ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
Collection
Keywords
  • 1
    facet.materialart.
    Unknown
    PANGAEA
    In:  Supplement to: Baldauf, Jack G; Thomas, Ellen; Clement, Bradford M; Takayama, Toshiaki; Weaver, Philip PE; Backman, Jan; Jenkins, G; Mudie, Peta J; Westberg-Smith, M J (1987): Magnetostratigraphic and biostratigraphic synthesis, Deep Sea Drilling Project Leg 94. In: Ruddiman, WF; Kidd, RB; Thomas, E; et al. (eds.), Initial Reports of the Deep Sea Drilling Project, Washington (U.S. Govt. Printing Office), 94, 1159-1205, https://doi.org/10.2973/dsdp.proc.94.146.1987
    Publication Date: 2023-05-12
    Description: During DSDP Leg 94 sediment was recovered from 22 holes at six sites situated between 37° and 53°N in the North Atlantic. Paleomagnetic, calcareous nannofossil, foraminiferal, diatom, radiolarian, and dinocyst stratigraphic studies were completed. The excellent magnetostratigraphic results, the near-complete recovery, and the abundant fossil content of the sediment allowed refinement of these stratigraphies, especially for the upper Pliocene-Holocene. Because the Leg 94 sites span middle and high North Atlantic latitudes, it is possible to use them to evaluate the synchrony of late Pliocene to Holocene datums.
    Keywords: Deep Sea Drilling Project; DSDP
    Type: Dataset
    Format: application/zip, 6 datasets
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Publication Date: 2023-06-27
    Keywords: 94-607; 94-607A; Age model; Age model, optional; Comment; Datum level; Deep Sea Drilling Project; Depth, bottom/max; DEPTH, sediment/rock; Depth, top/min; DRILL; Drilling/drill rig; DSDP; Event label; Glomar Challenger; Leg94; North Atlantic/FLANK
    Type: Dataset
    Format: text/tab-separated-values, 451 data points
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Publication Date: 2023-06-27
    Keywords: 94-606; 94-606A; Age model; Age model, optional; Comment; Datum level; Deep Sea Drilling Project; Depth, bottom/max; DEPTH, sediment/rock; Depth, top/min; DRILL; Drilling/drill rig; DSDP; Event label; Glomar Challenger; Leg94; North Atlantic/FLANK
    Type: Dataset
    Format: text/tab-separated-values, 474 data points
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    Publication Date: 2023-06-27
    Keywords: 94-610; 94-610A; 94-610B; 94-610E; Age model; Age model, optional; Comment; Datum level; Deep Sea Drilling Project; Depth, bottom/max; DEPTH, sediment/rock; Depth, top/min; DRILL; Drilling/drill rig; DSDP; Event label; Glomar Challenger; Leg94; North Atlantic/RIDGE
    Type: Dataset
    Format: text/tab-separated-values, 381 data points
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    Publication Date: 2023-06-27
    Keywords: 94-609; 94-609A; Age model; Age model, optional; Comment; Datum level; Deep Sea Drilling Project; Depth, bottom/max; DEPTH, sediment/rock; Depth, top/min; DRILL; Drilling/drill rig; DSDP; Event label; Glomar Challenger; Leg94; North Atlantic/FLANK
    Type: Dataset
    Format: text/tab-separated-values, 510 data points
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    Publication Date: 2023-06-27
    Keywords: 94-611; 94-611C; 94-611D; Age model; Age model, optional; Comment; Datum level; Deep Sea Drilling Project; Depth, bottom/max; DEPTH, sediment/rock; Depth, top/min; DRILL; Drilling/drill rig; DSDP; Event label; Glomar Challenger; Leg94; North Atlantic/RIDGE
    Type: Dataset
    Format: text/tab-separated-values, 406 data points
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 7
    Publication Date: 2023-06-27
    Keywords: 94-608; 94-608A; Age model; Age model, optional; Comment; Datum level; Deep Sea Drilling Project; Depth, bottom/max; DEPTH, sediment/rock; Depth, top/min; DRILL; Drilling/drill rig; DSDP; Event label; Glomar Challenger; Leg94; North Atlantic/FLANK
    Type: Dataset
    Format: text/tab-separated-values, 536 data points
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    ISSN: 1432-1793
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The spatial, diel and tidal variability in the abundance of piscivorous fishes and their teleost prey, and the dietary composition of predatory fishes were investigated in beds of Heterozostera tasmanica within Port Phillip Bay, Australia, from September 1997 to February 1998. Predatory and prey fish assemblages were sampled from beds of H. tasmanica at three locations during each combination of diel (day and night) and tidal (high and low) cycles. Pelagic and benthic crustaceans represented 〉60% by abundance of the diets of all predatory fishes. Seven species, 54% of all predatory fishes, were piscivorous. These piscivores consumed individuals from seven families, 36.8% of the fish families being associated with seagrass. Western Australian salmon, Arripis truttacea (Arripidae) (n = 174) and yank flathead, Platycephalus speculator (Platycephalidae) (n = 46) were the most abundant piscivores. A. truttacea consumed larval/post-larval atherinids, gobiids and sillaginids. P. speculator consumed late-juvenile/adult atherinids, clinids and gobiids. While the abundances of piscivores varied between locations (P 〈 0.001) and diel periods (P = 0.028), the relative differences in piscivore abundance between sites and diel periods were not consistent between tides. The abundances of A. truttacea varied in a complex way amongst sites, diel period and tidal cycle, as shown by a three-way interaction between these factors (P = 0.026). Only during diurnal periods at St. Leonards was the abundance of A. truttacea significantly higher during high than low tides (P 〈 0.001). During the other diel periods at each site, the abundance of A. truttacea did not vary. P. speculator was significantly more abundant nocturnally (P = 0.017). The abundance of small (prey) fishes varied significantly amongst sites (P 〈 0.001). During the day, the abundance of small fishes did not vary between high and low tides (P = 0.185), but their nocturnal abundance was greater during low tide (P 〈 0.001). Atherinids (n = 1732) and sillaginids (n = 1623) were the most abundant families of small fishes. Atherinids were significantly more abundant nocturnally (P = 0.005) and during low tides (P = 0.029), and varied significantly amongst sites (P 〈 0.001). Sillaginids varied significantly only amongst sites (P 〈 0.001). Seagrass beds provide a foraging habitat for a diverse assemblage of predatory fishes, many of which are piscivorous. Anti-predator behaviour and amongst-location variability in abundances of piscivorous fishes may explain some of the diel and tidal, and broad-scale spatial patterns in small-fish abundances.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Marine biology 95 (1987), S. 157-166 
    ISSN: 1432-1793
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Daily growth increments on otoliths were used to age larvae of the pleuronectid fluonders Rhombosolea tapirina Günther and Ammotretis rostratus Günther, collected from Port Phillip Bay, Victoria, Australia, in winter 1984. Daily formation of growth increments was confirmed for R. tapirina by examining the growth of the marginal increment on otoliths of larvae collected over two 24h periods in winter 1985. The first distinctive growth increment was laid down approximately 5 d after hatching, at the onset of external feeding. Growth of flounder larvae was exponential from an early feeding stage to notochord flexion at approximately 30 d after hatching. The specific growth rate was very similar for the two species, at slightly over 4% of standard length per day. Predicted absolute growth rate of R. tapirina larvae increased from approximately 0.10 mm d-1 in early feeding larvae to approximately 0.23 mm d-1 in flexion-stage larvae, compared with 0.12 to 0.28 mm d-1 for A. rostratus larvae of equivalent ages. Exponential models did not adequately describe growth of first-feeding larvae, which was slower than predicted. Growth in the field was faster than that recorded for the same species in the laboratory at higher water temperatures and prey abundances. Otolith growth accelerated markedly in relation to growth in length at the beginning of metamorphosis, causing a significant alteration in the morphology of growth increments, and eventually leading to the cessation of production of visible increments.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Chromosoma 93 (1986), S. 413-419 
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Comparisons were made between two kinds of tetraploids derived from the hybrid Lolium temulentum x L. perenne. One hybrid behaves like an autotetraploid with multivalents at first metaphase of meiosis in pollen mother cells. The other behaves like an allotetraploid, in which pairing at first metaphase is restricted to bivalents comprised of strictly homologous chromosomes. The “diploidisation” of the latter form is controlled by determinants located on both the normal, A chromosomes and on supernumary B chromosomes. Reconstruction of synaptonemal complexes and their elements, from serial sections through pollen mother cell nuclei examined under the electron microscope, reveals that at zygotene pairing in both forms results in multivalent formation involving non-homologous as well as homologous chromosomes. The mechanism responsible for the diploidisation is, therefore, not based on a restriction of pairing at early meiosis to homologous chromosomes but on a “correction” or transformation of the multivalent chromosome associations to bivalents subsequent to zygotene. The transformation is not completed until late pachytene. In the multivalent-forming tetraploid a maximum of four chromosomes are associated at first metaphase. Yet configurations of a higher valency are found at zygotene. There is, therefore, a partial transformation of multivalents even in this autotetraploid form which restricts configurations at metaphase I to homologous and homoeologous chromosomes only. In both hybrids some homologous bivalents are not the product of resolution of multivalents but result from two-by-two pairing from the beginning of zygotene.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...