91 research outputs found

    The effects of multiple trap spacing, baffles and brine volume on sediment trap collection efficiency

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    The hydrodynamic effects on trapping efficiency of sediment trap cross-frame position, baffles and brine volume were evaluated in three short-term (\u3c1 week) experiments in a temperate shallow marine environment (Evans Bay, Wellington Harbour, New Zealand). The effects of trap position and brine were further investigated during two open ocean, free-floating sediment trap deployments (1-2 days) near the Subtropical Front (STF), east of New Zealand. In the Evans Bay experiments (numbered I-III), cross-frames, each holding 12 cylindrical traps (inside diameter 9 cm, height 95 cm), were moored 3 meters above the seafloor in 15-18 m water depths at three randomly selected inner harbor sites. Triplicate subsamples from each cylinder were analyzed for total dry weight and mass fluxes calculated. The STF deployments utilized JGOFS MULTI-traps (inside diameter 7 cm, height 58 cm) attached to cross-frames moored at three depths (120, 300 and 550 m) on drifting arrays (Experiments IV and V). MULTI-trap samples were analyzed for total particulate mass, carbon and nitrogen. Results from Experiments I and V indicate that a spacing of about 3-trap diameters was sufficient to minimize inter-trap interactions and maintain trapping efficiency among traps suspended on a cross-frame at the same depth. Furthermore, baffles had no effect on trapping efficiency and an undetectable impact on zooplankton swimmer populations also collected in traps (Experiment II). In Experiment III, traps that were filled completely with high-density salt brine (50‰ excess NaCl) collected 2-3 times less material than traps with a basal brine height equivalent to 1- and 2.5-trap diameters. In contrast, high levels of inter-site variability confounded the STF MULTI-trap deployments during Experiment IV. However, variability in flux measurements from both Experiments III and IV increased 2 to 3-fold in brine-filled traps. Thus, the potential for brine-filled traps to undercollect material with higher levels of variability could possibly explain previously reported inaccuracies in the sediment trap method

    Abundance of small individuals influences the effectiveness of processing techniques for deep-sea nematodes

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    Nematodes are the most abundant metazoans of deep-sea benthic communities, but knowledge of their distribution is limited relative to larger organisms. Whilst some aspects of nematode processing techniques, such as extraction, have been extensively studied, other key elements have attracted little attention. We compared the effect of (1) mesh size (63, 45, and 32 μm) on estimates of nematode abundance, biomass, and body size, and (2) microscope magnification (50 and 100×) on estimates of nematode abundance at bathyal sites (250-3100 m water depth) on the Challenger Plateau and Chatham Rise, south-west Pacific Ocean. Variation in the effectiveness of these techniques was assessed in relation to nematode body size and environmental parameters (water depth, sediment organic matter content, %silt/clay, and chloroplastic pigments). The 63-μm mesh retained a relatively low proportion of total nematode abundance (mean ±SD = 55 ±9%), but most of nematode biomass (90 ± 4%). The proportion of nematode abundance retained on the 45-μm mesh in surface (0-1 cm) and subsurface (1-5 cm) sediment was significantly correlated (P < 0.01) with %silt/clay (R² = 0.39) and chloroplastic pigments (R² = 0.29), respectively. Variation in median nematode body weight showed similar trends, but relationships between mean nematode body weight and environmental parameters were either relatively weak (subsurface sediment) or not significant (surface sediment). Using a low magnification led to significantly lower (on average by 43%) nematode abundance estimates relative to high magnification (P < 0.001), and the magnitude of this difference was significantly correlated (P < 0.05) with total nematode abundance (R²p = 0.53) and the number of small (≤ 250 μm length) individuals (R²p = 0.05). Our results suggest that organic matter input and sediment characteristics influence the abundance of small nematodes in bathyal communities. The abundance of small individuals can, in turn, influence abundance estimates obtained using different mesh sizes and microscope magnifications

    Long-term slip rates and fault interactions under low contractional strain, Wanganui Basin, New Zealand

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    The newly mapped Kapiti-Manawatu Fault System (KMFS) in southern North Island, New Zealand, accommodated ∼3.5 km of basement throw over the last 3 Myr. Along-strike throw profiles are generated using seven stratigraphic markers, interpreted from seismic reflection profiles acquired <3 km apart. The profiles are symmetrical about their point of maximum displacement, and cumulative profiles suggest that the reverse fault system behaves coherently. The KMFS originates from the reactivation of extensional structures, with fault lengths remaining constant over time. Contractional deformation started at circa 1750 ± 400 ka. Maximum dip-slip rates along individual faults are 1.77 ± 0.53 and 0.74 ± 0.22 mm yr−1 for the 0–120 and 120–1350 ka periods, respectively. The maximum cumulative throw rates across the KMFS are 4.9 ± 1.5 and 1.5 ± 0.5 mm yr−1 for the same periods. Long-term strain rates across the KMFS are 2–5 times smaller than strain rates in the forearc basin of the Hikurangi subduction margin located less than 100 km to the east. The faults of the KMFS may extend to depth and link with the subducted Pacific plate

    Why are biotic iron pools uniform across high- and low-iron pelagic ecosystems?

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    Dissolved iron supply is pivotal in setting global phytoplankton productivity and pelagic ecosystem structure. However, most studies of the role of iron have focussed on carbon biogeochemistry within pelagic ecosystems, with less effort to quantify the iron biogeochemical cycle. Here we compare mixed-layer biotic iron inventories from a low-iron (~0.06nmol L-1) subantarctic (FeCycle study) and a seasonally high-iron (~0.6nmol L-1) subtropical (FeCycle II study) site. Both studies were quasi-Lagrangian, and had multi-day occupation, common sampling protocols, and indirect estimates of biotic iron (from a limited range of available published biovolume/carbon/iron quotas). Biotic iron pools were comparable (~100±30pmol L-1) for low- and high-iron waters, despite a tenfold difference in dissolved iron concentrations. Consistency in biotic iron inventories (~80±24pmol L-1, largely estimated using a limited range of available quotas) was also conspicuous for three Southern Ocean polar sites. Insights into the extent to which uniformity in biotic iron inventories was driven by the need to apply common iron quotas obtained from laboratory cultures were provided from FeCycle II. The observed twofold to threefold range of iron quotas during the evolution of FeCycle II subtropical bloom was much less than reported from laboratory monocultures. Furthermore, the iron recycling efficiency varied by fourfold during FeCycle II, increasing as stocks of new iron were depleted, suggesting that quotas and iron recycling efficiencies together set biotic iron pools. Hence, site-specific differences in iron recycling efficiencies (which provide 20-50% and 90% of total iron supply in high- and low-iron waters, respectively) help offset the differences in new iron inputs between low- and high-iron sites. Future parameterization of iron in biogeochemical models must focus on the drivers of biotic iron inventories, including the differing iron requirements of the resident biota, and the subsequent fate (retention/export/recycling) of the biotic iron

    Coccolithophore biodiversity controls carbonate export in the Southern Ocean

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    Southern Ocean waters are projected to undergo profound changes in their physical and chemical properties in the coming decades. Coccolithophore blooms in the Southern Ocean are thought to account for a major fraction of the global marine calcium carbonate (CaCO3) production and export to the deep sea. Therefore, changes in the composition and abundance of Southern Ocean coccolithophore populations are likely to alter the marine carbon cycle, with feedbacks to the rate of global climate change. However, the contribution of coccolithophores to CaCO3 export in the Southern Ocean is uncertain, particularly in the circumpolar subantarctic zone that represents about half of the areal extent of the Southern Ocean and where coccolithophores are most abundant. Here, we present measurements of annual CaCO3 flux and quantitatively partition them amongst coccolithophore species and heterotrophic calcifiers at two sites representative of a large portion of the subantarctic zone. We find that coccolithophores account for a major fraction of the annual CaCO3 export, with the highest contributions in waters with low algal biomass accumulations. Notably, our analysis reveals that although Emiliania huxleyi is an important vector for CaCO3 export to the deep sea, less abundant but larger species account for most of the annual coccolithophore CaCO3 flux. This observation contrasts with the generally accepted notion that high particulate inorganic carbon accumulations during the austral summer in the subantarctic Southern Ocean are mainly caused by E. huxleyi blooms. It appears likely that the climate-induced migration of oceanic fronts will initially result in the poleward expansion of large coccolithophore species increasing CaCO3 production. However, subantarctic coccolithophore populations will eventually diminish as acidification overwhelms those changes. Overall, our analysis emphasizes the need for species-centred studies to improve our ability to project future changes in phytoplankton communities and their influence on marine biogeochemical cycles.info:eu-repo/semantics/publishedVersio

    Giant depressions on the Chatham Rise offshore New Zealand – Morphology, structure and possible relation to fluid expulsion and bottom currents

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    Highlights • Large seafloor depressions with diameters of up 10 km across have been mapped on the southern Chatham Rise, New Zealand. • Seismic reflection data show scarce indications for vertical fluid flow but no clear link between fluid flow and depressions. • Methane gas or methane hydrates appear to be absent on the southern Chatham Rise. • Seismic evidence suggests that vertical fluid flow was likely fuelled by polygonal faulting and silica diagenesis • The depressions are the results of erosion and sediment drift deposition of bottom currents associated with the Subtropical Front. Abstract Several giant seafloor depressions were investigated on the Chatham Rise offshore New Zealand using mainly bathymetric and seismic data, supplemented by sediment cores and reported porewater geochemistry data. The depressions have diameters of up to 11 km and occur on the southern flank of the Chatham Rise in water depths between 600 and 900 m, i.e. roughly underneath the location of the strongest thermal gradients of the Subtropical Front (STF) and characterized by eastward flowing currents. With up to 150 m of relief the depressions cut into post-Miocene deposits. Some of the depressions are partially filled with drift deposits that have similar seismic characteristics as the surrounding sediments and consist of alternations of silty muds and silts. Seismic profiles also show completely filled depressions that no longer have a bathymetric expression. Despite several pipe structures indicating vertical fluid flow, neither active fluid seepage nor indications for past fluid seepage are present at the seafloor of the Chatham Rise. Also, both pore water geochemistry and geophysical data do not show indications for an existing or past gas hydrate system in the area. Instead, seismic data suggest widespread polygonal faulting and the presence of silica diagenetic fronts. The release of mineral-bound water during silica diagenesis or fluid expulsion during sediment compaction can explain the presence of vertical fluid flow features but not the giant depressions themselves. Instead, the depressions are interpreted as the result of scouring by strong bottom currents for which fluid venting may have created the nucleation points

    Microbial control of diatom bloom dynamics in the open ocean

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    Diatom blooms play a central role in supporting foodwebs and sequestering biogenic carbon to depth. Oceanic conditions set bloom initiation, whereas both environmental and ecological factors determine bloom magnitude and longevity. Our study reveals another fundamental determinant of bloom dynamics. A diatom spring bloom in offshore New Zealand waters was likely terminated by iron limitation, even though diatoms consumed <1/3 of the mixed-layer dissolved iron inventory. Thus, bloom duration and magnitude were primarily set by competition for dissolved iron between microbes and small phytoplankton versus diatoms. Significantly, such a microbial mode of control probably relies both upon out-competing diatoms for iron (i.e., K-strategy), and having high iron requirements (i.e., r-strategy). Such resource competition for iron has implications for carbon biogeochemistry, as, blooming diatoms fixed three-fold more carbon per unit iron than resident non-blooming microbes. Microbial sequestration of iron has major ramifications for determining the biogeochemical imprint of oceanic diatom blooms. Citation: Boyd, P. W., et al. (2012), Microbial control of diatom bloom dynamics in the open ocean, Geophys. Res. Lett., 39, L18601

    Full annual monitoring of Subantarctic Emiliania huxleyi populations reveals highly calcified morphotypes in high-CO2 winter conditions

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    Datos de investigación en: http://hdl.handle.net/10366/143074[EN]Ocean acidifcation is expected to have detrimental consequences for the most abundant calcifying phytoplankton species Emiliania huxleyi. However, this assumption is mainly based on laboratory manipulations that are unable to reproduce the complexity of natural ecosystems. Here, E. huxleyi coccolith assemblages collected over a year by an autonomous water sampler and sediment traps in the Subantarctic Zone were analysed. The combination of taxonomic and morphometric analyses together with in situ measurements of surface-water properties allowed us to monitor, with unprecedented detail, the seasonal cycle of E. huxleyi at two Subantarctic stations. E. huxleyi subantarctic assemblages were composed of a mixture of, at least, four diferent morphotypes. Heavier morphotypes exhibited their maximum relative abundances during winter, coinciding with peak annual TCO2 and nutrient concentrations, while lighter morphotypes dominated during summer, coinciding with lowest TCO2 and nutrients levels. The similar seasonality observed in both time-series suggests that it may be a circumpolar feature of the Subantarctic zone. Our results challenge the view that ocean acidifcation will necessarily lead to a replacement of heavily-calcifed coccolithophores by lightly-calcifed ones in subpolar ecosystems, and emphasize the need to consider the cumulative efect of multiple stressors on the probable succession of morphotypes.European Union's Horizon 2020, Marie Skłodowska-Curie Individual fellowshi

    Full annual monitoring of Subantarctic Emiliania huxleyi populations reveals highly calcified morphotypes in high-CO2 winter conditions [Dataset]

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    [EN]Supplement Table S1. a. Sampling dates and morphotype relative abundance of E. huxleyi coccolith assemblages collected in the surface layer at the SOTS site. b. Sampling intervals, fluxes and morphotype relative abundance and morphometric measurements of E. huxleyi coccolith assemblages intercepted by the sediment traps at the SOTS and SAM sites. Table S2. Environmental parameters measured at the surface layer of the SOTS site from August 2011 to July 2012.European Union's Horizon 2020, Marie Skłodowska-Curie Individual fellowshipThe dataset includes Supplementary Information, Table S1. : abundance, composition and morphometric data of E. huxleyi coccolith assemblages generated during the current study Table S2: environmental data Environmental parameters measured at the surface layer of the SOTS site from August 2011 to July 2012

    Insights Into the Biogeochemical Cycling of Iron, Nitrate, and Phosphate Across a 5,300 km South Pacific Zonal Section (153°E-150°W)

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    Iron, phosphate, and nitrate are essential nutrients for phytoplankton growth, and hence, their supply into the surface ocean controls oceanic primary production. Here we present a GEOTRACES zonal section (GP13; 30–33°S, 153°E–150°W) extending eastward from Australia to the oligotrophic South Pacific Ocean gyre outlining the concentrations of these key nutrients. Surface dissolved iron concentrations are elevated at >0.4 nmol L−1 near continental Australia (west of 165°E) and decreased eastward to ≤0.2 nmol L−1 (170°W–150°W). The supply of dissolved iron into the upper ocean (<100 m) from the atmosphere and vertical diffusivity averaged 11 ± 10 nmol m−2 d−1. In the remote South Pacific Ocean (170°W–150°W), atmospherically sourced iron is a significant contributor to the surface dissolved iron pool with average supply contribution of 23 ± 17% (range 3% to 55%). Surface water nitrate concentrations averaged 5 ± 4 nmol L−1 between 170°W and 150°W, while surface water phosphate concentrations averaged 58 ± 30 nmol L−1. The supply of nitrogen into the upper ocean is primarily from deeper waters (24–1647 μmol m−2 d−1) with atmospheric deposition and nitrogen fixation contributing <1% to the overall flux along the eastern part of the transect. The deep water N:P ratio averaged 14.5 ± 0.5 but declined to <1 above the deep chlorophyll maximum (DCM) indicating a high N:P assimilation ratio by phytoplankton leading to almost quantitative removal of nitrate. The supply stoichiometry for iron and nitrogen relative to phosphate at and above the DCM declines eastward leading to two biogeographical provinces: one with diazotroph production and the other without diazotroph production.This research was supported by the New Zealand Foundation for Research, Science and Technology Coasts and Oceans Outcome-Based Investment (COIX0501), and the Australian Research Council Discovery Projects (DP1092892 and DP110100108) and Future Fellowships (FT130100037) programs, University of Tasmania, internal grants to A. R. B. (refs B0018994, B0019024, and L0018934), and University of Technology Sydney Chancellor Fellowship to CSH
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