Biomedical subjects

Graham Bell

Publications and source records attributed to Graham Bell.

7 recordsLinked to original sources

PubMed2003

Divergent evolution during an experimental adaptive radiation.

How repeatable a process is evolution? Comparative studies of multicellular eukaryotes and experimental studies with unicellular prokaryotes document the repeated evolution of adaptive phenotypes during similar adaptive radiations, suggesting that the outcome of adaptive radiation is broadly reproducible. The goal of this study was to test this hypothesis by using phenotypic traits to infer the genetic basis of adaptation to simple carbon-limited environments in an extensive adaptive radiation. We used a clone of the bacterium Pseudomonas fluorescens to found two sets of experimental lines. The first set of lines was allowed to adapt to one of 23 novel environments for 1100 generations while the second set of lines was allowed to accumulate mutations by drift for 2000 generations. All lines were then assayed in the 95 environments provided by Biolog microplates to determine the phenotypic consequences of selection and drift. Replicate selection lines propagated in a common environment evolved similar adaptive components of their phenotype but showed extensive variation in non-adaptive phenotypic traits. This variation in non-adaptive phenotypic traits primarily resulted from the ascendance of different beneficial mutations in different lines. We argue that these results reconcile experimental and comparative approaches to studying adaptation by demonstrating that the convergent phenotypic evolution that occurs during adaptive radiation may be associated with radically different sets of beneficial mutations.

Adaptation, Biological↗

PubMed2003

Arming the enemy: the evolution of resistance to self-proteins.

A remarkable range of novel antibiotics is attracting increasing interest as a major new weapon in the campaign against bacterial infection. They are based on the toxic peptides that provide the innate immune system of animals, and it is claimed that bacteria will be unable to evolve resistance to them because they attack the 'Achilles' heel' of bacterial membrane structure. Both experimental evidence and theoretical arguments suggest that this claim is doubtful. If so, the introduction of these substances into general use may provoke the evolution of resistance to our own defence proteins and thus compromise our natural defences against infection.

Animals↗

PubMed2003

An experimental test of local adaptation in soil bacteria.

We extracted bacterial isolates of similar colony morphology from spatially located soil samples within 1 ha of old-growth forest. The same soil samples were used to prepare growth medium. Each isolate was then cultured in each medium and its growth recorded. There was no overall tendency for isolates to grow more successfully in their home site (i.e., the medium derived from the soil sample from which they had been extracted). Most isolates grew very poorly, however, and when the analysis was restricted to the minority of vigorous isolates there was clear evidence of local adaptation: isolates tended to grow better at their home site than did isolates from elsewhere and grew better at their home site than they did at other sites. The variation of growth within the 1-ha plot made up a complex fitness landscape of peaks, ridges, and valleys. Most of the vigorous isolates were found at or near a local fitness (growth) peak, although seldom at a global peak. In consequence, there was a tendency for growth to diminish away from the home site. The home isolate was about 50% more fit than average at its home site; fitness diminished exponentially away from the home site at a rate of 0.0577 per meter. These figures are similar to those previously reported for plants. This selection gradient has matched the bacterial assemblage to the edaphic structure of the environment, although the fit is far from perfect.

Adaptation, Physiological↗

PubMed2002

The ecology and genetics of fitness in Chlamydomonas. XII. Repeated sexual episodes increase rates of adaptation to novel environments.

We investigated the dynamics of adaptation of the unicellular chlorophyte Chlamydomonas reinhardtii to new and hostile conditions of growth provided by novel carbon substrates in the dark. The experiment was designed to contrast perennially asexual lines with lines that had experienced one or more sexual episodes. All lines were capable of adapting to the novel environment. The sexual lines, however, showed greater adaptation over the course of the experiment, especially in more complex environments. Moreover, the effect of sex on adaptation increased with the number of successive sexual episodes. The time-course of adaptation showed that sex initially caused an increase in the standardized variance of fitness and an initial drop in mean fitness, at least after a second or third sexual episode. These short-term effects were followed by a period of recovery during which the fitness of sexual lines eventually exceeded that of asexual lines. The increase in mean fitness was mirrored by a decrease in the standardized variance of fitness relative to asexuals, suggesting that directional selection used up the variation generated by meiotic recombination and thereby conferred a fitness advantage to the sexual lines. These results support the Weismann-Fisher-Muller hypothesis for the maintenance of sex in natural populations.

Adaptation, Physiological↗

PubMed2002

The ecology and genetics of fitness in Chlamydomonas. VIII. The dynamics of adaptation to novel environments after a single episode of sex.

According to classical evolutionary theory, sexual recombination can generate the variation necessary to adapt to changing environments and thereby confer an evolutionary advantage of sexual over asexual reproduction. Using the green alga, Chlamydomonas reinhardtii, we investigated the effect of a single sexual episode on adaptation of heterotrophic growth on different carbon sources. In an initial mixture of isolates, sex was induced and the resulting offspring constituted the sexual populations, along with any unmated vegetative cells; the unmated mixture of isolates represented the asexual populations. Mean and variance in division rates (i.e., fitness) were measured four times during approximately 50 generations of vegetative growth in the dark on all possible combinations of four carbon sources. Consistent with effects of recombination of epistatic genes in linkage disequilibrium, sexual populations initially had a higher variance in fitness, but their mean fitness was lower than that of asexual populations, possibly due to recombinational load. Subsequently, fitness of sexual populations exceeded that of asexual ones, but finally they regained parity in both mean and variance of fitness. Although recombination was not more effective on more complex substrates, these results generally support the idea that sex can accelerate adaptation to novel environments.

Adaptation, Physiological↗

PubMed2000

The Distribution of Abundance in Neutral Communities.

The patterns of abundance generated by a simple stochastic birth-death-immigration model are described in order to characterize the diversity of neutral communities of ecologically equivalent species. Diversity is described by species number S and the variance of frequency or log abundance q∼. The frequency distribution of abundance is very generally lognormal, skewed to the left by immigration and resembling descriptions of natural communities. Increased immigration and community size always cause S to increase. Their effect on q∼ is more complicated, but given biologically reasonable assumptions, S and q∼ will be positively correlated in most circumstances. Larger samples contain more species; the graph of log S on log individuals, equivalent to a species-area curve, is generally convex upward but becomes linear with a slope of about +0.25 when immigration is low and births exceed deaths. When individuals invade a new, vacant environment, both S and q∼ increase through time. Thus, a positive correlation between S and q∼ will usually be generated when sites of differing size or age are surveyed. At equilibrium, communities maintain roughly constant levels of S and q∼ but change in composition through time; composition may remain similar, however, for many generations. Many prominent patterns observed in natural communities can therefore be generated by a strictly neutral model. This does not show that community structure is determined exclusively by demographic stochasticity, but rather demonstrates the necessity for an appropriate null model when functional hypotheses are being tested.

abundance↗

PubMedDate not supplied

Macroevolution simulated with autonomously replicating computer programs.

The process of adaptation occurs on two timescales. In the short term, natural selection merely sorts the variation already present in a population, whereas in the longer term genotypes quite different from any that were initially present evolve through the cumulation of new mutations. The first process is described by the mathematical theory of population genetics. However, this theory begins by defining a fixed set of genotypes and cannot provide a satisfactory analysis of the second process because it does not permit any genuinely new type to arise. The evolutionary outcome of selection acting on novel variation arising over long periods is therefore difficult to predict. The classical problem of this kind is whether 'replaying the tape of life' would invariably lead to the familiar organisms of the modern biota. Here we study the long-term behaviour of populations of autonomously replicating computer programs and find that the same type, introduced into the same simple environment, evolves on any given occasion along a unique trajectory towards one of many well-adapted end points.

Adaptation, Biological↗