Skip to main content Skip to main navigation menu Skip to site footer
Type: Article
Published: 2019-05-20
Page range: 261–278
Abstract views: 135
PDF downloaded: 2

A new species of anole from Parque Nacional Volcán Arenal, Costa Rica (Reptilia, Squamata, Dactyloidae: Norops)

Senckenberg Forschungsinstitut und Naturmuseum, Senckenberganlage 25, 60325 Frankfurt a.M., Germany Goethe-University, Institute for Ecology, Evolution & Diversity, Biologicum, Building C, Max-von-Laue-Straße 13, 60438 Frankfurt am Main, Germany.
Senckenberg Forschungsinstitut und Naturmuseum, Senckenberganlage 25, 60325 Frankfurt a.M., Germany Internationales Hochschulinstitut Zittau, Markt 23, 02763 Zittau, Germany
Reptilia DNA barcoding hemipenis morphology Lower Central America mainland anoles Norops arenal Norops carpenteri taxonomy twig anole ecomorph 16S

Abstract

We describe the new species Norops arenal sp. nov. from Parque Nacional Volcán Arenal, north-central Costa Rica. In external morphology and genetic similarity of the 16S DNA barcode, Norops arenal is most similar to N. altae, N. fortunensis, N. fuscoauratus, N. gruuo, N. kemptoni, N. monteverde, N. pseudokemptoni, and N. tenorioensis. In morphology it shares with these species the following characteristics: (1) short hind limbs; (2) a single elongate prenasal scale; (3) tiny, smooth, often juxtaposed body scales; and (4) a slender habitus, often delicate. Norops arenal differs from these species, among several scalation details, by having a blackish central area in the male dewlap in life and in preservative (vs. no suffusion of black pigment on male dewlap in the other species), and a small red female dewlap in life (vs. dirty white, cream colored, or orange); extremely short hind legs with the tip of fourth toe of the adpressed hind leg reaching only to level of shoulder (vs. usually at least to level of ear in the other species); a short tail with a tail length/SVL ratio of 1.53 in single specimen with complete tail (vs. this ratio >1.6 in the other species); and a tiny size with 41.5 mm in single known adult male and 38.5 mm in single known adult female (vs. SVL of adults usually >42.0 mm). It further differs from N. altae, N. fuscoauratus, N. gruuo, N. pseudokemptoni, and N. tenorioensis by having a unilobed hemipenis (vs. bilobed in these five species).

 

References

  1. Arosemena, F.A. & Ibáñez, D.R. (1993) Una especie nueva de Anolis (Squamata: Iguanidae) del grupo fuscoauratus de Fortuna, Panamá. Revista de Biologia Tropical, 41, 267–272.

    Bouckaert, R. & Heled, J. (2014) DensiTree 2: Seeing trees through the forest. BioRxiv, 012401, 1–11.

    Castañeda, M.D.R. & De Queiroz, K. (2013) Phylogeny of the Dactyloa clade of Anolis lizards: new insights from combining morphological and molecular data. Bulletin of the Museum of Comparative Zoology, 160, 345–398.

    https://doi.org/10.3099/0027-4100-160.7.345

    Chaves, G., García-Rodríguez, A., Mora, A. & Leal, A. (2009) A new species of dink frog (Anura: Eleutherodactylidae: Diasporus) from Cordillera de Talamanca, Costa Rica. Zootaxa, 2088, 1–14.

    Cope, E.D. (1862) Contributions to Neotropical saurology. Proceedings of the Academy of Natural Sciences of Philadelphia, 14, 176–188.

    De Queiroz, K. (2007) Species concepts and species delimitation. Systematic Biology, 56, 879–886.

    https://doi.org/10.1080/10635150701701083

    Drummond, A.J., Ashton, B., Cheung, M., Heled, J., Kearse, M., Moir, R., Stones-Havas, S., Thierer, T. & Wilson, A. (2010) Geneious. Version 4.8.5. Available from: http://www.geneious.com (accessed 16 April 2019)

    Drummond, A.J., Suchard, M.A., Xie, D. & Rambaut, A. (2012) Bayesian phylogenetics with BEAUti and the BEAST 1.7. Molecular Biology and Evolution, 29, 1969–1973.

    https://doi.org/10.1093/molbev/mss075

    Duméril, A.M.C. & Bibron, G. (1837) Erpétologie générale ou histoire naturelle complète des reptiles. Tome 4. Librairie encyclopédique de Roret, Paris. ii + 571 pp.

    Dunn, E.R. (1930) Notes on Central American Anolis. Proceedings of the New England Zoölogical Club, 12, 15–24.

    Edgar, R.C. (2004) MUSCLE: a multiple sequence alignment method with reduced time and space complexity. BMC Bioinformatics, 5, 1–19.

    https://doi.org/10.1186/1471-2105-5-113

    Etheridge, R.E. (1959) The relationships of the anoles (Reptilia: Sauria: Iguanidae). An interpretation based on skeletal morphology (Unpublished doctoral dissertation). University of Michigan, Ann Arbor, Michigan, 236 pp.

    Ivanova, N.V., De Waard, J. & Hebert, P.D.N. (2006) An inexpensive, automation-friendly protocol for recovering high-quality DNA. Molecular Ecology Notes, 6, 998–1002.

    https://doi.org/10.1111/j.1471-8286.2006.01428.x

    Kekkonen, M., Mutanen, M., Kaila, L., Nieminen, M. & Hebert, P.D.N. (2015) Delineating species with DNA Barcodes: A case of taxon dependent method performance in moths. PloS ONE, Article ID e0122481.

    https://doi.org/10.1371/journal.pone.0122481

    Köhler, G. (2009) A new species of Anolis formerly referred to as Anolis altae from Monteverde, Costa Rica (Squamata: Polychrotidae). Journal of Herpetology, 43, 11–20.

    https://doi.org/10.1670/07-180R2.1

    Köhler, G. (2011) A new species of anole related to Anolis altae from Volcán Tenorio, Costa Rica (Reptilia, Squamata, Polychrotidae). Zootaxa, 3120, 29–42.

    https://doi.org/10.11646/zootaxa.3120.1.2

    Köhler, G. (2012) Color Catalogue for Field Biologists. Herpeton, Offenbach, Germany.

    Köhler, G. (2014) Characters of external morphology used in Norops taxonomy––Definition of terms, advice on usage, and illustrated examples. Zootaxa, 3774 (3), 201–257.

    https://doi.org/10.11646/zootaxa.3774.3.1

    Köhler, G., Batista, A., Vesely, M., Ponce, M., Carrizo, A. & Lotzkat, S. (2012) Evidence for the recognition of two species of Norops formerly referred to as A. tropidogaster (Squamata: Dactyloidae). Zootaxa, 3348, 1–23.

    https://doi.org/10.11646/zootaxa.3348.1.1

    Köhler, G., Gómez Trejo Pérez, R., Petersen, C.B.P. & Méndez de la Cruz, F.R. (2014a) A revision of the Mexican Norops (Reptilia, Squamata, Dactyloidae) from the Pacific versant west of the Isthmus de Tehuantepec in the states of Oaxaca, Guerrero, and Puebla, with the description of six new species. Zootaxa, 3862 (1), 1–210.

    https://doi.org/10.11646/zootaxa.3862.1.1

    Köhler, G., Ponce, M., Sunyer, J. & Batista, A. (2007) Four new species of anoles (genus Anolis) from the Serranía de Tabasará, west-central Panama (Squamata: Polychrotidae). Herpetologica, 63, 375–391.

    https://doi.org/10.1655/0018-0831(2007)63[375:FNSOAG]2.0.CO;2

    Köhler, G., Townsend, J.H. & Petersen, C.B.P. (2016) A taxonomic revision of the Norops tropidonotus complex (Squamata, Dactyloidae), with the resurrection of N. spilorhipis (Álvarez del Toro and Smith, 1956) and the description of two new species. Mesoamerican Herpetology, 3, 8–41.

    Köhler, G., Vargas, J. & Lotzkat, S. (2014b) Two new species of the Norops pachypus complex (Squamata, Dactyloidae) from Costa Rica. Mesoamerican Herpetology, 1: 254–280.

    Kubicki, B., Salazar, S. & Puschendorf, R. (2015) A new species of glassfrog, genus Hyalinobatrachium (Anura: Centrolenidae), from the Caribbean foothills of Costa Rica. Zootaxa, 3920 (1), 69–84.

    https://doi.org/10.11646/zootaxa.3920.1.4

    Losos, J.B. (2009) Lizards in an Evolutionary Tree. Ecology and Adaptive Radiation of Anoles. University of California Press, Berkley, 528 pp.

    Lotzkat, S., Bienentreu, J.-F., Hertz, A. & Köhler, G. (2011) A new species of Norops (Squamata: Iguania: Dactyloidae) formerly referred to as A. pachypus from the Cordillera de Talamanca of western Panama and adjacent Costa Rica. Zootaxa, 3125, 1–21.

    McCranie, J.R. & Köhler, G. (2015) The anoles of Honduras. Bulletin of the Museum of Comparative Zoology, Special Publications Series 1, 1–292.

    Nicholson, K.E., Crother, B.I., Guyer, C. & Savage, J.M. (2012) It is time for a new classification of anoles (Squamata: Dactyloidae). Zootaxa, 3477, 1–108.

    Nicholson, K.E., Crother, B.I., Guyer, C. & Savage, J.M. (2014) Anole classification: a response to Poe. Zootaxa, 3814 (1), 109–120.

    https://doi.org/10.11646/zootaxa.3814.1.6

    Ogilvie, H.A., Bouckaert, R.R. & Drummond, A.J. (2017) StarBEAST2 brings faster species tree inference and accurate estimates of substitution rates. Molecular Biology and Evolution, 34, 2101–2114.

    https://doi.org/10.1093/molbev/msx126

    Peters, W. (1863) Über einige Arten der Saurier-Gattung Anolis. Monatsberichte der Königlichen Preussischen Akademien der Wissenschaften zu Berlin, 1863, 135–149.

    Poe, S. (2013) 1986 redux: New genera of anoles (Squamata: Dactyloidae) are unwarranted. Zootaxa, 3626 (2), 295–299.

    https://doi.org/10.11646/zootaxa.3626.2.7

    Poe, S., Nieto-Montes de Oca, A., Torres-Carvajal, O., De Queiroz, K., Velasco, J.A., Truett, B., Gray, L.N., Ryan, M.J., Köhler, G., Ayala-Varela & F., Latell, I. (2017) A phylogenetic, biogeographic, and taxonomic study of all extant species of Anolis (Squamata; Iguanidae). Systematic Biology, 66 (5), 663–697.

    https://doi.org/10.1093/sysbio/syx029

    Puillandre, N., Lambert, A., Brouillet, S. & Achaz, G. (2012) ABGD, Automatic Barcode Gap Discovery for primary species delimitation. Molecular Ecology, 21, 1864–1877.

    https://doi.org/10.1111/j.1365-294X.2011.05239.x

    Sabaj-Pérez, M.H. (2016) Standard symbolic codes for institutional resource collections in herpetology and ichthyology. Version 6.5 (16 August 2016). An online reference. Available from: http://www.asih.org/ (accessed 18 November 2018)

    Savage, J.M. (2002) The amphibians and reptiles of Costa Rica. A herpetofauna between two continents, between two seas. University of Chicago Press, Chicago, Illinois, 954 pp.

    Schaad, E.W. & Poe, S. (2010) Patterns of ecomorphological convergence among mainland and island Anolis lizards. Biological Journal of the Linnean Society, 101, 852–859.

    https://doi.org/10.1111/j.1095-8312.2010.01538.x

    Tamura, K., Stecher, G., Peterson, D., Filipski, A. & Kumar, S. (2013) MEGA6: Molecular Evolutionary Genetics Analysis version 6.0. Molecular Biology and Evolution, 30, 2725–2729.

    https://doi.org/10.1093/molbev/mst197

    Vieites, D.R., Wollenberg, K.C., Andreone, F., Köhler, J., Glaw, F. & Vences, M. (2009) Vast underestimation of Madagascar’s biodiversity evidenced by an integrative amphibian inventory. Proceedings of the National Academy of Sciences of the United States of America, 106, 8267–8272.

    https://doi.org/10.1073/pnas.0810821106

    Wiegmann, A.F.A. (1834) Herpetologica Mexicana. Pars Prima, Saurorum Species. Sumptibus C. G. Lüderitz, Berlin, 54 pp.

    Williams, E.E. (1983) Ecomorphs, faunas, island size, and diverse end points in island radiations of Anolis. In: Huey, R.B., Pianka, E.R. & Schoener, T.W. (Eds.), Lizard ecology: studies of a model organism. Cambridge: Harvard University Press.

    https://doi.org/10.4159/harvard.9780674183384.c18

    Yang, Z., Landry, J.-F. & Hebert, P.D.N. (2016) A DNA barcode library for North American Pyraustinae (Lepidoptera: Pyraloidea: Crambidae). PloS ONE, 11, e0161449.

    https://doi.org/10.1371/journal.pone.0161449