Possible strategy for the survival of marine bacteria under starvation conditions

A population of a psychrophilic marine vibrio (Ant-300) suspended at a low cell density in natural seawater (SW) or artificial seawater (ASW) showed an initial 200-fold increase in cell numbers. Ant-300 suspended in ASW at various densities showed a magnified initial increase in numbers as well as increased longevity as the population density decreased. The magnitude of the initial increase and the viability of the cells after 7 weeks continued incubation were the same whether the cells were suspended in SW, ASW amended with amino acids, or organic-free ASW. Continued incubation (long-term starvation) of a culture of Ant-300 at low cell densities in ASW showed that after 70 weeks over 15 times the orginal number of cells were still viable. When compared to the starvation survival of other bacceria, Ant-300 exceeds the longest reported starvation survival by at least 2.5 times. Our data indicate that Ant-300 is especially adapted for survival at low nutrient concentrations and low population densities due to a sustained increase in cell numbers that may represent a species survival mechanism for marine bacteria.Technical Paper No. 4493, Oregon Agricultural Experiment Station.     

Tactics of whelks preying on limpets

Although holes drilled by the whelk Dicathais aegrota Reeve, 1846 in the limpet Patelloida alticostata (Angas, 1865) were not in the areas of thinnest shell, they were away from the margin, over the gonad and digestive gland, and in the segments where the predator fitted evenly onto the prey's shell. This complicated handling of prey provides access to energy-rich tissues and probably prevents dislodgement of the predator.     

Development and metamorphosis of the planktotrophic larvae of Rostanga pulchra (Mollusca: Nudibranchia)

Rostanga pulchra MacFarland, a small (1 to 2 cm) dorid nudibranch, lays an average of 7000 eggs in the laboratory during a period of 30 days in the summer. The veligers hatch 15 to 16 days after oviposition and it takes another 35 to 40 days to become competent for metamorphosis at a temperature of 10° to 15°C. Larval cultures were maintained initially at a concentration of 500 veligers per 100 ml of filtered sea water (antibiotics added). During the planktotrophic phase of development, the veliger grows from 150 to 300 m in shell length. Although the veligers are generalists in their food preference, the best result (faster growth) was achieved by feeding them with a combination of Monochrysis lutheri and Isochrysis galbana. The concentration of food cells was kept at 10⁴ cells per ml of culture media and was supplied every 2 to 3 days. A veliger which is competent to metamorphose is identifiable morphologically by its propodium, eyespots, rhinophores, and spiculated dorsal papillae. The entire metamorphic process lasts 24 h when a suitable substrate such as the food sponge Ophlitaspongia pennata is provided. The competent veliger is able to delay metamorphosis for at least 3 weeks. Juveniles were kept in the laboratory for 70 days and, during this period, grew to a length of 4.5 mm.     

Ethologie du stade infestant du copépode ascidicole Notodelphyidae Pachypygus gibber. I. Réactions à la lumière au cours de la vie larvaire pélagique

The phototropic reactions of pelagic larvae of Pachypygus gibber (Thorell) under laboratory conditions change according to their stage and their age. The behaviour of these larvae is described by 4 experimental parameters: threshold of the reaction, orientation towards the light or the opposite, speed and form of motility. Specimens were tested under different conditions of illumination. In the nauplii, the threshold reaction to light is higher than that in Copepodids 1 and 2. In the early planktonic stages (nauplii, Copepodids 1 and young Copepodids 2, from emergence to 3 days), most specimens respond positively to light, however the response is negative in older Copepodids 2 (4 to 10 days). There is a parallel evolution between the development of P. gibber and the change from positive to negative phototropism. The inversion of this response occurs in the developmental period between the 3-day old Copepodids 2 and the Copepodids 2 of 4 to 6 days of age. This reversal in vitro could correspond to the moment of penetration into the host. The average swimming speed is fastest in the positive phase of Copepodids 1, and is very slow in the older Copepodids 2. The form of the motility, rectilinear for most Copepodids 1, becomes increasingly winding as the Copepodids 2 grow. This random exploration of the environment would increase the possibility of finding the host. The evolution of phototropism is apparently related to the search for the host and its infestation.     

Phytoplankton in a temperate-zone salt marsh: Net production and exchanges with coastal waters

Phytoplankton production and associated variables were measured in Flax Pond, a 52 ha salt marsh on the north shore of Long Island, New York, from July 1972 to October 1973. Measurements made up to five times per day, once per week, yielded a mean annual net primary production, determined by the ¹⁴C technique, of 20.5 mg C/m³/h; daily means were as high as 60.0 mg C/m³/h. However, when productivity was calculated for the entire marsh ecosystem, the shallow water in the salt marsh produced only 11.7 g C/m² of marsh/year. There was a net flux of phytoplankton from the coastal waters into the marsh; during the summer up to 0.2 g chlorophy 11/m² of marsh was carried in with the tides daily and remained in the marsh. Analysis of the productivity data, as well as variables associated with productivity (pH, standing crop, nutrients, extinction coefficient), indicated that the aquatic portion of the marsh behaved more as a net consumer rather than a net producer of phytoplankton.Research carried out at Brookhaven National Laboratory, supported by the U.S. Atomic Energy Commission and the National Science Foundation under Grant No. AG-375.     

Etude des variations du poids sec et de la constitution chimique élémentaire de Tisbe holothuriae (Copepoda: Harpacticoïda) élevé sur différents régimes artificiels

Dry weight and body composition of C, H and N were investigated in male and female Tisbe holothuriae Humes fed 7 artificial compound diets and a living algal diet (Nannochloris sp.) over the whole biological cycle. No correlation was found between the respective proportion of C, H and N in the food and in the copepod body. Food quality had a significant effect on dry weight. Carbon content varied between 35.35 and 42.32% of body dry weight in females, and between 25.10 and 26.84% in males. Nitrogen values were 9.11 to 10.00% and 6.79 to 6.99%, respectively, varying with different diets. The C:N ratio varied between 3.74 and 4.28 in females and between 3.70 and 3.87 in males. Some diets had a significant effect on this ratio. In some experiments, three different temperatures were tested using the same diet. Body dry weight was inversely correlated with temperature, but no clear relation appeared between C:N and temperature. C:N variations were directly related to C concentration and seemed independent of N concentration. It is suggested that C variations correspond to different levels in lipid content under different trophic conditions. The relation between elementary chemical composition and fecundity in T. holothuriae fed different diets is discussed.     

Behavioral responses of larvae of the crab Rhithropanopeus harrisii (Brachyura: Xanthidae) during diel vertical migration

Larval Rhithropanopeus harrisii (Gould) show nocturnal vertical migration. Larval behavioral responses to different rates of increase and decrease in light intensity were measured in an apparatus with a natural angular light distribution. A central objective was to establish whether phototaxis actually participates in vertical migration. At sunset the level of light adaptation controlled the readiness of the larvae to migrate, while an ascent was initiated by a preductable relative decrease in intensity (e.g. 4.0x10^-3s^-1). Rates of relative decrease around sunset would evoke continuous upward swimming. Gravity was the orienting cue and there was no change in swimming speed during the ascent. At sunrise, the larval descent was initiated by exposure to an absolute light intensity of about 0.23 log unit above the lower visual threshold. Light served as an orienting cue, as larvae descended by a negative phototaxis. Thus, phototaxis is not a laboratory artifact and does participate in vertical migration. A consideration of behavioral responses of other crustacean zooplankton indicates there is considerable variation in the initiating and directing cues for vertical movements. The variety of behavioral responses of R. harrisii suggests that a synthesis of hypotheses about migration may provide the proper basis for explaining the mechanisms underlying diel vertical migration.     

New development in the MOCNESS,an apparatus for sampling zooplankton and micronekton

Four variants of the Multiple Opening/Closing Net and Environmental Sensing System (MOCNESS) have been constructed to sample a broad size spectrum of oceanic animals from microzooplankton to micronekton. The systems differ in mouth opening dimensions (ranging from 1/4 to 20 m²), the number of nets carried (from 5 to 20), and the mesh size of the netting (from 64 m to 3.0 mm). A new electronics package enables an operator to send commands down a single conductor, armored cable to open/close the nets and provides 12-bit resolution for the environmental (temperature, depth, conductivity) and net operation data (flow, net-frame angle, net-bar release), which are transmitted up the cable to the deck unit at 2-s intervals. A microcomputer system, interfaced to the deck unit, calculates salinity, volume filtered by a net, net trajectory velocity, and vertical velocity. The data are printed out and stored on disc, and profiles of temperature and salinity versus depth are plotted during the course of the tow. Analysis of the relationship between the geometry of the MOCNESS under tow and the past and present methods used to estimate the water filtered by a net revealed that significant bias is introduced when the ascent or descent angle of a net is disregarded. The bias is a function of the ratio of vertical velocity to net trajectory velocity and results in an underestimate of volume filtered while shooting a net and an overestimate while hauling.     

Parental investment decision rules and the Concorde fallacy

Summary Investment theory states that animals should base their parental investment decisions on expected benefits, and not on whether or not past investment will be wasted. Otherwise, they would comnit the Concorde fallacy. If reproduction has a cost, however, then past investment and expected benefits are necessarily confounded. Assuming a cost of reproduction, animals will be selected to maximize their remaining lifetime reproductive success, subject to a tradeoff between present and future reproduction (Williams' principle). We extend Williams' principle and develop an experimental design that would allow past investment and expected benefits to be varied independently. This design illustrates the importance of the value of the brood relative to the value of future reproduction.     

Occurrence and significance of nitrogen transport in the brown alga Laminaria digitata

Nitrogen transport in a Laminaria digitata (Huds.) Lamour population growing at Arbroath, Scotland has been investigated (during the period 3 June 1981 to 3 July 1981), using ¹⁵N as tracer. NO ₃ ^- was assimilated both by the blade meristem and by the mature blade. NO ₃ ^- uptake by the blade meristem alone was insufficient to supply the nitrogen demand for growth. This additional demand was met by nitrogen transport from the mature blade to the meristem. It was estimated that 70% of the nitrogen demand of the meristematic region was supplied by nitrogen transport from the mature blade. Although transport occurred, the size of the endogenous pool of stored nitrogen in the mature blade did not change, the quantity of nitrogen transported being equivalent to the amount of NO ₃ ^- assimilated during the experimental period. The possible co-transport of nitrogen and carbon is discussed.