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      Trends in shell fragmentation as evidence of mid-Paleozoic changes in marine predation

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          Abstract

          Recent observations indicate that shell fragmentation can be a useful tool in assessing crushing predation in marine communities. However, criteria for recognizing shell breakage caused by durophagous predators versus physical factors are still not well established. Here, we provide data from tumbling and aquarium experiments to argue that physical and biotic processes lead to different patterns of shell damage, specifically that angular shell fragments are good indicators of durophagous predation. Using such angular shell fragments as a predation proxy, we analyze data from 57 European Paleozoic localities spanning the Ordovician through the Mississippian. Our results reveal a significant increase in angular shell fragments (either occurring as isolated valves or present in regurgitalites) in the Mississippian. The timing of this increase is coincident with the increased diversity of crushing predators as well as marked anti-predatory changes in the architecture and mode of life of invertebrate prey observed after the end-Devonian Hangenberg extinction (359 Ma). More specifically, the observed trend in shell fragmentation constitutes strong and independent confirmation of a recently suggested end-Devonian changeover in the primary method of fish predation from shearing to crushing. These results also highlight the important effect of extinction events, not only on taxonomic diversity, but also on the nature of predator-prey interactions.

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          Most cited references26

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          The Mesozoic marine revolution: evidence from snails, predators and grazers

          Tertiary and Recent marine gastropods include in their ranks a complement of mechanically sturdy forms unknown in earlier epochs. Open coiling, planispiral coiling, and umbilici detract from shell sturdiness, and were commoner among Paleozoic and Early Mesozoic gastropods than among younger forms. Strong external sculpture, narrow elongate apertures, and apertural dentition promote resistance to crushing predation and are primarily associated with post-Jurassic mesogastropods, neogastropods, and neritaceans. The ability to remodel the interior of the shell, developed primarily in gastropods with a non-nacreous shell structure, has contributed greatly to the acquisition of these antipredatory features.
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            The mid-Paleozoic precursor to the Mesozoic marine revolution

            The mid-Paleozoic was punctuated by a rapid radiation of durophagous (shell-crushing) predators. These new predators were primarily placoderm and chondrichthyan fishes but probably also included phyllocarid and eumalacostracan arthropods. Coincident with the radiation of these durophages, beginning in the mid-Devonian, there was an increase in the frequency of predation-resistant morphologies in a variety of marine invertebrate taxa. Among bellerophontid molluscs, disjunct coiling disappeared and umbilici became less common while the frequency of genera with sculpture increased. The abundance of brachiopod genera with spines on one or both valves increased dramatically. Sculpture became more pronounced and common among genera of coiled nautiloids. Inadunate and camerate crinoids showed a marked increase in spinosity, and all three crinoid subclasses tended to develop thicker thecal plates.
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              Seafood through time: changes in biomass, energetics, and productivity in the marine ecosystem

              The biomass of marine consumers increased during the Phanerozoic. This is indicated by the increase in both fleshiness and average size of individuals of dominant organisms, coupled with the conservative estimate that dominant organisms in the Cenozoic are at least as abundant as those in the Paleozoic. As faunal dominants replaced one another during the Phanerozoic the general level of metabolic activity increased due to both increase in basal metabolism and increase in more energetic modes of life. This demonstrates that the expenditure of energy by marine consumers has increased with time as well. There is a time lag in the expansion of more energetic life habits from environmental settings known to have high food supply into regions expected to have lower rates of food supply (e.g., bivalves into offshore carbonate environments or deep burrowing deposit feeders into the full range of shelf environments), and a time lag in diversification of energetic modes of life (e.g., predation or deep burrowing deposit feeding) for long intervals after they first appeared. This suggests that the supply of food increased across the whole spectrum of marine habitats during the Phanerozoic. The great diversification of specialized predators especially suggests that biomass increase took place all the way down the food chain to the level of primary production. The development of plant life on land and the impact of land vegetation on stimulating productivity in coastal marine settings, coupled with the transfer of organic material and nutrients from coastal regions to the open ocean, and the increase through time in diversity and abundance of oceanic phytoplankton all point to increased productivity in the oceans through the Phanerozoic.
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                Author and article information

                Journal
                Paleobiology
                Paleobiology
                Paleontological Society
                0094-8373
                1938-5331
                2014
                April 08 2016
                2014
                : 40
                : 1
                : 14-23
                Article
                10.1666/13018
                2ed6f2b1-f32d-41f4-8231-a5fdb99ee931
                © 2014

                https://www.cambridge.org/core/terms

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