Influence of light on algal symbionts of the deep water coral Leptoseris fragilis

Photoadaptations of zooxanthellae living within the deep water coral Leptoseris fragilis taken from the Gulf of Aqaba (Red Sea) were studied. Specimens-collected in summer 1988 between 110 and 120 m depth —were transplanted to 70 and 160 m. At each depth individuals were exposed in their natural growth position (oral side facing the surface) or in a reverse growth position (oral side facing the bottom). After 1 yr of exposure the corals were collected and the zooxanthellae were isolated. As a function of the availability of light with depth and growth position several algal parameters showed changes which are related to photoadaptations. The relatively low density of zooxanthellae of 0.15x10⁶ cellsxcm^-2 at a natural growth depth of 116 m decreased to 0.0034x10⁶ cellsxcm^-2 (2%) at 160 m in specimens growing with a natural orientation. In corals with a downward-facing oral surface at the same depth (160 m) only degenerated algae could be observed. With respect to depth dependence the volume of the algae decreased from 728 m³ at 116 m to 406 m³ at a depth of 160 m and the content of pigments increased. The augmentation of peridinin per cell was low (two times at 160 m compared to 116 m). Chlorophyll a and in particular chlorophyll c ₂ concentrations per cell were enhanced. Compared to natural amounts at 116 m, chl a was five times and chl c ₂ eight times higher at 160 m. At all depths the chl c ₂ content per cell was higher than for chl a. The formation of chl a/chl c ₂ complexes as light harvestor is discussed. Light harvesting, with chl c ₂ prevailing may be explained as a special type of chromatic adaptation of L. fragilis in a double sense: (1) in the habitat light short wavelengths predominate. This light can be directly absorbed with pigments such as chl a and chl c ₂. (2) Host pigments absorb visible violet light and transform these wavelengths, less suitable for photosynthesis, into longer ones by means of autofluorescence. The emitted longer wavelengths fit the absorption maxima of the algal pigments. Thus the host supports photosynthesis of his symbionts. Corals exposed at 160 m depth with a downward facing oral surface were alive after 1 yr and the host wavelength transforming pigment system was still present, but zooxanthellae were absent or degenerated. The light field at 160 m seems therefore to be critical: the combined photoadaptations of host and symbionts, allowing photosynthesis under barren light conditions, seem to be exhausted. In L. fragilis the photoadaptive strategies of host and symbionts cooperate harmoniously. In addition, the adaptations are interlocked with the particular light situation of the habitat with respect to light quantity and quality. The cooperation of physical and organismic parameters examplifies how evolution and, in particular, coevolution has led to optimal fitness.     

Field survey of the occurrence and significance of regeneration in Amphiura chiajei (Echinodermata: Ophiuroidea) from Killary Habrour,west coast of Ireland

The boreo-Mediterranean amphiurid Amphiura chiajei Forbes occurs in high numbers (700 individuals/m²) in Killary Harbour, a fjordic inlet on the west coast of Ireland. 99.1% of the adult individuals show signs of arm regeneration, while 0.5% show regeneration of the disc. A study of the phenomenon commenced in November 1987 and continued on a seasonal basis until July 1989. Specimens were collected by SCUBA. The overall mean length of regenerated arm tissue over the 21 mo sampling period was 33.5±6.5 mm. Regeneration points were most common in the proximal and in the distal one-third of each arm. An overall mean of 4.21±0.3 arms per individual showed evidence of regeneration, while biomass assays revealed that regenerated tissue accounted for up to 57.9% of the total body weight. Anthropogenic activity (e.g. bottom trawling) may contribute to regeneration, although sub-lethal predation appears to be the main causitive factor of regeneration. Gut analyses of potential predators at the sampling station revealed that fish species (especially the Pleuronectidae) are particularly implicated. This predation seems to vary seasonally, being greatest in the summer months. Since the larger individuals showed the greatest evidence of arm regeneration, it is assumed that such sub-lethal damage is a persistent experience. Whatever the causality, the population of A. chiajei in Killary Harbour is deemed to be highly resilient.     

Constraints on group size in primates and carnivores: population density and day-range as assays of exploitation competition

Summary We hypothesise that foraging group size (FGS) and population group size (PGS) in primates and carnivores are related to quantifiable variables indexing the intensity of exploitative competition. Group size is predicted to increase with both food density and travel capabilities, as estimated by the constraint-free day-range (DR_s), i.e. the day-range of a solitary individual uninfluenced by competition from conspecifics. We test this exploitation competition hypothesis among primates and carnivores, using data on populations, species and genera. Food density was indexed by population density. Where DR_s could be estimated by regression it was found to be correlated with observed day-range (DR_m). DR_s was therefore indexed by DR_m in all species. Population density and DR_m were associated with each other, but in a multiple regression each variable contributed independently to explaining variation in group size. PGS was predicted better than FGS, but regressions involving either measure of group size were significant in all analyses. The multiple regression analyses were validated by the method of linear contrasts, which accounts for possible lack of independence among taxa. We conclude that species differences in group size are influenced by both food density and DR_s. This suggests that variation in the intensity of exploitation competition is partly responsible for differences in group size.Correspondence to: R.W. Wrangham     

Sex-biased lactational duration in a human population and its reproductive costs

Summary We tested the proposition that among humans (1) differences in lactational duration result in differences in costs of reproduction even under rich nutritional conditions; and (2) elimination of factors postulated to favor male-biased parental care will be reflected in elimination or reversal of sex-biased care. To do so, we examined the relationship between lactational duration and fertility among Hutterites, a communal-living human population in which the levels of nutritional resources and fertility are high, breast-feeding is the norm, contraceptive use is limited and the collective social and economic system results in low resource variance among individuals. We demonstrate that even under good nutritional conditions, duration of nursing was a significant predictor of the length of time to next pregnancy and that nursing continued to suppress fertility after the resumption of menses. Moreover, we find that daughters were nursed longer than sons, leading to a longer interval to next pregnancy. We examine this uncommon, but not unique, finding of female-biased human parental care in the light of Hutterite social structure, and we explore the consistency of this finding with the most applicable models of parental investment. Correspondence to: S.W. Margulis     

Threshold and dose response estimation using the “filter model”

The “filter model” has been developed to explain the biologic effects of radiation and chemicals. We have examined nearly 300 sets of dose response data, of which 50 are presented here. Responses (induced by radiation and chemicals) which have been examined include in vitro survival studies on animal and plant tissues, induction of cellular aberrations and time to tumor or death. Similar data from in vivo studies has also been examined. All of the data appear to fit the model R = a lnD + b(lnD)² + c, where R is the response, a and b are parameters fitted by regression to a particular set of data, and c is the response at zero (or lowest) dose. By writing this model in exponential form, it can be seen that the response R results from multistage filtering (by net amounts a and b) of the initial dose, D. The threshold is obtained from this model as the point, $\text{D}\text{?}{}_{\mathrm{T}}$, at which the second derivative becomes zero. This is given by $\text{D}\text{?}{}_{\mathrm{T}}\text{=}\text{exp}\text{(1 ?}\text{a}\text{2b}\text{)}$ when a and b are oppositelt signed.     

A note on the allocation of investment

It is shown by example that the results obtained by Gruver [11 concerning specialization of investment in either directly productive or pollution control capital arise because of an implicit linearity assumption on the underlying technology. Utilizing a strictly concave “eighth sphere” technology, results are obtained which imply joint investment in the two types of capital except in “rare” instances. The results indicate the need for incorporating more general technologies into the analysis of such problems.     

Counter-disaster training in developing countries

This paper discusses both the need for training within a wider context of community disaster preparedness and the major alternatives in methods of training. Emphasis is placed on the importance of compatibility between the resources within a given country and appropriate training programmes.