Not all written in stone: Interdisciplinary syntheses in echinoderm paleontology

Canadian Journal of Zoology

Volumn 79, Issue 7, 2001, Pages 1209-1231

  Mooi, R ^a  

^a CALIFORNIA ACADEMY OF SCIENCES   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BIOSYNTHESIS; ECOLOGY; ROCKS;

ECHINODERMATA;

BIODIVERSITY;

ECHINODERM; FOSSIL RECORD; PALEONTOLOGY;

ASTEROZOA; ECHINODERMATA; ECHINOIDEA; EDRIOASTEROIDEA; HOMALOZOA; INVERTEBRATA; PELMATOZOA;

EID: 0034860299     PISSN: 00084301     EISSN: None     Source Type: Journal    
DOI: 10.1139/z00-217     Document Type: Review

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50. Inferring substrate preferences from test morphology in echinoids, and interpreting spatial and temporal patterns of diversity
51. Substrate preferences and biofacies of Egyptian Eocene echinoids
52. Eocene echinoids, the Suwannee Strait, and biogeographic taphonomy
53. The fossil record and early evolution of the Metazoa
54. A new stem-craniate from the Ordovician of Morocco and the search for the sister group of the Craniata
55. A cladistic analysis of the cornutes (stem chordates)
56. Two cornutes from the Middle Ordovician (Llandeilo) of Normandy, France, and a reinterpretation of Milonicystis kerfornei
57. The anatomy of the solute Girvanicystis batheri (?Chordata) from the Upper Ordovician of Scotland and a new species of Girvanicystis from the Upper Ordovician of south Wales
58. Two new cornutes from the Lower Ordovician of Shropshire and southern France
59. Anatomy, locomotion and ontogeny of the solute Castericystis vali from the Middle Cambrian of Utah
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61. Embryology supports a new theory of skeletal homologies for the phylum Echinodermata
62. Major events in the evolution of echinoderms viewed by the light of embryology
63. Comprendre les Échinodermes: La contribution du modèle extraxial-axial
64. The ontogenetic basis of Lovén's Rule clarifies homologies of the echinoid peristome
65. Are homalozoans echinoderms? An answer from the extraxial-axial theory
66. What makes an ophiuroid? A morphological study of the problematic Ordovician stelleroid Stenaster and the palaeobiology of the earliest asteroids and ophiuroids
67. Oligocene echinoids of Jamaica
68. The early evolution of echinoderms: The class Ctenocystoidea and its closest relatives revisited
69. Functional morphology of synostosial articulations in the crinoid column
70. The taphonomy of echinoderms: Calcareous multi-element skeletons in the marine environment
71. Contractile tissues in the cirri of ancient crinoids: Criteria for recognition
72. Jamaican Cretaceous Echinoidea
73. Jamaican Cenozoic Echinoidea
74. Evolution of the Jamaican echinoid fauna during the Eocene-Oligocene extinction crisis
75. Some fossil echinoids (Echinodermata) from the Cenozoic of Jamaica, Cuba and Guadeloupe
76. Early Pleistocene echinoids of the Manchioneal Formation, Jamaica
77. Crinoids, asteroids, and ophiuroids in the Jamaican fossil record
78. Testing the marine continental fossil records: Comment and reply
79. Jamaican Cretaceous Crinoidea
80. Observations on the Early Cambrian helicoplacoid echinoderms
81. Diversification of disasteroids, holasteroids and spatangoids in the Mesozoic
82. The role of development in evolutionary radiations
83. Paleontology in academia II: The source and academic age of U.S. paleontologists
84. Paleontology in academia: Recent trends and future opportunities
85. Morphological and taxonomic diversity in a clade's history: The blastoid record and stochastic simulations
86. Paleozoic record of morphological diversity in blastozoan echinoderms
87. Rarefaction analysis of morphological and taxonomic diversity
88. Discordance and concordance between morphological and taxonomic diversity
89. Morphological disparity in Ordovician-Devonian crinoids and the early saturation of morphological space
90. Morphology of Ordovician-Devonian crinoids
91. Morphological diversification of Paleozoic crinoids
92. Morphology of Carboniferous and Permian crinoids
93. Ecological controls on the evolutionary recovery of post-Paleozoic crinoids
94. Perspective: Evolutionary patterns in the fossil record
95. Sampling, taxonomic description, and our evolving knowledge of morphological diversity
96. Dense beds of ophiuroids from the Paleozoic to the Recent: The significance of bathyal populations
97. Earliest known echinoderm - A new Ediacaran fossil from the Pound Subgroup of South Australia
98. Bohemiaecystis jefferiesi n.sp.: Primer Cornuta para el Ordovicio espanol
99. Holothurian faunal changes across the Triassic-Jurassic boundary
100. Holothurians in the Blue Lias of southern Britain
101. The skeletal morphology, systematics, and evolutionary history of holothurians
102. An integrated study of echinoid taphonomy: Predictions for the fossil record of four echinoid families
103. Agelacrinites curvatus n.sp., ein Edrioasteroide (Echinodermata) aus oberen siegener schichten des nordlichen westerwaldes, rheinisches schiefergebirge
104. Paleoecology of hardground encrusting and commensal crinoids, Middle Ordovician, Tennessee
105. Rise of echinoderms in the Paleozoic evolutionary fauna: Significance of paleoenvironmental controls
106. Revised phylogeny and functional interpretation of the Edrioasteroidea based on new taxa from the Early and Middle Ordovician of western Utah
107. Fossil holothurians: Constructional morphology of the sea cucumber, and the origin of the calcareous ring
108. Die holothurien-konstruktion: Evolutionsmodell und altester fossilbericht
109. Echinodermen aus dem Unter-Devon der argentinischen präkordillere
110. Nudicorona, eine devonische Holothurie
111. The descent of the Asteroidea and the reaffirmation of paxillosidan primitiveness
112. An edrioasteroid from the Silurian of Tasmania
113. Paleoecology and evolutionary ecology of Paleozoic crinoids
114. Lovén's law and adult ray homologies in echinoids, ophiuroids, edrioasteroids, and an ophiocistioid (Echinodermata: Eleutherozoa)
115. A "rays-as-appendages" model for the origin of pentamerism in echinoderms
116. Discussion on pentamerism: The five-part pattern of Stromatocystites, Asterozoa, and Echinozoa
117. Offshore-onshore trends in marine invertebrate evolution
118. Environmental patterns in the origins of higher taxa: The post-Paleozoic fossil record
119. An overview of Late Cretaceous and Early Palaeogene echinoderm faunas from Liège-Limburg (Belgium, the Netherlands)
120. Late Cretaceous - Early Palaeogene echinoderms and the K/T boundary in the southeast Netherlands and northeast Belgium. Part 1: Introduction and stratigraphy; Part 2: Crinoids
121. The subphylum Calcichordata (Jefferies, 1967) primitive fossil chordates with echinoderm affinities
122. How to characterize the Echinodermata - Some implications of the sister-group relationship between echinoderms and chordates
123. The echinoderm stem group
124. A defense of the calcichordates
125. How chordates and echinoderms separated from each other and the problem of dorso-ventral inversion
126. Which way up were the mitrates? - Flat surface up
127. An episode in the ancestry of vertebrates: From mitrate to crown-group craniate
128. All change at the Cretaceous-Tertiary boundary? Echinoids from the Maastrichtian and Danian of the Mangyshlak Peninsula, Kazakhstan
129. Dawn of echinoid nonplanktotrophy: Coordinated shifts in development indicate environmental instability prior to the K-T boundary
130. Revision of the echinoid Enallopneustes from the Upper Cretaceous of north Africa
131. Carrying on regardless: The echinoid genus Cyclaster at the Cretaceous-Tertiary boundary
132. Estimating extinction levels for echinoids across the Cretaceous-Tertiary boundary
133. Early Permian cladid crinoids from the Gharif Formation of Oman
134. Species longevity as a function of niche breadth: Evidence from fossil crinoids
135. Evolutionary significance of differential species longevity in Osagean-Meramecian (Mississippian) crinoid clades
136. Adaptation of test shape for burrowing and locomotion in spatangoid echinoids
137. Crinoids in a machine: Computer generation and enumeration of crinoid calyx morphologies and comparisons with real forms
138. Experimental disintegration of regular echinoids: Roles of temperature, oxygen and decay thresholds
139. The youngest carpoid occurrence affinities and life mode of a Pennsylvanian Morrowan mitrate from Oklahoma, U.S.A.
140. Ciliary bands in echinoderm larvae: Evidence for structural homologies and a common plan
141. A camerate-rich Late Carboniferous (Moscovian) crinoid fauna from volcanic conglomerate, Xinjiang, People's Republic of China
142. Echinoderm faunas of the Hongguleleng Formation, Late Devonian (Famennian), Xinjiang-Uygur Autonomous Region, People's Republic of China
143. New Ordovician cornutes (Echinodermata, Stylophora) from Montagne Noire and Brittany (France) and a revision of the order Cornuta Jaekel 1901
144. Homologies in stylophoran echinoderms
145. Echinoderm class relationships revisited
146. A combined morphological and molecular phylogeny for sea urchins (Echinoidea: Echinodermata)
147. The interrelationships of the echinoderm classes: Morphological and molecular evidence
148. Five classes of echinoderm and one school of thought
149. Compositional and taphonomic variations in modern crinoid-rich sediments from the deep-water margin of a carbonate bank
150. Radical alterations in the roles of homeobox genes during echinoderm evolution
151. Paleoautecology and systematic re-evaluation of Camptocrinus alabamensis (Mississippian: Chesterian) from northern Alabama
152. Morphology, systematics and phylogeny of schizasterid sea urchins
153. Echinoids at the Cretaceous-Paleogene boundary
154. Molecular approaches to echinoderm phylogeny
155. Echinoids from the La Meseta Formation (Eocene), Seymour Island, Antarctica
156. Evolution of Paleogene echinoids: A global and regional view
157. The significance of gastropod predation to patterns of evolution and extinction in Australian Tertiary echinoids
158. Relocation movement in a stalked crinoid (Echinodermata)
159. Evolutionary implications of predation on Recent comatulid crinoids from the Great Barrier Reef
160. Population paleoecology and comparative taphonomy of two edrioasteroid (Echinodermata) pavements: Upper Ordovician of Kentucky and Ohio
161. Adaptive radiation of the comatulid crinoids
162. Eocene crinoids from Seymour Island, Antarctic Peninsula: Paleobiogeographic and paleoecologic implications
163. Phylogeny and palaeobiology of Marsupites and Uintacrinus
164. Paleobiology of isocrinid crinoids from the Red Chalk (Albian, Lower Cretaceous) of north-east England
165. Skeletal homologies of echinoderms
166. Evolution within a bizarre phylum: Homologies of the first echinoderms
167. Echinoderm skeletal homologies: Classical morphology meets modern phylogenetics
168. Echinoid distribution by fragment identification in the northern Bay of Safaga, Red Sea, Egypt
169. The northern Bay of Safaga (Red Sea, Egypt): An actuopalaeontological approach. 3. Distribution of echinoids
170. Actuopalaentological investigations on echinoids: The potential for taphonomic interpretation
171. Comparative taphonomy of clypeasteroids
172. Uses and limitations of actuopalaeontological investigations of echinoids
173. Biodiversity of shallow-water Red Sea echinoids: Implications for the fossil record
174. Taphonomy of Clypeaster humilis and Echinodiscus auritus (Echinoidea, Clypeasteroida) from the Red Sea
175. The encrustation of fossil and recent sea-urchin tests: Ecological and taphonomic significance
176. Répartition demographique des Hemiaster (Echinoidea: Spatangoida) dans le Cenomanien de Charente-Maritime (France)
177. Transgressions-regressions and echinoid morphoclines
178. Hemiasterid echinoids (Echinodermata: Spatangoida) from the Cretaceous Tethys to the present-day Mediterranean
179. Diversité des échinides fossiles et reconstitutions paléoenvironnementales
180. Un assemblage de Macrogaster cf. polygonus, spatangoide primitif de l'Albien moyen de Saint-Jouin (Seine-Maritime): Developpement ontogénique, démographie, paléoecologie
181. Cenomanian and Turonian echinoids from Nigeria
182. The Cretaceous echinoids from central Saudi Arabia
183. Variation in echinoid biodiversity during the Cenomanian - Early Turonian transgressive episode in Charentes (France)
184. Comparative variation in asteroid and echinoid diversity during the Late Cenomanian transgression in Charentes (France)
185. The International Echinoderm Conferences - A retrospect
186. Is predation intensity reduced with increasing depth? Evidence from the west Atlantic stalked crinoid Endoxocrinus parrae (Gervais) and implications for the Mesozoic marine revolution
187. Survival of crinoid stalk fragments and its taphonomic implications
188. Survival of crinoid stalk fragments and its taphonomic implications: Additional discussion
189. Arm autotomy and arm branching pattern as anti-predatory adaptations in stalked and stalkless crinoids
190. Paracrinoids
191. Feeding and respiratory strategies in Stylophora
192. Aristocystites, a recumbent diploporid (Echinodermata) from the Middle and Late Ordovician of Bohemia, CSSR
193. Review of selected North American mitrate stylophorans (Homalozoa, Echinodermata)
194. Mitrocystitid functional morphology, evolution and their relationships with other primitive echinoderm classes
195. The echinoderm classes Stylophora and Homoiostelea: Non Calcichordata
196. Taxonomic revision of the Stylophora
197. The Cincta (Homostelea) as blastozoans
198. Functional inference in fossil echinoderms
199. The early radiation and phylogeny of echinoderms
200. A phylogenetic test of the calcichordate scenario
201. Set-aside cells in maximal indirect development: Evolutionary and developmental significance
202. Expression pattern of Brachyury and Not in the sea urchin: Comparative implications for the origins of mesoderm in the basal deuterostomes
203. A new echinoid from the Eocene La Meseta Formation of Seymour Island, Antarctic Peninsula
204. New representatives of the class Stylophora (Echinodermata)
205. The benthic adaptation of echinoderms during the Early Paleozoic
206. Comparative morphology of Rhipidocystis Jaekel, 1900 and Cryptocrinites von Buch, 1840 (Eocrinoidea; Ordovician)
207. A new stem-chordate solute from the Middle Ordovician of Estonia
208. Lower Cambrian echinoderms from Russia
209. A new mitrate from the Lower Ordovician of southern France
210. Brief review of the stylophoran debate
211. Protocytidium gen. nov., a new anomalocystitid mitrate from the Victorian Latest Ordovician and evolution of the Allanicytidiidae
212. Adoketocarpus gen. nov., a mitrate from the Ludlovian Kilmore siltstone and Lochkovian Humevale Formation of central Victoria
213. Two new anomalocystitid mitrates from the Lower Devonian Humevale Formation of central Victoria
214. A note on Victoriacystis wilkinsi (Anomalocystitida: Mitrata) from the Upper Silurian of Victoria
215. Revision of Silurian and Devonian Allanicytidiidae (Anomalocystitida: Mitrata) from southeastern Australia, Tasmania and New Zealand
216. Two Devonian mitrates from South Africa
217. A new interpretation of crinoid thecal plate homology and phylogeny
218. Reinterpretation of thecal plate homology and phylogeny in the class Crinoidea
219. Echinodermata
220. Classification of the Echinodermata
221. Evolutionary diversification of echinoderms during the early Paleozoic
222. Echinoderm phylogeny: Morphology and molecules approach accord
223. Echinoid distribution in the Cenomanian: An analytical study in biogeography
224. Triassic echinoids from Peru
225. Echinoids from the Jurassic Oxford Clay of England
226. Echinoderm larvae and phylogeny
227. Echinoderm phylogeny: How congruent are morphological and molecular estimates?
228. What does palaeontology contribute to systematics in a molecular world?
229. Cretaceous echinoids from north-eastern Brazil
230. Sea-levels, sequence stratigraphy and echinoid diversity through the Cretaceous
231. Middle Triassic holothurians from northern Spain
232. Selectivity of extinction among sea urchins at the end of the Cretaceous period
233. Cambrian edrioasteroids from Australia and the origin of starfishes
234. Paleontological data and molecular phylogenetic analysis
235. Molecular and morphological evolution during the post-Palaeozoic diversification of echinoids
236. British Cretaceous echinoids. Part 1. Introduction and Cidaroida
237. British Cretaceous echinoids. Part 2. Echinothurioida, Diadematoida and Stirodonta (1, Calycina)
238. British Cretaceous echinoids. Part 3. Stirodonta 2 (Hemicidaroida, Arbacioida and Phymosomatoida, part 1)
239. British Cretaceous echinoids. Part 4. Stirodonta 3 (Phymosomatidae, Pseudodiadematidae) and Camarodonta
240. Cenomanian and Lower Turonian echinoderms from Wilmington, south-east Devon, England
241. Cenomanian echinoids, larger foraminifera and calcareous algae from the Natih Formation, central Oman Mountains
242. Ophiuroid phylogeny and higher taxonomy: Morphological, molecular and palaeontological perspectives
243. Fossil pericosmid echinoids
244. Radiation of Echinodermata
245. Revision of Echmatocrinus from the Middle Cambrian Burgess Shale of British Columbia
246. Origin of echinoderms in the Paleozoic evolutionary fauna: The role of substrates
247. Early radiation of echinoderms
248. "Golf-ball" paracrinoid
249. New echinoderms from the Early Ordovician of west Texas
250. Spiraclavus nacoensis, a new species of clavate agelacrinitid edrioasteroid from central Arizona
251. Thecal designs in isorophinid edrioasteroids
252. Late Paleozoic edrioasteroids (Echinodermata) from the North American midcontinent
253. The role of fossils in the phylogenetic reconstruction of Echinodermata
254. Giganticlavus, a new genus of Pennsylvanian edrioasteroid from North America
255. Could edrioasteroids move?
256. Plating and pectinirhombs of the Ordovician rhombiferan Plethoschisma
257. Phylogenetic analysis of living Echinodermata based on primitive fossil taxa
258. Early ontogeny of the glyptocystitid rhombiferan Lepadocystis moorei
259. Ponticulocarpus, a new cornute-grade stylophoran from the Middle Cambrian Spence shale of Utah
260. Systematics and paleoecology of Late Cambrian echinoderms from the western United States
261. Early Paleozoic echinoderms
262. Réflexions sur la nature et la fonction de l'appendice articulé des "carpoïdes" Stylophora (Echinodermata)
263. Deux Stylophora (Homalozoa, Echinodermata) nouveaux pour l'Ordovicien inférieur de la Montagne Noir (France Méridionale)
264. Échinodermes nouveaux du Cambrien Supérieur de la Montagne Noire (France Méridionale)
265. Échinodermes nouveaux (Stylophora, Eocrinoidea) de l'Ordovicien inférieur de la Montagne Noire (France)
266. Brachiopods, archaeocyathids, and Pelmatozoa from the Minaret Formation of the Ellsworth Mountains, West Antarctica: Introduction, stratigraphy, and Pelmatozoa
267. Permian echinoderms from Western Australia
268. Early Permian inadunate crinoids from Thailand
269. The evolution of cell lineage in echinoderms
270. Origin and diversification of echinoderm body architecture: Insights from the expression of body patterning genes
271. Molecular evidence for deep Pre-Cambrian divergences among metazoan phyla