Ocean uptake of anthropogenic CO2 causes ocean acidification, a secular, global-scale decline in the pH of seawater. In order to better understand the implications of contemporary acidification for marine organisms and ecosystems, there is a need to better characterise natural variability in carbonate chemistry. In this thesis, climatological seasonal variability of sea surface pH and aragonite saturation state (OmegaA) in the open ocean is indirectly derived from other parameters of the marine CO2 system, namely total alkalinity (TA) and seawater pCO2/fCO2 (pCO2sw/fCO2sw). New monthly sea surface TA, fCO2sw and temperature climatologies are developed for this purpose, utilising newly-released observational synthesis products (PACIFICA for TA and SOCAT v2 for fCO2sw). Two versions of the new SST climatology are developed, referred to as upper and lower SST (USST and LSST), to test sensitivity to the depth range of the input observations. Annual ranges are generally found to be larger for the USST climatology, derived using observations from the upper 2 m, compared to LSST (which is based on deeper observations). Further, a seasonal cycle is found in the monthly average of the differences between these climatologies north of 30 degN, perhaps partly due to seasonal variation in near-surface stratification. The USST seasonal ranges are also found to be generally larger than in two previous SST climatologies, however, difference in the depth distribution of the input measurements is unlikely the main cause. The new monthly sea surface TA climatology extends coverage into the Nordic seas, excluded from previous climatologies. TA seasonality is found to be small outside of regions with large seasonal ranges in salinity. Large seasonal ranges in salinity and TA are found beneath the Intertropical Convergence Zone, in the Antarctic seasonal sea ice zone and in the western Greenland Sea. Non-salinity driven TA seasonality is found to be large in the Gulf of Alaska, eastern equatorial Pacific and western Greenland Sea. Compared to the Lee et al. (2006) TA climatology, substantially lower annual means and seasonal ranges are found for the subarctic Pacific, a region with greatly improved coverage courtesy of PACIFICA. The pH/OmegaA climatologies derived in the final chapter suggest pH seasonality is predominantly temperature driven in the subtropics and mainly driven by variation in salinity normalised dissolved inorganic carbon (sDIC) in the subpolar north Atlantic, western subarctic Pacific and Southern Ocean. Salinity variation is found to only exert a strong influence on pH seasonality in the western Greenland Sea. Climatological seasonal pH ranges are found to be mostly small in the tropics (<0.05), moderate in the subtropics (0.05-0.10) but very large (>0.1) in parts of the Ross, Weddell, Irminger and Iceland Seas and western subarctic Pacific gyre. OmegaA seasonality is found to be predominantly sDIC-driven everywhere except in the western Greenland Sea, with temperature variation generally being of modest influence. Seasonal cycles of pH and OmegaA are found to be in anti-phase where pH is mainly thermally driven and in-phase where pH is mainly sDIC-forced (both pH and OmegaA vary inversely with DIC). Comparison is made between the primary new pH/OmegaA climatology and various open ocean carbonate chemistry time-series. The climatology captures the general form of the climatological seasonal cycles of pH and OmegaA from the time-series, although with some differences in phasing and seasonal range. Analysing the time-series for long-term trends, I find that inter-decadal anthropogenic CO2 uptake driven pH and OmegaA declines can be modulated by trends in temperature, salinity or sTA. Investigation is also conducted into how the amplitude of pH and OmegaA seasonal cycles might change by 2100 for a subpolar and subtropical time-series. Under a high CO2 emissions scenario, the seasonal range of pH is found to be strongly enhanced for the subpolar time-series and moderately reduced for the subtropical time-series, with both being due to changes in seawater buffer capacity. / Graduate / 0425 / 0415 / robdj87@hotmail.com

The presence of annual density banding in certain long-lived reef-building corals provides a record of the coral’s growth rate over time in response to changing environmental conditions. Coral growth is best described by three parameters: linear extension, bulk density, and calcification. Coral growth is generally controlled by the combined influences of light, temperature, and water quality; however, corals are highly responsive to their surrounding conditions and thus record environmental variations through their rates and patterns of skeletal accretion. Because coral growth rates reflect environmental conditions over time, they allow testing of hypotheses regarding the effects of climate change, more specifically global warming which affects sea surface temperatures and rising atmospheric carbon dioxide which affect the aragonite saturation state of seawater. Influences on coral growth include local changes in sea surface temperature and rainfall as well as large scale climatic indices such as the Atlantic Multidecadal Oscillation (AMO), the North Atlantic Oscillation (NAO), and the Southern Oscillation Index (SOI). Chapter 1, Background, reviews the current state of knowledge in three primary areas: 1) coral biology, growth, density band formation, and measurement of extension, density, and calcification, 2) potential climate change impacts on coral growth, and 3) long-term coral growth records. This section is broadly intended to review the literature, identify possible information gaps, and recognize current debate within coral and climate change research. Chapter 2, Sample Size for Coral Sclerochronology, presents data of sample size correlations based on statistical analyses of annual extension rates. A standardized period (1970-1985) of annual extension rates from the largest number of Montastraea faveolata samples available from southeast Florida (136 corals) was used to test correlation on varying spatial scales and to determine sample size requirements for desired levels of correlation based on objective criteria. The results provide basic information on masterchronology construction for sclerochronological growth rate studies and provide a framework from which further growth rate variability can be assessed. Extension and bulk density can be measured from X-ray films of coral skeletal slabs and can be used to calculate calcification. Chapter 3, Relative Optical Densitometry, describes the techniques and associated errors through the process of coral coring, sectioning, X-raying, developing, digitizing, calibrating and analyzing. The principles of relative optical densitometry and the calculation of mass absorption coefficient ratios for aragonite and aluminum standards are explained. Calculated and measured errors are quantified to define the accuracy and precision of these techniques necessary to detect potentially subtle changes in coral growth caused by climate change. Coral cores from the Florida Key, USA, were used to construct growth records over a 60-yr period from 1973-1996. Chapter 4, Coral Growth Records and Climate Change, uses linear extension rate, bulk-density, and calcification rate from annual and sub-annual bands in order to assess: 1) growth averages, variability, and relationships between growth parameters, 2) long term trends with respect to rising carbon dioxide levels and sea surface temperature, 3) correlation with local environmental variables of temperature and rainfall, and 4) correlation with major climate indices of Atlantic Multidecadal Oscillation, North Atlantic Oscillation, and the Southern Oscillation.

Bacterioplankton are keystone organisms in marine ecosystems. They are important for element cycles, by transforming dissolved organic carbon and other nutrients. Bacterioplankton community composition and productivity rates change in surface waters over spatial and temporal scales. Yet, many underlying biological processes determining when, why and how bacterioplankton react to changes in environmental conditions are poorly understood. Here, I used experiments with model bacteria and natural assemblages as well as field studies to determine molecular, physiological and ecological responses allowing marine bacteria to adapt to their environment. Experiments with the flavobacterium Dokdonia sp. MED134 aimed to determine how the metabolism of bacteria is influenced by light and different organic matter. Under light exposure, Dokdonia sp. MED134 expressed proteorhodopsin and adjusted its metabolism to use resources more efficiently when growing with lower-quality organic matter. Similar expression patterns were found in oceanic datasets, implying a global importance of photoheterotrophic metabolisms for the ecology of bacterioplankton. Further, I investigated how the composition and physiology of bacterial assemblages are affected by elevated CO2 concentrations and inorganic nutrients. In a large-scale experiment, bacterioplankton could keep productivity and community structure unaltered by adapting the gene expression under CO2 stress. To maintain pH homeostasis, bacteria induced higher expression of genes related to respiration, membrane transport and light acquisition under low-nutrient conditions. Under high-nutrient conditions with phytoplankton blooms, such regulatory mechanisms were not necessary. These findings indicate that open ocean systems are more vulnerable to ocean acidification than coastal waters. Lastly, I used field studies to resolve how bacterioplankton is influenced by environmental changes, and how this leads to seasonal succession of marine bacteria. Using high frequency sampling over three years, we uncovered notable variability both between and within years in several biological features that rapidly changed over short time scales. These included potential phytoplankton-bacteria linkages, substrate uptake rates, and shifts in bacterial community structure. Thus, high resolution time series can provide important insights into the mechanisms controlling microbial communities. Overall, this thesis highlights the advantages of combining molecular and traditional oceanographic methodological approaches to study ecosystems at high resolution for improving our understanding of the physiology and ecology of microbial communities and, ultimately, how they influence biogeochemical processes.

A acidificação oceânica, resultante do aumento da concentração de CO2 atmosférico, vem alterando a química dos oceanos resultando na diminuição de seu pH. Diversos estudos avaliaram as consequências dessa diminuição no pH oceânico nas taxas de calcificação, reprodução e desenvolvimento em diversos modelos marinhos, entretanto estudos relacionados a outros processos fisiológicos, como a imunidade, e estudos com indivíduos adultos são escassos. Ouriços-do-mar são espécies aderidas ao substrato, importantes para a ciclagem de nutrientes no ambiente marinho, sendo também animais utilizados como bioindicadores para monitoramento ambiental; assim o estudo da resposta imune inata desses animais frente à acidificação dos oceanos é de extrema importância para prever possíveis alterações fisiológicas desses animais e sua capacidade de adaptação. O presente trabalho teve como objetivo avaliar as alterações provocadas pela acidificação oceânica na resposta imune e no balanço ácido base de duas espécies de ouriço-do-mar tropicais: Lytechinus variegatus e Echinometra lucunter durante as estações de verão e inverno; para isso foram analisados os índices fagocíticos, a capacidade de adesão e espraiamento celular dos amebócitos fagociticos além do balanço acido base do liquido celomático após o período de 24 horas e cinco dias de exposição aos pHs 7,6 e 7,3. Foi também avaliada a capacidade de recuperação dessas espécies com o objetivo de verificar se os parâmetros alterados pela exposição conseguiam ser reestabelecidos. Os resultados mostraram que a redução no pH da água do mar alterou a proporção celular, reduziu a capacidade de fagocitose e espraiamento dos amebócitos fagocíticos assim como também afetou o balanço ácido-base do líquido celomático. Foram encontradas diferenças também entre as estações do ano sendo estas encontradas apenas na espécie Lytechinus variegatus. O teste de recuperação mostrou que os parâmetros alterados pela exposição tendem a retornar aos valores controles, mostrando que em curto prazo essas alterações podem não ser irreversíveis, entretanto, mais estudos são necessários principalmente avaliando períodos de exposição prolongados. Juntos nossos resultados mostram que a acidificação oceânica prejudica parâmetros imunes extremamente importantes para a eliminação de patógenos e consequentemente a sobrevivência desses animais em um futuro oceano acidificado. / Ocean acidification due to increased atmospheric CO2 concentration is altering ocean chemistry resulting in the decrease of its pH. Several studies evaluated the effects of this decrease in ocean pH on calcification rates, reproduction and development in different marine models, however studies related to other physiological processes such as immunity and studies with adult animals are scarce. Sea urchins are species adhered to the substrate, important for nutrient cycling in the marine environment, also being used as bioindicators for environmental monitoring. Thus the study of the innate immune response of these animals due to the acidification of the oceans is extremely important to predict possible physiological changes of these animals and their ability to adapt to this condition. This study aimed to evaluate the changes caused by ocean acidification in the immune response and in the acid-base balance of two sea urchin tropical species: Lytechinus variegatus and Echinometra lucunter during seasons of summer and winter; for this, indexes of phagocytosis, cell adhesion and spreading ability were analyzed in addition to the acid-base balance of the coelomic fluid after 24 hours and five days of exposure to pH 7.6 and 7.3The recover ability of these species were also evaluated in order to verify if the parameters altered by exposition could be reestablished. The results shows that a reduction in the seawater pH changed the cell proportion, reduced the ability of phagocytosis and phagocytic amoebocyte spreading as well as affected the acid-base balance of the coelomic fluid. Differences were also found between seasons, but only in the specie Lytechinus variegatus. The recovery test showed that the parameters altered by exposure tend to return to control values, showing that in the short term these changes may not be irreversible, however, further studies are necessary mainly those related to prolonged periods of exposure. Together our results show that ocean acidification impairs immune parameters extremely important for the elimination of pathogens and consequently the survival of these animals in a future acidified ocean.

L’océan côtier occupe une position clé dans le cycle du carbone et est exposé à l’acidification des océans. Une grande partie de matière organique(MO) marine et continentale est minéralisée dans les sédiments estuariens par des voies aérobies ou anaérobies. Cette minéralisation produit du carbone inorganique dissous (DIC), mais aussi de l’alcalinité totale(TA) pour la partie anoxique, ce qui tamponne les variations de pH du système et augmente la capacitéde l’eau de mer à absorber du CO2. Des mesures dans les sédiments du prodelta du Rhône ont montré que la minéralisation anoxique, surtout la sulfato-réduction, y est dominante et produit des forts flux de TA et de DIC. Proche de l’embouchure, c’est surtout la MO continentale qui est minéralisée et la fraction marine augmente vers le large. Une expérience d’acidification des sédiments de la baie de Villefranche-sur-mer a montré que l’acidification des océans cause la dissolution des carbonates ce qui tamponne le pH dans les sédiments. / Continental shelves are key regions for theglobal carbon cycle and particularly exposed to oceanacidification. A large part of organic matter (OM) ofcontinental and marine origin is mineralized in estuarinesediments following oxic and anoxic pathways.This mineralization produces dissolved inorganic carbon(DIC) leading to acidification of the bottom waters.Anoxic mineralization can produce total alkalinity(TA) that can contribute to buffer bottom water pHand increase the CO2 storage capacity of seawater. Measurementsin the sediments of the Rhˆone River prodeltashowed that anoxic mineralization, especially sulfate reduction,are the major pathways of OM mineralizationand create high DIC and TA fluxes. Land derived OMis mineralized close to the river mouth and marine OMtakes over on the shelf. An acidification experiment withsediment cores from the bay of Villefranche evidencedthat acidification causes carbonate dissolution at thesediment surface that buffers porewater pH.

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Human activities have contributed to the increase in atmospheric greenhouse gases such as carbon dioxide (CO2). This anthropogenic gas emission has led to a rise in the average Earth temperature. Moreover, the ocean constitutes the major sink for anthropogenic CO2 and its dissolution in surface waters has already resulted in an increase of seawater acidity since the beginning of the industrial revolution. This is commonly called ocean acidification. The increase in water temperature could induce modifications of the physical and chemical characteristics of the ocean. Also, the structure and the functioning of marine ecosystems may be altered as a result of ocean acidification. <p>Phytoplankton productivity is one of the primary controls in regulating our climate, for instance via impact on atmospheric CO2 levels. Coccolithophores, of which Emiliania huxleyi is the most abundant species, are considered to be the most important pelagic calcifying organisms on Earth. Coccolithophores are characterized by calcium carbonate platelets (coccoliths) covering the exterior of the cells. They form massive blooms in temperate and sub-polar oceans and in particular along continental margin and in shelf seas. The intrinsic coupling of organic matter production and calcification in coccolithophores underlines their biogeochemical importance in the marine carbon cycle. Both processes are susceptible to change with ocean acidification and warming. Coccolithophores are further known to produce transparent exopolymer particles (TEP) that promote particle aggregation and related processes such as marine snow formation and sinking. Thus, the impact of ocean warming and acidification on coccolithophores needs to be studied and this can be carried out through a transdisciplinary approach.<p>The first part of this thesis consisted of laboratory experiments on E. huxleyi under controlled conditions. The aim was to estimate the effect of increasing water temperature and acidity on E. huxleyi and especially on the calcification. Cultures were conducted at different partial pressures of CO2 (pCO2); the values considered were 180, 380 and 750 ppm corresponding to past, present and future (year 2100) atmospheric pCO2. These experiments were conducted at 13°C and 18°C. The cellular calcite concentration decreases with increasing pCO2. In addition, it decreases by 34 % at 380 ppm and by 7 % at 750 ppm with an increase in temperature of 5°C. Changes in calcite production at future pCO2 values are reflected in deteriorated coccolith morphology, while temperature does not affect coccolith morphology. Our findings suggest that the sole future increase of pCO2 may have a larger negative impact on calcification than its interacting effect with temperature or the increase in temperature alone. The evolution of culture experiments allows a better comprehension of the development of a bloom in natural environments. Indeed, in order to predict the future evolution of calcifying organisms, it is required to better understand the present-day biogeochemistry and ecology of pelagic calcifying communities under field conditions.<p>The second part of this dissertation was dedicated to results obtained during field investigations in the northern Bay of Biscay, where frequent and recurrent coccolithophorid blooms were observed. Cruises, assisted by remote sensing, were carried out along the continental margin in 2006 (29 May – 10 June), 2007 (7 May – 24 May) and 2008 (5 May – 23 May). Relevant biogeochemical parameters were measured in the water column (temperature, salinity, dissolved oxygen, Chlorophyll-a and nutrient concentrations) in order to determine the status of the bloom at the time of the different campaigns. Calcification has been shown to be extremely important in the study area. In addition, TEP production was significant at some stations, suggesting that the northern Bay of Biscay could constitute an area of important carbon export. Mortality factors for coccolithophores were studied and the first results of lysis rates measured in this region were presented. <p>Results obtained during culture experiments and comparison with data reported in the literature help to better understand and to predict the future of coccolithophores in a context of climate change. Data obtained during either culture experiments or field investigations allowed a better understanding of the TEP dynamics. Finally, the high lysis rates obtained demonstrate the importance of this process in bloom decline. Nevertheless, it is clear that we only begin to understand the effects of global change on marine biogeochemistry, carbon cycling and potential feedbacks on increasing atmospheric CO2. Thus, further research with a combination of laboratory experiments, field measurements and modelling are encouraged.<p><p> / Doctorat en Sciences / info:eu-repo/semantics/nonPublished

L’acidification des océans provoquée par l’absorption du CO2 atmosphérique par l’eau de merest devenue une préoccupation écologique majeure et menace déjà les organismes calcifiants. Suiteà la révolution industrielle, le pH de l’océan de surface a diminué de 0,1 unité-pH. En revanche, celuides eaux profondes reste peu documenté. Les isotopes du bore (11B) dans les carbonatesbiogéniques se sont révélés être un puissant outil géochimique pour la reconstitution du pH, mais n’apas encore été appliqué aux coraux profonds. Un travail analytique sur MC-ICPMS Neptune et uneanalyse géochimique de ces coraux ont été effectués afin de reconstituer et quantifier l’acidificationdes océans. De même, la valeur 11B de l’eau de mer utilisée pour calculer les paléo-pH a étérevisitée et l’homogénéité des océans vérifiée.L’analyse de deux colonies modernes de Lophelia pertusa et Madrepora oculata a permis dequantifier un taux d’acidification pendant la fin du XXème siècle pour les eaux de sub-surface en mer deNorvège et cela après établissement d’une calibration expérimentale à partir de coraux de culture.L’analyse géochimique des coraux profonds a mis en évidence un effet vital lié à la physiologie quidoit être considéré pour quantifier avec précision la variabilité du pH. Celui-ci peut être en partiecorrigé par une analyse statistique des isotopes stables B, C et O. Cette étude a aussi révélél’influence de l’hydrodynamique régionale. Enfin les variations naturelles du pH pendant l’Holocène etle Dernier Maximum Glaciaire sur des coraux profonds fossiles méditerranéens ont été établies etcelles pendant l’aube de l’explosion de la diversité biologique. / Ocean acidification is caused by the absorption of rising atmospheric CO2 by seawater andrepresents a major environmental issue. Since the beginning of the industrial era, seawater pH hasdecreased by 0.1 pH units and is already threatening calcifying organisms. Boron isotopes (11B) haveproved to be a powerful geochemical tool for the reconstruction of pH variations, but has not yet beenapplied to deep-sea corals (DSC). Accurate and precise measurements of boron isotopes in coralsand seawaters were performed in order to measure small pH variations.The technique of pH reconstruction based on boron isotopes (pH-11B) was used on two specimens of the DSC Madrepora oculata and Lophelia pertusa collected alive in the Norwegian Sea and spanning an age of 40 (3) and 67 (3) years, respectively. Acidification rates were calculated by applying a new pH-11B calibration obtained from the geochemical analysis M. oculata and L. pertusa samples cultured under different pCO2 conditions. The contribution of a biological-related vital effect on d11B was observed at macrometer scale, and a correction was finally suggested based on oxygen and carbon isotopes. Overall, the coral δ 11B-based reconstructions show a pH decrease in the Norwegian Sea since the 1940s, which seems to be related to the local hydrodynamics. The pH-11B technique was also applied to fossil DSC fragments from two “on-mound sediment cores” retrieved in the Siculo-Tunisian Strait with the aim to reconstruct the pH during the Last Glacial Maximum and the Holocene periods. Finally, well-preserved limestone samples from the stratigraphic sequence Nama (551-543 Ma) in Namibia were investigated for 11B to study the pH variations at the beginning of the Cambrian evolutive radiation.

Radiative forcing by increased atmospheric levels of greenhouse gases (GHGs) produced by human activities could lead to strongly undesirable effects on oceans and their dependent human systems in the coming centuries. Such dangerous anthropogenic interference with the climate system is a possibility the UN Framework Convention on Climate Change (UNFCCC) calls on nations to avoid. Unacceptable consequences of such interference could include inundation of coastal areas and low-lying islands by rising sea level, the rate of which could exceed natural and human ability to adapt, and ocean acidification contributing to widespread disruption of marine and human food systems. Such consequences pose daunting socioeconomic costs, for developing nations in particular. Drawing on existing literature, we define example levels of acceptable global marine change in terms of global mean temperature rise, sea level rise and ocean acidification. A global-mean climate model (ACC2), is implemented in an optimizing environment, GAMS, and coupled to an economic model (DICE). Using cost-effectiveness analysis and the tolerable windows approach (TWA) allows for the computation of both economically optimal carbon dioxide emissions pathways as well as a range in carbon dioxide emissions (the so-called ``emissions corridor'') which respect the predetermined ceilings and take into account the socio-economically acceptable pace of emissions reductions. The German Advisory Council on Global Change (WBGU) has issued several guardrails focused on marine changes, of which we find the rate and absolute rise in global mean temperature to be the most restrictive (0.2 degrees Celsius per decade, 2 degrees Celsius total). Respecting these guardrails will require large reductions in both carbon and non-carbon GHGs over the next century, regardless of equilibrium climate sensitivity. WBGU sea level rise and rate of rise guardrails (1 meter absolute, 5 cm per decade) are substantially less restrictive, and respecting them does not require deviation from a business-as-usual path in the next couple hundred of years, provided common assumptions of Antarctic ice mass balance sensitivity are correct. The ocean acidification guardrail (0.2 unit decline relative to the pre-industrial value) is less restrictive than those for temperature, but does require emissions reductions into the coming century.

Anthropogenic carbon dioxide (CO2) emissions are increasing the atmospheric CO2 concentration and the oceans are absorbing around 1/3 them. The CO2 hydrolysis increases the H+ concentration, decreasing the pH, while the proportions of the HCO3- and CO32- ions are also affected. This process already led to a decrease of 0.1 pH units in surface seawater. According to "business-as-usual" models, provided by the Intergovernmental Panel on Climate Change (IPCC), the pH is expected to decrease 0.3-0.5 units by 2100 and 0.7-0.8 by 2300. As a result the surface ocean carbonates chemistry will also change: with increasing pCO2, dissolved inorganic carbon will increase and the equilibrium of the carbonate system will shift to higher CO2 and HCO3– levels, while CO32– concentration will decrease. Surface seawaters will progressively become less saturated towards calcite and aragonite saturation state and some particular polar and cold water regions could even become completely undersaturated within the next 50 years. <p>Responses of marine organisms to environmental hypercapnia, i.e. to an excess of CO2 in the aquatic environment, can be extremely variable and the degree of sensitivity varies between species and life stages. Sea urchins are key stone species in many marine ecosystems. They are considered to be particularly vulnerable to ocean acidification effects not only due to the nature of their skeleton (magnesium calcite) whose solubility is similar or higher than that of aragonite, but also because they lack an efficient ion regulatory machinery, being therefore considered poor acid-base regulators. Populations from polar regions are expected to be at an even higher risk since the carbonate chemical changes in surface ocean waters are happening there at a faster rate. <p>The goal of this work was to study the effects of low seawater pH exposure of different life stages of sea urchins, in order to better understand how species from different environments and/or geographic origins would respond and if there would be scope for possible adaptation and/or acclimatization.<p>In a first stage we investigated the effects of ocean acidification on the early stages of an intertidal species from temperate regions, the Atlantic Paracentrotus lividus sea urchin, and of a sub-Antarctic species, Arbacia dufresnei. The fertilization, larval development and larval growth were studied on specimens submitted through different pH experimental treatments. The fertilization rate of P. lividus gametes whose progenitors came from a tide pool with high pH decrease was significantly higher, indicating a possible acclimatization or adaptation of gametes to pH stress. Larval size in both species decreased significantly in low pH treatments. However, smaller A. dufresnei echinoplutei were isometric to those of control treatments, showing that size reduction was most likely due to a slower growth rate. In the pH 7.4 (predicted for 2300) treatment, P. lividus presented significantly more abnormal forms than control ones, but A. dufresnei did not. The latter does not seem to be more vulnerable than temperate species, most likely due to acclimatization/adaptation to lower pH seasonal fluctuations experienced by individuals of this population during spring time.<p>In a second stage, adult physiological responses of P. lividus and A. dufresnei to low pH seawaters were studied. Intertidal field P. lividus specimens can experience pH fluctuations of 0.4 units during low tidal cycles, but their coelomic fluid pH will not change. During experimental exposure to low pH, the coelomic fluid (extracellular) pH of both species decreased after weeks of exposure to low seawater pH. However, it owned a certain buffer capacity (higher than that of seawater) which did not seem to be related to passive skeleton dissolution. In laboratory studies, the feeding rate of P. lividus, the RNA/DNA ratio (proxy for protein synthesis and thus metabolism) of both the gonads and the body wall of the studied species and the carbonic anhydrase activity in the body wall (an enzyme involved in calcification and respiratory processes) of A. dufresnei did not differ according to seawater pH. The same was true for spine regeneration (a proxy for calcification) of both species. This shows that both P. lividus and A. dufresnei are able to cope when exposed to mild hypercapnia (lowest investigated pH 7.4) for a mid-term period of time (weeks). In a different set of experiments, pH effects were tested on P. lividus individuals together with two temperatures (10ºC and 16ºC). The pH decrease of the coelomic fluid did not vary between temperatures, neither did its buffer response. The oxygen uptake rates of P. lividus (as a proxy for global metabolic state of the whole organism) increased in lower pH treatments (7.7 and 7.4) in organisms exposed to lower temperatures (10ºC), showing that this was upregulated and that organisms experienced a higher energetic demand to maintain normal physiological functions. For instance, gonad production (given by the RNA/DNA ratio) was not affected neither by temperature, nor pH.<p>Finally, possible morphological and chemical adaptations of cidaroid (“naked”) spines, which are not covered by epidermis, to low magnesium calcite saturation states were investigated. Deep sea field specimens from the Weddell Sea (Antarctica), Ctenocidaris speciosa were studied. Cidaroid spines have an exterior skeleton layer with a polycrystalline constitution that apparently protects the interior part of the monocrystaline skeleton, the stereom (tridimensional magnesium calcite lattice). The cortex of C. speciosa was by its turn divided into two layers. From these, it presented a thicker inner cortex layer and a lower Mg content in specimens collected below the aragonite saturation horizon. The naked cortex seems able to resist to low calcium carbonate saturation state. We suggest that this could be linked to the important organic matrix that surrounds the crystallites of the cortex.<p>Some echinoid species present adaptive features that enable them to deal with low pH stresses. This seems to be related to the environmental conditions to which populations are submitted to. Therefore, organisms already submitted to pH daily or seasonal fluctuations or living in environments undersaturated in calcium carbonate seem to be able to cope with environmental conditions expected in an acidified ocean. Under the realistic scenario of a decrease of ca. 0.4 units of pH by 2100, sea urchins, and echinoderms in general, appear to be robust for most studied processes. Even thought, this general response can depend on different parameters such as exposure time, pH level tested, the process and the life stage considered, our results show that there is scope for echinoids to cope with ocean acidification.<p> / Doctorat en Sciences / info:eu-repo/semantics/nonPublished