Sediment release of dissolved organic matter in the oxygen minimum zone off Peru

In combination to sluggish ventilation by ocean currents, the nutrient upwelling and high surface productivity, followed by organic matter remineralization, leads to a pronounced oxygen minimum zone (OMZ) in the eastern tropical South Pacific (ETSP). There, oxygen concentrations drop below 1 �mol/kg at a water depth <80 m. The high productivity results in the supply of organic matter (OM) to the anoxic sediments and its utilization by heterotrophic communities. The microbial utilization of OM under anoxia leads to nitrogen loss processes, and an accumulation of sulphide and methane. The proximity of the OMZ to the ocean surface in the ETSP may lead to an active outgassing of climate relevant products of the anoxic OM remineralization. The degradation of OM in sediments is associated with production of dissolved organic matter (DOM) from organic particles (POM) that is further remineralized into inorganic nutrients and dissolved inorganic carbon, which then can be released back to the water column, fuelling productivity. Part of the DOM pool may be released to the overlying water column and serve as ligands for micronutrients, such as iron, or provide an additional substrate for microbial communities to respire, affecting overlying water column biogeochemistry. Despite the potential relevance for biogeochemical processes, the quality of the DOM in the pore waters that may be released to the overlying water column has been barely studied in the ETSP off Peru. High spatial resolution measurements of DOM fluorescence (FDOM) during the research cruise M93 (Feb-March 2013) indicated elevated intensities near the sediments in the ETSP off Peru. Those intensities were interpreted as a sediment release of DOM, the quantification of dissolved organic carbon (DOC) flux, however, was not possible at the time. To estimate DOM fluxes and DOM quality, DOC and DOM samples were collected from the sediment pore waters and from benthic incubation chambers from six stations along the 12°S transect in the Peruvian upwelling in 2017 (cruises M136, M137). Samples were collected using a multiple-corer and by Biogeochemical Observatories, respectively. Here, we evaluate DOC fluxes from the sediments and relate them to the measurements of FDOM. We evaluate the quality of DOM by Excitation Emission spectroscopy, followed by parallel factor analysis. The possible implications of the DOM release for water column biogeochemistry are discussed

Radiative forcing of natural forest disturbances

Forest disturbances are major sources of carbon dioxide to the atmosphere, and therefore impact global climate. Biogeophysical attributes, such as surface albedo (reflectivity), further control the climate-regulating properties of forests. Using both tower-based and remotely sensed data sets, we show that natural disturbances from wildfire, beetle outbreaks, and hurricane wind throw can significantly alter surface albedo, and the associated radiative forcing either offsets or enhances the CO2 forcing caused by reducing ecosystem carbon sequestration over multiple years. In the examined cases, the radiative forcing from albedo change is on the same order of magnitude as the CO2 forcing. The net radiative forcing resulting from these two factors leads to a local heating effect in a hurricane-damaged mangrove forest in the subtropics, and a cooling effect following wildfire and mountain pine beetle attack in boreal forests with winter snow. Although natural forest disturbances currently represent less than half of gross forest cover loss, that area will probably increase in the future under climate change, making it imperative to represent these processes accurately in global climate models

Structural Abnormalities at Neuromuscular Synapses Lacking Multiple Syntrophin Isoforms

The syntrophins are modular adapter proteins that function by recruiting signaling molecules to the cytoskeleton via their direct association with proteins of the dystrophin protein family. We investigated the physiological function of beta2-syntrophin by generating a line of mice lacking this syntrophin isoform. The beta2-syntrophin null mice show no overt phenotype, or muscular dystrophy, and form structurally normal neuromuscular junctions (NMJs). To determine whether physiological consequences caused by the lack of beta2-syntrophin were masked by compensation from the alpha-syntrophin isoform, we crossed these mice with our previously described alpha-syntrophin null mice to produce mice lacking both isoforms. The alpha/beta2-syntrophin null mice have NMJs that are structurally more aberrant than those lacking only alpha-syntrophin. The NMJs of the alpha/beta2-syntrophin null mice have fewer junctional folds than either parent strain, and the remaining folds are abnormally shaped with few openings to the synaptic space. The levels of acetylcholine receptors are reduced to 23% of wild type in mice lacking both syntrophin isoforms. Furthermore, the alpha/beta2-syntrophin null mice ran significantly shorter distances on voluntary exercise wheels despite having normal neuromuscular junction transmission as determined by micro-electrode recording of endplate potentials. We conclude that both alpha-syntrophin and beta2-syntrophin play distinct roles in forming and maintaining NMJ structure and that each syntrophin can partially compensate for the loss of the other

Simulating Electron Transport and Synchrotron Emission in Radio Galaxies: Shock Acceleration and Synchrotron Aging in Axis-Symmetric Flows

We introduce a simple and economical but effective method for including relativistic electron transport in multi-dimensional simulations of radio galaxies. The method is designed to follow explicitly diffusive acceleration at shocks, and, in smooth flows 2nd order Fermi acceleration plus adiabatic and synchrotron cooling. We are able to follow both the spatial and energy distributions of the electrons, so that direct synchrotron emission properties can be modeled in time-dependent flows for the first time. Here we present first results in the form of some axis-symmetric MHD simulations of Mach 20 light jet flows. These show clearly the importance of nonsteady terminal shocks that develop in such flows even when the jet inflow is steady. As a result of this and other consequences of the fundamentally driven character of jets, we find complex patterns of emissivities and synchrotron spectra, including steep spectral gradients in hot spots, islands of distinct spectra electrons within the lobes and spectral gradients coming from the dynamical histories of a given flow element rather than from synchrotron aging of the embedded electrons. In addition, spectral aging in the lobes tends to proceed more slowly than one would estimate from regions of high emissivity.Comment: 30 pages of Latex generated text plus 7 figures in gif format. Accepted for publication in the Astrophysical Journal. High resolution postscript figures available through anonymous ftp at ftp://ftp.msi.umn.edu/pub/users/twj/RGje

Triple negative breast cancers express receptors for LHRH and are potential therapeutic targets for cytotoxic LHRH-analogs, AEZS 108 and AEZS 125

Background Triple negative breast cancer (TNBC) is a distinct subtype of breast cancer burdened with a dismal prognosis due to the lack of effective therapeutic agents. Receptors for LHRH (luteinizing hormone-releasing hormone) can be successfully targeted with AEZS-108 [AN-152], an analog of LHRH conjugated to doxorubicin. Our study evaluates the presence of this target LHRH receptor in human specimens of TNBC and investigates the efficacy and toxicity of AEZS-108 in vivo. We also studied in vitro activity of AEZS-125, a new LHRH analog conjugated with the highly potent natural compound, Disorazol Z. Methods 69 human surgical specimens of TNBC were investigated for LHRH-R expression by immunohistochemistry. Expression of LHRH-R in two TNBC cell lines was evaluated by real time RT-PCR. Cytotoxicity of AEZS-125 was evaluated by Cell Titer Blue cytoxicity assay. LHRH- receptor expression was silenced with an siRNA in both cell lines. For the in vivo experiments an athymic nude mice model xenotransplanted with the cell lines, MDA-MB-231 and HCC 1806, was used. The animals were randomised to three groups receiving solvent only (d 1, 7, 14, i.v.) for control, AEZS-108 (d 1, 7, 14, i.v.) or doxorubicin at an equimolar dose (d 1, 7, 14, i.v.). Results In human clinical specimens of TNBC, expression of the LHRH-receptor was present in 49% (n = 69). HCC 1806 and MDA-MB-231 TNBC cells expressed mRNA for the LHRH-receptor. Silencing of the LHRH-receptor significantly decreased the cytotoxic effect of AEZS-108. MDA-MB-231 and HCC 1806 tumors xenografted into nude mice were significantly inhibited by treatment with AEZS-108; doxorubicin at equimolar doses was ineffective. As compared to AEZS 108, the Disorazol Z – LHRH conjugate, AEZS-125, demonstrated an increased cytotoxicity in vitro in HCC 1806 and MDA-MB-231 TNBC; this was diminished by receptor blockade with synthetic LHRH agonist (triptorelin) pretreatment. Conclusion The current study confirms that LHRH-receptors are expressed by a significant proportion of TNBC and can be successfully used as homing sites for cytotoxic analogs of LHRH, such as AEZS-108 and AEZS-125