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  • PANGAEA
  • 2015-2019  (3)
  • 2000-2004  (1)
  • 2016  (3)
  • 2001  (1)
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  • 2015-2019  (3)
  • 2000-2004  (1)
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  • 1
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    PANGAEA
    In:  Supplement to: Kaplan, Jed O; Pfeiffer, Mirjam; Kolen, Jan C A; Davis, Basil A S (2016): Large Scale Anthropogenic Reduction of Forest Cover in Last Glacial Maximum Europe. PLoS ONE, 11(11), e0166726, https://doi.org/10.1371/journal.pone.0166726
    Publication Date: 2023-01-13
    Description: Reconstructions of the vegetation of Europe during the Last Glacial Maximum (LGM) are an enigma. Pollen-based analyses have suggested that Europe was largely covered by steppe and tundra, and forests persisted only in small refugia. Climate-vegetation model simulations on the other hand have consistently suggested that broad areas of Europe would have been suitable for forest, even in the depths of the last glaciation. Here we reconcile models with data by demonstrating that the highly mobile groups of hunter-gatherers that inhabited Europe at the LGM could have substantially reduced forest cover through the ignition of wildfires. Similar to hunter-gatherers of the more recent past, Upper Paleolithic humans were masters of the use of fire, and preferred inhabiting semi-open landscapes to facilitate foraging, hunting and travel. Incorporating human agency into a dynamic vegetation-fire model and simulating forest cover shows that even small increases in wildfire frequency over natural background levels resulted in large changes in the forested area of Europe, in part because trees were already stressed by low atmospheric CO2 concentrations and the cold, dry, and highly variable climate. Our results suggest that the impact of humans on the glacial landscape of Europe may be one of the earliest large-scale anthropogenic modifications of the earth system.
    Type: Dataset
    Format: application/zip, 5.3 MBytes
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  • 2
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    PANGAEA
    In:  Supplement to: Elling, Felix J; Spiegel, Cornelia; Estrada, Solveig; Davis, Donald W; Reinhardt, Lutz; Henjes-Kunst, Friedhelm; Allroggen, Niklas; Dohrmann, Reiner; Piepjohn, Karsten; Lisker, Frank (2016): Origin of Bentonites and Detrital Zircons of the Paleocene Basilika Formation, Svalbard. Frontiers in Earth Science, 4:73, https://doi.org/10.3389/feart.2016.00073
    Publication Date: 2023-10-21
    Description: Major and trace element composition as well as Sm-Nd isotopes of whole-rock samples and clay fractions (〈2 µm) of bentonite layers and U-Pb ages of detrital zircons from the Paleogene Basilika Formation (Svalbard) and Mount Lawson Formation (Ellesmere Island).
    Keywords: Center for Marine Environmental Sciences; GeoB; Geosciences, University of Bremen; MARUM
    Type: Dataset
    Format: application/zip, 7 datasets
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  • 3
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    PANGAEA
    In:  Supplement to: Anderson, Linda Davis; Ravelo, Ana Christina (2001): Data report: Biogenic opal in Palmer Deep sediments, Site 1098, Leg 178. In: Barker, PF; Camerlenghi, A; Acton, GD; Ramsay, ATS (eds.) Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 178, 1-7, https://doi.org/10.2973/odp.proc.sr.178.216.2001
    Publication Date: 2024-01-09
    Description: High-resolution records of sedimentary proxies provide insights into fine-scale geochemical responses to climatic forcing. Gamma-ray attenuation (GRA) bulk-density data and magnetic stratigraphy records from Palmer Deep, Site 1098, show variability close to the same scale as ice cores, making this site ideal for high-resolution geochemical investigations. In conjunction with shipboard geophysical measurements, silica records allow high-resolution evaluation of the frequencies and amplitudes of biogenic variability. This provides investigators additional data sets to evaluate the global extent of climatic events that are presently defined by regional oceanic data sets (e.g., Younger Dryas in the North Atlantic) and to evaluate the potential mechanisms that link biological productivity and climate in the Southern Ocean. In addition, because of the observed links between diatom blooms and export productivity (Michaels and Silver, 1988, doi:10.1016/0198-0149(88)90126-4), biogenic silica may be an indicator of the efficiency of the biological pump (removal of organic carbon from the euphotic zone and burial within the sediments). Because the net removal of CO2 (on short time scales up to millennial, the balance between upwelled CO2, carbon fixation, and the removal of organic carbon from the surface ocean) can determine the atmospheric concentration; proxies that allow us to quantify export production yield insights into carbon cycle responses. In today's ocean, diatoms are integrally linked with new production (production based on the use of nitrate and molecular nitrogen rather than ammonium, which is generated by the microbial degradation of organic carbon) (Dugdale and Goering, 1967). Thus, as with nutrient utilization proxies, biogenic silica may be a good indicator of export production. The difficulties lie in translating the biogenic opal burial records to export production. Numerous factors control the preservation of sedimentary biogenic silica, including depth of the water column, water temperature, trace element chemistry, grazing pressure, bloom structure, and species composition of the diatom assemblage (Nelson et al., 1995, doi:10.1029/95GB01070). In addition, several recent investigations have noted additional complications. Iron limitation increases the uptake of Si relative to carbon (Hutchins et al., 1998, ; Takeda, 1998, doi:10.1038/31674). In the Southern Ocean, iron limitation could produce more robust, and thus better preserved, diatoms; thus, the burial record may be a record of iron limitation rather than of the export of organic carbon (Boyle, 1998). In addition, laboratory experiments show that bacteria accelerate the dissolution of biogenic silica (Bidle and Azam, 1999, doi:10.1038/17351). Both the species composition and temperature seem to influence the amount of dissolution. Evidence of recycling of silicic acid within the photic zone (Brzezinski et al., 1997) suggests that the silica pump (removal from the euphotic zone of silica relative to nitrogen and phosphorus) may work with variable efficiency. This becomes an issue when trying to reconstruct the removal of organic carbon from sedimentary biogenic silica records. In fact, there is a wide range in the Si:Corganic molar ratio in the Southern Ocean (0.18-0.81) (Nelson et al., 1995; Ragueneau et al., 2000, doi:10.1016/S0921-8181(00)00052-7). Thus, the presence (or absence) of biogenic silica alone may tell us little about the export productivity, complicating the interpretation of age-related trends. One recent assessment has added some hope to links between productivity and opal burial in the Southern Ocean (Pondaven et al., 2000). Quantitative comparison of different productivity proxies will greatly aid in this evaluation.
    Keywords: 178-1098; COMPCORE; Composite Core; Depth, composite; DEPTH, sediment/rock; Drake Passage; DSDP/ODP/IODP sample designation; Intercore correlation; Joides Resolution; Leg178; Ocean Drilling Program; ODP; Opal, biogenic silica; Opal, biogenic silica, standard deviation; Opal, extraction; Mortlock & Froelich, 1989; Sample code/label
    Type: Dataset
    Format: text/tab-separated-values, 2632 data points
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  • 4
    Publication Date: 2024-03-15
    Description: To date, numerous studies have shown negative impacts of CO2-acidified seawater (i.e. ocean acidification, OA) on marine organisms including calcifying invertebrates and fishes; however, limited research has been conducted on the physiological effects of OA on polar fishes and even less on the impacts of OA on early developmental stages of polar fishes. We evaluated aspects of aerobic metabolism and cardiorespiratory physiology of juvenile emerald rockcod Trematomus bernacchii, an abundant fish in the Ross Sea, Antarctica, to elevated partial pressure of carbon dioxide (pCO2) (420 [Ambient], 650 [Moderate] and 1050 [High] μtam pCO2) over a one-month period. We examined cardiorespiratory physiology including heart rate, stroke volume, cardiac output and ventilation, whole organism metabolism via oxygen consumption rate, and sub-organismal aerobic capacity by citrate synthase enzyme activity. Juvenile fish showed an increase in ventilation rate under High pCO2 compared to Ambient pCO2, while cardiac performance, oxygen consumption, and citrate synthase activity were not significantly affected by elevated pCO2. Acclimation time did have a significant effect on ventilation rate, stroke volume, cardiac output and citrate synthase activity, such that all metrics increased over the 4-week exposure period. These results suggest that juvenile emerald rockcod are robust to near-future increases in OA and may have the capacity to adjust for future increases in pCO2 by increasing acid-base compensation through increased ventilation.
    Keywords: Alkalinity, total; Alkalinity, total, standard deviation; Animalia; Antarctic; Aragonite saturation state; Aragonite saturation state, standard deviation; Behaviour; Bicarbonate ion; Bicarbonate ion, standard deviation; Bottles or small containers/Aquaria (〈20 L); Calcite saturation state; Calcite saturation state, standard deviation; Calculated using seacarb; Calculated using seacarb after Nisumaa et al. (2010); Calculated using seacarb after Orr et al. (2018); Cape_Evans_Ice_Wall; Carbon, inorganic, dissolved; Carbon, inorganic, dissolved, standard deviation; Carbonate ion; Carbonate ion, standard deviation; Carbonate system computation flag; Carbon dioxide; Carbon dioxide, standard deviation; Cardiac output; Chordata; Citrate synthase activity, per protein mass; Citrate synthase activity per fresh mass; Coast and continental shelf; Day of experiment; EXP; Experiment; File name; Fish, standard length; Fish, standard length, standard deviation; Fish, standard length, standard error; Fugacity of carbon dioxide (water) at sea surface temperature (wet air); Fugacity of carbon dioxide in seawater, standard deviation; Fulton's condition factor; Fulton's condition factor, standard deviation; Fulton's condition factor, standard error; Growth/Morphology; Heart rate; Heart rate, standard error; Identification; Laboratory experiment; Mass; Mass, standard deviation; Mass, standard error; Mass specific cardiac output; Mass specific stroke volume; Nekton; OA-ICC; Ocean Acidification International Coordination Centre; Other studied parameter or process; Partial pressure of carbon dioxide, standard deviation; Partial pressure of carbon dioxide (water) at sea surface temperature (wet air); Pelagos; pH; pH, standard deviation; Polar; Potentiometric; Potentiometric titration; Registration number of species; Replicate; Respiration; Respiration rate, oxygen; Salinity; Salinity, standard deviation; Single species; Species; Stroke volume; Temperature, water; Temperature, water, standard deviation; Treatment; Trematomus bernacchii; Type; Uniform resource locator/link to reference; Ventilation rate; Ventilation rate, standard error
    Type: Dataset
    Format: text/tab-separated-values, 16244 data points
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