167 resultados para SPIDER ARANEUS-DIADEMATUS


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A relatively complete lower Paleocene to lower Oligocene sequence was recovered from the Southern High of Shatsky Rise at Sites 1209, 1210, and 1211. The sequence consists of nannofossil ooze and clay-rich nannofossil ooze. Samples from these sites have been the target of intensive calcareous nannofossil biostratigraphic investigations. Calcareous nannofossils are moderately preserved in most of the recovered sequence, which extends from nannofossil Zones CP1 to CP16. Most traditional zonal markers are present; however, the rarity and poor preservation of key species in the uppermost Paleocene and lower Eocene inhibits zonal subdivision of part of this sequence.

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Six sites were drilled on the southern Iberia Abyssal Plain during Ocean Drilling Program (ODP) Leg 173. Three holes (1067A, 1068A, and 1069A) recovered Eocene sediments consisting of thinly bedded turbidite deposits with interbedded hemipelagic sediments (Bouma sequence Te) deposited near the calcite compensation depth. The hemipelagic sediments are barren of nannofossils, necessitating the use of the turbidite deposits to erect an Eocene biostratigraphy for these holes. Moderately preserved, diverse assemblages of nannofossils were recovered from silty clays (Bouma sequence Td) and poorly preserved, less diverse assemblages were recovered from sandy/silty clays (Bouma sequence Tc). Hole 1067A has a continuous record of sedimentation (Subzones CP9a-CP14a) and Holes 1068A and 1069A have similar continuous records (Subzones CP9a-CP12a), although all holes contain barren intervals. Holes 1067A, 1068A, 1069A, 900A (ODP Leg 149), and 398D (Deep Sea Drilling Project Leg 47B) display a similar increase in mass accumulation rates in the lowermost middle Eocene. A reliable Eocene biostratigraphy has been erected using nannofossil data from turbidite sequences, allowing for correlation between Iberia Abyssal Plain sites.

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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.

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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.