Forests are of major importance to human society, contributing several crucial ecosystem services. Biodiversity is suggested to positively influence multiple services but evidence from natural systems at scales relevant to management is scarce. Here, across a scale of 400,000 km2, we report that tree species richness in production forests shows positive to positively hump-shaped relationships with multiple ecosystem services. These include production of tree biomass, soil carbon storage, berry production and game production potential. For example, biomass production was approximately 50% greater with five than with one tree species. In addition, we show positive relationships between tree species richness and proxies for other biodiversity components. Importantly, no single tree species was able to promote all services, and some services were negatively correlated to each other. Management of production forests will therefore benefit from considering multiple tree species to sustain the full range of benefits that the society obtains from forests.
Numerous studies have estimated carbon exchanges at the land-atmosphere interface, more recently also including estimates at the freshwater-atmosphere interface. Less attention has been paid to lateral carbon fluxes, in particular to the fate of terrestrial carbon during transport from soils via surface waters to the sea. Using extensive datasets on soil, lake and river mouth chemistry of the boreal/hemiboreal region we determined organic carbon (OC) stocks of the O horizon from catchment soils, annual OC transports through more than 700 lakes (OC lakeflux ) and the total annual OC transport at Sweden's 53 river mouths (OC seaflux ). We show here that a minimum of 0.03-0.87% yr À1 of the OC soil stocks need to be exported to lakes in order to sustain the annual OC lakeflux . Across Sweden we estimated a total OC lakeflux of~2.9 Mtonne yr À1 , which corresponds to~10% of Sweden's total terrestrial net ecosystem production, and it is over 50% higher than the total OC seaflux . The OC loss during transport to the sea follows a simple exponential decay with an OC half-life of~12 years. Water colour, a proxy often used for dissolved humic matter, is similarly lost exponentially but about twice as fast as OC. Thus, we found a selective loss of the coloured portion of soil-derived OC during its transport through inland waters, prior to being discharged into the sea. The selective loss is water residence time dependent, resulting in that the faster the water flows through the landscape the less OC and colour is lost. We conclude that increases in runoff will result in less efficient losses of OC, and particularly of colour, if the time for OC transformations in the landscape shortens. Consequently, OC reaching the sea is likely to become more coloured, and less processed, which can have far-reaching effects on biogeochemical cycles.
Dissolved organic carbon (DOC) leached from recent litter in the forest floor has been suggested to be an important source of C to the mineral soil of forest ecosystems. To determine the rate at which this flux of C occurs, we have taken advantage of a local release of 14C at Oak Ridge National Laboratory Reservation, Oak Ridge, TN (35°58′N, 84°16′W). Eight replicate 7‐ by 7‐m plots were established at four field sites on the reservation in an upland oak forest setting. Half of the plots were provided with 14C‐enriched litter (Δ14C ≈ 1000‰), and the other half with near‐background litter (Δ14C ≈ 220‰) for multiple years. Differences in the labeled leaf litter were used to quantify the movement of litter‐derived DOC through the soil profile. Soil solutions were collected for several years with tension lysimeters at 15‐ and 70‐cm depths and measured for DOC concentration and 14C abundance. The net amount of DOC retained between 15 and 70 cm was between 2 and 10 g m−2 yr−1 There were significant effects of the litter additions on the 14C abundance in the DOC, but the net transport of 14C from the added litter was small. The difference in Δ14C between the treatments with enriched and near‐background litter was only about 130‰ at both depths, which is small compared with the difference in Δ14C in the added litter. The primary source of DOC within the mineral soil must therefore have been either the Oe or Oa horizon or the organic matter in the mineral soil. During a 2‐yr time frame, leaching of DOC from recent litter did not have a major impact on the C stock in the mineral soil below 15 cm in this ecosystem.
Leaching of dissolved organic carbon (DOC) from the forest floor and transport in soil solution into the mineral soil are important for carbon cycling in boreal forest ecosystems. We examined DOC concentrations in bulk deposition, throughfall and in soil solutions collected under the O and B horizons in three Norway spruce stands along a climatic gradient in Sweden. Mean annual temperature for the three sites was 5.5, 3.4 and 1.2°C. At each site we also examined the effect of soil moisture on DOC dynamics along a moisture gradient (dry, mesic and moist plots). To obtain information about the fate of DOC leached from the O horizon into the mineral soil, 14 C measurements were made on bulk organic matter and DOC. The concentration and fluxes of DOC in O horizon leachates were highest at the southern site and lowest at the northern. Average DOC concentrations at the southern, central and northern sites were 49, 39 and 30 mg l À1 , respectively. We suggest that DOC leaching rates from O horizons were related to the net primary production of the ecosystem. Soil temperature probably governed the within-year variation in DOC concentration in O horizon leachates, but the peak in DOC was delayed relative to that of temperature, probably due to sorption processes. Neither soil moisture regime (dry, mesic or moist plots) nor seasonal variation in soil moisture seemed to be of any significance for the concentration of DOC leached from the O horizon. The 14 C measurements showed that DOC in soil solution collected below the B horizon was derived mainly from the B horizon itself, rather than from the O horizon, indicating a substantial exchange (sorption-desorption reactions) between incoming DOC and soil organic carbon in the mineral soil.
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