Showing posts with label Cetacea. Show all posts
Showing posts with label Cetacea. Show all posts

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you from my usual boring wordiness, but also to protect the rights of authors of these presentations from having their unpublished material shared without their permission.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, August 19, 2009

Injured fossil mysticete and an investigation of osteosclerosis (and benthic feeding?) in fossil mysticetes

I'm sorry to have been inactive for so much of the last month, but I've been busily trying to get some papers completed before the all-consuming teaching schedule takes over my life (1st year Anatomy course started today). I will try to be more active and regular with the blog, I promise.

So, to kick off a rejuvenated series, I thought I'd post something new of mine. Below is a press release by the Virginia Museum of Natural History concerning a paper just published through their in-house journal by me and Alton "Butch" Dooley (which is open access at the Jeffersoniana page at the VMNH), a good friend and colleague. After my paper with Bruce Rothschild in 2008 on decompression syndrome in cetaceans, I've had lots of people approach me about paleopathology, and though I am cautious about doing more than I am comfortable with, this project was irresistible.



VMNH assistant curator of vertebrate paleontology, Dr. Alton Dooley, burshes off dirt from the jacket protecting the unearthed whale skull in July 2006 (VMNH)


Butch had been collecting from a Calvert Formation locality (middle Miocene) known as Carmel Church, in VA. He has a very active dig going on with loads of great finds and volunteers that make it really a spectacular piece of work. One of the more complete whales he uncovered was that of an animal known as Diorocetus. It is a mid-sized "cetothere"-grade mysticete whale and this was an exceptionally well preserved specimen, with much of the skeleton and skull intact.


A dorsal view of the baleen whale's skull (Credit VMNH)


First, the whale has an unusual partially-healed break in its mandible. That alone is curious and worth a little discussion. And although I still think we need to take any interpretations of its cause and implications for behavior with a good amount of caution, to me the best part of it has been that this fossil stimulated something else - a look at osteosclerosis in mysticetes. This animal, probably Diorocetus, has some seriously osteosclerotic ribs. It is hard to find good diagnostic specimens of mysticetes that have decent skulls with associated ribs (partly because they are a pain to collect), so when we looked at this we couldn't believe it when we saw this classic "cetothere" with ribs that almost have as much cortical bone thickness as a manatee! Ok, that is perhaps a bit exaggerated, but it is significantly thicker than that found in odontocetes.


An artist's rendition of the possible feeding habit of the baleen whale (Credit Michael Morriss-VMNH)


So then we decided to look for osteosclerosis in other mysticetes, especially fossil taxa, and found that in our preliminary sample that some of the oldest mysticetes, including toothed mysticetes like Aetiocetus, they had a very advanced form of osteosclerosis, and that only "modern" mysticetes, particularly rorquals, have more porous bones like those seen in odontocetes. What this implies for the evolution of benthic feeding and filter feeding in general with mysticetes is interesting, and discussed in the paper'sm discussion section.

In the end, I think we stumbled upon an interesting sort of data about osteosclerosis that we would not have thought to seriously investigate if not for this curious injured individual from Carmel Church. As you will see in the press release, the interpretation of this individual is what gets the hype, although I am personally more confident and thrilled by the osteosclerosis bit. Still, it is food for thought and reminds us that even filter feeding with baleen is not a simple, one-style-fits-all sort of feeding, and it may have started out in a much different way than we may have previously thought.

I would urge you to read the paper and judge it for yourself. The disucssion of the cause and behavior associated with this individual specimen is meant to be speculative, although an intriguing idea, but the best part is the osteosclerosis (in my opinion). Well enough of me, read on....!

*****ALSO - for another media release about this, see the article in the Virginia Pilot, including comments by Mark Uhen and Nick Pyenson.



VMNH PRESS RELEASE


CONTACT:
Ryan Barber
(276) 634-4163


Virginia Museum of Natural History releases 20th installment of the Jeffersoniana scientific publication series
Publication features first published evidence of bottom feeding habits in extinct whales.


MARTINSVILLE, Va. (August 19, 2009) - The Virginia Museum of Natural History has released the 20th installment of its Jeffersoniana scientific publication series, which is now available as a free download from the museum's online store. The publication, titled "Injuries in a Mysticete Skeleton from the Miocene of Virginia", focuses on the mostly complete fossil skeleton of a baleen whale discovered during a museum excavation at the Carmel Church Quarry in Caroline County, Virginia in 2006. Unique features from these particular remains had never been documented in any other fossil baleen whale and give evidence to suggest several previously unpublished theories of the feeding habits of this now extinct species.
Co-authors Dr. Brian Beatty, VMNH museum research associate and assistant professor of anatomy at the New York College of Osteopathic Medicine, and Dr. Alton Dooley, Jr., assistant curator of vertebrate paleontology at VMNH, suggest that the baleen whale was likely a benthic, or bottom feeding animal, primarily obtaining its food from scooping mud from the ocean floor and filtering the sediment from the plentiful fauna living in the sea floor. Such behavior is common in today's gray whales and to a lesser extent in humpback whales. The size and placement of a fracture on the left side of its jaw suggests that the injury likely had occurred during feeding. The characteristics of the injury indicate it was likely the result of a severe impact, likely trauma resulting from benthic feeding.
Supporting this theory is the density of the whale's rib bones. Dense ribs like those seen in this baleen whale are associated in bottom feeding in some other marine mammals, such as the manatee. Moreover, the presence of similar dense ribs in early baleen whale relatives suggests that baleen may have originally evolved to allow feeding from seafloor mud and only later was adapted for capturing fish and shrimp.
In addition, the publication documents the presence of lateralization in a fossil whale for the first time. Lateralization, or handedness, is well-known in humans and occurs in many animals, including modern gray and humpback whales. Like humans, whales are usually right-handed, and primarily feed from the right side of their mouths when they canvas the ocean floor. Such a fracture on the left side of the fossil whale's jaw indicates it favored eating from its left side, a much less frequent occurrence.
The museum has recently made select installments of the Jeffersoniana series available for free download from the museum Web site in an effort to make the scientific research of the museum's full-time curators more widely accessible to the public. Currently, the museum offers editions 17 to 20 of Jeffersoniana as free online downloads, with additional installments planned for release soon. Hardcopy versions of all museum publications are available for purchase from the museum's online store.
Visit www.vmnh.net or call 276-634-4141 for more information.

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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Barklow, W. E. 2004. Amphibious communication with sound in hippos, Hippopotamus amphibius. Animal Behaviour, 68:1125-1132.

Beatty, B. L., AND B. M. Rothschild. 2008. Decompression Syndrome and the Evolution of Deep Diving Physiology in the Cetacea. Naturwissenschaften, 95.

Bodyak, N. D., AND L. V. Stepanova. 1994. Harderian gland ultrastructure of the black sea bottlenose dolphin (Tursiops truncatus ponticus). Journal of Morphology, 220(2):207-221.

Burton, R. F. 2006. A new look at the scaling of size in mammalian eyes. Journal of Zoology, 269(2):225-232.

Denny, M. 1993. Air and Water: The Biology and Physics of Life's Media. Princeton University Press, Princeton, 341 p.

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Monday, June 22, 2009

Hippos prancing about underwater (Hippo-Ecomorph Rant #1)

The origin of most marine mammals invokes some imaginary semiaquatic transitional form. In the last decade, many of these transitional forms have actually been found, including the semiaquatic sirenian, Pezosiren portelli, which I had the honor of collecting with my master's advisor, Daryl Domning, in Jamaica at the end of my undergraduate studies and beginning of my MS in Anatomy at Howard University. Likewise, in 2001 two papers were published in the same week that described fossil ankle bones of whales that conclusively linked the origins of the Cetacea to the Artiodactyla. I remember that day, I think it was Sept 21, 2001, a Friday, because I was interviewing at Johns Hopkins that day. Shawn Zack (now at Marshall) picked me up at the train station and asked me if I had seen the paper by Thewissen and colleagues published on Thursday, and then said that there was another paper published that Friday by Gingerich and colleagues. Since then, the molecular phylogenetic assertions that hippos are the most closely related modern mammal to the Cetacea has gained much more backing, evn though these original papers in 2001 never inform us of what fossil group they are more closely aligned to. Some recent finds in Pakistan by Thewissen and colleagues have claimed an ancestor in an unusual group of terrestrial mammals known as raoellids, though further analysis by Geisler & Theodor calls some questions to exactly which fossil groups are related to cetaceans and which are not. Yet despite this rigor of questioning what are the real sister taxa to cetaceans, the message most in the public and media have gotten is that there is some connection to hippos. Unfortunately, the connection to hippos also leads some people to examine hippos as examples of what the origins of whales were like, even though the fossil record of hippos goes only into the Miocene and the understanding of whether these earliest forms were semiaquatic or not is still very rudimentary.

Hippos, in my opinion, should be considered the poster-child for how paleontologists take their overgeneralized views of modern animal biology/ecology and infer it for fossil organisms without much, if any fustification. I wont go into this too much further, as a hippo-ecomorph rant(s) is certainly already partly written and worth spending some time on.

But, in the hopes of starting the hippo discussion, how they might relate to cetacean origins and better understanding their roles as examples of the semiaquatic "transitional" mammal, and to relate to a very recent paper recently brought to my attention, it is worth discussing one key point, underwater locomotion in hippos.

A recent paper by Coughlin and Fish (2009) about underwater locomotion in the modern common hippo is an informative look at what many people often see as a "transitional state" for the terrestrial to aquatic transition. This paper is excellent, and in an elegant way really get to the heart of how hippo underwater locomotion is unique, and perhaps a good, or not so good, example of how transitional forms may have made it into the water. I am not sure the parallels they draw between hippos as raoellids, or Pezosiren portelli for that matter, are sufficiently supported, but they gently bring it up as a future avenue for research and should be commended for calling attention to the subject in a rigorous way.

The funny thing is, I have seen these sorts of results from a study of this sort many years ago in the work of a master's student from the University of Florida, Matthew Mihlbachler. In his work, notably done on a budget with a stopwatch and VHS recorder, Matt was able to come to much of the same conclusions as Coughlin and Fish (2009). Though his thesis entailed multiple aspects of the paleobiology of some fossil rhinos (which includes some interesting work about paleodemography) Mihlbachler has only published a small amount of this data in a paper about a fossil brontothere with curiously similar short limbs he named Aktautitan hippopotamopus (NOTE: hippopotamopus is not a typo, see the paper for the etymology).

The best part about these two studies is that they ultimately come to the same conclusion - when you look at hippo underwater locomotion, they are unique. Though there may be some parallels to be found in the hydrostasis controls found in either group someday (as Mihlbachler hints at with some data in his thesis), at present all we can say is that, if hippos are a good example of a transitional semiaquatic mammal (which I am not sure I would claim they are), then many of the characteristics we see in whales that lead from that negatively buoyant transitional form need to be further explored (although Sandy Madar has done some excellent work along these lines, as has Lisa Cooper).

All in all, hippos are an excellent source of information for trying to understand how large mammals might adapt to a life that involves more regular use of water, and in that way they may be good examples of the "transitional form" - BUT the notion that the ancestor of cetaceans was a hippo in the way they are today, or worse, the way we THINK they are today, is poorly conceived and unrealistic.

Tuesday, June 9, 2009

update on Cetacean response to climate change

I was just reading over another recent paper that may also prove relevant to this post as well as the previous one, so I thought I would post an update.
Site fidelity in cetaceans is not new, but a recent paper by Valenzuela et al (2009) does an excellent job showing that for at least some large mysticetes, site fidelity is a matter of cultural inheritance, and can cause a lack of flexibility (at least in the geologically speaking 'short term') of feeding grounds for some taxa even in bad years.
Obviously, this report does not bode well for balaenids in the oncoming global warming situation, though it may be another facet worth exploring when considering prehistoric cetacean distributions. It may ultimately be outside the realm of possibility to answer such questions, particularly when we still don't have good estimates of simple things like body size of fossil groups (though I know one person is working on that) or how far different taxa may have regularly migrated (which may or may not be consistently related to body size).