The Concept of Reproductive Effort and Its Relation to the Evolution of Life Histories of Lizards
1969; University of Chicago Press; Volume: 103; Issue: 933 Linguagem: Inglês
10.1086/282617
ISSN1537-5323
Autores Tópico(s)Species Distribution and Climate Change
ResumoPrevious articleNext article No AccessThe Concept of Reproductive Effort and Its Relation to the Evolution of Life Histories of LizardsDonald W. TinkleDonald W. Tinkle Search for more articles by this author PDFPDF PLUS Add to favoritesDownload CitationTrack CitationsPermissionsReprints Share onFacebookTwitterLinkedInRedditEmailPrint SectionsMoreDetailsFiguresReferencesCited by The American Naturalist Volume 103, Number 933Sep. - Oct., 1969 Published for The American Society of Naturalists Article DOIhttps://doi.org/10.1086/282617 Views: 32Total views on this site Citations: 208Citations are reported from Crossref Copyright 1969 University of ChicagoPDF download Crossref reports the following articles citing this article:Raciel Cruz-Elizalde, Aurelio Ramírez-Bautista, Uriel Hernández-Salinas, César A Díaz-Marín, Jonathon C Marshall, Jack W Sites JR, Dulce María Galván-Hernández, Aaron García-Rosales, Christian Berriozabal-Islas Variation in body size and reproductive characteristics among chromosomal races of the Sceloporus grammicus complex in México, Biological Journal of the Linnean Society 454 (Mar 2023).https://doi.org/10.1093/biolinnean/blac150Abdullah Altunışık, Mehmet Zülfü Yıldız, Fatma Üçeş, Mehmet Akif Bozkurt, Mehtap Sömer Altitude impacts body size but not age in the Asia Minor Thin-toed Gecko ( Mediodactylus heterocercus ), Canadian Journal of Zoology 100, no.55 (May 2022): 315–321.https://doi.org/10.1139/cjz-2021-0197Haiyan Nie, Jike Liu, Baoyang Chen Life‐history traits and fitness of plateau pika ( Ochotona curzoniae ) in alpine meadow ecosystem, Ecology and Evolution 12, no.11 (Jan 2022).https://doi.org/10.1002/ece3.8548Udita Bansal, Maria Thaker, Allen Hurlbert Diet influences latitudinal gradients in life‐history traits, but not reproductive output, in ectotherms, Global Ecology and Biogeography 30, no.1212 (Sep 2021): 2431–2441.https://doi.org/10.1111/geb.13396Gabriel Henrique De Oliveira Caetano, Guarino Rinaldi Colli Climate instability causing the decline of a Neotropical savanna lizard population (Squamata: Tropiduridae), Biological Journal of the Linnean Society 134, no.22 (Jul 2021): 474–485.https://doi.org/10.1093/biolinnean/blab084Jhan-Wei Lin, Ying-Rong Chen, Tsui-Wen Li, Pei-Jen L. Shaner, Si-Min Lin Long-term monitoring reveals invariant clutch size and unequal reproductive costs between sexes in a subtropical lacertid lizard, Zoological Letters 6, no.11 (Jan 2020).https://doi.org/10.1186/s40851-019-0152-0Eric Peña‐Herrera, Maricela Villagrán‐SantaCruz, Oswaldo Hernández‐Gallegos, Justin L. Rheubert, Kevin M. Gribbins, Gisela Granados‐González Reproductive activity in males of Sceloporus variabilis : Little time to rest, long time to breed, Acta Zoologica 101, no.11 (Sep 2018): 101–108.https://doi.org/10.1111/azo.12275Aaron M. Reedy, William J. Evans, Robert M. Cox Sexual dimorphism explains residual variance around the survival‐reproduction tradeoff in lizards: Implications for sexual conflict over life‐history evolution*, Evolution 73, no.1111 (Aug 2019): 2324–2332.https://doi.org/10.1111/evo.13799Yuping Li, Dmitri A. Petrov, Gavin Sherlock Single nucleotide mapping of trait space reveals Pareto fronts that constrain adaptation, Nature Ecology & Evolution 3, no.1111 (Oct 2019): 1539–1551.https://doi.org/10.1038/s41559-019-0993-0Gabriel Suárez-Varón, Orlando Suárez-Rodríguez, Gisela Granados-González, Maricela Villagrán-Santa Cruz, Kevin M. Gribbins, Diego Cortez-Quezada, Oswaldo Hernández-Gallegos Relative clutch mass of Basiliscus vittatus Wiegmann, 1828 (Squamata, Corytophanidae): female morphological constraints, Herpetozoa 32 (Sep 2019): 211–219.https://doi.org/10.3897/herpetozoa.32.e35910Hans Recknagel, Kathryn R. Elmer Differential reproductive investment in co-occurring oviparous and viviparous common lizards (Zootoca vivipara) and implications for life-history trade-offs with viviparity, Oecologia 190, no.11 (May 2019): 85–98.https://doi.org/10.1007/s00442-019-04398-wMelissa J. Griffin, Gregory I. Holwell, Matthew R. E. Symonds Insect harem polygyny: when is a harem not a harem?, Behavioral Ecology and Sociobiology 73, no.44 (Mar 2019).https://doi.org/10.1007/s00265-019-2652-5Jordi Alexis Garcia Marsà, Federico L. Agnolín, Fernando Novas Bone microstructure of Lewisuchus admixtus Romer, 1972 (Archosauria, Dinosauriformes), Historical Biology 31, no.22 (Jul 2017): 157–162.https://doi.org/10.1080/08912963.2017.1347646Uriel Hernández-Salinas, Aurelio Ramírez-Bautista, Raciel Cruz-Elizalde, Shai Meiri, Christian Berriozabal-Islas Ecology of the growth of Anolis nebulosus (Squamata: Dactyloidae) in a seasonal tropical environment in the Chamela region, Jalisco, Mexico, Ecology and Evolution 9, no.44 (Jan 2019): 2061–2071.https://doi.org/10.1002/ece3.4899Débora da Silva, Mônica Cassel, Mahmoud Mehanna, Adelina Ferreira, Mary Anne Heidi Dolder Follicular Development and Reproductive Characteristics in Four Species of Brazilian Tropidurus Lizards, Zoological Science 35, no.66 (Dec 2018): 553–563.https://doi.org/10.2108/zs180030Robin M. Andrews Changing Perspectives on Reptile Eggs: One Biologist's Journey from Demography to Development, Journal of Herpetology 52, no.33 (Jun 2018): 243–251.https://doi.org/10.1670/17-050Konstantin Hallmann, Eva Maria Griebeler An exploration of differences in the scaling of life history traits with body mass within reptiles and between amniotes, Ecology and Evolution 8, no.1111 (May 2018): 5480–5494.https://doi.org/10.1002/ece3.4069Erin A. Tripp, James C. Lendemer Twenty-seven modes of reproduction in the obligate lichen symbiosis, Brittonia 70, no.11 (Dec 2017): 1–14.https://doi.org/10.1007/s12228-017-9500-6Hibraim Adán Pérez-Mendoza, Salomón Rubén Sanabria-Tobón, José Luis Jaramillo-Alba, Israel Solano-Zavaleta, Luis Felipe Vázquez-Vega, Aníbal Helios Díaz de la Vega-Pérez Reproductive Traits of Dusky Rattlesnakes ( Crotalus triseriatus ) in Central Mexico, Journal of Herpetology 52, no.11 (Jan 2018): 6–11.https://doi.org/10.1670/16-003Michael A. Carlo, Eric A. Riddell, Ofir Levy, Michael W. Sears, John Wiens Recurrent sublethal warming reduces embryonic survival, inhibits juvenile growth, and alters species distribution projections under climate change, Ecology Letters 21, no.11 (Nov 2017): 104–116.https://doi.org/10.1111/ele.12877Eric R. Pianka, Laurie J. Vitt, Nicolás Pelegrin, Daniel B. Fitzgerald, and Kirk O. Winemiller Toward a Periodic Table of Niches, or Exploring the Lizard Niche Hypervolume, The American Naturalist 190, no.55 (Aug 2017): 601–616.https://doi.org/10.1086/693781Patrick William Hughes Between semelparity and iteroparity: Empirical evidence for a continuum of modes of parity, Ecology and Evolution 7, no.2020 (Sep 2017): 8232–8261.https://doi.org/10.1002/ece3.3341Nancy Greco, Nicolás Cluigt, Andrew Cline, Gerardo Liljesthröm, Guy Smagghe Life history traits and life table analysis of Lobiopa insularis (Coleoptera: Nitidulidae) fed on strawberry, PLOS ONE 12, no.77 (Jul 2017): e0180093.https://doi.org/10.1371/journal.pone.0180093Jimena B. FERNÁNDEZ, Marlin MEDINA, Erika L. KUBISCH, José A. SCOLARO, Nora R. IBARGÜENGOYTÍA Reproductive strategies in males of the world's southernmost lizards, Integrative Zoology 12, no.22 (Mar 2017): 132–147.https://doi.org/10.1111/1749-4877.12224J. M. Davenport, B. R. Hossack Reevaluating geographic variation in life‐history traits of a widespread Nearctic amphibian, Journal of Zoology 299, no.44 (May 2016): 304–310.https://doi.org/10.1111/jzo.12352Raciel Cruz‐Elizalde, Aurelio Ramírez‐Bautista Reproductive cycles and reproductive strategies among populations of the Rose‐bellied Lizard Sceloporus variabilis (Squamata: Phrynosomatidae) from central Mexico, Ecology and Evolution 6, no.66 (Feb 2016): 1753–1768.https://doi.org/10.1002/ece3.1998Daniel Oliveira Mesquita, Renato Gomes Faria, Guarino Rinaldi Colli, Laurie J. Vitt, Eric R. Pianka Lizard life-history strategies, Austral Ecology 41, no.11 (Sep 2015): 1–5.https://doi.org/10.1111/aec.12276D. Reznick Life History Evolution in Guppies, Experimental Studies of, (Jan 2016): 343–351.https://doi.org/10.1016/B978-0-12-800049-6.00100-1Konstantin Hallmann, Eva Maria Griebeler, Gregorio Moreno-Rueda Eggshell Types and Their Evolutionary Correlation with Life-History Strategies in Squamates, PLOS ONE 10, no.99 (Sep 2015): e0138785.https://doi.org/10.1371/journal.pone.0138785William J. Matthews Basic Biology, Good Field Notes, and Synthesizing across Your Career, Copeia 103, no.33 (Sep 2015): 495–501.https://doi.org/10.1643/OT-15-296Inon Scharf, Anat Feldman, Maria Novosolov, Daniel Pincheira-Donoso, Indraneil Das, Monika Böhm, Peter Uetz, Omar Torres-Carvajal, Aaron Bauer, Uri Roll, Shai Meiri Late bloomers and baby boomers: ecological drivers of longevity in squamates and the tuatara, Global Ecology and Biogeography 24, no.44 (Oct 2014): 396–405.https://doi.org/10.1111/geb.12244Justin L. Rheubert, Katherine Touzinsky, David M. Sever, Robert D. Aldridge, Anthony J. Wilmes, Dustin S. Siegel, Kevin M. Gribbins Reproductive Biology of Sceloporus consobrinus (Phrynosomatidae): Male Germ Cell Development and Reproductive Cycle Comparisons within Spiny Lizards, Journal of Herpetology 48, no.22 (Jun 2014): 162–171.https://doi.org/10.1670/12-156Laurie J. Vitt Walking the Natural-History Trail, Herpetologica 69, no.22 (Jun 2013): 105–117.https://doi.org/10.1655/HERPETOLOGICA-D-13-00027Wen-San Huang, David A. Pike, Cédric Sueur Testing Cost-Benefit Models of Parental Care Evolution Using Lizard Populations Differing in the Expression of Maternal Care, PLoS ONE 8, no.22 (Feb 2013): e54065.https://doi.org/10.1371/journal.pone.0054065Héctor Gadsden, Gamaliel Castañeda Demography of the Side-Blotched Lizard, Uta stansburiana , in Sand Dunes of the Central Chihuahuan Desert, The Southwestern Naturalist 57, no.33 (Sep 2012): 292–303.https://doi.org/10.1894/0038-4909-57.3.292Nicholas B. Pollock, Larisa K. Vredevoe, Emily N. Taylor How do host sex and reproductive state affect host preference and feeding duration of ticks?, Parasitology Research 111, no.22 (Apr 2012): 897–907.https://doi.org/10.1007/s00436-012-2916-8R. Sacchi, D. Pellitteri‐Rosa, A. Capelli, M. Ghitti, A. Di Paoli, A. Bellati, S. Scali, P. Galeotti, M. Fasola, Mark‐Oliver Rödel Studying the reproductive biology of the common wall lizard using ultrasonography, Journal of Zoology 287, no.44 (May 2012): 301–310.https://doi.org/10.1111/j.1469-7998.2012.00917.xRodrigo Caruccio, Renata Cardoso Vieira, Laura Verrastro, Denise Mello Machado, Thermal biology, activity, and population parameters of Cnemidophorus vacariensis (Squamata, Teiidae), a lizard endemic to southern Brazil, Iheringia. Série Zoologia 101, no.44 (Dec 2011): 283–295.https://doi.org/10.1590/S0073-47212011000300002Jennifer Botha-Brink, Roger M. H. Smith Osteohistology of the Triassic archosauromorphs Prolacerta , Proterosuchus , Euparkeria , and Erythrosuchus from the Karoo Basin of South Africa, Journal of Vertebrate Paleontology 31, no.66 (Nov 2011): 1238–1254.https://doi.org/10.1080/02724634.2011.621797Conrado A. B Galdino, Monique Van Sluys, , Clutch size in the small-sized lizard Eurolophosaurus nanuzae (Tropiduridae): does it vary along the geographic distribution of the species?, Iheringia. Série Zoologia 101, no.1-21-2 (Jun 2011): 61–64.https://doi.org/10.1590/S0073-47212011000100008Daniel Blackburn, James Stewart Viviparity and Placentation in Snakes, (May 2011): 119–181.https://doi.org/10.1201/b10879-6Robert M. Cox, Ryan Calsbeek SEVERE COSTS OF REPRODUCTION PERSIST IN ANOLIS LIZARDS DESPITE THE EVOLUTION OF A SINGLE-EGG CLUTCH, Evolution 55 (Dec 2009).https://doi.org/10.1111/j.1558-5646.2009.00906.xA. Ferreira, DN. Silva, M. Van Sluys, H. Dolder, , , Seasonal changes in testicular and epididymal histology of the tropical lizard, Tropidurus itambere (Rodrigues, 1987), during its reproductive cycle, Brazilian Journal of Biology 69, no.22 (May 2009): 429–435.https://doi.org/10.1590/S1519-69842009000200028Wei-Guo Du, Dan Lü An experimental test of body volume constraint on female reproductive output, Journal of Experimental Zoology Part A: Ecological Genetics and Physiology 9999A (Jan 2009): n/a–n/a.https://doi.org/10.1002/jez.583Kristopher B. Karsten, Laza N. Andriamandimbiarisoa, Stanley F. Fox, Christopher J. Raxworthy A unique life history among tetrapods: An annual chameleon living mostly as an egg, Proceedings of the National Academy of Sciences 105, no.2626 (Jul 2008): 8980–8984.https://doi.org/10.1073/pnas.0802468105A. I. Banet, D. N. Reznick Do placental species abort offspring? Testing an assumption of the Trexler–DeAngelis model, Functional Ecology 22, no.22 (Apr 2008): 323–331.https://doi.org/10.1111/j.1365-2435.2007.01367.xHéctor Gadsden, José L. Estrada-Rodríguez Demography of the Yarrow's Spiny Lizard, Sceloporus jarrovii, from the Central Chihuahuan Desert, Western North American Naturalist 68, no.11 (Mar 2008): 46–57.https://doi.org/10.3398/1527-0904(2008)68[46:DOTYSL]2.0.CO;2Gamaliel Castañeda, Héctor Gadsden, Armando J. Contreras-Balderas, Cristina GarcÍa-De la Peña VARIATION IN HOME RANGE OF THE SIDE-BLOTCHED LIZARD, UTA STEJNEGERI , IN COAHUILA, MEXICO, The Southwestern Naturalist 52, no.44 (Dec 2007): 461–467.https://doi.org/10.1894/0038-4909(2007)52[461:VIHROT]2.0.CO;2Héctor Gadsden, José L. Estrada-RodrÍguez ECOLOGY OF THE SPINY LIZARD SCELOPORUS JARROVII IN THE CENTRAL CHIHUAHUAN DESERT, The Southwestern Naturalist 52, no.44 (Dec 2007): 600–608.https://doi.org/10.1894/0038-4909(2007)52[600:EOTSLS]2.0.CO;2Domingos J. Rodrigues, Masao Uetanabaro, Frederico S. Lopes Breeding biology of Phyllomedusa azurea Cope, 1862 and P. sauvagii Boulenger, 1882 (Anura) from the Cerrado, Central Brazil, Journal of Natural History 41, no.29-3229-32 (Dec 2010): 1841–1851.https://doi.org/10.1080/00222930701507220Victor J. T. Loehr, Margaretha D. Hofmeyr, Brian T. Henen Growing and shrinking in the smallest tortoise, Homopus signatus signatus: the importance of rain, Oecologia 153, no.22 (Apr 2007): 479–488.https://doi.org/10.1007/s00442-007-0738-7Casey A. Gilman, Blair O. Wolf Use of portable ultrasonography as a nondestructive method for estimating reproductive effort in lizards, Journal of Experimental Biology 210, no.1111 (Jun 2007): 1859–1867.https://doi.org/10.1242/jeb.001875Cameron W. Barrows, Geoffrey C. Carpenter POPULATION DYNAMICS OF A THREATENED SAND DUNE LIZARD, The Southwestern Naturalist 51, no.44 (Dec 2006): 514–523.https://doi.org/10.1894/0038-4909(2006)51[514:PDOATS]2.0.CO;2Héctor Gadsden, María de la Luz Dávila-Carrazco, Rosalina Gil-Martínez Reproduction in the Arenicolous Mexican Lizard Uma exsul, Journal of Herpetology 40, no.11 (Mar 2006): 117–122.https://doi.org/10.1670/0022-1511(2006)40[117:RITAML]2.0.CO;2J. Jaime Zúñiga-Vega, R. Isaac Rojas-González, Julio A. Lemos-Espinal, M. Esther Pérez-Trejo Growth Ecology of the Lizard Xenosaurus grandis in Veracruz, México, Journal of Herpetology 39, no.33 (Sep 2005): 433–443.https://doi.org/10.1670/202-04A.1WEI-GUO DU, XIANG JI, YONG-PU ZHANG, XUE-FENG XU, RICHARD SHINE Identifying sources of variation in reproductive and life-history traits among five populations of a Chinese lizard (Takydromus septentrionalis, Lacertidae), Biological Journal of the Linnean Society 85, no.44 (Jul 2005): 443–453.https://doi.org/10.1111/j.1095-8312.2005.00508.xVicente Mata-Silva, Aurelio Ramírez-Bautista, Geoffrey C. Carpenter REPRODUCTIVE CHARACTERISTICS OF TWO SYNTOPIC, WIDELY FORAGING LIZARDS, ASPIDOSCELIS DEPPII AND ASPIDOSCELIS GUTTATA FROM OAXACA, MÉXICO, The Southwestern Naturalist 50, no.22 (Jun 2005): 262–267.https://doi.org/10.1894/0038-4909(2005)050[0262:RCOTSW]2.0.CO;2Laurie J. Vitt, Peter A. Zani Ecology and Reproduction of Anolis capito in Rain Forest of Southeastern Nicaragua, Journal of Herpetology 39, no.11 (Mar 2005): 36–42.https://doi.org/10.1670/0022-1511(2005)039[0036:EAROAC]2.0.CO;2Patricia A. Herrmann, Hans-Werner Herrmann Egg and Clutch Characteristics of the Mountain Chameleon, Chamaeleo montium, in Southwestern Cameroon, Journal of Herpetology 39, no.11 (Mar 2005): 154–157.https://doi.org/10.1670/0022-1511(2005)039[0154:EACCOT]2.0.CO;2Wei-Guo Du, Yi-Wei Lu, Jian-Yang Shen The influence of maternal thermal environments on reproductive traits and hatchling traits in a Lacertid lizard, Takydromus septentrionalis, Journal of Thermal Biology 30, no.22 (Feb 2005): 153–161.https://doi.org/10.1016/j.jtherbio.2004.09.005Héctor Gadsden, Fausto R. Méndez De La Cruz, Rosalina Gil Martínez CICLO REPRODUCTOR DE UTA STEJNEGERI SCHMIDT 1921 (SAURIA: PHRYNOSOMATIDAE) EN DUNAS DEL BOLSÓN DE MAPIMÍ; DURANGO; MÉXICO, ACTA ZOOLÓGICA MEXICANA (N.S.) 20, no.33 (Jun 2004): 127–138.https://doi.org/10.21829/azm.2004.2031586Clare Morrison, Jean-Marc Hero, Jay Browning ALTITUDINAL VARIATION IN THE AGE AT MATURITY, LONGEVITY, AND REPRODUCTIVE LIFESPAN OF ANURANS IN SUBTROPICAL QUEENSLAND, Herpetologica 60, no.11 (Mar 2004): 34–44.https://doi.org/10.1655/02-68Aurelio Ramírez-Bautista, Guadalupe Gutiérrez-Mayén Reproductive Ecology of Sceloporus utiformis (Sauria: Phrynosomatidae) from a Tropical Dry Forest of México, Journal of Herpetology 37, no.11 (Mar 2003): 1–10.https://doi.org/10.1670/0022-1511(2003)037[0001:REOSUS]2.0.CO;2X. Bonnet, R. Shine, O. Lourdais, G. Naulleau Measures of reproductive allometry are sensitive to sampling bias, Functional Ecology 17, no.11 (Feb 2003): 39–49.https://doi.org/10.1046/j.1365-2435.2003.00704.xM. Znari, E. El Mouden, H. Francillon‐Vieillot Long‐term variation in reproductive traits of Bibron's agama, agama impalearis, in Western Morocco, African Journal of Herpetology 51, no.11 (Jun 2002): 57–68.https://doi.org/10.1080/21564574.2002.9635462Helga C. Wiederhecker, Adriana C. S. Pinto, Guarino R. Colli Reproductive Ecology of Tropidurus torquatus (Squamata: Tropiduridae) in the Highly Seasonal Cerrado Biome of Central Brazil, Journal of Herpetology 36, no.11 (Mar 2002): 82–91.https://doi.org/10.1670/0022-1511(2002)036[0082:REOTTS]2.0.CO;2 David N. Penick , Justin Congdon , James R. Spotila , and Joseph B. Williams Microclimates and Energetics of Free‐Living Box Turtles, Terrapene carolina, in South Carolina D. N. Penick, J. Congdon, J. R. Spotila, and J. B. Williams, Physiological and Biochemical Zoology 75, no.11 (Jul 2015): 57–65.https://doi.org/10.1086/339219James R. Carey I NSECT B IODEMOGRAPHY, Annual Review of Entomology 46, no.11 (Jan 2001): 79–110.https://doi.org/10.1146/annurev.ento.46.1.79Daniel G Blackburn Reptilian viviparity: past research, future directions, and appropriate models, Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology 127, no.44 (Dec 2000): 391–409.https://doi.org/10.1016/S1095-6433(00)00272-5Aurelio Ramírez-Bautista, Carlos Balderas-Valdivia, Laurie J. Vitt, A. H. Price Reproductive Ecology of the Whiptail Lizard Cnemidophorus lineatissimus (Squamata: Teiidae) in a Tropical Dry Forest, Copeia 2000, no.33 (Aug 2000): 712–722.https://doi.org/10.1643/0045-8511(2000)000[0712:REOTWL]2.0.CO;2Pedro Galán Demography and population dynamics of the lacertid lizard Podarcis bocagei in north‐west Spain, Journal of Zoology 249, no.22 (Feb 2006): 203–218.https://doi.org/10.1111/j.1469-7998.1999.tb00759.x Mark J. Komoroski , Roy D. Nagle , and Justin D. Congdon Relationships of Lipids to Ovum Size in Amphibians M. J. Komoroski, R. D. Nagle, & J. D. Congdon, Physiological Zoology 71, no.66 (Sep 2015): 633–641.https://doi.org/10.1086/515989Pedro Galan Reproductive ecology of the lacertid lizard Podarcis bocagei, Ecography 20, no.22 (Apr 1997): 197–209.https://doi.org/10.1111/j.1600-0587.1997.tb00362.xAllan J. Landwer Manipulation of egg production reveals costs of reproduction in the tree lizard (Urosaurus ornatus), Oecologia 100, no.33 (Dec 1994): 243–249.https://doi.org/10.1007/BF00316951Hugh Griffith Body elongation and decreased reproductive output within a restricted clade of lizards (Reptilia: Scincidae), Journal of Zoology 233, no.44 (May 2009): 541–550.https://doi.org/10.1111/j.1469-7998.1994.tb05364.xAlison Cree Low annual reproductive output in female reptiles from New Zealand, New Zealand Journal of Zoology 21, no.44 (Jan 1994): 351–372.https://doi.org/10.1080/03014223.1994.9518005Xu Haigen, Yang Fengxiang Age classification and growth model of Phrynocephalus przewalskii, Ecological Modelling 70, no.1-21-2 (Nov 1993): 127–135.https://doi.org/10.1016/0304-3800(93)90076-5F K Kasule A quantitative genetic analysis of reproductive allocation in the cotton stainer bug Dysdercus fasciatus, Heredity 69, no.22 (Aug 1992): 141–149.https://doi.org/10.1038/hdy.1992.107Lin Schwarzkopf, Richard Shine Costs of reproduction in lizards: escape tactics and susceptibility to predation, Behavioral Ecology and Sociobiology 31, no.11 (Jul 1992): 17–25.https://doi.org/10.1007/BF00167812Richard Shine RELATIVE CLUTCH MASS AND BODY SHAPE IN LIZARDS AND SNAKES: IS REPRODUCTIVE INVESTMENT CONSTRAINED OR OPTIMIZED?, Evolution 46, no.33 (May 2017): 828–833.https://doi.org/10.1111/j.1558-5646.1992.tb02088.xDouglas T. Kenrick, Richard C. Keefe Age preferences in mates reflect sex differences in human reproductive strategies, Behavioral and Brain Sciences 15, no.11 (May 2011): 75–91.https://doi.org/10.1017/S0140525X00067595Thomas R. Alley Perceived age, physical attractiveness and sex differences in preferred mates' ages, Behavioral and Brain Sciences 15, no.11 (May 2011): 92–92.https://doi.org/10.1017/S0140525X00067601Betty M. Bayer On the separation of reproduction from mating preferences, Behavioral and Brain Sciences 15, no.11 (May 2011): 92–93.https://doi.org/10.1017/S0140525X00067613Peter Borkenau Age preferences: The crucial studies have yet to be done, Behavioral and Brain Sciences 15, no.11 (May 2011): 93–94.https://doi.org/10.1017/S0140525X00067625Gwen J. Broude The May-September algorithm meets the 20th century actuarial table, Behavioral and Brain Sciences 15, no.11 (May 2011): 94–95.https://doi.org/10.1017/S0140525X00067637Donn Byrne, Kathryn Kelley Differential age preferences: The need to test evolutionary versus alternative conceptualizations, Behavioral and Brain Sciences 15, no.11 (May 2011): 96–96.https://doi.org/10.1017/S0140525X00067649Charles Crawford Sex differences in age preferences for mates: Primary and secondary predictions from evolutionary theory, Behavioral and Brain Sciences 15, no.11 (May 2011): 97–98.https://doi.org/10.1017/S0140525X00067650Donald A. Dewsbury Continuing a long tradition, Behavioral and Brain Sciences 15, no.11 (May 2011): 98–98.https://doi.org/10.1017/S0140525X00067662John Dupré Arbitrariness and bias in evolutionary speculation, Behavioral and Brain Sciences 15, no.11 (May 2011): 98–99.https://doi.org/10.1017/S0140525X00067674David C. Funder Toward a nonarbitrary social psychology, Behavioral and Brain Sciences 15, no.11 (May 2011): 99–100.https://doi.org/10.1017/S0140525X00067686Norval D. Glenn Toward a more complete integration of evolutionary and other perspectives on age preferences in mates, Behavioral and Brain Sciences 15, no.11 (May 2011): 100–100.https://doi.org/10.1017/S0140525X00067698Karl Grammer Variations on a theme: Age dependent mate selection in humans, Behavioral and Brain Sciences 15, no.11 (May 2011): 100–102.https://doi.org/10.1017/S0140525X00067704Henry Harpending Age differences between mates in southern African pastoralists, Behavioral and Brain Sciences 15, no.11 (May 2011): 102–103.https://doi.org/10.1017/S0140525X00067716George Levinger, Lee A. Kirkpatrick Biological versus social psychological bases of mate selection, Behavioral and Brain Sciences 15, no.11 (May 2011): 103–104.https://doi.org/10.1017/S0140525X00067728Richard Lippa On building bridges between social psychology and evolutionary biology, Behavioral and Brain Sciences 15, no.11 (May 2011): 104–105.https://doi.org/10.1017/S0140525X0006773XLinda Mealey Individual differences in reproductive tactics: Cuing, assessment, and facultative strategies, Behavioral and Brain Sciences 15, no.11 (May 2011): 105–106.https://doi.org/10.1017/S0140525X00067741Christopher A. Moffatt, Randy J. Nelson May/December romance: Adaptive significance non probabilis est, Behavioral and Brain Sciences 15, no.11 (May 2011): 106–107.https://doi.org/10.1017/S0140525X00067753D. W. Rajecki, Jeffrey Lee Rasmussen Personal ads as deviant and unsatisfactory: Support for evolutionary hypotheses, Behavioral and Brain Sciences 15, no.11 (May 2011): 107–107.https://doi.org/10.1017/S0140525X00067765J. Philippe Rushton Age similarity is genetic similarity, Behavioral and Brain Sciences 15, no.11 (May 2011): 108–108.https://doi.org/10.1017/S0140525X00067777P. A. Russell The evolutionary model is synthetic not heuristic, Behavioral and Brain Sciences 15, no.11 (May 2011): 108–109.https://doi.org/10.1017/S0140525X00067789Robert Schoen Marital choice and reproductive strategies, Behavioral and Brain Sciences 15, no.11 (May 2011): 109–109.https://doi.org/10.1017/S0140525X00067790Jeffry A. Simpson Half a theory and half the data for half the people?, Behavioral and Brain Sciences 15, no.11 (May 2011): 109–110.https://doi.org/10.1017/S0140525X00067807Steven A. Sloman, Leon Sloman What does evolution tell us about age preferences?, Behavioral and Brain Sciences 15, no.11 (May 2011): 110–111.https://doi.org/10.1017/S0140525X00067819Walter G. Stephan Sexual motivation, patriarchy and compatibility, Behavioral and Brain Sciences 15, no.11 (May 2011): 111–112.https://doi.org/10.1017/S0140525X00067820Gillian Stevens Mortality and age-specific patterns of marriage, Behavioral and Brain Sciences 15, no.11 (May 2011): 112–113.https://doi.org/10.1017/S0140525X00067832Donald Symons What do men want?, Behavioral and Brain Sciences 15, no.11 (May 2011): 113–114.https://doi.org/10.1017/S0140525X00067844Nancy Wilmsen Thornhill, Patrick A. A. Thornhill The preferred age of a potential mate reflects evolved male sexual psychology, Behavioral and Brain Sciences 15, no.11 (May 2011): 114–115.https://doi.org/10.1017/S0140525X00067856John Marshall Townsend Measuring the magnitude of sex differences, Behavioral and Brain Sciences 15, no.11 (May 2011): 115–116.https://doi.org/10.1017/S0140525X00067868Pierre L. van den Berghe Wanting and getting ain't the same, Behavioral and Brain Sciences 15, no.11 (May 2011): 116–117.https://doi.org/10.1017/S0140525X0006787XArie J. van Noordwijk, Jacqui A. Shykoff Accounting for age preferences in sexual selection, Behavioral and Brain Sciences 15, no.11 (May 2011): 117–118.https://doi.org/10.1017/S0140525X00067881Kim Wallen Evolutionary hypothesis testing: Consistency is not enough, Behavioral and Brain Sciences 15, no.11 (May 2011): 118–119.https://doi.org/10.1017/S0140525X00067893Douglas T. Kenrick, Richard C. Keefe Sex differences in age preference: Universal reality or ephemeral construction?, Behavioral and Brain Sciences 15, no.11 (May 2011): 119–133.https://doi.org/10.1017/S0140525X0006790XRichard Shine, Lin Schwarzkopf THE EVOLUTION OF REPRODUCTIVE EFFORT IN LIZARDS AND SNAKES, Evolution 46, no.11 (May 2017): 62–75.https://doi.org/10.1111/j.1558-5646.1992.tb01985.xLin Schwarzkopf, Richard Shine Thermal biology of reproduction in viviparous skinks, Eulamprus tympanum: why do gravid females bask more?, Oecologia 88, no.44 (Dec 1991): 562–569.https://doi.org/10.1007/BF00317720JAMES R. KARR Avian Survival Rates and the Extinction Process on Barro Colorado Island, Panama, Conservation Biology 4, no.44 (Dec 1990): 391–397.https://doi.org/10.1111/j.1523-1739.1990.tb00313.xMasami Hasegawa Demography of an island population of the lizard, Eumeces okadae , on Miyake‐jima, Izu Islands, Population Ecology 32, no.11 (Nov 2018): 119–133.https://doi.org/10.1007/BF02512594Douglas J. Futuyma Anpassung, (Jan 1990): 283–322.https://doi.org/10.1007/978-3-0348-5235-7_9H. ELIZABETH BRAKER Evolution and ecology of oviposition on host plants by acridoid grasshoppers, Biological Journal of the Linnean Society 38, no.44 (Jan 2008): 389–406.https://doi.org/10.1111/j.1095-8312.1989.tb01584.xEric T. Schultz, Robert R. Warner PHENOTYPIC PLASTICITY IN LIFE‐HISTORY TRAITS OF FEMALE THALASSOMA BIFASCIATUM (PISCES: LABRIDAE). 1. MANIPULATIONS OF SOCIAL STRUCTURE IN TESTS FOR ADAPTIVE SHIFTS OF LIFE‐HISTORY ALLOCATIONS, Evolution 43, no.77 (May 2017): 1497–1506.https://doi.org/10.1111/j.1558-5646.1989.tb02599.xVincent G. DeMarco Annual variation in the seasonal shift in egg size and clutch size in Sceloporus woodi, Oecologia 80, no.44 (Sep 1989): 525–532.https://doi.org/10.1007/BF00380077Linda Partridge, Paul H. Harvey The Ecological Context of Life History Evolution, Science 241, no.48724872 (Sep 1988): 1449–1455.https://doi.org/10.1126/science.241.4872.1449H. Strijbosch, R. C. M. Creemers Comparative demography of sympatric populations of Lacerta vivipara and Lacerta agilis, Oecologia 76, no.11 (Jun 1988): 20–26.https://doi.org/10.1007/BF00379595Craig James, Richard Shine Life-history strategies of Australian lizards: a comparison between the tropics and the temperate zone, Oecologia 75, no.22 (Mar 1988): 307–316.https://doi.org/10.1007
Referência(s)