431 resultados para Galeus atlanticus
Resumo:
Abundant and diverse polycystine radiolarian faunas from ODP Leg 181, Site 1123 (0-1.2 Ma at ~21 kyr resolution) and Site 1124 (0-0.6 Ma, ~5 kyr resolution, with a disconformity between 0.42-0.22 Ma) have been used to infer Pleistocene-Holocene paleoceanographic changes north of the Subtropical Front (STF), offshore eastern New Zealand, southwest Pacific. The abundance of warm-water taxa relative to cool-water taxa was used to determine a radiolarian paleotemperature index, the Subtropical (ST) Index. ST Index variations show strong covariance with benthic foraminifera oxygen isotope records from Site 1123 and exhibit similar patterns through Glacial-Interglacial (G-I) cycles of marine isotope stages (MIS) 15-1. At Site 1123, warm-water taxa peak in abundance during Interglacials (reaching ~8% of the total fauna). Within Glacials cool-water taxa increase to ~15% (MIS2) of the fauna. Changes in radiolarian assemblages at Site 1124 indicate similar but much better resolved trends through MIS15-12 and 7-1. Pronounced increases in warm-water taxa occur at the onset of Interglacials (reaching ~15% of the fauna), whereas the abundance of cool-water taxa increases in Glacials peaking in MIS2 (~17% of the fauna). Overall warmer conditions at Site 1124 during the last 600 kyrs indicate sustained influence of the subtropical, warm East Cape Current (ECC). During Interglacials radiolarian assemblages suggest an increase in marine productivity at both sites which might be due to predominance of micronutrient-rich Subtropical Water. At Site 1123, an increased abundance of deep-dwelling taxa in MIS 13 and 9 suggests enhanced vertical mixing. During Glacials, reduced vigour of ECC flow combined with northward expansion of cool, micronutrient-poor Subantarctic Water occurs. Only at Site 1123 there is evidence of a longitudinal shift of the STF, reaching as far north as 41°S.
Resumo:
Presented are physical and biological data for the region extending from the Barents Sea to the Kara Sea during 158 scientific cruises for the period 1913-1999. Maps with the temporal distribution of physical and biological variables of the Barents and Kara Seas are presented, with proposed quality control criteria for phytoplankton and zooplankton data. Changes in the plankton community structure between the 1930s, 1950s, and 1990s are discussed. Multiple tables of Arctic Seas phytoplankton and zooplankton species are presented, containing ecological and geographic characteristics for each species, and images of live cells for the dominant phytoplankton species.
Resumo:
The Southern Ocean (SO) plays a key role in modulating atmospheric CO2 via physical and biological processes. However, over much of the SO, biological activity is iron-limited. New in situ data from the Antarctic zone south of Africa in a region centered at -20°E - 25°E reveal a previously overlooked region of high primary production, comparable in size to the northwest African upwelling region. Here, sea ice together with enclosed icebergs is channeled by prevailing winds to the eastern boundary of the Weddell Gyre, where a sharp transition to warmer waters causes melting. This cumulative melting provides a steady source of iron, fuelling an intense phytoplankton bloom that is not fully captured by monthly satellite production estimates. These findings imply that future changes in sea-ice cover and dynamics could have a significant effect on carbon sequestration in the SO.
Resumo:
The evolution of air-breathing organs (ABOs) is associated not only with hypoxic environments but also with activity. This investigation examines the effects of hypoxia and exercise on the partitioning of aquatic and aerial oxygen uptake in the Pacific tarpon. The two-species cosmopolitan genus Megalops is unique among teleosts in using swim bladder ABOs in the pelagic marine environment. Small fish ( 58 - 620 g) were swum at two sustainable speeds in a circulating flume respirometer in which dissolved oxygen was controlled. For fish swimming at 0.11 m s(-1) in normoxia (Po-2 = 21 kPa), there was practically no air breathing, and gill oxygen uptake was 1.53 mL kg(-0.67) min(-1). Air breathing occurred at 0.5 breaths min(-1) in hypoxia ( 8 kPa) at this speed, when the gills and ABOs accounted for 0.71 and 0.57 mL kg(-0.67) min(-1), respectively. At 0.22 m s(-1) in normoxia, breathing occurred at 0.1 breaths min(-1), and gill and ABO oxygen uptake were 2.08 and 0.08 mL kg(-0.67) min(-1), respectively. In hypoxia and 0.22 m s(-1), breathing increased to 0.6 breaths min(-1), and gill and ABO oxygen uptake were 1.39 and 1.28 mL kg(-0.67) min(-1), respectively. Aquatic hypoxia was therefore the primary stimulus for air breathing under the limited conditions of this study, but exercise augmented oxygen uptake by the ABOs, particularly in hypoxic water.