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Few studies to date have demonstrated widespread biological impacts of ocean acidification (OA) under conditions currently found in the natural environment. From a combined survey of physical and chemical water properties and biological sampling along the Washington-Oregon-California coast in August 2011, we show that large portions of the shelf waters are corrosive to pteropods in the natural environment. We show a strong positive correlation between the proportion of pteropod individuals with severe shell dissolution damage and the percentage of undersaturated water in the top 100 m with respect to aragonite. We found 53% of onshore individuals and 24% of offshore individuals on average to have severe dissolution damage. Relative to pre-industrial CO2 concentrations, the extent of undersaturated waters in the top 100 m of the water column has increased over sixfold along the California Current Ecosystem (CCE). We estimate that the incidence of severe pteropod shell dissolution owing to anthropogenic OA has doubled in near shore habitats since pre-industrial conditions across this region and is on track to triple by 2050. These results demonstrate that habitat suitability for pteropods in the coastal CCE is declining. The observed impacts represent a baseline for future observations towards understanding broader scale OA effects.
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Exoesqueleto/química , Cambio Climático , Ecosistema , Agua de Mar/química , Caracoles/crecimiento & desarrollo , Exoesqueleto/crecimiento & desarrollo , Animales , Calcificación Fisiológica , Carbonato de Calcio/análisis , California , Concentración de Iones de Hidrógeno , Oregon , Océano Pacífico , Solubilidad , WashingtónRESUMEN
Analyses of suspended particulate matter from the eastern equatorial Pacific Ocean have defined a 400-meter-thick benthic nepheloid layer enriched in aluminum, silicon, iron, and manganese relative to the overlying waters. Chemical mass-balance calculations suggest that the concentration increases in the benthic nepheloid layer are due to resuspension from the fraction of the local bottom sediments in the size range >/=1 micrometer.
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Fluxes of biogenic carbonates moving out of the euphotic zone and into deeper undersaturated waters of the North Pacific were estimated with free-drifting sediment traps. Short-duration (1 to 1.5 day) sampling between 100 and 2200 meters points to a major involvement in the oceanic carbonate system by a class of organisms which had been relegated to a secondary role-aragonitic pteropods. Pteropod fluxes through the base of the euphotic zone are almost large enough to balance the alkalinity budget for the Pacific Ocean. Dissolution experiments with freshly collected materials shed considerable light on a mystery surrounding these labile organisms: although plankton collections from net tows almost always contain large numbers of pteropods, these organisms are never a major component of biogenic materials in long-duration sediment trap collections. Their low abundance in long-duration collections results from dissolution subsequent to collection. Shortduration sampling showed significant increases in the ratio of calcitic foraminifera to aragonitic pteropods in undersaturated waters, indicating the more stable mineralogic form, calcite, was preserved relative to aragonite. Approximately 90 percent of the aragonite flux is remineralized in the upper 2.2 kilometers of the water column.
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The equatorial Pacific is the largest oceanic source of carbon dioxide to the atmosphere and has been proposed to be a major site of organic carbon export to the deep sea. Study of the chemistry and biology of this area from 170 degrees to 95 degrees W suggests that variability of remote winds in the western Pacific and tropical instability waves are the major factors controlling chemical and biological variability. The reason is that most of the biological production is based on recycled nutrients; only a few of the nutrients transported to the surface by upwelling are taken up by photosynthesis. Biological cycling within the euphotic zone is efficient, and the export of carbon fixed by photosynthesis is small. The fluxes of carbon dioxide to the atmosphere and particulate organic carbon to the deep sea were about 0.3 gigatons per year, and the production of dissolved organic carbon was about three times as large. The data establish El Niño events as the main source of interannual variability.
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Data on particulate strontium sulfate fluxes and strontium to chlorinity ratios were compared to provide insights into the strontium cycle of the North Pacific. Freedrifting sediment traps were used to derive large particle fluxes between depths of 100 and 3500 meters in the eastern and western North Pacific Ocean. Flux data revealed substantial quantities of acantharian skeletons and cysts (both made of strontium sulfate) settling through the upper kilometer of the water column. The greatest fluxes of celestite were detected at 400 meters. Minimal to nondetectable fluxes noted at and below 900 meters provide evidence that by this horizon, the majority of acantharian specimens had dissolved, thereby contributing to the pool of dissolved strontium. Growth and subsequent dissolution of acantharians in the upper kilometer are qualitatively consistent with the well-developed minimum and maximum strontium to chlorinity ratios that are consistently noted in these waters. These fluxes of particulate strontium and model calculations for fluxes of dissolved strontium indicate that acantharians play an important role in the ocean's strontium budget.
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A survey of hydrothermal activity along the superfast-spreading (approximately 150 millimeters per year) East Pacific Rise shows that hydrothermal plumes overlay approximately 60 percent of the ridge crest between 13 degrees 50' and 18 degrees 40'S, a plume abundance nearly twice that known from any other rige portion of comparable length. Plumes were most abundant where the axial cross section is inflated and an axial magma chamber is present. Plumes with high ratios of volatile ((3)He, CH(4), and H(2)S) to nonvolatile (Mn and Fe) species marked where hydrothermal circulation has been perturbed by recent magmatic activity. The high proportion of volatile-rich plumes observed implies that such episodes are more frequent here than on slower spreading ridges.
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We compare physiological responses of the crustacean copepod Calanus pacificus and pelagic pteropod mollusk Limacina helicina to ocean temperatures and pH by measuring biomarkers of oxidative stress, antioxidant defences, and the activity of the respiratory electron transport system in organisms collected on the 2016 West Coast Ocean Acidification cruise in the California Current System. Copepods and pteropods exhibited strong but divergent responses in the same habitat; copepods had higher oxygen-reactive absorbance capacity, glutathione-S-transferase, and total glutathione content. The ratio between reduced to oxidised glutathione was higher in copepods than in pteropods, indicating lower oxidative stress in copepods. Pteropods showed higher activities of glutathione reductase, catalase, and lipid peroxidation, indicating increased antioxidant defences and oxidative stress. Thus, the antioxidant defence system of the copepods has a greater capacity to respond to oxidative stress, while pteropods already face severe stress and show limited capacity to deal with further changes. The results suggest that copepods have higher adaptive potential, owing to their stronger vertical migration behaviour and efficient glutathione metabolism, whereas pteropods run the risk of oxidative stress and mortality under high CO2 conditions. Our results provide a unique dataset and evidence of stress-inducing mechanisms behind pteropod ocean acidification responses.
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Adaptación Fisiológica/fisiología , Copépodos/fisiología , Calentamiento Global , Concentración de Iones de Hidrógeno , Moluscos/fisiología , Animales , Antioxidantes , Transporte de Electrón , Gastrópodos , Océanos y Mares , Estrés OxidativoRESUMEN
Spaceborne observations of carbon dioxide (CO2) from the Orbiting Carbon Observatory-2 are used to characterize the response of tropical atmospheric CO2 concentrations to the strong El Niño event of 2015-2016. Although correlations between the growth rate of atmospheric CO2 concentrations and the El Niño-Southern Oscillation are well known, the magnitude of the correlation and the timing of the responses of oceanic and terrestrial carbon cycle remain poorly constrained in space and time. We used space-based CO2 observations to confirm that the tropical Pacific Ocean does play an early and important role in modulating the changes in atmospheric CO2 concentrations during El Niño events-a phenomenon inferred but not previously observed because of insufficient high-density, broad-scale CO2 observations over the tropics.
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The pteropod Limacina helicina frequently experiences seasonal exposure to corrosive conditions (Ωar < 1) along the US West Coast and is recognized as one of the species most susceptible to ocean acidification (OA). Yet, little is known about their capacity to acclimatize to such conditions. We collected pteropods in the California Current Ecosystem (CCE) that differed in the severity of exposure to Ωar conditions in the natural environment. Combining field observations, high-CO2 perturbation experiment results, and retrospective ocean transport simulations, we investigated biological responses based on histories of magnitude and duration of exposure to Ωar < 1. Our results suggest that both exposure magnitude and duration affect pteropod responses in the natural environment. However, observed declines in calcification performance and survival probability under high CO2 experimental conditions do not show acclimatization capacity or physiological tolerance related to history of exposure to corrosive conditions. Pteropods from the coastal CCE appear to be at or near the limit of their physiological capacity, and consequently, are already at extinction risk under projected acceleration of OA over the next 30 years. Our results demonstrate that Ωar exposure history largely determines pteropod response to experimental conditions and is essential to the interpretation of biological observations and experimental results.
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Exposición a Riesgos Ambientales , Gastrópodos , Concentración de Iones de Hidrógeno , Agua de Mar , Animales , Calcificación Fisiológica , Carbonatos/química , Océanos y Mares , Estados del Pacífico , Agua de Mar/análisisRESUMEN
The near-term progression of ocean acidification (OA) is projected to bring about sharp changes in the chemistry of coastal upwelling ecosystems. The distribution of OA exposure across these early-impact systems, however, is highly uncertain and limits our understanding of whether and how spatial management actions can be deployed to ameliorate future impacts. Through a novel coastal OA observing network, we have uncovered a remarkably persistent spatial mosaic in the penetration of acidified waters into ecologically-important nearshore habitats across 1,000 km of the California Current Large Marine Ecosystem. In the most severe exposure hotspots, suboptimal conditions for calcifying organisms encompassed up to 56% of the summer season, and were accompanied by some of the lowest and most variable pH environments known for the surface ocean. Persistent refuge areas were also found, highlighting new opportunities for local adaptation to address the global challenge of OA in productive coastal systems.
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Global ship-based programs, with highly accurate, full water column physical and biogeochemical observations repeated decadally since the 1970s, provide a crucial resource for documenting ocean change. The ocean, a central component of Earth's climate system, is taking up most of Earth's excess anthropogenic heat, with about 19% of this excess in the abyssal ocean beneath 2,000 m, dominated by Southern Ocean warming. The ocean also has taken up about 27% of anthropogenic carbon, resulting in acidification of the upper ocean. Increased stratification has resulted in a decline in oxygen and increase in nutrients in the Northern Hemisphere thermocline and an expansion of tropical oxygen minimum zones. Southern Hemisphere thermocline oxygen increased in the 2000s owing to stronger wind forcing and ventilation. The most recent decade of global hydrography has mapped dissolved organic carbon, a large, bioactive reservoir, for the first time and quantified its contribution to export production (â¼20%) and deep-ocean oxygen utilization. Ship-based measurements also show that vertical diffusivity increases from a minimum in the thermocline to a maximum within the bottom 1,500 m, shifting our physical paradigm of the ocean's overturning circulation.
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Carbono/análisis , Agua de Mar/química , Clima , Oceanografía/instrumentación , Navíos , Temperatura , Movimientos del AguaRESUMEN
The sources and sinks of dissolved and particulate Pb, Cu and Zn were determined for the main basin of Puget Sound to understand the effect man has had on metal concentrations in both the water column and in the sediments. Municipal, industrial and atmospheric sources contributed about 66% of the total Pb added to the main basin of Puget Sound during the early 1980s. Advective inputs were the major sources of total Cu and Zn (approximately 40%) while riverine and erosional sources contributed about 30%. The discharge of the particle-bound trace metals from rivers minimized the influence of particulate anthropogenic sources, which constituted 50%, 23% and 18% of the total particulate Pb, Cu and Zn inputs, respectively. While advective transport was the major source of dissolved Cu and Zn (approximately 60% of all dissolved inputs), industrial, municipal and atmospheric inputs contributed about 85%, 30% and 38% of the dissolved Pb, Cu and Zn inputs, respectively. The sources of dissolved and particulate Cu and Zn were comparable with the sinks within the errors of the analyses indicating their quasi-conservative nature. Advection removed about 60% of the total Cu and Zn added to the main basin while 40% was deposited in the sediments of Puget Sound. Because of this quasi-conservative nature of Cu and Zn, anthropogenic inputs of Cu and Zn were dispersed from the system more than they were contained within main basin sediments. About 75% of the dissolved Pb discharged into the main basin of Puget Sound was lost from the dissolved phase and was balanced by a similar gain in the particulate phase. Because of this extensive scavenging and the effective retention of particles within the main basin, about 70% of the total Pb added to the main basin was retained within its sediments. These separate mass balances have utility in management decisions because they show the relative contributions from different sources and demonstrate whether the influences of dissolved and particulate inputs are reflected solely in the water column or the sediments, respectively.
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The DRG/OMT [Diagnosis-Related Groups/Osteopathic Manipulative Treatment] Master Matrix is a tabulated guideline for helping osteopathic physicians and hospitals document their unique form of health-care. The DRG/OMT Master Matrix is a quality management tool designed for osteopathic physician care of hospitalized patients. It furnishes a mechanism for relating various diagnostic entities to probable areas of somatic dysfunction. This matrix and the accompanying patient record aid the physician in recording diagnosis and treatment, thus providing the hospital with documentation of osteopathic patient care's competitive advantage. In a hospital record review, OMT use increased from 5% to 15% of patients after the DRG/OMT Master Matrix was introduced.
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Grupos Diagnósticos Relacionados/normas , Hospitales Traumatológicos/normas , Manipulación Ortopédica/normas , Guías de Práctica Clínica como Asunto , Protocolos Clínicos , Documentación , Control de Formularios y Registros , Humanos , Estados UnidosAsunto(s)
Cambio Climático , Monitoreo del Ambiente/métodos , Invertebrados/metabolismo , Agua de Mar/química , Contaminantes Químicos del Agua/análisis , Animales , Dióxido de Carbono/análisis , Ácido Carbónico/análisis , Concentración de Iones de Hidrógeno , Invertebrados/efectos de los fármacos , Océanos y Mares , Contaminantes Químicos del Agua/toxicidadRESUMEN
Approximately 250,000 measurements made for the pCO2 difference between surface water and the marine atmosphere, DeltapCO2, have been assembled for the global oceans. Observations made in the equatorial Pacific during El Nino events have been excluded from the data set. These observations are mapped on the global 4 degrees x 5 degrees grid for a single virtual calendar year (chosen arbitrarily to be 1990) representing a non-El Nino year. Monthly global distributions of DeltapCO2 have been constructed using an interpolation method based on a lateral advection-diffusion transport equation. The net flux of CO2 across the sea surface has been computed using DeltapCO2 distributions and CO2 gas transfer coefficients across sea surface. The annual net uptake flux of CO2 by the global oceans thus estimated ranges from 0.60 to 1.34 Gt-Cyr-1 depending on different formulations used for wind speed dependence on the gas transfer coefficient. These estimates are subject to an error of up to 75% resulting from the numerical interpolation method used to estimate the distribution of DeltapCO2 over the global oceans. Temperate and polar oceans of the both hemispheres are the major sinks for atmospheric CO2, whereas the equatorial oceans are the major sources for CO2. The Atlantic Ocean is the most important CO2 sink, providing about 60% of the global ocean uptake, while the Pacific Ocean is neutral because of its equatorial source flux being balanced by the sink flux of the temperate oceans. The Indian and Southern Oceans take up about 20% each.