11 results on '"seawater pH"'
Search Results
2. Two new coastal time-series of seawater carbonate system variables in the NW Mediterranean Sea: rates and mechanisms controlling pH changes.
- Author
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Garcıá-Ibáñez, Maribel I., Guallart, Elisa F., Lucas, Arturo, Pascual, Josep, Gasol, Josep M., Marrasé, Cèlia, Calvo, Eva, and Pelejero, Carles
- Subjects
OCEAN temperature ,SEAWATER ,ATMOSPHERIC carbon dioxide ,OCEAN acidification ,ARTIFICIAL seawater ,CARBON dioxide ,SALINE water conversion - Abstract
In this work, we present, for the first time, the seawater carbonate system measurements of two coastal time-series in the NW Mediterranean Sea, L'Estartit Oceanographic Station (EOS; 42.05°N 3.2542°E) and the Blanes Bay Microbial Observatory (BBMO; 41.665°N 2.805°E). At these two time-series, measurements of total alkalinity (TA), pH, and associated variables, such as dissolved inorganic nutrients, temperature, and salinity, have been performed monthly since 2010 in surface seawater. Seasonality and seasonal amplitude are analogous in both time-series, with seasonality in pH
T in situ (pH at in situ seawater conditions on the total hydrogen ion scale) primarily determined by seasonality in sea surface temperature. The evaluated pHT in situ trends at BBMO (-0.0021 ± 0.0003 yr-1 ) and EOS (-0.0028 ± 0.0005 yr-1 ) agree with those reported for coastal and open ocean surface waters in the Mediterranean Sea and open ocean surface waters of the global ocean, therefore indicating that these time-series are representative of global ocean acidification signals despite being coastal. The decreases in pHT in situ can be attributed to increases in total dissolved inorganic carbon (DIC; 1.5 ± 0.4 µmol kg-1 yr-1 at BBMO and 1.6 ± 0.6 µmolESkg-1 yr-1 at EOS) and sea surface temperature (0.08 ± 0.02℃ yr-1 at BBMOand 0.08 ± 0.04℃ yr-1 at EOS). The increases in carbon dioxide fugacity (fCO2 ; 2.4 ± 0.3 µmol kg-1 yr-1 at BBMO and 2.9 ± 0.6 µmol kg-1 yr-1 at EOS) follow the atmospheric CO2 forcing, thus indicating the observed DIC increase is related to anthropogenic CO2 uptake. The increasing trends in TA (1.2 ± 0.3 µmol kg-1 yr-1 at BBMO and 1.0 ± 0.5 µmol kg-1 yr-1 at EOS) buffered the acidification rates, counteracting 60% and 72% of the pHT in situ decrease caused by increasing DIC at EOS and BBMO, respectively. Once accounted for the neutralizing effect of TA increase, the rapid sea surface warming plays a larger role in the observed pH decreases (43% at EOS and 62% at BBMO) than the DIC increase (36% at EOS and 33% at BBMO). [ABSTRACT FROM AUTHOR]- Published
- 2024
- Full Text
- View/download PDF
3. Two new coastal time-series of seawater carbonate system variables in the NW Mediterranean Sea: rates and mechanisms controlling pH changes
- Author
-
Maribel I. García-Ibáñez, Elisa F. Guallart, Arturo Lucas, Josep Pascual, Josep M. Gasol, Cèlia Marrasé, Eva Calvo, and Carles Pelejero
- Subjects
ocean acidification ,Mediterranean Sea ,time series ,seawater pH ,ocean warming ,Science ,General. Including nature conservation, geographical distribution ,QH1-199.5 - Abstract
In this work, we present, for the first time, the seawater carbonate system measurements of two coastal time-series in the NW Mediterranean Sea, L’Estartit Oceanographic Station (EOS; 42.05°N 3.2542°E) and the Blanes Bay Microbial Observatory (BBMO; 41.665°N 2.805°E). At these two time-series, measurements of total alkalinity (TA), pH, and associated variables, such as dissolved inorganic nutrients, temperature, and salinity, have been performed monthly since 2010 in surface seawater. Seasonality and seasonal amplitude are analogous in both time-series, with seasonality in pHTin situ(pH at in situ seawater conditions on the total hydrogen ion scale) primarily determined by seasonality in sea surface temperature. The evaluated pHTin situtrends at BBMO (-0.0021 ± 0.0003 yr-1) and EOS (-0.0028 ± 0.0005 yr-1) agree with those reported for coastal and open ocean surface waters in the Mediterranean Sea and open ocean surface waters of the global ocean, therefore indicating that these time-series are representative of global ocean acidification signals despite being coastal. The decreases in pHTin situcan be attributed to increases in total dissolved inorganic carbon (DIC; 1.5 ± 0.4 µmol kg-1 yr-1 at BBMO and 1.6 ± 0.6 µmolESkg-1 yr-1 at EOS) and sea surface temperature (0.08 ± 0.02 °C yr-1 at BBMO and 0.08 ± 0.04 °C yr-1 at EOS). The increases in carbon dioxide fugacity (fCO2; 2.4 ± 0.3 µmol kg-1 yr-1 at BBMO and 2.9 ± 0.6 µmol kg-1 yr-1 at EOS) follow the atmospheric CO2 forcing, thus indicating the observed DIC increase is related to anthropogenic CO2 uptake. The increasing trends in TA (1.2 ± 0.3 µmol kg-1 yr-1 at BBMO and 1.0 ± 0.5 µmol kg-1 yr-1 at EOS) buffered the acidification rates, counteracting 60% and 72% of the pHTin situdecrease caused by increasing DIC at EOS and BBMO, respectively. Once accounted for the neutralizing effect of TA increase, the rapid sea surface warming plays a larger role in the observed pH decreases (43% at EOS and 62% at BBMO) than the DIC increase (36% at EOS and 33% at BBMO).
- Published
- 2024
- Full Text
- View/download PDF
4. Processes Controlling the Carbonate Chemistry of Surface Seawater Along the 150°E Transect in the Northwest Pacific Ocean.
- Author
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Mou, Liang, Zhang, Honghai, Chen, Zhaohui, and Hu, Yubin
- Abstract
The problem of ocean acidification caused by the increase of atmospheric carbon dioxide concentration is becoming increasingly prominent. Field observation in the northwest Pacific Ocean was carried out along the 150°E transect in November 2019. The distribution characteristics and influencing factors of the surface seawater carbonate chemistry, including dissolved inorganic carbon (DIC), total alkalinity (TA), pH, partial pressure of carbon dioxide (pCO
2 ) and aragonite saturation state (Ωarag ) were investigated. DIC and TA ranged from 1915 to 2014 µmol kg−1 and 2243 to 2291 µmol kg−1 , respectively; DIC in general decreased with decreasing latitude, but TA had no clear latitudinal gradient. pCO2 values increased with the decrease of latitude and were all below the atmospheric pCO2 level, ranging from 332 to 387 µatm. pH on the total hydrogen ion concentration scale (pHT ) decreased with the decrease of latitude in the range of 8.044–8.110, while Ωarag increased with the decrease of latitude in the range of 2.61–3.88, suggesting that the spatial distributions of pHT and Ωarag were out of phase. Compared with the present, the predicted values of pHT and Ωarag by the end of this century would decrease remarkedly; larger declines were found in the higher pHT and Ωarag regions, resulting in the differences along the meridional gradient becoming smaller for both pHT and Ωarag . [ABSTRACT FROM AUTHOR]- Published
- 2022
- Full Text
- View/download PDF
5. Photosynthetic performance of the red algae Gracilariopsis lemaneiformis under high seawater pH: Excess reactive oxygen production due to carbon limitation.
- Author
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Xu H, Pang T, Zhang L, and Liu J
- Subjects
- Hydrogen-Ion Concentration, Malondialdehyde metabolism, Hydrogen Peroxide metabolism, Lipid Peroxidation, Electron Transport, Photosynthesis, Seawater, Rhodophyta metabolism, Rhodophyta physiology, Reactive Oxygen Species metabolism, Carbon metabolism
- Abstract
The red algae Gracilariopsis lemaneiformis is extensively cultivated at high densities, leading to significant increases in regional seawater pH due to its photosynthetic removal of inorganic carbon. We conducted a study on G. lemaneiformis cultured under various pH conditions (normal pH, pH 9.3, and pH 9.6) and light levels (dark and 100 μmol photons m
-2 s-1 ) to investigate how high pH seawater environments affect the metabolic processes of G. lemaneiformis. The high pH did not directly damage the photosynthetic light reactions or the Calvin cycle. Instead, the observed reduction in photosynthetic rates was primarily due to CO2 limitation. However, under illuminated conditions, a high pH environment leads to a decrease in electron transport efficiency (ETo/RC) and reaction center density (RC/CSo), while simultaneously increasing the levels of hydrogen peroxide (H2 O2 ), malondialdehyde (MDA), and the activity of antioxidant enzymes. Under illuminated conditions, the limitation of inhibit the photosynthetic electron transport process, leading to energy imbalance and excessive production of reactive oxygen species, which in turn resulted in lipid peroxidation of the cell membrane. This might be one of the inducing factors responsible for the bleaching in sea-farmed G. lemaneiformis plants., (© 2024 American Society for Photobiology.)- Published
- 2025
- Full Text
- View/download PDF
6. Decreases in pH from effluent had a devastating but reversible impact on the coastal plankton communities.
- Author
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Lin YJ, Chen TC, Chen CA, Wong SL, Meng PJ, and Chen MH
- Abstract
An event of releasing untreated effluent caused serious decreases in surface seawater pH from 8.1 to lower than 7.5 in seven years and increased back to prior levels after 15 years. It gives us a rare natural experiment to examine the impacts of decreases in pH on the marine plankton communities (phytoplanktons, zooplanktons, shrimp larvae, crab larvae, fish eggs, and larvae) in the natural environment. Observed decreases in pH had a nonlinear effect ubiquitous on all plankton groups, leading to a reduction of approximately 50 % in their density and abundance compared to the level at pH 8.1. Non-linear responses of planktons implied the existence of specific groups more robust to decreases in pH. As pH bounced back to normal levels, the density and abundance of the plankton communities also recovered, further indicating that the negative impacts of decreases in pH on the marine plankton communities were reversible., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024. Published by Elsevier Ltd.)
- Published
- 2024
- Full Text
- View/download PDF
7. Two new coastal time-series of seawater carbonate system variables in the NW Mediterranean Sea: rates and mechanisms controlling pH changes
- Author
-
European Commission, Ministerio de Transición Ecológica (España), Ministerio de Ciencia e Innovación (España), Agencia Estatal de Investigación (España), Generalitat de Catalunya, García-Ibáñez, Maribel I., Fernández-Guallart, Elisa, Lucas Forcadell, Arturo, Pascual, Josep, Gasol, Josep M., Marrasé, Cèlia, Calvo, Eva María, Pelejero, Carles, European Commission, Ministerio de Transición Ecológica (España), Ministerio de Ciencia e Innovación (España), Agencia Estatal de Investigación (España), Generalitat de Catalunya, García-Ibáñez, Maribel I., Fernández-Guallart, Elisa, Lucas Forcadell, Arturo, Pascual, Josep, Gasol, Josep M., Marrasé, Cèlia, Calvo, Eva María, and Pelejero, Carles
- Abstract
In this work, we present, for the first time, the seawater carbonate system measurements of two coastal time-series in the NW Mediterranean Sea, L’Estartit Oceanographic Station (EOS; 42.05°N 3.2542°E) and the Blanes Bay Microbial Observatory (BBMO; 41.665°N 2.805°E). At these two time-series, measurements of total alkalinity (TA), pH, and associated variables, such as dissolved inorganic nutrients, temperature, and salinity, have been performed monthly since 2010 in surface seawater. Seasonality and seasonal amplitude are analogous in both time-series, with seasonality in pHT in situ(pH at in situ seawater conditions on the total hydrogen ion scale) primarily determined by seasonality in sea surface temperature. The evaluated pHT in situtrends at BBMO (-0.0021 ± 0.0003 yr-1) and EOS (-0.0028 ± 0.0005 yr-1) agree with those reported for coastal and open ocean surface waters in the Mediterranean Sea and open ocean surface waters of the global ocean, therefore indicating that these time-series are representative of global ocean acidification signals despite being coastal. The decreases in pHT in situcan be attributed to increases in total dissolved inorganic carbon (DIC; 1.5 ± 0.4 µmol kg-1 yr-1 at BBMO and 1.6 ± 0.6 µmolESkg-1 yr-1 at EOS) and sea surface temperature (0.08 ± 0.02 °C yr-1 at BBMO and 0.08 ± 0.04 °C yr-1 at EOS). The increases in carbon dioxide fugacity (fCO2; 2.4 ± 0.3 µmol kg-1 yr-1 at BBMO and 2.9 ± 0.6 µmol kg-1 yr-1 at EOS) follow the atmospheric CO2 forcing, thus indicating the observed DIC increase is related to anthropogenic CO2 uptake. The increasing trends in TA (1.2 ± 0.3 µmol kg-1 yr-1 at BBMO and 1.0 ± 0.5 µmol kg-1 yr-1 at EOS) buffered the acidification rates, counteracting 60% and 72% of the pHT in situdecrease caused by increasing DIC at EOS and BBMO, respectively. Once accounted for the neutralizing effect of TA increase, the rapid sea surface warming plays a larger role in the observed pH decreases (43% at EOS and 62% at BBMO) than t
- Published
- 2024
8. Is the relative thickness of ammonoid septa influenced by ocean acidification, phylogenetic relationships and palaeogeographic position?
- Author
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Weber, Céline, Hautmann, Michael, Tajika, Amane, and Klug, Christian
- Published
- 2022
- Full Text
- View/download PDF
9. Detection of impurities in m-cresol purple with Soft Independent Modeling of Class Analogy for the quality control of spectrophotometric pH measurements in seawater.
- Author
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Fong, Michael B., Takeshita, Yuichiro, Easley, Regina A., and Waters, Jason F.
- Subjects
- *
ARTIFICIAL seawater , *QUALITY control , *SEAWATER , *HIGH performance liquid chromatography , *SEAWATER salinity , *MARINE west coast climate - Abstract
Accurate spectrophotometric pH measurements in seawater are critical to documenting long-term changes in ocean acidity and carbon chemistry, and for calibration of autonomous pH sensors. The recent development of purified indicator dyes greatly improved the accuracy of spectrophotometric pH measurements by removing interfering impurities that cause biases in pH that can grow over the seawater pH range to > 0.01 above pH 8. However, some batches of purified indicators still contain significant residual impurities that lead to unacceptably large biases in pH for oceanic and estuarine climate quality measurements. While high-performance liquid chromatography (HPLC) is the standard method for verifying dye purity, alternative approaches that are simple to implement and require less specialized equipment are desirable. We developed a model to detect impurities in the pH indicator m- cresol purple (m CP) using a variant of the classification technique Soft Independent Modeling of Class Analogy (SIMCA). The classification model was trained with pure m CP spectra (350 nm to 750 nm at 1 nm resolution) at pH 12 and tested on independent samples of unpurified and purified m CP with varying levels of impurities (determined by HPLC) and measured on two different spectrophotometers. All the dyes identified as pure by the SIMCA model were sufficiently low in residual impurities that their apparent biases in pH were < 0.002 in buffered artificial seawater solutions at a salinity of 35 and over a pH range of 7.2 to 8.2. Other methods that can also detect residual impurities relevant to climate quality measurements include estimating the impurity absorption at 434 nm and assessing the apparent pH biases relative to a reference purified dye in buffered solutions or natural seawater. Laboratories that produce and distribute purified m CP should apply the SIMCA method or other suitable methods to verify that residual impurities do not significantly bias pH measurements. To apply the SIMCA method, users should download the data and model developed in this work and measure a small number of instrument standardization and model validation samples. This method represents a key step in the development of a measurement quality framework necessary to attain the uncertainty goals articulated by the Global Ocean Acidification Observing Network (GOA-ON) for climate quality measurements (i.e., ±0.003 in pH). • We developed a chemometric model to detect impurities in a pH indicator dye. • The model was developed for m -cresol purple, a widely used dye for seawater pH. • The model can verify a dye is pure enough for "climate quality" pH measurements. • Other spectrophotometric methods can also be used to assess dye purity. [ABSTRACT FROM AUTHOR]
- Published
- 2024
- Full Text
- View/download PDF
10. Upwelling as a stressor event during embryonic development: Consequences for encapsulated and early juvenile stages of the marine gastropod Acanthina monodon.
- Author
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Paredes-Molina, F.J., Chaparro, O.R., Navarro, J.M., Cubillos, V.M., Paschke, K., Márquez, F., Averbuj, A., Zabala, M.S., Bökenhans, V., and Pechenik, J.A.
- Subjects
- *
EMBRYOLOGY , *GASTROPODA , *GEOMETRIC analysis , *INDIVIDUAL development , *MARINE organisms , *SEASHELLS , *HATCHABILITY of eggs - Abstract
Upwelling phenomena alter the physical and chemical parameters of the sea's subsurface waters, producing low levels of temperature, pH and dissolved oxygen, which can seriously impact the early developmental stages of marine organisms. To understand how upwelling can affect the encapsulated development of the gastropod Acanthina monodon, capsules containing embryos at different stages of development (initial, intermediate and advanced) were exposed to upwelling conditions (pH = 7.6; O 2 = 3 mg L−1; T° = 9 °C) for a period of 7 days. Effects of treatment were determined by estimating parameters such as time to hatching, number of hatchlings per capsule, percentage of individuals with incomplete development, and shell parameters such as shell shape and size, shell strength, and the percentage of the organic/inorganic content. We found no significant impacts on hatching time, number of hatchlings per capsule, or percentage of incomplete development in either the presence or absence of upwelling, regardless of developmental stage. On the other hand, latent effects on encapsulated stages of A. monodon were detected in embryos that had been exposed to upwelling stress in the initial embryonic stage. The juveniles from this treatment hatched at smaller sizes and with higher organic content in their shells, resulting in a higher resistance to cracking 30 days after hatching, due to greater elasticity. Geometric morphometric analysis showed that exposure to upwelling condition induced a change in the morphology of shell growth in all post-hatching juveniles (0–30 days), regardless of embryonic developmental stage at the time of exposure. Thus, more elongated shells (siphonal canal and posterior region) and more globular shells were observed in newly hatched juveniles that had been exposed to the upwelling condition. The neutral or even positive upwelling exposure results suggests that exposure to upwelling events during the encapsulated embryonic phase of A. monodon development might not have major impacts on the future juvenile stages. However, this should be taken with caution in consideration of the increased frequency and intensity of upwelling events predicted for the coming decades. • More advanced embryos exposed to upwelling conditions delayed the time to hatching. • Juveniles that hatched at smaller sizes were more resistant to cracking. • Exposure of encapsulated embryos to upwelling conditions altered the juvenile morphology. • Latent effects were found mainly when embryos were exposed to upwelling stress during initial stages of development. [ABSTRACT FROM AUTHOR]
- Published
- 2024
- Full Text
- View/download PDF
11. Warmer and more acidic conditions enhance performance of an endemic low-shore gastropod.
- Author
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Martin N, Robinson TB, and Clusella-Trullas S
- Subjects
- Animals, Hydrogen-Ion Concentration, Temperature, Acclimatization physiology, Seawater chemistry, Gastropoda
- Abstract
Changing ocean temperatures are predicted to challenge marine organisms, especially when combined with other factors, such as ocean acidification. Acclimation, as a form of phenotypic plasticity, can moderate the consequences of changing environments for biota. Our understanding of how altered temperature and acidification together influence species' acclimation responses is, however, limited compared with that of responses to single stressors. This study investigated how temperature and acidification affect the thermal tolerance and righting speed of the girdled dogwhelk, Trochia cingulata. Whelks were acclimated for 2 weeks to combinations of three temperatures (11°C: cold, 13°C: moderate and 15°C: warm) and two pH regimes (8.0: moderate and 7.5: acidic). We measured the temperature sensitivity of the righting response by generating thermal performance curves from individual data collected at seven test temperatures and determined critical thermal minima (CTmin) and maxima (CTmax). We found that T. cingulata has a broad basal thermal tolerance range (∼38°C) and after acclimation to the warm temperature regime, both the optimal temperature for maximum righting speed and CTmax increased. Contrary to predictions, acidification did not narrow this population's thermal tolerance but increased CTmax. These plastic responses are likely driven by the predictable exposure to temperature extremes measured in the field which originate from the local tidal cycle and the periodic acidification associated with ocean upwelling in the region. This acclimation ability suggests that T. cingulata has at least some capacity to buffer the thermal changes and increased acidification predicted to occur with climate change., Competing Interests: Competing interests The authors declare no competing or financial interests., (© 2023. Published by The Company of Biologists Ltd.)
- Published
- 2023
- Full Text
- View/download PDF
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