273 D17. Paleontology, Paleoecology B
Wednesday, 7 November 2018
1:30 PM - 5:30 PM
Room 142
A REASSESSMENT OF DUROPHAGOUS PREDATION ON BRACHIOPODS THROUGH THE PALEOZOIC
Paper number: 273-2
Program: Technical Sessions
Time: 1:45 PM – 2:00 PM
Authors
-
Steven E. MendoncaUniversity of Alberta, Edmonton, AB
-
Matthew J. PrudenUniversity of Alberta, Edmonton, AB
-
Rylan V. DievertUniversity of Alberta, Edmonton, AB
Abstract
The percent of scarred individuals, and the per capita scar frequency, follow similar U-shaped trends: high values (usually > 40%) before the Devonian, low values (usually < 35%) during the Devonian, and a return to higher values post-Devonian. As repairs indicate failed attacks, changes in repairs through time can be either due to predator success (with evolutionary implications) or to attack rate (can be ecological without invoking evolution). Based on changes in the size of the prey at the time of attack (not to be confused with the size at death, which might have happened much later, subsequent to additional growth), we interpret the decline in repairs during the Devonian to be related to the Paleozoic Revolution, when new and stronger durophages, including vertebrates, diversified. As durophages grew stronger, they were able to take larger prey, success increased, and thus repair frequency declined. The largely post-Devonian adaptive radiation of the order Productida, strophomenates with spines, and the Orthotetidina, cementing strophomenates, may have been evolutionary responses to the rise of stronger durophages. Spines and cementation have been demonstrated to inhibit predation, and may have forced predators to take smaller prey. Overall success may have declined, resulting in greater repair frequencies. The temporal pattern of Paleozoic repairs is consistent with hypothesized evolutionary trends.
Geological Society of America Abstracts with Programs. Vol. 50, No. 6
doi: 10.1130/abs/2018AM-325042
© Copyright 2018 The Geological Society of America (GSA), all rights reserved. Permission is hereby granted to the author(s) of this abstract to reproduce and distribute it freely, for noncommercial purposes. Permission is hereby granted to any individual scientist to download a single copy of this electronic file and reproduce up to 20 paper copies for noncommercial purposes advancing science and education, including classroom use, providing all reproductions include the complete content shown here, including the author information. All other forms of reproduction and/or transmittal are prohibited without written permission from GSA Copyright Permissions.