Author: Christian Perez

Ecomorphology of La Selva Anoles

Ever since the seminal papers by Williams and Rand [1,2], the Anolis radiation across the West Indies has increasingly established itself as an alluring example of ecomorphological convergence. Considering an Anolis community on one island, sympatric species have undergone niche partitioning, whereby each species has evolved particular behavioral, morphological, and ecological traits well-adapted for the microhabitat it occupies. Pop over to another island, and voilà, similar sets of ecomorphs can be found— their resemblance so striking and uncanny.

But the Anolis story isn’t clean cut. Studies of mainland anoles have yielded equivocal findings for whether they also conform to the beautiful patterns observed in the Caribbean. Much baseline data on mainland Anolis communities are needed to determine the extent to which convergence occurs and what factors drive differences in community structure. To partly address this gap, Jonathan Losos, Anthony Herrel, Ambika Kamath, and I recently published a paper describing the ecological morphology of anoles in a lowland tropical rainforest in Costa Rica, at La Selva Biological Station.

Accumulating field observations from four field seasons ranging from 2005 to 2017, we draw from over 1000 observations to characterize the habitat use of eight Anolis species that occur at La Selva. These species include Anolis humilis, Anolis limifrons, Anolis lemurinus, Anolis oxylophus, Anolis capito, Anolis carpenteri, Anolis biporcatus, and Anolis pentaprion, and we opted to devote a brief section to the co-occurring Polychrus gutturosus. Our results revealed overlapping niches and substantial variability in habitat use across many species. Furthermore, the morphologies of A. humilis and A. limifrons were at odds with microhabitat use following the predictions of Caribbean anole ecomorphology. Among the two most abundant species, relative hindlimb length was greater for the more arboreal A. limifrons, whereas it was shorter for the more terrestrial A. humilis.

If mainland and island anoles exhibit divergent ecomorphological patterns, this begs the question of how selective pressures differ between mainland and island habitats to drive these differences. Andrews [3] proposed that predation may more strongly influence Anolis diversification on the mainland, because in comparison to islands, predators are far more abundant, anole population densities are lower, and arthropod prey is plentiful. In contrast, Caribbean anoles are thought to be food limited and there may be stronger selection for niche partitioning. Through examining variation in species’ habitat use relative to the abundance of other co-occurring species at La Selva, our data suggests a low level of interspecific competition for this mainland community, corroborating the hypotheses Andrews set forth.

In recent years, the study of mainland anoles has received more attention. We are in great need of ecological, morphological, and life history trait data for Anolis communities throughout Central and South America to further our understanding of the evolutionary trajectories of mainland and island anoles. So, anole biologists, you can throw out your boats and steer clear of the oceanic divide!

 

[1] Rand, A. S., and E. E. Williams. 1969. The anoles of La Palma: aspects of their ecological relationships. Breviora 327:1–17.

[2] Williams, E. E. 1972. The origin of faunas. Evolution of lizard congeners in a complex island fauna: a trial analysis. Evolutionary Biology 6: 47–89.

[3] Andrews, R. M. 1979. Evolution of life histories: a comparison of Anolis lizards from matched island and mainland habitats. Breviora 454: 1–51.

Arthropod Predators of Anoles

Orange-legged wandering spider (Cupiennius coccineus) consuming house gecko (Hemidactylus frenatus) at Sirena Biological Station, Corcovado, Costa Rica

Red-legged wandering spider (Cupiennius coccineus) consuming a house gecko (Hemidactylus frenatus) at Sirena Biological Station, Corcovado, Costa Rica

When someone first asked me about the major predators of anoles, my first thought was to talk about curly-tailed lizards (Leiocephalus carinatus) in the Caribbean, vine snakes (Oxybelis spp.) in the neotropics [see my previous post on anole predation by O. aeneus at La Selva], and birds. I think that as herpetologists, we tend to fall into the trap of thinking of invertebrates as “lesser” taxa to be preyed upon by small vertebrates like lizards, and in turn for small vertebrates to be eaten by larger vertebrates.

I, too, when thinking about how selective pressures shape morphological variation in mainland and island habitats turned to fellow herps and birds as the primary predation pressure for mainland anoles. However, it wasn’t until I arrived in Costa Rica that I discovered the high prevalence of voracious arthropods, and I realized that our beloved lizards had much more to fear!

Orange wandering spider (Cupiennius getazi) with egg sac at La Selva Biological Station, Costa Rica

Orange wandering spider (Cupiennius getazi) with egg sac at La Selva Biological Station, Costa Rica

Red-legged wandering spider (Cupiennius coccineus) eating a pink katydid (Tettigoniidae: Phaneropterinae) at La Selva Biological Station, Costa Rica

Red-legged wandering spider (Cupiennius coccineus) eating a pink katydid (Tettigoniidae: Phaneropterinae) at La Selva Biological Station, Costa Rica

A large adult female mantis (Phasmomantis championi) at La Selva Biological Station, Costa Rica

A large adult female mantis (Phasmomantis championi) at La Selva Biological Station, Costa Rica

Conehead katydid (Tettigoniidae: Conocephalinae: Vestria sp.) at La Tarde, Osa Peninsula, Costa Rica

Conehead katydid (Tettigoniidae: Conocephalinae: Vestria sp.) at La Tarde, Osa Peninsula, Costa Rica

In a single night at La Selva, I could easily find dozens of large wandering spiders (Ctenidae), and if I pointed my headlamp higher in the trees I could see eyeshine from hundreds of spiders. Given the high density of large ctenids at La Selva, it is not unlikely that anoles and small tree frogs constitute a major portion of their diet. In fact, I wouldn’t be surprised if large arthropods are one of the most common predators of mainland anoles in some regions.

The same might be the case for giant mantids of the genera Macromantis and Phasmomantis, and conocephaline katydids sporting fearsome mandibles (e.g. Copiphora spp.). Since the invasive Chinese mantids (Tenodera sinensis) in North America are well documented to prey on hummingbirds almost equal in size to the mantids [see Nyffeler et al. 2017], surely larger and bulkier species in the neotropics can take lizards much smaller than themselves. Even though wandering spiders and conehead katydids are primarily nocturnal hunters, I have heard many stories of these arthropods being implicated in anole and tree frog predation. Research looking into how ctenids and nocturnal katydids forage would help determine if they can actually detect sleeping anoles or if predation events occur from the arthropods simply running in to the anoles while on the move.

If anyone here on Anole Annals has any anecdotal or photographic records, please comment below.

To throw a twist on this discussion, is it possible for a spider to prey on a lizard two and a half times its size? A new paper about a vertebrate-eating jumping spider (Salticidae) describes just that! Considering arthropods as possible major players in anole predation could shed light on behavioral and ecological studies of mainland anoles.

Figure 1 from Nyfeller et al. 2017, showing female jumping spiders (Phidippus regius) consuming Carolina anoles (Anolis carolinensis) and Cuban tree frogs (Osteopilus septentrionalis)

Figure 1 from Nyfeller et al. 2017, showing female jumping spiders (Phidippus regius) consuming Carolina anoles (Anolis carolinensis) and Cuban tree frogs (Osteopilus septentrionalis)

Here are a few more spider photos to wrap up this blog post.

Jumping spider (Salticidae: Phiale cf. guttata) eating an assassin bug (Reduviidae)

Jumping spider (Salticidae: Phiale cf. guttata) eating an assassin bug (Reduviidae)

Red-legged wandering spider (Cupiennius coccineus) consuming house gecko (Hemidactylus frenatus) at Sirena Biological Station, Corcovado, Costa Rica

Another angle of a red-legged wandering spider (Cupiennius coccineus) consuming a house gecko (Hemidactylus frenatus) at Sirena Biological Station, Corcovado, Costa Rica

Threat display of a Brazilian wandering spider (Phoneutria boliviensis) from Tárcoles, Costa Rica. A ctenid with medically significant venom.

Threat display of a Brazilian wandering spider (Phoneutria boliviensis) from Tárcoles, Costa Rica. A ctenid with medically significant venom.

Identification Request for Panamanian Anole

 

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Last month I spent a week in Bocas del Toro for a marine invertebrate biology course. However, I made some obligatory terrestrial excursions in search of our favorite vertebrate, the anoles! The habitat surrounding the STRI facility was secondary forest, and anoles were most commonly seen at forest edges. On one tree I found two A. limifrons scurrying about. They both promptly flattened their bodies against the thin branches when they detected my presence. A few seconds later, I noticed that a slightly larger anole was staring right at me from several inches away. I haven’t been able to get a solid ID on this female yet, and I would appreciate any input!

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