Data from: Macroevolutionary patterns in Rhynchocephalia: is the tuatara (Sphenodon punctatus) a living fossil?

负责人：

关键词：

Mesozoic;Sphenodontia;Sphenodon punctatus;Rhynchocephalia;rates of evolution;living fossils;Holocene;morphospace

DOI：

doi:10.5061/dryad.568jh

摘要：

, rhynchocephalians had heterogeneous rates of morphological evolution and occupied wide morphospaces during the Triassic and Jurassic, and these then decline

Data from: Cope’s Rule in a modular organism: directional evolution without an overarching macroevolutionary trend

负责人：

关键词：

Macroevolution;Paleogene;Neogene;module size;Morphological Evolution;Bryozoa;Macroevolution;fossils;Cope's Rule;Bergmann's rule;Bryozoa;fossils;modular organisms;Recent;Jurassic;Triassic;Cheilostomatida;Holocene;paleobiology;Pleistocene

DOI：

doi:10.5061/dryad.nv89424

摘要：

simply comprises repeated rounds of microevolution, evolutionary processes occurring with lineages are not always detectable from macroevolutionary patterns.

Data from: Intraspecific variation in cephalopod conchs changes during ontogeny: perspectives from three-dimensional morphometry

负责人：

关键词：

Jurassic;Devonian;Tomography;cephalopods;Nautilus pompilius;intraspecific variation;Holocene

DOI：

doi:10.5061/dryad.4cb86

摘要：

phalopods (ammonoids and nautiloids), in which an excessive number of taxa were established during the past centuries. Since intraspecific variation of fossi

Data from: Rates of evolution: a quantitative synthesis

负责人：

关键词：

Brachycrus wilsoni;Mesozoic;Otomys auretus;Experimental Selection;Paleocene;Longitudinal time series;Merycochoerus proprius;Ectocion parvus;Passer montanus;Petrochelidon pyrrhonota;Metrarabdotos volkesorum;Metrarabdotos cubaguaense;Anolis carolinensis;Anakosmoceras sp.;Globoratalia tumida;Oligocene;Cervus elaphus;Rattus rattus;Ursavus elmensis;Merychippus paniensis;Longitudinal field study;cross-sectional field study;Merychyus elegans;Mesohippus bairdi;Hyracotherium sandrae;Hyopsodus latidens;Cantius trigonodus;Cantius ralstoni;Kosmoceras sp.;Passer domesticus;Pliocene;Merycochoerus matthewi;Stephanodiscus yellowstonensis;Eocoelia sp.;Hyopsodus pauxillus;Jurassic;Merychyus crabilli;Neotoma albigula;Branta leucopsis;Scathophaga stercoraria;Mus sp.;Metrarabdotos colligatum;Peromyscus maniculatus;Loxodonta sp.;Mollusca;Holocene;Mesomyla sclateri;Homo erectus;Brassica rapa;Mammuthus sp.;Artificial selection;Haplomylus simpsoni;Cormohipparion occidentale;Peromyscus leucopus;Cosomys primus;Hyracotherium grangeri;Parapelomys sp.;Globorotalia conoidea;Eohippus resartus;Vulpes vulpes;Hyopsodus miticulus;Zea mays;Dipodomys merriami;Urocitellus beldingi;Amara quenseli;Eocene;Herpestes auropunctatus;Otomys angoniensis;Hyopsodus powellianus;Hirundo rustica;Elephas sp.;Poseidonamicus spp.;Paleozoic;Primelephas sp.;Euryderus grossus;Globoratalia plesiotumida;Merychyus relictus;Ursus etruscus;Cantius mckennai;Gyretes sinuatus;Gambusia affinis;Globorotalia inflata;Gasterosteus aculeatus;Pleistocene;Drepanis coccinea;Gymnodactylus amarali;Carabus nemoralis;Chlorocebus sabaeus;Experimental field study;Ursus spelaeus;Myzomela pammelaena;Cymindis planipennis;Thymallus thymallus;Ectocion ralstonensis;Haplomylus speirianus;Pseudocubus vema;Pterostichus algidus;Dinosauria;Pterostichus melanarius;Equus germanicus;Cenozoic;Globorotalia puncticulata;Gallus gallus;Merychyus minimus;Cryptopecten vesicululosus;Equidae;Hyopsodus minor;Hyracotherium borealis;Oncorhyncus nerka;Ovis aries;Fringilla coelebs;fossil record;Anser caerulescens;Haplomylus scottianus;drosophila melanogaster;Brachycrus siouense;Cantius torresi;Hyopsodus lysitensis;Ficedula albicollis;Ectocion osbornianus;Mus musculus;Silurian;Bison bison;Metrarabdotos saundersi;Zugokosmoceras sp.;Bison priscus;Metrarabdotos auriculatum;Bison latifrons;Mandarina chichijimana;Gasterosteus doryssus;Geospiza scandens;Scaphinotus angusticollis;Telespyza canans;Recent;Oryctolagus cuniculus;Jadera haematoloma;Antemus sp.;Hyopsodus loomisi;Progonomys sp.;Drosophila subobscura;Harpalus fraternus;introduced species;Laboratory selection;Haplomylus palustris;Haplomylus zalmouti;Cyclostephanos andinus;Loxodonta africana;Globorotalia conomiozea;Karnimata sp.;Plethodon spp.;natural selection;Geospiza fortis;Ursus arctos;Bison antiquus;Metrarabdotos boldi;Metrarabdotos coatesi;Drosophila pseudoobscura;Littorina obtusata;Parus caeruleus;Poecilia reticulata;Miocene

DOI：

doi:10.5061/dryad.1tn7123

摘要：

s, and rates for selection experiments (file 1: 15,431 rates), field studies (file 2: 12,461 rates), and fossil studies (file 3: 47,854 rates).

Data from: Empirical and theoretical study of Atelostomate (Echinoidea, Echinodermata) plate architecture: using graph analysis to reveal

负责人：

关键词：

Jurassic to Holocene;morphological disparity;graph theory;structural constraints;Echinoidea;plate topologies

DOI：

doi:10.5061/dryad.2t30k

摘要：

morphogenetic processes and the associated constraints that control the morphological diversification of clades. This is particularly relevant for studies

Data from: Evidence for complex life cycle constraints on salamander body form diversification

负责人：

关键词：

Jurassic;salamanders;direct development;Caudata;trait evolution;Amphibia;metamorphosis;Constraints;paedomorphosis;Holocene

DOI：

doi:10.5061/dryad.pn5kg

摘要：

d an increased rate of vertebral column and body form diversification compared to lineages with a complex, aquatic-terrestrial (biphasic) life cycle. These