Biomarkers in surface sediments from the Ob and Yenisei estuaries and the southern Kara Sea

Organic-geochemical bulk parameter (Total organic carbon contents, C/N ratios and d13Corg values), biogenic opal and biomarkers (n-alkanes, fatty acids, sterols and amino acids) were determined in surface sediments from the Ob and Yenisei estuaries and the adjacent southern Kara Sea. Maximum TOC contents were determined in both estuaries, reaching up to 3 %. Relatively high C/N ratios around 10, light d13Corg values of -26.5 per mil (Yenisei) and -28 to -28.7 per mil (Ob), and maximum concentrations of long-chain n-alkanes of up to about 10 µg/g Sed clearly show the predominance of terrigenous organic matter in the sediments from the estuaries. Towards the open Kara Sea, all p arameters indicate a decrease in terrigenous organic carbon. Brassicasterol as well as the short-chain n-alkanes parallel this trend, suggesting that these biomarkers are probably also related to a terrigenous (fresh-water phytoplankton) source. Amino acid spectra show characteristic trends from the Yenisei Estuary to the open Kara Sea revealing increasing state of degradation. Sedimentary organic matter in the Yenisei Estuary is relatively less degraded compared to the Ob Estuary and the open Kara Sea.

Global Ocean Biomes: Mean and time-varying maps (NetCDF 7.8 MB)

Large-scale studies of ocean biogeochemistry and carbon cycling have often partitioned the ocean into regions along lines of latitude and longitude despite the fact that spatially more complex boundaries would be closer to the true biogeography of the ocean. Herein, we define 17 open-ocean biomes classified from four observational data sets: sea surface temperature (SST), spring/summer chlorophyll a concentrations (Chl a), ice fraction, and maximum mixed layer depth (maxMLD) on a 1° × 1° grid. By considering interannual variability for each input, we create dynamic ocean biome boundaries that shift annually between 1998 and 2010. Additionally we create a core biome map, which includes only the grid cells that do not change biome assignment across the 13 years of the time-varying biomes. These biomes can be used in future studies to distinguish large-scale ocean regions based on biogeochemical function.

(Table 2) Particulate organic carbon concentrations in the water column of the Barents Sea in August-September 1997

A comparative estimation of particulate organic matter concentration in seawater in various regions of the Barents Sea was carried out on the basis of materials collected by authors in August-September 1997. It is shown that the major feature of near-bottom distribution of particulate organic matter is distinct decrease in its concentration from off-shore areas of the Murman and Novaya Zemlya coasts and the Franz Josef Land Archipelago toward the central part of the Barents Sea. Using a method of mean and maximum concentrations of particulate organic matter, an attempt was made to estimate its fluxes from the surface to the bottom.

The third glacier inventory of North Tyrol, Austria, for 2006

A new, third, glacier inventory (GI3) is presented for North Tyrol, which is based on Airborne Laser Scanning for the year 2006. 447 glaciers covering 235 km**2 are included. 4 small, formerly neglected glaciers have been added. Basic quantities such as size, maximum, minimum and median elevation show large variances. Very recent glacier changes between the former inventory (GI2: 1998) and GI3 show a strong reduction in area (-8%) and mean thickness (-7 m). An asymmetry of mean maximum, minimum and median elevation is quantified with approximately 200 m higher values for south-exposed glaciers. Rates of changes are around 1% per year and 1 m per year between GI2 and GI3. The strongest volume losses occurred for glaciers between 5 and 10 km**2.

Sea surface temperature reconstruction for the LGM

The southwest Pacific Ocean covers a broad range of surface-water conditions ranging from warm, salty water in the subtropical East Australian Current to fresher, cold water in the Circumpolar Current. Using a new database of planktonic foraminifera assemblages (AUSMAT-F2), we demonstrate that the modern analog technique can be used to accurately reconstruct the magnitude of sea-surfacetemperature (SST) in this region. We apply this technique to data from 29 deep-sea cores along a meridional transect of the southwest Pacific Ocean to estimate the magnitude of SST cooling during the Last Glacial Maximum. We find minimal cooling in the tropics (0°-2°C), moderate cooling in the subtropical midlatitudes (2°-6°C), and maximum cooling to the southeast of New Zealand (6°-10°C). The magnitude of cooling at the sea surface from the tropics to the temperate latitudes is found to generally be less than cooling at the surface of adjacent land masses.

Seawater carbonate chemistry, thickness and carbonate elemental composition of the test of juvenile sea urchins in a laboratory experiment

Ocean surface CO2 levels are increasing in line with rising atmospheric CO2 and could exceed 900 µatm by year 2100, with extremes above 2000 µatm in some coastal habitats. The imminent increase in ocean pCO2 is predicted to have negative consequences for marine fishes, including reduced aerobic performance, but variability among species could be expected. Understanding interspecific responses to ocean acidification is important for predicting the consequences of ocean acidification on communities and ecosystems. In the present study, the effects of exposure to near-future seawater CO2 (860 µatm) on resting (M O2rest) and maximum (M O2max) oxygen consumption rates were determined for three tropical coral reef fish species interlinked through predator-prey relationships: juvenile Pomacentrus moluccensis and Pomacentrus amboinensis, and one of their predators: adult Pseudochromis fuscus. Contrary to predictions, one of the prey species, P. amboinensis, displayed a 28-39% increase in M O2max after both an acute and four-day exposure to near-future CO2 seawater, while maintaining M O2rest. By contrast, the same treatment had no significant effects on M O2rest or M O2max of the other two species. However, acute exposure of P. amboinensis to 1400 and 2400 µatm CO2 resulted in M O2max returning to control values. Overall, the findings suggest that: (1) the metabolic costs of living in a near-future CO2 seawater environment were insignificant for the species examined at rest; (2) the M O2max response of tropical reef species to near-future CO2 seawater can be dependent on the severity of external hypercapnia; and (3) near-future ocean pCO2 may not be detrimental to aerobic scope of all fish species and it may even augment aerobic scope of some species. The present results also highlight that close phylogenetic relatedness and living in the same environment, does not necessarily imply similar physiological responses to near-future CO2.

Data compilation of respiration, feeding, and growth rates of marine pelagic organisms

The metabolic rate of organisms may either be viewed as a basic property from which other vital rates and many ecological patterns emerge and that follows a universal allometric mass scaling law; or it may be considered a property of the organism that emerges as a result of the organism's adaptation to the environment, with consequently less universal mass scaling properties. Data on body mass, maximum ingestion and clearance rates, respiration rates and maximum growth rates of animals living in the ocean epipelagic were compiled from the literature, mainly from original papers but also from previous compilations by other authors. Data were read from tables or digitized from graphs. Only measurements made on individuals of know size, or groups of individuals of similar and known size were included. We show that clearance and respiration rates have life-form-dependent allometries that have similar scaling but different elevations, such that the mass-specific rates converge on a rather narrow size-independent range. In contrast, ingestion and growth rates follow a near-universal taxa-independent ~3/4 mass scaling power law. We argue that the declining mass-specific clearance rates with size within taxa is related to the inherent decrease in feeding efficiency of any particular feeding mode. The transitions between feeding mode and simultaneous transitions in clearance and respiration rates may then represent adaptations to the food environment and be the result of the optimization of tradeoffs that allow sufficient feeding and growth rates to balance mortality.

Planktonic foraminifera in Core ML2_66, North Atlantic

Evolution of approaches and methods for reconstruction of paleoenvironmental conditions from microfossils contained in bottom sediments is assessed. Authors elaborated a new actualistic basis for such reconstructions, consisting of a database on contents of tests of planktonic foraminifers in the surface layer of Atlantic sediments and a package of mathematical tools for computer data processing. Structure of the database is described. It contains data on test contents for 29 species and varieties of planktonic foraminifers in 381 samples. A mathematical model designed for reconstructions is based on factor analysis and multidimensional spline interpolation. The model allows one to deduce Quaternary hydrological parameters (paleotemperature, paleosalinity) for standard hydrological levels down to depth of 250 m for the four seasons of the year. Reconstructions are illustrated by an example of a sedimentary core from the North Atlantic representing a period of 300 ky. During the next to last and the last maxima of continental glaciation (oxygen isotope stages 8, 6, 4, and 2), the subarctic water mass was spread here. Winter and summer surface water temperatures comprised 1-5° and 5-7°C, respectively. During interglacials and in Holocene the conditions were close to present ones: winter and summer surface water temperatures comprised 10-12 and 15-17°C, respectively. Vertical paleohydrological profiles compiled for peaks of climatostratigraphic intervals suggest that during cold intervals water stratification was stronger than during the warm ones. At depth 50 m seasonal salinity oscillations did not exceed 0.4 per mil and commonly salinity was minimum in winter and maximum in summer.