Effect of enhanced water exchange on ecosystem functions in backwaters of an urban floodplain

This study evaluated the effects of a controlled surface water connectivity scheme on several backwaters in an urban floodplain within the city limits of Vienna, the Upper Lobau. A phosphorus budget and ecosystem metabolism measurements were used to assess the reaction of two trophically distinct floodplain backwater sections on changed connectivity conditions. The surface water connection led to a reduction of the retention times in the backwater system. The water column nutrient concentrations in the individual backwater sections approached those of the source water body. The significance of these effects, however, depends on the historical and current trophic situation of the respective water bodies. Generally, the surface water connectivity introduced particulate phosphorus export up to 30% increase over the influent loading and dissolved phosphorus up to 14% increase over the influent loading. However, in sections with submersed macrophyte development, which provided enhanced filtering capacities for particulate matter, sediment and phosphorus accumulation rates were increased. At the same time, water transparency increased resulting in a positive feedback supporting further macrophyte development. Based on these findings, the evaluation of restoration measures in urban floodplains needs to consider the spatial and temporal dynamics of nutrients and ecosystem processes such as gross primary production and community respiration to predict long-term development.     

Platinum group elements and gold in ferromanganese crusts from Afanasiy-Nikitin seamount,equatorial Indian Ocean: Sources and fractionation

The major element relationships in ferromanganese (Fe-Mn) crusts from Afanasiy-Nikitin seamount (ANS), eastern equatorial Indian Ocean, appear to be atypical. High positive correlations (r = 0.99) between Mn/Co and Fe/Co ratios, and lack of correlation of those ratios with Co, Ce, and Ce/Co, indicate that the ANS Fe-Mn crusts are distinct from Pacific seamount Fe-Mn crusts, and reflect region-specific chemical characteristics. The platinum group elements (PGE: Ir, Ru, Rh, Pt, and Pd) and Au in ANS Fe-Mn crusts are derived from seawater and are mainly of terrestrial origin, with a minor cosmogenic component. The Ru/Rh (0.5–2) and Pt/Ru ratios (7–28) are closely comparable to ratios in continental basalts, whereas Pd/Ir ratios exhibit values (<2) similar to CI-chondrite (∼1). The chondrite-normalized PGE patterns are similar to those of igneous rocks, except that Pd is relatively depleted. The water depth of Fe-Mn crust formation appears to have a first-order control on both major element and PGE enrichments. These relationships are defined statistically by significant (r > 0.75) correlations between water depth and Mn/Co, Fe/Co, Ce/Co, Co, and the PGEs. Fractionation of the PGE-Au from seawater during colloidal precipitation of the major-oxide phases is indicated by well-defined linear positive correlations (r > 0.8) of Co and Ce with Ir, Ru, Rh, and Pt; Au/Co with Mn/Co; and by weak or no correlations of Pd with water depth, Co-normalized major-element ratios, and with the other PGE (r < 0.5). The strong enrichment of Pt (up to 1 ppm) relative to the other PGE and its positive correlations with Ce and Co demonstrate a common link for the high concentrations of all three elements, which likely involves an oxidation reaction on the Mn-oxide and Fe-oxyhydroxide surfaces. The documented fractionation of PGE-Au and their positive association with redox sensitive Co and Ce may have applications in reconstructing past-ocean redox conditions and water masses.     

The local impacts of climate change in the Ferlo, Western Sahel

Recent increases in the accuracy of climate models have enhanced the possibilities for analyzing the impacts of climate change on society. This paper explores how the local, economic impacts of climate change can be modeled for a specific eco-region, the Western Sahel. The people in the Sahel are highly dependent on their natural resource base, and these resources are highly vulnerable to climate change, in particular to changes in rainfall. Climate models project substantial changes in rainfall in the Sahel in the coming 50 years, with most models predicting a reduction in rainfall. To connect climate change to changes in ecosystem productivity and local income, we construct an ecological–economic model that incorporates rangeland dynamics, grazing and livestock prices. The model shows that decreased rainfall in the Sahel will considerably reduce local incomes, in particular if combined with increases in rainfall variability. Adaptation to these climate change projections is possible if reductions in rainfall are followed by destocking to reach efficient grazing levels. However, while such a strategy is optimal from the perspective of society, the stocking rate is determined by individual pastoralists that face few incentives to destock.     

Pliocene clays from Aegina (Greece): Reference material for chemical provenance studies on bronze age pottery from the Island

Normally, the use of clays as reference materials in chemical provenance studies of ancient ceramics is complicated due to the original clay paste processing. The primary mixing and/or refining of raw materials during pottery production makes a straightforward comparison of archaeological ceramics with extant geological materials difficult if not impossible in many cases. However, in the case of Pliocene clays from Aegina (Greece), which were examined chemically and mineralogically and compared with Bronze Age pottery produced on the island, a successful exception can be presented. The chemical composition of a large group of Aeginetan pottery resembles the chemical composition of clays from a deposit in close vicinity to the main Bronze Age settlement of the island. Clays from specific outcrops exhibit considerable chemical and mineralogical homogeneity, and the suitability of those clays for pottery production apparently made substantial clay paste processing unnecessary. © 2004 Wiley Periodicals, Inc.     

The molecular mechanism of Mo isotope fractionation during adsorption to birnessite

Fractionation of Mo isotopes during adsorption to manganese oxides is a primary control on the global ocean Mo isotope budget. Previous attempts to explain what drives the surprisingly large isotope effect δ^97/95Mo_dissolved-δ^97/95Mo_adsorbed=1.8‰ have not successfully resolved the fractionation mechanism. New evidence from extended X-ray absorption fine structure analysis and density functional theory suggests that Mo forms a polymolybdate complex on the surfaces of experimental and natural samples. Mo in this polynuclear structure is in distorted octahedral coordination, while Mo remaining in solution is predominantly in tetrahedral coordination as . Our results indicate that the difference in coordination environment between dissolved Mo and adsorbed Mo is the cause of isotope fractionation. The molecular mechanism of metal isotope fractionation in this system should enable us to explain and possibly predict metal isotope effects in other systems where transition metals adsorb to mineral surfaces.     

Hydrothermal mineralization along submarine rift zones,Hawaii

This is the first article to describe mineralization of midplate submarine rift zones and hydrothermal manganese oxide mineralization of midplate volcanic edifices. Hydrothermal Mn oxides were recovered from submarine extensions of two Hawaiian rift zones, along Haleakala and Puna Ridges. These Mn oxides form two types of deposits, metallic stratiform layers in volcaniclastic rocks and cement for clastic rocks; both deposit types are composed of todorokite and bimessite. Thin Fe‐Mn crusts that coat some rocks formed by a combination of hydrogenetic and hydrothermal processes and are composed of δ‐MnO₂. The stratiform layers have high Mn contents (mean 40%) and a large fractionation between Mn and Fe (Fe/Mn = 0.04). Unlike most other hydrothermal Mn oxide deposits, those from Hawaiian rift zones are enriched in the trace metals Zn, Co, Ba, Mo, Sr, V, and especially Ni (mean 0.16%). Metals are derived from three sources: mafic and ultramafic rocks leached by circulating hydrothermal fluids, clastic material (in Mn‐cemented sandstone), and seawater that mixed with the hydrothermal fluids. Mineralization on Haleakala Ridge occurred sometime during the past 200 to 400 ka, when the summit was at a water depth of more than 1,000 m. Hydrothermal circulation was probably driven by heat produced by intrusion of dikces, magma reservoirs, and flow of magma through axial and lateral conduits. The supply of seawater to ridge interiors must be extensive because of their high porosity and permeability. Precipitation of Mn oxide below the seafloor is indicated by its occurrence as cement, growth textures that show mineralizing fluids were introduced from below, and pervasive replacement of original matrix of clastic rocks.     

Ferromanganese crusts as indicators for paleoceanographic events in the NE Atlantic

Hydrogenetic ferromanganese crusts reflect the chemical conditions of the sewater from which they formed. Fine-scale geochemical analysis of crust layers in combination with age determinations can therefore be used to investigate paleoceanographic changes which are recorded in geochemical gradients in the crusts. At Tropic seamount (off northwest Africa), uniform crust growth influenced by terrigenous input from the African continent occurred during approximately the past 12 Ma. Phosphatization of these crusts is minor. In contrast, crusts from Lion seamount, located between Madeira and the Portuguese coast, display a much more variable growth history. A pronounced increase in Ni, Cu, and Zn is observed in some intervals of the crusts, which probably reflects increased surface productivity. A thick older phosphatized generation occurs in many samples. Hydrographic profiles indicate that Mediterranean outflow water (MOW) may play an important role in the composition of these crusts.¹⁰Be dating of one sample confirms that the interruption of the MOW during the Messinian salinity crisis (6.2–5 Ma ago) resulted in changes in element composition. Sr-isotope dating of the apatite phase of the old crust generation has been carried out to obtain a minimum age for the older generation of Atlantic crusts and to determine whether crust phosphatization in the Atlantic can be related to phosphatization episodes recorded in Pacific crusts. The preliminary data show that the old phosphatized crust generation might be as old as approximately 30–40 Ma.     

Sea floor gouges and pits in deep fjords,Baffin Island: Possible mammalian feeding traces

Pisces submersible dives within Baffin Island fjords have revealed the common occurrence of pits on the sea floor, at water depths between 40 and 326 m. The size of these pits are in the decimeter to meter range. Through indirect evidence (by comparison of morphologic features to pits or gouges of known origin) they are believed to be feeding traces of narwhal, beluga, or bowhead whales. If so, they are the deepest mammalian feeding traces yet reported. Bioerosion by large foraging mammals may be a more common sea floor process than previously thought.     

Influence of atmospheric inputs on the iron distribution in the subtropical North-East Atlantic Ocean

Aerosol (soluble and total) iron and water-column dissolved (DFe, < 0.2 μm) and total dissolvable (TDFe, unfiltered) iron concentrations were determined in the Canary Basin and along a transect towards the Strait of Gibraltar, in order to sample across the Saharan dust plume. Cumulative dust deposition fluxes estimated from direct aerosol sampling during our one-month cruise are representative of the estimated deposition fluxes based on near surface water dissolved aluminium concentrations measured on board. Iron inventories in near surface waters combined with flux estimates confirmed the relatively short residence time of DFe in waters influenced by the Saharan dust plume (6–14 months). Enhanced near surface water concentrations of DFe (5.90–6.99 nM) were observed at the Strait of Gibraltar mainly due to inputs from metal-rich rivers. In the Canary Basin and the transect towards Gibraltar, DFe concentrations (0.07–0.76 nM) were typical of concentrations observed in the surface North Atlantic Waters, with the highest concentrations associated with higher atmospheric inputs in the Canary Basin. Depth profiles showed that DFe and TDFe were influenced by atmospheric inputs in this area with an accumulation of aeolian Fe in the surface waters. The sub-surface minimum of both DFe and TDFe suggests that a simple partitioning between dissolved and particulate Fe is not obvious there and that export may occur for both phases. At depths of around 1000–1300 m, both regeneration and Meddies may explain the observed maximum. Our data suggest that, in deep waters, higher particle concentrations likely due to dust storms may increase the scavenging flux and thus decrease DFe concentrations in deep waters.