997 resultados para Intercellular CO2 concentration
Resumo:
We measured the relationship between CO2-induced seawater acidification, photo-physiological performance and intracellular pH (pHi) in a model cnidarian-dinoflagellate symbiosis - the sea anemone Aiptasia sp. -under ambient (289.94 ± 12.54 µatm), intermediate (687.40 ± 25.10 µatm) and high (1459.92 ± 65.51 µatm) CO2 conditions. These treatments represented current CO2 levels, in addition to CO2 stabilisation scenarios IV and VI provided by the Intergovernmental Panel on Climate Change (IPCC). Anemones were exposed to each treatment for two months and sampled at regular intervals. At each time-point we measured a series of physiological responses: maximum dark-adapted fluorescent yield of PSII (Fv/Fm), gross photosynthetic rate, respiration rate, symbiont population density, and light-adapted pHi of both the dinoflagellate symbiont and isolated host anemone cell. We observed increases in all but one photo-physiological parameter (Pgross:R ratio). At the cellular level, increases in light-adapted symbiont pHi were observed under both intermediate and high CO2 treatments, relative to control conditions (pHi 7.35 and 7.46 versus pHi 7.25, respectively). The response of light-adapted host pHi was more complex, however, with no change observed under the intermediate CO2 treatment, but a 0.3 pH-unit increase under the high CO2 treatment (pHi 7.19 and 7.48, respectively). This difference is likely a result of a disproportionate increase in photosynthesis relative to respiration at the higher CO2 concentration. Our results suggest that, rather than causing cellular acidosis, the addition of CO2 will enhance photosynthetic performance, enabling both the symbiont and host cell to withstand predicted ocean acidification scenarios.
Resumo:
Since pre-industrial times, uptake of anthropogenic CO2 by surface ocean waters has caused a documented change of 0.1 pH units. Calcifying organisms are sensitive to elevated CO2 concentrations due to their calcium carbonate skeletons. In temperate rocky intertidal environments, calcifying and noncalcifying macroalgae make up diverse benthic photoautotrophic communities. These communities may change as calcifiers and noncalcifiers respond differently to rising CO2 concentrations. In order to test this hypothesis, we conducted an 86?d mesocosm experiment to investigate the physiological and competitive responses of calcifying and noncalcifying temperate marine macroalgae to 385, 665, and 1486 µatm CO2. We focused on comparing 2 abundant red algae in the Northeast Atlantic: Corallina officinalis (calcifying) and Chondrus crispus (noncalcifying). We found an interactive effect of CO2 concentration and exposure time on growth rates of C. officinalis, and total protein and carbohydrate concentrations in both species. Photosynthetic rates did not show a strong response. Calcification in C. officinalis showed a parabolic response, while skeletal inorganic carbon decreased with increasing CO2. Community structure changed, as Chondrus crispus cover increased in all treatments, while C. officinalis cover decreased in both elevated-CO2 treatments. Photochemical parameters of other species are also presented. Our results suggest that CO2 will alter the competitive strengths of calcifying and noncalcifying temperate benthic macroalgae, resulting in different community structures, unless these species are able to adapt at a rate similar to or faster than the current rate of increasing sea-surface CO2 concentrations.
Resumo:
The effects of CO2-induced seawater acidification on plankton communities were also addressed in a series of 3 mesocosm experiments, called the Pelagic Ecosystem CO2 Enrichment (PeECE I-III) studies, which were conducted in the Large-Scale Mesocosm Facilities of the University of Bergen, Norway in 2001, 2003 and 2005, respectively. Each experiment consisted of 9 mesocosms, in which CO2 was manipulated to initial concentrations of 190, 350 and 750 µatm in 2001 and 2003, and 350, 700 and 1050 µatm in 2005. The present dataset concerns PeECE I.
Resumo:
Ocean acidification studies in the past decade have greatly improved our knowledge of how calcifying organisms respond to increased surface ocean CO2 levels. It has become evident that, for many organisms, nutrient availability is an important factor that influences their physiological responses and competitive interactions with other species. Therefore, we tested how simulated ocean acidification and eutrophication (nitrate and phosphate enrichment) interact to affect the physiology and ecology of a calcifying chlorophyte macroalga (Halimeda opuntia (L.) J.V. Lamouroux) and its common noncalcifying epiphyte (Dictyota sp.) in a 4-week fully crossed multifactorial experiment. Inorganic nutrient enrichment (+NP) had a strong influence on all responses measured with the exception of net calcification. Elevated CO2 alone significantly decreased electron transport rates of the photosynthetic apparatus and resulted in phosphorus limitation in both species, but had no effect on oxygen production or respiration. The combination of CO2 and +NP significantly increased electron transport rates in both species. While +NP alone stimulated H. opuntia growth rates, Dictyota growth was significantly stimulated by nutrient enrichment only at elevated CO2, which led to the highest biomass ratios of Dictyota to Halimeda. Our results suggest that inorganic nutrient enrichment alone stimulates several aspects of H. opuntia physiology, but nutrient enrichment at a CO2 concentration predicted for the end of the century benefits Dictyota sp. and hinders its calcifying basibiont H. opuntia.
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Ocean acidification substantially alters ocean carbon chemistry and hence pH but the effects on sea ice formation and the CO2 concentration in the enclosed brine channels are unknown. Microbial communities inhabiting sea ice ecosystems currently contribute 10-50% of the annual primary production of polar seas, supporting overwintering zooplankton species, especially Antarctic krill, and seeding spring phytoplankton blooms. Ocean acidification is occurring in all surface waters but the strongest effects will be experienced in polar ecosystems with significant effects on all trophic levels. Brine algae collected from McMurdo Sound (Antarctica) sea ice was incubated in situ under various carbonate chemistry conditions. The carbon chemistry was manipulated with acid, bicarbonate and bases to produce a pCO2 and pH range from 238 to 6066 µatm and 7.19 to 8.66, respectively. Elevated pCO2 positively affected the growth rate of the brine algal community, dominated by the unique ice dinoflagellate, Polarella glacialis. Growth rates were significantly reduced when pH dropped below 7.6. However, when the pH was held constant and the pCO2 increased, growth rates of the brine algae increased by more than 20% and showed no decline at pCO2 values more than five times current ambient levels. We suggest that projected increases in seawater pCO2, associated with OA, will not adversely impact brine algal communities.
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Increased atmospheric carbon dioxide leads to ocean acidification and carbon dioxide (CO2) enrichment of seawater. Given the important ecological functions of seagrass meadows, understanding their responses to CO2 will be critical for the management of coastal ecosystems. This study examined the physiological responses of three tropical seagrasses to a range of seawater pCO2 levels in a laboratory. Cymodocea serrulata, Halodule uninervis and Thalassia hemprichii were exposed to four different pCO2 treatments (442-1204 µatm) for 2 weeks, approximating the range of end-of-century emission scenarios. Photosynthetic responses were quantified using optode-based oxygen flux measurements. Across all three species, net productivity and energetic surplus (PG:R) significantly increased with a rise in pCO2 (linear models, P < 0.05). Photosynthesis-irradiance curve-derived photosynthetic parameters-maximum photosynthetic rates (P max) and efficiency (alpha) also increased as pCO2 increased (linear models, P < 0.05). The response for productivity measures was similar across species, i.e. similar slopes in linear models. A decrease in compensation light requirement (Ec) with increasing pCO2 was evident in C. serrulata and H. uninervis, but not in T. hemprichii. Despite higher productivity with pCO2 enrichment, leaf growth rates in C. serrulata did not increase, while those in H. uninervis and T. hemprichii significantly increased with increasing pCO2 levels. While seagrasses can be carbon-limited and productivity can respond positively to CO2 enrichment, varying carbon allocation strategies amongst species suggest differential growth response between species. Thus, future increase in seawater CO2 concentration may lead to an overall increase in seagrass biomass and productivity, as well as community changes in seagrass meadows.
Resumo:
The effects of CO2-induced seawater acidification on plankton communities were also addressed in a series of 3 mesocosm experiments, called the Pelagic Ecosystem CO2 Enrichment (PeECE I-III) studies, which were conducted in the Large-Scale Mesocosm Facilities of the University of Bergen, Norway in 2001, 2003 and 2005, respectively. Each experiment consisted of 9 mesocosms, in which CO2 was manipulated to initial concentrations of 190, 350 and 750 µatm in 2001 and 2003, and 350, 700 and 1050 µatm in 2005. The present dataset concerns PeECE II.
Resumo:
In the present uncertain global context of reaching an equal social stability and steady thriving economy, power demand expected to grow and global electricity generation could nearly double from 2005 to 2030. Fossil fuels will remain a significant contribution on this energy mix up to 2050, with an expected part of around 70% of global and ca. 60% of European electricity generation. Coal will remain a key player. Hence, a direct effect on the considered CO2 emissions business-as-usual scenario is expected, forecasting three times the present CO2 concentration values up to 1,200ppm by the end of this century. Kyoto protocol was the first approach to take global responsibility onto CO2 emissions monitoring and cap targets by 2012 with reference to 1990. Some of principal CO2emitters did not ratify the reduction targets. Although USA and China spur are taking its own actions and parallel reduction measures. More efficient combustion processes comprising less fuel consuming, a significant contribution from the electricity generation sector to a CO2 dwindling concentration levels, might not be sufficient. Carbon Capture and Storage (CCS) technologies have started to gain more importance from the beginning of the decade, with research and funds coming out to drive its come in useful. After first researching projects and initial scale testing, three principal capture processes came out available today with first figures showing up to 90% CO2 removal by its standard applications in coal fired power stations. Regarding last part of CO2 reduction chain, two options could be considered worthy, reusing (EOR & EGR) and storage. The study evaluates the state of the CO2 capture technology development, availability and investment cost of the different technologies, with few operation cost analysis possible at the time. Main findings and the abatement potential for coal applications are presented. DOE, NETL, MIT, European universities and research institutions, key technology enterprises and utilities, and key technology suppliers are the main sources of this study. A vision of the technology deployment is presented.
Resumo:
La conciencia de la crisis de la modernidad -que comienza ya a finales del siglo XIX- ha cobrado más experiencia debido al conocimiento de los límites del desarrollo económico, ya que como parecía razonable pensar, también los recursos naturales son finitos. En 1972, el Club de Roma analizó las distintas opciones disponibles para conseguir armonizar el desarrollo sostenible y las limitaciones medioambientales. Fue en 1987 cuando la Comisión Mundial para el Medio Ambiente y el Desarrollo de la ONU definía por primera vez el concepto de desarrollo sostenible. Definición que posteriormente fue incorporada en todos los programas de la ONU y sirvió de eje, por ejemplo, a la Cumbre de la Tierra celebrada en Río de Janeiro en 1992. Parece evidente que satisfacer la demanda energética, fundamentalmente desde la Revolución Industrial en el s XIX, trajo consigo un creciente uso de los combustibles fósiles, con la consiguiente emisión de los gases de efecto invernadero (GEI) y el aumento de la temperatura global media terrestre. Esta temperatura se incrementó en los últimos cien años en una media de 0.74ºC. La mayor parte del incremento observado desde la mitad del siglo XX en esta temperatura media se debe, con una probabilidad de al menos el 90%, al aumento observado en los GEI antropogénicos, siendo uno de ellos el CO2 que proviene de la transformación del carbono de los combustibles fósiles durante su combustión. Ante el creciente uso de los combustibles fósiles, los proyectos CAC, proyectos de captura, transporte y almacenamiento, se presentan como una contribución al desarrollo sostenible ya que se trata de una tecnología que permite mitigar el cambio climático. Para valorar si la tecnología CAC es sostenible, habrá que comprobar si existe o no capacidad para almacenar el CO2 en una cantidad mayor a la de producción y durante el tiempo necesario que impone la evolución de la concentración de CO2 en la atmósfera para mantenerla por debajo de las 450ppmv (concentración de CO2 que propone el Panel Intergubernamental para el Cambio Climático). El desarrollo de los proyectos CAC completos pasa por la necesaria selección de adecuados almacenes de CO2 que sean capaces de soportar los efectos de las presiones de inyección, así como asegurar la capacidad de dichos almacenes y la estanqueidad del CO2 en los mismos. La caracterización geológica de un acuífero susceptible de ser almacén de CO2 debe conducir a determinar las propiedades que dicho almacén posee para asegurar un volumen adecuado de almacenamiento, una inyectabilidad del CO2 en el mismo a un ritmo adecuado y la estanqueidad del CO2 en dicho acuífero a largo plazo. El presente trabajo pretende estudiar los parámetros que tienen influencia en el cálculo de la capacidad del almacén, para lo que en primer lugar se ha desarrollado la tecnología necesaria para llevar a cabo la investigación mediante ensayos de laboratorio. Así, se ha desarrollado una patente, "ATAP, equipo para ensayos petrofísicos (P201231913)", con la que se ha llevado a cabo la parte experimental de este trabajo para la caracterización de los parámetros que tienen influencia en el cálculo de la capacidad del almacén. Una vez desarrollada la tecnología, se aborda el estudio de los distintos parámetros que tienen influencia en la capacidad del almacén realizando ensayos con ATAP. Estos ensayos definen el volumen del almacenamiento, llegándose a la conclusión de que en la determinación de este volumen, juegan un papel importante el alcance de los mecanismos trampa, físicos o químicos, del CO2 en el almacén. Ensayos que definen la capacidad del almacén de "aceptar" o "rechazar" el CO2 inyectado, la inyectabilidad, y por último, ensayos encaminados a determinar posibles fugas que se pueden dar a través de los pozos de inyección, definidos estos como caminos preferenciales de fugas en un almacén subterráneo de CO2. Queda de este modo caracterizada la estanqueidad del CO2 en el acuífero a largo plazo y su influencia obvia en la determinación de la capacidad del almacén. Unido al propósito de la estimación de la capacidad del almacén, se encuentra el propósito de asegurar la estanqueidad de dichos almacenes en el tiempo, y adelantarse a la evolución de la pluma de CO2 en el interior de dichos almacenes. Para cumplir este propósito, se ha desarrollado un modelo dinámico a escala de laboratorio, mediante el programa ECLIPSE 300, con el fin de establecer una metodología para el cálculo de la capacidad estimada del almacén, así como el estudio de la evolución de la pluma de CO2 dentro del acuífero a lo largo del tiempo, partiendo de los resultados obtenidos en los ensayos realizados en ATAP y con la modelización de la probeta de roca almacén empleada en dichos ensayos. Presentamos por tanto un trabajo que establece las bases metodológicas para el estudio de la influencia de distintos parámetros petrofísicos en el cálculo de la capacidad del almacén unidos al desarrollo tecnológico de ATAP y su utilización para la determinación de dichos parámetros aplicables a cada acuífero concreto de estudio. ABSTRACT The crisis of modernity –which begins at the end of 19th Century- has been more important due to the knowledge of the limits of economic development, since it appeared to be thought reasonable, the natural resources are finite. In 1972, The Club of Rome analyzed the different options available in order to harmonize the sustainability and the environment development. It was in 1987 when The Global Commission on The Environment and the Development of UN, defined for the first time the concept of Sustainable Development. This definition that was fully incorporated in all the UN programs and it was useful as an axis, for example, in La Cumbre de la Tierra summit in Río de Janeiro in 1992. It seems obvious to satisfy energetic demand, basically after The Industrial Revolution in 19th Century, which represented an increasing use of fossil fuels, therefore greenhouse gases emission and the increasing of global average temperature. This temperature increased in the last 100 years up to 0.74ºC. The major part of the temperature increase is due to the increase observed in Greenhouse gases with human origin, at least with 90% of probability. The most important gas is the CO2 because of its quantity. In the face of the increasing use of fossil fuels, the CCS projects, Carbon Capture and Storage projects, appear as a contribution of sustainable development since it is a technology for avoiding the climate change. In order to evaluate if CCS technology is sustainable, it will be necessary to prove if the capacity for CO2 storage is available or not in a quantity greater than the production one and during the time necessary to keep the CO2 concentration in the atmosphere lower than 450ppmv (concentration imposed by IPCC). The development of full CCS projects goes through the selection of good CO2 storages that are able to support the effects of pressure injection, and assure the capacity of such storages and the watertightness of CO2. The geological characterization of the aquifer that could be potential CO2 storage should lead to determine the properties that such storage has in order to assure the adequate storage volume, the CO2 injectivity in a good rate, and the watertightness of the CO2 in the long term. The present work aims to study the parameters that have influence on the calculation of storage capacity, and for that purpose the appropriate technology has been developed for carrying out the research by mean of laboratory tests. Thus, a patent has been developed, "ATAP, equipo para ensayos petrofísicos (P201231913)", that has been used for developing the experimental part of this work. Once the technology has been developed, the study of different parameters, that have influence on the capacity of the storage, has been addressed developing different tests in ATAP. These tests define the storage volume which is related to the scope of different CO2 trap mechanisms, physical or chemical, in the storage. Tests that define the capacity of the storage to “accept” or “reject” the injected CO2, the injectivity, and tests led to determine possible leakages through injection wells. In this way we could talk about the watertightness in the aquifer in the long term and its influence on the storage capacity estimation. Together with the purpose of the storage capacity estimation, is the purpose of assuring the watertightness of such storages in the long term and anticipating the evolution of CO2 plume inside such aquifers. In order to fulfill this purpose, a dynamic model has been developed with ECLIPSE 300, for stablishing the methodology for the calculation of storage capacity estimation and the evolution of the CO2 plume, starting out with the tests carried out in ATAP. We present this work that establishes the methodology bases for the study of the influence of different petrophysics parameters in the calculation of the capacity of the storage together with the technological development of ATAP and its utilization for the determination of such parameters applicable to each aquifer.
Resumo:
Net photosynthesis (Pn) is inhibited by moderate heat stress. To elucidate the mechanism of inhibition, we examined the effects of temperature on gas exchange and ribulose 1,5-bisphosphate carboxylase/oxygenase (Rubisco) activation in cotton and tobacco leaves and compared the responses to those of the isolated enzymes. Depending on the CO2 concentration, Pn decreased when temperatures exceeded 35–40°C. This response was inconsistent with the response predicted from the properties of fully activated Rubisco. Rubisco deactivated in leaves when temperature was increased and also in response to high CO2 or low O2. The decrease in Rubisco activation occurred when leaf temperatures exceeded 35°C, whereas the activities of isolated activase and Rubisco were highest at 42°C and >50°C, respectively. In the absence of activase, isolated Rubisco deactivated under catalytic conditions and the rate of deactivation increased with temperature but not with CO2. The ability of activase to maintain or promote Rubisco activation in vitro also decreased with temperature but was not affected by CO2. Increasing the activase/Rubisco ratio reduced Rubisco deactivation at higher temperatures. The results indicate that, as temperature increases, the rate of Rubisco deactivation exceeds the capacity of activase to promote activation. The decrease in Rubisco activation that occurred in leaves at high CO2 was not caused by a faster rate of deactivation, but by reduced activase activity possibly in response to unfavorable ATP/ADP ratios. When adjustments were made for changes in activation state, the kinetic properties of Rubisco predicted the response of Pn at high temperature and CO2.
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It is not certain whether coral reefs are sources of or sinks for atmospheric CO2. Air–sea exchange of CO2 over reefs has been measured directly and inferred from changes in the seawater carbonate equilibrium. Such measurements have provided conflicting results. We provide community metabolic data that indicate that large changes in CO2 concentration can occur in coral reef waters via biogeochemical processes not directly associated with photosynthesis, respiration, calcification, and CaCO3 dissolution. These processes can significantly distort estimates of reef calcification and net productivity and obscure the contribution of coral reefs to global air–sea exchange of CO2. They may, nonetheless, explain apparent anomalies in the metabolic performance of reefs close to land and reconcile the differing experimental findings that have given rise to the CO2 debate.
Resumo:
It has been reported that carbonic anhydrase (CA) activity in plant leaves is decreased by Zn deficiency. We examined the effects of Zn deficiency on the activity of CA and on photosynthesis by leaves in rice plants (Oryza sativa L.). Zn deficiency increased the transfer resistance from the stomatal cavity to the site of CO2 fixation 2.3-fold and, consequently, the value of the transfer resistance relative to the total resistance in the CO2-assimilation process increased from 10% to 21%. This change led to a reduced CO2 concentration at the site of CO2 fixation, resulting in an increased gradient of CO2 between the stomatal cavity and this site. The present findings support the hypothesis that CA functions to facilitate the supply of CO2 from the stomatal cavity to the site of CO2 fixation. We also showed that the level of mRNA for CA decreased to 13% of the control level during Zn deficiency. This decrease resembled the decrease in CA activity, suggesting the possible involvement of the CA mRNA level in the regulation of CA activity.
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The accumulation of soluble carbohydrates resulting from growth under elevated CO2 may potentially signal the repression of gene activity for the small subunit of ribulose-1,5-bisphosphate carboxylase/oxygenase (rbcS). To test this hypothesis we grew rice (Oryza sativa L.) under ambient (350 μL L−1) and high (700 μL L−1) CO2 in outdoor, sunlit, environment-controlled chambers and performed a cross-switching of growth CO2 concentration at the late-vegetative phase. Within 24 h, plants switched to high CO2 showed a 15% and 23% decrease in rbcS mRNA, whereas plants switched to ambient CO2 increased 27% and 11% in expanding and mature leaves, respectively. Ribulose-1,5-bisphosphate carboxylase/oxygenase total activity and protein content 8 d after the switch increased up to 27% and 20%, respectively, in plants switched to ambient CO2, but changed very little in plants switched to high CO2. Plants maintained at high CO2 showed greater carbohydrate pool sizes and lower rbcS transcript levels than plants kept at ambient CO2. However, after switching growth CO2 concentration, there was not a simple correlation between carbohydrate and rbcS transcript levels. We conclude that although carbohydrates may be important in the regulation of rbcS expression, changes in total pool size alone could not predict the rapid changes in expression that we observed.