Simulated decadal oscillations of the Atlantic meridional overturning circulation in a cold climate state

The significance of the Atlantic meridional overturning circulation (MOC) for regional and hemispheric climate change requires a complete understanding using fully coupled climate models. Here we present a persistent, decadal oscillation in a coupled atmosphere–ocean general circulation model. While the present study is limited by the lack of comparisons with paleo-proxy records, the purpose is to reveal a new theoretically interesting solution found in the fully-coupled climate model. The model exhibits two multi-century-long stable states with one dominated by decadal MOC oscillations. The oscillations involve an interaction between anomalous advective transport of salt and surface density in the North Atlantic subpolar gyre. Their time scale is fundamentally determined by the advection. In addition, there is a link between the MOC oscillations and North Atlantic Oscillation (NAO)-like sea level pressure anomalies. The analysis suggests an interaction between the NAO and an anomalous subpolar gyre circulation in which sea ice near and south of the Labrador Sea plays an important role in generating a large local thermal anomaly and a meridional temperature gradient. The latter induces a positive feedback via synoptic eddy activity in the atmosphere. In addition, the oscillation only appears when the Nordic Sea is completely covered by sea ice in winter, and deep convection is active only near the Irminger Sea. Such conditions are provided by a substantially colder North Atlantic climate than today.     

Water sorption on martian regolith analogs: Thermodynamics and near-infrared reflectance spectroscopy

The near-infrared reflectance spectra of the martian surface present strong absorption features attributed to hydration water present in the regolith. In order to characterize the relationships between this water and atmospheric vapor and decipher the physical state of water molecules in martian regolith analogs, we designed and built an experimental setup to measure near-IR reflectance spectra under martian atmospheric conditions. Six samples were studied that cover part of the diversity of Mars surface mineralogy: a hydrated ferric oxide (ferrihydrite), two igneous samples (volcanic tuff, and dunite sand), and three potential water rich soil materials (Mg-sulfate, smectite powder and a palagonitic soil, the JSC Mars-1 regolith stimulant). Sorption and desorption isotherms were measured at 243 K for water vapor pressure varying from 10⁻⁵ to ∼0.3 mbar (relative humidity: 10⁻⁴ to 75%). These measurements reveal a large diversity of behavior among the sample suite in terms of absolute amount of water adsorbed, shape of the isotherm and hysteresis between the adsorption and desorption branches. Simultaneous in situ spectroscopic observations permit a detailed analysis of the spectral signature of adsorbed water and also point to clear differences between the samples. Ferric (oxy)hydroxides like ferrihydrite or other phases present in palagonitic soils are very strong water adsorbent and may play an important role in the current martian water cycle by allowing large exchange of water between dust-covered regions and atmosphere at diurnal and seasonal scales.     

Field reconnaissance of the Anti-Atlas coastline, Morocco: Fluvial and marine evidence for Late Cenozoic uplift

The available evidence regarding the disposition and chronology of Pliocene–Pleistocene fluvial terraces, coastal rock flats, raised beaches and lacustrine sediments adjoining the Anti-Atlas coastline of Morocco has been reviewed and supplemented by additional information from our own field reconnaissance. It is thus suggested that the study region has experienced uplift by  130 m since the Mid-Pliocene climatic optimum ( 3.1 Ma), by  90 m since the latest Pliocene ( 2 Ma), and by  45 m since the Mid-Pleistocene Revolution ( 0.9 Ma). Each of these phases of uplift correlates with a phase of global climate change known independently, and it is thus inferred that the observed uplift is being driven by climate through mechanisms such as erosional isostasy and the associated induced lower-crustal flow. Numerical modelling of the observed uplift history indicates that the mobile lower-crustal layer in the study region is  9 km thick, with a temperature at its base of  500 °C. The base of this mobile layer is inferred to be at  24 km depth, the deepest crust consisting of a layer of mafic underplating that does not flow under ambient conditions. The principal landform in the study region, the coastal rock platform at  60 m a.s.l., thus formed during a succession of interglacial marine highstands in the late Early Pleistocene when uplift rates were low. Although control on the ages of young sediments and landforms is currently extremely limited, being dependent on regional correlation schemes rather than on absolute dating, the study region fits the pattern, emerging worldwide, that climate change is driving the systematic growth of topographic relief evident during the Late Cenozoic.     

Moisture sorption behaviour of salt mixtures in porous stone

Moisture in stone material is the key factor for all stone deterioration processes and also in weathering of cultural heritage. With additional presence of salts in the material the situation gets even more critical. While the properties of pure salts with moisture are well known, knowledge about the interaction of salt mixtures with moisture is still poor. In different approaches the reactions of salt-contaminated stone material on changing moisture were tested in the laboratory. Experiments with different solutions in the Na-Mg-SO₄-NO₃-H₂O system revealed interesting new results on the moisture behaviour of salt-contaminated samples. Theoretical considerations and computer simulations are helpful to interpret the data obtained, but are not yet sufficient to explain the real processes acting on site at the monuments. More encouraging to this fact are complementary studies on visible efflorescences in the same salt system. It is shown how by experimental approaches the understanding on salt-induced stone deterioration is strongly complemented.     

Landscape variations in stream water SO4 and δSSO4 in a boreal stream network

Despite reduced anthropogenic deposition during the last decades, deposition sulphate may still play an important role in the biogeochemical cycles of S and many catchments may act as net sources of S that may remain for several decades. The aim of this study is to elucidate the temporal and spatial dynamics of both SO₄²⁻ and δ³⁴S_SO4 in stream water from catchments with varying percentage of wetland and forest coverage and to determine their relative importance for catchment losses of S. Stream water samples were collected from 15 subcatchments ranging in size from 3 to 6780 ha, in a boreal stream network, northern Sweden. In forested catchments (<2% wetland cover) S-SO₄²⁻ concentrations in stream water averaged 1.7 mg L⁻¹ whereas in wetland dominated catchments (>30% wetland cover) the concentrations averaged 0.3 mg L⁻¹. A significant negative relationship was observed between S-SO₄²⁻ and percentage wetland coverage (r² = 0.77, p < 0.001) and the annual export of stream water SO₄²⁻ and wetland coverage (r² = 0.76, p < 0.001). The percentage forest coverage was on the other hand positively related to stream water SO₄²⁻ concentrations and the annual export of stream water SO₄²⁻ (r² = 0.77 and r² = 0.79, respectively). The annual average δ³⁴S_SO4 value in wetland dominated streams was +7.6‰ and in streams of forested catchments +6.7‰. At spring flood the δ³⁴S_SO4 values decreased in all streams by 1‰ to 5‰. The δ³⁴S_SO4 values in all streams were higher than the δ³⁴S_SO4 value of +4.7‰ in precipitation (snow). The export of S ranged from 0.5 kg S ha⁻¹ yr⁻¹ (wetland headwater stream) to 3.8 kg S ha⁻¹ yr⁻¹ (forested headwater stream). With an average S deposition in open field of 1.3 kg S ha⁻¹ yr⁻¹ (2002-2006) the mass balance results in a net export of S from all catchments, except in catchments with >30% wetland. The high temporal and spatial resolution of this study demonstrates that the reducing environments of wetlands play a key role for the biogeochemistry of S in boreal landscapes and are net sinks of S. Forested areas, on the other hand were net sources of S.     

Objectives of fisheries management: case studies from the UK, France, Spain and Denmark

The main objectives of fisheries management are generally similar throughout the world. These are often stated in policy documents such as the Common Fisheries Policy and the Magnuson–Stevens Fishery Conservation and Management Act. However, at the local level often the key objectives of management are more detailed, characterised by both the overriding management structure and the status and type of fishery concerned. In this paper, we consider case study fisheries from the UK, France, Spain and Denmark to compare some of the various types of fisheries and fisheries management systems that exist in the European Union. From this, we define the key objectives for each management system.     

蔗渣生物质炭对喀斯特农田石灰性土壤氮转化过程的短期影响

生物质炭对于土壤中不同形态氮库的含量影响已有较多研究,但对西南喀斯特区石灰性土壤氮素形态,尤其是控制氮素形态的转化过程研究较为缺乏。本研究设置土壤中添加1%(C1)和3%(C2)蔗渣生物质炭2个用量水平,并以不施用蔗渣生物质炭作为对照(CK),共3个处理,通过 15 NH 4 NO 3 和NH^15 4 NO 3 成对标记技术,结合MCMC氮素转化模型研究了不同用量的蔗渣生物质炭对石灰性土壤氮转化过程的短期影响,为该地区蔗渣资源化利用和土壤氮保持提供理论支撑。结果表明,与CK相比,添加蔗渣生物质炭能够快速提高土壤pH和有机碳含量。添加生物质炭并没有显著改变土壤氮的矿化、铵态氮(NH^+ 4 )和硝态氮(NO^- 3 )的微生物同化和异养硝化速率,但NH^+ 4 吸附速率随生物质炭用量的增加而提高,以添加量最高的C2处理最大。添加生物质炭同样提高了土壤NH^+ 4 释放速率,但C1和C2处理的土壤NH^+ 4 释放速率并无显著性差异。与CK和C1处理相比,施用高量蔗渣生物质炭通过抑制自养硝化速率而显著降低了硝态氮净产生速率。这些结果表明,施用高量蔗渣生物质炭于石灰性土壤中可快速实现对NH^+ 4 吸附,降低自养硝化速率,减少NO^- 3 产生,从而降低了其损耗和淋失风险。