10 research outputs found
Initial planetary base construction techniques and machine implementation
Conceptual designs of (1) initial planetary base structures, and (2) an unmanned machine to perform the construction of these structures using materials local to the planet are presented. Rock melting is suggested as a possible technique to be used by the machine in fabricating roads, platforms, and interlocking bricks. Identification of problem areas in machine design and materials processing is accomplished. The feasibility of the designs is contingent upon favorable results of an analysis of the engineering behavior of the product materials. The analysis requires knowledge of several parameters for solution of the constitutive equations of the theory of elasticity. An initial collection of these parameters is presented which helps to define research needed to perform a realistic feasibility study. A qualitative approach to estimating power and mass lift requirements for the proposed machine is used which employs specifications of currently available equipment. An initial, unmanned mission scenario is discussed with emphasis on identifying uncompleted tasks and suggesting design considerations for vehicles and primitive structures which use the products of the machine processing
Molecular mechanisms of cell death: recommendations of the Nomenclature Committee on Cell Death 2018.
Over the past decade, the Nomenclature Committee on Cell Death (NCCD) has formulated guidelines for the definition and interpretation of cell death from morphological, biochemical, and functional perspectives. Since the field continues to expand and novel mechanisms that orchestrate multiple cell death pathways are unveiled, we propose an updated classification of cell death subroutines focusing on mechanistic and essential (as opposed to correlative and dispensable) aspects of the process. As we provide molecularly oriented definitions of terms including intrinsic apoptosis, extrinsic apoptosis, mitochondrial permeability transition (MPT)-driven necrosis, necroptosis, ferroptosis, pyroptosis, parthanatos, entotic cell death, NETotic cell death, lysosome-dependent cell death, autophagy-dependent cell death, immunogenic cell death, cellular senescence, and mitotic catastrophe, we discuss the utility of neologisms that refer to highly specialized instances of these processes. The mission of the NCCD is to provide a widely accepted nomenclature on cell death in support of the continued development of the field
Trace Element Geochemistry in North Pacific Red Clay Sediment Porewaters and Implications for WaterâColumn Studies
Geochemical analyses of trace elements in the ocean water column have suggested that pelagic clayârich sediments are a major source of various elements to bottomâwaters. However, corresponding highâquality measurements of trace element concentrations in porewaters of pelagic clayârich sediments are scarce, making it difficult to evaluate the contributions from benthic processes to global oceanic cycles of trace elements. To bridge this gap, we analyzed porewater and bulk sediment concentrations of vanadium, chromium, cobalt, nickel, copper, arsenic, molybdenum, barium and uranium, as well as concentrations of the major oxidants nitrate, manganese, iron, and sulfate in the top 30 cm of cores collected along a transect from Hawaii to Alaska. The data show large increases in porewater concentrations of vanadium, manganese, cobalt, nickel, copper, and arsenic within the top cm of the sediment, consistent with the release of these elements from remineralized organic matter. The sediments are a sink for sulfate, uranium, and molybdenum, even though conditions within the sampled top 30 cm remain aerobic. Porewater chromium concentrations generally increase with depth due to release from sediment particles. Extrapolated to the global aerial extent of pelagic clay sediment, the benthic fluxes in mol yr â1 are Ba 3.9 ± 3.6 Ă 10 9 , Mn 3.4 ± 3.5 Ă 10 8 , Co 2.6 ± 1.3 Ă 10 7 , Ni 9.6 ± 8.6 Ă 10 8 , Cu 4.6 ± 2.4 Ă 10 9 , Cr 1.7 ± 1.1 Ă 10 8 , As 6.1 ± 7.0 Ă 10 8 , V 6.0 ± 2.5 Ă 10 9 . With the exception of vanadium, calculated fluxes across the sedimentâwater interface are consistent with the variability in bottomâwater concentrations and ocean residence time of the studied elements
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Trace Element Geochemistry in North Pacific Red Clay Sediment Porewaters and Implications for WaterâColumn Studies
Publication status: PublishedAbstractGeochemical analyses of trace elements in the ocean water column have suggested that pelagic clayârich sediments are a major source of various elements to bottomâwaters. However, corresponding highâquality measurements of trace element concentrations in porewaters of pelagic clayârich sediments are scarce, making it difficult to evaluate the contributions from benthic processes to global oceanic cycles of trace elements. To bridge this gap, we analyzed porewater and bulk sediment concentrations of vanadium, chromium, cobalt, nickel, copper, arsenic, molybdenum, barium and uranium, as well as concentrations of the major oxidants nitrate, manganese, iron, and sulfate in the top 30 cm of cores collected along a transect from Hawaii to Alaska. The data show large increases in porewater concentrations of vanadium, manganese, cobalt, nickel, copper, and arsenic within the top cm of the sediment, consistent with the release of these elements from remineralized organic matter. The sediments are a sink for sulfate, uranium, and molybdenum, even though conditions within the sampled top 30 cm remain aerobic. Porewater chromium concentrations generally increase with depth due to release from sediment particles. Extrapolated to the global aerial extent of pelagic clay sediment, the benthic fluxes in mol yrâ1 are Ba 3.9 ± 3.6 Ă 109, Mn 3.4 ± 3.5 Ă 108, Co 2.6 ± 1.3 Ă 107, Ni 9.6 ± 8.6 Ă 108, Cu 4.6 ± 2.4 Ă 109, Cr 1.7 ± 1.1 Ă 108, As 6.1 ± 7.0 Ă 108, V 6.0 ± 2.5 Ă 109. With the exception of vanadium, calculated fluxes across the sedimentâwater interface are consistent with the variability in bottomâwater concentrations and ocean residence time of the studied elements.</jats:p