Tag: Anolis baleatus

Cranial Ornamentation in Anolis baleatus

When I first encountered Anolis baleatus, this Hispaniolan crown-giant was mostly an inconvenience. At the time I was gathering data for my doctoral thesis by cycling preserved anoles through a µCT-scanner. Most of the adult specimens of A. baleatus were just too large to easily fit into the scan chamber, so it took a lot of patience and creativity to acquire any decent images of the appendicular girdles, which are the body parts I was interested in.

During that process I also acquired radiographic images of the head skeleton, and found unusual patterns of crenulation in this species. The cranium of Anolis baleatus displays a great degree of seemingly asymmetrical (or at least somewhat irregular) ornamentation across its dorsal surface. This is especially pronounced on the prefrontal and frontal bones, and completely obscures all superficial distinction between them in adult lizards. In adults, cranial ornamentation is also borne by the paired nasals, maxillae, and postorbitals, and the parietal (see figure).

Both Steven Poe (1998) and Susan Evans (2008) mentioned this ossified garnish, but a thorough account of their variation among anoles remains absent from the primary literature. Richard Etheridge and Kevin de Queiroz (1988) were probably the first to report on skull ornaments in anoles (as part of a discussion of several iguanian lizards with similar cranial adornments), and remarked that the distribution patterns of dermal rugae may reflect those of the topographically associated epidermal scales.

Overall, this ornamentation appears to be relatively uncommon among anoles, especially to the degree expressed in Anolis baleatus (and several other crown-giant ecomorph anoles). Considering the osteologically robust appearance of crown-giants, even at early stages of ontogenetic development, this gives rise to questions regarding the development of these ornamental patterns. Thanks to the collection efforts of Luke Mahler (University of Toronto), and a postdoctoral position in his lab, I was able to acquire CT-image data representing an ontogenetic series of this species, ranging from very young juveniles to skeletally mature adults.

While parts of the paired frontals of juveniles are covered in modest eminences, prominent cranial ornamentation is absent from small specimens (see figure). Likely, growth of these ornaments begins very late during ontogenetic development. Ornaments on the prefrontals and parietal are only evident in specimens that, to the best of our judgement, are approaching sexual maturity. We looked at fifteen specimens per sex, representing a range of juvenile and subadult sizes, and this general pattern is consistent throughout the image data. Schwartz (1974) inferred that anoles in the ricordii group reach sexual maturity between 100 and 110 mm snout-vent length (SVL), and we observed the first prominent ornaments at sizes between 90 and 95 mm SVL. Assuming that differences in size directly represent ontogenetic growth, these findings imply that Anolis baleatus starts to grow elaborate ornamentation as it approaches sexual maturity, and that expansion and growth of these ornaments then continues into skeletal maturity. Interestingly, both males and females appear to develop them at roughly the same body size.

The function and evolutionary cause of these structures remain unknown, and these are questions we are currently investigating. Body size is an important correlate for the occurrence of cranial ornaments, but these structures may also conceivably play roles in defense, feeding, or intraspecific agonistic interactions. Stay tuned!

Videos

A. baleatus, female, 55 mm SVL
A. baleatus, female, 65 mm SVL
A. baleatus, female, 96 mm SVL
A. baleatus, female, 126 mm SVL

References

Etheridge, R. & de Queiroz, K. (1988): A phylogeny of Iguanidae.─ [In:] Estes, R.D. & Pregill, G.K. (eds.): Phylogenetic Relationships of the Lizard Families: Essays Commemorating Charles L Camp, 283-367; Stanford: Stanford University Press.

Evans, S. (2008): The skull of lizards and tuatara.─ [In:] Gans, C., Gaunt, A.S. & Adler, K. (eds.), Biology of the Reptilia, vol. 20:1-347; Society for the Study of Amphibians and Reptiles, Ithaca, New York.

Poe, S. (1998): Skull characters and the cladistic relationships of the Hispaniolan dwarf twig Anolis.─ Herpetological Monographs, 12:192-236; The Herpetologists’ League.

Schwartz, A. (1974): An analysis of variation in the Hispaniolan giant anole, Anolis ricordi Dumeril and Bibron.─ Bull. Mus. Comp. Zool., 146:89-146.

Fill In The Blank: Obscure Anole Life History Traits

In collaboration with the Conservation Biology course taught by Dr. Karen Beard here at Utah State University, where I am a Ph.D. student, I have been involved in gathering life history data on ~400 species of reptiles that have been introduced outside of their native ranges for an analysis of how life history traits (e.g., diet, fecundity, longevity) interact with other factors to influence the likelihood of successful establishment. Appendix A of Fred Kraus’ 2009 book Alien Reptiles and Amphibians is the source of the species list we are using, and included in this analysis are 26 species of Anolis. This is where you come in.

First, we coded all anoles as (i) sexually-dichromatic, (ii) diurnal, (iii) non-venomous, (iv) oviparous, (v) omnivores that lack (vi) temperature-dependent sex determination and (vii) parthenogenesis. Is anyone aware of any exceptions to these seven generalizations?

Second, we searched for data on clutch size, clutch frequency, incubation time, and longevity. The Anole Classics section of this site and the Biodiversity Heritage Library were particularly useful. After conducting what I feel to be a pretty thorough literature scavenger hunt, I am forced to conclude that some of these data simply do not exist at the species level for all of the species we’re interested in, or are not explicitly stated in a way that is obvious to a non-anole-expert. Of course, there is a lot of literature, including many books that I don’t have access to, and there are also lots of credible observations that don’t get published. I’m hoping that some of the readership here can help fill in at least some of the blanks in the table below. As one member of the team, I did not collect all of the data that are filled in myself, nor have I personally vetted every value, so if you spot an error please do point it out.

Two important points:

  1. Many environmental factors obviously influence the life history parameters of our beloved and wonderfully plastic reptiles, so we appreciate that many of these values would be better represented by ranges and are dependent on latitude, altitude, climate, and many other factors. Where a range is published, we are using its median value.
  2. I should also emphasize that, because of the large size of this study and the diversity of taxa included (ranging in size from giants like Burmese Pythons, Nile Crocodiles, and Aldabra Tortoises to, well, anoles and blindsnakes), it is more important for the data to reflect the relative values of these life history parameters across all anoles (and all reptiles) than it is to specifically and precisely represent all known variation within a given species of anole.

Without further ado (for your enjoyment, and because I know from my own blog that nobody reads posts lacking pictures, I’ve embedded an image of each species):

Species Median clutch size Median clutches per year Incubation time (days) Maximum longevity (months)
A aeneus
A. aeneus
2
A baleatus
A. baleatus
A bimaculatus
A.bimaculatus            
2 43 84
A carolinensis
A. carolinensis
1.15 6  41.5 65
A chlorocyanus
A.chlorocyanus
1 18
A conspersus
A. conspersus
1
A cristatellus
A. cristatellus
2.5 18 83
A cybotes
A. cybotes
1 18 45
A distichus
A. distichus
1 16 45.5
A equestris
A. equestris
1 1 48 149
A extremus
A. extremus
A ferreus
A. ferreus
1 18
A garmani
A. garmani
1.5 18 67
A grahami
A. grahami
1
A leachii
A. leachii
A lineatus
A. lineatus
A lucius
A. lucius
1 3.5 60
A marmoratus
A. marmoratus
2  50
A maynardi
A. maynardi
A porcatus
A. porcatus
1 18 63.5
A pulchellus
A. pulchellus
1
A richardii
A. richardii
1
A sagrei
A. sagrei
2 20  32 22
A stratulus
A. stratulus
A trinitatis
A. trinitatis
2  50
A wattsi
A. wattsi
1

Thanks in advance. I think this is a great blog and I hope to post something more interesting on here soon.

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