The multiple chronological techniques applied to the Lake Suigetsu SG06 sediment core,central Japan

The varved sediment of Lake Suigetsu (central Japan) provides a valuable opportunity to obtain high‐resolution, multi‐proxy palaeoenvironmental data across the last glacial/interglacial cycle. In order to maximize the potential of this archive, a well‐constrained chronology is required. This paper outlines the multiple geochronological techniques being applied – namely varve counting, radiocarbon dating, tephrochronology (including argon–argon dating) and optically stimulated luminescence (OSL) – and the approaches by which these techniques are being integrated to form a single, coherent, robust chronology. Importantly, we also describe here the linkage of the floating Lake Suigetsu (SG06) varve chronology and the absolute (IntCal09 tree‐ring) time scale, as derived using radiocarbon data from the uppermost (non‐varved) portion of the core. This tie‐point, defined as a distinct (flood) marker horizon in SG06 (event layer B‐07–08 at 1397.4 cm composite depth), is thus derived to be 11 255 to 11 222 IntCal09 cal. years BP (68.2% probability range).     

Market access,population density,and socioeconomic development explain diversity and functional group biomass of coral reef fish assemblages

There is overwhelming evidence that many local-scale human activities (e.g. fishing) have a deleterious effect on coral reef fish assemblages. Our understanding of how broad social phenomena (e.g. socioeconomic development) affect the diversity and function of coral reef fish assemblages however, is still poor. Here, we use structural equation models to reveal how human population density, socioeconomic development, and market access affect fishing pressure and coral cover to, in turn, explain the diversity and biomass of key functional groups of reef fish assemblages within Solomon Islands. Fishing pressure is predominantly driven by both market access and local population density, and has a clear negative effect on the diversity and function of coral reef fishes. The strong positive effect of market access on fishing pressure makes clear the importance of understanding social-ecological linkages in the context of increasingly connected societies. This study highlights the need to address broad social phenomena rather than focusing on proximate threats such as fishing pressure, to ensure the continued flow of coral reef goods and services in this time of rapid global social and environmental change.     

Sustaining trajectories towards Sustainability: Dynamics and diversity in UK communal growing activities

Civil society is a critical arena both for exploring Sustainability itself and for sustaining trajectories towards it through innovation, experimentation and debate. Innovations can be mould breaking and can challenge local institutions. Concurrently, initiatives may be fragile due to the development of new working relationships, reliance on voluntary labour and goodwill, and dependence on grant funding. Here we examine different aspects of what it takes to sustain grassroots trajectories for ‘communal growing’, given the pressures that groups and intermediary organisations practicing and supporting this activity experience, and the consequential need to build qualities like ‘resilience’. Attending carefully to the definition of this otherwise slippery concept, a particular focus is given to how contrasting aspects of temporality and agency lead to divergent constructions of ‘resilience’ and strategies for sustaining growing. We draw on fieldwork that explores the practice and support of communal growing in East Sussex, England, and directly associated activities at a national level.We find important interdependencies between communal growing projects and the intermediary organisations supporting them. Additionally there is huge diversity within and between both projects and the organisations that support them, including with respect to the ends to which growing is seen as a means. These ends link growing initiatives – both antagonistically and synergistically – to food, education and health systems. This diversity can be seen positively as: a source of innovation; facilitating the open and bottom up nature of growing; and, enabling the securing of greater financial support for the endeavour. What is less clear is how this plays into framing and configuring communal growing specifically in relation to achieving a more Sustainable and localised food system. We discuss the conceptual and methodological implications of these empirically derived observations with regards future research on grassroots innovations.     

The role of tides in redistributing macrodetrital aggregates within the Swartvlei estuary

The Swartvlei estuary possesses a prolific growth of both intertidal and subtidal eelgrass,Zostera capensis. During 1984 less than 12% of the eelgrass beds were located in the upper half of the estuary, yet deposition ofZostera/macroalgal wrack in this region, when the estuary was linked to the sea (open phase), was similar to that in the lower half. Over a period of 20 semidiurnal tidal cycles there was a net gain of 2.5 tonnes dry mass of plant material into the upper reaches. Export of aquatic macrophytes and filamentous algae from the lower reaches toward the sea over 20 tidal cycles amounted to 1.6 tonnes dry mass. The amount of plant material transported during spring tides was 2 to 3 times greater than that carried during neap tides. Shallowing of the estuary mouth due to sand deposition resulted in a decline in the tidal prism and a decrease in macrodetrital flux. Total export ofZostera and associated algae amounted to 0.87 g ash-free dry mass m^?2d^?1 and represented a monthly export of 18% ofZostera bed biomass. Deposition of plant wrack during the 1984–1985 closed phase amounted to 63 g dry mass per meter of shore per day at the lower reaches site but only 10 g m^?1d^?1 was recorded at the upper reaches site. The relatively low latter value was attributed to the absence of tidal action which transports macrodetritus from the lower and middle reaches into the upper part of the system. During the 1984 open phase 70 g m^?1d^?1 was deposited at the lower reaches site and 68 g m^?1d^?1 at the upper reaches site. The role of tides in the redistribution of aquatic macrophyte primary production in the Swartvlei estuary was therefore clearly underscored.     

Direct measurements of latent heat during crystallization and melting of a ugandite and an olivine basalt

Step-scanning calorimetric measurements using a Setaram HT1500 calorimeter were performed between 800 and 1400°C on two natural samples: a ugandite from the East African rift and an olivine basalt from the western Mexican arc. Our measurements provide the first in-situ quantitative assessment of enthalpy during melting of initially crystalline natural samples. The distribution of latent heat across the liquidus-solidus intervals of the two samples is distinctly different, reflecting significant variation in the sequence and abundance of mineral phases during melting (clinopyroxene and leucite in the ugandite; olivine, clinopyroxene, and plagioclase in the basalt). Our data further indicate that the common assumption of a uniform distribution of latent heat across the liquidus-solidus interval of a magma is a reasonable approximation for the olivine basalt, but is grossly in error for the ugandite. This is due to cotectic precipitation of leucite and clinopyroxene, leading to a large, disproportionate release of latent heat early in the crystallization sequence. The implication for the thermal history of a crystallizing ugandite magma is that therate of heat loss during conductive cooling will unitially be more rapid than the average rate. The net result will be to produce lower magmatic temperatures after a given cooling interval relative to models assuming a uniform release of latent heat. An additional series of scanning calorimetric experiments were performed at variable rates (1,2 and 3°/min) to evaluate the role of kinetics on the distribution of enthalpy during both melting and crystallization of the ugandite and olivine basalt. The results indicate that clinopyroxene is the most important mineral phase in controlling the shapes of the enthalpy profiles during cooling; this is due to its large enthalpy of fusion and its tendency for sluggish nucleation, followed by rapid crystallization at temperatures that vary with cooling rate. The resolution of the calorimeter (in terms of heat detected per unit time) is also important in determining the shapes of theobserved enthalpy profiles during these rapid scans. Estimates based on the observed calorimetric signal associated with melting of olivine, and the lack of a calorimetric signal during melting of leucite, combined with known enthalpies of fusion for the two phases, indicate detection limits of approximately 0.6–1.2 kJ per 5 min increments.     

Ultimate removal mechanisms of elements from the ocean—a comment

Li (1981) has proposed a surface complexation model to rationalise the partitioning of the elements between the oceans and pelagic clays. In this comment we compare the resulting scattered correlations with the coherent and statistically significant correlations obtained from a simple electrostatic model.     

New density measurements on carbonate liquids and the partial molar volume of the CaCO<Subscript>3</Subscript> component

Density measurements on nine liquids in the CaCO₃–Li₂CO₃–Na₂CO₃–K₂CO₃ quaternary system were performed at 1 bar between 555 and 969 °C using the double-bob Archimedean method. Our density data on the end-member alkali carbonate liquids are in excellent agreement with the NIST standards compiled by Janz (1992). The results were fitted to a volume equation that is linear in composition and temperature; this model recovers the measured volumes within experimental error (±0.18% on average, with a maximum residual of ±0.50%). Our results indicate that the density of the CaCO₃ component in natrocarbonate liquids is 2.502 (±0.014) g/cm³ at 800 °C and 1 bar, which is within the range of silicate melts; its coefficient of thermal expansion is 1.8 (±0.5)×10^–4 K^–1 at 800 °C. Although the volumes of carbonate liquids mix linearly with respect to carbonate components, they do not mix linearly with silicate liquids. Our data are used with those in the literature to estimate the value of in alkaline silicate magmas (20 cm³/mol at 1400 °C and 20 kbar), where CO₂ is dissolved as carbonate in close association with Ca. Our volume measurements are combined with sound speed data in the literature to derive the compressibility of the end-member liquids Li₂CO₃, Na₂CO₃, and K₂CO₃. These results are combined with calorimetric data to calculate the fusion curves for Li₂CO₃, Na₂CO₃, and K₂CO₃ to 5 kbar; the calculations are in excellent agreement with experimental determinations of the respective melting reactions.Editorial responsibility: I Carmichael     

Inter-relationships of MnO2 precipitation, siderophore-Mn complex formation, siderophore degradation, and iron limitation in Mn-oxidizing bacterial cultures

To examine the pathways that form Mn^(III) and Mn^(IV) in the Mn^(II)-oxidizing bacterial strains Pseudomonas putida GB-1 and MnB1, and to test whether the siderophore pyoverdine (PVD) inhibits Mn^(IV)O₂ formation, cultures were subjected to various protocols at known concentrations of iron and PVD. Depending on growth conditions, P. putida produced one of two oxidized Mn species - either soluble PVD-Mn^(III) complex or insoluble Mn^(IV)O₂ minerals - but not both simultaneously. PVD-Mn^(III) was present, and MnO₂ precipitation was inhibited, both in iron-limited cultures that had synthesized 26-50 μM PVD and in iron-replete (non-PVD-producing) cultures that were supplemented with 10-550 μM purified PVD. PVD-Mn^(III) arose by predominantly ligand-mediated air oxidation of Mn^(II) in the presence of PVD, based on the following evidence: (a) yields and rates of this reaction were similar in sterile media and in cultures, and (b) GB-1 mutants deficient in enzymatic Mn oxidation produced PVD-Mn^(III) as efficiently as wild type. Only wild type, however, could degrade PVD-Mn^(III), a process linked to the production of both MnO₂ and an altered PVD with absorbance and fluorescence spectra markedly different from those of either PVD or PVD-Mn^(III). Two conditions, the presence of bioavailable iron and the absence of PVD at concentrations exceeding those of Mn, both had to be satisfied for MnO₂ to appear. These results suggest that P. putida cultures produce soluble Mn^(III) or MnO₂ by different and mutually inhibitory pathways: enzymatic catalysis yielding MnO₂ under iron sufficiency or PVD-promoted oxidation yielding PVD-Mn^(III) under iron limitation. Since PVD-producing Pseudomonas species are environmentally prevalent Mn oxidizers, these data predict influences of iron (via PVD-Mn^(III) versus MnO₂) on the global oxidation/reduction cycling of various pollutants, recalcitrant organic matter, and elements such as C, S, N, Cr, U, and Mn.