Browning of surface waters, as a result of increasing dissolved organic carbon and iron concentrations, is a widespread phenomenon with implications to the structure and function of aquatic ecosystems. In this article, we provide an overview of the consequences of browning in relation to ecosystem services, outline what the underlying drivers and mechanisms of browning are, and specifically focus on exploring potential mitigation measures to locally counteract browning. These topical concepts are discussed with a focus on Scandinavia, but are of relevance also to other regions. Browning is of environmental concern as it leads to, e.g., increasing costs and risks for drinking water production, and reduced fish production in lakes by limiting light penetration. While climate change, recovery from acidification, and land-use change are all likely factors contributing to the observed browning, managing the land use in the hydrologically connected parts of the landscape may be the most feasible way to counteract browning of natural waters.
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The term browning (or brownification) refers to a considerable increase in water color (Fig. 1) reported for a vast number of northern freshwaters during recent decades (Monteith et al. 2007; de Wit et al. 2016). This browning has been mainly attributed to rising concentrations of terrestrially derived dissolved organic carbon (DOC), but rising iron (Fe) concentrations also contribute to the increase in water color (Weyhenmeyer et al. 2014; Fig. 2). Browning is an environmental concern in many freshwaters, since it has important ecological consequences by affecting water quality as well as the structure and function of the aquatic ecosystems (Solomon et al. 2015; Creed et al. 2018). Previous studies have suggested important implications also for ecosystem services that freshwaters provide, e.g., by affecting the fish community and production, and other aspects linking to recreational values (Van Dorst et al. 2018). Moreover, many freshwaters that are sources of drinking water are undergoing browning, with associated health risks and enhanced costs for production of clean and safe potable water (Lavonen et al. 2013).
While browning is observed on a vast geographical scale, not all waters are subject to this change. For instance, significant increases in DOC and Fe were found in 59 and 28% of investigated sites, respectively, in a study covering 340 surface waters in northern Europe and North America (Björnerås et al. 2017). Some of the largest and most dramatic increases have been recorded in boreal regions, which is likely due to the high amounts of organic carbon available for transport to water bodies. The boreal region is characterized by enormous stores of peat, containing at least one-third of the world’s terrestrial carbon pool (Bradshaw and Warkentin 2015). This large pool of soil carbon is several orders of magnitude more prone to degradation from climate warming than in other biomes (Crowther et al. 2016). Increases in DOC and Fe concentrations are also more frequent in freshwaters where coniferous tree covers dominate than in areas where, e.g., agriculture is the major land use (Björnerås et al. 2017), reflecting the relationship between soil pools and export of DOC and Fe to freshwaters (Weyhenmeyer et al. 2012). Furthermore, hydrological connectivity also regulates how DOC is transported from organic soils to streams (Laudon et al. 2011), suggesting that local and regional differences in climate and land use can enhance or reduce the effect on freshwaters. Finally, waters with a longer residence time, allowing for in-water processing and loss of DOC and Fe from the water column (Weyhenmeyer et al. 2014; Tiwari et al. 2017), are generally less responsive to browning.
There are still many uncertainties regarding the actual drivers and mechanisms behind browning, and consequently also pertaining to any measures that may be implemented to mitigate the continuing trend. It has been argued that the observed trajectory is driven by processes associated to climate change, which enhance terrestrial productivity, alter vegetation cover, and affect the hydrological control on production and transport of terrestrial DOC (de Wit et al. 2016; Finstad et al. 2016). Another proposed driver is the long-term change in atmospheric sulfur (S) deposition—which has declined strongly since the peak in the 1980s—allowing for recovery from acidification and increasing the solubility and transport of DOC from soils (Monteith et al. 2007; de Wit et al. 2016). Finally, a few recent studies invoke that land-use change may have a more important role to browning of freshwaters than previously thought (Schelker et al. 2012; Meyer-Jacob et al. 2015; Kritzberg 2017).
Sediment records indicate that DOC concentrations were significantly higher before the widespread human catchment disturbance, including forest grazing, farming, and land drainage, which intensified around ad 1500, and air pollution effects from around 1900, and these studies identify a DOC minimum around the early or mid-twentieth century (Meyer-Jacob et al. 2015). Regardless if current browning represents a return to what may be viewed as a more “natural state,” it has important negative consequences at several different levels. Thus, the motivation for this review is not to identify or strive toward a reference state with regards to water color, but to explore options to counteract browning. If land use and management are indeed factors involved, opportunities arise for local actions in order to mitigate browning.
Browning has been subject to considerable interest, and several scientific reviews effectively address its ecological effects and various aspects thereof (Solomon et al. 2015; Creed et al. 2018). Here, we aim at providing an interface between scientific knowledge and societal demands, i.e., to provide stakeholders and decision makers with potential measures to counteract browning, and thereby improve the ecosystem services provided by freshwater ecosystems. To this effect, we have organized the paper to provide an overview of consequences of browning for ecosystem services (Why is it a problem?) and of the underlying drivers and mechanisms (Where does the problem come from?), and with the emphasis on a discussion of possible mitigation measures (Are there ways to solve the problem?). We also address broader implications in terms of synergies and conflicts with other environmental issues. The options to mitigate browning should be viewed as hypotheses based on our current knowledge about controls of production and export of DOC and Fe in the landscape. In our final remarks, we provide specific suggestions for further research efforts and policy recommendations. Consequences, drivers, and mitigation measures of browning are vast areas to summarize, and therefore only a selection of relevant articles are cited, with priority laid to studies that are central and of relevance to environmental conditions of Sweden.
While browning is a problem in many regions, the initiative for this paper came from stakeholders in Sweden with interests in systems where browning has a tangible negative effect on ecosystem services, such as drinking water production, biodiversity, and recreational values. Therefore, we use Sweden as a starting point for our discussion, but most conclusions and suggestions apply to a wide range of lakes, streams, and rivers in boreal regions, and to browning as a general concern.
Consequences of browning for ecosystem services
Numerous studies reveal strong impacts of browning on the organism structure and ecological processes in freshwaters. The concept of ecosystem services links ecological processes with human well-being, and is used here to illustrate which human benefits may be reduced or lost as browning proceeds. The consequences of browning are discussed following the four categories of ecosystem services—provisionary (drinking water production), cultural (outdoor experience), supportive (biodiversity), and regulating (biogeochemical processes). Moreover, browning may also have synergistic effects with other environmental threats, such as warming and eutrophication.
Drinking water production
Clean water is one of the 16 UN sustainably development goals and plays a fundamental role for the development of societies, industrial and economic growth, as well as for human health. This imposes a strong incentive for society to provide drinking water of high quality. In many countries, surface waters (lakes and rivers) are the main source for drinking water production. In Sweden, for instance, 50% of the drinking water produced is drawn from surface waters, 25% from artificial infiltration of surface water, and 25% from groundwater (http://www.svensktvatten.se), suggesting that 75% of the drinking water supply is potentially influenced by browning (Fig. 3). In addition, lowering of groundwater levels, which is widely observed as a result of climate change and human outtake, will further increase our reliance on surface waters for drinking water production.
In drinking water-treatment plants (DWTPs), steps are included to reduce DOC concentrations. There are no legislative limits regarding DOC in drinking water, but there are recommendations, e.g. in Sweden, it is recommended that DOC concentrations stay below 4 mg L−1 (Köhler et al. 2016). Commonly, DOC is reduced in DWTP by chemical precipitation with FeCl3, AlCl3, or Al2(SO4)3. With browning, DOC concentrations in the incoming water increases, and more chemicals are required for precipitation, which is in direct conflict with general international legislation and recommendations to reduce chemical usage. The enhanced use of chemicals due to browning is estimated to increase the cost of producing drinking water by approximately 5% in Sweden. Moreover, precipitation of DOC with chemicals is never complete, and the remaining DOC interferes with subsequent purification steps, such as active carbon filters, UV-disinfection, and chlorination. Therefore, browning is also associated with risks that the drinking water contains elevated levels of pharmaceutical residues and potentially carcinogenic chlorinated organic compounds (Lavonen et al. 2013), and that microbial growth in the distribution network is enhanced. In addition to increasing concentrations of DOC, browning also comes with a change in the chemical character of DOC, and the chemical fractions differ in their amenability to removal and formation of disinfection byproducts (Ritson et al. 2014). Finally, if DOC concentrations are high (> 15 mg DOC L−1), chemical precipitation is no longer efficient, forcing DWTPs either to change their raw water source, which comes with major infrastructural costs, or to invest in ultra- or nanofiltration techniques.
Brown water is seen as a negative factor for recreational value
There are general concerns about the impact of browning on recreational use and tourism (Valinia et al. 2012). Several studies have identified human preferences for clear water, for example, on Fraser Island in Australia, where only 1% of the respondents preferred to swim in brown lakes, whereas most people preferred clear lakes, streams, swimming pools, or the ocean (Hadwen and Arthington 2003). Moreover, in a study using geotagged photographs from social media, clear water increased the perceived recreational value of lakes, and visitors were willing to travel 56 min extra for every meter increase in water clarity (Keeler et al. 2015). Browning is also sometimes associated with increased abundances of the algae Gonyostomum semen (Rengefors et al. 2012), which can cause skin irritation and allergic reaction, thereby strongly reducing the recreational value.
Effects on fish and angling opportunities
At moderate levels, browning can promote fish production since terrestrially derived organic matter may act as an energy and nutrient subsidy (Finstad et al. 2014), and also reduce harmful UV radiation from the sun (Williamson et al. 1996). However, when the visibility for predatory fish decreases beyond a threshold level because of browning, their growth is impaired (Ranåker et al. 2014), rendering brown-water lakes less attractive for anglers. Moreover, primary production declines at high water color leading to lower overall food web production, including fish biomass (Karlsson et al. 2009). Algae produce unsaturated fatty acids essential for birds and mammals, and because browning often promotes phytoplankton species that produce less fatty acids, fish in brown lakes are less “nutritious” than fish in other lakes (Taipale et al. 2016). Humic substances, which dominate terrestrially derived DOC, also exert a mild chemical stress on many aquatic organisms (Steinberg et al. 2006), and have a complex role by both lowering pH and protecting against aluminum toxicity in fish (Serrano et al. 2008). Hence, the relation between water color and fish biomass is often described as hump shaped, where a mild browning increases fish production, whereas highly brown water reduces fish production (Finstad et al. 2014), and thereby angling opportunities.
Brown water and high DOC concentrations are generally associated with low productivity and diversity of phytoplankton communities (Jones, 1992), which often become dominated by mixotrophic species, i.e., algae that rely both on photosynthesis and heterotrophic uptake of bacteria or other algae (Wilken et al. 2018). One such species is G. semen, which often dominates in brown-water lakes (Trigal et al. 2011). However, although browning may have some effect on the phytoplankton species composition, it has a relatively limited effect on the diversity (Lebret et al. 2018). Moreover, a direct effect of the reduced light penetration is that pelagic species become favored over benthic species (Ask et al. 2009), and that macrophyte species with capacity to elongate their stem and reach the surface, such as Elodea canadensis, may become dominant (Mormul et al. 2012).
Biogeochemical consequences that follow with browning
In the last decade, freshwater DOC has been recognized as a major component of the global carbon cycle, and inland waters have been identified as key contributors to C emissions (as a greenhouse gas) to the atmosphere (Tranvik et al. 2009). The terrestrial DOC that is exported to surface waters is to a large extent processed there, either mineralized to carbon dioxide or methane that is emitted to the atmosphere, or aggregated and sedimented (Tranvik et al. 2009). Browning and rising DOC concentrations could therefore increase the flux of greenhouse gases to the atmosphere.
Since both DOC and Fe act as carriers of other elements, changes in many chemical variables occur as a consequence of browning. For instance, DOC influences the speciation, mobility, and bioavailability of most cationic metals including mercury (Hg; Lydersen et al. 2002). Higher Hg levels in fish and invertebrates are generally found in aquatic systems with higher DOC concentration (Creed et al. 2018). Aluminum, zinc, and copper have increased widely, partly linked to the increased browning as DOC forms strong organic complexes, which favor mobilization and transport from soils to surface waters (Oni et al. 2013). Iron also acts as an important vector of highly toxic metals such as lead, arsenic, and vanadium, which have increased in concentrations in many waters (Wällstedt et al. 2010). Browning also brings micro- and macronutrients that can support phytoplankton production, although it is only at rather low DOC concentrations that this fueling effect on primary production overrides that of increased light attenuation (Creed et al. 2018). Finally, browning affects the recovery from acidification as DOC acts as an organic acid and hence reduces the expected recovery associated with the decline in mineral acid deposition (Futter et al. 2014).
Synergies with other aspects of environmental change
Browning interacts with other large-scale environmental changes, such as climate warming and eutrophication, which may lead to additive or even synergistic effects. For example, eutrophication and browning will together reduce water clarity more than each of them alone and thereby reduce the area available for benthic macrophytes, and the feeding success of predatory fish (Ranåker et al. 2014). Although browning alone may not always stimulate cyanobacteria (Hansson et al. 2013), the cyanobacteria Microcystis spp. benefit when climate warming and browning act together (Urrutia-Cordero et al. 2016). Most studies on browning have been performed in freshwater systems, but large amounts of humic substances also enter the sea through rivers (Svedäng et al. 2018). Although browning effects in saltwater are still less pronounced than in freshwaters, phytoplankton production is suppressed, thereby shifting the carbon flow toward microbial heterotrophy also in coastal areas of the sea (Wikner and Andersson 2012). In coastal regions where climate warming will lead to higher precipitation, and thereby higher runoff, this may eventually result in reduced fish production.
Drivers and mechanisms
The principal drivers that have been proposed to contribute to the widespread browning are climate change/weather patterns, acid deposition, and land cover/land use. The mechanisms by which these different drivers may affect export of DOC and Fe from surrounding soils are outlined in Fig. 4 and Box 1. To the extent that reduced acid deposition has been the major driver, browning will likely eventually level off and represent a return to a more “natural state” (Monteith et al. 2007; de Wit et al. 2016). If reduced acid deposition were the sole driver of browning, we would stand without measures to counteract it. However, some historical records do not corroborate that water color was suppressed in response to increasing S deposition (Kritzberg 2017), pointing to the role of other drivers than just recovery from acidification to browning. Other studies suggest that increasing primary production and accumulation of soil organic carbon, driven primarily by expanding intensive coniferous forestry and amplified by longer growing seasons and varying precipitation patterns, are major factors behind the current browning trend (Finstad et al. 2016).
Time series analyses clearly demonstrate that oscillations in water color with rather large amplitude relate to weather/climate variability, e.g., dry versus wet periods (Erlandsson et al. 2008). While browning on the centennial scale thus far does not seem to be primarily explained by any long-term trend in precipitation (Kritzberg 2017), a further increase in precipitation will likely enhance browning, except for systems in high precipitation areas (de Wit et al. 2016).
Thus, what we can say with certainty, based on current knowledge about DOC and Fe mobilization, is that water color will continue to vary widely in response to variable weather and air pollution loads, and is likely to continue to pose environmental and aesthetic problems. Acknowledging the human influence on terrestrial primary production and organic carbon accumulation means that our best chance to control/mitigate browning is by managing the land use in the hydrologically connected parts of the landscape (Fig. 4).
The DOC flux to headwater streams is largely determined by the quantity and quality of organic matter in wetlands (Creed et al. 2008) and organic-rich riparian forest soils (McGlynn and McDonnell 2003), which provide the main sources for downstream environments (Tiwari et al. 2017). Thus, to properly understand the spatial and temporal aspects of DOC in surface waters hydrological connectivity and transport mechanisms between soil organic matter (SOM) sources and surface waters must be considered simultaneously (Laudon et al. 2011). The quantity and quality of the exported DOC depend largely on land use that dictates the type of vegetation cover (Kothawala et al. 2015; Kritzberg 2017). How and when SOM pools are linked to surface waters depends on the groundwater level and subsurface groundwater flow paths (Laudon et al. 2011). When the groundwater level is high and the organic soil layers saturated, water is in close contact with relatively recently deposited organic matter within the surface peat that leaches from the SOM pool (Nieminen et al. 2018). During precipitation events, or snowmelt, groundwater levels peak and DOC export to surface waters is at its highest (Laudon et al. 2011). Generally, subsurface groundwater flow paths follow surface topography and are concentrated in localized areas in the glacial till landscape, which feed into streams at discrete points (Ploum et al. 2018), making them important controls for water quality. Once in the surface water, the retention time affects the time during which DOC can be processed and lost (Stanley et al. 2012).
Understanding the linkages between the distribution and quality of the SOM, groundwater level and flow paths, and in-water processing, can help us to identify ways in which they can be managed to counteract ongoing and future browning. Below we discuss a number of potential mitigation measures related to altered land use (i.e., vegetation type) in hydrologically connected areas, modifying hydrological connectivity in itself, and restoring retention time, all as measures to reduce browning of waters.
Using hydrological connectivity to target changes in land-use management
The importance of the riparian zone, both in terms of providing a major source of DOC and controlling and buffering hydrological connectivity and DOC fluxes from surrounding hillslopes, has been highlighted in various environments (McGlynn and McDonnell 2003; Marwick et al. 2014; Musolff et al. 2018). This is especially true in boreal regions where the riparian zone has a critical role in DOC export because of high accumulation of SOM (Dick et al. 2015). Boreal soils tend to generate significantly higher DOC concentrations than other forested biomes because of high conifer cover with poor litter quality and relatively wet and cold soils with slow decomposition. The increased cover of Norway spruce (sometimes termed “sprucification”) that has occurred since pre-industrial times due to forest industry demands and modern forest management practices (Hellberg et al. 2009), has important implications for DOC dynamics. In addition, suppression of natural disturbance regimes, such as recurrent wildfires in upland forests (Hellberg et al. 2009) and seasonal floods in riparian environments (e.g., Johansson and Nilsson 2002), have favored the species composition toward conifers. This shift from deciduous to conifer tree dominance is particularly important for riparian areas and may therefore be an important player in the browning of surface waters.
However, not all riparian zones behave the same way, and are therefore not equally important for the DOC export. Recent work has illustrated this by quantifying the contribution of water from the riparian zone, showing that 70% of hydrologic inputs into a 1400 m stream segment enter at only a few distinct groundwater input zones, which constitute less than 10% of the channel length (Leach et al. 2017). These so-called discrete riparian input points (DRIPS, Ploum et al. 2018) are the result of the topography channelizing groundwater water into specific areas, acting as hotspots for water and solute input to streams (Fig. 5). As such, these highly organic sites are also likely to contribute with large amounts of DOC to surface waters and thus, are suitable targets for active management.
Riparian zones: Shift species composition to deciduous
The century-long transition toward dominance of conifers has likely resulted in increased DOC concentrations in many surface waters. In general, litter from coniferous species, such as spruce and pine, is a lower-quality substrate for microbial processes compared to deciduous trees (Duan et al. 2014), and more DOC leaches from coniferous forests than from deciduous (Camino-Serrano et al. 2014). Thus, the ongoing browning trend may be halted or even reversed by management of spruce via thinning and actively planting deciduous broadleaf tree species in riparian areas and DRIPS, thereby reducing the DOC entering freshwaters (Fig. 5). A higher density of deciduous streamside vegetation may, besides lowering stream DOC export, also promote headwater biodiversity (Jonsson et al. 2017). Hence, although management actions toward more deciduous riparian forest cover could potentially take decades (Hasselquist et al. 2015) or up to centuries to affect the DOC concentration in surface waters, such a transition would also have several other more instant positive ecosystem effects.
Manipulating hydrological connectivity
Extensive peatland areas throughout Fennoscandia have been drained, in more or less systematic ways, with the purpose to improve forest production (Päivänen and Hånell 2012; Sikström and Hökkä 2016). Area drained for peatland forestry has been positively correlated with TOC and DOC (Marttila et al. 2018) and drained peatland forests have been shown to be significantly greater sources of DOC to receiving waters than undrained peatlands and upland forest soils (Rantakari et al. 2010). Päivänen and Hånell (2012) suggested that in drained peatlands, aeration promotes microbial processes and solubility, and thereby increases peat mineralization, resulting in the increasing DOC concentration. This increase in peat decomposition level due to drainage, combined with naturally fluctuating water tables, creates a condition with increased loads of DOC and nutrients from drained peatlands (Marttila et al. 2018; Nieminen et al. 2018).
Ditch network maintenance (DNM)
In Sweden, there is currently no new drainage ditch digging performed in pristine peatlands. However, DNM is done to restore the drainage functions of degraded ditches in order to improve and maintain the forest production achieved by the first-time drainage (Fig. 6; Sikström and Hökkä 2016). DNM can also involve digging of supplementary ditches in-between existing ones to increase the drainage function. DNM in Sweden is typically done at stand rotation to lower groundwater levels in order to allow for seedling establishment, since the removal of the mature tree stands reduces evapotranspiration (Sikström and Hökkä 2016). In Finland, it is more common that DNM is done every 20 years, typically in connection with thinning operations (Sikström and Hökkä 2016). It should be noted that environmentally responsible drainage becomes more difficult to implement with the increasing time after drainage because peat decomposition increases its erodibility as well as the peat subsidence (Päivänen and Hånell 2012).
How DNM affects water quality is a hot topic, and a recent review on the subject summarized the current understanding of the impact of DNM on water quality, including DOC concentrations (Nieminen et al. 2018). In general, the effect of DNM on DOC export depends on the underlying soil type. For peat covering fine-textured mineral soils or deep peat soil, a significant decrease in DOC concentrations after DNM has been found to continue for up to two decades, while no such effect has been observed for peat covering coarse-textured mineral soils (Nieminen et al. 2018). Nieminen et al. (2018) also summarized the proposed hypotheses for the processes likely causing decreased DOC exports from DNM areas. They argued that the most frequently suggested mechanism is that DNM changes the water pathways so that it no longer comes into close contact with high-quality, recently deposited organic matter within the surface peat (Fig. 6). Instead, water flows in deep soil, where it can interact with positively charged mineral soil oxyhydroxides that act as sorption sites for negatively charged organic moieties (Åstrom et al. 2001). If the water table is already low due to high evaporative demand from mature trees (Fig. 6; Sarkkola et al. 2010), negligible changes in DOC exports are to be expected (Nieminen et al. 2018). DNM may, however, induce other water-quality problems primarily related to erosion of suspended solids (Nieminen et al. 2018). Hence, remedial actions against browning must be valued against other negative water-quality impacts.
Forestry methods: Reduce disturbance and hydrological connectivity of production peatland forests
Even-aged forest management, which includes clear-cutting, site preparation to create planting spots, and sometimes DNM, has been shown to increase DOC export to streams significantly. In northern Sweden, clear-cutting increased downstream DOC export by 92%, and site preparation increased it by 195%, compared to pretreatment conditions (Schelker et al. 2012). The increase in DOC export is likely primarily due to the raised groundwater level following harvesting (Fig. 6; Schelker et al. 2012), which during high-flow conditions are caused by the lateral flow through riparian zones that exponentially increases DOC concentrations of riparian soil water near the soil surface. In Finland, where the typical forest regeneration phase in even-aged forest management includes clear-cutting, soil preparation for planting as well as management of the existing ditch networks, DOC exports increase, especially from the most fertile sites (Nieminen 2004; Kaila et al. 2016). If continuous cover forestry was implemented, the rise in groundwater level due to forest harvest would be reduced due to the evapotranspiration of the remaining tree stand (Fig. 6; Sarkkola et al. 2010). This would plausibly result in less flow through the most peat-rich riparian zone layers and hence reduce the mobilization and release of DOC, redox-sensitive nutrients and metals (Nieminen et al. 2018). Recent studies have indicated that it is a change in redox-conditions in surface peat that is the key factor controlling the enhanced DOC exports (Nieminen et al. 2018) from drained peatland forests after clear-cutting.
Manipulating water residence time
Human impact has in many cases caused reduction of water residence time through channelization, construction of canals and levees, as well as elimination of wetlands or floodplains that would otherwise slow water movement (Stanley et al. 2012). Decreases in residence times are particularly pronounced in urban settings, where impervious surfaces result in rapid downstream routing of water by preventing infiltration into soils and groundwater (Stanley et al. 2012). Similar hydrologic short-circuiting also occurs in agricultural areas with tile drains and forest drainage ditches through peatlands described above.
Once terrestrial DOC is delivered to the aquatic environment, its quantity and quality can be modified by microbial processing, respiration, sedimentation, adsorption/desorption, photobleaching, and photooxidation (Stanley et al. 2012). A few active measures are available to increase the retention time of water in a system and thereby enhance these processes. Some key actions are to restore the long residence time associated with a hydrological regime more typical of natural peatlands or to increase geomorphic complexity of streams through re-meandering or restoring in-stream heterogeneity.
Restoration of historically drained peatlands is often performed in order to improve water quality, but there are conflicting results on how restoration affects DOC export. Restoration is a disturbance in itself; ditches are blocked by damming and in-filling usually using peat material in order to raise the water table level back to the level prior to drainage (Fig. 6; Laine et al. 2011). In the first few years after restoration, DOC exports can sum up to several years’ worth of background export (Koskinen et al. 2017). This has primarily been the case in drained nutrient-rich peatlands where there is a significant risk for increased short-term export of DOC. In contrast, restoration of nutrient-poor peatlands has been shown to pose less risk (Koskinen et al. 2017). Over the long-term, the reduction of DOC may counterbalance this initial pulse, but how long this takes is still unclear. After 4 years, DOC had recovered to near natural conditions in one study (Koskinen et al. 2017), while in a study of 24 restored peatlands, restoration reduced DOC concentrations to near natural or reference levels in most mire types within 6 years (Menberu et al. 2017). Further support for reduced DOC from restored peatlands comes from a national survey in the UK suggesting that the water sampled from restored drainage ditches tended to be less colored than that from unblocked drains (Armstrong et al. 2010). Furthermore, the degree of restoration also affects DOC in peatlands. Hydrologically over-restored sites (inundated) have significantly higher concentrations of pore water DOC than less restored sites (Menberu et al. 2017), indicating the importance of achieving a hydrological regime typical of natural peatlands during restoration.
Overall, streams and rivers are increasingly being recognized for their significant role in the processing of organic matter and DOC (Mineau et al. 2016). In a study of seven watersheds in the northeastern US, between 27 and 45% of the water column DOC was removed by in-stream processing during transport (Mineau et al. 2016). In contrast, other studies have shown that there is little or no processing of DOC relative to water residence time. For example, first to fourth order (< 0.5–4 m wide) boreal streams were found to act as passive pipes since in‐stream processing of DOM was restricted by short water residence times (Kothawala et al. 2015).
Theoretically, increasing residence time of water in the stream system through increasing hydrogeomorphic complexity should lead to reduction of DOC, but it is unclear to what extent restoration can affect this, and little empirical work has been done to test this in a restoration context. Changing the load or concentration of DOC in streams and rivers rarely motivates management activities—rather reduction in nutrients such as nitrogen and phosphorus are commonly stated goals (Stanley et al. 2012). However, restoration through addition of large boulders and in-stream wood has been shown to increase the retention of allochthonous organic matter (Frainer et al. 2018), as well as affect hydrodynamics and surface water–ground water interactions of streams (Kupilas et al. 2017). For example, stream widening reduces flow velocity and creates backwaters and pools which could change the size and location of transient storage zones, which in turn would enhance carbon processing and nutrients (Kupilas et al. 2017). Little work has been done in boreal and temperate contexts, but in the subtropical, low gradient, blackwater-type (high DOC) Kissimmee River in Florida, USA, primary production and respiration were estimated before and after canal backfilling and restoration of continuous flow in the natural stream channel (Colangelo 2007). After the restoration, net daily metabolism values indicated an increase in the amount of organic matter being processed, likely originating from the reconnected floodplain. DOC values decreased after restoration, but not significantly in the short 3-year period of postrestoration measurements (Colangelo 2007). As more restoration is planned at the watershed scale, more research is needed on how restoration of in-stream complexity affects ecosystem processes such as metabolism, and specifically, DOC processing.
Changing climate/weather, reversed acidification, and altered land-use and management practices have acted in concert to generate the increased browning of inland waters observed over the last few decades. Although it is difficult to disentangle the individual importance of each of these drivers in space and time—making it difficult to predict future trajectories for water color—variability in climate drivers will continue to promote high concentrations of DOC and Fe at levels that pose a problem to stakeholders and impair ecosystem services. However, the growing recognition that land use and management are significant drivers provides us with the potential measures to mitigate or reduce browning. Unfortunately, as the role of land use and management has been largely overlooked, research has not been directed toward evaluating such measures.
Therefore, the options to mitigate browning, which are highlighted and discussed here, should be regarded as hypotheses based on the contemporary understanding of what factors govern the production and export of DOC in the boreal landscape and its loss in the aquatic system. Interestingly, several of the proposed interventions are being implemented at small scales, but for other purposes. Actively promoting deciduous broadleaf tree species in riparian areas, for instance, is becoming a more common practice, since there are known benefits for biodiversity and fishing opportunities. Similarly, restorations of peatlands and wetlands are performed both in the agricultural and forested landscape, with the aims to increase biodiversity and nutrient retention, as well as to reduce greenhouse gas emissions from decomposing peat. For an optimized management perspective, it is imperative that funding is allocated to evaluate the multiple consequences of such interventions, including DOC and Fe export. A dialog between land owners, forest companies, scientists, and policy makers should be promoted in order to improve and spread knowledge about how land-use management affects water quality and other ecosystem services, and to build commitment. Finally, funding to perform large-scale and long-term experiments, designed to test the efficiency and response over time is crucial for providing decision support regarding management practices. Some measures may be in conflict with other water-quality issues such as erosion of suspended solids, or other ecosystem services, such as forest production and associated carbon sequestration. However, if measures can be efficiently assessed and directed toward hydrologically connected areas only, such conflicts may potentially be overcome.
Akselsson, C., H. Hultberg, P.E. Karlsson, G.P. Karlsson, and S. Hellsten. 2013. Acidification trends in south Swedish forest soils 1986–2008—Slow recovery and high sensitivity to sea-salt episodes. Science of the Total Environment 444: 271–287.
Armstrong, A., J. Holden, P. Kay, B. Francis, M. Foulger, S. Gledhill, A.T. McDonald, and A. Walker. 2010. The impact of peatland drain-blocking on dissolved organic carbon loss and discolouration of water; results from a national survey. Journal of Hydrology 381: 112–120.
Ask, J., J. Karlsson, L. Persson, P. Ask, P. Bystrom, and M. Jansson. 2009. Terrestrial organic matter and light penetration: Effects on bacterial and primary production in lakes. Limnology and Oceanography 54: 2034–2040.
Åstrom, M., E.K. Aaltonen, and J. Koivusaari. 2001. Impact of ditching in a small forested catchment on concentrations of suspended material, organic carbon, hydrogen ions and metals in stream water. Aquatic Geochemistry 7: 57–73.
Björnerås, C., G.A. Weyhenmeyer, C.D. Evans, M.O. Gessner, H.-P. Grossart, K. Kangur, P. Kortelainen, et al. 2017. Widespread increases in iron concentration in European and North American freshwaters. Global Biogeochemical Cycles. https://doi.org/10.1002/2017gb005749.
Bradshaw, C.J.A., and I.G. Warkentin. 2015. Global estimates of boreal forest carbon stocks and flux. Global and Planetary Change 128: 24–30.
Camino-Serrano, M., B. Gielen, S. Luyssaert, P. Ciais, S. Vicca, B. Guenet, B. De Vos, N. Cools, et al. 2014. Linking variability in soil solution dissolved organic carbon to climate, soil type, and vegetation type. Global Biogeochemical Cycles. https://doi.org/10.1002/2013gb004726.
Clark, J.M., A. Heinimeyer, P. Martin, and S.H. Bottrell. 2012. Processes controlling DOC in pore water during simulated drought cycles in six different UK peats. Biogeochemistry 109: 253–270.
Colangelo, D.J. 2007. Response of river metabolism to restoration of flow in the Kissimmee River, Florida, USA. Freshwater Biology 52: 459–470.
Creed, I.F., F.D. Beall, T.A. Clair, P.J. Dillon, and R.H. Hesslein. 2008. Predicting export of dissolved organic carbon from forested catchments in glaciated landscapes with shallow soils. Global Biogeochemical Cycles. https://doi.org/10.1029/2008gb003294.
Creed, I.F., A.K. Bergström, C.G. Trick, N.B. Grimm, D.O. Hessen, J. Karlsson, K.A. Kidd, et al. 2018. Global change-driven effects on dissolved organic matter composition: Implications for food webs of northern lakes. Global Change Biology 24: 3692–3714.
Crowther, T.W., K.E.O. Todd-Brown, C.W. Rowe, W.R. Wieder, J.C. Carey, M.B. Machmuller, B.L. Snoek, S. Fang, et al. 2016. Quantifying global soil carbon losses in response to warming. Nature 540: 104–108.
De Wit, H.H., S. Valinia, G.A. Weyhenmeyer, M.N. Futter, P. Kortelainen, K. Austnes, D.O. Hessen, A. Räike, et al. 2016. Current browning of surface waters will be further promoted by water climate. Environmental Science and Technology 3: 430–435.
Dick, J.J., D. Tetzlaff, C. Birkel, and C. Soulsby. 2015. Modelling landscape controls on dissolved organic carbon sources and fluxes to streams. Biogeochemistry 122: 361–374.
Duan, S.W., K. Delaney-Newcomb, S.S. Kaushal, S.E.G. Findlay, and K.T. Belt. 2014. Potential effects of leaf litter on water quality in urban watersheds. Biogeochemistry 121: 61–80.
Ekström, S.M., E.S. Kritzberg, D.B. Kleja, N. Larsson, P.A. Nilsson, W. Granéli, and B. Bergkvist. 2011. Effect of acid deposition on quantity and quality of dissolved organic matter in soil-water. Environmental Science and Technology 45: 4733–4739.
Erlandsson, M., I. Buffam, J. Fölster, H. Laudon, J. Temnerud, G.A. Weyhenmeyer, and K. Bishop. 2008. Thirty-five years of synchrony in the organic matter concentrations of Swedish rivers explained by variation in flow and sulfate. Global Change Biology 14: 1191–1198.
Finstad, A.G., T. Andersen, S. Larsen, K. Tominage, S. Blumentrath, H.A. de Wit, H. Tømmervik, and D.O. Hessen. 2016. From greening to browning: Catchment vegetation development and reduced S-deposition promote organic carbon load on decadal time scales in Nordic lakes. Scientific Reports 6: 31944.
Finstad, A.G., I.P. Helland, O. Ugedal, T. Hesthagen, and D.O. Hessen. 2014. Unimodal response of fish yield to dissolved organic carbon. Ecology Letters 17: 36–43.
Frainer, A., L.E. Polvi, R. Jansson, and B.G. McKie. 2018. Enhanced ecosystem functioning following stream restoration: The roles of habitat heterogeneity and invertebrate species traits. Journal of Applied Ecology 55: 377–385.
Futter, M.N., S. Valinia, S. Löfgren, S.J. Köhler, and J. Fölster. 2014. Long-term trends in water chemistry of acid-sensitive Swedish lakes show slow recovery from historic acidification. Ambio 43: 77–90.
Hadwen, W.L., and A.H. Arthington. 2003. The significance and management implications of perched dune lakes as swimming and recreation sites on Fraser Island, Australia. Journal of Tourism Studies 14: 35–44.
Hansson, L.-A., A. Nicolle, W. Granéli, P. Hallgren, E. Kritzberg, A. Persson, J. Björk, P.A. Nilsson, et al. 2013. Food-chain length alters community responses to global change in aquatic systems. Nature Climate Change 3: 228–233.
Hasselquist, E.M., C. Nilsson, J. Hjältén, D. Jørgensen, L. Lind, and L.E. Polvi. 2015. Time for recovery of riparian plants in restored northern Swedish streams: A chronosequence study. Ecological Applications 25: 1373–1389.
Hellberg, E., T. Josefsson, and L. Östlund. 2009. The transformation of a Norway spruce dominated landscape since pre-industrial times in northern Sweden: The influence of modern forest management on forest structure. Silva Fennica 43: 783–797.
Johansson, M.E., and C. Nilsson. 2002. Responses of riparian plants to flooding in free-flowing and regulated boreal rivers: An experimental study. Journal of Applied Ecology 39: 971–986.
Johansson, L., J. Temnerud, J. Abrahamsson, and D.B. Kleja. 2010. Variation in organic matter and water color in Lake Mälaren during the past 70 years. Ambio 39: 116–125.
Jones, R.I. 1992. The influence of humic substances on lacustrine planktonic food-chains. Hydrobiologia 229: 73–91.
Jonsson, M., R.M. Burrows, J. Lidman, E. Fältström, H. Laudon, and R.A. Sponseller. 2017. Land use influences macroinvertebrate community composition in boreal headwaters through altered stream conditions. Ambio 46: 311–323.
Karlsson, J., P. Bystrom, J. Ask, P. Ask, L. Persson, M. Jansson. 2009. Light limitation of nutrient-poor lake ecosystems. Nature 460: 506–509.
Kaila, A., Z. Asam, M. Koskinen, R. Uusitalo, A. Smolander, O. Kiikkilä, S. Sarkkola, C. O’Driscoll, et al. 2016. Impact of re-wetting of forestry-drained peatlands on water quality—A laboratory approach assessing the release of P, N, Fe, and dissolved organic carbon. Water, Air Soil and Pollution 227: 292.
Keeler, B.L., S.A. Wood, S. Polasky, C. Kling, C.T. Filstrup, and J.A. Downing. 2015. Recreational demand for clean water: Evidence from geotagged photographs by visitors to lakes. Frontiers in Ecology and the Environment 13: 76–81.
Knorr, K.-H. 2013. DOC-dynamics in a small headwater catchment as driven by redox fluctuations and hydrological flow paths—Are DOC exports mediated by iron reduction/oxidation cycles? Biogeosciences 10: 891–904.
Koskinen, M., T. Tahvanainen, S. Sarkkola, M.W. Menberu, A. Lauren, T. Sallantaus, H. Marttila, A.-K. Ronkanen, et al. 2017. Restoration of fertile peatlands poses a risk for high exports of dissolved organic carbon, nitrogen, and phosphorus. Science of the Total Environment 586: 858–869.
Kothawala, D.N., X. Ji, H. Laudon, A.M. Ågren, M.N. Futter, S.J. Köhler, and L.J. Tranvik. 2015. The relative influence of land cover, hydrology, and in-stream processing on the composition of dissolved organic matter in boreal streams. Journal of Geophysical Research: Biogeosciences 120: 1491–1505.
Kritzberg, E.S. 2017. Centennial-long trends of lake browning show major effect of afforestation. Limnology and Oceanography Letters 2: 105–112.
Kupilas, B., D. Hering, A.W. Lorenz, C. Knuth, and B. Gücker. 2017. Hydromorphological restoration stimulates river ecosystem metabolism. Biogeosciences 14: 1989–2002.
Köhler, S.J., E. Lavonen, A. Keucken, P. Schmitt-Kopplin, T. Spanjer, and K.M. Persson. 2016. Upgrading coagulation with hollow-fibre nanofiltration for improved organic matter removal during surface water treatment. Water Research 89: 232–240.
Laine, A.M., M. Leppälä, O. Tarvainen, M.L. Päätalo, R. Seppänen, and A. Tolvanen. 2011. Restoration of managed pine fens: Effect on hydrology and vegetation. Applied Vegetation Science 14: 340–349.
Laudon, H., M. Berggren, A. Ågren, I. Buffam, K. Bishop, T. Grabs, M. Jansson, and S. Köhler. 2011. Patterns and dynamics of dissolved organic carbon (DOC) in boreal streams: The role of processes, connectivity, and scaling. Ecosystems 14: 880–893.
Lavonen, E.E., M. Gonsior, L.J. Tranvik, P. Schmitt-Kopplin, and S.J. Köhler. 2013. Selective chlorination of natural organic matter: Identification of previously unknown disinfection byproducts. Environmental Science and Technology 47: 2264–2271.
Leach, J.A., W. Lidberg, L. Kuglerová, A. Peralta-Tapia, A. Ågren, and H. Laudon. 2017. Evaluating topography-based predictions of shallow lateral groundwater discharge zones for a boreal lake-stream system. Water Resources Research 53: 5420–5437.
Lebret, K., S. Langenheder, N. Colinas, Ö. Östman, and E.S. Lindstrom. 2018. Increased water colour affects freshwater plankton communities in a mesocosm study. Aquatic Microbial Ecology 81: 1–17.
Li, J., and D.D. Richter. 2012. Effects of two-century land use changes on soil iron crystallinity and accumulation in Southeastern Piedmont region, USA. Geoderma 173–174: 184–191.
Lindbladh, M., A.-L. Axelsson, T. Hultberg, J. Brunet, and A. Felton. 2014. From broadleaves to spruce—The borealization of southern Sweden. Scandinavian Journal of Forest Research 29: 686–696.
Lydersen, E., S. Löfgren, and R.T. Arnesen. 2002. Metals in Scandinavian surface waters: Effects of acidification, liming, and potential reacidification. Critical Reviews in Environmental Science and Technology 32: 73–295.
Löfgren, S., and T. Zetterberg. 2011. Decreased DOC concentrations in soil water in forested areas in southern Sweden during 1987–2008. Science of the Total Environment 409: 1916–1926.
Marttila, H., S.-M. Karjalainen, M. Kuoppala, M.L. Nieminen, A.-K. Ronkanen, B. Kløve, and S. Hellsten. 2018. Elevated nutrient concentrations in headwaters affected by drained peatland. Science of the Total Environment 643: 1304–1313.
Marwick, T.R., A.V. Borges, K. Van Acker, F. Darchambeau, and S. Bouillon. 2014. Disproportionate contribution of riparian inputs to organic carbon pools in freshwater systems. Ecosystems 17: 974–989.
McGlynn, B.L., and J.J. McDonnell. 2003. Role of discrete landscape units in controlling catchment dissolved organic carbon dynamics. Water Resources Research. https://doi.org/10.1029/2002wr001525.
Mattsson, T., P. Koretelainen, A. Laubel, D. Evans, M. Pujo-Pay, A. Råike, and P. Conan. 2009. Export of dissolved organic matter in relation to land use along a European climatic gradient. Science of the Total Environment 407: 1967–1976.
Menberu, M.W., H. Marttila, T. Tahvanainen, J.S. Kotiaho, R. Hokkanen, B. Kløve, and A.-K. Ronkanen. 2017. Changes in pore water quality after peatland restoration: Assessment of a large-scale, replicated Before-After-Control-Impact study in Finland. Water Resources Research 53: 8327–8343.
Meyer-Jacob, C., J. Tolu, C. Bigler, H. Yang, and R. Bindler. 2015. Early land use and centennial scale changes in lake-water organic carbon prior to contemporary monitoring. Proceedings of the National Academy of Sciences of the United States of America 112: 6579–6584.
Mineau, M.M., W.M. Wollheim, I. Buffam, S.E.G. Findlay, R.O. Hall, E.R. Hotchkiss, L.E. Koenig, W.H. McDowell, and T.B. Parr. 2016. Dissolved organic carbon uptake in streams: A review and assessment of reach-scale measurements. Journal of Geophysical Research: Biogeosciences 121: 2019–2029.
Monteith, D.T., J.L. Stoddard, C.D. Evans, H.A. de Wit, M. Forsius, T. Høgåsen, A. Wilander, et al. 2007. Dissolved organic carbon trends resulting from changes in atmospheric deposition chemistry. Nature 450: 537–540.
Mormul, R.P., J. Ahlgren, M.K. Ekvall, L.A. Hansson, and C. Brönmark. 2012. Water brownification may increase the invasibility of a submerged non-native macrophyte. Biological Invasions 14: 2091–2099.
Musolff, A., J.H. Fleckenstein, M. Opitz, O. Buttner, R. Kumar, and J. Tittel. 2018. Spatio-temporal controls of dissolved organic carbon stream water concentrations. Journal of Hydrology 566: 205–215.
Nieminen, M. 2004. Export of dissolved organic carbon, nitrogen and phosphorus following clear-cutting of three Norway spruce forests growing on drained peatlands in southern Finland. Silva Fennica 38: 123–132.
Nieminen, M., M. Palviainen, S. Sarkkola, A. Laurén, H. Marttila, and L. Finér. 2018. A synthesis of the impacts of ditch network maintenance on the quantity and quality of runoff from drained boreal peatland forests. Ambio 47: 523–534.
Nikulin, G., E. Kjellström, U. Hansson, G. Strandberg, and A. Ullerstig. 2016. Evaluation and future projections of temperature, precipitation and wind extremes over Europe in an ensemble of regional climate simulations. Tellus A: Dynamic Meteorology and Oceanography 63: 41–55.
Oni, S.K., M.N. Futter, K. Bishop, S.J. Köhler, M. Ottosson-Löfvenius, and H. Laudon. 2013. Long-term patterns in dissolved organic carbon, major elements and trace metals in boreal headwater catchments: Trends, mechanisms and heterogeneity. Biogeosciences 10: 2315–2330.
Päivänen, J., and B. Hånell. 2012. Peatland ecology and Forestry—A sound approach. University of Helsinki Department of Forest Sciences Publications 3.
Ploum, S.W., J.A. Leach, L. Kuglerová, and H. Laudon. 2018. Thermal detection of discrete riparian inflow points (DRIPs) during contrasting hydrological events. Hydrological Processes 32: 3049–3050.
Rantakari, M., T. Mattsson, P. Kortelainen, S. Piirainen, L. Finér, and M. Ahtiainen. 2010. Organic and inorganic carbon concentrations and fluxes from managed and unmanaged boreal first-order catchments. Science of the Total Environment 408: 1649–1658.
Ranåker, L., J. Persson, M. Jönsson, P.A. Nilsson, and C. Brönmark. 2014. Piscivore-prey fish interactions: Mechanisms behind diurnal patterns in prey selectivity in brown and clear water. PLoS ONE. https://doi.org/10.1371/journal.pone.0102002.
Rengefors, K., G.A. Weyhenmeyer, and I. Bloch. 2012. Temperature as a driver for the expansion of the microalga Gonyostomum semen in Swedish lakes. Harmful Algae 18: 65–73.
Ritson, J.P., N.J.D. Graham, M.R. Templeton, J.M. Clark, R. Gough, and C. Freeman. 2014. The impact of climate change on the treatability of dissolved organic matter (DOM) in upland water supplies: A UK perspective. Science of the Total Environment 473–474: 714–730.
Sarkkola, S., H. Hökkä, H. Koivusalo, M. Nieminen, E. Ahti, J. Päivänen, and J. Laine. 2010. Role of tree stand evapotranspiration in maintaining satisfactory drainage conditions in drained peatlands. Canadian Journal of Forest Research 40: 1485–1496.
Schelker, J., K. Eklöf, K. Bishop, and H. Laudon. 2012. Effects of forestry operations on dissolved organic carbon concentrations and export in boreal first-order streams. Journal of Geophysical Research: Biogeosciences. https://doi.org/10.1029/2011jg001827.
Serrano, I., I. Buffam, D. Palm, E. Brannas, and H. Laudon. 2008. Thresholds for survival of brown trout during the spring flood acid pulse in streams high in dissolved organic carbon. Transactions of the American Fisheries Society 137: 1363–1377.
Sikström, U., and H. Hökkä. 2016. Interactions between soil water conditions and forest stands in boreal forests with implications for ditch network maintenance. Silva Fennica 50: article id 1416.
Solomon, C.T., S.E. Jones, B.C. Weidel, I. Buffam, M.L. Fork, J. Karlsson, S. Larsen, J.T. Lennon, et al. 2015. Ecosystem consequences of changing inputs of terrestrial dissolved organic matter to lakes: Current knowledge and future challenges. Ecosystems 18: 376–389.
Stanley, E.H., S.M. Powers, N.R. Lottig, I. Buffam, and J.T. Crawford. 2012. Contemporary changes in dissolved organic carbon (DOC) in human-dominated rivers: Is there a role for DOC management? Freshwater Biology 57: 26–42.
Steinberg, C.E.W., S. Kamara, V.Y. Prokhotskaya, L. Manusadzianas, T.A. Karasyova, M.A. Timofeyev, Z. Jie, A. Paul, T. Meinelt, et al. 2006. Dissolved humic substances—Ecological driving forces from the individual to the ecosystem level? Freshwater Biology 51: 1189–1210.
Svedäng, H., E.J. Sundblad, and A. Grimvall. 2018. The Hanö Bay—A warning bell. Swedish Institute for the Marine Environment, Report 2018:2, Gothenburg (in Swedish).
Taipale, S.J., K. Vuorio, U. Strandberg, K.K. Kahilainen, M. Jarvinen, M. Hiltunen, E. Peltomaa, and P. Kankaala. 2016. Lake eutrophication and brownification downgrade availability and transfer of essential fatty acids for human consumption. Environment International 96: 156–166.
Tiwari, T., F. Lidman, H. Laudon, W. Lidberg, and A.M. Ågren. 2017. GIS-based prediction of stream chemistry using landscape composition, wet areas, and hydrological flow pathways. Journal of Geophysical Research: Biogeosciences 122: 65–79.
Tranvik, L.J., J.A. Downing, J.B. Cotner, S.A. Loiselle, R.G. Striegl, T.J. Ballatore, P. Dillon, K. Finlay, et al. 2009. Lakes and reservoirs as regulators of carbon cycling and climate. Limnology and Oceanography 54: 2298–2314.
Trigal, C., W. Goedkoop, and R.K. Johnson. 2011. Changes in phytoplankton, benthic invertebrate and fish assemblages of boreal lakes following invasion by Gonyostomum semen. Freshwater Biology 56: 1937–1948.
Urrutia-Cordero, P., M.K. Ekvall, and L.-A. Hansson. 2016. Local food web management increases resilience and buffers against global change effects on freshwaters. Scientific Reports 6: 29542. https://doi.org/10.1038/srep29542.
Van Dorst, R.M., A. Gårdmark, R. Svanbäck, U. Beier, G.A. Weyhenmeyer, and M. Huss. 2018. Warmer and browner waters decrease fish biomass production. Global Change Biology. https://doi.org/10.1111/gcb.14551.
Valinia, S., H.P. Hansson, M.N. Futter, K. Bishop, N. Sriskandarajah, and J. Fölster. 2012. Problems with the reconciliation of good ecological status and public participation in the Water Framework Directive. Science of the Total Environment 433: 482–490.
Wällstedt, T., L. Björkvald, and J.P. Gustafsson. 2010. Increasing concentrations of arsenic and vanadinium in (south) Swedish streams. Applied Geochemistry 25: 1162–1175.
Weyhenmeyer, G.A., M. Fröberg, E. Karltun, M. Khalili, D. Kothawala, J. Temnerud, and L.J. Tranvik. 2012. Selective decay of terrestrial organic carbon during transport from land to sea. Global Change Biology 18: 349–355.
Weyhenmeyer, G.A., Y.T. Prairie, and L.J. Tranvik. 2014. Browning of boreal freshwaters coupled to carbon-iron interactions along the aquatic continuum. PLoS ONE 9: 1965–1976.
Wikner, J., and A. Andersson. 2012. Increased freshwater discharge shifts the trophic balance in the coastal zone of the northern Baltic Sea. Global Change Biology 18: 2509–2519.
Wilken, S., M. Soares, P. Urrutia-Cordero, J. Ratcovich, M.K. Ekvall, E. Van Donk, and L.A. Hansson. 2018. Primary producers or consumers? Increasing phytoplankton bacterivory along a gradient of lake warming and browning. Limnology and Oceanography 63: S142–S155.
Williamson, C.E., R.S. Stemberger, D.P. Morris, T.M. Frost, and S.G. Paulsen. 1996. Ultraviolet radiation in North American lakes: Attenuation estimates from doc measurements and implications for plankton communities. Limnology and Oceanography 41: 1024–1034.
Open access funding provided by Lund University. This paper was initiated at a Workshop at Stockholm Environment Institute, involving scientists, stakeholders, and managing authorities, by Initiative from Helge Model Forest. We want to thank all participants in the workshop: Jan Lannér, Anders Esselin, Susanna Hogdin, Kenneth Persson, Agne Andersson, Anja Lomander, Carina Wettemark, Andreas Jezek, Stephan Köhler, Per-Erik Larsson, Karin Olsson, Kevin Bishop, Karin Eklöf, Emil Grönkvist, Henrik Gustafsson, and Bengt Olsson. This workshop was supported by Region Skånes Miljövårdsfond, Helgeåns vattenråd, Swedish Forest Agency, Sydvatten, SEI, Biosphere Reserve Vattenriket, Swedish Water Research AB, and the Swedish Agency for Marine and Water Management. ESK was funded by Formas (Grant Number 2015-01407); HL and EMH by the Healthy Waters Project (Formas 2013-01650), Skogssällskapet, and the Mistra Future Forest Program; SL by the Environmental Assessment Program on Acidification at SLU; SV by the Research Council of Norway KLIMAFORSK Project (SURFER: 267481); LAH from Formas (2018-00800 and 2018-02426; LimnoScenES, BiodivERsA); and OO by the MIRACLE Project, funded by BONUS—The Joint Baltic Sea Research and Development Programme. The data in Fig. 3 were kindly furnished by Eva Steiner at the Municipality of Karlskrona for River Lyckeby, and by Per Ericsson and Anna Jansson at Norrvatten for Lake Görveln.
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Kritzberg, E.S., Hasselquist, E.M., Škerlep, M. et al. Browning of freshwaters: Consequences to ecosystem services, underlying drivers, and potential mitigation measures. Ambio 49, 375–390 (2020). https://doi.org/10.1007/s13280-019-01227-5