Friday, April 11, 2008

On Cellular Scaling Rules for Primate Brains

ResearchBlogging.orgStudent post submitted by Heidi K. Rivera.


Why are primates smarter than rodents with similar-sized brains? To get the full explanation read this paper. Or, in short, read on. This paper analyzed the cellular scaling rules of primate brain sizes and cellular composition across six species of primates (marmoset (pictured here), galagos, owl monkey, squirrel monkey, rhesus monkey and the tree shrew). In a previous paper, the authors described the cellular scaling rules that apply to rodent brains. That research showed that rodent brain scales hypermetrically as a function of its numbers of neurons and that the average of neuronal size is bigger in larger brains, while the average nonneuronal cell size remains relatively stable.Marmoset.jpg


The results of that study encouraged the scientists to extend their research to other mammalian species. Would this reflect the characteristics or traits inherited from a common ancestor? This begged the question, “what rules differ across orders of mammals, and thus might account for phylogenetic variance across groups?” After doing some calculations, they found that if the same cellular scaling rules for rodents applied to primate brains, “a brain comparable to ours, with approximately 100 billion neurons, would weigh >45 kg and belong to a body of 109 tons, about the mass of the heaviest living mammal, the blue whale!” Realizing this obviously indicated that the cellular scaling rules differ between rodents and primates. This is also supported by the fact that it is know that rodents and primates have very different cognitive abilities even when they have a similar brain size. The main difference in the cellular scaling rules for building rodent and primate brains is that increased numbers of neurons in primates are not accompanied by decreased neuronal densities, indicating that the average neuronal cell size remains stable across primate species. After completing their research, they found that primate brain sizes increase isometrically with body size across primate species. Primate brains increase in size as a linear function while rodent brains hyperscale as they gain neurons. This suggests that, “there has been a selective pressure against increase in average neuronal size with brain size.” This type of increase allowed primate brains to accumulate large numbers of neurons without becoming prohibitively large. If the rodent cellular scaling model applied to say, the macaque brain, which has approximately 6.4 billion neurons, would weigh about 575g instead of it’s actual weight of 87g! “These findings suggest that the divergence of primate evolution away from the common ancestor with rodents involved mechanisms that favored the concentration of larger numbers of neurons per unit volume of brain tissue.” The larger number of neurons per unit volume apparently provides primates with a larger computational capacity than rodent brains of the same size. This answers the question of why primates are smarter than rodents with similar-sized brains. They concluded with possibly applying the research found from both the rodent paper and this paper to apes and humans. My question is whether this “model” of cellular scaling and cellular composition can be applied to other species. What about reptiles or amphibians? What do you think?


Reference:


Herculano-Houzel, S., Collins, C.E., Wong, P., Kaas, J.H. (2007). Cellular scaling rules for primate brains. Proceedings of the National Academy of Sciences, 104(9), 3562-3567. DOI: 10.1073/pnas.0611396104


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Chimps cracking nuts with stone tools

And of course, YouTube has the video to go along with Scott Brown's post about percussive tool using chimpanzees!








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Exposing Deeper Roots of Chimpanzee Culture

ResearchBlogging.orgStudent post submitted by Scott Brown.


kanziknappingb.jpgA recent study performed in the tropical rain forests of Western Africa has generated a lot of interest and discussion into ancient chimpanzee cultures. The excavation of stone tools dating back 4,300 years has changed a lot of preconceived notions about how chimps acquired this food gathering technique. Modern chimps use large, heavy granite stones to pummel Panda nuts to extract the fruit within the hard exterior shell. The history of chimps performing this task previously dated back only to the 19th century, so many experts believed that this technique was developed from chimps imitating humans. The new stones, excavated by a team led by Julio Mercader of the University of Calgary, predate any known human inhabitants of Noulo at Cote d'Ivoire in the Ivory Coast's Tai National Park. Researchers had previously theorized that chimps learned this technique from ancient humans, and this imitation was passed down through generations. If chimps manufactured and used tools without the presence of humans, it can now be theorized that chimps either developed this idea independently as a result of independent technological convergence, or chimps may share a common ancestor with early humans that first learned this pummelling technique.


070212184608.jpg The dig was conducted in the only known ancient chimpanzee rain forest settlement. Researchers dug down several meters to find charcoal samples that indicated that sedimentary depositions from the area dated back 4,300 years. From the dig, researchers collected 206 stones that exhibited unnatural chipping characteristic of repetitive pummelling. These stones were mixed with other similar naturally broken stones and tested by three examiners. These specialists of ancient stones proved the collected stones were not geofacts and indeed broken by a physical force applied by an agent. The stones averaged 12.6 inches in length, 4.5 pounds in weight, and most of them were Granite. All three of these characteristics correlate to the average rock parameters preferred by modern local chimps when choosing a pummelling stone. The size of hands required to slam such a large stone and the starch residues found on the rocks indicate that the original agent was chimp rather than human. So if these stones were in fact used by ancient chimps in the late stone age, what light can be shed onto the development of their culture and intellect during this prehistoric time.


In order to smash a fruit with a stone, a certain extent of socialization and culture must be implied. Simple tasks such as selection of proper rocks and movement of the rock to where the fruit is located is somewhat simple. But the social network that is required for the passing down of this complicated action from one generation to the next should not be underestimated. Previous studies conducted by one of the scientists involved with the dig, Christoph Boesch, suggest that modern chimps undergo a seven year internship with elder members of the troop in order to successfully pummel their own fruit. There would need to be a significant accumulation of generations practicing this technique before it became established enough to generate 206 pummeling stones in the same area. If you consider the rocks dated back 4,300 years, they should indicate that the roots of primate intelligence run much deeper and older than previously estimated. It was found in the 1980's by Jane Goodall that chimps are capable of considerable understanding, but it is now apparent that they have been exhibiting characteristics of established culture for thousands of years.


Reference:





Mercader, J., Barton, H., Gillespie, J., Harris, J., Kuhn, S., Tyler, R., Boesch, C. (2007). 4,300-Year-old chimpanzee sites and the origins of percussive stone technology. Proceedings of the National Academy of Sciences, 104(9), 3043-3048. DOI: 10.1073/pnas.0607909104




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On parasite-host coevolution

ResearchBlogging.orgStudent post submitted by Toua Chang.


The interactions between a parasite and its host are not completely understood. Though conventional wisdom of parasitology and medicine suggests the net effect of a parasite on its host (virulence) to be little or none, recent data suggest there may be many possible coevolutionary outcomes. These outcomes, as outlined by Andrew J. Karter and Catherine A. Toft, include the settlement of virulence to intermediate levels, high levels, or zero.


According to Karter and Toft settlement of virulence to intermediate levels is more readily accepted due to the fact that the best-documented cases of coevolution are primarily of virulence settling to intermediate levels. One such case includes the introduction of avian malaria to Hawaii, in which native birds became extinct upon introduction of the disease. As time progressed, however, some native birds evolved resistant to avian malaria; therefore, reducing the virulence of Plasmodium.


Given other factors such as vectors, however, virulence may potentially rise to high levels. One argument for potential high virulence is that vector-borne parasites are able to increasingly exploit their hosts without penalty. Such parasites include the acute Plasmodium strain that infects humans, in which immobilization due to the host immune response allows the parasite to be transmitted through a feeding arthropod vector. In this case, if the host’s immune system is unable to counter the parasite, then the parasite’s virulence would have increased significantly.


When virulence is zero, the parasite and its host are considered to be in a commensal relationship. Commensalism, in this case, does not imply a peaceful coexistence, but rather a stand-off between parasite attack and host counterattack. It is, therefore, evolutionarily possible for either the host or the parasite to overcome the other at any time. Examples include the evolution of eukaryotes relative to mitochondria and chloroplasts.


Karter and Toft suggests that anyone of these outcomes may occur at anytime. In African trypanosomiasis, for example, one “species”, Trypanosma brucei, is able to infect a variety of mammals and cause varying degrees of diseases. Tryanosoma brucei brucei is non-infective to humans, but T. b. gambiense and T. b. rhodiense causes chronic and acute forms of the disease, respectively. Conventional wisdom suggests that the resistance of humans to the brucei strain occurred earlier on in evolutionary history, and that the acute strain occurred later. Though this may be conventionally reasonable, enzymatic and molecular techniques have proven otherwise, suggesting a different order of evolutionary history. Based solely on symptoms and geographical locations, it is difficult to determine what constitutes a species in T. brucei. This is due to the fact that all strains of T. brucei are morphologically indistinguishable.


As stated, Karter and Toft suggests three outcomes pertaining to the interactions between parasite and host. There is currently no sufficient evidence to suggest any sole outcome as the correct one. To further evaluate the coevolution of virulence between two interacting species it is important to gather more empirical data on the parasite-host association.


Reference:


Toft, C.A., Karter, A.J. (1990). Parasite-host coevolution. Trends in Ecology & Evolution, 5(10), 326-329.



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Of California Tiger Salamanders

ResearchBlogging.orgStudent post submitted by Christian Ramirez


The larval stage of amphibians is often used as a model for ecological processes. However, the demography, ecology, and life history of amphibians after their larval stage is not well known. The article I read focuses on describing the life history and demography of the California Tiger Salamander as well as the effects the environment has on both. The California Tiger Salamander is found mainly in the grasslands of the Central Valley as well as in the surrounding foothills and valleys.


TigerSalamanderSm.jpgThe data presented by the authors dealt with variations in the timing and magnitude of the breeding migrations. The size and age structure of breeding adults as well as the production of juveniles were also observed. Mortality rates were recorded from the metamorphic stages to adulthood. The data was collected over a seven-year time period in Carmel Valley located in Monterey County.


The test area was a pond that was fenced off from larger animals. The pond would dry up each summer and refill during the fall. There were additional ponds near the test area which provided other breeding grounds. The distance of the ponds from the test area varied from 550-3000m.


The data was collected by using drift fences surrounding the pond which would direct the salamanders into irregularly placed pitfalls. The pitfalls were placed on the outside and inside of the pond in order to record the amount of salamanders entering and leaving the pond. The pitfalls were checked every morning and captures were recorded and tagged.


The authors also used skeletochronology to estimate the individual ages of the salamanders. Skeletochronology is a technique which estimates the salamander’s age by counting lines of arrested growth (LAG) in thin cross-sections of elongate bones mostly located in the toe. It should be noted that few investigators have validated the assumptions formed by skeletochronology.


The data showed that the researchers captured and observed approximately 20% of the population. The data also showed that the males were usually the first to arrive when the pond began to fill up and stayed much later than the females. The ratio of sex usually stayed around 1:1, except for years in which the pond was not completely filled by rainfall. This was attributed to surviving females skipping breeding opportunities in years with later rainfall. When breeding occurred, the females bred an average of 1.4 times and produced an average of 8.5 young.


The data also showed that the mortality for the metamorphs in their first summer was extremely high. This was due to a low percentage of first year metamorphs being recaptured in comparison to mature salamander recapture rates. The overall estimate of juveniles that reached maturity was approximately 5%.


The conclusions that the authors came to were that an isolated breeding pond on its own is not able to sustain a long term population. In order for a population to remain stable, a female must reproduce at least one male and female offspring. Calculating the numbers, at least 18.2% of the juvenile population would have to survive in order to maintain population stability.


Because less than 50% of the population bred at the pond more than once, the authors also considered the test area as a sink habitat rather than a source habitat meaning the population at the pond was not a major one.

Although the data was well prepared and the paper well written, there are some problems with this paper. First, the authors did not study the salamanders in their terrestrial habitats. They even say that a greater focus should be put on the time salamanders spend in terrestrial areas as the population greatly decreases during that time. There could be many different evolutionary factors which play into the overall fitness of the salamanders as their size was proven to be a neglible factor. These factors could be selected for or against in the terrestrial habitats.


Another problem was that the drift fence was ineffective at times. During flooding, the salamanders were able to climb over the fence, effectively escaping capture and observation. This could have skewed the mortality, return, trespassing and breeding rates that the authors gathered over the seven year period. Mortality and survivorship were also hard to determine because adults chose to skip breeding in certain years, which could have also yielded incorrect data.


Even when they were captured, the authors had to use skeletochronology at times when the salamanders were unmarked or immigrants from the other ponds. Although the authors found that there was little error, this is still considered a new form of data analysis and is still unproven.


The authors chose to use skeletochronology because it was quicker and tagging the salamanders seemed to cause an increase in mortality. This assumption was made because the authors found they recaptured a greater amount of salamanders that were untagged in comparison to tagged salamanders.


That being said, this paper is still well done. Because less attention is given to amphibians in juvenile and adult stages of life as well as in their terrestrial habitats, there was not much precedent for the authors to draw from. By looking at what was done correctly and incorrectly in this study other researchers can formulate better experiments. This paper was a step in the right direction for the study of amphibians in the later stages of life and helped to show that all facets of life as well as all habitats should be studied in order to better understand a species.


Reference:





Trenham, P.C., Bradley Shaffer, H., Koenig, W.D., Stromberg, M.R. (2000). Life History and Demographic Variation in the California Tiger Salamander (Ambystoma californiense). Copeia, 2000(2), 365. DOI: 10.1643/0045-8511(2000)000[0365:LHADVI]2.0.CO;2




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Thursday, April 10, 2008

And now, a frog with no lungs!

080407-lungless-frog-02.jpg

Such a biological wonder has indeed now been discovered lurking in the rainforests of Borneo, as you may have read in the science blogosphere and even mainstream news channels already!


Ain't evolution cool! Its never about "progress" in a certain direction, or increasing complexity, or any other "upward" trajectory we may think of. Its always about what works best for a given organism in its particular environmental circumstance: if a trait (such as lungs or skin to breathe through) works well enough to let you survive and make lots of babies, it may prevail and become the norm in your lineage; OTOH, if an existing trait (such as your newly evolved lungs) get in the way of surviving and procreating, natural selection might well get rid of it! Sometimes, your entire lineage goes with the trait - natural selection isn't really all that particular in that way. But if, like this frog, you have one troublesome big trait that is chafing against the filter of selection, and also have a backup system to perform the same physiological function, you may get away with losing the big new innovation!


These frogs apparently live in fast, cold, mountain streams rich enough in oxygen that they can get enough through their skins. Of course all amphibians can breathe through their skin to some extent, but the big innovation that allowed them to plant the tetrapod flag in the terrestrial realm in the first place, was of course lungs! Yet these little guys have given up on lungs, and, unable to re-invent more ancestral gills, reverted to the skin - and it'll be fascinating now to study how that skin has evolved in this species.


Meanwhile, the serendipitous discovery of this wonder must give pause to my friends who are against vivisection (for many good reasons, and some poor ones), and even against collecting specimens at all for museum collections or scientific study. And it becomes harder to argue with activists of that persuasion when it comes to rare new species. Yet, this amazing discovery would not have been possible if someone hadn't thought to look inside the body of the frog! Contrary to what the romantic Wordsworth wrote, I have to contend that we biologists do not always "murder to dissect"!



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Remember when snakes had legs?

ResearchBlogging.orgCan't remember? Well, it was a while back, and fossils of legged snakes have been hard to come by. Another one of those pesky gaps in the fossil record, although we know from the precious few specimens we have and a whole range of other evidence that snakes evolved from lizards that had legs. Not just that - loss of limbs is a recurring theme among a bunch of squamate lineages with snakes being the most prominent. And one of the problems with fossils, especially when you don't have many specimens to play with, is that its not easy to study anatomical detail without risking destroying the fossil! And without such detail, it is difficult to reconstruct exactly what might have happened in the evolutionary trajectory from lizards to snakes. What to do? Well, high energy physics to the rescue, of course!


As reported today by the BBC, a new study used intense X-rays - with much higher energy, one guesses, than found in your dentist's office - to examine one such rare snake fossil to look beneath the surface of the fossil and take a picture of a hidden leg! Here's an excerpt (with photo below the fold):


Researchers at the European Light Source (ESRF) in Grenoble, France, used intense X-rays to confirm that a creature imprinted on a rock, and with one visible leg, had another appendage buried just under the surface of the slab.


"We were sure he had two legs but it was great to see it, and we hope to find other characteristics that we couldn't see on the other limb," said Alexandra Houssaye from the National Museum of Natural History, Paris.


The 85cm-long (33in) creature, known as Eupodophis descouensi, comes from the Late Cretaceous, about 92 million years ago.


Unearthed near the village of al-Nammoura [in Lebanon], it was originally described in 2000.


Its remains are divided across the two interior faces of a thin limestone block that has been broken apart.


A portion of the vertebral column is missing; and in the process of preservation, the "tail" has become detached and positioned near the head.


But it is the unmistakable leg bones - fibula, tibia and femur - that catch the eye. The stumpy hind-limb is only 2cm (0.8in) long, and was presumably utterly useless to the animal in life.



Still how much can one do with one such tantalizing glimpse from a single fossil?


_44555496_snake_fossil466x400.gif
The top picture is a synchrotron view of the visible snake leg;
Synchrotron light in the bottom view illuminates the hidden limb



"Every detail can be very important in establishing the great relationships and that's why we must know them very well," explained Ms Houssaye.


"I wanted to study the inner structure of different bones and so for that you would usually use destructive methods; but given that this is the only specimen [of E. descouensi ], it is totally impossible to do that.


"3D reconstruction techniques were the only solution. We needed a good resolution and only this machine can do that," she told BBC News.


That machine is the European Synchrotron Radiation Facility. This giant complex on the edge of the Alps produces an intense, high-energy light that can pierce just about any material, revealing its inner structure.


For this study, the fossil snake was clamped to an inclined table and rotated in front of the facility's brilliant X-ray beam.


In a process known as computed laminography, many hundreds of 2D images are produced which can be woven, with the aid of a smart algorithm, into a detailed 3D picture.


The finished product, which can be spun around on a computer screen, reveals details that will be measured in just millionths of a metre.


The E. descouensi investigation shows the second leg hidden inside the limestone is bent at the knee.


"We can even see ankle bones," ESRF's resident palaeontologist Paul Tafforeau said.


"In most cases, we can't find digits; but that may be because they are not preserved or because, as this is a vestigial leg, they were never present."


Cool, huh? The only uncool part of the story is that the BBC does not tell us where this is being published in the peer-reviewed literature! I suppose we'll know soon enough. Meanwhile, check out these earlier papers, linked above:


Apesteguí­a, S., Zaher, H. (2006). A Cretaceous terrestrial snake with robust hindlimbs and a sacrum. Nature, 440(7087), 1037-1040. DOI: 10.1038/nature04413


Wiens, J.J., Brandley, M.C., Reeder, T.W. (2006). Why does a trait evolve multiple times within a clade? Repeated evolution of snakelike body form in squamate reptiles. Evolution, 60(1), 123. DOI: 10.1554/05-328.1



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Wednesday, April 9, 2008

An ancient reptile challenges some modern hypotheses about molecular evolution rates

ResearchBlogging.orgStudent post submitted by Nathan S. Sunderson.


A recent study by Jennifer Hay and colleagues at the Allan Wilson Centre for Molecular Ecology and Evolution in New Zealand has found that unexpectedly, the Tuatara (Sphenodon punctatus ) may have some of the fastest rates of molecular evolution seen in the animal kingdom. The two species of tuatara have long been a fascination in the realm of herpetology because they have changed little since the time of the dinosaurs and are the sole living members of a sister clade to the familiar squamata (snakes and lizards). Tuataras have many “primitive” characteristics such as low metabolism, slow growth, and slow reproduction: all of which are expected to correspond to slow mutation rates. How can an animal with such historically slow morphological evolution have high rates of molecular evolution?


By sequencing the mitochondrial DNA hypervariable regions (HVRs) of the control region of modern and fossilized tuataras and radiodating the fossils examined, the group calculated an evolution rate of 1.56 (0.83-2.34) substitutions per nucleotide per million years. This is the highest rate seen among the 10 animal species studied to-date using similar statistical techniques.


These findings contradict the assertions that: 1) there is an inverse relationship between generation time and molecular evolution rate, 2) rate of evolution corresponds to body size, and 3) there is a direct correlation between metabolic and evolutionary rates. The most important implication of this study is that the rates of neutral molecular and phenotypic evolution may be decoupled. Indeed, previous studies on other living fossils (coelacanth and horseshoe crab) suggest that they may similarly have high evolutionary rates. The group has suggested that perhaps genome structure and replication processes (not metabolism, body mass, and generation time) are the key to understanding the diversity of evolutionary rates among animals.


Reference:


HAY, J., SUBRAMANIAN, S., MILLAR, C., MOHANDESAN, E., LAMBERT, D. (2008). Rapid molecular evolution in a living fossil. Trends in Genetics, 24(3), 106-109. DOI: 10.1016/j.tig.2007.12.002


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Monday, April 7, 2008

The Ecological Strategies of Sea Turtles

ResearchBlogging.orgStudent posting by Rebecca Bellamy


Since the Triassic, sea turtles have not changed a great deal. About 200 million years ago, the common ancestor to today’s Chelonians developed an “armored tank” body form, enclosing its body inside a tough shell as a mode of defense from large toothed predators. This was one of the early steps that led to the evolution of the sea turtle. The development of this hard encasing was achieved by many other anatomical changes. Many vertebrae from the trunk region were done away with and the ribs were no longer attached to the sternum. Because of the fusion of the axial skeleton to the shell, almost all of the dorsal trunk muscles were lost or became modified to aid in respiration. These many changes of body form also led to the development of a new swimming mode, since undulatory swimming was no longer an option. This new swimming mode came from modifications of the forelimbs, which became stiffened and elongated. Now the animal could move through the water by propulsion from up and down strokes of the modified front limbs, while using its back flippers as a rudder.


These modifications of body form allowed the Chelonians to move into an unoccupied niche space in the marine environment. However, because of the restrictions of hardened shell, there was not sufficient room to expand the cloacal area, and so the Chelonians were still dependent on the terrestrial environment for the laying of eggs and development of their offspring. But with the new modifications to the limbs sea turtles were no longer able to move very well on land. This makes them extremely vulnerable to predators when it comes time for them to lay their eggs. Therefore sea turtles developed the behavior of choosing remote beaches as their nesting sites and do not care for their nests. This in turn, leaves the eggs very vulnerable to predation during incubation, as well as the hatchlings as they make their way to the ocean. Thus, there is a high mortality rate in the early life stages of the Chelonian. This is somewhat compensated for by the laying of larger numbers of eggs.


The most commonly recognized species of sea turtles are all very similar, but each has minor differences in morphology and each occupies its own ecological niche. Some of the species are migratory between feeding and nesting sites, some species are neritic and one species is strictly pelagic. However, all species are dependent on land for their nesting sites. Most Chelonians are herbivores, with a few species being carnivorous. The pelagic species feed on planktonic jelly fish, while the neritic species feed either on mollusks or crustaceans. The migratory species consist mostly of the herbivores, as well as one species that is omnivorous and another species that is carnivorous.


According to Hendrickson, the leathery sea turtle, Dermochelys coriacea, is more adapted to its pelagic lifestyle because of more powerfully developed front flippers, which are proportioned and structured differently from those of any other sea turtle. He also believes the carapace ridges found on their shells to be adaptations for dealing with the laminar flow associated with a sustained swimming speed. Because of their life in the open ocean, these turtles are obligate jelly fish feeders.


The green sea turtle, Chelonia mydas, is one of the species that migrates between feeding and nesting sites. Some populations of this species migrate longer distances than others, while some species practice a coastal-oriented migration and never cross open ocean waters to get to their nesting sites. The populations that live in Hawaii and the Galapagos, however, seem to be permanent residents of these islands. Thus, Hendrickson states that this species seems to be divided in to distinct variant populations, more so than the other species of sea turtles.


The flatback sea turtle, Chelonia depressa, is an Australian species that is characterized by its large head and flattened shell. Hendrickson believes that this Chelonian evolved to species status from a population of C. mydas fairly recently. This species is one of the non-migratory species of sea turtles and is thought to subsist on a diet of sea cucumbers. Interestingly, C. depressa has lost a majority of its hard shell, so much so that even a light scratch can draw blood. Hendrickson attributes this to the fact that this Chelonian evolved in the absence of placental carnivores.


Eretmochelys imbricata is better known as the hawksbill turtle. It is thought that this species separated from C. mydas earlier than C. depressa and intergenic breeding of E. imbricata and C. mydas produces viable offspring. These turtles are omnivorous, feeding on coral reefs. This species is also a solitary nester and does not do long migrations. They nest mainly on islands near the coral reefs in which they feed.


The neritic sea turtle, Caretta caretta, is a carnivore feeding on mollusks. This turtle is distributed mainly along the eastern coasts of continents over productive sea bottoms and characteristically nest on beaches of the mainland. Hendrickson states that their large head and jaw structure is a direct adaptation to their diet of mollusks, however they have been known to eat jellyfish and mangrove leaves. This species is the only other species besides D. coriacea that can tolerate lower water temperatures.


The olive ridley turtle, or Lepidochelys olivacea, shares a similar distribution and diet as the loggerhead turtle, but during the non-breeding portion of its life it is thought to reside farther offshore than the loggerhead. Hendrickson believes that reported sightings of green sea turtles far out at sea in the eastern Pacific are actually olive ridley turtles. He also suspects that these turtles, in addition to long dives to feed on the benthic crustaceans of the neritic waters, will float above abyssal waters and feed on the crustaceans that surface at night.


Hendrickson believes that the Kemp ridley turtle, Lepidochelys kempi, is a recent offshoot of the L. olivacea line after the Panamanian land barrier isolated these turtles from the rest of the population of L. olivacea. This turtle is only found in the Gulf of Mexico and the entire population nests in a small section of coast in Mexico. This species will come ashore to nest in enormous arribadas during the day, unlike the olive ridley turtle which does this at night. A problem these turtles encounter is being swept up the eastern coast of the U.S. and as far away as Europe in the strong Gulf currents. It is not known whether these turtles are ever able to make their way back to their home to participate in the reproduction of the species.


Reference:


Hendrickson, J.R. (1980). The Ecological Strategies of Sea Turtles. American Zoology, 20, 597-608.



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