Showing posts with label Charles Darwin. Show all posts
Showing posts with label Charles Darwin. Show all posts

Friday, June 19, 2009

Humans More Related To Orangutans Than Chimps, Study Suggests


ScienceDaily (June 18, 2009) — New evidence underscores the theory of human origin that suggests humans most likely share a common ancestor with orangutans, according to research from the University of Pittsburgh and the Buffalo Museum of Science. Reporting in the June 18 edition of the Journal of Biogeography, the researchers reject as "problematic" the popular suggestion, based on DNA analysis, that humans are most closely related to chimpanzees, which they maintain is not supported by fossil evidence.
Jeffrey H. Schwartz, professor of anthropology in Pitt's School of Arts and Sciences and president of the World Academy of Art and Science, and John Grehan, director of science at the Buffalo Museum, conducted a detailed analysis of the physical features of living and fossil apes that suggested humans, orangutans, and early apes belong to a group separate from chimpanzees and gorillas. They then constructed a scenario for how the human-orangutan common ancestor migrated between Southeast Asia—where modern orangutans are from—and other parts of the world and evolved into now-extinct apes and early humans.
The study provides further evidence of the human-orangutan connection that Schwartz first proposed in his book "The Red Ape: Orangutans and Human Origins, Revised and Updated" (Westview Press, 2005).
Schwartz and Grehan scrutinized the hundreds of physical characteristics often cited as evidence of evolutionary relationships among humans and other great apes—chimps, gorillas, and orangutans—and selected 63 that could be verified as unique within this group (i.e., they do not appear in other primates). Of these features, the analysis found that humans shared 28 unique physical characteristics with orangutans, compared to only two features with chimpanzees, seven with gorillas, and seven with all three apes (chimpanzees, gorillas, and orangutans). Gorillas and chimpanzees shared 11 unique characteristics.
Schwartz and Grehan then examined 56 features uniquely shared among modern humans, fossil hominids—ancestral humans such as Australopithecus—and fossil apes. They found that orangutans shared eight features with early humans and Australopithecus and seven with Australopithecus alone. The occurrence of orangutan features in Australopithecus contradicts the expectation generated by DNA analysis that ancestral humans should have chimpanzee similarities, Schwartz and Grehan write. Chimpanzees and gorillas were found to share only those features found in all great apes.
Schwartz and Grehan pooled humans, orangutans, and the fossil apes into a new group called "dental hominoids," named for their similarly thick-enameled teeth. They labeled chimpanzees and gorillas as African apes and wrote in Biogeography that although they are a sister group of dental hominoids, "the African apes are not only less closely related to humans than are orangutans, but also less closely related to humans than are many" fossil apes.
The researchers acknowledge, however, that early human and ape fossils are largely found in Africa, whereas modern orangutans are found in Southeast Asia. To account for the separation, they propose that the last common human-orangutan ancestor migrated between Africa, Europe, and Asia at some point that ended at least 12 million to 13 million years ago. Plant fossils suggest that forests once extended from southern Europe, through Central Asia, and into China prior to the formation of the Himalayas, Schwartz and Grehan write, proposing that the ancestral dental hominoid lived and roamed throughout this vast area; as the Earth's surface and local ecosystems changed, descendant dental hominoids became geographically isolated from one another.
Schwartz and Grehan compare this theory of ancestral distribution with one designed to accommodate a presumed human-chimpanzee relationship. They write that in the absence of African ape fossils more than 500,000 years old, a series of "complicated and convoluted" scenarios were invented to suggest that African apes had descended from earlier apes that migrated from Africa to Europe. According to these scenarios, European apes then diverged into apes that moved on to Asia and into apes that returned to Africa to later become humans and modern apes. Schwartz and Grehan challenge these theories as incompatible with the morphological and biogeographic evidence.
Paleoanthropologist Peter Andrews, a past head of Human Origins at the London Natural History Museum and coauthor of "The Complete World of Human Evolution" (Thames & Hudson, 2005), said that Schwartz and Grehan provide good evidence to support their theory. Andrews had no part in the research, but is familiar with it.
"They have good morphological evidence in support of their interpretation, so that it must be taken seriously, and if it reopens the debate between molecular biologists and morphologists, so much the better," Andrews said. "They are going against accepted interpretations of human and ape relationships, and there's no doubt their conclusions will be challenged. But I hope it will be done in a constructive way, for science progresses by asking questions and testing results."
Schwartz and Grehan contend in the Journal of Biogeography that the clear physical similarities between humans and orangutans have long been overshadowed by molecular analyses that link humans to chimpanzees, but that those molecular comparisons are often flawed: There is no theory holding that molecular similarity necessarily implies an evolutionary relationship; molecular studies often exclude orangutans and focus on a limited selection of primates without an adequate "outgroup" for comparison; and molecular data that contradict the idea that genetic similarity denotes relation are often dismissed.
"They criticize molecular data where criticism is due," said Malte Ebach, a researcher at Arizona State University's International Institute for Species Exploration who also was not involved in the project but is familiar with it.
"Palaeoanthropology is based solely on morphology, and there is no scientific justification to favor DNA over morphological data. Yet the human-chimp relationship, generated by molecular data, has been accepted without any scrutiny. Grehan and Schwartz are not just suggesting an orangutan–human relationship—they're reaffirming an established scientific practice of questioning data."
Journal reference:
John R. Grehan1 and Jeffrey H. Schwartz. Evolution of the second orangutan: phylogeny and biogeography of hominid origins. Journal of Biogeography, 2009 DOI: 10.1111/j.1365-2699.2009.02141.x
Adapted from materials provided by University of Pittsburgh.

Friday, June 12, 2009

Biologist Discovers Pink-winged Moth In Chiracahua Mountains

SOURCE

ScienceDaily (June 12, 2009) — University of Arizona biologist Bruce Walsh has identified a new species of moth in southern Arizona. Normally, this is not a big deal. The region is one of the most biologically rich areas in the country and collectors have been finding hundreds of new species for decades. This one, however, is different.
Walsh is a professor of ecology and evolutionary biology and a member of the UA's BIO5 Institute. He is best known in the science community as an authority on plant and animal breeding, having written one of the leading textbooks on the subject.
His work also spans several departments and programs, including statistics, applied math, insect science and genetics. He also teaching biostatistics in the UA Zuckerman College of Public Health and has worked with trial attorneys on interpreting DNA evidence. Collecting moths is a hobby.
His new discovery is Lithophane leeae. Walsh found it in the Chiracahua mountains east of Tucson, and reported it in the journal Zoo Keys.
Lithophane moths are members of the noctuid family, which often are dull colored. Walsh's moth, in contrast, is bright pink. He also named it after his wife, Lee, who has an affinity for the color.
Walsh discovered L. leeae while collecting one evening at Onion Saddle, at about 7,700 feet in the Chiracahuas. Collecting involves illuminating a sheet with mercury vapor lamps. Moths are attracted by the lights and will land on the sheet.
"This large moth flew in and we didn't think much of it because there is a silk moth very much like it, a Doris silk moth that feeds on pines that has dark wings with pink on the hind wings. It's fairly common there."
On closer inspection, though, the moth, a female, appeared to be an entirely different species from an entirely different family. Walsh said it currently is the only known individual.
Scientists are generally reluctant to identify a new species based on one individual, but L. leeae appears so distinct from others that Walsh said it is highly unlikely that it is an aberration of an existing species. A DNA barcode later confirmed it as a distinct species.
Walsh said he is confident there are bound to be more. "If this thing is flying at the top of the Chiracahuas, it's probably pretty common," he said.
Finding it is another matter because moths like Lithophane tend to over-winter at higher elevations, hibernating when there is snow on the ground and flying off at the first signs of spring. Walsh said bats are the primary predators of moths, and so if the insects can make it through the winter, when bats hibernate, they will likely do well as the weather gets warmer.
As to why L. leeae hasn't been found before, Walsh theorized that his specimen simply emerged late from hibernation when it was caught. Another theory is that it could be a stray from another mountain range in the region. He said there are a number of species that fly early in the summer and are rare in collections and not often seen in most years.
"We can now add L. leeae to this group of large, but quite elusive, species," he said.
Adapted from materials provided by University of Arizona.

Sunday, May 10, 2009

Communal Stomach Of An Ant Colony

SOURCE

ScienceDaily (May 11, 2009) — How do ant colonies manage the nutrients in their food? Audrey Dussutour from the Centre de recherche sur la cognition animale (CNRS/Université Paul Sabatier) and Steve Simpson from Sydney University have shown that an ant colony functions like a “collective mouth and gut”. The members of a colony are capable of dealing with the nutritional needs of their social structure by sharing tasks (foraging, digestion and excretion).
In an ants' nest, food is brought home by only 10% of the colony members - the foragers. This food is then regurgitated and shared among all the ants in the colony. Nutritional needs differ, however, between the young (larvae) and adults of the colony.
Audrey Dussutour and Steve Simpson have recently shown that the larvae, which cannot move or leave the nest, are capable of communicating their nutritional needs to forager ants, who adapt their gathering strategy accordingly. These researchers provided sugar- or protein-rich foods for ant colonies with and without larvae, and observed that ant behaviour differed. When a colony had larvae, high protein foods were preferentially gathered that could sustain larval growth. Inversely, when there were no larvae, the ants preferentially gathered sugar-rich foods.
In a second experiment, the researchers showed that sugar is the key nutrient regulating gathering in ants. Provided with a range of food containing varying proportions of protein and sugar, foragers are capable of harvesting the same quantity of sugar. These researchers also observed that when the food was rich in protein and poor in sugar, the excess of proteins was ejected from the nest. Ants are therefore capable of extracting sugar from food and regurgitating protein in the form of waste pellets.
However, despite this food manipulation, the colonies reared with protein-rich food had extremely high mortality due to protein toxicity and suffered losses of up to 75%. In comparison, the ant colonies reared on food of lower protein content lost less than 5% of their numbers.
The scientists noticed that the mortality was lower in colonies with larvae. They demonstrated that the ants in these colonies managed to partially escape the toxic effects of proteins by giving the work of nutrient processing to the larvae, which are better equipped for protein digestion. The researchers also confirmed the highly toxic effect of protein-rich food on ants, as they had previously demonstrated in fruit flies.
Journal reference:
Dussutour et al. Communal Nutrition in Ants. Current Biology, May 12, 2009; DOI: 10.1016/j.cub.2009.03.015
Adapted from materials provided by CNRS.

Monday, September 3, 2007

Male Deer Are Born To Live Fast, Die Young


Source:

Science Daily — In the September issue of The American Naturalist, Juan Carranza (Biology and Ethology Unit, University of Extremadura, Spain) and Javier Pérez-Barbería (Macaulay Institute, United Kingdom) offer a new explanation for why males of ungulate species subjected to intense competition are born with lower survival expectancies than females.
The research reveals that male ungulates have smaller molars relative to their body size -- and hence less durable teeth that will wear out sooner, which might contribute to their shorter lives compared with females.
Natural selection favors reproduction rather than survival; the cost of reproduction compromises survival. Males of species subjected to intense male-male competition for access to females are known to have shorter life expectancies than females. Earlier aging in males might be related to higher reproductive costs, especially when lifetime reproductive success in males takes place within the few years when they can win contests and maintain their dominance.
By comparing body and dental size of males and females of 123 species of ungulates, the authors offer another compelling explanation for why male ungulates lead shorter lives. They estimated the pattern of change of these traits along the evolutionary development of the group and found that for species where a single male has many females and where the males and females are different sizes, the rate of increase of dental size was lower than that of body size.
As a result, smaller teeth (in comparison to body size) are produced in males. It is possible that natural selection did not produce larger, more durable teeth because there was no reproductive return from it, since males in these species do not generally increase their success by living longer after prime age.
"These findings," the authors state, "provide us with interesting insights into how natural and sexual selection design our bodies and their longevity."
Reference: Juan Carranza and F. Javier Pérez-Barbería, "Sexual selection and senescence: male size-dimorphic ungulates evolved relatively smaller molars than females", The American Naturalist (2007) volume 170:370--380. DOI: 10.1086/519852
Note: This story has been adapted from a news release issued by University of Chicago Press Journals.

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