Description: A general study of structure, biomass estimates and dynamics on the macrofauna was carried out in August 1975 and March 1976 during PREFLEX (1975) and FLEX (1976), the Fladen Ground Experiment. On the basis of these data an attempt was made to estimate macrobenthic production expressed as minimum production (MP). The macrobenthic production is discussed together with meiobenthic annual production (FAUBEL, HARTWIG & THIEL 1983) and with indirectly estimated microbenthic production in relation to an energy input from the water column of about 25g C m-2 year-1 (STEELE 1974). From the production estimates of the three benthic components a rough energy budget is proposed. Sampling was performed at five Stations for endofauna twice during the time of investigation and for epifauna once. At each station two replicate box core samples (30 X 20 cm) were taken for endofauna. Epifauna was sampled with an Agassiz trawl once at each Station. The total numbers of endofauna increased from station l to 5. This was valid as well for August 1975 (4,233-12,166 individuals per m2 and 10 cm sediment depth) as for March 1976 (1,008-2,925 individuals). The polychaetes were the dominant organisms with a share of 33 to 62%. The densities for the endofauna decreased from August 1975 to March 1976 by a mean factor of 2.8. Abundances of epifauna amounted to values between 11 and 102 individuals per 1000 m2. The biomass dry weights (DWT) for macrobenthic endofauna varied between 0.97g DWT m-2 and 6.42g DWT m-2 in August 1975 and between 0.27g DWT m-2 and 2.64g DWT m-2 in March 1976. The mean amounted to 1.74g DWT m-2. Dry weights of epifauna biomass gave values between 4.9 and 83.1g DWT, 1000 m-2. The minimum production for the total macro-endofauna at Fladen Ground amounted to 1.43g DWT m-2 yr-1 or 0.82g C m-2 yr-1. This resulted in a minimum turnover rate (P/B) of 0.8. The share produced by the polychaetes amounted to 1.06g DWT m-2 yr-1 or 74%.

Description: A general study of structure, biomass, and dynamic estimates on meiofauna was carried out during PREFLEX (1975) and FLEX (1976), in 117-141 m water depth. On the basis of these data an attempt was made to estimate meiofauna production, and this is discussed in relation to the energy input from the spring phytoplankton bloom. Sampling was performed at five stations, but only the stations 1, 4, and 5 were covered by a complete series from August 1975 to July 1976. At each station, from four replicate box core samples, two were withdrawn to study the abundance, distribution, and biomass of meiofauna, the content of chloroplastic pigment equivalents (CPE), and chemical and grain size analyses. At all stations grain size feil in the range of fine sand having median diameters (MD) of 〈125 μm. From Station 1 to 5 an increase in MD was observed. Highest values of CPE (7.81 μg ml-1) and organic matter (4.7%) were obtained in June and July (1976)/August (1975), respectively. Meiofauna abundance was fairly uniform at all stations examined. Station 1 displayed maximal numbers during the whole investigation period. The abundance per 100 cm2 varied between 15,550 and 34,900 organisms. All meiofauna studied both in total and as separate taxa showed annual cycles of abundance. Low abundance values were recorded during early summer, and maximum values during winter. High numbers of Foraminifera were obtained for August 1975 (9,460 per 100 cm2) and July 1976 (9,710 per 100 cm2). From December to June the values decreased from 3,280 to 1,030 per 100 cm2. At station 1 maximum values of meiofauna biomass were recorded ranging from 1.5 to 2.7 g DWT m-2. The mean meiofauna dry weight amounted to 2.1 g DWT m-2. Based on minimum production, the P/B ratio for the area of Station 1 might have a mean of 1.4. Taking into consideration generation times we believe that a turnover ratio of 2 is a conservative value for the Fladen Ground meiofauna. The annual production would amount to 4.2 g DWT m-2 yr-1. This is 27.5% of the energy supply during the spring phytoplankton bloom, which is channelled into the meiofauna. The hypothesis is put forward that the energetic strategy of deep offshore meiofauna differs distinctively from that of shallow inshore meiofauna. While the shallow inshore meiofauna show a relatively fast response to organic matter input, the deep offshore meiofauna reacts much more slowly, the food energy consumption seems to be spread out over a longer period.

Description: Macro- and meiobenthic abundance and biomass as well as metabolic activity (respiration, ETS activity) have been studied along a transect ranging from 130 to 3000 m water depth off northern Morocco (35° N) during "Meteor" cruise No. 53 (1980). The distribution of chloroplastic pigment concentration (chlorophyll a, pheophytins) in the sediment has been investigated as a measure of sedimented primary organic matter. High chloroplastic pigment concentrations were found on the shelf and around the shelf break, but values declined rapidly between 200 and 600 m depth. Below 1200 m pigment concentrations remained at a relatively uniform low level. Macrobenthic abundance and biomass (wet weight) decreased with increasing water depth and with distance from the shore. Significant changes occurred between the shelf and upper slope and below 2000 m depth. Meiobenthic abundance and biomass (ash free dry weight) followed the same general pattern, but changes were found below 400 and 800 m depth. In the depth range of 1200 to 3000 m values differ only slightly. Meiofauna abundance and biomass show a good correlation with the sedimentary chloroplastic pigment concentrations. Respiratory activity of sediment cores, measured by a shipboard technique at ambient temperatures, decreased with water depth and shows a good correlation with the pigment concentrations. ETS activity was highest on the shelf and decreased with water depth, with significant changes between 200 and 400 m, and below 1200 m depth, respectively. Activity was generally highest in the top 5 cm of the sediment and was measurable, at all Stations, down to 15 cm sediment depth. Shelf and upper slope stations exhibited a vertical distribution pattern of ETS activity in the sediment column, different from that of deeper Stations. The importance of biological activity measurements as an estimate of productivity is discussed. To prove the thesis that differences in benthic abundance, biomass and activity reflect differences in pelagic surface primary production, in the case of the NW-African coast caused by different upwelling intensities, the values from 35° N were compared with data from 21° N (permanent upwelling activity) and 17° N (ca. 9 months upwelling per year). On the shelf and upper slope (〈 500 m) hydrographical conditions (currents, internal waves) influence the deposition of organic matter and cause a biomass minimum between 200 and 400 m depth in some regions. But, in general, macrobenthic abundance and biomass increases with enhanced upwelling activity and reaches a maximum in the area off Cape Blanc (21° N). On the shelf and in the shelf break region meiofauna densities are higher at 35° N in comparison to 21° N; but in contrast to the decreasing meiofauna abundance with increasing water depth at 35° N, an abundance maximum between 400 and 1200 m depth is formed in the Cape Blanc region; this maximum coincides with the maximum of sedimenta1y chloroplastic pigment equivalents. The comparison of ETS activities between 35° N and 21° N shows on the shelf activity at 21° N is up to 14 times higher and on the slope 4-9 times higher, which demonstrates that benthic activity responds to the surface productivity regime.

Description: 1. On the cruises 3 and 15 of R.V. "Meteor" 6 grab samples, and 6 hauls with the 6 m Agassiztrawl were taken and at 2 stations the deep sea camera was lowered. This material gave quantitative results on the meiofauna and minimum counts of the macrofauna. 2. The nematodes constitute nearly 95% of the meiofauna, the copepoda only 2%, With increasing sediment depth the density of animals decreases gradually. In the uppermost centimeter of sediment (layer A) 42.6% of the meiofauna are found while only 3.7% live in layer G (tab. 6). Meiofauna weight ranges from 0.6-5.7 mg/25 m2 sediment surface i.e. 0.24-2.8 g/m2. 3. Mean numbers of individuals (tab. 3) and weights (tab. 5 for nematodes) show standard errors of 20-30%. As an approximate average value for further considerations the weight of the meiofauna in the area was taken as 1 g/m2. 4. Quantitative information on the macrofauna is derived from the trawls and the photographs for the actinia Chitonanthus abyssorum only, which is found in the rate of 1 individual/36-72 m 2, but seems to be less abundant generally. 5. Animal density does not decrease steadily from nearshore to offshore biocoenoses, i.e. generally with increasing depth. The decrease is more pronounced for macro- than for meiofauna. For the deep sea the weight proportion of macrofauna : meiofauna is of the order of 1 : 1. 6. With the assumption, that adaptation of metabolism to deep sea conditions is similar in macro- and meiofauna total metabolism of invertebrates is ascribed to meiofauna to more than 80%. 7. The structure of the biocoenosis of the deep sea floor is characterized by the meiofauna living on and in the sediment and by the dominance of sediment feeders in the macrofauna. 8. Considering the large numbets and high partition rates of bacteria a comparative large part of the metabolism in the deep sea sediment must be ascribed to bacteria. This favours the hypothesis, that with increasing depth and decreasing addition of organic material to the sediment, the importance of meiofauna and microorganisms for total metabolism increases. 9. Considering the different modes of food transport to the deep sea environment, i.e. sinking of dead particles, transport by vertical migration of organisms, aggregation of organic particles, adsorption of dissoloved organic substance to inorganic particles, and heterotrophy, the sediment may be assumed to contain more food for invertebrates than the water above the bottom. 10. Suspensionfeeders of macrofauna are fixed to hard substrates in the sediment surface. Same of them are shown to bend themselves down to the bottom in underwater photographs. This suggests the idea that some deep sea suspension feeders partly depend on food from the sediment surface, on which they feed directly.

Description: This report deals in its first part with problems concerning the settlement of animals and the establishment of populations on seamounts. Ideas on habitat and productivity as well as systematic and zoogeographic questions are discussed. Besides the plans for the expeditions, the second part contains a cruise report with the participants in the benthos programme; the station list and a description of the gear and the methods employed are also given. The results will be worked out by several specialists. After the samples have been sorted and quantitative determinations of animals groups are carried out, these will be sent to four German museums, which will take charge of the material and try to find specialists for the systematics. Publication of the results is planned in "Meteor" Forschungsergebnisse, Series D (Biology).

Description: During the years 1968-1980 R.V. "Meteor" worked off Northwest Africa on several occasions and four expeditions were partly devoted to sample the benthos. This paper elucidates the questions asked in this benthic programme, it lists the participants (Table 1), gives information on sampling areas (Fig. 1, Table 2), presents Station, sampling and subsampling lists (Tables 4-10), and shortly describes the methods used on board ship.

Description: 1. Coeloplana meteoris is described as a new platyctene ctenophore (with 11 photographs and 1 coloured figure). 2. Its systematic position is discussed and understood as preliminary. 3. A comparison is made of the gastrovascularsystem of the Platyctenea. These can be used for systematic characterisation.