I Recent Interactions and Their Preservation |
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Chapter 1 Biotic Interactions in Recent Marine Sedimentary Environments |
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3 | (7) |
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1.1 Common Units of Measure |
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5 | (1) |
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6 | (1) |
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1.3 Categories of Infauna |
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7 | (3) |
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10 | (9) |
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2.1 Competition in the Recent |
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10 | (5) |
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2.2 Competition in the Paleozoic |
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15 | (4) |
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19 | (8) |
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3.1 Types of Predators in the Recent |
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19 | (6) |
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3.2 Predation in the Paleozoic |
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25 | (2) |
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4 Pattern Differentiation: Competition or Predation? |
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27 | (3) |
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30 | (1) |
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31 | (8) |
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Chapter 2 Biological Determinants of Present and Past Sessile Animal Distributions |
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39 | (2) |
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2 Organisms and Their Environments |
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41 | (4) |
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3 Causes of Distributions |
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45 | (36) |
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47 | (1) |
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3.2 Larval Habitat Selection and Interactions with Previously Settled Organisms |
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48 | (8) |
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56 | (14) |
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70 | (6) |
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76 | (1) |
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77 | (4) |
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4 Fossil Evidence for Causes of Distributions |
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81 | (25) |
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4.1 Some Criteria for Recognition of Past Habitat Selection and Mortality Processes in Fossils |
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81 | (8) |
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4.2 Examples of Ancient Interactions |
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89 | (17) |
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106 | (1) |
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107 | (14) |
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Chapter 3 Seasonality: Effects in Marine Benthic Communities |
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121 | (6) |
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123 | (2) |
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125 | (2) |
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2 Seasonal Parameters with Primary Density-Independent Effects |
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127 | (8) |
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127 | (4) |
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2.2 Salinity and Other Physical Variables |
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131 | (1) |
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132 | (3) |
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3 Seasonal Parameters with Primarily Density-Dependent Effects |
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135 | (7) |
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135 | (1) |
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135 | (1) |
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136 | (5) |
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141 | (1) |
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4 Processes That Mediate Density-Dependent Effects |
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142 | (5) |
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142 | (2) |
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4.2 Reproduction and Development: Seasonal Strategies in z |
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144 | (1) |
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4.3 Niche Expansion: Seasonal Strategies in X |
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145 | (1) |
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146 | (1) |
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5 Consequences for Biotic Patterns |
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147 | (5) |
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147 | (1) |
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148 | (3) |
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151 | (1) |
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152 | (5) |
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Chapter 4 Soft-Bottom Succession and the Fossil Record |
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157 | (1) |
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158 | (2) |
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160 | (1) |
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4 Nearshore Benthic Succession |
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161 | (8) |
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161 | (2) |
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163 | (6) |
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5 Succession in Other Environments |
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169 | (2) |
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6 Preservation of Soft-Bottom Succession |
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171 | (12) |
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6.1 Taphonomic Losses and Mixing |
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171 | (4) |
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175 | (1) |
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6.3 Comparison Of Life and Death Assemblages |
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176 | (7) |
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7 Relation to Geologic Examples |
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183 | (4) |
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187 | (1) |
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188 | (7) |
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Chapter 5 Taphonomic Feedback: Ecological Consequences of Shell Accumulation |
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195 | (1) |
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2 Recent and Fossil Examples of Taphonomic Feedback |
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196 | (12) |
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2.1 Taphonomic Facilitation |
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197 | (9) |
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2.2 Taphonomic Inhibition |
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206 | (2) |
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3 Expected Patterns in the Stratigraphic Record |
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208 | (12) |
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212 | (1) |
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213 | (2) |
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215 | (2) |
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217 | (1) |
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218 | (2) |
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4 Case Study: Neogene Chesapeake Group, Atlantic Coastal Plain |
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220 | (13) |
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4.1 Evidence of Taphonomic Feedback |
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223 | (6) |
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229 | (4) |
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233 | (2) |
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235 | (16) |
II Interactions among Selected Taxa |
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Chapter 6 Biological Interactions and Precambrian Eukaryotes |
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251 | (2) |
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2 Hypotheses of Eukaryotic Origins |
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253 | (5) |
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3 A Scenario for Early Eukaryotic Evolution |
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258 | (6) |
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4 The Fossil Record of Early Eukaryotes |
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264 | (10) |
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265 | (3) |
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268 | (1) |
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4.3 Filamentous Microfossils |
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268 | (1) |
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4.4 Size Distribution Data |
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269 | (1) |
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270 | (3) |
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4.6 Vase-Shaped Microfossils |
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273 | (1) |
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4.7 Precambrian Macrofossils |
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273 | (1) |
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5 Ecological Consequences of Early Eukaryote Evolution |
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274 | (2) |
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276 | (1) |
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277 | (8) |
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Chapter 7 Biotic Interactions and Siliceous Marine Phytoplankton: An Ecological and Evolutionary Perspective |
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285 | (2) |
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2 Competition and Coexistence |
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287 | (10) |
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2.1 Nutrient Uptake Kinetics |
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287 | (4) |
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2.2 Coexistence of Competing Species |
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291 | (3) |
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2.3 The Paradox of Enrichment |
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294 | (2) |
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2.4 Nonequilibrium Theories of Competitive Coexistence |
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296 | (1) |
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3 PredatorPrey Interactions |
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297 | (7) |
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3.1 Predation as a Selective Force |
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297 | (5) |
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3.2 Predation and the Maintenance of Diversity |
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302 | (1) |
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3.3 Predation and the Sediment Record |
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303 | (1) |
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4 Life History Strategies |
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304 | (5) |
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5 Evolutionary Mode of Phytoplankton |
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309 | (3) |
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6 Paleontological Applications |
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312 | (8) |
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6.1 Competitive Displacement in Evolutionary Time |
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313 | (1) |
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6.2 Character Divergence and Convergence |
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313 | (1) |
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314 | (6) |
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320 | (11) |
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Chapter 8 Biotic Interactions in Benthic Foraminifera |
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331 | (1) |
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332 | (27) |
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332 | (2) |
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2.2 Trophic Mechanisms in Foraminifera |
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334 | (18) |
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2.3 Consumption of Foraminifera by Other Organisms |
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352 | (7) |
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359 | (4) |
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3.1 Foraminifera as Epibionts |
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359 | (4) |
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3.2 Foraminfera as Substrata |
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363 | (1) |
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363 | (1) |
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364 | (2) |
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6 Taphonomic Aspects of Foraminiferal Biotic Interactions |
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366 | (3) |
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369 | (1) |
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370 | (8) |
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Chapter 9 Biotic Interactions among Recent and among Fossil Crinoids |
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378 | (1) |
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378 | (7) |
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2.1 Sources of Predation on Living Crinoids |
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378 | (2) |
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2.2 Possible Antipredator Adaptations of Living Crinoids |
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380 | (1) |
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2.3 Predation on Ancient Crinoids |
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381 | (2) |
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2.4 Possible Antipredator Morphology in Ancient Crinoids |
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383 | (2) |
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2.5 Regeneration and Nonlethal Predation |
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385 | (1) |
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385 | (7) |
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3.1 Possible Mechanisms of Competition |
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387 | (1) |
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3.2 Niche Differentiation among Living and among Ancient Crinoids |
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388 | (4) |
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4 Associations of Living Crinoids with Other Organisms |
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392 | (6) |
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395 | (1) |
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396 | (1) |
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396 | (1) |
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397 | (1) |
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5 Associations of Ancient Crinoids with Other Organisms |
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398 | (16) |
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5.1 Nature of Associations |
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398 | (1) |
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399 | (7) |
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5.3 Stereomic Malformations |
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406 | (5) |
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411 | (1) |
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412 | (2) |
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414 | (1) |
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7 Habitat Modification by Crinoids |
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415 | (3) |
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7.1 Contribution to Sediment |
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415 | (1) |
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416 | (2) |
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7.3 Consequences for Community Succession |
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418 | (1) |
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8 Role of Biotic Interactions in Crinoid Evolution |
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418 | (2) |
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420 | (11) |
III Biotic Interactions through Time |
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Chapter 10 Algal Symbiosis and Its Recognition in the Fossil Record |
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431 | (1) |
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432 | (4) |
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433 | (2) |
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2.2 Phyletic Distribution of Hosts of Algal Symbionts |
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435 | (1) |
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2.3 Geographical and Ecological Distribution |
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435 | (1) |
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3 The Origin of Algal Symbiosis |
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436 | (3) |
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4 Characters Associated with Symbiosis |
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439 | (10) |
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4.1 Characters That Promote Symbiosis |
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440 | (6) |
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4.2 Characters That Result from Symbiosis |
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446 | (3) |
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5 Recognition of Algal Symbiosis in the Fossil Record |
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449 | (13) |
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449 | (4) |
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453 | (1) |
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454 | (2) |
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5.4 Fossil Cardiacean Bivalves |
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456 | (1) |
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456 | (4) |
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460 | (2) |
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5.7 Recalcitrant Groups: The Planktonic Syndrome |
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462 | (1) |
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6 Case Study of Symbiosis in Permian Brachiopods |
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462 | (12) |
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6.1 The Feeding Mechanism of the Richthofeniacea |
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463 | (2) |
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6.2 Symbiosis in the Richthofeniacea |
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465 | (6) |
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6.3 Symbiosis in the Teguliferinidae |
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471 | (1) |
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6.4 Symbiosis in the Lyttoniacea |
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472 | (1) |
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6.5 The Origins of Symbiosis in Brachiopods |
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473 | (1) |
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474 | (6) |
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Chapter 11 Sediment-Mediated Biological Disturbance and the Evolution of Marine Benthos |
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480 | (1) |
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2 Disturbance of Recent Sediments: Villains, Victims and Modi Operandi |
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481 | (26) |
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487 | (1) |
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2.2 Modes of Sediment-Mediated Interaction |
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487 | (3) |
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2.3 Ranking of Modes of Disturbance |
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490 | (10) |
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2.4 Effects of Bulldozing on IMOUS |
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500 | (1) |
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2.5 Determinants of Bioturbation Rates |
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501 | (4) |
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2.6 Significance of Trophic Group Amensalism |
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505 | (2) |
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3 Rise of the Bulldozers: Paleontological Perspective and Neontological Insight |
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507 | (13) |
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3.1 Diversification and Deductions from Recent Reworking |
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507 | (10) |
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3.2 Evidence from Morphology, Traces, and Behavior |
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517 | (3) |
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4 More Evidence from Trace Fossils: Tracking Villains through Geologic Time |
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520 | (2) |
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5 Physical Disturbance and Biotic Stabilization: How Shifting Were the Sands of Time? |
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522 | (2) |
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6 Phanerozoic Patterns: Restructuring the Benthos |
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524 | (20) |
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531 | (4) |
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535 | (1) |
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536 | (1) |
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6.4 Statistical Summary of Diversity Data |
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537 | (2) |
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539 | (1) |
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539 | (5) |
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544 | (1) |
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544 | (3) |
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8 Archaic IMOUS in Recent Refugia: Avoiding the Bulldozers |
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547 | (6) |
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547 | (1) |
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548 | (1) |
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549 | (3) |
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552 | (1) |
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552 | (1) |
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8.6 Corais: Refugia in Excelcis |
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553 | (1) |
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9 Geological and Paleontological Consequences |
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553 | (4) |
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9.1 Sedimentology and Stratigraphy |
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553 | (1) |
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554 | (1) |
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9.3 Preservation of Fossils |
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555 | (2) |
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10 Speculation on Causes and Consequences |
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557 | (5) |
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10.1 Land Plants and Their Ramifications |
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557 | (1) |
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558 | (1) |
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10.3 Infaunal vs. Epifaunal Suspension-Feeders |
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559 | (1) |
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560 | (1) |
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560 | (1) |
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10.6 Substrate Specificity |
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561 | (1) |
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561 | (1) |
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562 | (6) |
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562 | (1) |
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563 | (1) |
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11.3 Implications for Paleoecologic Methods: Generic Duration, Diversity, and Abundance |
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564 | (1) |
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565 | (1) |
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566 | (2) |
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568 | (27) |
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595 | (32) |
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Chapter 12 The Evolution of Infaunal Communities and Sedimentary Fabrics |
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627 | (1) |
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2 Infaunal Life and Sediment Reworking |
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628 | (1) |
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3 Comparison of Sedimentary Fabrics |
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629 | (13) |
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631 | (2) |
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3.2 Effect of Bioturbation |
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633 | (9) |
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642 | (4) |
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642 | (1) |
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4.2 Evolution of Infaunal Communities |
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642 | (4) |
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646 | (1) |
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646 | (3) |
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Chapter 13 Shell-Breaking Predation through Time |
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649 | (1) |
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2 Breakage as Agent of Mortality and Selection |
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650 | (2) |
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3 Adaptations against Breakage |
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652 | (3) |
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4 Gastropod Shell Form through Geological Time |
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655 | (5) |
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660 | (1) |
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6 The Geological Record of Shell-Breakers |
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661 | (2) |
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7 Alternative and Additional Interpretations |
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663 | (1) |
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664 | (9) |
IV Effects of Interactions on Community Evolution |
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Chapter 14 Diversification, Faunal Change, and Community Replacement during the Ordovician Radiations |
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673 | (1) |
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2 Patterns of Diversification and Faunal Change during the Ordovician |
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674 | (10) |
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2.1 Global Diversity and the Three "Great Evolutionary Faunas" |
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675 | (5) |
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2.2 Modeling Paleozoic Diversity Patterns |
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680 | (4) |
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3 Distributional Ecology of the Ordovician Radiations |
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684 | (13) |
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684 | (3) |
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687 | (2) |
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3.3 Cluster Analysis of Cambro-Ordovician Communities |
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689 | (6) |
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3.4 Factor Analysis of Cambro-Ordovician Communities |
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695 | (2) |
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697 | (8) |
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4.1 Generality of Results |
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699 | (2) |
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4.2 Mechanisms of OnshoreOffshore Change |
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701 | (4) |
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705 | (2) |
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707 | (3) |
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710 | (9) |
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Chapter 15 Ecospace Utilization and Guilds in Marine Communities through the Phanerozoic |
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719 | (3) |
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1.1 Diversity Change through the Phanerozoic |
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720 | (1) |
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1.2 The Question of an Ecologic Role in Controlling Diversity Patterns |
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721 | (1) |
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2 General Pattern of Ecospace Utilization |
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722 | (6) |
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2.1 Turnover of Class-Level Taxa through Time |
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722 | (3) |
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2.2 Change in General Ecospace Utilization |
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725 | (3) |
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3 The Guild Concept and Its Application to Paleocommunities |
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728 | (5) |
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3.1 Extension of the Guild Concept |
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728 | (2) |
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3.2 Defining Guilds in Paleocommunities |
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730 | (3) |
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4 Guilds in Paleocommunities |
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733 | (9) |
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733 | (1) |
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4.2 Differences in Guild Structures of Paleozoic and Neogene Communities |
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733 | (3) |
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4.3 Similarities in Species Distribution within Guilds |
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736 | (4) |
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740 | (2) |
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742 | (2) |
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744 | (3) |
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Chapter 16 Soft-Bottom Epifaunal Suspension-Feeding Assemblages in the Late Cretaceous: Implications for the Evolution of Benthic Paleocommunities |
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747 | (2) |
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2 Late Cretaceous Offshore Benthic Assemblages |
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749 | (22) |
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2.1 Gulf and Atlantic Coastal Plain |
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749 | (13) |
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762 | (9) |
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3 Late Cretaceous Nearshore Benthic Assemblages |
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771 | (5) |
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3.1 Gulf and Atlantic Coastal Plain |
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771 | (4) |
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3.2 Other Nearshore Faunas |
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775 | (1) |
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4 Structure of Late Cretaceous Assemblages |
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776 | (5) |
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776 | (2) |
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4.2 The Taphonomic Overprint |
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778 | (3) |
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5 Evolutionary History and Mechanisms |
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781 | (12) |
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781 | (6) |
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5.2 Evolutionary Mechanisms |
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787 | (6) |
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793 | (2) |
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795 | (2) |
Index |
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797 | |