The nitrogen status of Austrian forest ecosystems as influenced by atmospheric deposition,biomass harvesting and lateral organomass exchange

Measurements of the deposition rates of atmospheric trace constituents to forest ecosystems in Austria have shown that the deposition of plant utilizable nitrogen compounds is in the range from 12 kg N to more than 30 kg N ha^-1 a^-1. Locally, even higher deposition rates are encountered as a consequence of point sources or special deposition mechanisms such as fog interception, hoar frost formation, and accumulation in snow drifts. In order to place these values into perspective, they are compared with the nitrogen demand of past and present forest land use and with natural processes of nitrogen depletion and accumulation in forest ecosystems. During wind erosion of forest litter, woody material with a wide C/N-ratio remains on the windward side of ridges, while nutrient-rich material with a narrow C/N-ratio is deposited on the leeward side. As a result, total nitrogen storage in the forest soil as well as overall C/N-ratios change dramatically along a transect over a ridge, thus indicating a strong influence of litter C/N ratio on nitrogen retention in the forest soil. A study of nitrogen stores in the soil of beech ecosystems of the same yield class in the Vienna Woods showed a significant correlation of total N-content with base saturation. These results suggest that nitrogen storage capacity of forest soils may be managed by liming and tree species selection. As knowledge is still meagre, a special study on factors which determine nitrogen storage in forest soils is proposed within the FERN-programme.     

Nitrogen yields from undisturbed watersheds in the Americas

Yields of total fixed nitrogen and nitrogen fractions are summarized for thirty-one watersheds in which anthropogenic disturbance of the nitrogen cycle, either through land use or atmospheric deposition, is negligible or slight. These yields are taken as representative of background conditions over a broad range of watershed areas, elevations, and vegetation types. The data set focuses on watersheds of the American tropics, but also includes information on the Gambia River (Africa) and some small watersheds in the Sierra Nevada of California. For the tropical watersheds, total nitrogen yield averages 5.1 kg ha^–1 y^–1. On average, 30% of the total is particulate and 70% is dissolved. Of the dissolved fraction, an average of 50% is organic and 50% is inorganic, of which 20% is ammonium and 80% is nitrate. Yields are substantially lower than previously estimated for background conditions. Yields of all nitrogen fractions are strongly related to runoff, which also explains a large percentage of variance in yield of total nitrogen (r²=0.85). For total nitrogen and nitrogen fractions, yield increases at about two-thirds the rate of runoff; concentration decreases as runoff increases. There is a secondary but significant positive relationship between elevation and yield of DIN. Ratios DON/TDN and PN/TN both are related to watershed area rather than runoff; DON/TDN decreases and PN/TN increases toward higher stream orders. The analysis suggests for tropical watersheds the existence of mechanisms promoting strong homeostasis in the yield of N and its fractions for a given moisture regime, as well as predictable downstream change in proportionate representation N fractions. Yields and concentrations for small tropical watersheds are much larger than for the few temperate ones with which comparisons are possible.     

The impact of humans on the nitrogen cycle,with focus on temperate arable agriculture

The 6 billion people alive today consume about 25 million tonnes of protein nitrogen each year, a requirement that could well increase to 40–45 million tonnes by 2050. Most of them ultimately depend on the Haber-Bosch process to fix the atmospheric N₂ needed to grow at least part of their protein and, over the earth as a whole, this dependency is likely to increase. Humans now fix some 160 million tonnes of nitrogen per year, of which 98 are fixed industrially by the Haber-Bosch process (83 for use as agricultural fertilizer, 15 for industry), 22 during combustion and the rest is fixed during the cultivation of leguminous crops and fodders. These 160 million tonnes have markedly increased the burden of combined nitrogen entering rivers, lakes and shallow seas, as well as increasing the input of NH₃, N₂O, NO and NO₂ to the atmosphere. Nitrogen fertilizers give large economic gains in modern farming systems and under favourable conditions can be used very efficiently. Losses of nitrogen occur from all systems of agriculture, with organic manures being particularly difficult to use efficiently. Although nitrate leaching has received much attention as an economic loss, a cause of eutrophication and a health hazard, gaseous emissions may eventually prove to be the most serious environmentally. Scientists working on the use and fate of nitrogen fertilizers must be careful, clear headed and vigilant in looking for unexpected side effects.     

Yield of nitrogen from minimally disturbed watersheds of the United States

Watersheds of the US Geological Survey's Hydrologic Benchmark Network program were used in estimating annual yield of total nitrogen and nitrogen fractions (ammonium, nitrate, dissolved organic N, particulate N) in relation to amount of runoff, elevation, and watershed area. Only watersheds minimally disturbed with respect to the nitrogen cycle were used in the analysis (mostly natural vegetation cover, no point sources of N, atmospheric deposition of inorganic N < 10 kg ha^–1 y^–1). Statistical analysis of the yields of total nitrogen and nitrogen fractions showed that elevation and watershed area bear no significant relationship to nitrogen yield for these watersheds. The yields of total nitrogen and nitrogen fractions are, however, strongly related to runoff (r ² = 0.91 for total N). Annual yield increases as runoff increases, but at a rate lower than runoff; annual discharge-weighted mean concentrations decline as annual runoff increases. Yields of total nitrogen and most nitrogen fractions bear a relationship to runoff that is nearly indistinguishable from a relationship that was documented previously for minimally disturbed watersheds of the American tropics. Overall, the results suggest strong interlatitudinal convergence of yields and percent fractionation for nitrogen in relation to runoff.     

Nitrogen outputs from fecal and urine deposition of small mammals: implications for nitrogen cycling

The contribution of small mammals to nitrogen cycling could have repercussions for the producer community in the maintaining or perhaps magnifying of nitrogen availability. Our objective was to model nitrogen outputs (deposition of feces and urine) of small mammals in an old-field ecosystem and estimate the amount of fecal and urinary nitrogen deposited annually. To address this objective, we used models from laboratory studies and combined these with data from field studies to estimate dietary nitrogen and monthly and annual nitrogen outputs from fecal and urine deposition of five rodent species. The models accounted for monthly fluctuations in density and biomass of small-mammal populations. We estimated that the minimal amount of nitrogen deposited by rodents was 1.0 (0.9–1.1) and 2.7 (2.6–2.9) kg Nha⁻¹ year⁻¹ from feces and urine, respectively, for a total contribution of 3.7 (3.5–4.0) kg Nha⁻¹ year⁻¹. Hispid cotton rats (Sigmodon hispidus) accounted for >75% of the total nitrogen output by small mammals. Our estimates of annual fecal and urinary nitrogen deposited by rodents were comparable to nitrogen deposits by larger herbivores and other nitrogen fluxes in grassland ecosystems and should be considered when assessing the potential effects of herbivory on terrestrial nitrogen cycles.     

Available soil nitrogen in relation to fractions of soil nitrogen and other soil properties

The available N of 27 soils from England and Wales was assessed from the amounts of N taken up over a 6-month period by perennial ryegrass grown in pots under uniform environmental conditions. Relationships between availability and the distribution of soil N amongst various fractions were then examined using multiple regression. The relationship: available soil N (mg kg^–1 dry soil)=(N_min×0.672)+(N_inc×0.840)+(N_mom×0.227)–5.12 was found to account for 91% of the variance in available soil N, where N_min=mineral N, N_inc=N mineralized on incubation and N_mom=N in macro-organic matter. The N mineralized on incubation appeared to be derived largely from sources other than the macro-organic matter because these two fractions were poorly correlated. When availability was expressed in terms of available organic N as % of soil organic N (N_ao) the closest relationship with other soil characteristics was: N_ao=[N_inc×(1.395–0.0347×CN_mom]+[N_mom×0.1416], where CN_mom=CN ratio of the macro-organic matter. This relationship accounted for 81% of the variance in the availability of the soil organic N.The conclusion that the macro-organic matter may contribute substantially to the available N was confirmed by a subsidiary experiment in which the macro-organic fraction was separated from about 20 kg of a grassland soil. The uptake of N by ryegrass was then assessed on two subsamples of this soil, one without the macro-organic matter and the other with this fraction returned: uptake was appreciably increased by the macro-organic matter.     

Time course of N2 fixation in common bean (Phaseolus vulgaris L.)

Field and greenhouse experiments were conducted to assess the nitrogen fixation rates of four cultivars of common bean (Phaseolus vulgaris L.) at different growth stages. The ¹⁵N isotope dilution technique was used to quantify biological nitrogen fixation. In the greenhouse, cultivars M4403 and Kallmet accumulated 301 and 189 mg N plant^–1, respectively, up to 63 days after planting (DAP) of which 57 and 43% was derived from atmosphere. Under field conditions, cultivars Bayocel and Flor de Mayo RMC accumulated in 77 DAP, 147 and 135 kg N ha^–1, respectively, of which approximately one-half was derived from the atmosphere. The rates of N₂ fixation determined at different growth stages increased as the plants developed, and reached a maximum during the reproductive stage both under field and greenhouse conditions. Differences in translocation of N were observed between the cultivars tested, particularly under field conditions. Thus, the fixed N harvest index was 93 and 60 for cultivars Flor de Mayo and Bayocel, respectively. In early stages of growth, the total content of ureides in the plants correlated with the N fixation rates. The findings reported in the present paper can be used to build a strategy for enhancing biological N₂ fixation in common bean.     

嫁接与施氮对甜瓜产量和氮素吸收、利用的影响

通过裂区设计田间试验,主区为2种栽培方式(嫁接栽培和自根栽培),副区为4个施氮水平(0、120、240、360 kg N·hm^-2),研究了栽培方式和施氮量对甜瓜产量和品质、氮素运移和分配,以及氮素利用率的影响.结果表明: 嫁接栽培的甜瓜商品瓜产量较自根甜瓜提高了7.3%,可溶性固形物含量降低了0.16%～3.28%;生长前期嫁接栽培甜瓜氮素累积量较自根栽培低,结果后嫁接栽培氮素累积量显著升高,收获时植株氮素累积量较自根栽培增加了5.2%,果实中的氮素累积量提高了10.3%;嫁接栽培植株氮素向果实的转移量较自根栽培提高了20.9%,嫁接栽培果实中的氮素分配率在80%以上,自根栽培的分配率在80%以下;在同一施氮水平下,嫁接栽培的甜瓜氮素吸收利用率较自根栽培提高了1.3%～4.2%,氮素农学效率提高了2.73～5.56 kg·kg^-1,氮素生理利用率提高了7.39～16.18 kg·kg^-1;从商品瓜产量、氮素吸收量和氮素利用率综合考虑,施氮量240 kg·hm^-2为本区域嫁接甜瓜较适宜的氮素用量.     

Nitrogen inputs to a marine embayment: the importance of groundwater

We examined the importance of nitrogen inputs from groundwater and runoff in a small coastal marine cove on Cape Cod, MA, USA. We evaluated groundwater inputs by three different methods: a water budget, assuming discharge equals recharge; direct measurements of discharge using bell jars; and a budget of water and salt at the mouth of the Cove over several tidal cycles. The lowest estimates were obtained by using a water budget and the highest estimates were obtained using a budget of water and salt at the Cove mouth. Overall there was more than a five fold difference in the freshwater inputs calculated by using these methods. Nitrogen in groundwater appears to be largely derived from on site septic systems. Average nitrate concentrations were highest in the region where building density was greatest. Nitrate in groundwater appeared to behave conservatively in sandy sediments where groundwater flow rates were high (> 11/m²/h), indicating that denitrification was not substantially reducing external nitrogen loading to the Cove. Nitrogen inputs from groundwater were approximately 300 mmol-N/m³/y of Cove water. Road runoff contributed an additional 60 mmol/m³/y. Total nitrogen inputs from groundwater and road runoff to this cove were similar in magnitude to river dominated estuaries in urbanized areas in the United States.     

Nitrogen deposition and forest nitrogen cycling along an urban–rural transect in southern China

There is increasing concern over the impact of atmospheric nitrogen (N) deposition on forest ecosystems in the tropical and subtropical areas. In this study, we quantified atmospheric N deposition and revealed current plant and soil N status in 14 forests along a 150 km urban to rural transect in southern China, with an emphasis on examining whether foliar δ¹⁵N can be used as an indicator of N saturation. Bulk deposition ranged from 16.2 to 38.2 kg N ha^?1 yr^?1, while the throughfall covered a larger range of 11.7–65.1 kg N ha^?1 yr^?1. Foliar N concentration, NO₃^? leaching to stream, and soil NO₃^? concentration were low and NO₃^? production was negligible in some rural forests, indicating that primary production in these forests may be limited by N supply. But all these N variables were enhanced in suburban and urban forests. Across the study transect, throughfall N input was correlated positively with soil nitrification and NO₃^? leaching to stream, and negatively with pH values in soil and stream water. Foliar δ¹⁵N was between ?6.6‰ and 0.7‰, and was negatively correlated with soil NO₃^? concentration and NO₃^? leaching to stream across the entire transect, demonstrating that an increased N supply does not necessarily increase forest δ¹⁵N values. We proposed several potential mechanism that could contribute to the δ¹⁵N pattern, including (1) increased plant uptake of ¹⁵N‐depleted soil NO₃^?, (2) foliage uptake of ¹⁵N‐depleted NH₄⁺, (3) increased utilization of soil inorganic N relative to dissolved organic N, and (4) increased fractionation during plant N uptake under higher soil N availability.