In situ estimates of annual net nitrogen mineralization and nitrification in a subarctic watershed

Summary Annual estimates of surface soil nitrogen transformations were determined using an in situ method in four different subarctic vegetation types within a watershed in southwestern Alaska. The net nitrogen mineralization estimates were 22.5, 0.5, 4.7, and 2.7 kg-N ha^-1 yr^-1 for the alder, dry tundra, moist tundra, and white spruce sites, respectively. Only the soil from the alder site showed net nitrification (about 10 kg-N ha^-1 yr^-1). Annual inogranic nitrogen flux from the overlying organic layer to the mineral soil was almost seven times greater than net N production in the surface mineral soil in the alder site, indicating that the alder forest floor is potentially a substantial source for plant-available N. Rates of mobilization of N from the surface organic layers of the other sites were similar to net N production rates in surface mineral soils. In situ rates of N transformations showed a similar trend among sites as did laboratory estimates conducted in a previous study, suggesting a strong substrate control of N transformations in these soils.     

Nitrogen transformations in two nitrogen saturated forest ecosystems subjected to an experimental decrease in nitrogen deposition

Nitrogen transformations were studied in the forest floor and mineral soil (0–5 cm) of a Douglas fir forest (Pseudotsuga menziesii (Mirb.) Franco.) and a Scots pine forest (Pinus sylvestris L.) in the Netherlands. Curren nitrogen depositions (40 and 56 kg N ha^-1 yr^-1, respectively) were reduced to natural background levels (1–2 kg N ha^-1 yr^-1) by a roof construction. The study concentrated on rates and dynamic properties of nitrogen transformations and their link with the leaching pattern and nitrogen uptake of the vegetation under high and reduced nitrogen deposition levels. Results of an in situ field incubation experiment and laboratory incubations were compared. No effect of the reduced N deposition on nitrogen transformations was found in the Douglas fir forest. In the Scots pine forest, however, during some periods of the year nitrogen transformations were significantly decreased under the low nitrogen deposition level. At low nitrogen inputs a net immobilization occurred during most of the year leading to a very small net mineralization for the whole year. In laboratory and in individual field plots nitrogen transformations were negatively correlated with initial inorganic nitrogen concentrations. Nitrogen budget estimates showed that nitrogen transformations were probably underestimated by the in situ incubation technique. Nevertheless less nitrogen was available for plant uptake and leaching at the low deposition plots.     

Nitrogen cycling in an acid forest ecosystem in the Netherlands under increased atmospheric nitrogen input

Within a long-term research project studying the biogeochemical budget of an oak-beech forest ecosystem in the eastern part of the Netherlands, the nitrogen transformations and solute fluxes were determined in order to trace the fate of atmospherically deposited NH₄ ⁺ and to determine the contribution of nitrogen transformations to soil acidification.The oak-beech forest studied received an annual input of nitrogen via throughfall and stemflow of 45 kg N ha^–1 yr^–1, mainly as NH₄ ⁺, whereas 8 kg N ha^–1 yr^–1 was taken up by the canopy. Due to the specific hydrological regime resulting in periodically occurring high groundwater levels, denitrification was found to be the dominant output flux (35 kg N ha^–1 yr^–1). N₂0 emmission rate measurements indicated that 57% of this gaseous nitrogen loss (20 kg N ha^–1 yr^–1) was as N₂O. The forest lost an annual amount of 11 kg N ha^–1 yr^–1 via streamwater output, mainly as N0₃ ^–.Despite the acid conditions, high nitrification rates were measured. Nitrification occurred mainly in the litter layer and in the organic rich part of the mineral soil and was found to be closely correlated with soil temperature. The large amount of NH₄ ⁺ deposited on the forest floor via atmospheric deposition and produced by mineralization was to a large extent nitrified in the litter layer. Almost no NH₄ ⁺ reached the subsurface soil horizons. The N0₃ ^– was retained, taken up or transformed mainly in the mineral soil. A small amount of N0₃ ^– (9 kg N ha^–1 yr^–1) was removed from the system in streamwater output. A relatively small amount of nitrogen was measured in the soil water as Dissolved Organic Nitrogen.On the basis of these data the proton budget of the system was calculated using two different approaches. In both cases net proton production rates were high in the vegetation and in the litter layer of the forest ecosystem. Nitrogen transformations induced a net proton production rate of 2.4 kmol ha^–1 yr^–1 in the soil compartment.     

Forest floor-mineral soil interactions in the internal nitrogen cycle of an old-growth forest

Seasonal patterns and annual rates of N inputs, outputs, and internal cycling were determined for an old-growth mixed-conifer forest floor in the Sierra Nevada Mountains of California. Rates of net N mineralization within the forest floor, and plant N-uptake and leaching of inorganic N from the forest floor were 13, 10, and 9 kg-N ha^-1 yr^-1, respectively. The Mediterranean-type climate appeared to have a significant effect on N cycling within this forest, such that all N-process and flow rates showed distrinct seasonal patterns. We estimated the forest floor supplies less than one-third of the total aboveground plant N-uptake in this forest. The rate of net nitrification within the forest floor was always low (1 kg-NO₃ ^--N ha^-1 30d^-1). Mean residence times for organic matter and N in the forest floor were 13 and 34 years, respectively, suggesting that this forest floor layer is a site of net N immobilization within this ecosystem. We examined the influence of the forest floor on mineral soil N dynamics by injecting small amounts of¹⁵N-enriched (NH₄)₂SO₄ solutions into the surface mineral soil with the forest floor present (+FF) or removed (-FF). K₂SO₄-extractable NO₃ ^--N, total inorganic-N, and total-N pool sizes in the mineral soil were initially increased after forest floor removal (after 4 months), but NO₃ ^--N and total inorganic-N were not significantly different thereafter. Microbial biomass-N and K₂SO₄-extractable total-N pool sizes were also found to be larger in mineral soils without a forest floor after 1 and 1.3 years, respectively. Total¹⁵N-recovery was greater in the +FF treatment compared to the -FF treatment after 1-year (about 50% and 35%, respectively) but did not differ after 1.3 years (both about 35%), suggesting that the forest floor delays but does not prevent the N-loss from the surface mineral soil of this forest. We estimated using our¹⁵N data that fungal translocation from the mineral soil to the forest floor may be as large as 9 kg-N ha^-1 yr^-1 (similar in magnitude to other N flows in this forest), and may account for all of the observed absolute increase of N in litter during the early stages of decomposition at this site. Our results suggest that the forest floor acts both as a source and sink for N in the mineral soil.     

Nitrogen deposition,distribution and cycling in a subalpine spruce-fir forest in the Adirondacks,New York,USA

Nitrogen inputs, fluxes, internal generation and consumption, and outputs were monitored in a subalpine spruce-fir forest at approximately 1000-m elevation on Whiteface Mountain in the Adirondacks of New York, USA. Nitrogen in precipitation, cloudwater and dry deposition was collected on an event basis and quantified as an input. Throughfall, stemflow, litterfall and soil water were measured to determine fluxes within the forest. Nitrogen mineralization in the forest floor was estimated to determine internal sources of available N. Lower mineral horizon soil water was used to estimate output from the ecosystem. Vegetation and soil N pools were determined.During four years of continuous monitoring, an average of 16 kg N ha^–1 yr^–1 was delivered to the forest canopy as precipitation, cloudwater and dry deposition from the atmosphere. Approximately 30% of the input was retained by the canopy. Canopy retention is likely the result of both foliar uptake and immobilization by bark, foliage and microorganisms. Approximately 40 kg of N was made available within the forest floor from mineralization of organic matter. Virtually all the available ammonium (mineralized plus input from throughfall) is utilized in the forest floor, either by microorganisms or through uptake by vegetation. The most abundant N component of soil water solutions leaving the system was nitrate. Net ecosystem fluxes indicate accumulation of both ammonium and nitrate. There is a small net loss of organic N from the ecosystem. Some nitrate leaves the bottom of the B horizon throughout the year. Comparisons with other temperate coniferous sites and examination of the ecosystem N mass balance indicate that N use efficiency is less at our site, which suggests that the site is not severely limited by N.     

Cation distribution,cycling, and removal from mineral soil in Douglas-fir and red alder forests

Overstory species influence the distribution and dynamics of nutrients in forest ecosystems. Ecosystem-level estimates of Ca, Mg, and K pools and cycles in 50-year old Douglas-fir and red alder stands were used to determine the effect of overstory composition on net cation removal from the mineral soil, i.e. cation export from the soil in excess of additions. Net cation removal from Douglas-fir soil was 8 kg Ca ha^–1 yr^–1, 1 kg Mg ha^–1 yr^–1, and 0.3 kg K ha^–1 yr^–1. Annual cation export from soil by uptake and accumulation in live woody tissue and O horizon was of similar magnitude to leaching in soil solution. Atmospheric deposition partially off-set export by adding cations equivalent to 28–88% of cation export. Net cation removal from red alder soil was 58 kg Ca ha^–1 yr^–1, 9 kg Mg ha^–1 yr^–1, and 11 kg K ha^–1 yr^–1. Annual cation accumulation in live woody tissue and O horizon was three times greater than in Douglas-fir, while cation leaching in soil solution was five to eight times greater. The lack of excessive depletion of exchangeable cations in the red alder soil suggests that mineral weathering, rather than exchangeable cations, was the source of most of the removed cations. Nitric acid generated during nitrification in red alder soil led to high rates of weathering and NO₃-driven cation leaching.     

Nitrogen mineralization and H+ transfers in a Scots pine (Pinus sylvestris L.) forest soil as affected by liming

H⁺ production due to N uptake in a mature Scots pine stand subjected to high NH₄ ⁺ deposition was previously estimated to amount to approx. 2.2 kmol ha^-1 y^-1. The question whether H⁺ transfers related to N mineralization (ammonification and nitrification) offset or corroborate this proton production is investigated in the present research. To determine N mineralization, soil cores were used of which both ends were closed with layers of ion exchange resin (IER) to prevent influx and efflux of ions. The effect of liming on N mineralization and the resulting H⁺ production was investigated in 7 incubation periods of each ca. 8 wk. Because of its high mobility NO₃ accumulated in both IER layers at the expense of that in the incubated forest floor and mineral soil. Net N mineralization in the soil cores as a whole amounted to 40 and 77 kg N ha^-1 in 384 d in the control and limed plots, respectively. In both treatments ca. 65% of mineralized N was nitrified. H⁺ production due to N mineralization amounted to approx. 1.2 kmol ha^-1 y^-1 in the control and limed plots. Liming reduced the amount of C in the forest floor, but not forest floor mass, because of an increased mixing with mineral particles.     

Changes in ecosystem functioning after replacement of forest by Lantana shrubland in Kumaun Himalaya

Abstract. Lantana camara shrubland is compared with the adjacent Quercus leucotrichophora and Pinus roxburghii forests to understand changes occurring in net primary productivity and nutrient cycling, as a consequence of degradation of these forests. The total net primary productivity of Lantana camara shrubland was 17 t ha^-1 yr^-1, which is similar to the values reported for forests: 16 - 21 t ha^-1 yr^-1. Total nutrient content (N, P) in the soil in the L. camara shrubland: 2932 kg ha^-1 N and 111 kg ha^-1 P, was lower than that of the forest soils.     

Variation in biomass and carbon storage by stand age in pine (Pinus tabulaeformis) planted ecosystem in Mt. Taiyue,Shanxi, China

Forest ecosystems play dominant roles in global carbon budget because of the large quantities stored in live biomass, detritus, and soil organic matter. Researchers in various countries have investigated regional and continental scale patterns of carbon (C) stocks in forest ecosystems; however, the relationship between stand age in different components (vegetation, forest floor detritus, and mineral soil) and C storage and sequestration remains poorly understood. In this paper, we assessed an age sequence of 18-, 20-, 25-, 38-, and 42-year-old Pinus tabulaeformis planted by analyzing the vertical distribution of different components biomass with similar site conditions on Mt. Taiyue, Shanxi, China. The results showed that biomass of P. tabulaeformis planted stands was ranged from 88.59 Mg ha^?1 for the 25-year-old stand to 231.05 Mg ha^?1 for the 42-year-old stand and the major biomass was in the stems. Biomass of the ground vegetation varied from 0.51 to 1.35 Mg C ha^?1 between the five stands. The forest floor biomass increased with increasing stand age. The mean C concentration of total tree was 49.94%, which was higher than C concentrations of ground vegetation and forest floor. Different organs of trees C concentration were between 54.14% and 47.74%. C concentrations stored in the mineral soil for each stand experienced decline with increasing soil depth, but were age-independent. Total C storage of five planted forests ranged from 122.15 to 229.85 Mg C ha^?1, of which 51.44–68.38% of C storage was in the soil and 28.46–45.21% in vegetation. The study provided not only with an estimation biomass of P. tabulaeformis planted forest in Mt. Taiyue, Shanxi, China, but also with accurately estimating forest C storage at ecosystem scale.     

Relationships between soil microbial properties and aboveground stand characteristics of conifer forests in Oregon

Eight forest sites representing a large range of climate, vegetation, and productivity were sampled in a transect across Oregon to study the relationships between aboveground stand characteristics and soil microbial properties. These sites had a range in leaf area index of 0.6 to 16 m² m^–2 and net primary productivity of 0.3 to 14 Mg ha^–1 yr^–1.Measurements of soil and forest floor inorganic N concentrations and in situ net N mineralization, nitrification, denitrification, and soil respiration were made monthly for one year. Microbial biomass C and anaerobic N mineralization, an index of N availability, were also measured. Annual mean concentrations of NH ₄ ⁺ ranged from 37 to 96 mg N kg^–1 in the forest floor and from 1.7 to 10.7 mg N kg^–1 in the mineral soil. Concentrations of NO ₃ ^– were low ( < 1 mg N kg^–1) at all sites. Net N mineralization and nitrification, as measured by the buried bag technique, were low on most sites and denitrification was not detected at any site. Available N varied from 17 to 101 mg N kg^–1, microbial biomass C ranged from 190 to 1230 mg Ckg^–1, and soil respiration rates varied from 1.3 to 49 mg C kg^–1 day^–1 across these sites. Seasonal peaks in NH ₄ ⁺ concentrations and soil respiration rates were usually observed in the spring and fall.The soils data were positively correlated with several aboveground variables, including leaf area index and net primary productivity, and the near infrared-to-red reflectance ratio obtained from the airborne simulator of the Thematic Mapper satellite. The data suggest that close relationships between aboveground productivity and soil microbial processes exist in forests approaching semi-equilibrium conditions.Abbreviations IR infrared - LAI leaf area index - k _c proportion of microbial biomass C mineralized to CO₂ - NPP net primary productivity - TM Thematic Mapper     

Mineralization of nitrogen in long-term pasture soils: effects of management

A field incubation technique with acetylene to inhibit nitrification was used to estimate net N mineralization rates in some grassland soils through an annual cycle. Measurements were made on previously long-term grazed pastures on a silty clay loam soil in S.W. England which had background managements of +/– drainage and +/– fertilizer (200 kg N ha^–1 yr^–1). The effect of fertilizer addition on mineralization during the year of measurement was also determined. Small plots with animals excluded, and with herbage clipped and removed were used as treatment areas and measurements were made using an incubation period of 7 days at intervals of 7 or 14 days through the year. Soil temperature, moisture and mineral N contents were also determined. Mineralization rates fluctuated considerably in each treatment. Maximum daily rates ranged from 1.01 to 3.19 kg N ha^–1, and there was substantial net release of N through the winter period (representing, on average, 27% of the annual release). Changes in temperature accounted for 35% of the variability but there was little significant effect of soil moisture. Annual net release of N ranged from 135 kg ha^–1 (undrained soil, no previous or current fertilizer) to 376 (drained soil, +200 kg N ha^–1 yr^–1 previous and current fertilizer addition). Addition of fertilizer N to a previously unfertilized sward significantly increased the net release of N but there was no immediate effect of withholding fertilizer on mineralization during the year in which measurements were made.     

The biogeochemistry of pristine,headwater Precambrian shield watersheds: an analysis of material transport within a heterogeneous landscape

The hydrology and elemental transport within five low order Precambrian shield catchments was investigated during 1988–90. Catchments were subdivided and instrumented to examine the vertical and horizontal fluxes of elements within and between two distinct landscape types: open, lichen-covered bedrock outcrops and patches of conifer forest. The dominant hydrologic pathways were Horton overland flow in the lichen-bedrock areas and shallow subsurface flow through organic rich LFH (forest floor) and Ah soil horizons in the forested areas. Annual runoff coefficients ranged from 0.3 to 0.7. Runoff chemistry was acidic (pH 4.01–4.72), with organic anion equivalents (RCOO^-), comprising 60 and 69% of the anion charge total for bedrock and forest runoff, respectively. Forested plots exported more H⁺ (2.6x), DOC (1.4x), Al (1.6x) and Fe (1.8x) and less N (0.40x), P (0.13x), particulate C (0.08x), Ca²⁺ (0.38x), Mg²⁺ (0.83x), Na⁺ (0.85x) and K⁺ (0.32x) per unit area than the bedrock-lichen plots. The catchments exhibited a net export of H⁺ (34), Mg²⁺ (24), Na⁺ (20), K⁺ (4) (units in eq ha^-1 yr^-1) and C (16), Si (5.6), Al (1.6) and Fe (0.47) (units kg ha^-1 yr^-1). The catchments retained N (5.66), P (0.08), Mn (0.03) (units kg ha^-1 yr^-1), and Ca²⁺ (37), and Cl^- (3) (units eq ha^-1 yr^-1). The strong retention of Ca²⁺ within the treed soil islands resulted in extremely low export rates of base cations (-15 to 38 eq ha^-1 yr^-1). The spatial distribution and hydrologic and biogeochemical linkages associated with each landscape unit interact to control element transport within the study catchments.     

Nitrogen cycling and dynamic analysis of man made larch forest ecosystem

Nitrogen cycling process and dynamic change over 2 years were studied in 21-year-old planted dahurian larch (Lurix gmelinii (Rupr) Rupr.) in the eastern part of northern China. N concentrations in the plants varied by tissue, age, position in tree and season. In the aboveground components the N concentration was highest in foliage, followed by live branches, bolebark and bolewood. The organic N concentrations in undergrowth and herbs were higher than that in larch tree. The total amount of N accumulated in the larch ecosystem was 13167 kg.ha^-1, in which the percentages of N storage in soil, living plants, dead standing and litter were 94.7%, 2.8%, 0.1% and 2.4%, respectively. The uptake of N by vegetation was 56 kg.ha^-1.y^-1, in which the retention and return were 24 kg.ha^-1.y^-1 and 32 kg. ha^-1 y^-1, respectively. Precipitation provided 13 kg.ha^-1.y^-1 of N, while N loss via runoff was 4 kg.ha^-1.y^-1 and therefore, the net gain of N by ecosystem was 9 kg.ha^-1.y^-1.The simulation of N dynamic change showed that an increase in the age of stand was accompanied by a concomitant increase in N storage in the forest floor, whereas N flux from forest floor organic matter into soil would decrease, and consequently, growth rate of larch stands would reduce owing to the inadequacy of available N in the soil. The prediction indicated that the degradation of soil fertility in larch plantation might occur under continuous cropping. The study implied that release rate of N from litter into soil was the key factor in determining and regulating N cycling in larch plantation.The understory minor vegetation in the larch stand plays an important role in speeding up N cycling. The timely thinning is needed to improve growth and development of shrubs and herbs, and to avert the potential soil degradation. The mixed stand of larch with either a certain proportion of broad-leaved or a moderately well developed understory vegetation should be encouraged.     

Soil N mineralization and nitrification in relation to nitrogen solution chemistry in a small forested watershed

Spatial variations in soil processes regulating mineral N losses to streams were studied in a small watershed near Toronto, Ontario. Annual net N mineralization in the 0–8 cm soil was measured in adjacent upland and riparian forest stands using in situ soil incubations from April 1985 to 1987. Mean annual rates of soil N mineralization and nitrification were higher in a maple soil (93.8 and 87.0 kg.ha^–1) than in a pine soil (23.3 and 8.2 kg.ha^–1 ). Very low mean rates of mineralization (3.3 kg.ha^–1) and nitrification (3.4 kg.ha^–1) were found in a riparian hemlock stand. Average NO₃-N concentrations in soil solutions were 0.3–1.0 mg.L^–1 in the maple stand and >0.06mg.L^–1 in the pine stand. Concentrations of NO₃–N in shallow ground water and stream water were 3–4× greater in a maple subwatershed than in a pine subwatershed. Rapid N uptake by vegetation was an important mechanism reducing solution losses of NO₃–N in the maple stand. Low rates of nitrification were mainly responsible for negligible NO₃–N solution losses in the pine stand.     

Forest floor biomass,litter fall and nutrient return in Central Himalayan oak forests

The seasonal dynamics of forest floor biomass, pattern of litter fall and nutrient return in Central Himalayan oak forests are described. Fresh and partially decomposed litter layers occur throughout the whole year in addition to herbaceous vegetation. The highest leaf litter value is found in April and May and the minimum in September. Partially and largely decomposed litter tended to increase from January to May with a slight decline in June. The wood litter peaked in March and April. The relative contribution of partially decomposed litter to the forest floor remains greatest the year round. The maximum herbaceous vegetation development was found in September with a total annual net production of 104.3 g m^-2yr^-1. The total calculated input of litter was 480.8 g m^-2yr^-1. About 68% of the forest floor was replaced each year with a subsequent turnover time of 1.47 yr. The total annual input of litter ranged from 664 (Quercus floribunda site) –952 g m^-2 (Q. lanuginosa site), of which tree, shrub and herbaceous litter accounted for respectively 72.0–86.3%, 6.4 – 19.4% and 5.2 – 8.6%. The annual nutrient return through litter fall amounted to (kg ha^-1) 178.0 – 291.0 N, 10.0 – 26.9 P, 176.8 – 301.6 Ca, 43.9 – 64.1 K and 3.98 – 6.45 Na. The tree litter showed an annual replacement of 66.0 – 70.0%, for different nutrients the range was 64 and 84%.     

Land-use change effects on soil C and N transformations in soils of high N status: comparisons under indigenous forest, pasture and pine plantation

Globally, land-use change is occurring rapidly, and impacts on biogeochemical cycling may be influenced by previous land uses. We examined differences in soil C and N cycling during long-term laboratory incubations for the following land-use sequence: indigenous forest (soil age = 1800 yr); 70-year-old pasture planted after forest clearance; 22-year-old pine (Pinus radiata) planted into pasture. No N fertilizer had been applied but the pasture contained N-fixing legumes. The sites were adjacent and received 3–6 kg ha^–1 yr^–1volcanic N in rain; NO₃ ^–-N leaching losses to streamwater were 5–21 kg ha^–1 yr^–1, and followed the order forest < pasture = pine. Soil C concentration in 0–10 cm mineral soil followed the order: pasture > pine = forest, and total N: pasture > pine > forest. Nitrogen mineralization followed the order: pasture > pine > forest for mineral soil, and was weakly related to C mineralization. Based on radiocarbon data, the indigenous forest 0–10 cm soil contained more pre-bomb C than the other soils, partly as a result of microbial processing of recent C in the surface litter layer. Heterotrophic activity appeared to be somewhat N limited in the indigenous forest soil, and gross nitrification was delayed. In contrast, the pasture soil was rich in labile N arising from N fixation by clover, and net nitrification occurred readily. Gross N cycling rates in the pine mineral soil (per unit N) were similar to those under pasture, reflecting the legacy of N inputs by the previous pasture. Change in land use from indigenous forest to pasture and pine resulted in increased gross nitrification, net nitrification and thence leaching of NO₃ ^–-N.     

Effects of soil freezing disturbance on soil solution nitrogen, phosphorus, and carbon chemistry in a northern hardwood ecosystem

Reductions in snow cover undera warmer climate may cause soil freezing eventsto become more common in northern temperateecosystems. In this experiment, snow cover wasmanipulated to simulate the late development ofsnowpack and to induce soil freezing. Thismanipulation was used to examine the effects ofsoil freezing disturbance on soil solutionnitrogen (N), phosphorus (P), and carbon (C)chemistry in four experimental stands (twosugar maple and two yellow birch) at theHubbard Brook Experimental Forest (HBEF) in theWhite Mountains of New Hampshire. Soilfreezing enhanced soil solution Nconcentrations and transport from the forestfloor. Nitrate (NO₃ ^–) was thedominant N species mobilized in the forestfloor of sugar maple stands after soilfreezing, while ammonium (NH₄ ⁺) anddissolved organic nitrogen (DON) were thedominant forms of N leaching from the forestfloor of treated yellow birch stands. Rates ofN leaching at stands subjected to soil freezingranged from 490 to 4,600 mol ha^–1yr^–1, significant in comparison to wet Ndeposition (530 mol ha^–1 yr^–1) andstream NO₃ ^– export (25 mol ha^–1yr^–1) in this northern forest ecosystem. Soil solution fluxes of P_i from the forestfloor of sugar maple stands after soil freezingranged from 15 to 32 mol ha^–1 yr^–1;this elevated mobilization of P_i coincidedwith heightened NO₃ ^– leaching. Elevated leaching of P_i from the forestfloor was coupled with enhanced retention ofP_i in the mineral soil Bs horizon. Thequantities of P_i mobilized from the forestfloor were significant relative to theavailable P pool (22 mol ha^–1) as well asnet P mineralization rates in the forest floor(180 mol ha^–1 yr^–1). Increased fineroot mortality was likely an important sourceof mobile N and P_i from the forest floor,but other factors (decreased N and P uptake byroots and increased physical disruption of soilaggregates) may also have contributed to theenhanced leaching of nutrients. Microbialmortality did not contribute to the acceleratedN and P leaching after soil freezing. Resultssuggest that soil freezing events may increaserates of N and P loss, with potential effectson soil N and P availability, ecosystemproductivity, as well as surface wateracidification and eutrophication.     

Decline of soil nitrogen mineralization and nitrification during forest conversion of evergreen broad-leaved forest to plantations in the subtropical area of Eastern China

We examined soil nitrogen (N) mineralization and nitrification rates, and soil and forest floor properties in one native forest: evergreen broad-leaved forest (EBLF), one secondary shrubs (SS), and three adjacent plantation forests: Chinese fir plantation (CFP), bamboo plantation (BP) and waxberry groves (WG) in Tiantong National Forest Park, Eastern China. All forests showed seasonal dynamics of N mineralization and nitrification rates. Soil N mineralization rate was highest in EBLF (1.6 ± 0.3 mg-N kg⁻¹ yr⁻¹) and lowest in CFP (0.4 ± 0.1 mg-N kg⁻¹ yr⁻¹). Soil nitrification rate was also highest in EBLF (0.6 ± 0.1 mg-N kg⁻¹ yr⁻¹), but lowest in SS (0.02 ± 0.01 mg-N kg⁻¹ yr⁻¹). During forest conversion of EBLF to SS, CFP, BP and WG, soil N mineralization rate (10.7%, 73%, 40.3% and 69.8%, respectively), soil nitrification rate (94.9%, 32.2%, 33.9% and 39%, respectively), and soil N concentration (50%, 65.4%, 78.9% and 51.9%, respectively) declined significantly. Annual soil N mineralization was positively correlated with total C and N concentrations of surface soil and total N concentration of forest floor, and negatively correlated with soil bulk density, soil pH and C:N ratio of forest floor across the five forests. Annual soil nitrification was positively correlated with total C concentration of surface soil and N concentration of forest floor, and negatively correlated with soil bulk density and forest floor mass. In contrast, annual soil nitrification was not correlated to pH value, total N concentration, C:N ratio of surface soil and total C concentration and C:N ratio of forest floor.     

Soil nitrogen mineralization in plantations ofJuglans nigra interplanted with actinorhizalElaeagnus umbellata orAlnus glutinosa

Nitrogen mineralization rates were estimated in 19-year-old interplantings of black walnut (Juglans nigra L.) with dinitrogen fixing autumn-olive (Elaeagnus umbellata Thunb.) or black alder (Alnus glutinosa L. Gaertn.) and in pure walnut plantings at two locations in Illinois USA. N mineralization rates were measured repeatedly over a one year period usingin situ incubations of soil cores in oxygen-permeable polyethylene bags at 0–10 and 10–20 cm soil depths, and also by burying mixed-bed ion-exchange resin in soil. Mineralization rates were highest in summer and in plots containing actinorhizal Elaeagnus and Alnus in contrast with pure walnut plots. Elaeagnus plots at one location yielded 236 kg of mineral N ha^–1 yr^–1 in the upper 20 cm of soil, a value higher than previously reported for temperate decidous forest soils in North America. The highest mean plot values for N mineralization in soil at a location were 185 kg ha^–1 yr^–1 for Alnus interplantings and 90 kg ha^–1 yr^–1 for pure walnut plots. Plots which had high N mineralization rates also had the largest walnut trees. Despite low pH (4.1 and 6.5) and low extractable P concentrations (1.4 and 0.7 mg kg^–1 dry mass) at the two locations, nitrification occurred in all plots throughout the growing season. NO ₃ ^– –N was the major form of mineralized N in soil in the actinorhizal interplantings, with NH ₄ ⁺ –N being the major form of mineral N in control plots. Walnut size was highly correlated with soil nitrogen mineralization, particularly soil NO ₃ ^– –N production in a plot.     

Residual phosphorus in runoff from successional forest on abandoned agricultural land: 2. Hydrological and soluble reactive P Budgets

Residual P from historical farm practices hasbeen linked to elevated soluble reactivephosphorus (SRP) transport in runoff from afield study site in the Catskills Mountains,New York, U.S.A., with a P source assay indicatingthat successional forest floor biomass was themajor contributor to runoff SRP. In thispaper, we assemble hydrological and SRP budgetsthat indicate net SRP loss of 0.123 kgha^–1 yr^–1 occurs from the site(composed of 0.044 kg ha^–1 yr^–1precipitation input, with 0.143 kg ha^–1yr^–1 and 0.024 kg ha^–1 yr^–1losses in runoff and groundwater,respectively). These findings contrast withconservative P cycling reported for undisturbedforests. Coupled hydrological and SRP data areanalyzed suggesting that catchment ambient andequilibrium SRP concentrations corresponding togroundwater and long-term average runoffconcentrations are in the range capable ofcontributing to eutrophication of receivingwaters. A physically based variable sourcearea hydrological model is tested to simulateSRP export using deterministic concentrations. The three-layer model (surface runoff, shallowlateral flow, and groundwater) is parameterizedusing spatially distributed data fromadditional P source assays and fieldhydrological monitoring for the site. Differences in simulated and observed outflowand SRP export are partially explained byforest evapotranspiration and frozen soilprocesses. The field data, SRP budgets andsimulations show that sufficient residual Ppools exist to prolong net SRP loss rates untilecosystem processes re-establish moreconservative P cycling.