Dense bones in benthic dive foraging archaic (but not recent pelagic odontocetes &) mysticetes:
The Aquatic Amniote: Injured fossil mysticete and an investigation of osteosclerosis (and benthic feeding?) in fossil mysticetes
[Possible stone swallowing for ballast as well, as in crocs, penguins and seals?]
Decompression sickness signs and deep diving evolution in whales
http://www.ncbi.nlm.nih.gov/pubmed/18446257
http://www.ncbi.nlm.nih.gov/pubmed/19427415?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_SingleItemSupl.Pubmed_Discovery_RA&linkpos=1&log$=relatedarticles&logdbfrom=pubmed
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The problem in identifying dental microwear characteristics in aquatic herbivory: differentiating signs, similar patterns, different quantities of phytoliths, broad spectrum herbivory/omnivory vs single species diet.
http://aquaticamniotes.blogspot.com/2009/10/problem-with-microwear-1-of-many-to.html
[Congo gorillas consume much aquatic floating herb hydrocharis with some sedges, modern humans consume much wetland rice and variably water lily (pond lily) and sedge (chufa) benthic rhyzomes, whilst archaic hominoids probably consumed all of these in addition to invertebrates and waterside tree fruits.]
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"Instead of studies of nociception, thermoreception, muscle spindles, or even general spinal nerve mechanoreceptors, Denhardt & Mauck’s (chapter 17) introduction to the physics and physiology of mechanoreception, as well as their following chapter (18) on mechanoreception in secondarily aquatic vertebrates, focus almost entirely on the trigeminal system of mechanoreception that innervates facial areas. The reason for this becomes clear, as this is where most aquatic specializations exist for actively seeking prey items. [Note: not same as chasing mobile prey.] The attention to the work of Daphne Soares and the folks at the University of Maryland on dome pressure receptors in Alligator is particularly striking, as is Denhardt’s own work on pinniped vibrissae."
http://aquaticamniotes.blogspot.com/2009/07/review-of-sensory-evolution-on.html
The Aquatic Amniote: Injured fossil mysticete and an investigation of osteosclerosis (and benthic feeding?) in fossil mysticetes
[Possible stone swallowing for ballast as well, as in crocs, penguins and seals?]
Decompression sickness signs and deep diving evolution in whales
http://www.ncbi.nlm.nih.gov/pubmed/18446257
http://www.ncbi.nlm.nih.gov/pubmed/19427415?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_SingleItemSupl.Pubmed_Discovery_RA&linkpos=1&log$=relatedarticles&logdbfrom=pubmed
-
The problem in identifying dental microwear characteristics in aquatic herbivory: differentiating signs, similar patterns, different quantities of phytoliths, broad spectrum herbivory/omnivory vs single species diet.
http://aquaticamniotes.blogspot.com/2009/10/problem-with-microwear-1-of-many-to.html
[Congo gorillas consume much aquatic floating herb hydrocharis with some sedges, modern humans consume much wetland rice and variably water lily (pond lily) and sedge (chufa) benthic rhyzomes, whilst archaic hominoids probably consumed all of these in addition to invertebrates and waterside tree fruits.]
-
"Instead of studies of nociception, thermoreception, muscle spindles, or even general spinal nerve mechanoreceptors, Denhardt & Mauck’s (chapter 17) introduction to the physics and physiology of mechanoreception, as well as their following chapter (18) on mechanoreception in secondarily aquatic vertebrates, focus almost entirely on the trigeminal system of mechanoreception that innervates facial areas. The reason for this becomes clear, as this is where most aquatic specializations exist for actively seeking prey items. [Note: not same as chasing mobile prey.] The attention to the work of Daphne Soares and the folks at the University of Maryland on dome pressure receptors in Alligator is particularly striking, as is Denhardt’s own work on pinniped vibrissae."
http://aquaticamniotes.blogspot.com/2009/07/review-of-sensory-evolution-on.html
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