Publications by authors named "Marcus B Wallin"

Unlabelled: Wetlands cover a small portion of the world, but have disproportionate influence on global carbon (C) sequestration, carbon dioxide and methane emissions, and aquatic C fluxes. However, the underlying biogeochemical processes that affect wetland C pools and fluxes are complex and dynamic, making measurements of wetland C challenging. Over decades of research, many observational, experimental, and analytical approaches have been developed to understand and quantify pools and fluxes of wetland C.

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Drainage for forestry has created ~ 1 million km of artificial waterways in Sweden, making it one of the largest human-induced environmental disturbances in the country. These extensive modifications of both peatland and mineral soil dominated landscapes still carry largely unknown, but potentially enormous environmental legacy effects. However, the consequences of contemporary ditch management strategies, such as hydrological restoration via ditch blocking or enhancing forest drainage to promote biomass production via ditch cleaning, on water resources and greenhouse gas (GHG) fluxes are unclear.

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Widespread increases in organic matter (OM) content of surface waters, as measured by color and organic carbon (OC), are a major issue for aquatic ecosystems. Long-term monitoring programs revealed the issue of "brownification", with climate change, land cover changes and recovery from acidification all suspected to be major drivers or contributing factors. While many studies have focused on the impact and drivers, fewer have followed up on whether brownification is continuing.

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Article Synopsis
  • - The study investigates the hydrological and biogeochemical processes of tropical rivers in Hainan Island, China, focusing on aspects like evaporation and aquatic photosynthesis.
  • - Measurements revealed that about 95% of dissolved inorganic carbon (DIC) in these rivers comes from modern, biogenic sources, indicating significant water turnover and changes in carbon balance.
  • - High rates of evaporation and aquatic primary production were predominantly found in narrow headwater segments, affecting spatial variations in dissolved solutes and providing insights into global carbon cycling.
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Streams and river networks are increasingly recognized as significant sources for the greenhouse gas nitrous oxide (N O). N O is a transformation product of nitrogenous compounds in soil, sediment and water. Agricultural areas are considered a particular hotspot for emissions because of the large input of nitrogen (N) fertilizers applied on arable land.

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Dissolved organic matter (DOM) from soils enters the aquatic environment via headwater streams. Thereafter, it is gradually transformed, removed by sedimentation, and mineralised. Due to the proximity to the terrestrial source and short water residence time, the extent of transformation is minimal in headwaters.

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It is well established that stream dissolved inorganic carbon (DIC) fluxes play a central role in the global C cycle, yet the sources of stream DIC remain to a large extent unresolved. Here, we explore large-scale patterns in δC-DIC from streams across Sweden to separate and further quantify the sources and sinks of stream DIC. We found that stream DIC is governed by a variety of sources and sinks including biogenic and geogenic sources, CO evasion, as well as in-stream processes.

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The stability of northern peatland's carbon (C) store under changing climate is of major concern for the global C cycle. The aquatic export of C from boreal peatlands is recognized as both a critical pathway for the remobilization of peat C stocks as well as a major component of the net ecosystem C balance (NECB). Here, we present a full year characterization of radiocarbon content ( C) of dissolved organic carbon (DOC), carbon dioxide (CO ), and methane (CH ) exported from a boreal peatland catchment coupled with C characterization of the catchment's peat profile of the same C species.

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Global stream and river greenhouse gas emissions seem to be as large as the oceanic C uptake. However, stream and river emissions are uncertain until both spatial and temporal variability have been quantified. Here we investigated in detail the stream CH and CO emissions within a hemiboreal catchment in Southwest Sweden primarily covered by coniferous forest.

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Half of the world's forest is in boreal and sub-boreal ecozones, containing large carbon stores and fluxes. Carbon lost from headwater streams in these forests is underestimated. We apply a simple stable carbon isotope idea for quantifying the CO2 loss from these small streams; it is based only on in-stream samples and integrates over a significant distance upstream.

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Evasion of gaseous carbon (C) from streams is often poorly quantified in landscape C budgets. Even though the potential importance of the capillary network of streams as C conduits across the land-water-atmosphere interfaces is sometimes mentioned, low-order streams are often left out of budget estimates due to being poorly characterized in terms of gas exchange and even areal surface coverage. We show that evasion of C is greater than all the total dissolved C (both organic and inorganic) exported downstream in the waters of a boreal landscape.

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