Spatial and temporal dynamics of forest canopy gaps following selective logging in the eastern Amazon

Selective logging is a dominant form of land use in the Amazon basin and throughout the humid tropics, yet little is known about the spatial variability of forest canopy gap formation and closure following timber harvests. We established chronosequences of large‐area (14–158 ha) selective logging sites spanning a 3.5‐year period of forest regeneration and two distinct harvest methods: conventional logging (CL) and reduced‐impact logging (RIL). Our goals were to: (1) determine the spatial characteristics of canopy gap fraction immediately following selective logging in the eastern Amazon; (2) determine the degree and rate of canopy closure in early years following harvest among the major landscape features associated with logging – tree falls, roads, skid trails and log decks; and (3) quantify spatial and temporal differences in canopy opening and closure in high‐ and low‐damage harvests (CL vs. RIL). Across a wide range of harvest intensities (2.6–6.4 felled trees ha^?1), the majority of ground damage occurred as skid trails (4–12%), whereas log decks and roads were only a small contributor to the total ground damage (<2%). Despite similar timber harvest intensities, CL resulted in more ground damage than RIL. Neither the number of log decks nor their individual or total area was correlated with the number of trees removed or intensity of tree harvesting (trees ha^?1). The area of skids was well correlated with the ground area damaged (m²) per tree felled. In recently logged forest (0.5 years postharvest), gap fractions were highest in log decks (mean RIL=0.83, CL=0.99) and lowest in tree‐fall areas (RIL: 0.26, CL: 0.41). However, the small surface area of log decks made their contribution to the total area‐integrated forest gap fraction minor. In contrast, tree falls accounted for more than two‐thirds of the area disturbed, but the canopy gaps associated with felled trees were much smaller than for log decks, roads and skids. Canopy openings decreased in size with distance from each felled tree crown. At 0.5 years postharvest, the area initially affected by the felling of each tree was approximately 100 m in radius for CL and 50 m for RIL. Initial decreases in gap fraction during the first 1.5 years of regrowth diminished in subsequent years. Throughout the 3.5‐year period of forest recovery, tree‐fall gap fractions remained higher in CL than in RIL treatments, but canopy gap closure rates were higher in CL than in RIL areas. During the observed recovery period, the canopy gap area affected by harvesting decreased in radius around each felled tree from 100 to 40 m in CL, and from 50 to 10 m in RIL. The results suggest that the full spatial and temporal dynamics of canopy gap fraction must be understood and monitored to predict the effects of selective logging on regional energy balance and climate regimes, biogeochemical processes including carbon cycling, and plant and faunal population dynamics. This paper also shows that remote sensing of log decks alone will not provide an accurate assessment of total forest area impacted by selective logging, nor will it be closely correlated to damage levels and canopy gap closure rates.     

Coarse woody debris in undisturbed and logged forests in the eastern Brazilian Amazon

Coarse woody debris (CWD) is an important component of the carbon cycle in tropical forests. We measured the volume and density of fallen CWD at two sites, Cauaxi and Tapajós in the Eastern Amazon. At both sites we studied undisturbed forests (UFs) and logged forests 1 year after harvest. Conventional logging (CL) and reduced impact logging (RIL) were used for management on areas where the geometric volumes of logs harvested was about 25–30 m³ ha^?1. Density for five classes of fallen CWD for large material (>10 cm diameter) ranged from 0.71 to 0.28 Mg m^?3 depending upon the degree of decomposition. Density of wood within large fallen logs varied with position relative to the ground and with distance from the center of the log. Densities for materials with diameters from 2 to 5 and 5 to 10 cm were 0.36 and 0.45 Mg m^?3, respectively. The average mass (±SE) of fallen CWD at Cauaxi was 55.2 (4.7), 74.7 (0.6), and 107.8 (10.5) Mg ha^?1 for duplicate UF, RIL, and CL sites, respectively. At Tapajós, the average mass of fallen CWD was 50.7 (1.1) Mg ha^?1 for UF and 76.2 (10.2) Mg ha^?1 for RIL for duplicate sites compared with 282 Mg ha^?1 for live aboveground biomass. Small‐ and medium‐sized material (<10 cm dia.) accounted for 8–18% of the total fallen CWD mass. The large amount of fallen CWD at these UF sites relative to standing aboveground biomass suggests either that the forests have recently been subjected to a pulse of high mortality or that they normally suffer a high mortality rate in the range of 0.03 per year. Accounting for background CWD in UF, CL management produced 2.7 times as much CWD as RIL management. Excess CWD at logging sites would generate a substantial CO₂ emission given the high rates of decay in moist tropical forests.     

Net primary productivity allocation and cycling of carbon along a tropical forest elevational transect in the Peruvian Andes

The net primary productivity, carbon (C) stocks and turnover rates (i.e. C dynamics) of tropical forests are an important aspect of the global C cycle. These variables have been investigated in lowland tropical forests, but they have rarely been studied in tropical montane forests (TMFs). This study examines spatial patterns of above‐ and belowground C dynamics along a transect ranging from lowland Amazonia to the high Andes in SE Peru. Fine root biomass values increased from 1.50 Mg C ha^?1 at 194 m to 4.95 ± 0.62 Mg C ha^?1 at 3020 m, reaching a maximum of 6.83 ± 1.13 Mg C ha^?1 at the 2020 m elevation site. Aboveground biomass values decreased from 123.50 Mg C ha^?1 at 194 m to 47.03 Mg C ha^?1 at 3020 m. Mean annual belowground productivity was highest in the most fertile lowland plots (7.40 ± 1.00 Mg C ha^?1 yr^?1) and ranged between 3.43 ± 0.73 and 1.48 ± 0.40 Mg C ha^?1 yr^?1 in the premontane and montane plots. Mean annual aboveground productivity was estimated to vary between 9.50 ± 1.08 Mg C ha^?1 yr^?1 (210 m) and 2.59 ± 0.40 Mg C ha^?1 yr^?1 (2020 m), with consistently lower values observed in the cloud immersion zone of the montane forest. Fine root C residence time increased from 0.31 years in lowland Amazonia to 3.78 ± 0.81 years at 3020 m and stem C residence time remained constant along the elevational transect, with a mean of 54 ± 4 years. The ratio of fine root biomass to stem biomass increased significantly with increasing elevation, whereas the allocation of net primary productivity above‐ and belowground remained approximately constant at all elevations. Although net primary productivity declined in the TMF, the partitioning of productivity between the ecosystem subcomponents remained the same in lowland, premontane and montane forests.     

Water chemistry and nutrient budgets in an undisturbed evergreen rainforest of Southern Chile

In a pristine evergreen rainforest of Nothofagus betuloides, located at the Cordillera de los Andes in southern Chile (41?°S), concentrations and fluxes of nutrients in bulk precipitation, cloud water, throughfall water, stemflow water, soil infiltration and percolation water and runoff water were measured. The main objectives of this study were to investigate canopy–soil–atmosphere interactions and to calculate input–output budgets. From May 1999 till April 2000, the experimental watershed received 8121?mm water (86% incident precipitation, 14% cloud water), of which the canopy intercepted 16%. Runoff water volume amounted 9527?mm. Bulk deposition of inorganic (DIN) and organic (DON) nitrogen amounted 3.6?kg?ha^?1?year^?1 and 8.2?kg?ha^?1?year^?1 respectively. Occult deposition (clouds?+?fog) contributes for 40% to the atmospheric nitrogen input (bulk?+?occult deposition) of the forest. An important part of the atmospheric ammonium deposition is retained within the canopy or converted to nitrate or organic nitrogen by epiphytic bacteria or lichens. Also the export of inorganic (0.9?kg?ha^?1?year^?1) and organic (5.2?kg?ha^?1?year^?1) nitrogen via runoff is lower than the input to the forest floor via throughfall and stemflow water (3.2?kg?DIN?ha^?1?year^?1 and 5.6?kg?DON?ha^?1?year^?1). The low concentrations of NO-₃ and NH+₄ under the rooting depth suggest an effective biological immobilization by vegetation and soil microflora. Dry deposition and foliar leaching of base cations (K⁺, Ca²⁺, Mg²⁺) was estimated using a canopy budget model. Bulk deposition accounted for about 50% of the total atmospheric input. Calculated dry and occult deposition are both of equal value (about 25%). Foliar leaching of K⁺, Ca²⁺, and Mg²⁺ accounted for 45%, 38% and 6% of throughfall deposition respectively. On an annual basis, the experimental watershed was a net source for Na⁺, Ca²⁺ and Mg²⁺.     

The Role of Dissolved Organic Carbon, Dissolved Organic Nitrogen, and Dissolved Inorganic Nitrogen in a Tropical Wet Forest Ecosystem

Although tropical wet forests play an important role in the global carbon (C) and nitrogen (N) cycles, little is known about the origin, composition, and fate of dissolved organic C (DOC) and N (DON) in these ecosystems. We quantified and characterized fluxes of DOC, DON, and dissolved inorganic N (DIN) in throughfall, litter leachate, and soil solution of an old-growth tropical wet forest to assess their contribution to C stabilization (DOC) and to N export (DON and DIN) from this ecosystem. We found that the forest canopy was a major source of DOC (232 kg C ha^–1 y^–1). Dissolved organic C fluxes decreased with soil depth from 277 kg C ha^–1 y^–1 below the litter layer to around 50 kg C kg C ha^–1 y^–1 between 0.75 and 3.5m depth. Laboratory experiments to quantify biodegradable DOC and DON and to estimate the DOC sorption capacity of the soil, combined with chemical analyses of DOC, revealed that sorption was the dominant process controlling the observed DOC profiles in the soil. This sorption of DOC by the soil matrix has probably led to large soil organic C stores, especially below the rooting zone. Dissolved N fluxes in all strata were dominated by mineral N (mainly NO₃⁻). The dominance of NO₃^– relative to the total amount nitrate of N leaching from the soil shows that NO₃^– is dominant not only in forest ecosystems receiving large anthropogenic nitrogen inputs but also in this old-growth forest ecosystem, which is not N-limited.     

Fine Root Biomass,Production, Turnover Rates,and Nutrient Contents in Boreal Forest Ecosystems in Relation to Species,Climate, Fertility,and Stand Age: Literature Review and Meta-Analyses

Fine roots <2 mm in diameter play a key role in regulating the biogeochemical cycles of ecosystems and are important to our understanding of ecosystem responses to global climate changes. Given the sensitivity of fine roots, especially in boreal region, to climate changes, it is important to assess whether and to what extent fine roots in this region change with climates. Here, in this synthesis, a data set of 218 root studies were complied to examine fine root patterns in the boreal forest in relation to site and climatic factors. The mean fine root biomass in the boreal forest was 5.28 Mg ha^?1, and the production of fine roots was 2.82 Mg ha^?1 yr^?1, accounting for 32% of annual net primary production of the boreal forest. Fine roots in the boreal forest on average turned over 1.07 times per year. Fine roots contained 50.9 kg ha^?1 of nitrogen (N) and 3.63 kg ha^?1 of phosphorous (P). In total, fine roots in the boreal forest ecosystems contain 6.1 × 10⁷ Mg N and 4.4×10⁶Mg P pools, respectively, about 10% of the global nutrients of fine roots. Fine root biomass, production, and turnover rate generally increased with increasing mean annual temperature and precipitation. Fine root biomass in the boreal forest decreased significantly with soil N and P availability. With increasing stand age, fine root biomass increased until about 100 years old for forest stands and then leveled off or decreased thereafter. These results of meta analysis suggest that environmental factors strongly influence fine root biomass, production, and turnover in boreal forest, and future studies should place a particular emphasis on the root-environment relationships.     

Nitrogen deposition in tropical forests from savanna and deforestation fires

We used satellite‐derived estimates of global fire emissions and a chemical transport model to estimate atmospheric nitrogen (N) fluxes from savanna and deforestation fires in tropical ecosystems. N emissions and reactive N deposition led to a net transport of N equatorward, from savannas and areas undergoing deforestation to tropical forests. Deposition of fire‐emitted N in savannas was only 26% of emissions – indicating a net export from this biome. On average, net N loss from fires (the sum of emissions and deposition) was equivalent to approximately 22% of biological N fixation (BNF) in savannas (4.0 kg N ha^?1 yr^?1) and 38% of BNF in ecosystems at the deforestation frontier (9.3 kg N ha^?1 yr^?1). Net N gains from fires occurred in interior tropical forests at a rate equivalent to 3% of their BNF (0.8 kg N ha^?1 yr^?1). This percentage was highest for African tropical forests in the Congo Basin (15%; 3.4 kg N ha^?1 yr^?1) owing to equatorward transport from frequently burning savannas north and south of the basin. These results provide evidence for cross‐biome atmospheric fluxes of N that may help to sustain productivity in some tropical forest ecosystems on millennial timescales. Anthropogenic fires associated with slash and burn agriculture and deforestation in the southern part of the Amazon Basin and across Southeast Asia have substantially increased N deposition in these regions in recent decades and may contribute to increased rates of carbon accumulation in secondary forests and other N‐limited ecosystems.     

Removal of carbon and mineral nutrients upon clear felling of spruce forests in the middle taiga

We obtain an estimate of the influence of localized clear felling in a middle taiga spruce forest on the dynamics of organic mass and its content of carbon and elements of mineral nutrition. In an old-age myrtillus bilberry moist spruce stand, in which the reserve of organic mass is 180 t ha^?1, there are concentrated 86 t of carbon, 508 kg of nitrogen, and 904 kg of ash elements. On the logging area of this spruce forest in the undercut (incomplete felling), roots, and logging slash, there are 112 t ha^?1 of phytomass, where 53 t C ha^?1, 308 kg of nitrogen, and 723 kg of ash elements are concentrated. Upon the localized clear felling with removal of tree-length logs, the loss of carbon is 44%, nitrogen 28.3%, and ash elements 22.3% of their overall reserve in the myrtillus moist spruce stand. In the spruce-sphagnum forest, the phytomass of the stand is 194 t ha^?1 and contains 92 t ha^?1 of carbon, 580 kg of nitrogen, and 974 kg of ash elements. Upon cutting of the stand in this spruce forest, 77 t ha^?1 of organic mass were taken away, including 37 t of carbon, 140 kg of nitrogen, and 215 kg of ash elements, which are 39.5, 24.2, and 22% of their overall mass in woody plants of the cenosis, respectively.     

Effects of experimental N addition on plant diversity in an old‐growth temperate forest

Temperate forest ecosystems have experienced mounting negative effects due to increasing levels of nitrogen (N) deposition. We examined the effects of experimental N addition on plant diversity in an old‐growth temperate forest to test the following hypothesis: Long‐term excessive N addition decreases plant diversity by affecting the growth of plants, which results from changes in the soil nutrient content and a decrease in the soil pH in temperate forests. Experimental N additions were administered at the following levels since 2008: control (0 kg N ha^?1 year^?1), low N (30 kg N ha^?1 year^?1), medium N (60 kg N ha^?1 year^?1), and high N (120 kg N ha^?1 year^?1). Additionally, plant diversity was studied from 2014 to 2016. The results showed that the experimental N additions had significant effects on plant diversity and soil properties in an old‐growth temperate forest. The high‐N treatment decreased the density, cover, and diversity of understory plants, and some herbs even appeared to undergo premature aging, whereas the species diversity of herbs and ferns in the low‐N treatment plots showed a slight increasing tendency. This may have been because the old‐growth temperate forest is an N‐limited ecosystem, so the moderate N input did not show a large influence on plant diversity. However, the long‐term high‐N treatment ultimately reduced plant diversity by changing the soil nutrient contents, decreasing the pH values, and damaging plant growth. Our results suggested that the long‐term excessive N addition negatively affected the forest ecosystem in an N‐limited temperature forest.     

Primary production and carbon allocation in relation to nutrient supply in a tropical experimental forest

Nutrient supply commonly limits aboveground plant productivity in forests, but the effects of an altered nutrient supply on gross primary production (GPP) and patterns of carbon (C) allocation remain poorly characterized. Increased nutrient supply may lead to a higher aboveground net primary production (ANPP), but a lower total belowground carbon allocation (TBCA), with little change in either aboveground plant respiration (APR) or GPP. Alternatively, increases in nutrient supply may increase GPP, with the quantity of GPP allocated aboveground increasing more steeply than the quantity of GPP allocated belowground. To examine the effects of an elevated nutrient supply on the C allocation patterns in forests, we determined whole‐ecosystem C budgets in unfertilized plots of Eucalyptus saligna and in adjacent plots receiving regular additions of 65 kg N ha^?1, 31 kg P ha^?1, 46 kg K ha^?1, and macro‐ and micronutrients. We measured the absolute flux of C allocated to the components of GPP (ANPP, TBCA and APR), as well as the fraction of GPP allocated to these components. Fertilization dramatically increased GPP. Averaged over 3 years, GPP in the fertilized plots was 34% higher than that in the unfertilized controls (3.95 vs. 2.95 kg C m^?2 yr^?1). Fertilization‐related increases in GPP were allocated entirely aboveground – ANPP was 85% higher and APR was 57% higher in the fertilized than in the control plots, while TBCA did not differ significantly between treatments. Carbon use efficiency (NPP/GPP) was slightly higher in the fertilized (0.53) compared with the control plots (0.51). Overall, fertilization increased ANPP and APR, and these increases were related to a greater GPP and an increase in the fraction of GPP allocated aboveground.     

Biomass,Carbon, and Nitrogen Pools in Mexican Tropical Dry Forest Landscapes

Tropical dry forest is the most widely distributed land-cover type in the tropics. As the rate of land-use/land-cover change from forest to pasture or agriculture accelerates worldwide, it is becoming increasingly important to quantify the ecosystem biomass and carbon (C) and nitrogen (N) pools of both intact forests and converted sites. In the central coastal region of México, we sampled total aboveground biomass (TAGB), and the N and C pools of two floodplain forests, three upland dry forests, and four pastures converted from dry forest. We also sampled belowground biomass and soil C and N pools in two sites of each land-cover type. The TAGB of floodplain forests was as high as 416 Mg ha^–1, whereas the TAGB of the dry forest ranged from 94 to 126 Mg ha^–1. The TAGB of pastures derived from dry forest ranged from 20 to 34 Mg ha^–1. Dead wood (standing and downed combined) comprised 27%–29% of the TABG of dry forest but only about 10% in floodplain forest. Root biomass averaged 32.0 Mg ha^–1 in floodplain forest, 17.1 Mg ha^–1 in dry forest, and 5.8 Mg ha^–1 in pasture. Although total root biomass was similar between sites within land-cover types, root distribution varied by depth and by size class. The highest proportion of root biomass occurred in the top 20 cm of soil in all sites. Total aboveground and root C pools, respectively, were 12 and 2.2 Mg ha^–1 in pasture and reached 180 and 12.9 Mg ha^–1 in floodplain forest. Total aboveground and root pools, respectively, were 149 and 47 kg ha^–1 in pasture and reached 2623 and 264 kg ha^–1 in floodplain forest. Soil organic C pools were greater in pastures than in dry forest, but soil N pools were similar when calculated for the same soil depths. Total ecosystem C pools were 306. The Mg ha^–1 in floodplain forest, 141 Mg ha^–1 in dry forest, and 124 Mg ha^–1 in pasture. Soil C comprised 37%–90% of the total ecosystem C, whereas soil N comprised 85%–98% of the total. The N pools lack of a consistent decrease in soil pools caused by land-use change suggests that C and N losses result from the burning of aboveground biomass. We estimate that in México, dry forest landscapes store approximately 2.3 Pg C, which is about equal to the C stored by the evergreen forests of that country (approximately 2.4 Pg C). Potential C emissions to the atmosphere from the burning of biomass in the dry tropical landscapes of México may amount to 708 Tg C, as compared with 569 Tg C from evergreen forests.     

Effects of Soil Texture on Belowground Carbon and Nutrient Storage in a Lowland Amazonian Forest Ecosystem

Soil texture plays a key role in belowground C storage in forest ecosystems and strongly influences nutrient availability and retention, particularly in highly weathered soils. We used field data and the Century ecosystem model to explore the role of soil texture in belowground C storage, nutrient pool sizes, and N fluxes in highly weathered soils in an Amazonian forest ecosystem. Our field results showed that sandy soils stored approximately 113 Mg C ha^-1 to a 1-m depth versus 101 Mg C ha^-1 in clay soils. Coarse root C represented a large and significant ecosystem C pool, amounting to 62% and 48% of the surface soil C pool on sands and clays, respectively, and 34% and 22% of the soil C pool on sands and clays to 1-m depth. The quantity of labile soil P, the soil C:N ratio, and live and dead fine root biomass in the 0–10-cm soil depth decreased along a gradient from sands to clays, whereas the opposite trend was observed for total P, mineral N, potential N mineralization, and denitrification enzyme activity. The Century model was able to predict the observed trends in surface soil C and N in loams and sands but underestimated C and N pools in the sands by approximately 45%. The model predicted that total belowground C (0–20 cm depth) in sands would be approximately half that of the clays, in contrast to the 89% we measured. This discrepancy is likely to be due to an underestimation of the role of belowground C allocation with low litter quality in sands, as well as an overestimation of the role of physical C protection by clays in this ecosystem. Changes in P and water availability had little effect on model outputs, whereas adding N greatly increased soil organic matter pools and productivity, illustrating the need for further integration of model structure and tropical forest biogeochemical cycling. Received 3 March 1999; accepted 27 August 1999.     

Nitrate leaching and soil nitrous oxide emissions diminish with time in a hybrid poplar short‐rotation coppice in southern Germany

Hybrid poplar short‐rotation coppices (SRC) provide feedstocks for bioenergy production and can be established on lands that are suboptimal for food production. The environmental consequences of deploying this production system on marginal agricultural land need to be evaluated, including the investigation of common management practices i.e., fertilization and irrigation. In this work, we evaluated (1) the soil‐atmosphere exchange of carbon dioxide, methane, and nitrous oxide (N₂O); (2) the changes in soil organic carbon (SOC) stocks; (3) the gross ammonification and nitrification rates; and (4) the nitrate leaching as affected by the establishment of a hybrid poplar SRC on a marginal agricultural land in southern Germany. Our study covered one 3‐year rotation period and 2 years after the first coppicing. We combined field and laboratory experiments with modeling. The soil N₂O emissions decreased from 2.2 kg N₂O‐N ha^?1 a^?1 in the year of SRC establishment to 1.1–1.4 kg N₂O‐N ha^?1 a^?1 after 4 years. Likewise, nitrate leaching reduced from 13 to 1.5–8 kg N ha^?1 a^?1. Tree coppicing induced a brief pulse of soil N₂O flux and marginal effects on gross N turnover rates. Overall, the N losses diminished within 4 years by 80% without fertilization (irrespective of irrigation) and by 40% when 40–50 kg N ha^?1 a^?1 were applied. Enhanced N losses due to fertilization and the minor effect of fertilization and irrigation on tree growth discourage its use during the first rotation period after SRC establishment. A SOC accrual rate of 0.4 Mg C ha^?1 a^?1 (uppermost 25 cm, P = 0.2) was observed 5 years after the SRC establishment. Overall, our data suggest that SRC cultivation on marginal agricultural land in the region is a promising option for increasing the share of renewable energy sources due to its net positive environmental effects.     

Nutrient constraints to tropical agroecosystem productivity in long‐term degrading soils

Soil degradation is one of the most serious threats to sustainable crop production in many tropical agroecosystems where extensification rather than intensification of agriculture has occurred. In the highlands of western Kenya, we investigated soil nitrogen (N) and phosphorus (P) constraints to maize productivity across a cultivation chronosequence in which land‐use history ranged from recent conversion from primary forest to 100 years in continuous cropping. Nutrient treatments included a range of N and P fertilizer rates applied separately and in combination. Maize productivity without fertilizer was used as a proxy measure for indigenous soil fertility (ISF). Soil pools of mineral nitrogen, strongly bound P and plant‐available P decreased by 82%, 31% and 36%, and P adsorption capacity increased by 51% after 100 years of continuous cultivation. For the long rainy season (LR), grain yield without fertilizer declined rapidly as cultivation age increased from 0 to 25 years and then gradually declined to a yield of 1.6 Mg ha^?1, which was maintained as time under cultivation increased from 60 to 100 years. LR grain yield in the old conversions was only 24% of the average young conversion grain yield (6.4 Mg ha^?1). Application of either N or P alone significantly increased grain yield in both the LR and short rainy (SR) seasons, but only application of 120 kg N ha^?1 on the old conversion increased yield by >1 Mg ha^?1. In both SR and LR, there was a greater average yield increment response to N and P when applied together (ranging from 1 to 3.8 Mg ha^?1 for the LR), with the greatest responses on the old conversions. The benefit–cost ratio (BCR) for applying 120 kg N ha^?1 alone was <1 except on the old conversions, while BCRs were>1 for applying 25 kg P ha^?1 alone at all levels of conversion for both seasons. Application of both N (120 kg N ha^?1) and P (25 kg P ha^?1) on the old conversions resulted in the greatest BCRs. This study clearly indicates that maize productivity responses to N and P fertilizer are significantly affected by the age of cultivation and its influence on ISF, but that loss of productivity can be restored rapidly when these limiting nutrients are applied. Management strategies should consider ISF and economic factors to determine optimal N and P input requirements for achieving and sustaining profitable crop production on degraded soils.     

Slow response of soil organic matter to the reduction in atmospheric nitrogen deposition in a Norway spruce forest

Global nitrogen (N) deposition rates in terrestrial environments have quadrupled since preindustrial times, causing structural and functional changes of ecosystems. Different emission reduction policies were therefore devised. The aim of our study was to investigate if, and over what timescale, processes of soil organic matter (OM) transformation respond to a decline in atmospheric N deposition. A N‐saturated spruce forest (current N deposition: 34 kg ha^?1 yr^?1; critical N load: 14 kg ha^?1 yr^?1), where N deposition has been reduced to 11.5 kg ha^?1 yr^?1 since 1991, was studied. Besides organic C and organic and inorganic N, noncellulosic carbohydrates, amino sugars and amino acids were determined. A decline in organic N in litter indicated initial effects at plant level. However, there were no changes in biomarkers upon the reduction in N deposition. In addition, inorganic N was not affected by reduced N deposition. The results showed that OM cycling and transformation processes have not responded so far. It was concluded that no direct N deposition effects have occurred due to the large amount of stored organic N, which seems to compensate for the reduction in deposited N. Obviously, the time span of atmospheric N reduction (about 14.5 years) is too short compared with the mean turnover time of litter to cause indirect effects on the composition of organic C and N compounds. It is assumed that ecological processes, such as microbial decomposition or recycling of organic N and C, react slowly, but may start within the next decade with the incorporation of the new litter.     

Regional gains and losses of nitrogen in the Amazon basin

In order to better understand the relative importance of different ecosystems and nitrogen cycling processes within the Amazon basin to the nitrogen economy of this region, we constructed a generalized nitrogen budget for the region based on data for hydrologic losses of nitrogen and nitrogen fixation in Amazon forests. Data included information available for nitrogen in water entering and leaving both the entire basin and watersheds on oxisol and ultisol soils near Manaus, Brazil, in addition to biological nitrogen fixation in forests on ultisol, oxisol and entisol (‘varzea’) soils in Central Amazonia. Available data indicate that 4–6 kg N ha^?1 yr^?1 are lost via the River Amazonas, and that a similar amount enters in rainfall. Root-associated biological nitrogen fixation contributesca. 2 kg N ha^?1 yr^?1 to forests on oxisols, 20 kg N ha^?1 yr^?1 to forests on utisols, and 200 kg N ha^?1 yr^?1 to forests on fertile varzea soils. There is 5–10 fold more NH₄ ⁺?N than NO₃?N in rain and stream water entering and leaving the waterbasin near Manaus. Calculations based on these data plus certain assumption yield the following regional nitrogen balance estimate: inputs through bulk deposition of 36×10⁸ kg N yr^?1 and through biological nitrogen fixation of 120×10⁸ kg N yr^?1, and outputsvia the River Amazonas of 36×10⁸ kg N yr^?1 andvia denitrification and volatization (by difference) of 120×10⁸ kg N yr^?1.     

Impacts of climate and land use on N2O and CH4 fluxes from tropical ecosystems in the Mt. Kilimanjaro region,Tanzania

In this study, we quantify the impacts of climate and land use on soil N₂O and CH₄ fluxes from tropical forest, agroforest, arable and savanna ecosystems in Africa. To do so, we measured greenhouse gases (GHG) fluxes from 12 different ecosystems along climate and land‐use gradients at Mt. Kilimanjaro, combining long‐term in situ chamber and laboratory soil core incubation techniques. Both methods showed similar patterns of GHG exchange. Although there were distinct differences from ecosystem to ecosystem, soils generally functioned as net sources and sinks for N₂O and CH₄ respectively. N₂O emissions correlated positively with soil moisture and total soil nitrogen content. CH₄ uptake rates correlated negatively with soil moisture and clay content and positively with SOC. Due to moderate soil moisture contents and the dominance of nitrification in soil N turnover, N₂O emissions of tropical montane forests were generally low (<1.2 kg N ha^?1 year^?1), and it is likely that ecosystem N losses are driven instead by nitrate leaching (~10 kg N ha^?1 year^?1). Forest soils with well‐aerated litter layers were a significant sink for atmospheric CH₄ (up to 4 kg C ha^?1 year^?1) regardless of low mean annual temperatures at higher elevations. Land‐use intensification significantly increased the soil N₂O source strength and significantly decreased the soil CH₄ sink. Compared to decreases in aboveground and belowground carbon stocks enhanced soil non‐CO₂ GHG emissions following land‐use conversion from tropical forests to homegardens and coffee plantations were only a small factor in the total GHG budget. However, due to lower ecosystem carbon stock changes, enhanced N₂O emissions significantly contributed to total GHG emissions following conversion of savanna into grassland and particularly maize. Overall, we found that the protection and sustainable management of aboveground and belowground carbon and nitrogen stocks of agroforestry and arable systems is most crucial for mitigating GHG emissions from land‐use change.     

Nitrate leaching from three afforestation chronosequences on former arable land in Denmark

In regions dominated by agricultural activities, nitrogen (N) is recognized as a major pollutant in aquatic environments. In north‐western Europe, afforestation of agricultural land is part of a strategy to improve water quality. In Denmark, former arable land has been afforested during the past 40–50 years. This study evaluated the effect of afforestation of former arable land on nitrate leaching, based on three afforestation chronosequences. Precipitation, canopy throughfall and soil water were collected and soil moisture was monitored at two Danish locations, Vestskoven (nutrient‐rich, medium deposition) and Gejlvang (nutrient‐poor, high deposition). Afforestation was performed using Norway spruce [Picea abies (Karst.) L.] and common oak (Quercus robur L.) at Vestskoven and Norway spruce at Gejlvang. The results suggest that afforestation of former arable land initially leads to lower nitrate leaching than that occurring under the former agricultural land use, and largely below the standard of 50 mg NO⁻₃ L⁻¹ for groundwater to be utilized as drinking water. Nitrate concentrations became almost negligible in forest stands of 5–20 years of age. However, after canopy closure (>20 years) nitrate concentrations below the root zone and nitrate leaching tended to increase. This was attributed to increased N deposition with increasing canopy development and decreased N demand once the most N‐rich biomass compartments had been built up. Nitrate leaching started to increase at a throughfall deposition level of about 10 kg N ha⁻¹ yr⁻¹. Compared with nutrient‐poor sandy soils, nutrient‐rich clayey soils appeared more vulnerable to disturbance of the N cycle and to increased N deposition, leading to N saturation and enhanced nitrate leaching. In approximately the first 35 years after afforestation, nitrate leaching below the root zone was generally higher below oak than below Norway spruce.     

The effects of gap disturbance on nitrogen cycling and retention in late-successional northern hardwood–hemlock forests

Late-successional forests in the upper Great Lakes region are susceptible to nitrogen (N) saturation and subsequent nitrate (NO₃⁻) leaching loss. Endemic wind disturbances (i.e., treefall gaps) alter tree uptake and soil N dynamics; and, gaps are particular susceptible to NO₃⁻ leaching loss. Inorganic N was measured throughout two snow-free periods in throughfall, forest floor leachates, and mineral soil leachates in gaps (300–2,000 m², 6–9 years old), gap-edges, and closed forest plots in late-successional northern hardwood, hemlock, and northern hardwood–hemlock stands. Differences in forest water inorganic N among gaps, edges, and closed forest plots were consistent across these cover types: NO₃⁻ inputs in throughfall were significantly greater in undisturbed forest plots compared with gaps and edges; forest floor leachate NO₃⁻ was significantly greater in gaps compared to edges and closed forest plots; and soil leachate NO₃⁻ was significantly greater in gaps compared to the closed forest. Significant differences in forest water ammonium and pH were not detected. Compared to suspected N-saturated forests with high soil NO₃⁻ leaching, undisturbed forest plots in these late-successional forests are not losing NO₃⁻ (net annual gain of 2.8 kg ha⁻¹) and are likely not N-saturated. Net annual NO₃⁻ losses were observed in gaps (1.3 kg ha⁻¹) and gap-edges (0.2 kg ha⁻¹), but we suspect these N leaching losses are a result of decreased plant uptake and increased soil N mineralization associated with disturbance, and not N-saturation.