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  • Wiley  (191.939)
  • American Physical Society  (105.684)
  • American Chemical Society (ACS)  (66.957)
  • 2015-2019  (347.023)
  • 1950-1954  (17.557)
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  • 11
    Publikationsdatum: 2024-03-22
    Beschreibung: The complex deglacial to Holocene oceanographic development in the Gulf of Guayaquil (Eastern Equatorial Pacific) is reconstructed for sea surface and subsurface ocean levels from (isotope) geochemical proxies based on marine sediment cores. At sea surface, southern sourced Cold Coastal Water and tropical Equatorial Surface Water/Tropical Surface Water are intimately related. In particular since ~10 ka, independent sea surface temperature proxies capturing different seasons emphasize the growing seasonal contrast in the Gulf of Guayaquil, which is in contrast to ocean areas further offshore. Cold Coastal Water became rapidly present in the Gulf of Guayaquil during the austral winter season in line with the strengthening of the Southeast Trades, while coastal upwelling off Peru gradually intensified and expanded northward in response to a seasonally changing atmospheric circulation pattern affecting the core locations intensively since 4 ka BP. Equatorial Surface Water, instead, was displaced and Tropical Surface Water moved northward together with the Equatorial Front. At subsurface, the presence of Equatorial Under Current-sourced Equatorial Subsurface Water was continuously growing, prominently since ~10–8 ka B.P. During Heinrich Stadial 1 and large parts of the Bølling/Allerød, and similarly during short Holocene time intervals at ~5.1–4 ka B.P. and ~1.5–0.5 ka B.P., the admixture of Equatorial Subsurface Water was reduced in response to both short-term weakening of Equatorial Under Current strength from the northwest and emplacement by tropical Equatorial Surface Water, considerably warming the uppermost ocean layers.
    Materialart: Article , PeerReviewed
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  • 12
    Publikationsdatum: 2024-03-22
    Beschreibung: High-latitude cold-water coral (CWC) reefs are particularly susceptible due to enhanced CO2 uptake in these regions. Using precisely dated (U/Th) CWCs (Lophelia pertusa) retrieved during research cruise POS 391 (Lopphavet 70.6°N, Oslofjord 59°N) we applied boron isotopes (δ11B), Ba/Ca, Li/Mg and U/Ca ratios to reconstruct the environmental boundary conditions of CWC reef growth. The sedimentary record from these CWC reefs reveals a lack of corals between ∼ 6.4 and 4.8 ka. The question remains if this phenomenon is related to changes in the carbonate system or other causes. The initial postglacial setting had elevated Ba/Ca ratios, indicative of meltwater fluxes showing a decreasing trend towards cessation at 6.4 ka with a oscillation pattern similar to continental glacier fluctuations. Downcore U/Ca ratios reveal an increasing trend, which is outside the range of modern U/Ca variability in L. pertusa, suggesting changes of seawater pH near 6.4 ka. The reconstructed BWT at Lopphavet reveals a striking similarity to Barent Sea-Surface and sub-Sea-Surface-Temperature records. We infer that meltwater pulses weakened the North Atlantic Current system resulting in southward advances of cold and CO2 rich Arctic waters. A corresponding shift in the δ11B record from ∼ 25.0‰ to ∼ 27.0 ‰ probably implies enhanced pH-up regulation of the CWCs due to the higher pCO2 concentrations of ambient seawater, which hastened Mid-Holocene CWC reef decline on the Norwegian Margin.
    Materialart: Article , PeerReviewed
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  • 13
    Publikationsdatum: 2024-02-29
    Beschreibung: Continental slopes are areas of high primary productivity, in particular where strong winds allow cold, nutrient‐laden deep water to upwell. The seafloor in upwelling areas is affected by repeated large submarine landslides, but the special environmental conditions have as yet not been taken into account in the analysis of these landslides. We show evidence for a potential link between environmental conditions and landslide occurrence for the Cap Blanc Slide Complex in the center of the Cap Blanc upwelling zone. Ocean Drilling Program Site 658 was drilled inside the slide complex, and its integration with high‐resolution seismic lines reveals that the onset of sliding postdates the onset of glaciations in the Northern Hemisphere. The sediment associated with failure surfaces of all seven slide events comprises of diatom ooze, the conditions for the formation of which are only met at the end of glacials. Preconditioning of the slope in the Cap Blanc Slide Complex is thus climatically controlled. We conclude that the presence of ooze formed under specific environmental conditions is an important factor in preconditioning slopes to fail in the Cap Blanc Slide Complex and potentially also at other continental slopes with high primary productivity.
    Materialart: Book chapter , NonPeerReviewed
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  • 14
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    Unbekannt
    Wiley
    In:  EPIC3Transactions of the Institute of British Geographers, Wiley, 43(1), pp. 61-78, ISSN: 0020-2754
    Publikationsdatum: 2024-02-07
    Beschreibung: The Pacific region of Colombia, like many sparsely populated places in developing countries, has been imagined as empty in social terms, and yet full in terms of natural resources and biodiversity. These imaginaries have enabled the creation of frontiers of land and sea control, where the state as well as private and illegal actors have historically dispossessed Afro-descendant and indigenous peoples. This paper contributes to the understanding of territorialisation in the oceans, where political and legal framings of the sea as an open-access public good have neglected the existence of marine social processes. It shows how Afro-descendant communities and non-state actors are required to use the language of resources, rather than socio-cultural attachment, to negotiate state marine territorialisation processes. Drawing on a case study on the Pacific coast of Colombia, we demonstrate that Afro-descendant communities hold local aquatic epistemologies, in which knowledge and the production of space are entangled in fluid and volumetric spatio-temporal dynamics. However, despite the social importance of aquatic environments, they were excluded from Afro-descendants' collective territorial rights in the 1990s. Driven by their local aquatic epistemologies, coastal communities are reclaiming authority over the seascape through the creation of a marine protected area. We argue that they have transformed relations of authority at sea to ensure local access and control, using state institutional instruments to subvert and challenge the legal framing of the sea as an open access public good. As such, this marine protected area represents a place of resistance that ironically subjects coastal communities to disciplinary technologies of conservation.
    Repository-Name: EPIC Alfred Wegener Institut
    Materialart: Article , isiRev
    Format: application/pdf
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  • 15
    Publikationsdatum: 2024-01-29
    Beschreibung: Marine sediments host large amounts of methane (CH4), which is a potent greenhouse gas. Quantitative estimates for methane release from marine sediments are scarce, and a poorly constrained temporal variability leads to large uncertainties in methane emission scenarios. Here, we use 2D and 3D seismic reflection, multibeam bathymetric, geochemical and sedimentological data to (I) map and describe pockmarks in the Witch Ground Basin (central North Sea), (II) characterize associated sedimentological and fluid migration structures, and (III) analyze the related methane release. More than 1500 pockmarks of two distinct morphological classes spread over an area of 225 km2. The two classes form independently from another and are corresponding to at least two different sources of fluids. Class 1 pockmarks are large in size (〉 6 m deep, 〉 250 m long, and 〉 75 m wide), show active venting, and are located above vertical fluid conduits that hydraulically connect the seafloor with deep methane sources. Class 2 pockmarks, which comprise 99.5 % of all pockmarks, are smaller (0.9‐3.1 m deep, 26‐140 m long, and 14‐57 m wide) and are limited to the soft, fine‐grained sediments of the Witch Ground Formation and possibly sourced by compaction‐related dewatering. Buried pockmarks within the Witch Ground Formation document distinct phases of pockmark formation, likely triggered by external forces related to environmental changes after deglaciation. Thus, greenhouse gas emissions from pockmark fields cannot be based on pockmark numbers and present‐day fluxes but require an analysis of the pockmark forming processes through geological time.
    Materialart: Article , PeerReviewed , info:eu-repo/semantics/article
    Format: text
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  • 16
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    Unbekannt
    Wiley
    In:  EPIC3Forschung, Wiley, 43(1), pp. 16-21, ISSN: 0172-1518
    Publikationsdatum: 2024-01-22
    Beschreibung: 〈jats:title〉Abstract〈/jats:title〉〈jats:p〉Plattentektonik, vulkanische Aktivität und Spreizung des Ozeanbodens in der Arktis: Die Emmy Noether‐Gruppe MOVE gewinnt nach aufwendigen Forschungs‐expeditionen und Erdbebenmessungen überraschende Erkenntnisse zur Entstehung und Struktur der Ozeanlithosphäre. Ein Werkstattbericht〈/jats:p〉
    Repository-Name: EPIC Alfred Wegener Institut
    Materialart: Article , notRev
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  • 17
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    Unbekannt
    Wiley
    In:  EPIC3German Research, Wiley, 41(2), pp. 8-13, ISSN: 0172-1526
    Publikationsdatum: 2024-01-22
    Beschreibung: 〈jats:title〉Abstract〈/jats:title〉〈jats:p〉Plate tectonics, volcanic activity and ocean floor spreading in the Arctic: Following several complex research expeditions and earthquake measurements, the Emmy Noether group MOVE has obtained some surprising findings about the formation and structure of the ocean lithosphere. A look at the results so far〈/jats:p〉
    Repository-Name: EPIC Alfred Wegener Institut
    Materialart: Article , notRev
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  • 18
    Publikationsdatum: 2024-01-12
    Beschreibung: We present a phylogenetic analysis of spiders using a dataset of 932 spider species, representing 115 families (only the family Synaphridae is unrepresented), 700 known genera, and additional representatives of 26 unidentified or undescribed genera. Eleven genera of the orders Amblypygi, Palpigradi, Schizomida and Uropygi are included as outgroups. The dataset includes six markers from the mitochondrial (12S, 16S, COI) and nuclear (histone H3, 18S, 28S) genomes, and was analysed by multiple methods, including constrained analyses using a highly supported backbone tree from transcriptomic data. We recover most of the higher-level structure of the spider tree with good support, including Mesothelae, Opisthothelae, Mygalomorphae and Araneomorphae. Several of our analyses recover Hypochilidae and Filistatidae as sister groups, as suggested by previous transcriptomic analyses. The Synspermiata are robustly supported, and the families Trogloraptoridae and Caponiidae are found as sister to the Dysderoidea. Our results support the Lost Tracheae clade, including Pholcidae, Tetrablemmidae, Diguetidae, Plectreuridae and the family Pacullidae (restored status) separate from Tetrablemmidae. The Scytodoidea include Ochyroceratidae along with Sicariidae, Scytodidae, Drymusidae and Periegopidae; our results are inconclusive about the separation of these last two families. We did not recover monophyletic Austrochiloidea and Leptonetidae, but our data suggest that both groups are more closely related to the Cylindrical Gland Spigot clade rather than to Synspermiata. Palpimanoidea is not recovered by our analyses, but also not strongly contradicted. We find support for Entelegynae and Oecobioidea (Oecobiidae plus Hersiliidae), and ambiguous placement of cribellate orb-weavers, compatible with their non-monophyly. Nicodamoidea (Nicodamidae plus Megadictynidae) and Araneoidea composition and relationships are consistent with recent analyses. We did not obtain resolution for the titanoecoids (Titanoecidae and Phyxelididae), but the Retrolateral Tibial Apophysis clade is well supported. Penestomidae, and probably Homalonychidae, are part of Zodarioidea, although the latter family was set apart by recent transcriptomic analyses. Our data support a large group that we call the marronoid clade (including the families Amaurobiidae, Desidae, Dictynidae, Hahniidae, Stiphidiidae, Agelenidae and Toxopidae). The circumscription of most marronoid families is redefined here. Amaurobiidae include the Amaurobiinae and provisionally Macrobuninae. We transfer Malenellinae (Malenella, from Anyphaenidae), Chummidae (Chumma) (new syn.) and Tasmarubriinae (Tasmarubrius, Tasmabrochus and Teeatta, from Amphinectidae) to Macrobuninae. Cybaeidae are redefined to include Calymmaria, Cryphoeca, Ethobuella and Willisius (transferred from Hahniidae), and Blabomma and Yorima (transferred from Dictynidae). Cycloctenidae are redefined to include Orepukia (transferred from Agelenidae) and Pakeha and Paravoca (transferred from Amaurobiidae). Desidae are redefined to include five subfamilies: Amphinectinae, with Amphinecta, Mamoea, Maniho, Paramamoea and Rangitata (transferred from Amphinectidae); Ischaleinae, with Bakala and Manjala (transferred from Amaurobiidae) and Ischalea (transferred from Stiphidiidae); Metaltellinae, with Austmusia, Buyina, Calacadia, Cunnawarra, Jalkaraburra, Keera, Magua, Metaltella, Penaoola and Quemusia; Porteriinae (new rank), with Baiami, Cambridgea, Corasoides and Nanocambridgea (transferred from Stiphidiidae); and Desinae, with Desis, and provisionally Poaka (transferred from Amaurobiidae) and Barahna (transferred from Stiphidiidae). Argyroneta is transferred from Cybaeidae to Dictynidae. Cicurina is transferred from Dictynidae to Hahniidae. The genera Neoramia (from Agelenidae) and Aorangia, Marplesia and Neolana (from Amphinectidae) are transferred to Stiphidiidae. The family Toxopidae (restored status) includes two subfamilies: Myroinae, with Gasparia, Gohia, Hulua, Neomyro, Myro, Ommatauxesis and Otagoa (transferred from Desidae); and Toxopinae, with Midgee and Jamara, formerly Midgeeinae, new syn. (transferred from Amaurobiidae) and Hapona, Laestrygones, Lamina, Toxops and Toxopsoides (transferred from Desidae). We obtain a monophyletic Oval Calamistrum clade and Dionycha; Sparassidae, however, are not dionychans, but probably the sister group of those two clades. The composition of the Oval Calamistrum clade is confirmed (including Zoropsidae, Udubidae, Ctenidae, Oxyopidae, Senoculidae, Pisauridae, Trechaleidae, Lycosidae, Psechridae and Thomisidae), affirming previous findings on the uncertain relationships of the \xe2\x80\x9cctenids\xe2\x80\x9d Ancylometes and Cupiennius, although a core group of Ctenidae are well supported. Our data were ambiguous as to the monophyly of Oxyopidae. In Dionycha, we found a first split of core Prodidomidae, excluding the Australian Molycriinae, which fall distantly from core prodidomids, among gnaphosoids. The rest of the dionychans form two main groups, Dionycha part A and part B. The former includes much of the Oblique Median Tapetum clade (Trochanteriidae, Gnaphosidae, Gallieniellidae, Phrurolithidae, Trachelidae, Gnaphosidae, Ammoxenidae, Lamponidae and the Molycriinae), and also Anyphaenidae and Clubionidae. Orthobula is transferred from Phrurolithidae to Trachelidae. Our data did not allow for complete resolution for the gnaphosoid families. Dionycha part B includes the families Salticidae, Eutichuridae, Miturgidae, Philodromidae, Viridasiidae, Selenopidae, Corinnidae and Xenoctenidae (new fam., including Xenoctenus, Paravulsor and Odo, transferred from Miturgidae, as well as Incasoctenus from Ctenidae). We confirm the inclusion of Zora (formerly Zoridae) within Miturgidae.
    Schlagwort(e): Ecology ; Evolution ; Behavior and Systematics
    Repository-Name: National Museum of Natural History, Netherlands
    Materialart: info:eu-repo/semantics/article
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  • 19
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    AGU (American Geophysical Union) | Wiley
    Publikationsdatum: 2023-11-08
    Beschreibung: We use a simple 1-D model representing an isolated density surface in the ocean and 3-D global ocean biogeochemical models to evaluate the concept of computing the subsurface oceanic oxygen utilization rate (OUR) from the changes of apparent oxygen utilization (AOU) and water age. The distribution of AOU in the ocean is not only the imprint of respiration in the ocean's interior but is strongly influenced by transport processes and eventually loss at the ocean surface. Since AOU and water age are subject to advection and diffusive mixing, it is only when they are affected both in the same way that OUR represents the correct rate of oxygen consumption. This is the case only when advection prevails or with uniform respiration rates, when the proportions of AOU and age are not changed by transport. In experiments with the 1-D tube model, OUR underestimates respiration when maximum respiration rates occur near the outcrops of isopycnals and overestimates when maxima occur far from the outcrops. Given the distribution of respiration in the ocean, i.e., elevated rates near high-latitude outcrops of isopycnals and low rates below the oligotrophic gyres, underestimates are the rule. Integrating these effects globally in three coupled ocean biogeochemical and circulation models, we find that AOU-over-age based calculations underestimate true model respiration by a factor of 3. Most of this difference is observed in the upper 1000 m of the ocean with the discrepancies increasing toward the surface where OUR underestimates respiration by as much as factor of 4.
    Materialart: Article , PeerReviewed
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  • 20
    Publikationsdatum: 2023-11-08
    Beschreibung: Upper‐plate normal faults are a widespread structural element in erosive plate margins. Increasing coverage of marine geophysical data has proven that similar features also exist in accretionary margins where horizontal compression usually results in folding and thrust‐faulting. There is a general lack of understanding of the role and importance of normal faulting for the structural and tectonic evolution of accretionary margins. Here, we use high‐resolution 2D and 3D seismic reflection data and derived seismic attributes to map and analyze upper‐plate normal faulting in the marine forearc of the accretionary Hikurangi margin, New Zealand. We document extension of the marine forearc over a wide area along the upper continental slope. The seismically imaged normal faults show low vertical displacements, high dip angles, a preference for landward dip and often en echelon patterns. We evaluate different processes, which may cause the observed extension, including (1) stress change during the earthquake cycle, (2) regional or local uplift and decoupling of shallow strata from compression at depth, as well as (3) rotation of crustal blocks and resulting differential stresses at the block boundaries. The results suggest that normal faults play an important role in the structural and tectonic evolution of accretionary margins, including the northern Hikurangi forearc.
    Materialart: Article , PeerReviewed
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