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  • Other Sources  (9)
  • American Institute of Physics
  • Periodicals Archive Online (PAO)
  • Wiley-Blackwell
  • 1985-1989  (8)
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  • 1950-1954
  • 1
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    Wiley-Blackwell
    In:  Journal of Zoology, 218 (4). pp. 603-608.
    Publication Date: 2020-07-17
    Type: Article , PeerReviewed
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  • 2
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    Wiley-Blackwell
    In:  Journal of Zoology, 214 (2). pp. 189-197.
    Publication Date: 2020-07-17
    Description: The cuttlefish ingests much skeleton from the crustaceans and fish it preys upon. The skeletal pieces are relatively large and their dimensions bear a close relationship to the length of the buccal mass and diameter of the oesophagus. The structures of the buccal mass are instrumental in the breakdown of prey and orientation of long pieces of skeleton to ensure their entry into the oesophagus. Many pieces of skeletal material present in the stomach contents still have attached muscles, showing that there is little, or no, external digestion. Skeletal material may be important for long-term maintenance of young Sepia in captivity.
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  • 3
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    Wiley-Blackwell
    In:  Lethaia, 21 (4). pp. 375-382.
    Publication Date: 2020-07-15
    Description: In the animal kingdom evolutionary size changes involved increasing, decreasing and stationary patterns. Planktic and benthic Foraminifera chiefly increased their size during evolution. This increase, however, did not always occur gradually, but could be interrupted by periods when the animals maintained or even decreased in size. The rate of the size increase is different for the various species examined, some benthic forms grew only 10% during the Oligocene-Pleistocene interval, while for others this figure was up to 96%. Some benthic species increased in size in certain areas, but not in others. It is not improbable that some phylogenetic trends of planktic Foraminifera representing, according to stratigraphers, the evolution of one species into another, represent in reality, from the biological point of view, specimens of the same species which changed their size and in addition some minor morphological traits which are encompassed by the normal span of intraspecific variability. A comprehensive understanding and explanation of the size change of Foraminifera needs much additional research.
    Type: Article , PeerReviewed
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  • 4
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    Wiley-Blackwell
    In:  Marine Ecology, 8 . pp. 1-20.
    Publication Date: 2017-10-05
    Description: Benthic metabolism and standing stocks were investigated in the deep Red Sea between 21o and 27oN, Activity was assessed by the determination of respiration rates with a shipboard method and by calculating oxygen consumption from the activity in the electron transport system. We attempted to compare results from different latitudes within the warm Red Sea and with data from cold Atlantic environments. Our investigations were part of an environmental risk assessment to evaluate future mining of metalliferous sediments from the Atlantis II Deep.
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  • 5
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    Wiley-Blackwell
    In:  Journal of Zoology, 212 (2). pp. 303-324.
    Publication Date: 2020-07-17
    Description: The diet of the king penguin Aptenodytes patagonicus at Marion Island was examined throughout the year by analysis of stomach samples. Fish accounted for 87% by wet mass, 75% by numbers and 69% by reconstituted mass. Their proportional importance by wet mass increased from 68% during winter to almost 100% in summer and probably reflects a real increase in their local availability. Squid comprised most of the remainder with crustaceans forming less than 1% of the diet by numbers. Prey items were generally small, the most abundant being three species of myctophid fish, Krefftichthys anderssoni, Protomyctophum tenisonì and Electrona carlsbergi, and a squid Kondakovia longimana. King penguins took both juvenile and adult Krefftichthys anderssoni and P. tenisoni, but only adult E. carlshergi. The juvenile and adult modal size classes of K. anderssoni and P. tenisoni increased from March through to February and the proportion of juvenile to adult fish increased in winter. The increase in the modal size class of the K. anderssoni/P. tenisoni complex during the year probably reflects growth of the fish, rather than movement of different populations in and out of the area exploited by king penguins. All squid consumed were probably juveniles. The modal size class of Kondakovia longimana increased from March to August, but in September to October smaller squid again formed a large proportion of the squid component of the diet. Numbers of measurable squid beaks recovered from November to February were low. This is the first time that mesopelagic myctophid fish have been shown to comprise a major component of the diet of a vertebrate predator in the Southern Ocean.
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  • 6
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    Wiley-Blackwell
    In:  Nordic Journal of Botany, 7 (3). pp. 359-363.
    Publication Date: 2018-10-02
    Description: Blidingia minima var. ramifera is reported for the first time in eastern North America. It occurs in the Gulf of St. Lawrence, Nova Scotia and in Maine. In the estuary of the West and Rights Rivers (Antigonish Harbour, Nova Scotia) it is the most common intertidal alga and during its maximum growth period (June‐August) covers 75–90% of the intertidal zone for several km of shoreline at the mouth of the Rights River. In culture, spore germination and early development were typical of the taxon as described from Europe. The taxon is raised to specific status as Blidingia ramifera stat. nov. Blidingia subsalsa is confirmed from New England based on observations of spore germination in plants from Maine and Connecticut.
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  • 7
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    American Institute of Physics
    In:  The Journal of the Acoustical Society of America, 78 (6). pp. 2115-2121.
    Publication Date: 2020-05-11
    Description: The acoustic backscatter of eight well‐curated ferromanganese nodules has been measured in 1 °C seawater at frequencies from 45 to 167 kHz. The nodules have diameters from 37 to 121 mm and are thought to be representative of the Cu–Ni–Co‐rich nodules from the area around 14° 40’ N, 125° 25’ W (DOMES site C). They had been collected in box cores on the Echo 1 expedition and were kept refrigerated and water soaked in air‐tight plastic bags. Acoustic backscatter variations of over 10 dB were observed while the nodule was rotated 10° to 30° about one of its principal axes. The complicated fine structure, as well as the target strength, makes it clear that nodules cannot be modeled as simple spheres.
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  • 8
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    American Institute of Physics
    In:  Journal of the Acoustical Society of America, 78 (4). pp. 1348-1355.
    Publication Date: 2020-07-16
    Description: Additional data from sonobuoys and the Deep Sea Drilling Project (DSDP) justify separating sound‐velocity‐depth functions and velocity gradients (in the first layer of soft marine sediments) into some geographic areas and sediment types. Based on sonobuoy and core measurements (where V is sound velocity in km/s, and h is depth in sediments in km), the following data are obtained: continental shelf basins off Sumatra and Java—V=1.484+0.710h−0.085h2; U. S. Atlantic continental rise—V=1.513+0.828h−0.138h2; deep‐sea terrigenous sediments—V=1.519+1.227h−0.473h2; and siliceous sediments of the Bering Sea— V=1.509+0.869h−0.267h2. Selected DSDP data (through leg 74) in similar areas yield: continental terrace silt–clays—V=1.505+0.712h; deep‐sea terrigenous sediments—V=1.510+1.019h; and deep‐sea siliceous sediments—V=1.533+0.761h. Computed velocity gradients from sonobuoy measurements are generally supported by the DSDP gradients. Only DSDP data give the following: hemipelagic sediments—V=1.501+1.151h; deep‐sea calcareous sediments—V=1.541+0.928h; and deep‐sea pelagic clay—V=1.526+1.046h. Where fast sediment accumulation occurs, there has not been enough time to reduce sediment pore spaces under overburden pressure; areas of slow accumulation may have relatively high sediment structural strength. Both cases have lower velocity gradients because higher porosities and consequent lower velocities persist to deeper depths.
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  • 9
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    American Institute of Physics
    In:  Journal of the Acoustical Society of America, 32 (6). pp. 641-644.
    Publication Date: 2020-07-16
    Description: Tables for the speed of sound in sea water are presented. These tables have been prepared from an empirical formula which was derived to fit measured sound‐speed data obtained over the temperature range −3°C to 30°C, the pressure range 1.033 kg/cm2 to 1000 kg/cm2, and the salinity range 33‰ to 37‰. The discrepancy of −3.0 m/sec found by Del Grosso at 1 atm., as compared to the tables of Kuwahara, is substantiated. In addition, the pressure coefficient of sound speed observed in the present work differs from that predicted by Kuwahara.
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