Variability in fire frequency and forest composition in Canada's Southeastern Boreal Forest: A challenge for sustainable forest management

Because some consequences of fire resemble the effects of industrial forest harvesting, forest management is often considered as a disturbance having effects similar to those of natural disturbances. Although the analogy between forest management and fire disturbance in boreal ecosystems has some merit, it is important to recognize that it has limitations. First, normal forest rotations truncate the natural forest stand age distribution and eliminate over-mature forests from the landscape. Second, in the boreal mixedwoods, natural forest dynamics following fire may involve a gradual replacement of stands of intolerant broadleaf species by mixedwood and then softwood stands, whereas current silvicultural practices promote successive rotations of similarly composed stands. Third, the large fluctuations observed in fire frequency during the Holocene limit the use of a single fire cycle to characterize natural fire regimes. Short fire cycles generally described for boreal ecosystems do not appear to be universal; rather, shifts between short and long fire cycles have been observed. These shifts imply important changes in forest composition at the landscape and regional levels. All of these factors create a natural variability in forest composition that should be maintained by forest managers concerned with the conservation of biodiversity. One avenue is to develop silvicultural techniques that maintain a spectrum of forest compositions over the landscape

Large increases in carbon burial in northern lakes during the Anthropocene

Northern forests are important ecosystems for carbon (C) cycling and lakes within them process and bury large amounts of organic-C. Current burial estimates are poorly constrained and may discount other shifts in organic-C burial driven by global change. Here we analyse a suite of northern lakes to determine trends in organic-C burial throughout the Anthropocene. We found burial rates increased significantly over the last century and are up to five times greater than previous estimates. Despite a correlation with temperature, warming alone did not explain the increase in burial, suggesting the importance of other drivers including atmospherically deposited reactive nitrogen. Upscaling mean lake burial rates for each time period to global northern forests yields up to 4.5 Pg C accumulated in the last 100 years—20% of the total burial over the Holocene. Our results indicate that lakes will become increasingly important for C burial under future global change scenarios

Global abundance and size distribution of streams and rivers

To better integrate lotic ecosystems into global cycles and budgets, we provide approximations of the size-distribution and areal extent of streams and rivers. One approach we used was to employ stream network theory combined with data on stream width. We also used detailed stream networks on 2 continents to estimate the fraction of continental area occupied by streams worldwide and corrected remote sensing stream inventories for unresolved small streams. Our estimates of global fluvial area are 485 000 to 662 000 km2 and are +30–300% of published appraisals. Moderately sized rivers (orders 5–9) seem to comprise the greatest global area, with less area covered by low and high order streams, while global stream length, and therefore the riparian interface, is dominated by 1st order streams. Rivers and streams are likely to cover 0.30–0.56% of the land surface and make contributions to global processes and greenhouse gas emissions that may be +20–200% greater than those implied by previous estimates

Net greenhouse gas balance of fibre wood plantation on peat in Indonesia

Tropical peatlands cycle and store large amounts of carbon in their soil and biomass1,2,3,4,5. Climate and land-use change alters greenhouse gas (GHG) fluxes of tropical peatlands, but the magnitude of these changes remains highly uncertain6,7,8,9,10,11,12,13,14,15,16,17,18,19. Here we measure net ecosystem exchanges of carbon dioxide, methane and soil nitrous oxide fluxes between October 2016 and May 2022 from Acacia crassicarpa plantation, degraded forest and intact forest within the same peat landscape, representing land-cover-change trajectories in Sumatra, Indonesia. This allows us to present a full plantation rotation GHG flux balance in a fibre wood plantation on peatland. We find that the Acacia plantation has lower GHG emissions than the degraded site with a similar average groundwater level (GWL), despite more intensive land use. The GHG emissions from the Acacia plantation over a full plantation rotation (35.2 ± 4.7 tCO2-eq ha−1 year−1, average ± standard deviation) were around two times higher than those from the intact forest (20.3 ± 3.7 tCO2-eq ha−1 year−1), but only half of the current Intergovernmental Panel on Climate Change (IPCC) Tier 1 emission factor (EF)20 for this land use. Our results can help to reduce the uncertainty in GHG emissions estimates, provide an estimate of the impact of land-use change on tropical peat and develop science-based peatland management practices as nature-based climate solutions

Anthropogenic perturbation of the carbon fluxes from land to ocean

A substantial amount of the atmospheric carbon taken up on land through photosynthesis and chemical weathering is transported laterally along the aquatic continuum from upland terrestrial ecosystems to the ocean. So far, global carbon budget estimates have implicitly assumed that the transformation and lateral transport of carbon along this aquatic continuum has remained unchanged since pre-industrial times. A synthesis of published work reveals the magnitude of present-day lateral carbon fluxes from land to ocean, and the extent to which human activities have altered these fluxes. We show that anthropogenic perturbation may have increased the flux of carbon to inland waters by as much as 1.0 Pg C yr-1 since pre-industrial times, mainly owing to enhanced carbon export from soils. Most of this additional carbon input to upstream rivers is either emitted back to the atmosphere as carbon dioxide (~0.4 Pg C yr-1) or sequestered in sediments (~0.5 Pg C yr-1) along the continuum of freshwater bodies, estuaries and coastal waters, leaving only a perturbation carbon input of ~0.1 Pg C yr-1 to the open ocean. According to our analysis, terrestrial ecosystems store ~0.9 Pg C yr-1 at present, which is in agreement with results from forest inventories but significantly differs from the figure of 1.5 Pg C yr-1 previously estimated when ignoring changes in lateral carbon fluxes. We suggest that carbon fluxes along the land–ocean aquatic continuum need to be included in global carbon dioxide budgets.Peer reviewe

Direct and indirect metabolic CO2 release by humanity

The direct CO2 released by respiration of humans and domesticated animals, as well as CO2 derived from the decomposition of their resulting wastes was calculated in order to ascertain the direct and indirect metabolic contribution of humanity to CO2 release. Human respiration was estimated to release 0.6 Gt C year-1 and that of their associated domestic animals was estimated to release 1.5 GtC year -1, to which an indirect release of 1.0 Gt C year-1, derived from decomposition of the organic waste and garbage produced by humans and their domestic animals, must be added. These combined direct and indirect metabolic sources, estimated at 3.1 GtC year-1, have increased 7 fold since pre-industrial times and are predicted to continue to rise over the 21st century.Peer Reviewe

Mesozooplankton grazing and primary production: Reply to the comment by Laws

4 pages, 1 figure, 1 tablePeer Reviewe

The ecosystem size and shape dependence of gas transfer velocity versus wind speed relationships in lakes

Air–water diffusive gas flux is commonly determined using measurements of gas concentrations and an estimate of gas transfer velocity (k600) usually derived from wind speed. The great heterogeneity of aquatic systems raises questions about the appropriateness of using a single wind-based model to predict k600 in all aquatic systems. Theoretical considerations suggest that wind speed to k600 relationships should instead be system-specific. Using data collected from aquatic systems of different sizes, we show that k600 is related to fetch and other measures of ecosystem size. Lake area together with wind speed provided the best predictive model of gas transfer velocity and explained 68% of the variability in individual k600 measurements. For a moderate wind speed of 5 m·s−1, predicted k600 varied from 6 cm·h−1 in a small 1 ha lake to over 13 cm·h−1 in a 100 km2 system. Wave height is also shown to be a promising integrative predictor variable. The modulating influence of system size on wind speed – gas transfer velocity relationships can have a large impact on upscaling exercises of gas exchange at the whole landscape level