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The paper examines the consequences of reliability adaptation which is considered as a preadaptation to enhanced cognitive powers of Homo sapiens. At the same time it is an answer to Eckhardt's (1987) critique of the reliability adaptation.
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The capacity for spoken language in the human is a genetic trait, but the information communicated by this means is to a large extent culturally determined. Using a gene-culture coevolutionary approach, we model the hypothesis that speech evolved as a channel for the communication of adaptive cultural traits from parent to offspring. The motivation for this paper is a condition obtained previously that initial increase of communication would require at least a two-fold advantage for the transmitted trait. Here, we show that under reasonable assumptions the invasion condition becomes less stringent. In Model 1, we assume that two adaptive cultural traits can be transmitted. A gene which permits communication of the second adaptive trait. In Model 2, we assume that a related function such as greater memory capacity is a prerequisite for speech, and that this function confers an advantage independent of its association with speech. In both models we assume haploid sexual genetics and a simple scheme of vertical transmission. The stability properties of all corner and edge equilibria of the models are analyzed. The two models taken together suggest a possible scenario for the initial stages of the evolution of speech.
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Explore the source record for details and available documents.
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Dark adaptation curves were determined for an amblyopic and a normal control subject following a variety of preadaptation conditions. Sizable between-eye differences were found in the dark adaptation functions of only the amblyope; the magnitude of such differences varied with this subject's distance from the light preadapting screen and with the effective size of his pupils during the light preadaptation period. Marked differences were also found between the dark adaptation functions of both eyes of the amblyopic subject and those of the normal subject. The preadaptation-dependent changes in the dark adaptation function of the amblyopic subject are hypothesized to result from anomalies of amblyopic eye light adaptation which are referable to disturbances of retinal receptor alignment.
The mutual adjustment of glucose uptake and metabolism in the insect stage of the protozoan parasite Trypanosoma brucei was studied. T. brucei was preadapted in the chemostat to conditions in which either glucose or proline served as the major carbon and energy source. Cells were grown and adapted to either energy or non-energy limitation at a low dilution rate (0.5 day-1) or a high dilution rate (1 day-1). The cells were then used in short- to medium-term uptake experiments with D-[14C]glucose as a tracer. In time course experiments a steady state was reached after 15 min regardless of the preadaptation conditions. This steady-state level increased with increasing glucose availability during preadaptation. The rate of glucose uptake and the hexokinase activity were linearly correlated. In short-term 5- to 90-s) uptake experiments a high transport rate was measured with cultures grown in excess glucose, an intermediate rate was measured with proline-grown cultures, and a low rate was measured in organisms grown under glucose limitation. Glucose metabolism and proline metabolism did not affect each other during the 15-min incubations. Glucose uptake, as a function of the external glucose concentration, did not obey simple Michaelis-Menten kinetics but could be described by a two-step mechanism: (i) transport of glucose by facilitated diffusion and (ii) subsequent metabolism of glucose. The respective rates of the two steps were adjusted to each other. It is concluded that T. brucei is capable of adjusting the different metabolic processes in a way that gives maximum energy efficiency at the cost of short-term flexibility.
Among extant taxa it appears that cyclic parthenogenesis has evolved on fewer than ten occasions. Evidence suggests that these groups are all derived from bisexual ancestors with genetic systems possessing specific preadaptations for the breeding system shift. Its apparently independent origin in two cecidomyiid lineages suggests that, when such preadaptations exist, the adoption of cyclic parthenogenesis may be a highly probable event. The genetic consequences of this transition are not dramatic; the genotypic characteristics of most cyclic parthenogens are similar to those of bisexuals. Specifically, genotypic frequencies at polymorphic loci are generally in Hardy-Weinberg equilibrium and linkage disequilibrium between variants at different loci is rare. Levels of variation in local populations of cyclic parthenogens are lower than those typical of sexual outcrossers, but the lack of variation appears to be a consequence of founder effects, as regional gene pool diversity is not similarly impoverished. An unusual genotypic structure occasionally develops in populations from habitats in which sustained parthenogenetic reproduction is possible and sexual recruitment is low. Under these circumstances low fitness genotypes are winnowed from the population by natural selection. The truncation of genotypic diversity often produces Hardy-Weinberg deviations and linkage disequilibrium. The depletion of clonal diversity rarely leads to the domination of a habitat by a single clone; an array of ecologically diversified clonal variants remains. The level of clonal variation in such populations is occasionally augmented by sexual recruitment, but the persistence of clonal diversity in local populations of obligate parthenogens makes it clear that clonal coexistence is not a consequence of such recruitment. Cyclic parthenogens have made the transition to obligate asexuality with high frequency, but there is little evidence to support the argument (Williams, 1975) that such shifts result from the relaxation of the short-term selection pressures supposedly necessary to sustain the sexual phase of the life cycle. Maynard Smith (1978) has recognized that in groups such as the aphids, which have never evolved the ability to produce their diapausing eggs asexually, sexuality may simply be retained as a consequence of its role in the formation of these eggs. However, he accepted that short-term selection was required to maintain sexuality in groups such as the cladocerans in which asexual forms have demonstrated their ability to retain life cycle complexity.(ABSTRACT TRUNCATED AT 400 WORDS)
The electro-oculogram is variable as a clinical test, but the recording technique has not been standardized, and differences in the protocols for adaptation and stimulation among laboratories may contribute to the variability. To analyze some of these factors, we performed more than 100 electro-oculograms on a single subject under different conditions. Both the Arden ratio and the ratio of light peak amplitude to a stable dark-adapted baseline were independent of pupillary dilation but linearly related to retinal illumination measured in trolands. Between 3.0 and 4.0 log trolands, the values began to level off, but they were difficult to interpret because of subject discomfort above 3.5 log trolands. The Arden ratios were influenced by preadaptation light levels and were roughly 20% higher above 90 cd/m2 than below 45 cd/m2. There was a circadian rhythm in dark trough, baseline and light peak values, but the composite Arden ratio and light peak/baseline ratio showed little circadian effect. The light peak/baseline ratios were slightly more stable than the Arden ratios; the variability (defined as [standard deviation x 100]/mean) was 6.6% and 12.5%, respectively. Our results suggest that stimulus intensities for clinical electro-oculographic testing should be between 3.0 and 3.5 log trolands; pupil dilation is optional. This translates into light levels of 141-447 cd/m2 for a 3-mm pupil and 20-63 cd/m2 for an 8-mm pupil. The reduction in variability and independence from preadaptation achieved by using the light peak/baseline ratio instead of the Arden ratio must be weighed against the time required to achieve a stable dark baseline.
A comparative study has been performed on test methods for assessing the biodegradability of chemicals in seawater environments. A simple shake flask die-away test with natural seawater and 14C-labeled chemicals added in microgram/liter concentrations is proposed as a "simulation" test. The analytical parameter used in this test is residual dissolved 14C activity. The performance of the simulation test has been compared with the performance of similar screening tests with dissolved organic carbon analysis and test compounds added in mg/liter concentrations to nutrient-enriched seawater. All chemicals investigated that passed the screening tests were also degradable in the simulation test and some results with simulation tests were positive; even screening tests were negative, while some compounds, including maleinhydrazide, known to be degradable in soil, remained undegraded in either type of test. Disappearance times after the ended lag time were smaller in screening tests than in simulation tests, but the rates of biodegradation cannot be meaningfully compared, as zero-order kinetics in combination with an exponentially growing population of degraders prevail in screening tests, while first-order kinetics and frequently a constant activity of degraders (cooxidation) prevail in simulation tests where the test material is a secondary substrate only. In screening tests, lag times are sometimes excessively long and highly variable. Whether the lag times could be decreased and their variability narrowed by supplementation with a cosubstrate (yeast extract) or by inoculation with seawater that had been preadapted to the test material was investigated. In most experiments such test modifications had no significant effect but in one experiment with 4-nitrophenol, inoculation with 1% preadapted seawater decreased the lag phase from greater than 35 to 9 days.
Adaptation to convergence-altering prism spectacles was studied. The subjects were trained for 8 min with either convergence-increasing or convergence-decreasing prisms. Before and after training they estimated the distance to a binocular dot varying in the stimulus it provided to convergence. Both the preadaptation and postadaptation estimates showed that the reciprocal of estimated target distance is linearly related to convergence. Further there was a consistent change in the direction of adaptation expected from the preadaptation to the postadaptation test. This change was accounted for in terms of a recalibration of the effective absolute convergence level.