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Aim: Although running waters are getting recognized as important methane sources, large‐scale geographical patterns of microorganisms controlling the net methane balance of streams are still unknown. Here we aim at describing community compositions of methanogenic and methanotrophic microorganisms at large spatial scales and at linking their abundances to potential sediment methane production (PMP) and oxidation rates (PMO). Location: The study spans across 16 European streams from northern Spain to northern Sweden and from western Ireland to western Bulgaria. Taxon: Methanogenic archaea and methane‐oxidizing microorganisms. Methods: To provide a geographical overview of both groups in a single approach, microbial communities and abundances were investigated via 16S rRNA gene sequencing, extracting relevant OTUs based on literature; both groups were quantified via quantitative PCR targeting mcrA and pmoA genes and studied in relation to environmental parameters, sediment PMP and PMO, and land use. Results: Diversity of methanogenic archaea was higher in warmer streams and of methanotrophic communities in southern sampling sites and in larger streams. Anthropogenically altered, warm and oxygen‐poor streams were dominated by the highly efficient methanogenic families Methanospirillaceae, Methanosarcinaceae and Methanobacteriaceae, but did not harbour any specific methanotrophic organisms. Contrastingly, sediment communities in colder, oxygen‐rich waters with little anthropogenic impact were characterized by methanogenic Methanosaetaceae, Methanocellaceae and Methanoflorentaceae and methanotrophic Methylococcaceae and Cd. Methanoperedens. Representatives of the methanotrophic Crenotrichaceae and Methylococcaceae as well as the methanogenic Methanoregulaceae were characteristic for environments with larger catchment area and higher discharge. PMP increased with increasing abundance of methanogenic archaea, while PMO rates did not show correlations with abundances of met

Aim: Although running waters are getting recognized as important methane sources, large‐scale geographical patterns of microorganisms controlling the net methane balance of streams are still unknown. Here we aim at describing community compositions of methanogenic and methanotrophic microorganisms at large spatial scales and at linking their abundances to potential sediment methane production (PMP) and oxidation rates (PMO). Location: The study spans across 16 European streams from northern Spain to northern Sweden and from western Ireland to western Bulgaria. Taxon: Methanogenic archaea and methane‐oxidizing microorganisms. Methods: To provide a geographical overview of both groups in a single approach, microbial communities and abundances were investigated via 16S rRNA gene sequencing, extracting relevant OTUs based on literature; both groups were quantified via quantitative PCR targeting mcrA and pmoA genes and studied in relation to environmental parameters, sediment PMP and PMO, and land use. Results: Diversity of methanogenic archaea was higher in warmer streams and of methanotrophic communities in southern sampling sites and in larger streams. Anthropogenically altered, warm and oxygen‐poor streams were dominated by the highly efficient methanogenic families Methanospirillaceae, Methanosarcinaceae and Methanobacteriaceae, but did not harbour any specific methanotrophic organisms. Contrastingly, sediment communities in colder, oxygen‐rich waters with little anthropogenic impact were characterized by methanogenic Methanosaetaceae, Methanocellaceae and Methanoflorentaceae and methanotrophic Methylococcaceae and Cd. Methanoperedens. Representatives of the methanotrophic Crenotrichaceae and Methylococcaceae as well as the methanogenic Methanoregulaceae were characteristic for environments with larger catchment area and higher discharge. PMP increased with increasing abundance of methanogenic archaea, while PMO rates did not show correlations with abundances of met

Aim: Although running waters are getting recognized as important methane sources, large‐scale geographical patterns of microorganisms controlling the net methane balance of streams are still unknown. Here we aim at describing community compositions of methanogenic and methanotrophic microorganisms at large spatial scales and at linking their abundances to potential sediment methane production (PMP) and oxidation rates (PMO). Location: The study spans across 16 European streams from northern Spain to northern Sweden and from western Ireland to western Bulgaria. Taxon: Methanogenic archaea and methane‐oxidizing microorganisms. Methods: To provide a geographical overview of both groups in a single approach, microbial communities and abundances were investigated via 16S rRNA gene sequencing, extracting relevant OTUs based on literature; both groups were quantified via quantitative PCR targeting mcrA and pmoA genes and studied in relation to environmental parameters, sediment PMP and PMO, and land use. Results: Diversity of methanogenic archaea was higher in warmer streams and of methanotrophic communities in southern sampling sites and in larger streams. Anthropogenically altered, warm and oxygen‐poor streams were dominated by the highly efficient methanogenic families Methanospirillaceae, Methanosarcinaceae and Methanobacteriaceae, but did not harbour any specific methanotrophic organisms. Contrastingly, sediment communities in colder, oxygen‐rich waters with little anthropogenic impact were characterized by methanogenic Methanosaetaceae, Methanocellaceae and Methanoflorentaceae and methanotrophic Methylococcaceae and Cd. Methanoperedens. Representatives of the methanotrophic Crenotrichaceae and Methylococcaceae as well as the methanogenic Methanoregulaceae were characteristic for environments with larger catchment area and higher discharge. PMP increased with increasing abundance of methanogenic archaea, while PMO rates did not show correlations with abundances of met

Globally, inland waters emit over 2 Pg of carbon per year as carbon dioxide, of which the majority originates from streams and rivers. Despite the global significance of fluvial carbon dioxide emissions, little is known about their diel dynamics. Here we present a large-scale assessment of day- and night-time carbon dioxide fluxes at the water-air interface across 34 European streams. We directly measured fluxes four times between October 2016 and July 2017 using drifting chambers. Median fluxes are 1.4 and 2.1mmolm(-2) h(-1) at midday and midnight, respectively, with night fluxes exceeding those during the day by 39%. We attribute diel carbon dioxide flux variability mainly to changes in the water partial pressure of carbon dioxide. However, no consistent drivers could be identified across sites. Our findings highlight widespread day-night changes in fluvial carbon dioxide fluxes and suggest that the time of day greatly influences measured carbon dioxide fluxes across European streams. Diel patterns can greatly impact total stream carbon dioxide emissions, with 39% greater carbon dioxide flux during the night-time relative to the day-time, according to a study of 34 streams across Europe.

Globally, inland waters emit over 2 Pg of carbon per year as carbon dioxide, of which the majority originates from streams and rivers. Despite the global significance of fluvial carbon dioxide emissions, little is known about their diel dynamics. Here we present a large-scale assessment of day- and night-time carbon dioxide fluxes at the water-air interface across 34 European streams. We directly measured fluxes four times between October 2016 and July 2017 using drifting chambers. Median fluxes are 1.4 and 2.1mmolm(-2) h(-1) at midday and midnight, respectively, with night fluxes exceeding those during the day by 39%. We attribute diel carbon dioxide flux variability mainly to changes in the water partial pressure of carbon dioxide. However, no consistent drivers could be identified across sites. Our findings highlight widespread day-night changes in fluvial carbon dioxide fluxes and suggest that the time of day greatly influences measured carbon dioxide fluxes across European streams. Diel patterns can greatly impact total stream carbon dioxide emissions, with 39% greater carbon dioxide flux during the night-time relative to the day-time, according to a study of 34 streams across Europe.

Globally, inland waters emit over 2 Pg of carbon per year as carbon dioxide, of which the majority originates from streams and rivers. Despite the global significance of fluvial carbon dioxide emissions, little is known about their diel dynamics. Here we present a large-scale assessment of day- and night-time carbon dioxide fluxes at the water-air interface across 34 European streams. We directly measured fluxes four times between October 2016 and July 2017 using drifting chambers. Median fluxes are 1.4 and 2.1mmolm(-2) h(-1) at midday and midnight, respectively, with night fluxes exceeding those during the day by 39%. We attribute diel carbon dioxide flux variability mainly to changes in the water partial pressure of carbon dioxide. However, no consistent drivers could be identified across sites. Our findings highlight widespread day-night changes in fluvial carbon dioxide fluxes and suggest that the time of day greatly influences measured carbon dioxide fluxes across European streams. Diel patterns can greatly impact total stream carbon dioxide emissions, with 39% greater carbon dioxide flux during the night-time relative to the day-time, according to a study of 34 streams across Europe.

Aim: Although running waters are getting recognized as important methane sources, large‐scale geographical patterns of microorganisms controlling the net methane balance of streams are still unknown. Here we aim at describing community compositions of methanogenic and methanotrophic microorganisms at large spatial scales and at linking their abundances to potential sediment methane production (PMP) and oxidation rates (PMO). Location: The study spans across 16 European streams from northern Spain to northern Sweden and from western Ireland to western Bulgaria. Taxon: Methanogenic archaea and methane‐oxidizing microorganisms. Methods: To provide a geographical overview of both groups in a single approach, microbial communities and abundances were investigated via 16S rRNA gene sequencing, extracting relevant OTUs based on literature; both groups were quantified via quantitative PCR targeting mcrA and pmoA genes and studied in relation to environmental parameters, sediment PMP and PMO, and land use. Results: Diversity of methanogenic archaea was higher in warmer streams and of methanotrophic communities in southern sampling sites and in larger streams. Anthropogenically altered, warm and oxygen‐poor streams were dominated by the highly efficient methanogenic families Methanospirillaceae, Methanosarcinaceae and Methanobacteriaceae, but did not harbour any specific methanotrophic organisms. Contrastingly, sediment communities in colder, oxygen‐rich waters with little anthropogenic impact were characterized by methanogenic Methanosaetaceae, Methanocellaceae and Methanoflorentaceae and methanotrophic Methylococcaceae and Cd. Methanoperedens. Representatives of the methanotrophic Crenotrichaceae and Methylococcaceae as well as the methanogenic Methanoregulaceae were characteristic for environments with larger catchment area and higher discharge. PMP increased with increasing abundance of methanogenic archaea, while PMO rates did not show correlations with abundances of met

Globally, inland waters emit over 2 Pg of carbon per year as carbon dioxide, of which the majority originates from streams and rivers. Despite the global significance of fluvial carbon dioxide emissions, little is known about their diel dynamics. Here we present a large-scale assessment of day- and night-time carbon dioxide fluxes at the water-air interface across 34 European streams. We directly measured fluxes four times between October 2016 and July 2017 using drifting chambers. Median fluxes are 1.4 and 2.1mmolm(-2) h(-1) at midday and midnight, respectively, with night fluxes exceeding those during the day by 39%. We attribute diel carbon dioxide flux variability mainly to changes in the water partial pressure of carbon dioxide. However, no consistent drivers could be identified across sites. Our findings highlight widespread day-night changes in fluvial carbon dioxide fluxes and suggest that the time of day greatly influences measured carbon dioxide fluxes across European streams. Diel patterns can greatly impact total stream carbon dioxide emissions, with 39% greater carbon dioxide flux during the night-time relative to the day-time, according to a study of 34 streams across Europe.

Globally, inland waters emit over 2 Pg of carbon per year as carbon dioxide, of which the majority originates from streams and rivers. Despite the global significance of fluvial carbon dioxide emissions, little is known about their diel dynamics. Here we present a large-scale assessment of day- and night-time carbon dioxide fluxes at the water-air interface across 34 European streams. We directly measured fluxes four times between October 2016 and July 2017 using drifting chambers. Median fluxes are 1.4 and 2.1mmolm(-2) h(-1) at midday and midnight, respectively, with night fluxes exceeding those during the day by 39%. We attribute diel carbon dioxide flux variability mainly to changes in the water partial pressure of carbon dioxide. However, no consistent drivers could be identified across sites. Our findings highlight widespread day-night changes in fluvial carbon dioxide fluxes and suggest that the time of day greatly influences measured carbon dioxide fluxes across European streams. Diel patterns can greatly impact total stream carbon dioxide emissions, with 39% greater carbon dioxide flux during the night-time relative to the day-time, according to a study of 34 streams across Europe.

Aim: Although running waters are getting recognized as important methane sources, large‐scale geographical patterns of microorganisms controlling the net methane balance of streams are still unknown. Here we aim at describing community compositions of methanogenic and methanotrophic microorganisms at large spatial scales and at linking their abundances to potential sediment methane production (PMP) and oxidation rates (PMO). Location: The study spans across 16 European streams from northern Spain to northern Sweden and from western Ireland to western Bulgaria. Taxon: Methanogenic archaea and methane‐oxidizing microorganisms. Methods: To provide a geographical overview of both groups in a single approach, microbial communities and abundances were investigated via 16S rRNA gene sequencing, extracting relevant OTUs based on literature; both groups were quantified via quantitative PCR targeting mcrA and pmoA genes and studied in relation to environmental parameters, sediment PMP and PMO, and land use. Results: Diversity of methanogenic archaea was higher in warmer streams and of methanotrophic communities in southern sampling sites and in larger streams. Anthropogenically altered, warm and oxygen‐poor streams were dominated by the highly efficient methanogenic families Methanospirillaceae, Methanosarcinaceae and Methanobacteriaceae, but did not harbour any specific methanotrophic organisms. Contrastingly, sediment communities in colder, oxygen‐rich waters with little anthropogenic impact were characterized by methanogenic Methanosaetaceae, Methanocellaceae and Methanoflorentaceae and methanotrophic Methylococcaceae and Cd. Methanoperedens. Representatives of the methanotrophic Crenotrichaceae and Methylococcaceae as well as the methanogenic Methanoregulaceae were characteristic for environments with larger catchment area and higher discharge. PMP increased with increasing abundance of methanogenic archaea, while PMO rates did not show correlations with abundances of met

Groundwater is an essential resource providing water for societies and sustaining surface waters. Although groundwater at intermediate depth could be highly influential at regulating lake and river surface water chemistry, studies quantifying organic and inorganic carbon (C) species in intermediate depth groundwater are still rare. Here, we quantified dissolved and gaseous C species in the groundwater of a boreal catchment at 3- to 20-m depth. We found that the partial pressure of carbon dioxide (pCO(2)), the stable carbon isotopic composition of dissolved inorganic carbon (delta C-13-DIC), and pH showed a dependency with depth. Along the depth profile, a negative relationship was observed between pCO(2) and delta C-13-DIC and between pCO(2) and pH. We attribute the negative pCO(2)-pH relationship along the depth gradient to increased silicate weathering and decreased soil respiration. Silicate weathering consumes carbon dioxide (CO2) and release base cations, leading to increased pH and decreased pCO(2). We observed a positive relationship between delta C-13-DIC and depth, potentially due to diffusion-related fractionation in addition to isotopic discrimination during soil respiration. Soil CO2 may diffuse downward, resulting in a fractionation of the delta C-13-DIC. Additionally, the dissolved organic carbon at greater depth may be recalcitrant consisting of old degraded material with a greater fraction of the heavier C isotope. Our study provides increased knowledge about the C biogeochemistry of groundwater at intermediate depth, which is important since these waters likely contribute to the widespread CO2 oversaturation in boreal surface waters.

Groundwater is an essential resource providing water for societies and sustaining surface waters. Although groundwater at intermediate depth could be highly influential at regulating lake and river surface water chemistry, studies quantifying organic and inorganic carbon (C) species in intermediate depth groundwater are still rare. Here, we quantified dissolved and gaseous C species in the groundwater of a boreal catchment at 3- to 20-m depth. We found that the partial pressure of carbon dioxide (pCO(2)), the stable carbon isotopic composition of dissolved inorganic carbon (delta C-13-DIC), and pH showed a dependency with depth. Along the depth profile, a negative relationship was observed between pCO(2) and delta C-13-DIC and between pCO(2) and pH. We attribute the negative pCO(2)-pH relationship along the depth gradient to increased silicate weathering and decreased soil respiration. Silicate weathering consumes carbon dioxide (CO2) and release base cations, leading to increased pH and decreased pCO(2). We observed a positive relationship between delta C-13-DIC and depth, potentially due to diffusion-related fractionation in addition to isotopic discrimination during soil respiration. Soil CO2 may diffuse downward, resulting in a fractionation of the delta C-13-DIC. Additionally, the dissolved organic carbon at greater depth may be recalcitrant consisting of old degraded material with a greater fraction of the heavier C isotope. Our study provides increased knowledge about the C biogeochemistry of groundwater at intermediate depth, which is important since these waters likely contribute to the widespread CO2 oversaturation in boreal surface waters.

Groundwater is an essential resource providing water for societies and sustaining surface waters. Although groundwater at intermediate depth could be highly influential at regulating lake and river surface water chemistry, studies quantifying organic and inorganic carbon (C) species in intermediate depth groundwater are still rare. Here, we quantified dissolved and gaseous C species in the groundwater of a boreal catchment at 3- to 20-m depth. We found that the partial pressure of carbon dioxide (pCO(2)), the stable carbon isotopic composition of dissolved inorganic carbon (delta C-13-DIC), and pH showed a dependency with depth. Along the depth profile, a negative relationship was observed between pCO(2) and delta C-13-DIC and between pCO(2) and pH. We attribute the negative pCO(2)-pH relationship along the depth gradient to increased silicate weathering and decreased soil respiration. Silicate weathering consumes carbon dioxide (CO2) and release base cations, leading to increased pH and decreased pCO(2). We observed a positive relationship between delta C-13-DIC and depth, potentially due to diffusion-related fractionation in addition to isotopic discrimination during soil respiration. Soil CO2 may diffuse downward, resulting in a fractionation of the delta C-13-DIC. Additionally, the dissolved organic carbon at greater depth may be recalcitrant consisting of old degraded material with a greater fraction of the heavier C isotope. Our study provides increased knowledge about the C biogeochemistry of groundwater at intermediate depth, which is important since these waters likely contribute to the widespread CO2 oversaturation in boreal surface waters.

Groundwater is an essential resource providing water for societies and sustaining surface waters. Although groundwater at intermediate depth could be highly influential at regulating lake and river surface water chemistry, studies quantifying organic and inorganic carbon (C) species in intermediate depth groundwater are still rare. Here, we quantified dissolved and gaseous C species in the groundwater of a boreal catchment at 3- to 20-m depth. We found that the partial pressure of carbon dioxide (pCO(2)), the stable carbon isotopic composition of dissolved inorganic carbon (delta C-13-DIC), and pH showed a dependency with depth. Along the depth profile, a negative relationship was observed between pCO(2) and delta C-13-DIC and between pCO(2) and pH. We attribute the negative pCO(2)-pH relationship along the depth gradient to increased silicate weathering and decreased soil respiration. Silicate weathering consumes carbon dioxide (CO2) and release base cations, leading to increased pH and decreased pCO(2). We observed a positive relationship between delta C-13-DIC and depth, potentially due to diffusion-related fractionation in addition to isotopic discrimination during soil respiration. Soil CO2 may diffuse downward, resulting in a fractionation of the delta C-13-DIC. Additionally, the dissolved organic carbon at greater depth may be recalcitrant consisting of old degraded material with a greater fraction of the heavier C isotope. Our study provides increased knowledge about the C biogeochemistry of groundwater at intermediate depth, which is important since these waters likely contribute to the widespread CO2 oversaturation in boreal surface waters.

Groundwater is an essential resource providing water for societies and sustaining surface waters. Although groundwater at intermediate depth could be highly influential at regulating lake and river surface water chemistry, studies quantifying organic and inorganic carbon (C) species in intermediate depth groundwater are still rare. Here, we quantified dissolved and gaseous C species in the groundwater of a boreal catchment at 3- to 20-m depth. We found that the partial pressure of carbon dioxide (pCO(2)), the stable carbon isotopic composition of dissolved inorganic carbon (delta C-13-DIC), and pH showed a dependency with depth. Along the depth profile, a negative relationship was observed between pCO(2) and delta C-13-DIC and between pCO(2) and pH. We attribute the negative pCO(2)-pH relationship along the depth gradient to increased silicate weathering and decreased soil respiration. Silicate weathering consumes carbon dioxide (CO2) and release base cations, leading to increased pH and decreased pCO(2). We observed a positive relationship between delta C-13-DIC and depth, potentially due to diffusion-related fractionation in addition to isotopic discrimination during soil respiration. Soil CO2 may diffuse downward, resulting in a fractionation of the delta C-13-DIC. Additionally, the dissolved organic carbon at greater depth may be recalcitrant consisting of old degraded material with a greater fraction of the heavier C isotope. Our study provides increased knowledge about the C biogeochemistry of groundwater at intermediate depth, which is important since these waters likely contribute to the widespread CO2 oversaturation in boreal surface waters.

Large-scale studies are needed to identify the drivers of total mercury (THg) and monomethyl-mercury (MeHg) concentrations in aquatic ecosystems. Studies attempting to link dissolved organic matter (DOM) to levels of THg or MeHg are few and geographically constrained. Additionally, stream and river systems have been understudied as compared to lakes. Hence, the aim of this study was to examine the influence of DOM concentration and composition, morphological descriptors, land uses and water chemistry on THg and MeHg concentrations and the percentage of THg as MeHg (%MeHg) in 29 streams across Europe spanning from 41°N to 64°N. THg concentrations (0.06–2.78 ng L−1) were highest in streams characterized by DOM with a high terrestrial soil signature and low nutrient content. MeHg concentrations (7.8–159 pg L−1) varied non-systematically across systems. Relationships between DOM bulk characteristics and THg and MeHg suggest that while soil derived DOM inputs control THg concentrations, autochthonous DOM (aquatically produced) and the availability of electron acceptors for Hg methylating microorganisms (e.g. sulfate) drive %MeHg and potentially MeHg concentration. Overall, these results highlight the large spatial variability in THg and MeHg concentrations at the European scale, and underscore the importance of DOM composition on mercury cycling in fluvial systems.