Showing posts with label Chelonia. Show all posts
Showing posts with label Chelonia. Show all posts

Thursday, November 4, 2010

Emerging New Research 1 – Recent Aquatic Amniote Literature Reviewed

Now that I have gotten the news of the recent symposium out of the way, I’d like to present a new type of post for me – an annotated review of recent literature on aquatic amniotes and matters relevant to the study of their paleobiology. My intention with this is to highlight the primary utility I see in recently published work, including some curious details that seem often get ignored, and occasionally review an “oldie but goodie” from among the pieces of less-cited literature that I worry hasn’t gotten the recognition it deserves. I will do my best to be open and honest, but don’t want this to be a way of building a long list of enemies either, so if I do not nitpick every paper’s problems and instead focus on what strengths it has, I hope you’ll forgive me. If you are the author of one of these papers and feel I haven’t gotten the point of it, or misrepresented it in some way, I would really appreciate your comments on the blog, or a direct message to me. This is not meant as a critique of research, only a way of pointing out some recent work that might have been missed by the greater aquatic amniote paleontological community. The literature is vast and growing everyday, and I’d like to consider this an aspect of service to our community of scientists – I’m going to read these anyway, so I may as well save you all the trouble of finding these papers and get the news out.

Each of these will have a link to a journal site (or preferably a site at which the paper is available open access), so I hope that this will serve as an aid for all of you that haven’t the time to review all the literature. Though many of these papers I get directly from authors or through journal subscriptions, many of the papers I review I received thanks to the gracious efforts of David Janiger (LACM). David lists recent papers and offers pdfs to people on the MARMAM listserv (by the way, Academia.edu has a Marmam listserv section). If you already get papers thanks to his help, or are reading this blog, thank him already! He has been doing this for a while, and it is incredibly valuable.

Fourteen nuclear genes provide phylogenetic resolution for difficult nodes in the turtle tree of life.
Anthony J. Barley, Phillip Q. Spinks, Robert C. Thomson, H. Bradley Shaffer
Molecular Phylogenetics and Evolution 55:1189-1194

Bradley Shaffer Lab page
author's page for pdf

This short and sweet paper about a nuclear gene-based phylogeny of modern turtles nicely resolves some of the persistent problems of the relationships among turtle families, particularly due to the taxon Platysternon (big-headed turtle). The taxon sampling here isn’t extremely extensive (19), but it gets at least two taxa from each family of interest, particularly with respect to the Kinosternidae, Chelydridae, Emydidae, and Chelonioidea. As a start at getting a molecular phylogeny that can resolve these contentious relationships, this study does well. I found it particularly satisfying that kinosternids and chelydrids are sister taxa here, together as sister taxa to the Chelonioidea. Parham et al (2006) found similar, but not the same results, having these three clades not as a monophyletic group, but paraphyletic nested sister taxa to the Emydidae, Platysternon, Geomydidae, and Testudinidae (for more papers by Jim Parham related to this, visit his site). The taxon sampling of the present study is not extensive, so ultimately after many more taxa are sampled for these same genes and other molecular and morphological data, we may find this remains stable, or not. Either way, this has some interesting relevance to the origins of sea turtles, and the relative age of these clades.

Understanding the diet composition of marine mammals: grey seals (Halichoerus grypus) in the Baltic Sea).
Karl Lundström, Olle Hjerne, Sven-Gunnar Lunneryd, Olle Karlsson
ICES Journal of Marine Science 67:1230-1239

Author's Academia.edu page

The literature on the diets of marine mammals is huge, even though a concrete idea of exactly what animals eat (taxonomic diversity, abundance) and how this diet varies with age and distribution is a difficult matter to resolve. The best global look at this I know of is a paper more than 10 years old (Pauly et al 1998), even though copious reports on stomach contents exist. Large-scale studies are difficult to coordinate in this way because so much of the existing literature on diet is uneven in its quality and coverage, often sampling only strandings or not accounting for abundance or taxonomic diversity. Here, this group has done so for the grey seal, Halichoerus grypus, in the Baltic Sea. The divided their sample of hunted seal specimens (which they got in cooperation with hunters and fisheries sources) by regions of the Baltic and age categories. What I really love is their care for the data on abundance AND diversity of stomach AND intestinal contents, and that they report all their data, and even correct it for Erosion-class-specific size and numerical correction factors. As one might predict from the nature of biology, when they looked closely at these details, they found differences in the diets of young and old, and between regions. These differences seem largely to be concerned with commercially caught fishes, which is of practical importance, but one could easily envision using this same data to compare paleodietary measures of the same specimens (isotopes, dental microwear, etc.). Gosh, I need to contact some people in Sweden!

Mid-Cenomanian vertebrate faunas of the Western Interior Seaway of North America and their evolutionary, paleobiogeographical, and paleoecological implications
Stephen L. Cumbaa, Kenshu Shimada, Todd D. Cook
Palaeogeography, Palaeoclimatology, Palaeoecology 295:199-214

Stephen Cumbaa's page
Kenshu Shimada's page
Todd Cook's page

This is a much-needed review of the copious marine vertebrate fauna of the Western Interior Seaway by some of the best people on this topic I know. Though this is obviously of interest here because of the numbers of marine reptiles many of us think of living in the Western Interior Seaway, this sea was obviously more densely populated with bony and cartilaginous fishes. These authors know these fishes well, and being a little familiar with these collections and taxa, I can see that this was a terribly massive amount of work to compile all of these faunal distributions, primarily because of the care it would take to go through all the hundreds and thousands of tiny fish teeth from these sites. Even though they only report on diversity of each site, not abundance, it is because of the clear limitation that these sites are biased by some degree of time-averaging. Without knowing how long each deposit/accumulation took to get there, abundance is a difficult thing to assess. In the end, this thorough study of the faunas of the WIS is incredibly useful and should play a part in estimates of biodiversity of marine reptiles as well, which presumably preyed on these taxa.

Single source sound production and dynamic beam formation in echolocating harbour porpoises (Phocoena phocoena)
P. T. Madsen, D. Wisniewska, K. Beedholm
The Journal of Experimental Biology 213:3105-3110

Author's page with pdf

I believe that this might be one of the less-conspicuous papers to those that study fossil cetaceans, as it could easily be misconstrued as simply another paper studying the acoustics of echolocation. But these researchers did something very clever – they attached suction-cupped microphones to both pairs of phonic lips of a porpoise to basically see whether both pairs were functioning to produce whistles. They weren’t, as one could glean from the title, and this has major implications for the functional role of the second pair of phonic lips, as well as questions about the evolutionary loss of them in sperm whales. Sperm whales usually fall out as primitive whales in most phylogenetic studies, and because of that one might consider it because they lack the second phonic lips that this is a primitive trait. But some (Cranford et al, 1996) have suggested it was secondarily lost, and this may be the case. If you are working on fossil cetaceans, this study itself may not be directly useful to your work with fossils, but it is important to your understanding of the adaptive and non-adaptive roles of anatomical structures, and how that might influence your perception of how structures associated with echolocation may be retained. I hope those looking into the evolution of echolocation will seriously consider this work.

Hydrodynamics of a ship/whale collision
Gregory K. Silber, Jonathan Slutsky, Shannon Bettridge
Journal of Experimental Marine Biology and Ecology 391:10-19

Author's page with pdf

This study utilized models in a flow tank to simulate the effects of the bow wave of a vessel and how that might interact with a whale. The model of the whale was outfitted with an accelerometer, and though not dynamic itself (no autonomous movement, and obviously no behavior), the accelerometer helped convey the data about how the whale model responded to wave propagation around the vessel as it passed. I’m personally more keen on seeing further data on whale strikes in real situations, but this study goes as far as one could without using living animals to get at some fundamental questions about flow around boats and whether whales are in any special danger of impact due to hydrodynamics. Though the authors stress how this might affect policies about vessel speed in whale-inhabited waterways (which is important), I would argue that one also must use this to consider how to modify vessel design to minimize the hydrodynamics that enhance the danger of collisions with whales. The former is obviously cheaper and easier to implement, but the latter is certainly worth considering.

Change in the foraging strategy of female South American sea lions (Carnivora: Pinnipedia) after partutition
Massimilliano Drago, Luis Cardona, Enrique A. Crespo, Nestor Garcia, Santiago Ameghino, Alex Aguilar
Scientia Marina 74(3):589-598
(free pdf at journal site)

The study of stable isotopes as a proxy for diet is widely recognized as a good technique for sorting out not only the diets of modern marine mammals, but those of fossil taxa as well. Curiously enough, much of the data on the isotopic composition of primary producers and potential prey species that are the sources of these isotopes in marine mammals is lacking for many environments, as is data on how the diets of these animals can change in small ways for short periods of time that may or may not be reflected in tooth enamel. If the changes are temporary, serial sampling may pickup some oddity, but without the sort of data that would answer the question. Plus, tooth enamel records only the isotopic record of the individual while the tooth is being formed, and the data presented here about the isotopic signature of coastal-benthic predation by post-partum female Otaria is likely never to be recorded in their teeth because their teeth have already developed. If one were to study the dental microwear of these same individuals and compare it with the data from their tooth-enamel based isotopes, one would find conflicting signals. It isn’t that either method is wrong, but that they sample the diet of the animal in different temporal and life history scales, which should be seen as an opportunity, not a limitation. In this case, these authors focus their work on the immediately relevant results of how these sea lions’ diets change after giving birth, but I would argue that for the paleobiologist, this is a clear reminder of the need for consideration of the minor changes in behavior that come with life history events that can have a big impact on the dental microwear or isotope record of individual specimens being studied. Hence, the most obvious solution to that is to consider these limitations when dealing with small samples (which some fossil taxa force us to work with), and when possible, use large samples.

Age and growth of franciscana dolphins, Pontoporia blainvillei (Cetacea: Pontoporiidae) incidentally caught off southern Brazile and northern Argentina
Silvina Botta, Eduardo R. Secchi, Monica M. C. Muelbert, Daniel Danilewicz, Maria Fernanda Negri, Humberto Luis Cappozzo, Aleta A. Hohn
Journal of the Marine Biological Association of the United Kingdom

With a large sample size (N=291) incidentally caught in fishing nets over an 11 year period, the authors were able to report the rate of growth for this species in a detailed fashion, with care taken for how gender may have a role. Though they found no significant differences between genders, their data seem to show that females start out consistently a little larger than males, even though their rates of growth do not seem to differ, except perhaps in the first two years of life (after which female growth rates are slightly greater than males). Although this is of minimal interest to a paleobiologist, it is important data to keep straight when further discussions about sexual dimorphism are brought up for fossil cetaceans.

Does dispersal across an aquatic geographic barrier obscure phylogeographic structure in the diamond-backed watersnake (Nerodia rhombifer)?
Matthew C. Brandley, Tim J. Guiher, R. Alexander Pyron, Christopher T. Winne, Frank T. Burbrink
Molecular Phylogenetics and Evolution 57(552-560)

Frank Burbrink's page

Ok, this may be mistaken for something marginally related to aquatic amniotes, but this is getting at something worth understanding with regard to the origins of aquatic amniotes – how can freshwater systems be a barrier or a habitat, and when does it matter? Joshua Samuels (John Day) and I have been talking about this together for years, and hopefully we’ll come to writing something about it someday, but in the meantime, let’s focus on the paper. The authors here simply compared the relatedness of populations of watersnakes around the Mississippi River, finding that the best explanation for the divide in the genotypes of populations was the Mississippi River as a barrier. Not only that, but that the divergence date of this barrier is likely to have been during the Pleistocene, during an interglacial when the river may have been much wider. This is particularly compelling, considering that this is a watersnake, not a dry-desert-loving rattlesnake. This taxon can cross the Mississippi River, yet reproduction must be a behaviorally complex enough event that the river has succeeded in being a barrier to these populations sharing with each other reproductively. What does this mean to the paleobiologist? Perhaps the notion of a river as a barrier, at least in some fashion (perhaps not distribution, but widespread dispersal) is possible not only for fully terrestrial taxa, but semiaquatic ones as well.


There are plenty more reviews coming, and I hope to have some new material on Eocene Sirenia and trichechid tooth development to share soon as well.
Cheers!

Brian

Wednesday, October 27, 2010

Recent Events: Physical Drivers and Marine Tetrapod Evolution – Symposium at the Society of Vertebrate Paleontology

It has been WAY too long since my last post, my sincerest apologies. I was consumed with a handful of projects, some of which are submitted, and some of which I presented at the Society of Vertebrate Paleontology meeting in Pittsbugh, PA this past October 10-13.

I fully intend to blog on some of this new material soon, but want to start with a couple of things. 1) A report on a symposium held at the recent Society of Vertebrate Paleontology meeting, and 2) a new series of blog posts reviewing recent literature and its relevance to the study of aquatic amniote evolution studies. I’ll get to the latter in my next post, but let me get started with this report on the recent (October 11, 2010) SVP Symposium titled, “Physical Drivers in Marine Tetrapod Evolution”. I’m keeping this brief, not only to save you from my usual boring wordiness, but also to protect the rights of authors of these presentations from having their unpublished material shared without their permission.

The symposium was organized by Neil Kelley (UC Davis) and R. Ewan Fordyce (University of Otago). Neil is a promising graduate student studying Triassic marine reptiles, and Ewan is one of the world’s leading experts on fossil cetaceans, and together it was a good match that brought lots of good minds together.


Neil Kelley and R. Ewan Fordyce, the organizers of the symposium, "Physical Drivers and Marine Tetrapod Evolution"


Among the minds brought together were (presented listed here only, though obviously many had co-authors that significantly contributed):

Neil Kelley (UC Davis, USA)

R. Ewan Fordyce (University of Otago, New Zealand)

Olivier Rieppel (Field Museum, USA)

Valentin Fischer (Royal Belgian Institute for Natural Science, Belgium)

Michael Polcyn (Southern Methodist University, USA)

Louis Jacobs (Southern Methodist University, USA)

James Parham (Alabama Museum of Natural History, USA)

Sanja Hinic-Frlog (Carleton University, Canada)

Tatsuro Ando (Ashoro Museum, Japan)

Brian Beatty (New York College of Osteopathic Medicine, USA)

Naoki Kohno (National Museum of Nature and Science, Japan)

Edward Davis (University of Oregon, USA)

Carolina Gutstein (Universidad de Chile, Chile)

Erich Fitzgerald (Museum Victoria, Australia)

Felix Marx (University of Otago, New Zealand)

Nicholas Pyenson (Smithsonian Institution, USA)


Topics covered included a variety of methods, details, and scales, though some common themes were:

  • How aquatic tetrapod groups have and have not been affected by the changing coastlines, chemistry, and productivity of the world’s oceans. I found it dumbfounding that so many variables affect diversity and distributions of these groups, and controlling for them is the challenge we all faced. Some did so by looking at distribution correlations, others by ecological variables such as isotope geochemistry or dental microwear. Methods here included:
    • Morphometrics of locomotor adaptations
    • Dental microwear
    • Stable isotope geochemistry
    • Distribution patterns
    • Bottom-up or top-down ecosystem design
    • Sea level changes and its effect on available habitat, and the use of freshwater by some usually marine groups.
    • Associations of taxa as implications of their ecology
    • Spatial and temporal changes in diversity correlating with global climate events

  • Some authors reviewed some unrecognized diversity, not only taxonomically but also in terms of ecological roles, that revise our understanding of how earth history may or may not have affected these groups. One compelling message of this was a clear reminder that we all need to come back to finding more fossils and describing them before jumping into complex analyses of existing records from databases alone.

  • In a surprising, but great twist, some made a point of looking at the way that some of the diversity and distribution of groups were or weren’t affected by how the animals themselves dealt with the physical environment in terms of sensory perceptions. Thus, not only did we see distribution and ecological variables discussed, but aspects of sensory modalities in some groups and how that could tell us more about where and how they lived and dealt with the changing environment.
Me (Beatty) finishing my talk on dental microwear in the Sirenia (photo by Michael Ayoub)

In the end, the topics covered all had one common theme – that the evolution of aquatic amniotes is very closely linked with the evolution of the Earth. Despite what one might see as an interesting lesson in history, I think that many of these talks demonstrated that for many of the taxa still living today, we can only hope that these lessons learned will help us avoid reliving history, especially those parts that ended in extinction. These are the sorts of studies that make paleontology relevant to modern ecologists and conservationists in the face of global warming.

I think that the symposium was a massive success, particularly because it seems to have encompassed a huge diversity of methods, taxa, and times, and brought people together to share ideas and potentially collaborate. I know I’m already going down the road of starting some new projects with people I spoke with just after the symposium. That is, after all, the more proximate goal of these symposia, and I am glad to have been part of it. I would like to thank Neil and Ewan for inviting me, and thank you for sharing my interest in keeping current with what is going on among aquatic amniotes.

Until next time... which will be soon!

Wednesday, July 1, 2009

Review of "Sensory Evolution on the Threshold"

Last year Hans Thewissen and Sirpa Nummela published an edited volume with Springer Verlag entitled, "Sensory Evolution on the Theshold". The text covers how sensory biology in aquatic amniotes (and other secondarily aquatic tetrapods) copes with perceiving the world around them.
It is an excellent, uncommon resource, and I highly recommend it. In fact, I reviewed it for the Journal of Mammalian Evolution, and it was published online in October 2008. But, as we all know, printed journals are limited to page charges. Being the wordy sort I am, my initial draft was MUCH longer. Although not as cleanly written, I strove in that version to go through the text in detail and do what I wish more book reviews did - fill in the gaps. That is not to say that this book has many gaps at all, it is really an impressive collection full of details. But being a human endeavor, error is inevitable, and though I doubt I could do as good a job of the book myself, I'm afforded the luxury of simply reading it and noticing some references that are missing. So, herewith I present the full version of the review as a wrote it initially. Though the starting phrases are similar, the content is vastly different in its scope, mainly because large parts had to be edited out to fit within the limitations of a printed journal. This is NOT the same text as the printed review, but I hope it might be useful, mainly for the additional references, so that students of these subjects might have less searching to do.

(NOTE: I would strongly suggest that if this interests you, that you consider joining the Society for the Study of Mammalian Evolution - the membership is only $35, you get the journal and would be in some rare company because the membership of the group is unusually small, considering how many folks study mammal evolution. So join the group!)

So, here is the unabridged version of the review:

Adaptive Convergences in Perception Recognized

Sensory Evolution on the Threshold – Adaptations in Secondarily Aquatic Vertebrates. Edited by J. G. M. Thewissen and Sirpa Nummela. Berkeley: University of California Press. 2008. 351 pp., $75 (cloth). ISBN 978-0-520-252783.

by Brian Lee Beatty

Functional morphology has its limitations, partly because of the inability to divorce the influences of ancestry from function in understanding the form of a given structure. For instance, hypsodonty in a horses, camels, and oreodonts are commonly given examples of adaptation to grazing, yet once evolved, hypsodonty may have simply added to niche breadth and not restricted an animal’s diet to grass exclusively (Feranec, 2003; Mihlbachler and Solounias, 2006). Though the source of morphology can never reasonably be categorized as “inherited” versus “functional”, as these two are not likely to exist without each other, the study of how distinct clades converge on similar forms and specializations is perhaps the best way in which to understand how organisms adapt to different foods, environments, and lifestyles. Once one gets past their charismatic megafauna role in popular culture, marine mammals can be seen as ideal study animals for looking at such convergences because of the numerous times they have returned to an aquatic lifestyle. The physical and chemical environments of air versus water are very, very different (Denny, 1993), and the body forms of marine mammals have proven to be exemplars of convergence in form for functional reasons (Fish, 2000; Pabst et al., 1999). Though marine mammals are similar in physiology and anatomy to the best known vertebrates, mice and men, they are not a natural group and focusing only on them leaves out the majority of vertebrates and far more than half of the clades that have returned to an aquatic lifestyle. The editors of Sensory Evolution on the Threshold, J. G. M. Thewissen and Sirpa Nummela, are known for their work on marine mammals (Nummela et al., 2004), but it is clear from this book that they recognize the importance of having a broader view of secondarily aquatic vertebrates and how many have converged on similar forms despite very disparate ancestries.

In Sensory Evolution on the Threshold, we get the most complete review I have seen of sensory biology and physics in secondarily aquatic vertebrates, from lissamphibia to squamates, birds, and mammals with no particular bias toward one group. The book starts with a concise, but detailed account of the diversity of secondarily aquatic vertebrates, with sections for each major group of vertebrates written by separate authors, some of which are authors of separate chapters in the book. These short sections detailing groups such as lissamphibia, birds, and mammals are nice brief summaries and do the most comprehensive job of reviewing the diversity of secondarily aquatic vertebrates that I have ever seen. I could envision myself citing them frequently, if it weren’t for the complicated act of citing a section within a chapter within an edited volume, each with separate authors/editors. Though they may be complicated to cite, each of these sections is worth it as a starting point for anyone starting work on these groups.


After this brief introductory chapter, the text is broken down into six sections, one for each sense: chemical senses, vision, hearing, balance, mechanoreception, as well as magnetoreception and electroreception. Each of these sections begins with a chapter on the physics and biology of that sensory modality in water. At first I found myself frustrated by reading so many reviews of topics already familiar from other books on specific sensory systems (Land and Nilsson, 2002; Smith, 2000; Stebbins, 1983), but realized that not only do these chapters help ease readers not familiar with these other works, but it also helps the reader construct ideas about what information is important to understanding the discussions of the anatomy and physiology that follow in chapters detailing how these senses work in various aquatic groups.

Chemical senses comprise seven chapters of their own, giving them more pages than any other sensory modality covered in this book. Though not as important to marine mammals as to other aquatic vertebrates, chemical senses are so complex and important to virtually all other vertebrates that they certainly warrant the attention.

For example, in Chapters 2, 3, 4 and 5 the detailed account of the role of the primary olfactory nerves and the vomeronasal organ in the reception of different stimuli really conveys how vomeronasal function is not cut-and-dry. In Chapters 4 (by Reiss and Eisthen) and 5 (by Schwenk), we get a glimpse of how nasal cavities in lissamphibians and nonavian reptiles can link subtle features of internal morphology to chemoreceptive abilities and the interplay between breathing, eating, and olfaction. Chapters such as this make it easy to imagine this as a starting point for people working on sensory adaptations in tetrapod origins or even Sauropterygia. Schwenk even provides a page or two on mosasaurs, phytosaurs, and plesiosaurs, full of inferences and insights that cannot help but stimulate speculation.

Chapter 6 (by Hieronymous) covers aquatic birds in a brief, detailed anatomical way. Though there is no doubt that many birds are aquatic, the amount of time and manner in which they use water is so diverse that birds (Hémery, 2001; Kristoffersen, 2001), perhaps like large ungulates, make it hard to narrowly define ‘semiaquatic’. This problem itself is probably responsible for many paleoecological misunderstandings about the Neornithes, as well as pterosaurs (Mazin, 2001). Hieronymous is an example of clarity when it comes to restricting how he partitions the continuum from terrestrial to fully aquatic. Hieronymous starts out defining what he means by ‘aquatic’ and keeps the chapter limited to a review of general details of what is known for major groups and points out what research is sorely lacking. These gaps in the knowledge of bird biology must be systemic, as even though Hieronymous provides far more details, this chapter reminds me of reviews on bird feeding biology (Rubega, 2000) that also point out the large gaps in our knowledge of modern taxa. Like many of the chapters in this volume, perhaps excluding those on vision, Hieronymous places this limited data optimized on a cladogram, hinting at what may be assumed and what work there is to be done.

Pihlström’s chapter (7) on chemical sense in aquatic mammals touches on the little published information there is for fossil groups briefly, but focuses on modern mammal groups. Pihlström demonstrates his attention to detail in noting the difference between mysticete and odontocete olfactory anatomy, adding to the growing amount of evidence informing us about the big physiological differences between these two groups as they diverged in the late Eocene and early Oligocene (Beatty and Rothschild, 2008; Fitzgerald, 2006; Lindberg and Pyenson, 2007). The only modern aquatic non-cetacean artiodactyls are the Hippopotamidae, and it is unfortunate that Pihlström’s review of this family does not more thoroughly include some significant findings of the role of olfaction in behavior (Zapico, 1999) that demonstrate how terrestrial these animals really are. Still, Pihlström demonstrates his mastery over this topic in his analysis of olfactory bulb volume with respect to body size of some of the smaller semiaquatic mammals in the conclusion of this chapter. Despite how anecdotal the data may suggest a reduction in olfactory bulb volume with becoming semiaquatic, he deftly conveys a need for caution in light of the fact that many semiaquatic taxa are larger than other non-semiaquatic sister taxa, as his data suggests that the only significant differences in olfactory bulb size seem to occur with fully aquatic taxa. Though this leaves more questions than answers, it gives me hope that chemoreception may be a possible dividing line between aquatic and semiaquatic mammals.

The second sensory modality covered is vision. Starting with Kröger’s chapter (8) on the physics of light in air and water, he brings up quite a number of important and novel concerns about vision underwater as compared to terrestrial environments. And though he succeeds in addressing the importance of pressure, sediment loads and salinity in how it may affect eyes as organs when exposed to different aquatic environments, the differences among aquatic habitats with respect to the role of temperature or salinity on the refractive index was not mentioned, even though this data is available (Denny, 1993). Though this does not devalue this useful chapter significantly, this information could be important to animals that move between environments of different temperature and/or osmolarity (e.g., deep diving cetaceans, manatees, possibly many transitional forms). Perhaps more importantly, though subsequent chapters make use of diopters as important units of vision, this chapter does not describe what they are or how they are measured. Even though not important to explain methodologically here, it would have been a better use of the space given to the speed of light in air and water, which has less relevance to the comparative anatomy.

Kröger and Katzir’s chapter (9) on the anatomy and physiology of eyes in aquatic tetrapods reviews specializations of the eyes of modern aquatic tetrapods for not only being fully aquatic, but also goes into detailed discussions of how a number of groups deal with vision when in water as well as when in air. In addition, their discussion of the meaning of eye size for vision in ichthyosaurs is expertly executed, as are the lengthy discussions of how many birds correct for the refraction of underwater prey when hunting from the air, and how odontocete eyes function. For the sake of completeness I feel it useful to report some recent references to the anatomy of Harderian glands in odontocetes (Bodyak and Stepanova, 1994; Ortiz et al., 2007) that are lacking in their discussion of the so-called ‘whale tear’, though this is hardly an oversight of much importance. Likewise, the hypothesis that Platanista (the South Asian river dolphin) may be able to use its light sensitive eyes to form an image in air (Waller, 1983) is not evaluated, and discussion of the use of these eyes as means to identify the surface during side-swimming (Purves and Pilleri, 1973) is absent, despite its relevance when comparing these with other river dolphins whose environments are similarly murky but lack such visual atrophy. The review of vision in sirenians is very thorough, in particular with its reference to findings about manatee corneal vascularity, which has recently been shown to be the result of a lack of expression of sflt-1, which is the normal means of suppressing vascularity in the cornea of all other mammals (Ambati et al., 2006).

Regarding perhaps the most obvious question that comes to mind when one sees this book, the position of orbits on the skull of aquatic and semiaquatic taxa (such as the hippopotamus staring at you from the cover of the book), the authors here only devote a brief discussion. This discussion is unfortunately very superficial, with apparently little care to discern between the derived states of the position of the orbits in the examples they provide to determine the ancestral state of Cetaceans. I believe the authors would not be so likely to continue to draw comparisons to hippos if they had been more careful to note that orbit position Hippopotamus is much more dorsal and derived than in Choeropsis or the putative ancestors of hippos, anthracotheriids. Similarly, there is very little reason to believe that the ‘transitional form’ Ambulocetus represents the ancestral state of subsequent archaeocetes, as all putative sister taxa to cetaceans have laterally-oriented orbits, including anthracotheriids, cebochoerids (Theodor and Foss, 2005), and raoellids (Thewissen et al., 2007) (though it is clear that the authors could not have included this latter reference in the time frame of publishing this chapter). Still, this chapter should be recognized for being a detailed review of a very complex and important subject in the study of aquatic tetrapods, and these omissions should be seen as stimuli for research, not faults.

Hearing is perhaps the sensory modality that has received the most attention with respect to aquatic mammals, particularly because of specializations for echolocation found in cetaceans. Nummela and Thewissen’s chapter on the physics of sound in air and water is the most clear and concise explanations of this topic I have seen, particularly with respect to the importance of acoustic impedance. This chapter is deficient in data comparing how the speed of sound varies in water of different salinities and temperatures, even though its importance is acknowledged in the text and data of this sort is available (Denny, 1993). The chapters on hearing in aquatic amphibians, reptiles, and birds by Hetherington, and mammals by Nummela are not only thorough in their descriptions of data for modern taxa, but Hetherington’s chapter is particularly attentive to fossil amniote taxa as well. I was a bit disappointed that no discussion of hearing in hippopotamids was included in Nummela’s chapter, especially with regard to new information on underwater hearing in common hippos that has recently come to light (Barklow, 2004).

The sense of balance is started with a chapter (14) by Sipla and Spoor on “The Physics and Physiology of Balance”, which is kept concise and clear. Georgi and Sipla’s following chapter (15) on balance in aquatic reptiles and birds avoids repeating details of how semicircular canals work and gets straight to exploring how canal shape changes may reflect aquatic specializations. In so doing, they help convey the importance of phylogenetic context, as the aquatic specializations of many non-mammalian amniotes can only be recognized in comparison with other close relatives, and not necessarily as “rules of construction” of their own. But some patterns do emerge from their presentation of original data and discriminant function analyses, making this chapter a valuable early look at their research that can be found nowhere else.

Likewise, Spoor & Thewissen’s chapter (16) on the semicircular canals of aquatic and semiaquatic mammals presents not only a complete review of previous research, but adds considerably more new data and analysis as well. Of particular interest are the new, conservative estimates about semicircular duct lumen size and how it may affect a canal’s response speed, as well as new data and analysis of pinnipeds, otters, and other semiaquatic rodents and monotremes. One minor technical error is the omission of one citation from the literature cited that is referenced in the text (Jansen and Jansen, 1969), an error so minor it is only worth noting here for the sake of completeness.

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. 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. This chapter has an enticing number of notes on what we still need to know, as well as small tastes of unpublished research by Denhardt and Mauck that make it a stimulating read.

The chapter (19) on magnetoreception by Hofmann and Wilkens is brief, but highlights the significant data on magnetoreception in sea turtles as well as the scant data for cetaceans. Though it is disappointing to read that so little research as been done outside of birds due to logistical difficulties in the study of magnetoreception, I suspect someone reading this chapter will be stimulated to invent new ways of exploring this topic and astound us in the future.

Chapter 20 on electroreception is equally brief, primarily because it is a sense largely lost in amniotes even though it is known to have evolved early on in vertebrate evolution. The data presented on monotremes, particularly the platypus, is excellent, though the suggestion that some dolphins (Sotalia) have electrosense is reported based primarily on similarities in vascularity of their vestigial hairless follicles (Mauck et al., 2000) and unpublished research by Denhardt (which is also brought up in Denhardt and Mauck’s chapter on mechanoreception). In addition to these unusual compelling cases, Wilkens and Hofmann do something rare, they report on other aquatic mammals that are known NOT to have electrosensory abilities.

The concluding chapter, by Thewissen and Nummela, presents new preliminary findings concerning the evolution of sensory systems in fossil cetaceans. They manage an exemplary job of applying the concepts for modern animals laid out in the previous chapters, particularly with vision. I was disappointed that for all of the data on fossil whales presented that their only analyses were of absolute eye size and eye size scaled to body size (with a following statement that increased eye size = increased vision), even though recent studies indicate that eye size scales with brain size quite well with little or no indication of visual specializations (Burton, 2006). Likewise, the inference of enhanced mechanoreception based on the pits and grooves on the rostrum of pakicetids is poorly supported. The statement that manatee rostra are densely pitted where their fields of vibrissae occur is inaccurate, and in general comparisons of a pakicetid rostrum’s pits to the muscular hydrostat of a manatee are poorly conceived. In contrast, their discussion of the sensory landscape of cetaceans, especially their figure illustrating their ideas, is compelling. Their overall scenario regarding this landscape is plausible, even though in this context they seem to be treating early cetaceans as a lineage instead of a number of groups that may not represent the ancestral condition of later taxa. The dichotomy did not start with the advent of the Neoceti, and I am surprised that no cladogram with sensory system data optimized on it was presented to depict the diversity of archaeocetes and early Neoceti.

In their approach to coordinating comprehensive reviews of sensory systems in all secondarily aquatic vertebrates, what Thewissen and Nummela have coordinated here can only be compared to other great integrative biology or functional morphology volumes such Feeding (Schwenk, 2000), The Skull: Volume 3 (Hanken and Hall, 1993), Mechanics and Physiology of Animal Swimming (Maddock et al., 1994), or Secondary Adaptation of Tetrapods to Life in Water (Mazin and Buffrénil, 2001). Though it seems like a plethora of details largely concerning modern vertebrates, it is apparent from these authors that there is still much to be done for modern and especially fossil vertebrates. In this volume I hope that current and incoming generations of paleontologists and organismal biologists will see golden opportunities and inspirations for future paths of study. Now, with this book in hand, I hope that path will be taken by many more.

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