The Mesozoic Marine Revolution is the rapid adaption to shell-crushing and boring predation in benthic organisms throughout the Mesozoic era. The term was first coined by Geerat J. Vermeij, who based his work on that of Steven M. Stanley. While initially restricted to the Late Cretaceous, more recent studies have suggested that the beginning of this ecological arms race extends back into the Norian It is the important transition between the Palaeozoicevolutionary fauna and the Cenozoic evolutionary fauna that occurred throughout the Mesozoic. The Mesozoic Marine Revolution was not the first bout of increased predation pressure; this also occurred around the end of the Ordovician. There appears to be some evidence of adaption to durophagy during the Palaeozoic, particularly in crinoids.
Causes
The Mesozoic Marine Revolution was driven by the evolution of shell-crushing behaviour among Mesozoic marine predators, the technique being perfected in the Late Cretaceous. This forced shelled marine invertebrates to develop defences against this mode of predation or be wiped out. The consequences of this can be seen in many invertebrates today. Such predators are thought to include: Triassic placodonts, Triassic ichthyosaurs, Triassic Omphalosaurus, Triassic plesiosaurs, Jurassic pliosaurs, Late Cretaceous mosasaurs and Cretaceous ptychodontoid sharks. It is also thought that the break-up of Pangaea throughout the Mesozoic brought together previously isolated communities, forcing them to adapt. The increased shelf space caused by sea-level rise and a hyper-greenhouse climate provided more iterations and chances to evolve, resulting in increasing diversity. Another proposal is the evolution of hermit crabs. These exploit the shells of dead gastropods, effectively doubling the life-span of the shell. This allows durophagous predators nearly twice the prey, making it a viable niche to exploit.
Effects
The net result of the Mesozoic Marine Revolution was a change from the sedentaryepifaunal mode of life of the Palaeozoic Evolutionary Fauna to the infaunal/planktonic mode of life of the Modern Evolutionary Fauna. Non-mobile types that failed to re-attach to their substrate when removed were picked off as easy prey, whereas those that could hide from predation or be mobile enough to escape had an evolutionary advantage. Three major trends can be associated with this: 1) Reduction in suspension feedingepifauna 2) Increasing abundance of infauna 3) An intermediate stage of mobile epifauna. Major casualties of the Mesozoic Marine Revolution include: sessile crinoids, gastropods, brachiopods and epifaunal bivalves.
Affected Taxa
Gastropods
Benthic gastropods were heavily preyed upon throughout the MMR, the weaker shelled types being pushed out of the benthic zone into more isolated habitats. The Palaeozoic archaeogastropods were subsequently replaced by neritaceans, mesogastropods and neogastropods. The former typically have symmetrical, umbilicate shells that are mechanically weaker than the latter. These lack an umbilicus and also developed the ability to modify the interior of their shells, allowing them to develop sculptures on their exterior to act as defence against predators. Another development among Muricidae was the ability to bore through shells and consume prey. These marks generally occur on sessile invertebrates, implying that they put pressure on Palaeozoic-type faunas during the MMR
Crinoids
The MMR heavily affected the crinoids, making the majority of forms extinct. Their sessile nature made them easy prey for durophagous predators since the Triassic. Survivors could swim or crawl, behaved nocturnally or had autotomy. The shift in the range of sessile stalked crinoids during the late Mesozoic from the shallow shelf to habitats further offshore suggests that they were forced by increased predation pressure in shallow water to migrate to a deep water refuge environment where predation pressure is lower and their mode of life more viable.
Brachiopods
Brachiopods, the dominant benthic organism of the Palaeozoic, suffered badly during the MMR. Their sessile foot-attached nature made them easy prey to durophagous predators. The fact that they could not re-attach to a substrate if an attack failed meant their chances of survival were slim. Unlike bivalves, brachiopods never adapted to an infaunal habit and so remained vulnerable throughout the MMR.
Bivalves
Bivalves adapted more readily than the Brachiopods to this transition. The majority of bivalves adopted an infaunal habit, using their siphons to gather nutrients from the sediment-water interface while remaining safe. Others like Pecten developed the ability to jump a short distance away from predators by contracting their valves. Like brachiopods, epifaunal varieties of bivalves were preyed upon heavily. Among epifaunal types, the ability to fuse to the substrate made them more difficult to consume for smaller predators. Epifaunal bivalves were preyed on heavily pre-Norian but extinction rates diminish after this.
Echinoids
do not suffer major predation during the MMR but it is clear from bromalites that cidaroids were consumed by predators. Echinoids radiate into predatory niches and are thought to have perfected coral grazing in the Late Cretaceous. Cidaroids also are thought to have contributed to the downfall of the crinoids.
