaborating with Habana University and The National Museum and Natural History of Cuba. Prof. Losos asked us to describe our research projects in Cuba for communication among anole biologists. Thus, we would like to inform our ongoing projects on Anolis lizards in Cuba, and we are very grateful if you have any suggestions and comments on our projects. Also, your suggestion of collaborating research projects will be welcome.

1. Searching for the genetic basis determining differences in hindlimb length between the trunk-ground anole A. sagrei and the twig anole A. angusticeps. Similar to Sanger et al. (2012), we have tried to determine the developmental timing for divergence of hindlimb length between twig and trunk-ground anoles. The manuscript on this subject was submitted and is now under review.

2.  The effects of microhabitat use, range expansion and the number of speciation events on local species richness of trunk-ground Anolis lizards in Cuba. We examined the species richness and thermal microhabitat partitioning (considered to be a measure of ecological interaction) of 12 trunk-ground anole species in 11 local assemblages in Cuba, covering nearly the entire geographic range of all these species. Our results suggest that the species composition and richness in local assemblages could be explained by both evolutionary history (the number of speciation events and limits to range expansion) and ecological processes (habitat partitioning). This research is a part of Ph.D. thesis of Antonio Cadiz (Tohoku University and Havana University). The manuscript on this subject was accepted by Ecosphere and will be available soon.

3. We reconstructed a phylogeny using almost all Cuban Anolis lizards and also analyzed the genetic distances between populations within Cuban islands for these species. This project aims not only to construct the comprehensive phylogeny, but to understand ecomorph evolution within Cuban island.

4. Genetic basis for adaptation to different thermal environments. Multiple trunk-ground species can coexist since they inhabit different thermal environments. Anolis sagrei was found in open locations with high levels of light intensity and temperature. In contrast, A. allogus was found in shaded locations within forests with low levels of both light and temperature. Anolis homolechis was typically found at the edges of forests or in open locations in forests with intermediate environmental conditions. We try to examine genetic basis for these different thermal adaptation by using both  a candidate gene approach and whole transcriptome analysis.

5. Other research projects will be started this year, although we do not specify the detailed plan.

In addition to Cuban Anoles, we are investigating the evolution of Anolis carolinensis introduced into the Bonin islands (Ogasawara islands) about 50 years ago (from either Guam, Hawaii or Florida).

Masakado Kawata, Graduate School of Life Sciences, Tohoku University, Sendai, Japan (kawata ‘at’ m.tohoku.ac.jp)

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