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Michael R. Rose | |
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Born | 25 July 1955 |
Occupation | Evolutionary biologist |
Michael R. Rose (born 25 July 1955) is a Professor in the Department of Ecology and Evolutionary Biology at the University of California, Irvine.
Michael Roberson Rose was born on July 25, 1955. He obtained his B.S. in 1975 from Queen's University, Kingston, Ontario, Canada. In 1976 he obtained his M.S.. In 1978 he obtained his Ph.D from the University of Sussex. [1]
His Ph.D. advisor was Brian Charlesworth. His main area of work has been the evolution of aging, approached both theoretically and empirically via the technique of experimental evolution. In 1991, he published Evolutionary Biology of Aging exploring a view of the subject based on antagonistic pleiotropy, the hypothesis that aging is caused by genes that have two effects, one acting early in life and the other much later. The genes are favored by natural selection as a result of their early-life benefits, and the costs that accrue much later appear as incidental side-effects that we identify as aging. Dr. Rose has also suggested that aging can stop in a latter stage of life. The field of aging biology is divided between those who think that it will be very difficult to develop technology to postpone human aging and those who expect breakthroughs in this field in the near future. Rose is an outspoken advocate for the former position.
The phenomenon was first described by George C. Williams in 1957, but it was Rose who coined the phrase "antagonistic pleiotropy". Rose's laboratory has conducted the longest-running experimental evolution experiment designed to test the theory of antagonistic pleiotropy. Fruit flies (Drosophila melanogaster) are being bred for longevity by collecting eggs from the longest-lived flies in each generation. The experiment has run since 1981, and has produced flies with quadruple the original life span[ citation needed ]. The prediction of the antagonistic pleiotropy hypothesis was that these long-lived flies would have much lower fertility early in life. The result has been the opposite - that the long-lived flies actually lay more eggs at every stage of life. Rose explains this result in terms of an interaction between genotype and environment. The long-lived flies show other weaknesses that would make them poor competitors in the wild, and perhaps these traits are the true areas of antagonistic pleiotropy. He is one of the biologists featured in the 1995 science documentary Death by Design/The Life and Times of Life and Times. In 1997, Rose was awarded the Busse Research Prize by the World Congress of Gerontology. He has authored The Long Tomorrow: How Advances in Evolutionary Biology Can Help Us Postpone Aging.
If the effect on fitness of increase in mortality is zero, as is the case after the age when survival affects reproduction, then natural selection does not weed out the tendency for rates of mortality to accelerate with age. The idea that selection for reproduction in youth causes accumulating dysfunction in later adulthood is a commonly accepted explanation for aging. Protagonistic pleiotropy is the opposite effect: beneficial effects in later life as a result of selection for reproduction in earlier life. Rose contends that a correct understanding of Hamilton's equations through mathematical modeling show that protagonistic pleiotropy is plausible. [2]
Rose's most recent book is Does Aging Stop?. [2] W. D. Hamilton advanced the idea that any gene killing an organism before it reproduced would be weeded out by natural selection. However, genes that kill later in life, after reproduction ceases, can remain in the population. For Rose, this suggests that aging is a result of "declining forces of natural selection." He points to studies of the demographic data in large-scale fruit fly experiments and actuarial data for humans which he believes support the hypothesis that acceleration in death rates can halt in later life. According to Rose, mortality-rate plateaus have not often been noticed in humans because they are only seen in specific-age cohorts of the very old. His proposed explanation is that at a stage of life beyond the potential to reproduce, the effect of natural selection is no longer falling as it has 'bottomed out'. Rose suggests that if a decline in the effect of natural selection is responsible for aging, then when this decline finally ends, at post-reproductive age, aging could halt. He reasons it follows that aging is "not a cumulative process of progressive chemical damage, like rust, at late ages, aging can stop". [2]
According to Rose, relative to the age of reproductive maturity a transition to the late-life stage of life occurs much later in humans than in the populations of flies for which there are data. In humans, the 'late-life' stage of life is only reached at 90 years old, whereas the data for flies scaled to humans would predict a 'late-life' stage for humans at 40–50 years old. Rose suggests that human populations' adoption of agriculture led to more children surviving to adulthood, and to reproduction occurring later in life. Agriculture is also hypothesized by Rose to have resulted in high population density, thereby increasing the range of ages not under selection. [2]
British Commonwealth Scholar, 1976–79; NATO Science Fellow, 1979-1981, NSERC of Canada University Research Fellow, 1981–88; President's Prize, American Society of Naturalists, 1992; Excellence in Teaching Award, University of California, Irvine Biological Sciences, 1996; Busse Prize, World Congress of Gerontology, 1997.
Senescence or biologicalaging is the gradual deterioration of functional characteristics in living organisms. The word senescence can refer to either cellular senescence or to senescence of the whole organism. Organismal senescence involves an increase in death rates and/or a decrease in fecundity with increasing age, at least in the latter part of an organism's life cycle.
George Christopher Williams was an American evolutionary biologist.
Sexual reproduction is an adaptive feature which is common to almost all multicellular organisms and various unicellular organisms, with some organisms being incapable of asexual reproduction. Currently the adaptive advantage of sexual reproduction is widely regarded as a major unsolved problem in biology. As discussed below, one prominent theory is that sex evolved as an efficient mechanism for producing variation, and this had the advantage of enabling organisms to adapt to changing environments. Another prominent theory, also discussed below, is that a primary advantage of outcrossing sex is the masking of the expression of deleterious mutations. Additional theories concerning the adaptive advantage of sex are also discussed below. Sex does, however, come with a cost. In reproducing asexually, no time nor energy needs to be expended in choosing a mate. And if the environment has not changed, then there may be little reason for variation, as the organism may already be well adapted. Sex also halves the amount of offspring a given population is able to produce. Sex, however, has evolved as the most prolific means of species branching into the tree of life. Diversification into the phylogenetic tree happens much more rapidly via sexual reproduction than it does by way of asexual reproduction.
Experimental evolution is the use of laboratory experiments or controlled field manipulations to explore evolutionary dynamics. Evolution may be observed in the laboratory as individuals/populations adapt to new environmental conditions by natural selection.
Reproductive success is an individual's production of offspring per breeding event or lifetime. This is not limited by the number of offspring produced by one individual, but also the reproductive success of these offspring themselves.
Pleiotropy occurs when one gene influences two or more seemingly unrelated phenotypic traits. Such a gene that exhibits multiple phenotypic expression is called a pleiotropic gene. Mutation in a pleiotropic gene may have an effect on several traits simultaneously, due to the gene coding for a product used by a myriad of cells or different targets that have the same signaling function.
The grandmother hypothesis is a hypothesis to explain the existence of menopause in human life history by identifying the adaptive value of extended kin networking. It builds on the previously postulated "mother hypothesis" which states that as mothers age, the costs of reproducing become greater, and energy devoted to those activities would be better spent helping her offspring in their reproductive efforts. It suggests that by redirecting their energy onto those of their offspring, grandmothers can better ensure the survival of their genes through younger generations. By providing sustenance and support to their kin, grandmothers not only ensure that their genetic interests are met, but they also enhance their social networks which could translate into better immediate resource acquisition. This effect could extend past kin into larger community networks and benefit wider group fitness.
The age of onset is the age at which an individual acquires, develops, or first experiences a condition or symptoms of a disease or disorder. For instance, the general age of onset for the spinal disease scoliosis is "10-15 years old," meaning that most people develop scoliosis when they are of an age between ten and fifteen years.
Life history theory is an analytical framework designed to study the diversity of life history strategies used by different organisms throughout the world, as well as the causes and results of the variation in their life cycles. It is a theory of biological evolution that seeks to explain aspects of organisms' anatomy and behavior by reference to the way that their life histories—including their reproductive development and behaviors, post-reproductive behaviors, and lifespan —have been shaped by natural selection. A life history strategy is the "age- and stage-specific patterns" and timing of events that make up an organism's life, such as birth, weaning, maturation, death, etc. These events, notably juvenile development, age of sexual maturity, first reproduction, number of offspring and level of parental investment, senescence and death, depend on the physical and ecological environment of the organism.
Optimal virulence is a concept relating to the ecology of hosts and parasites. One definition of virulence is the host's parasite-induced loss of fitness. The parasite's fitness is determined by its success in transmitting offspring to other hosts. For about 100 years, the consensus was that virulence decreased and parasitic relationships evolved toward symbiosis. This was even called the law of declining virulence despite being a hypothesis, not even a theory. It has been challenged since the 1980s and has been disproved.
Modularity refers to the ability of a system to organize discrete, individual units that can overall increase the efficiency of network activity and, in a biological sense, facilitates selective forces upon the network. Modularity is observed in all model systems, and can be studied at nearly every scale of biological organization, from molecular interactions all the way up to the whole organism.
Enquiry into the evolution of ageing, or aging, aims to explain why a detrimental process such as ageing would evolve, and why there is so much variability in the lifespans of organisms. The classical theories of evolution suggest that environmental factors, such as predation, accidents, disease, starvation, ensure that most organisms living in natural settings will not live until old age, and so there will be very little pressure to conserve genetic changes that increase longevity. Natural selection will instead strongly favor genes which ensure early maturation and rapid reproduction, and the selection for genetic traits which promote molecular and cellular self-maintenance will decline with age for most organisms.
The Red Queen hypothesis is a hypothesis in evolutionary biology proposed in 1973, that species must constantly adapt, evolve, and proliferate in order to survive while pitted against ever-evolving opposing species. The hypothesis was intended to explain the constant (age-independent) extinction probability as observed in the paleontological record caused by co-evolution between competing species; however, it has also been suggested that the Red Queen hypothesis explains the advantage of sexual reproduction at the level of individuals, and the positive correlation between speciation and extinction rates in most higher taxa.
The antagonistic pleiotropy hypothesis was first proposed by George C. Williams in 1957 as an evolutionary explanation for senescence. Pleiotropy is the phenomenon where one gene controls for more than one phenotypic trait in an organism. Antagonistic pleiotropy is when one gene controls for more than one trait, where at least one of these traits is beneficial to the organism's fitness early on in life and at least one is detrimental to the organism's fitness later on due to a decline in the force of natural selection. The theme of G.C. William's idea about antagonistic pleiotropy was that if a gene caused both increased reproduction in early life and aging in later life, then senescence would be adaptive in evolution. For example, one study suggests that since follicular depletion in human females causes both more regular cycles in early life and loss of fertility later in life through menopause, it can be selected for by having its early benefits outweigh its late costs.
Evolutionary thought, the recognition that species change over time and the perceived understanding of how such processes work, has roots in antiquity—in the ideas of the ancient Greeks, Romans, Chinese, Church Fathers as well as in medieval Islamic science. With the beginnings of modern biological taxonomy in the late 17th century, two opposed ideas influenced Western biological thinking: essentialism, the belief that every species has essential characteristics that are unalterable, a concept which had developed from medieval Aristotelian metaphysics, and that fit well with natural theology; and the development of the new anti-Aristotelian approach to modern science: as the Enlightenment progressed, evolutionary cosmology and the mechanical philosophy spread from the physical sciences to natural history. Naturalists began to focus on the variability of species; the emergence of palaeontology with the concept of extinction further undermined static views of nature. In the early 19th century prior to Darwinism, Jean-Baptiste Lamarck (1744–1829) proposed his theory of the transmutation of species, the first fully formed theory of evolution.
Host–parasite coevolution is a special case of coevolution, where a host and a parasite continually adapt to each other. This can create an evolutionary arms race between them. A more benign possibility is of an evolutionary trade-off between transmission and virulence in the parasite, as if it kills its host too quickly, the parasite will not be able to reproduce either. Another theory, the Red Queen hypothesis, proposes that since both host and parasite have to keep on evolving to keep up with each other, and since sexual reproduction continually creates new combinations of genes, parasitism favours sexual reproduction in the host.
The theoretical foundations of evolutionary psychology are the general and specific scientific theories that explain the ultimate origins of psychological traits in terms of evolution. These theories originated with Charles Darwin's work, including his speculations about the evolutionary origins of social instincts in humans. Modern evolutionary psychology, however, is possible only because of advances in evolutionary theory in the 20th century.
The following outline is provided as an overview of and topical guide to evolution:
Extrinsic mortality is the sum of the effects of external factors, such as predation, starvation and other environmental factors not under control of the individual that cause death. This is opposed to intrinsic mortality, which is the sum of the effects of internal factors contributing to normal, chronologic aging, such as, for example, mutations due to DNA replication errors, and which determined species maximum lifespan. Extrinsic mortality plays a significant role in evolutionary theories of aging, as well as the discussion of health barriers across socioeconomic borders.
The mutation accumulation theory of ageing was first proposed by Peter Medawar in 1952 as an evolutionary explanation for biological ageing and the associated decline in fitness that accompanies it. Medawar used the term 'senescence' to refer to this process. The theory explains that, in the case where harmful mutations are only expressed later in life, when reproduction has ceased and future survival is increasingly unlikely, then these mutations are likely to be unknowingly passed on to future generations. In this situation the force of natural selection will be weak, and so insufficient to consistently eliminate these mutations. Medawar posited that over time these mutations would accumulate due to genetic drift and lead to the evolution of what is now referred to as ageing.