994 resultados para Kernel Records v Mosley


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The Andorra family of languages (which includes the Andorra Kernel Language -AKL) is aimed, in principie, at simultaneously supporting the programming styles of Prolog and committed choice languages. On the other hand, AKL requires a somewhat detailed specification of control by the user. This could be avoided by programming in Prolog to run on AKL. However, Prolog programs cannot be executed directly on AKL. This is due to a number of factors, from more or less trivial syntactic differences to more involved issues such as the treatment of cut and making the exploitation of certain types of parallelism possible. This paper provides basic guidelines for constructing an automatic compiler of Prolog programs into AKL, which can bridge those differences. In addition to supporting Prolog, our style of translation achieves independent and-parallel execution where possible, which is relevant since this type of parallel execution preserves, through the translation, the user-perceived "complexity" of the original Prolog program.

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The present work reports on the extended distribution of nineteen species in the Mediterranean. These are: Upeneus pori (Fish:Turkey), Bursatella leachii (Mollusca, Opisthobranchia: eastern coast of Spain), Sparisoma cretense (Fish: Ionian coast of Greece), Pseudobryopsis myura (Chlorophyta:Turkey), Aplysia dactylomela (Mollusca, Opisthobranchia: Karpathos island, and Kyklades Archipelago, Greece), Asparagopsis armata and Botryocladia madagascariensis (Rhodophyta: South Peloponnesos, Greece), Oxynotus centrina (Fish: Greece), Caulerpa racemosa var. cylindracea (Chlorophyta ), Stypopodium schimperi (Phaeophyta ) Siganus luridus and Stephanolepis diaspros (Fish) Percnon gibbesi (Decapoda, Brachyura) (Kyklades Archipelago, Greece), Cerithium scabridum (Mollusca, Prosobranchia: Anavissos: Greece) and Cerithium renovatum (Mollusca, Prosobranchia: N. Κriti), Cassiopea andromeda (Scyphomedusa: Rhodos Island, Greece), Abra tenuis (Mollusca Bivalvia: Vouliagmeni Lake, Greece) Lagocephalus lagocephalus (Fish: Calabrian coast, Italy) and Plocamopherus ocellatus (Mollusca, Opisthobranchia: İskenderun Bay, Turkey).

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Reduced nitrate supply to the subarctic North Pacific (SNP) surface during the last ice age has been inferred from coupled changes in diatom-bound d15N (DB-d15N), bulk sedimentary d15N, and biogenic fluxes. However, the reliability of bulk sedimentary and DB-d15N has been questioned, and a previously reported d15N minimum during Heinrich Stadial 1 (HS1) has proven difficult to explain. In a core from the western SNP, we report the foraminifera-bound d15N (FB-d15N) in Neogloboquadrina pachyderma and Globigerina bulloides, comparing them with DB-d15N in the same core over the past 25 kyr. The d15N of all recorders is higher during the Last Glacial Maximum (LGM) than in the Holocene, indicating more complete nitrate consumption. N. pachyderma FB-d15N is similar to DB-d15N in the Holocene but 2.2 per mil higher during the LGM. This difference suggests a greater sensitivity of FB-d15N to changes in summertime nitrate drawdown and d15N rise, consistent with a lag of the foraminifera relative to diatoms in reaching their summertime production peak in this highly seasonal environment. Unlike DB-d15N, FB-d15N does not decrease from the LGM into HS1, which supports a previous suggestion that the HS1 DB-d15N minimum is due to contamination by sponge spicules. FB-d15N drops in the latter half of the Bølling/Allerød warm period and rises briefly in the Younger Dryas cold period, followed by a decline into the mid-Holocene. The FB-d15N records suggest that the coupling among cold climate, reduced nitrate supply, and more complete nitrate consumption that characterized the LGM also applied to the deglacial cold events.

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Late Weichselian and Holocene dinoflagellate cyst assemblages have been investigated at two stations situated close to the modern Polar Front at the continental margin oft East Greenland. Both the concentrations of dinoflagelate cysts and the assemblage composition reflect changes in the surface water conditions, occurring in distinct steps during the past 15,000 years. Low concentrations of dinoflagellate cysts during Termination Ia suggest harsh environmental conditions, most probably caused by an extensive sea-ice cover and/or a high influx of low salinity meltwater. A surface water warming was recorded from 13,000 - 12,000 years BP, related to the inflow of warmer water trom the North Atlantic into the western Norwegian-Greenland Sea. The interval between Terminations la and Ib was characterized by a strong seasonality with an extensive sea-ice cover in winter and relatively warm surface waters in summer. At the transition to the Holocene, a reorganisation of the hydrography resulted in surface water conditions characteristic for the Holocene with three well-defined major water masses and oceanographic fronts The modern water mass conditions at both stations were established at the end of Termination Ib, around 6,400 to 6,800 years BP. In general, the influence of colder surface waters was more pronounced at the location off Scoresby Sund throughout the Holocene. Arctic water had the strongest influence at both stations in the middle Holocene. A progressive cooling with an increase in sea-ice cover is time-transgressivelyrecorded at both stations during the Holocene, indicating that the Polar Front moved to its present position or that branches of the zonal currents expanded from the East Greenland shell eastward during tlie last 3,000 years.

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Reliable information of past vegetation changes are important to project future changes, especially for areas undergoing rapid transitioning such as the boreal treeline. The application of detailed sedDNA records has the potential to enhance our understanding of vegetation changes gained mainly from pollen studies of lake sediments. This study investigates sedDNA and pollen records from 31 lakes along a gradient of increasing larch forest cover in northern Siberia (Taymyr Peninsula) and compares them with vegetation field surveys within the lake's catchment. With respect to vegetation richness, sedDNA recorded 114 taxa, about half of them to species level, while pollen analyses identified 43 pollen taxa. Both approaches exceed the 31 taxa revealed by vegetation field surveys of 400 m**2 plots. From north to south, Larix percentages increase, as is consistently recorded by all three methods. Furthermore, tundra sites are separated from forested sites in the plots of the principal component analyses. Comparison of ordination results by Procrustes and Protest analyses yields a significant fit among all compared pairs of records. Despite the overall comparability of sedDNA and pollen analyses certain idiosyncrasies in the compositional signal are observed, such as high percentages of Alnus and Betula in all pollen spectra and high percentages of Salix in all sedDNA spectra. In conclusion, our results from the treeline show that sedDNA analyses perform better than pollen in recording site-specific richness (i.e. presence/absence of certain vegetation taxa in the direct vicinity of the lake) and perform as good as pollen in tracing regional vegetation composition.

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Hydrogen isotope values (dD) of sedimentary terrestrial leaf wax such as n-alkanes or n-acids have been used to map and understand past changes in rainfall amount in the tropics because dD of precipitation is commonly assumed as the first order controlling factor of leaf wax dD. Plant functional types and their photosynthetic pathways can also affect leaf wax dD but these biological effects are rarely taken into account in paleo studies relying on this rainfall proxy. To investigate how biological effects may influence dD values we here present a 37,000-year old record of dD and stable carbon isotopes (d13C) measured on four n-alkanes (n-C27, n-C29, n-C31, n-C33) from a marine sediment core collected off the Zambezi River mouth. Our paleo d13C records suggest that each individual n-alkanes had different C3/C4 proportional contributions. n-C29 was mostly derived from a C3 dicots (trees, shrubs and forbs) dominant vegetation throughout the entire record. In contrast, the longer chain n-C33 and n-C31 were mostly contributed by C4 grasses during the Glacial period but shifted to a mixture of C4 grasses and C3 dicots during the Holocene. Strong correlations between dD and d13C values of n-C33 (correlation coefficient R2 = 0.75, n = 58) and n-C31 (R2 = 0.48, n = 58) suggest that their dD values were strongly influenced by changes in the relative contributions of C3/C4 plant types in contrast to n-C29 (R2 = 0.07, n = 58). Within regions with variable C3/C4 input, we conclude that dD values of n-C29 are the most reliable and unbiased indicator for past changes in rainfall, and that dD and d13C values of n-C31 and n-C33 are sensitive to C3/C4 vegetation changes. Our results demonstrate that a robust interpretation of palaeohydrological data using n-alkane dD requires additional knowledge of regional vegetation changes from which nalkanes are synthesized, and that the combination of dD and d13C values of multiple n-alkanes can help to differentiate biological effects from those related to the hydrological cycle.

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The deep-sea cores M 16415-2 and M 16416-2 at about 9°N off Sierra Leone were analysed palynologically for the time interval 140,000-70,000 yr B.P. Results were presented in absolute (pollen concentration and pollen influx) and relative diagrams (pollen percentage). In a previous study it was evidenced that in northwest Africa pollen is mainly transported to the Atlantic by wind, so that the efficiency of aeolian pollen transport (pollen flux) could be used to evaluate changes in the intensity of the northeast trade winds. The glacial episodes (represented by the oxygen isotope stages 6 and 4) are characterized by strong northeast trade winds, whereas the last interglacial (stage 5) is characterized by weak trade winds. The pollen influx diagram shows that the intensity of the trade winds increased slightly during the relatively cool intervals of stage 5 (viz. 5.4 and 5.2). Tropical forest had maximally expanded around 124,000 yr B.P. (stage 5.5), around 98,000 yr B.P. (transition of stage 5.3 to 5.2), and around 70,000 yr B.P. (first part of stage 4): an increasing delay of the response of tropical forest to global intervals with maximum temperature is apparent during the last interglacial. As tropical forests need continuous humidity, the record of tropical forest monitors changes in climatic humidity south of the Sahara. During the last interglacial, the southern boundary of the Sahara shifted only little: expansions and contractions of the tropical forest area are correlated with contra-oscillations of the grass-dominated savanna zone. Great latitudinal shifts of the desert savanna boundary, on the contrary, occurred during the penultimate glacial interglacial transition (around 128,000 yr B.P.) to the north, and during the last interglacial-glacial transition (around 65,000 yr B.P.) to the south.

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Vols. 1-2 have imprint: Cairo, Printed by the French Institute of Oriental Archaeology.