Abundance and biomass of macrobenthos in the Black Sea during Mare Nigrum cruise S-RO1

Dataset containing macrobenthos data for samples collected during April 2008 in the North-West Black Sea (between 44°46' - 43°45' N latitude and 30° 11' - 29°35' E longitude). Macrobenthos sampling was done in 4 stations using a 0.14 m**2 Van Veen grab. Washing of the sample through two sieves - 1 mm and 0.25 mm mesh size; the material retained by the two sieves was examined at the binocular microscope; all animals were extracted, using fine tweezers and the species or group of species were identified and counted (in order to determine the density of populations); the larger organisms were measured and weighed (structure and biomass); for smaller organisms, the average wet weights inscribed in standard tables were used to calculate the biomass. Taxonomic identification was done at the GeoEcoMar by A. Teaca and T. Begun using the relevant taxonomic literature (Key-book for the identification of the Black Sea and Sea of Azov Fauna, 1968 -1972, Kiev - in Russian, V 1-4; BACESCU, M.C., MÜLLER, G. I., GOMOIU, M.-T., 1971 and BACESCU, M.C., MÜLLER, G. I., GOMOIU, M.-T., 1971-Benthic ecological research to Black Sea. Comparative quantitative and qualitative analyse of pontic benthic fauna. Marine Ecology, 4, 1-357 (in Romanian).

Abundance and biomass of meiobenthos in the Black Sea during Mare Nigrum cruise S-RO2

Dataset containing meiobenthos data for samples collected during the September 2008 Sesame Cruise in the North-West Black Sea on board of the Romanian R/V Mare Nigrum. Meiobenthos samples were collected in 5 stations, using a multicorer MARK II-400. The dataset includes 5 samples analysed for meiobenthos species composition, abundance and biomass. The entire washed sample was analyzed under the binocular stereomicroscope. Meiobenthic species were identified and enumerated; some meiobenthic species were identified and enumerated only at higher taxonomic level. Taxonomic identification was done at GEOECOMAR.

Abundance and biomass of meiobenthos in the Black Sea during Mare Nigrum cruise S-RO1

Dataset containing meiobenthos data for samples collected during the September 2008 Sesame Cruise in the North-West Black Sea on board of the Romanian R/V Mare Nigrum. Meiobenthos samples were collected in 5 stations, using a multicorer MARK II-400. The dataset includes 5 samples analysed for meiobenthos species composition, abundance and biomass. The entire washed sample was analyzed under the binocular stereomicroscope. Meiobenthic species were identified and enumerated; some meiobenthic species were identified and enumerated only at higher taxonomic level. Taxonomic identification was done at GEOECOMAR.

Abundance of mesozooplankton in the western part of the Black Sea during Mare Nigrum cruise S-RO1

The SESAME dataset contains mesozooplankton data collected during April 2008 in the North-Western part of Black Sea (between 44°46' N and 42°29'N latitude and 28°64'E and 30°59'E longitude). Mesozooplankton sampling was undertaken at 9 stations where samples were collected using a Hensen net in the 0-10, 10-25, 25-50, 50-100, 100-150, 150-200 m layer. The dataset includes 29 samples analysed for mesozooplankton species composition and abundance. The entire sample or an aliquot (1/2 to 1/4) was analyzed under the binocular microscope. Calculations of zooplankton abundance are made by the following formulae, in accordance with the Report of the third ICES/HELCOM workshop on quality assurance of Biological measurements Warnemünde, Germany, 1996. M - number of counted specimens (ind.), Vf - volume of filtrated water (m³), and K - counted part of sample. (http://www2008.io-warnemuende.de/research/helcom_zp/documents/qa_zp_part.pdf)

Abundance and biomass of macrobenthos in the western part of the Black Sea during Mare Nigrum cruise S-RO2

Dataset containing macrobenthos data for samples collected during September 2008 in the North-West Black Sea (between 44°46' - 43°45' N latitude and 30° 11' - 29°35' E longitude). Macrobenthos sampling was done in 4 stations using a 0.14 m**2 Van Veen grab. Washing of the sample through two sieves - 1 mm and 0.25 mm mesh size; the material retained by the two sieves was examined at the binocular microscope; all animals were extracted, using fine tweezers and the species or group of species were identified and counted (in order to determine the density of populations); the larger organisms were measured and weighed (structure and biomass); for smaller organisms, the average wet weights inscribed in standard tables were used to calculate the biomass. Taxonomic identification was done at the GeoEcoMar by A. Teaca and T. Begun using the relevant taxonomic literature ( "Key-book for the identification of the Black Sea and Sea of Azov Fauna, 1968 -1972, Kiev - in Russian, V 1-4; BACESCU, M.C., MÜLLER, G. I., GOMOIU, M.-T., 1971). BACESCU, M.C., MÜLLER, G. I., GOMOIU, M.-T., 1971-Benthic ecological research to Black Sea. Comparative quantitative and qualitative analyse of pontic benthic fauna. Marine Ecology, 4, 1-357 (in Romanian). Key-book for the identification of the Black Sea and Sea of Azov Fauna, 1968 -1972, Kiev, V. 1-4 (in Russian).

(Table 1) Normalized difference vegetation index in control and warming plots, Abisco Research Station

Extreme winter warming events in the sub-Arctic have caused considerable vegetation damage due to rapid changes in temperature and loss of snow cover. The frequency of extreme weather is expected to increase due to climate change thereby increasing the potential for recurring vegetation damage in Arctic regions. Here we present data on vegetation recovery from one such natural event and multiple experimental simulations in the sub-Arctic using remote sensing, handheld passive proximal sensors and ground surveys. Normalized difference vegetation index (NDVI) recovered fast (2 years), from the 26% decline following one natural extreme winter warming event. Recovery was associated with declines in dead Empetrum nigrum (dominant dwarf shrub) from ground surveys. However, E. nigrum healthy leaf NDVI was also reduced (16%) following this winter warming event in experimental plots (both control and treatments), suggesting that non-obvious plant damage (i.e., physiological stress) had occurred in addition to the dead E. nigrum shoots that was considered responsible for the regional 26% NDVI decline. Plot and leaf level NDVI provided useful additional information that could not be obtained from vegetation surveys and regional remote sensing (MODIS) alone. The major damage of an extreme winter warming event appears to be relatively transitory. However, potential knock-on effects on higher trophic levels (e.g., rodents, reindeer, and bear) could be unpredictable and large. Repeated warming events year after year, which can be expected under winter climate warming, could result in damage that may take much longer to recover.

Mean cover and frequencies of vascular plant species during three decades around Abisko Scientific Research Station

Plant species distributions are expected to shift and diversity is expected to decline as a result of global climate change, particularly in the Arctic where climate warming is amplified. We have recorded the changes in richness and abundance of vascular plants at Abisko, sub-Arctic Sweden, by re-sampling five studies consisting of seven datasets; one in the mountain birch forest and six at open sites. The oldest study was initiated in 1977-1979 and the latest in 1992. Total species number increased at all sites except for the birch forest site where richness decreased. We found no general pattern in how composition of vascular plants has changed over time. Three species, Calamagrostis lapponica, Carex vaginata and Salix reticulata, showed an overall increase in cover/frequency, while two Equisetum taxa decreased. Instead, we showed that the magnitude and direction of changes in species richness and composition differ among sites.

Pollen record and lithology of a profile from Dumfriesshire, Scotland

Four samples, G5, G7, G8, and G10, collected by Dr W. W. Bishop from an exposed section in the bank of the River Annan, at Roberthill Farm, Dumfriesshire (S35, 110794) were submitted for pollen analysis (Table I.). The samples, with the exception of the uppermost, were from thin peat layers that lie in the middle of a series of water- laid sands, silts and clays several feet in thickness and now rather strongly arched. The lowermost sample, G5, was taken from an organic layer about | in. thick overlying fine sand and underlying some 2.5 in. of grey, silty fine sand. A narrow layer of sandy peat immediately above the silty, fine sand yielded sample G7, and G8 was collected from a similar peaty layer separated from G7 by more sandy- silty peat. The uppermost sample, G10, was taken from light grey clay 13 in. above sample G8.

Abundance of plant macrofossils, mollusca and ostracoda in sediments obtained near Tessin, north Germany

A depression filled with Late Glacial and Holocene sediments was excavated during the geological exploration and recovery of a dump area near Tessin close to Rostock, and initiated the studies of the present paper. Pebble analysis of three exposed or respectively drilled till horizons as well as pollenanalytical, carpological and faunistical studies carried out allow the stratigraphical subdivision of the Quaternary sequence of the dump area. The basal till was probably the result of dead ice decay, and was lithostratigraphically assigned to the Pomerian Stage (qw2). The palynological results of boreholes RKS 19/93 and A/92 reveal pre-Allerod and other sediments instead of the expected interweichselian deposits. Based on the palynological and carpological findings, we correlated the beginning of the late glacial development in the locality with the end of the Meiendorf-lnterstadial sensu Menke in Bock et al. (1985, doi:10.3285/eg.35.1.18). The limnic-telmatic sedimentation could be observed pollen floristically probably starting with the Meiendorf-lnterstadial (Hippophae-Betula nana-phase) followed by the Bolling-(Betula nana-B. alba s.l.-Artemisia-Helianthemum-Poaceae-phase) and the Allerad-lnterstadial [Betula alba s.l.-(Pinus)-Cyperaceae-phase] lasting up to the Younger Dryas (Juniperus-Artemisia-Poaceae-phase). Sedimentation closed during the Younger Dryas with the accumulation of fine sands. It was reactivated later during the Holocene due to the anthropogene influence (Older and Younger Subatlantic, dampness of the depression by clearing).