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Lakes in permafrost regions are dynamic landscape components and play an important role for climate change feedbacks. Lake processes such as mineralization and flocculation of dissolved organic carbon (DOC), one of the main carbon fractions in lakes, contribute to the greenhouse effect and are part of the global carbon cycle. These processes are in the focus of climate research, but studies so far are limited to specific study regions. In our synthesis, we analyzed 2167 water samples from 1833 lakes across the Arctic in permafrost regions of Alaska, Canada, Greenland, and Siberia to provide first pan-Arctic insights for linkages between DOC concentrations and the environment. Using published data and unpublished datasets from the author team, we report regional DOC differences linked to latitude, permafrost zones, ecoregions, geology, near-surface soil organic carbon contents, and ground ice classification of each lake region. The lake DOC concentrations in our dataset range from 0 to 1130 mg L−1 (10.8 mg L−1 median DOC concentration). Regarding the permafrost regions of our synthesis, we found median lake DOC concentrations of 12.4 mg L−1 (Siberia), 12.3 mg L−1 (Alaska), 10.3 mg L−1 (Greenland), and 4.5 mg L−1 (Canada). Our synthesis shows a significant relationship between lake DOC concentration and lake ecoregion. We found higher lake DOC concentrations at boreal permafrost sites compared to tundra sites. We found significantly higher DOC concentrations in lakes in regions with ice-rich syngenetic permafrost deposits (yedoma) compared to non-yedoma lakes and a weak but significant relationship between soil organic carbon content and lake DOC concentration as well as between ground ice content and lake DOC. Our pan-Arctic dataset shows that the DOC concentration of a lake depends on its environmental properties, especially on permafrost extent and ecoregion, as well as vegetation, which is the most important driver of lake DOC in this study. This new dataset will be fundamental to quantify a pan-Arctic lake DOC pool for estimations of the impact of lake DOC on the global carbon cycle and climate change.

Coccolithophores are globally important marine calcifying phytoplankton that utilize a haplo-diplontic life cycle. The haplo-diplontic life cycle allows coccolithophores to divide in both life cycle phases and potentially expands coccolithophore niche volume. Research has, however, to date largely overlooked the life cycle of coccolithophores and has instead focused on the diploid life cycle phase of coccolithophores. Through the synthesis and analysis of global scanning electron microscopy (SEM) coccolithophore abundance data (n=2534), we find that calcified haploid coccolithophores generally constitute a minor component of the total coccolithophore abundance (≈ 2 %–15 % depending on season). However, using case studies in the Atlantic Ocean and Mediterranean Sea, we show that, depending on environmental conditions, calcifying haploid coccolithophores can be significant contributors to the coccolithophore standing stock (up to ≈30 %). Furthermore, using hypervolumes to quantify the niche of coccolithophores, we illustrate that the haploid and diploid life cycle phases inhabit contrasting niches and that on average this allows coccolithophores to expand their niche by ≈18.8 %, with a range of 3 %–76 % for individual species. Our results highlight that future coccolithophore research should consider both life cycle stages, as omission of the haploid life cycle phase in current research limits our understanding of coccolithophore ecology. Our results furthermore suggest a different response to nutrient limitation and stratification, which may be of relevance for further climate scenarios. Our compilation highlights the spatial and temporal sparsity of SEM measurements and the need for new molecular techniques to identify uncalcified haploid coccolithophores. Our work also emphasizes the need for further work on the carbonate chemistry niche of the coccolithophore life cycle.

Lakes in permafrost regions are dynamic landscape components and play an important role for climate change feedbacks. Lake processes such as mineralization and flocculation of dissolved organic carbon (DOC), one of the main carbon fractions in lakes, contribute to the greenhouse effect and are part of the global carbon cycle. These processes are in focus of climate research but studies so far are limited to specific study regions. In our synthesis, we analysed 2,167 water samples from 1,833 lakes across the Arctic in permafrost regions of Alaska, Canada, Greenland, and Siberia to provide first pan-Arctic insights for linkages between DOC concentrations and the environment. Using published data and unpublished datasets from the author team we report regional DOC differences linked to latitude, permafrost zones, ecoregions, geology, near-surface soil organic carbon contents, and ground ice classification of each lake region. The lake DOC concentrations in our dataset range from 0 mg L−1 to 1,130 mg L−1 (10.8 mg L−1 median DOC concentration). Regarding the permafrost regions of our synthesis, we found median lake DOC concentrations of 12.4 mg L−1 (Siberia), 12.3 mg L−1 (Alaska), 10.3 mg L−1 (Greenland), and 4.5 mg L−1 (Canada). Our synthesis shows a significant relationship of lake DOC concentration and ecoregion of the lake. We found higher lake DOC concentrations in boreal permafrost sites compared to tundra sites. About 22 % of the lakes in our extensive dataset are located in regions with ice-rich syngenetic permafrost deposits (yedoma). Yedoma contains large amounts of easily erodible organic carbon and we found significantly higher DOC concentrations in yedoma lakes compared to non-yedoma lakes. Compared to previous studies we found a weak significant relationship of soil organic carbon content and lake DOC concentration as well as between ground-ice content and lake DOC. Our pan-Arctic dataset shows that the DOC concentration of a lake strongly depends on its environmental properties, especially on permafrost extent and ecoregion, as well as vegetation, which is the most important driver of lake DOC in this study. This new dataset will be fundamental to quantify a pan-Arctic lake DOC pool for estimations of the impact of lake DOC on the global carbon cycle and climate change.

Permafrost ground is one of the largest repositories of terrestrial organic carbon and might become or already is a carbon source in response to ongoing global warming. With this study of syngenetically frozen, ice-rich and organic carbon (OC)-bearing Yedoma and associated alas deposits in central Yakutia (Republic of Sakha), we aimed to assess the local sediment deposition regime and its impact on permafrost carbon storage. For this purpose, we investigated the Yukechi alas area (61.76495∘ N, 130.46664∘ E), which is a thermokarst landscape degrading into Yedoma in central Yakutia. We retrieved two sediment cores (Yedoma upland, 22.35 m deep, and alas basin, 19.80 m deep) in 2015 and analyzed the biogeochemistry, sedimentology, radiocarbon dates and stable isotope geochemistry. The laboratory analyses of both cores revealed very low total OC (TOC) contents (<0.1 wt %) for a 12 m section in each core, whereas the remaining sections ranged from 0.1 wt % to 2.4 wt % TOC. The core sections holding very little to no detectable OC consisted of coarser sandy material were estimated to be between 39 000 and 18 000 BP (years before present) in age. For this period, we assume the deposition of organic-poor material. Pore water stable isotope data from the Yedoma core indicated a continuously frozen state except for the surface sample, thereby ruling out Holocene reworking. In consequence, we see evidence that no strong organic matter (OM) decomposition took place in the sediments of the Yedoma core until today. The alas core from an adjacent thermokarst basin was strongly disturbed by lake development and permafrost thaw. Similar to the Yedoma core, some sections of the alas core were also OC poor (<0.1 wt %) in 17 out of 28 samples. The Yedoma deposition was likely influenced by fluvial regimes in nearby streams and the Lena River shifting with climate. With its coarse sediments with low OC content (OC mean of 5.27 kg m−3), the Yedoma deposits in the Yukechi area differ from other Yedoma sites in North Yakutia that were generally characterized by silty sediments with higher OC contents (OC mean of 19 kg m−3 for the non-ice wedge sediment). Therefore, we conclude that sedimentary composition and deposition regimes of Yedoma may differ considerably within the Yedoma domain. The resulting heterogeneity should be taken into account for future upscaling approaches on the Yedoma carbon stock. The alas core, strongly affected by extensive thawing processes during the Holocene, indicates a possible future pathway of ground subsidence and further OC decomposition for thawing central Yakutian Yedoma deposits.

Industrial-scale mining of deep-sea polymetallic nodules will remove nodules in large areas of the sea floor. The regrowth of the nodules by metal precipitation is estimated to take millions of years. Thus, for future mining impact studies, it is crucial to understand the role of nodules in shaping microbial diversity and function in deep-sea environments. Here we investigated microbial-community composition based on 16S rRNA gene sequences retrieved from sediments and nodules of the Peru Basin (4130–4198 m water depth). The nodule field of the Peru Basin showed a typical deep-sea microbiome, with dominance of the classes Gammaproteobacteria, Alphaproteobacteria, Deltaproteobacteria, and Acidimicrobiia. Nodules and sediments host distinct bacterial and archaeal communities, with nodules showing lower diversity and a higher proportion of sequences related to potential metal-cycling Bacteria (i.e. Magnetospiraceae, Hyphomicrobiaceae), bacterial and archaeal nitrifiers (i.e. AqS1, unclassified Nitrosomonadaceae, Nitrosopumilus, Nitrospina, Nitrospira), and bacterial sequences found in the oceanic crust, nodules, hydrothermal deposits, and sessile fauna. Sediment and nodule communities overall shared a low proportion of operational taxonomic units (OTUs; 21 % for Bacteria and 19 % for Archaea). Our results show that nodules represent a specific ecological niche (i.e. hard substrate, high metal concentrations, and sessile fauna), with a potentially relevant role in organic-carbon degradation. Differences in nodule community composition (e.g. Mn-cycling bacteria, nitrifiers) between the Clarion–Clipperton Fracture Zone (CCZ) and the Peru Basin suggest that changes in environmental setting (e.g. sedimentation rates) also play a significant role in structuring the nodule microbiome.

The extracellular concentration of H2O2 in surface aquatic environments is controlled by a balance between photochemical production and the microbial synthesis of catalase and peroxidase enzymes to remove H2O2 from solution. In any kind of incubation experiment, the formation rates and equilibrium concentrations of reactive oxygen species (ROSs) such as H2O2 may be sensitive to both the experiment design, particularly to the regulation of incident light, and the abundance of different microbial groups, as both cellular H2O2 production and catalase–peroxidase enzyme production rates differ between species. Whilst there are extensive measurements of photochemical H2O2 formation rates and the distribution of H2O2 in the marine environment, it is poorly constrained how different microbial groups affect extracellular H2O2 concentrations, how comparable extracellular H2O2 concentrations within large-scale incubation experiments are to those observed in the surface-mixed layer, and to what extent a mismatch with environmentally relevant concentrations of ROS in incubations could influence biological processes differently to what would be observed in nature. Here we show that both experiment design and bacterial abundance consistently exert control on extracellular H2O2 concentrations across a range of incubation experiments in diverse marine environments. During four large-scale (>1000 L) mesocosm experiments (in Gran Canaria, the Mediterranean, Patagonia and Svalbard) most experimental factors appeared to exert only minor, or no, direct effect on H2O2 concentrations. For example, in three of four experiments where pH was manipulated to 0.4–0.5 below ambient pH, no significant change was evident in extracellular H2O2 concentrations relative to controls. An influence was sometimes inferred from zooplankton density, but not consistently between different incubation experiments, and no change in H2O2 was evident in controlled experiments using different densities of the copepod Calanus finmarchicus grazing on the diatom Skeletonema costatum (<1 % change in [H2O2] comparing copepod densities from 1 to 10 L−1). Instead, the changes in H2O2 concentration contrasting high- and low-zooplankton incubations appeared to arise from the resulting changes in bacterial activity. The correlation between bacterial abundance and extracellular H2O2 was stronger in some incubations than others (R2 range 0.09 to 0.55), yet high bacterial densities were consistently associated with low H2O2. Nonetheless, the main control on H2O2 concentrations during incubation experiments relative to those in ambient, unenclosed waters was the regulation of incident light. In an open (lidless) mesocosm experiment in Gran Canaria, H2O2 was persistently elevated (2–6-fold) above ambient concentrations; whereas using closed high-density polyethylene mesocosms in Crete, Svalbard and Patagonia H2O2 within incubations was always reduced (median 10 %–90 %) relative to ambient waters.

The speciation of dissolved iron (DFe) in the ocean is widely assumed to consist almost exclusively of Fe(III)-ligand complexes. Yet in most aqueous environments a poorly defined fraction of DFe also exists as Fe(II), the speciation of which is uncertain. Here we deploy flow injection analysis to measure in situ Fe(II) concentrations during a series of mesocosm/microcosm/multistressor experiments in coastal environments in addition to the decay rate of this Fe(II) when moved into the dark. During five mesocosm/microcosm/multistressor experiments in Svalbard and Patagonia, where dissolved (0.2 µm) Fe and Fe(II) were quantified simultaneously, Fe(II) constituted 24 %–65 % of DFe, suggesting that Fe(II) was a large fraction of the DFe pool. When this Fe(II) was allowed to decay in the dark, the vast majority of measured oxidation rate constants were less than calculated constants derived from ambient temperature, salinity, pH, and dissolved O2. The oxidation rates of Fe(II) spikes added to Atlantic seawater more closely matched calculated rate constants. The difference between observed and theoretical decay rates in Svalbard and Patagonia was most pronounced at Fe(II) concentrations <2 nM, suggesting that the effect may have arisen from organic Fe(II) ligands. This apparent enhancement of Fe(II) stability under post-bloom conditions and the existence of such a high fraction of DFe as Fe(II) challenge the assumption that DFe speciation in coastal seawater is dominated by ligand bound-Fe(III) species.

Permafrost ground is one of the largest repositories of stored terrestrial natural carbon and might become a carbon source with ongoing global warming. In particular, syngenetically frozen ice-rich Yedoma deposits originating from the late Pleistocene store a large amount of carbon. This carbon has not yet become part of the recent carbon cycle. With this study of Yedoma and associated Alas deposits in Central Yakutia we aim to understand the local sediment genesis and its effect on permafrost carbon storage. For this purpose, we investigated the Yukechi Alas area (61.76495° N, 130.46664° E), a thermokarst landscape degrading into Yedoma in Central Yakutia. Two sediment cores (Yedoma upland, 22.35 m depth, and Alas basin, 19.80 m depth) were drilled in 2015. We analyzed for ice content, total carbon and total nitrogen content, total organic carbon content, stable oxygen and hydrogen isotopes, stable carbon isotopes, mass specific magnetic susceptibility, grain size distribution, and radiocarbon ages. Samples taken from both cores were radiocarbon-dated up to 50,000 years before present. The laboratory analyses of both cores revealed very low carbon contents down to several meters depth. Those core parts holding very little to no detectable carbon consist of coarser sandy material estimated to an age between 39,000 and 18,000 years before present. For this period we assume sediment input of organic-poor material. Water isotope data derived from pore ice within the Yedoma core indicate a continuously cold state of the lower core parts, thereby ruling out a potential theory of Holocene influence. In consequence, we conclude that no strong organic matter decomposition took place in the sediments of the Yedoma core until today. In contrast, the Alas core from an adjacent thermokarst basin was strongly disturbed by lake development and permafrost thaw, and accordingly its sediment and carbon characteristics differed from those of the Yedoma core. The Alas core shows homogeneous ice content and the water isotope characteristics of a slightly more decomposed organic material; the findings of very carbon-poor core sections from the Yedoma core can be duplicated. The Yedoma deposition was likely influenced by fluvial regimes in nearby streams and the Lena River shifting with climate. The low carbon content and the clear stratigraphical layering of different sediment types suggest that the Yedoma deposits in the Yukechi area differ from other Yedoma sites regarding carbon stock and sedimentological composition. We conclude that sedimentary composition and deposition regimes of Yedoma may differ significantly within the Yedoma domain. The resulting heterogeneity should be taken into account for upscaling approaches on the Yedoma carbon stock. The Alas core gives clear insights into the future development of Cenral Yakutian Yedoma deposits.

The marine silicon cycle is intrinsically linked with carbon cycling in the oceans via biological production of silica by a wide range of organisms. The stable silicon isotopic composition (denoted by δ30Si) of siliceous microfossils extracted from sediment cores can be used as an archive of past oceanic silicon cycling. However, the silicon isotopic composition of biogenic silica has only been measured in diatoms, sponges and radiolarians, and isotopic fractionation relative to seawater is entirely unknown for many other silicifiers. Furthermore, the biochemical pathways and mechanisms that determine isotopic fractionation during biosilicification remain poorly understood. Here, we present the first measurements of the silicon isotopic fractionation during biosilicification by loricate choanoflagellates, a group of protists closely related to animals. We cultured two species of choanoflagellates, Diaphanoeca grandis and Stephanoeca diplocostata, which showed consistently greater isotopic fractionation (approximately −5 ‰ to −7 ‰) than cultured diatoms (−0.5 ‰ to −2.1 ‰). Instead, choanoflagellate silicon isotopic fractionation appears to be more similar to sponges grown under similar dissolved silica concentrations. Our results highlight that there is a taxonomic component to silicon isotope fractionation during biosilicification, possibly via a shared or related biochemical transport pathway. These findings have implications for the use of biogenic silica δ30Si produced by different silicifiers as proxies for past oceanic change.

Bottom trawling in the deep sea is one of the main drivers of sediment resuspension, eroding the seafloor and altering the content and composition of sedimentary organic matter (OM). The physical and biogeochemical impacts of bottom trawling were studied on the continental slope of the Gulf of Castellammare, Sicily (southwestern Mediterranean), through the analysis of two triplicate sediment cores collected at trawled and untrawled sites (∼550 m water depth) during the summer of 2016. Geochemical and sedimentological parameters (excess 210Pb, excess 234Th, 137Cs, dry bulk density, and grain size), elemental (organic carbon and nitrogen) and biochemical composition of sedimentary OM (proteins, carbohydrates, lipids), as well as its freshness (phytopigments) and degradation rates were determined in both coring locations. The untrawled site had a sedimentation rate of 0.15 cm yr−1 and presented a 6 cm thick surface mixed layer that contained siltier sediment with low excess 210Pb concentrations, possibly resulting from the resuspension, posterior advection, and eventual deposition of coarser and older sediment from adjacent trawling grounds. In contrast, the trawled site was eroded and presented compacted century-old sediment highly depleted in OM components, which were between 20 % and 60 % lower than those in the untrawled site. However, the upper 2 cm of the trawled site consisted of recently accumulated sediments enriched in excess 234Th, excess 210Pb, and phytopigments, while OM contents were similar to those from the untrawled core. This fresh sediment supported protein turnover rates of 0.025 d−1, which doubled those quantified in surface sediments of the untrawled site. The enhancement of remineralization rates in surface sediment of the trawled site was associated with the arrival of fresh particles on a chronically trawled deep-sea region that is generally deprived of OM. We conclude that the detrimental effects of bottom trawling can be temporarily and partially abated by the arrival of fresh and nutritionally rich OM, which stimulate the response of benthic communities. However, these ephemeral deposits are likely to be swiftly eroded due to the high trawling frequency over fishing grounds, highlighting the importance of establishing science-based management strategies to mitigate the impacts of bottom trawling.