Differences across the ITCZ in the chemical characteristics of the Indian Ocean MBL aerosol during INDOEX

International audienceThe water soluble inorganic part of the sub-micrometer aerosol was measured from two research vessels over the Indian Ocean during the winter monsoon season (February and March) as part of the INDOEX project in 1998 and 1999. Additional measurements were made of gas phase SO2 from one of the vessels in 1999. All samples collected north of the Inter Tropical Convergence Zone, ITCZ, were clearly affected by continental, anthropogenic sources. A sharp transition occurred across the ITCZ with concentrations of nss-SO42-, NH4+ and nss-K+ being lower by a factor of 7-15, >20 and >40, respectively, on the southern side of the ITCZ. The contribution from DMS to the sub-micrometer nss-SO42- was estimated to be up to 40% in clean air north of the ITCZ but less than 10% in polluted air originating from India. South of the ITCZ virtually all nss-SO42- was likely to be derived from oxidation of DMS. The concentration of SO2 decreased rapidly with distance from the Indian coast, the molar ratio SO2/nss-SO42- reaching values below 5% after 35 h travel time over the ocean. Surprisingly, MSA, which is derived from DMS, also showed higher concentrations in the sub-micrometer aerosol north of the ITCZ than south of it. This could be explained by the larger sub-micrometer surface area available north of the ITCZ for the condensation of MSA. South of the ITCZ a major part of the MSA was found on the super-micrometer particles. An analysis based on the air trajectories showed that systematic variation in the observed concentrations was associated with variations in the transport from source regions. For example, differences in time since air parcels left the Arabian or Indian coasts was shown to be an important factor for explaining the substantial differences in absolute concentrations

Interhemispheric differences in the chemical characteristics of the Indian Ocean aerosol during INDOEX

International audienceThe water soluble inorganic part of the sub-micrometer aerosol was measured from two research vessels over the Indian Ocean during the winter monsoon season (February and March) as part of the INDOEX project in 1998 and 1999. Additional measurements were made of gas phase SO2 from one of the vessels in 1999. All samples collected north of the ITCZ were clearly affected by continental, anthropogenic sources. A sharp transition occurred across the ITCZ with concentrations of nss-SO42, NH4+ and nss-K+ being lower by a factor of 7--15, >20 and >40, respectively, on the southern side of the ITCZ. The contribution from DMS to the sub-micrometer nss-SO42 was estimated to be up to 40% in clean air north of the ITCZ but less than 10% in polluted air originating from India. South of the ITCZ virtually all nss-SO42 was likely to be derived from oxidation of DMS. The concentration of \chem{SO_2} decreased rapidly with distance from the Indian coast, the ratio \SO2nss-SO42 reaching values below 5% after 35 h travel time over the ocean. Surprisingly, MSA, which is derived from DMS, also showed higher concentrations in the sub-micrometer aerosol north of the ITCZ than south of it. This could be explained by the larger sub-micrometer surface area available north of the ITCZ for the condensation of MSA. South of the ITCZ a major part of the MSA was found on the super-micrometer particles. The total amount of MSA, on both sub-micrometer and super-micrometer particles, varied little across the ITCZ. An analysis based on the air trajectories showed that systematic variation in the observed concentrations was associated with variations in the transport from source regions. For example, differences in time since air parcels left the Arabian or Indian coasts was shown to be an important factor for explaining the substantial differences in absolute concentrations

The maintenance and monitoring of perioperative blood volume

The assessment and maintenance of perioperative blood volume is important because fluid therapy is a routine part of intraoperative care. In the past, patients undergoing major surgery were given large amounts of fluids because health-care providers were concerned about preoperative dehydration and intraoperative losses to a third space. In the last decade it has become clear that fluid therapy has to be more individualized. Because the exact determination of blood volume is not clinically possible at every timepoint, there have been different approaches to assess fluid requirements, such as goal-directed protocols guided by invasive and less invasive devices. This article focuses on laboratory volume determination, capillary dynamics, aspects of different fluids and how to clinically assess and monitor perioperative blood volume

Theory and observations: Model simulations of the period 1955-1985

The main objective of the theoretical studies presented here is to apply models of stratospheric chemistry and transport in order to understand the processes that control stratospheric ozone and that are responsible for the observed variations. The model calculations are intended to simulate the observed behavior of atmospheric ozone over the past three decades (1955-1985), for which there exists a substantial record of both ground-based and, more recently, satellite measurements. Ozone concentrations in the atmosphere vary on different time scales and for several different causes. The models described here were designed to simulate the effect on ozone of changes in the concentration of such trace gases as CFC, CH4, N2O, and CO2. Changes from year to year in ultraviolet radiation associated with the solar cycle are also included in the models. A third source of variability explicitly considered is the sporadic introduction of large amounts of NO sub x into the stratosphere during atmospheric nuclear tests

Temperature-dependent quantum pair potentials and their application to dense partially ionized hydrogen plasmas

Extending our previous work \cite{filinov-etal.jpa03ik} we present a detailed discussion of accuracy and practical applications of finite-temperature pseudopotentials for two-component Coulomb systems. Different pseudopotentials are discussed: i) the diagonal Kelbg potential, ii) the off-diagonal Kelbg potential iii) the {\em improved} diagonal Kelbg potential, iv) an effective potential obtained with the Feynman-Kleinert variational principle v) the ``exact'' quantum pair potential derived from the two-particle density matrix. For the {\em improved} diagonal Kelbg potential a simple temperature dependent fit is derived which accurately reproduces the ``exact'' pair potential in the whole temperature range. The derived pseudopotentials are then used in path integral Monte Carlo (PIMC) and molecular dynamics (MD) simulations to obtain thermodynamical properties of strongly coupled hydrogen. It is demonstrated that classical MD simulations with spin-dependent interaction potentials for the electrons allow for an accurate description of the internal energy of hydrogen in the difficult regime of partial ionization down to the temperatures of about $60 000$ K. Finally, we point out an interesting relation between the quantum potentials and effective potentials used in density functional theory.Comment: 18 pages, 11 figure

Modelling of Peripheral Fluid Accumulation after a Crystalloid Bolus in Female Volunteers – A Mathematical Study

Objective. To simultaneously model plasma dilution and urinary output in female volunteers

Toward catchment hydro-biogeochemical theories

Headwater catchments are the fundamental units that connect the land to the ocean. Hydrological flow and biogeochemical processes are intricately coupled, yet their respective sciences have progressed without much integration. Reaction kinetic theories that prescribe rate dependence on environmental variables (e.g., temperature and water content) have advanced substantially, mostly in well-mixed reactors, columns, and warming experiments without considering the characteristics of hydrological flow at the catchment scale. These theories have shown significant divergence from observations in natural systems. On the other hand, hydrological theories, including transit time theory, have progressed substantially yet have not been incorporated into understanding reactions at the catchment scale. Here we advocate for the development of integrated hydro-biogeochemical theories across gradients of climate, vegetation, and geology conditions. The lack of such theories presents barriers for understanding mechanisms and forecasting the future of the Critical Zone under human- and climate-induced perturbations. Although integration has started and co-located measurements are well under way, tremendous challenges remain. In particular, even in this era of "big data," we are still limited by data and will need to (1) intensify measurements beyond river channels and characterize the vertical connectivity and broadly the shallow and deep subsurface; (2) expand to older water dating beyond the time scales reflected in stable water isotopes; (3) combine the use of reactive solutes, nonreactive tracers, and isotopes; and (4) augment measurements in environments that are undergoing rapid changes. To develop integrated theories, it is essential to (1) engage models at all stages to develop model-informed data collection strategies and to maximize data usage; (2) adopt a "simple but not simplistic," or fit-for-purpose approach to include essential processes in process-based models; (3) blend the use of process-based and data-driven models in the framework of "theory-guided data science." Within the framework of hypothesis testing, model-data fusion can advance integrated theories that mechanistically link catchments' internal structures and external drivers to their functioning. It can not only advance the field of hydro-biogeochemistry, but also enable hind- and fore-casting and serve the society at large. Broadly, future education will need to cultivate thinkers at the intersections of traditional disciplines with hollistic approaches for understanding interacting processes in complex earth systems.This article is categorized under:Science of Water > Method