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Notes: Zusammenfassung Es wird darauf hingewiesen, dass die Formel $$\frac{{k - k_1 }}{{k + xk_1 }} = \varrho \frac{{k_2 - k_1 }}{{k_2 + xk_1 }}$$ (k: dielektrische Konstante bzw. Leitfähigkeit) für die elektrischen Eigenschaften einer Suspension auch dann gilt, wenn diek komplex sind. Verschiedene Anwendungen dieser verallgemeinerten Formel werden besprochen, die für elektrische Messungen an zellularen Substraten biologischer Herkunft bei Ultrahochfrequenzen von Interesse sind. Diese umfassen Suspensionen orientierter Rotationsellipsoide. In Weiterführung früherer Arbeiten werden Kurven angegeben, diex für solche Systeme darstellen.

Notes: Abstract A new type of animal community has been found near hot vents in the subpolar Atlantic at 100 to 106 m depth off Kolbeinsey on the Jan-Mayen ridge. Incubation of high temperature fluids yielded cultures of undescribed hyperthermophilic eu- and archaebacteria, growing in a temperature range between 70° and 110°C depending on the isolates. Bacteria are closely related to species occurring within deep sea hydrothermal areas. In contrast to deep-sea vent sites of the Mid-Atlantic and other oceans, the Kolbeinsey macro- and meiofauna consists of species reported from non-vent areas in the boreal Atlantic and adjacent polar seas. The most abundant forms are a solitary hydroid polyp and two sponges. Kolbeinsey is an isolated and young area of hydrothermal activity at relatively low depth and in highly productive waters; these findings could indicate a model for an early evolutionary step towards the formation of a genuine specialized vent community.

Notes: Abstract 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 (Δ2%) 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 μm3 at 116 m to 406 μm3 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.

Notes: Abstract The home range system of the coelacanth Latimeria chalumnae was investigated along 11 km coastline at Grande Comore, Western Indian Ocean, between 1987 and 1991. 67 individuals were identified on individual white dot patterns. The home range consisted of daytime caves where fish aggregated in groups of up to 14 individuals while at night individuals moved singly downwards to a depth of 250 to 300 m in search of food. Site fidelity of at least 5 yr was found. The coelacanths used several caves within their home ranges. Cave size, cave occupation rate, average and maximum group size and cave preferences were studied. Tracking experiments with ultrasonic transmitters revealed horizontal home ranges of at least 8 km width. Population estimates of 200 to 230 individuals at Grande Comore confirm earlier counts. Large home ranges and highly mobility in a topographically narrow habitat apparently favoured inbreeding of the small local island population.

Notes: Abstract In the Indian Ocean, the fish Siphamia argentea usually lives in small groups within the interradial spaces of the sea urchin Astropyga radiata. The fish has a colouration similar to that of the sea urchin and is thus protected from predators both by camouflage and the physical barrier of the sea urchin's spines. If the fish do not keep to the interradial spaces, the urchin can prick them with its spines. When the fish groups become too large, there is not enough space for them in these protected interradial spaces. Individuals which cannot be accomodated, form a dense group around the sea urchin which resembles a large urchin. Such dense groups are also known to occur in the fish Plotosus anguillaris where the individuals actually touch each other. The relationship between fish and sea urchin is described and discussed as an example of collective mimetic behaviour. This is the first record of collective mimetic behaviour in a marine environment. It is difficult to decide whether this is mimicry or mimese, as detailed research on the predators of both the sea urchin and the fish has not been carried out.

Notes: Abstract A method for attaching acoustic transmitters externally to deep-water fishes in situ is described. Tags, each comprising a transmitter connected to a dart, were fired at fish from a pneumatic gun held by the manipulator arm of a submersible. The method was applied successfully for tagging coelacanths and may have application for use with other species of fishes living at depths to about 1000 m. The usefulness of direct observation for monitoring the effects of tags on fish is evaluated in relation to the effects of the tagging method on coelacanths.

Notes: Abstract Acoustic telemetry was used to examine patterns of activity and space utilisation of coelacanths, nocturnal predators which spend the day in submarine caves. Nine coelacanths (Latimeria chalumnae) were tracked, each for a period of 1 to 16 nights at Grande Comore, West Indian Ocean. Activities lasted on average 9 h, usually starting shortly after sunset and ending before sunrise. Vertically, coelacanths moved up and down at and below cave level by following the bottom contour, mainly between 180 and 400 m depth. The deepest record was 698 m, the shallowest 133 m. Most time was spent between 200 and 300 m depth. Large individuals performed deep excursions to depths below 400 m, usually once per night. The fish spent most time in water temperatures of 15 to 19 °C; they rarely ventured into waters warmer than 22 °C measured at depths shallower than 160 m depth. Horizontally, coelacanths stayed in narrow areas ranging from 〈1 to 10 km of coastline. Coelacanths are extremely slow drift-hunters with an estimated average swimming speed of 3.2 m min−1, often travelling not more than 3 km per night. They probably take advantage of local upwelling and downwelling and slow currents occurring parallel to the steep slopes. This study shows that coelacanths are inhabitants of the subphotic zone, where they are active mainly below the depth of their daytime refuges.

Notes: Abstract At Aldabra Atoll, the shrimp Ligur uvea inhabits a land-locked marine pool which is connected to the sea by a subterranean fissure. The shrimps migrate daily with the tide from a hole in the subterranean labyrinth to a feeding area at the bottom of the pool. The timing of the migration is tidal-linked and independent of light and temperature. With each incoming tide, tagged individuals return to a definite feeding ground. Such homing has not been reported from other L. uvea pools. Feeding activity was quantitatively measured, differences between day and night activity are interpreted as adaptations against predators (terrestrial wading birds). Compared to other L. uvea pools, the shrimps at Aldabra Atoll are exposed to a more rigorous environmental situation, which probably influences the tidal-linked behaviour of the local shrimp population.