ALBERT

Description: Carbonate buildups and mounds are impressive biogenic structures throughout Earth history. In the recent NE Atlantic, cold-water coral (CWC) reefs form giant carbonate mounds of up to 300 m of elevation. The expansion of these coral carbonate mounds is paced by climatic changes during the past 2.7 Myr. Environmental control on their development is directly linked to controls on its main constructors, the reef-building CWCs. Seawater density has been identified as one of the main controlling parameter of CWC growth in the NE Atlantic. One possibility is the formation of a pycnocline above the carbonate mounds, which is increasing the hydrodynamic regime, supporting elevated food supply, and possibly facilitating the distribution of coral larvae. The potential to reconstruct past seawater densities from stable oxygen isotopes of benthic foraminifera has been further developed: a regional equation gives reliable results for three different settings, peak interglacials (e.g., Holocene), peak glacials (e.g., Last Glacial Maximum), and intermediate setting (between the two extremes). Seawater densities are reconstructed for two different NE Atlantic CWC carbonate mounds in the Porcupine Seabight indicating that the development of carbonate mounds is predominantly found at a seawater density range between 27.3 and 27.7 kg m−3 (σΘ notation). Comparable to recent conditions, we interpret the reconstructed density range as a pycnocline serving as boundary layer, on which currents develop, carrying nutrition and possibly coral larvae. The close correlation of CWC reef growth with reconstructed seawater densities through the Pleistocene highlights the importance of pycnoclines and intermediate water mass dynamics.

Description: 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.

Description: 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.

Description: 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.

Description: There is still considerable debate about which mechanisms drive the relationship between biodiversity and ecosystem function (BEF). Although most scientists agree on the existence of two underlying mechanisms, complementarity and selection, experimental studies keep producing contrasting results on the relative contributions of the two effects. We present a spatially explicit resource competition model and investigate how the strength of these effects is influenced by trait and environmental variability, resource distribution, and species pool size. Our results demonstrate that the increase of biomass production with increasing species numbers depends on the concurrence of environmental and trait variability: BEF relationships are stronger if functionally different species coexist in a landscape with heterogeneous resource supply. These large biodiversity effects arise from complementarity effects, whereas selection effects are maximized when broad trait ranges coincide with narrow ranges of resource supply ratios. Our results will therefore help to resolve the debate on complementarity and selection mechanisms.

Description: The δ30Si of biogenic silica ( urn:x-wiley:gbc:media:gbc20388:gbc20388-math-0001) in marine sediments is a promising proxy for the reconstruction of silicic acid utilization by diatoms in the geological past. The application of this proxy, however, requires an understanding of the modern δ30Si distributions and their controlling mechanisms. Here we present results from a modern climate simulation with a coupled ocean‐sediment model that includes a prognostic formulation of biogenic silica production with concurrent silicon isotopic fractionation. In agreement with previous studies, biological fractionation combined with physical transport and mixing determines the oceanic distribution of simulated δ30Si. A new finding is a distinct seasonal cycle of δ30Si in the surface ocean, which is inversely related to that of silicic acid concentration and mixed layer depth. We also provide the first simulation results of sedimentary δ30Si, which reveal that (1) the urn:x-wiley:gbc:media:gbc20388:gbc20388-math-0002 distribution in the surface sediment reflects the exported urn:x-wiley:gbc:media:gbc20388:gbc20388-math-0003 signal from the euphotic zone and (2) the dissolution of biogenic silica in the sediment acts as a source of relatively light δ30Si into the bottom waters of the polar oceans, while it is a source of heavier δ30Si to the subtropical South Atlantic and South Pacific.

Description: Simulations with a free-running coupled climate model show that heat release associated with Southern Ocean deep convection variability can drive centennial-scale Antarctic temperature variations of up to 2.0 °C. The mechanism involves three steps: Preconditioning: heat accumulates at depth in the Southern Ocean; Convection onset: wind and/or sea-ice changes tip the buoyantly unstable system into the convective state; Antarctic warming: fast sea-ice–albedo feedbacks (on annual–decadal timescales) and slow Southern Ocean frontal and sea-surface temperature adjustments to convective heat release (on multidecadal–century timescales) drive an increase in atmospheric heat and moisture transport toward Antarctica. We discuss the potential of this mechanism to help drive and amplify climate variability as observed in Antarctic ice-core records.

Description: Changes of the Atlantic meridional overturning circulation (AMOC) in the mid‐Holocene compared to the preindustrial state are explored in different coupled climate models. Using time‐slice integrations by a newly developed global finite‐element model ECHAM6‐FESOM with unstructured mesh and high resolution, our simulations show an enhanced mid‐Holocene AMOC, accompanied by an increase in the ocean salinity over regions of deep water formation. We identify two different processes affecting the AMOC: (1) a more positive phase of North Atlantic Oscillation (NAO) increased water density over the Labrador Sea through anomalous net evaporation and surface heat loss; (2) a decreased import of sea ice from the Arctic causes a freshwater reduction in the northern North Atlantic Ocean. Using the coupled model ECHAM6‐MPIOM in T63GR15 and T31GR30 grids, we find that the simulated AMOC has significant discrepancy with different model resolutions. In detail, stronger‐than‐present mid‐Holocene AMOC is revealed by simulations with the T63GR15 grid, which resembles the result of ECHAM6‐FESOM, while a decline of the mid‐Holocene AMOC is simulated by the low resolution model with the T31GR30 grid. Such discrepancy can be attributed to different changes in Labrador Sea density which is mainly affected by (1) NAO‐induced net precipitation and deep water convection, (2) freshwater transport from the Arctic Ocean, and (3) the strength of AMOC itself. Finally, we analyzed available coupled climate models showing a diversity of responses of AMOC to mid‐Holocene forcings, most of which reveal positive AMOC changes related to northern high latitudes salinification.

Description: Key Points: • Little deep water circulation changes in the past 240,000 years in the central South Pacific • Reduced North Atlantic Deep Water admixture during glacials to the Southern Ocean • South Pacific lithogenic material mainly sourced from SE Australia and South New Zealand The South Pacific is a sensitive location for the variability of the global oceanic thermohaline circulation given that deep waters from the Atlantic Ocean, the Southern Ocean, and the Pacific basin are exchanged. Here we reconstruct the deep-water circulation of the central South Pacific for the last two glacial cycles (from 240,000 years ago to the Holocene) based on radiogenic neodymium (Nd) and lead (Pb) isotope records complemented by benthic stable carbon data obtained from two sediment cores located on the flanks of the East Pacific Rise. The records show small but consistent glacial/interglacial changes in all three isotopic systems with interglacial average values of -5.8 and 18.757 for εNd and 206Pb/204Pb, respectively, whereas glacial averages are -5.3 and 18.744. Comparison of this variability of Circumpolar Deep Water (CDW) to previously published records along the pathway of the global thermohaline circulation is consistent with reduced admixture of North Atlantic Deep Water (NADW) to CDW during cold stages. The absolute values and amplitudes of the benthic δ13C variations are essentially indistinguishable from other records of the Southern Hemisphere and confirm that the low central South Pacific sedimentation rates did not result in a significant reduction of the amplitude of any of the measured proxies. In addition, the combined detrital Nd and strontium (87Sr/86Sr) isotope signatures imply that Australian and New Zealand dust has remained the principal contributor of lithogenic material to the central South Pacific.

Description: Ice-rich permafrost coasts in the Arctic are highly sensitive to climate warming and erode at a pace that exceeds the global average. Permafrost coasts deliver vast amounts of organic carbon into the nearshore zone of the Arctic Ocean. Numbers on flux exist for particulate organic carbon (POC) and total or soil organic carbon (TOC, SOC). However, they do not exist for dissolved organic carbon (DOC), which is known to be highly bioavailable. This study aims to estimate DOC stocks in coastal permafrost as well as the annual flux into the ocean. DOC concentrations in ground ice were analyzed along the ice-rich Yukon coast (YC) in the western Canadian Arctic. The annual DOC flux was estimated using available numbers for coast length, cliff height, annual erosion rate, and volumetric ice content in different stratigraphic horizons. Our results showed that DOC concentrations in ground ice range between 0.3 and 347.0 mg L^-1 with an estimated stock of 13.6 ± 3.0 g m^-3 along the YC. An annual DOC flux of 54.9 ± 0.9 Mg yr^-1 was computed. These DOC fluxes are low compared to POC and SOC fluxes from coastal erosion or POC and DOC fluxes from Arctic rivers. We conclude that DOC fluxes from permafrost coasts play a secondary role in the Arctic carbon budget. However, this DOC is assumed to be highly bioavailable. We hypothesize that DOC from coastal erosion is important for ecosystems in the Arctic nearshore zones, particularly in summer when river discharge is low, and in areas where rivers are absent.