While it is not the most abundant greenhouse gas, a significant portion of the greenhouse effect is caused by methane. The amount of methane in the atmosphere is increasing, indicating that there is a continuous source of methane to the atmosphere. One significant source of methane is freshwater lakes, even though they cover only a small portion of the Earth’s surface. Because of this, it is important to monitor methane fluxes from lakes in order to understand the processes which affect the magnitude of these fluxes. Methane is produced in the sediment at the bottom of the lake, and transported through the water by ebullition, diffusive flux, storage flux, or plant mediated emission. This study looked to examine the amount of methane transmitted to the atmosphere by these processes on Lake Erken in eastern Sweden. Using the eddy covariance method, we can study the methane flux with good spatial and temporal resolution. Regular sampling of lake water, both from the surface and depths of 5 and 10 meters, also helps us to understand the amount of methane dissolved in the lake. These measurements can help us to better understand the transfer velocity, or the efficiency of the exchange between water and air, as well as the amount of methane transported from lakes to the atmosphere. Water sampling showed that there is very little variation in methane concentration between different parts of the lake. Concentrations at four surface locations are nearly identical. These surface measurements are also similar to concentrations at different depths. Over time, the concentrations generally stayed the same, with isolated high and low concentration events. The amount of methane emitted by the lake was studied with the lake divided into a shallow water area, and a deep water area. The magnitude of fluxes from both areas was very similar, but the area of shallow water had a higher total flux. The fluxes were well correlated with wind speed; higher fluxes coming during times with higher wind speed. This relates well to the transfer velocity theory, and the bulk flux approximation. However, there was no clear diurnal cycle in methane fluxes. The fluxes during the night were similar to daytime fluxes. Atmospheric pressure also had an impact on fluxes, with greater fluxes coming at times of lower pressure. A large seasonal variation was clear. More methane escaped the water in autumn and winter than in spring or summer. This is due in part to the fluxes from when the lake freezes over/thaws and the water in the lake turns over, bringing methane rich water from the lake’s bottom to the surface. As expected, the waterside concentration of methane also had a strong correlation with the fluxes. The main conclusions of this study are: 1) Methane fluxes are variable with wind speed, waterside concentrations, and the seasons 2) Water depth and diurnal cycles do not affect methane fluxes as strongly. Keywords: methane, transfer velocity, flux, waterside concentration, eddy covariance

World oceans cover more than 70% of the earth surface and constitutes a major sink of atmospheric CO2. Two of the most important gases in the marine carbon cycling are O2 and CO2 and hence accurate descriptions of the air-sea gas exchange of these gases are crucial. Still there is a lack of knowledge of the relative importance of processes controlling the efficiency of the air-sea gas transfer. This is especially true for Arctic and high latitude seas were studies on air-sea gas exchange are few. By studying processes causing water-side turbulence, using gases of different solubility and various measurement techniques, more knowledge on the governing processes can be obtained. Here we present the very first air-sea fluxes of O2 using atmospheric eddy covariance measurements and investigate the dependence between the gas transfer velocity of O2 and turbulence generated by the mean wind. The instrument was found to suffer from the limited precision and time response, causing significant corrections on the O2 flux. After correcting for this, the O2 fluxes displays an anti-correlation with the air-sea fluxes of CO2 in agreement with the measured air-sea gradient of O2. The transfer velocities for O2 indicates a stronger wind dependence than other commonly used parameterizations of the transfer velocity for CO2 and O2, this especially for wind speeds > 5 m s-1 where the typical onset of wave breaking occur. During two winter months eddy covariance measurements were taken over a high Arctic fjord. The data revealed a significant enhancement of the gas transfer velocity for CO2 from water-side convection, generated by cooling of surface waters. The dependence between water-side convection and gas transfer velocity were found for winds as high as 9 m s-1, but were strongest for wind speeds< 7  m s-1.  The data also showed on enhanced air-sea gas transfer of CO2 when conditions were unstable very close to neutral. This enhanced transfer were associated to increased contribution to the CO2 flux from downdraft of air with higher concentrations of CO2.  The combined effect of water-side convection and turbulence generated by wind results in a very effective transfer, thus the air-sea gas exchange at these latitudes may be significantly underestimated.

<p>This thesis aims to measure the rate of radon loss from water in a systematic way. The dependence on surface area, temperature and concentration will be investigated. The experiments were done at UWC by creating radon using radium sources and then measuring the radon concentrations inside a vacuum chamber to obtain the speed of radon escape from the water. The results are compared to a model [Cal 2002] where the radon concentration in the air and hence the transfer rate is measured using a RAD7 radon detector. Since the equations cannot be solved analytically, a numerical solution is employed. The radon transfer velocity coefficient is found to be (1.9&plusmn / 0.5)&times / 10-6m/s. This value indicates that the escape of radon should not be a problem when a sample is open to the air for a minute or two.</p>

<p>This thesis aims to measure the rate of radon loss from water in a systematic way. The dependence on surface area, temperature and concentration will be investigated. The experiments were done at UWC by creating radon using radium sources and then measuring the radon concentrations inside a vacuum chamber to obtain the speed of radon escape from the water. The results are compared to a model [Cal 2002] where the radon concentration in the air and hence the transfer rate is measured using a RAD7 radon detector. Since the equations cannot be solved analytically, a numerical solution is employed. The radon transfer velocity coefficient is found to be (1.9&plusmn / 0.5)&times / 10-6m/s. This value indicates that the escape of radon should not be a problem when a sample is open to the air for a minute or two.</p>

Magister Scientiae - MSc / This thesis aims to measure the rate of radon loss from water in a systematic way. The dependence on surface area, temperature and concentration will be investigated. The experiments were done at UWC by creating radon using radium sources and then measuring the radon concentrations inside a vacuum chamber to obtain the speed of radon escape from the water. The results are compared to a model [Cal 2002] where the radon concentration in the air and hence the transfer rate is measured using a RAD7 radon detector. Since the equations cannot be solved analytically, a numerical solution is employed. The radon transfer velocity coefficient is found to be (1.9±0.5)×10-6m/s. This value indicates that the escape of radon should not be a problem when a sample is open to the air for a minute or two. / South Africa

Since the beginning of the industrial revolution, a large amount of greenhouse gases such as carbon dioxide (CO2) have been emitted into the atmosphere due to human activities. One of the main consequences of these emissions is a rapid increase in atmospheric CO2 concentration and a profound modification of the Earth's climate system. The ocean plays an important role in the Earth radiative balance since it acts as an important CO2 sink for the atmosphere. By currently absorbing about 25 % of the CO2 emitted by humans it considerably slows down climate change. Understanding the present-day spatial and temporal dynamics of the air-sea CO2 exchange and the different processes that govern this exchange is of critical importance to anticipate the evolution of the oceanic CO2 sink in the future.This thesis was realized in this context and focused on an improved quantification of the exchange of CO2 through the air-sea interface (FCO2) of the global ocean, embracing open ocean waters and coastal regions. The main objective was to fill knowledge gaps in our understanding of the processes that govern the spatial and temporal distribution of FCO2. This objective was mainly achieved through observational approaches and addressed three main aspects: a quantification of the different sources of FCO2 uncertainties at the global scale, an analysis of spatial distribution of the oceanic CO2 exchange with a strong focus on the coastal ocean and a first assessment of the coastal seasonal FCO2 dynamics and its underlying drivers. The latter relied on a data-model fusion approach allowing to decompose the FCO2 seasonality into its main physical and biogeochemical drivers. The quantification of the oceanic FCO2 from observations consists in calculating an air-sea partial pressure CO2 gradient (ΔpCO2) between the atmosphere and the sea surface. Global monthly continuous partial pressure of CO2 (pCO2) products can for example be derived from observational pCO2 databases and statistical interpolation methods. This ΔpCO2 is then multiplied by a gas exchange transfer rate coefficient (k), which depends on wind speed. However, the parametrization of k is still entailed with poorly quantified uncertainties. From a literature review of all k parameterizations available in the literature over the past 25 years, I first quantified the FCO2 uncertainties associated with k globally and regionally for the open ocean. I also quantified the uncertainties associated with the choice of a wind product over another. Our results show that the range of global FCO2, calculated with these k relationships, diverge by 12 % when using CCMP, ERA or NCEP1. Regional discrepancies in FCO2 are more pronounced than global. These global and regional differences significantly increase when using NCEP2 or other k formulations. To minimize uncertainties associated with the choice of wind product, it is possible to recalculate the parametrization of k globally for a given wind product and its spatio-temporal resolution, in order to match the last evaluation of the global k value. In a second step, we improved the quantification and analysis of the dominant patterns and drivers of the FCO2 spatial distribution for the coastal ocean worldwide. This analysis was performed globally (at 0.25° spatial resolution), using a regional segmentation of the coastal ocean, and latitudinally. I found that coastal regions at high latitudes act as a CO2 sink while tropical regions and along the equator tend to act as an atmospheric CO2 source. Globally integrated, I quantified that the coastal seas act currently as a CO2 sink with a value of -0.20 ± 0.02 Pg C yr-1. For the first time, I also compared the spatial patterns of coastal FCO2 to that of the adjacent open ocean, globally. With the exception of some regions such as those dominated by riverine inputs, I demonstrated that they present similar latitudinal distribution of their FCO2 density per unit of surface area, suggesting analogous responses to increasing atmospheric CO2. I also reevaluated the global ocean CO2 budget and estimated a global anthropogenic CO2 uptake ranging between -2.6 ± 0.4 Pg C yr-1 and -2.9 ± 0.5 Pg C yr-1 for the 1998-2015 period. In a third step, I contributed to the first continuous observational pCO2 data product merging the coastal and open ocean in a consistent manner. This study showed that difference between open ocean and coastal ocean estimates along the overlap area increases with latitude but remains close to 0 µatm globally. Stronger discrepancies, however, exist on the regional level resulting in differences that exceed 10 % of the climatological mean pCO2, particularly in regions constrained by fewer observations, paired with biogeochemical complexity, such as the Peruvian upwelling system and ice covered regions.In a fourth step, a temporal analysis of the FCO2 seasonality was performed for the coastal ocean based on an observational approach. I analyzed and quantified the FCO2 seasonal dynamics globally and for different latitudinal bands. Globally, coastal regions act as a CO2 sink with a more intense uptake occurring in summer (-21 Tg C month-1) because of the disproportionate influence of high latitude shelves in the Northern Hemisphere. I also estimated the contribution of different drivers (sea-ice coverage, wind speed, and ΔpCO2 change) to the FCO2 seasonal amplitude. This data-driven approach allowed me to conclude that the ΔpCO2 is the main driver of the FCO2 variability at the seasonal timescale. I then used a global oceanic biogeochemical model to decompose the seasonal coastal pCO2 variability further into its driving physical and biological processes. From a first qualitative assessment, I concluded that the thermal effect associated to sea surface temperature changes is the main effect governing the coastal seasonal pCO2 variability except at high latitudes where the non-thermal effect associated to changes in biology, circulation, fresh water and the air-sea CO2 exchange itself dominate. I also found that, overall, the thermal effect alone should lead to larger seasonal fluctuations, but its influence is partly offset by the non-thermal effect. Throughout this thesis, I also evaluated the extent to which the continuous observational pCO2 products derived from an artificial neuronal network approach and from the global ocean biogeochemical model MOM6-COBALT could reproduce the raw pCO2 fields extracted from global databases. Overall, I showed that at the regional scale, the two products are in relatively good agreement compared to observations. I also identified regions where discrepancies are the largest and where future observational data are needed in the future, as well as regions where agreement is the most satisfactory and, thus, most suitable for further process-based analyses. / Depuis le début de la révolution industrielle, une grande quantité de gaz à effet de serre tels que le dioxyde de carbone (CO2) a été émise dans l'atmosphère en raison des activités humaines. L'une des principales conséquences de ces émissions est une augmentation rapide de la concentration en CO2 atmosphérique et une modification profonde du système climatique de la Terre. L'océan joue un rôle important dans l'équilibre radiatif de la Terre car il agit comme un important puits de CO2 pour l'atmosphère. En absorbant actuellement environ 25 % du CO2 émis par l'homme, il ralentit considérablement le changement climatique. Comprendre la dynamique spatiale et temporelle actuelle de l'échange de CO2 air-mer et les différents processus qui régissent cet échange est d'une importance cruciale pour anticiper l'évolution du puits océanique de CO2 à l'avenir.Cette thèse a été réalisée dans ce contexte et s'est concentrée sur une meilleure quantification de l'échange de CO2 à travers l'interface air-mer (FCO2) de l'océan global, considérant à la fois l’océan ouvert et les régions côtières. L'objectif principal était de combler les lacunes dans notre compréhension des processus qui régissent la distribution spatiale et temporelle du FCO2. Cet objectif a été principalement atteint grâce à des approches observationnelles et a abordé trois aspects principaux: une quantification des différentes sources d'incertitudes du FCO2 à l'échelle globale, une analyse de la distribution spatiale de l'échange de CO2 océanique avec un fort accent sur l'océan côtier et une première évaluation de la dynamique saisonnière du FCO2 côtier et de ses moteurs sous-jacents. Ce dernier s'est appuyé sur une approche de fusion de modèles et d’approches observationnelles permettant de décomposer la saisonnalité du FCO2 en ses principaux moteurs physiques et biogéochimiques.La quantification du FCO2 océanique à partir d’observations consiste à calculer un gradient de pression partielle air-mer de CO2 (ΔpCO2) entre l'atmosphère et la surface de la mer. Des produits globaux continus mensuels de la pression partielle de CO2 (pCO2) peuvent par exemple être dérivés à partir de bases de données observationnelles de pCO2 et de méthodes d'interpolation statistique. ΔpCO2 est ensuite multiplié par un coefficient de vitesse de transfert d'échange gazeux (k), qui dépend de la vitesse du vent. Cependant, la paramétrisation de k est sujette à de larges incertitudes et mal quantifiées. À partir d'une synthèse de la littérature de toutes les paramétrisations de k disponibles dans la littérature au cours des 25 dernières années, j'ai d'abord quantifié les incertitudes sur FCO2 associées à k à l'échelle globale et régionale pour l'océan ouvert. J'ai également quantifié les incertitudes associées au choix d'un produit éolien par rapport à un autre. Nos résultats montrent que la gamme du FCO2 global, calculée avec ces différentes paramétrisations de k, diverge de 12 % lors de l'utilisation de CCMP, ERA ou NCEP1. En raison des différences dans les pattern de vent régionaux, les différences régionales sur le FCO2 sont plus prononcés que globalement. Ces différences globales et régionales augmentent de manière significative lors de l'utilisation de NCEP2 ou d'autres formulations de k. Afin de réduire les incertitudes associées au choix du produit de vent, il est possible de recalculer la paramétrisation de k pour un produit de vent donné et à une résolution spatio temporelle.Dans un deuxième temps, nous avons amélioré la quantification et l'analyse des principaux pattern et des différents processus sur la distribution spatiale du FCO2 pour l’ensemble des régions côtières. Cette analyse a été réalisée à l'échelle globale (à une résolution spatiale de 0.25°), en utilisant une segmentation régionale de l'océan côtier, et latitudinalement. J'ai trouvé que les régions côtières aux hautes latitudes agissent comme un puits de CO2 tandis que les régions côtières tropicales et le long de l'équateur ont tendance à agir comme une source de CO2 atmosphérique. Globalement, j'ai quantifié que les régions côtières agissent actuellement en tant que puits de CO2 avec une valeur de -0.20 ± 0.02 Pg C an-1. Pour la première fois, j'ai également comparé la distribution spatiale du FCO2 côtier à celle de l'océan ouvert adjacent, à l'échelle globale. À l'exception de certaines régions telles que celles dominées par les apports fluviaux, j'ai démontré que les régions côtières et l’océan ouvert adjacent présentaient une distribution latitudinale similaire sur leur densité de FCO2 par unité de surface, suggérant des réponses analogues à l'augmentation du CO2 atmosphérique. J'ai également réévalué le budget mondial de CO2 de l'océan et estimé une absorption mondiale de CO2 anthropique comprise entre -2.6 ± 0.4 Pg C an-1 et -2.9 ± 0.5 Pg C an-1 pour la période 1998-2015. Dans un troisième temps, j'ai contribué à la création du premier produit continu de pCO2 observationnelles fusionnant le domaine côtier et l'océan ouvert de manière cohérente. Cette étude a montré que la différence entre les estimations provenant du produit de pCO2 de l’océan ouvert à celles dérivant du produit de pCO2 de l’océan côtier le long de leur zone de chevauchement augmente avec la latitude mais reste proche de 0 µatm globallement. Des divergences plus fortes existent cependant au niveau régional, entraînant des différences qui dépassent 10 % sur la moyenne climatologique de pCO2, en particulier dans les régions contraintes par moins d'observations, associées à une complexité biogéochimique, comme le système d'upwelling péruvien et les régions couvertes de glace.Dans une quatrième étape, une analyse temporelle de la saisonnalité du FCO2 a été réalisée pour l'océan côtier sur la base d'une approche observationnelle. J'ai analysé et quantifié la dynamique saisonnière du FCO2 à l'échelle globale et pour différentes bandes latitudinales. À l'échelle globale, les régions côtières agissent comme un puits de CO2 avec une absorption plus intense se produisant en été (-21 Tg C mois-1) en raison de l'influence disproportionnée des régions côtières des hautes latitudes dans l'hémisphère Nord. J'ai également estimé la contribution de différents processus (couverture de glace de mer, vitesse du vent et changement de ΔpCO2) à l'amplitude saisonnière du FCO2. Cette approche basée sur les données observationnelles m'a permis de conclure que ΔpCO2 est le principal moteur de la variabilité du FCO2 à l'échelle saisonnière. J'ai ensuite utilisé un modèle biogéochimique océanique global pour décomposer davantage la variabilité saisonnière du pCO2 côtier en ses processus physiques et biologiques. À partir d'une première évaluation qualitative, j'ai conclu que l'effet thermique associé aux changements de température de la surface de la mer est le principal effet régissant la variabilité côtière saisonnière du pCO2 sauf aux hautes latitudes où l'effet non thermique associé aux changements de biologie, de circulation, d'eau douce et de l’échange de CO2 air-mer domine. J'ai également constaté que, globalement, l'effet thermique à lui seul devrait entraîner des fluctuations saisonnières plus importantes, mais son influence est en partie compensée par l'effet non thermique.Tout au long de cette thèse, j'ai également évalué dans quelle mesure les produits continus de pCO2 observationnelles dérivés d'une approche de réseau de neurones artificiels et du modèle biogéochimique océanique global MOM6-COBALT pourraient reproduire les champs de pCO2 bruts extraits des bases de données globale. Dans l'ensemble, j'ai montré qu'à l'échelle régionale, les deux produits sont relativement en bon accord par rapport aux observations. J'ai également identifié les régions où les différences sont les plus importantes et où de futures données observationnelles sont nécessaires à l'avenir, ainsi que les régions où les deux produits présentent un accord le plus satisfaisant et, par conséquent, le plus approprié pour de futures analyses de compréhension des différents processus. / Doctorat en Sciences / info:eu-repo/semantics/nonPublished

Freshwater bodies such as lakes and streams release the greenhouse gases methane (CH4) and carbon dioxide (CO2) into the atmosphere. Global freshwater CH4 and CO2 emissions have been estimated to be of a similar magnitude to the global land or ocean carbon sink, and are thus significant components of global carbon budgets. However, the data supporting global estimates frequently lacks information regarding spatial and temporal variability and are thus highly inaccurate. In this thesis, detailed studies of the spatio-temporal variability of CH4 and CO2 fluxes were conducted in the open water areas of lakes and streams within a whole catchment in Sweden. One aim was also to evaluate the importance of spatio-temporal variability in lake and stream fluxes when making whole catchment aquatic or large scale assessments. Apart from the expected large spatio-temporal variability in lake fluxes, interactions between spatial and temporal variability in CH4 fluxes were found. Shallow lakes and shallow areas of lakes were observed to emit more CH4 as compared to their deeper counterparts. This spatial variability interacted with the temporal variability driven by an exponential temperature response of the fluxes, which meant that shallow waters were more sensitive to warming than deeper ones. Such interactions may be important for climate feedbacks. Surface water CO2 in lakes showed significant spatio-temporal variability and, when considering variability in both space and time, CO2 fluxes were largely controlled by concentrations, rather than gas transfer velocities. Stream fluxes were also highly variable in space and time and in particular, stream CH4 fluxes were surprisingly large and more variable than CO2 fluxes. Fluxes were large from stream areas with steep slopes and periods of high discharge which occupied a small fraction of the total stream area and the total measurement period, respectively, and a failure to account for these spatially distinct or episodic high fluxes could lead to underestimates. The total aquatic fluxes from the whole catchment were estimated by combining the measurements in open waters of lakes and streams. Using our data, recommendations on improved study designs for representative measurements in lakes and streams were provided for future studies. Thus, this thesis presents findings relating to flux regulation in lakes and streams, and urges forthcoming studies to better consider spatio-temporal variability so as to achieve unbiased large-scale estimates. / Sötvatten som sjöar och vattendrag är källor till växthusgaserna metan (CH4) och koldioxid (CO2) i atmosfären. De globala utsläppen av CH4 och CO2 från sötvatten har uppskattats vara av samma storleksordning som den globala land- eller havskolsänkan och är därmed viktiga delar av jordens växthusgasbudget. De globala uppskattningarna saknar ofta information om variation i tid och rum och är därmed mycket osäkra. Denna avhandling behandlar hur CH4- och CO2-flöden från öppet vatten i sjöar och vattendrag i ett avrinningsområde varierar rumsligt och tidsmässigt. Ett syfte var också att utvärdera betydelsen av dessa variationer när data extrapoleras för att göra storskaliga uppskattningar av växthusgasflöden från vattenmiljöer. Förutom de förväntade stora rumsliga och tidsmässiga variationerna i sjöars gasflöden identifierades interaktioner mellan rumsliga och tidsmässiga variation för CH4-flöden. Den rumsliga variabiliteten med högre CH4-flöden från grunda vatten interagerade med tidsvariationen, som i sin tur drevs av en exponentiell temperaturrespons av gasflödena. Det betyder att grunda vattenområden var mer känsliga för uppvärmning än djupare vatten och därmed att vattendjupet har betydelse för hur sjöars CH4-utsläpp påverkas av klimatet. Koncentrationer av CO2 i sjöars ytvatten uppvisade också en betydande rumslig och tidsmässig variation som tillsammans visar att CO2-flöden över längre perioder till stor del styrs av koncentrationer snarare än av gasutbyteshastigheter. Vattendragens gasflöden varierade också mycket i tid och rum. Detta gällde i synnerhet CH4-flödena vilka var förvånansvärt stora och mer varierande än CO2-flödena. Gasflödena var höga från områden i vattendrag med högre lutning och då det var höga vattenflöden, trots att dessa områden och tidsperioder utgjorde en bråkdel av den totala arean och mätperioden. Att inte räkna med dessa gasflöden från bäcksektioner med höga vattenhastigheter eller korta perioder med höga flöden, leder till underskattningar. De totala CH4- och CO2-flödena från öppet vatten i hela avrinningsområdet uppskattades genom att kombinera mätningar i sjöar och vattendrag. Denna avhandling visar att rumslig och tidsmässig variabilitet har stor betydelse, och den ger information om hur denna variation kan beaktas för bättre framtida mätningar och storskaliga uppskattningar av växthusgasflöden från sjöar och vattendrag.

O ciclo diurno do fluxo de CO2 no oceano Atlântico equatorial para o mês de agosto é estimado utilizando um algoritmo de transferência de gases. O algoritmo é baseado na teoria de similaridade de Monin-Obukhov para fluxos turbulentos na interface ar-mar e na física da transferência de CO2 na camada molecular oceânica. O ciclo diurno do fluxo de CO2, obtido na região, caracteriza o oceano Atlântico equatorial, durante o período, como fonte de CO2 para a atmosfera e seus valores estão entre 0,71 e 0,85 mol CO2 m^-2 ano^-1. / The diurnal cycle of CO2 is estimated for the month of August on the Atlantic Ocean using a gas transfer algorithm. The algorithm is based on the Monin-Obukhov similarity theory for turbulent transfer at the air-sea interface and the physics of the CO2 transfer at the oceanic molecular layer.

River, lakes and   streams account for more carbon dioxide emissions than all other freshwater   reservoirs together. However, there is still lack of knowledge of the   physical processes that control the efficiency of the air-water exchange of   CO2 in these aquatic systems. In the more turbulent water sections   of a river, the gas transfer is thought to be governed by the river’s   morphology such as bottom topography, slope and stream flow. Whiles for wider   sections of the river, the gas transfer could potentially be influenced by   atmospheric forcing (e.g. Wind speed). The main purpose of this project is to   study the fluxes of carbon dioxide and how (wind speed and stream discharge)   influence the CO2 fluxes in the river. In this study, direct and   continuous measurements of CO2 emission was conducted for the   first time in a controlled boreal river in Kattstrupeforsen (Sweden) from   18th April to 10th May 2018. A unique measurement setup which combines eddy   covariance techniques, general meteorology and in situ water variables (for   high accuracy emission measurements) was used. The results show that   in the late winter, an   upward directed CO2 fluxes measured in the river was approximately   2.2 μmol m−2 s−1. This value agrees with many other small and   large rivers where CO2 fluxes has been studied. The river can be   said to serve as source of CO2 to the atmosphere in the day due to   the dominant upward fluxes recorded during the daytime. The results also show   that carbon dioxide fluxes increase with increasing wind speed notably at   wind speed above 2 m s-1. There   was no relation between CO2 fluxes and stream discharge. This   indicates that wind speed could be one principal factor for air- river gas   exchange. The findings in this work on river gas exchange will provide   a basis for a regional estimate and be applicable for many river systems on a   global scale. / <p>2018-07-09</p>

O ciclo diurno do fluxo de CO2 no oceano Atlântico equatorial para o mês de agosto é estimado utilizando um algoritmo de transferência de gases. O algoritmo é baseado na teoria de similaridade de Monin-Obukhov para fluxos turbulentos na interface ar-mar e na física da transferência de CO2 na camada molecular oceânica. O ciclo diurno do fluxo de CO2, obtido na região, caracteriza o oceano Atlântico equatorial, durante o período, como fonte de CO2 para a atmosfera e seus valores estão entre 0,71 e 0,85 mol CO2 m^-2 ano^-1. / The diurnal cycle of CO2 is estimated for the month of August on the Atlantic Ocean using a gas transfer algorithm. The algorithm is based on the Monin-Obukhov similarity theory for turbulent transfer at the air-sea interface and the physics of the CO2 transfer at the oceanic molecular layer.