Daniel O. Mesquita,^1,7 Guarino R. Colli,² Gabriel C. Costa,³ Taís B. Costa,¹ Donald B. Shepard,⁴ Laurie J. Vitt,⁵ and Eric R. Pianka⁶

1 Departamento de Sistemática e Ecologia, Centro de Ciências Exatas e da Natureza, Universidade Federal da Paraíba, Av. Castelo Branco, s/n, João Pessoa, PB, 58000-000, Brazil

2 Departamento de Zoologia, Instituto de Ciências Biológicas, Universidade de Brasília, Brasília, DF, 70910-900, Brazil

3 Departamento de Ecologia, Centro de Biociências, Universidade Federal do Rio Grande do Norte, Lagoa Nova, Natal, RN, 59072-970, Brazil

4 Department of Biology, University of Central Arkansas, 201 Donaghey Avenue, LSC 180, Conway, Arkansas 72035 USA

5 Sam Noble Oklahoma Museum of Natural History and Department of Zoology, University of Oklahoma, Norman, Oklahoma 73019 USA

6 Department of Integrative Biology, C0930, University of Texas at Austin, One University Station, Austin, Texas 78712-0253 USA

Life_history_data_of_lizards_of_the_world.txt.zip (MD5: 13aa07593aa81a05423bbd0ffc9392cc)

Life is defined by a capacity for reproduction, yet the ways in which animals reproduce vary tremendously among species. Reproductive life histories are complex phenomena influenced by a variety of factors, such as physical condition of individuals, food supply, bauplan, and phylogenetic history, which are often correlated. Understanding life histories is crucial in evolutionary ecology, because they represent different strategies that evolved to maximize individual fitness. Variation in life history can be attributed to both historical (= phylogenetic) and non-historical (= environmental) causes. We compiled a large data set on lizard life history variables. Our data set consists of life history data for 737 lizard populations, representing 337 species in 33 families from 280 study sites globally. About 64% of these data were collected directly by the authors. Regarding data collected by authors, we sexed lizards by dissection and direct examination of gonads. Females were considered reproductive if vitellogenic follicles or oviductal eggs were present. We regarded the simultaneous presence of enlarged vitellogenic follicles and either oviductal eggs or corpora lutea as evidence for the sequential production of more than one clutch of eggs per year. We considered clutch size as the number of vitellogenic follicles or oviductal eggs in mature females. For each population, we recorded the following variables, if available: adult female mass (g), adult female SVL (mm), female SVL at maturity (based on SVL of smallest reproductive female), offspring SVL (based on hatchling size or smallest individual in population), clutch or litter size (number of offspring per clutch or litter for all reproductive females in the population), total number of clutches or litters per year, clutch frequency (single- or multiple-brooded), relative clutch or litter mass [total volume of eggs or embryos (cc) divided by adult female mass (g)], reproductive mode (oviparous or viviparous), foraging mode (sit-and-wait or active), distribution (tropical or temperate), and preferred habitat type (aquatic, arboreal, bromelicolous, fossorial, psammophilous, saxicolous, semi-arboreal, or terrestrial). These data are valuable to test various life history hypotheses, including phylogenetic design constraints and effects of ecology and climate on reproductive tactics.

Key words: ecology; reproduction; Squamata.