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.     

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.     

The cycling of organic nitrogen through the atmosphere

Atmospheric organic nitrogen (ON) appears to be a ubiquitous but poorly understood component of the atmospheric nitrogen deposition flux. Here, we focus on the ON components that dominate deposition and do not consider reactive atmospheric gases containing ON such as peroxyacyl nitrates that are important in atmospheric nitrogen transport, but are probably not particularly important in deposition. We first review the approaches to the analysis and characterization of atmospheric ON. We then briefly summarize the available data on the concentrations of ON in both aerosols and rainwater from around the world, and the limited information available on its chemical characterization. This evidence clearly shows that atmospheric aerosol and rainwater ON is a complex mixture of material from multiple sources. This synthesis of available information is then used to try and identify some of the important sources of this material, in particular, if it is of predominantly natural or anthropogenic origin. Finally, we suggest that the flux of ON is about 25 per cent of the total nitrogen deposition flux.     

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.     

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.     

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.     

Mechanisms of plant species impacts on ecosystem nitrogen cycling

Plant species are hypothesized to impact ecosystem nitrogen cycling in two distinctly different ways. First, differences in nitrogen use efficiency can lead to positive feedbacks on the rate of nitrogen cycling. Alternatively, plant species can also control the inputs and losses of nitrogen from ecosystems. Our current understanding of litter decomposition shows that most nitrogen present within litter is not released during decomposition but incorporated into soil organic matter. This nitrogen retention is caused by an increase in the relative nitrogen content in decomposing litter and a much lower carbon‐to‐nitrogen ratio of soil organic matter. The long time lag between plant litter formation and the actual release of nitrogen from the litter results in a bottleneck, which prevents feedbacks of plant quality differences on nitrogen cycling. Instead, rates of gross nitrogen mineralization, which are often an order of magnitude higher than net mineralization, indicate that nitrogen cycling within ecosystems is dominated by a microbial nitrogen loop. Nitrogen is released from the soil organic matter and incorporated into microbial biomass. Upon their death, the nitrogen is again incorporated into the soil organic matter. However, this microbial nitrogen loop is driven by plant‐supplied carbon and provides a strong negative feedback through nitrogen cycling on plant productivity. Evidence supporting this hypothesis is strong for temperate grassland ecosystems. For other terrestrial ecosystems, such as forests, tropical and boreal regions, the data are much more limited. Thus, current evidence does not support the view that differences in the efficiency of plant nitrogen use lead to positive feedbacks. In contrast, soil microbes are the dominant factor structuring ecosystem nitrogen cycling. Soil microbes derive nitrogen from the decomposition of soil organic matter, but this microbial activity is driven by recent plant carbon inputs. Changes in plant carbon inputs, resulting from plant species shifts, lead to a negative feedback through microbial nitrogen immobilization. In contrast, there is abundant evidence that plant species impact nitrogen inputs and losses, such as: atmospheric deposition, fire‐induced losses, nitrogen leaching, and nitrogen fixation, which is driven by carbon supply from plants to nitrogen fixers. Additionally, plants can influence the activity and composition of soil microbial communities, which has the potential to lead to differences in nitrification, denitrification and trace nitrogen gas losses. Plant species also impact herbivore behaviour and thereby have the potential to lead to animal‐facilitated movement of nitrogen between ecosystems. Thus, current evidence supports the view that plant species can have large impacts on ecosystem nitrogen cycling. However, species impacts are not caused by differences in plant quantity and quality, but by plant species impacts on nitrogen inputs and losses.     

Sustainable forestry: A model of the effects of nitrogen removals in wood harvesting and fire on the nitrogen balance of regrowth eucalypt stands

Abstract Sustainable forest use is an integral part of Australia's recently adopted National Forest Policy; consequently, there is an urgent need for quantitative, ecologically based measures of sustainability. One process that may affect ecosystem sustainability is the removal of nutrients through forest harvesting and fire. This paper presents a model-based analysis of the combined consequences of harvesting and fire management practices for the nitrogen (N) budgets of managed forest ecosystems. The model, called N-BAL, evaluates the balance between N removals due to harvesting and fire (prescribed and regeneration burns), and N inputs (both natural and as added fertilizer), and leads to a criterion for the maintenance of site N reserves. That criterion can be used to estimate the accretion (or depletion) of site N over a single forest rotation, or to predict sustainable stem productivity for given N inputs and management practices. The analysis is applied to managed stands of karri (Eucalyptus diversicolor F. Muell.) in southwestern Australia to investigate whether natural N inputs are sufficient to maintain site N capital under current harvesting and fire practices. Model predictions for stands harvested at age 100 years with slash burns and regular prescribed burns range from a rotation-averaged depletion rate of 22 kg ha^?1 year^?1 to an annual accretion of 14 kg ha^?1 year^?1, depending on assumed N inputs and fire frequency and intensity. The mean annual N balance is highly sensitive to rates of natural N inputs, fire intensity and inter-fire period, and less sensitive to rotation length. These results are tentative and highlight the need for further research to improve estimates of several key model parameters and relationships.     

沉积物氮形态与测定方法研究进展

长期以来,国内外学者对沉积物中氮进行了大量的研究,在氮生物地球化学循环和生态学效应方面取得了重要进展.然而,现有关于氮赋存形态的研究主要集中在总氮和无机氮方面,还不能深入阐明沉积物氮的生物和生态学机制.分析了沉积物和土壤氮赋存形态划分和测定方法的研究进展,研究表明:沉积物氮的形态划分与测定方法基本上还是借鉴了土壤氮的研究方法;无机态氮的研究多集中在可交换态氮方面,对固定铵的研究相对较少;在可交换态氮提取方法上并没有针对沉积物与土壤的差异进行必要的论证和改进,沉积物中可溶态氮对可交换态氮测定的影响还不明确;有机氮的测定方法基本上是经验方法,目前还无针对有机氮生态学效应的分类及测定方法;连续分级浸提方法从生态学效应的角度对沉积物氮的研究进行了有益的探索,为深入揭示氮的生态学机制提供了新的思路,但是此类方法目前还集中在国内学者的相关研究中.     

模拟氮沉降对杉木幼苗细根化学计量学特征的影响

为了揭示全球氮(N)沉降对杉木人工林细根碳(C)、N、磷(P)元素组成的影响,在福建三明陈大国有林场开展杉木(Cunninghamia lanceolata)幼苗模拟N沉降试验,设置了对照(CK)、低N(LN,40 kg N hm~(-2)a~(-1))、高N(HN,80 kg N hm~(-2)a~(-1))3个处理,每个处理5个重复。采用内生长环法通过2年4次取样探讨N沉降对细根C、N、P化学计量学的影响。结果显示:(1) N添加在2015年降低细根C浓度,此后低N处理无影响,高N添加在2016年增加了细根C浓度;高N添加提高了细根(特别是0—1 mm细根) N浓度,但低N添加则无显著影响,甚至在2016年7月显著降低细根N浓度; N添加在2015年对细根P浓度无显著影响,但在2016年导致细根(特别是0—1 mm细根) P浓度降低。(2)低N添加在2016年显著提高细根的C∶N比,而高N添加则在2015年1月显著降低细根的C∶N比;低N添加对细根N∶P比没有显著影响,而高N添加则在大部分取样时间里显著增加了细根N∶P比。(3)不同处理细根C浓度、C∶N比均随着时间的增加呈增加趋势,而细根N浓度和N∶P比呈降低趋势。本研究表明,N添加对杉木细根化学计量学特征的影响因不同N添加水平而异,并受苗木生长的稀释效应所调节。     

大气NO2影响植物生长与代谢的研究进展

二氧化氮(NO₂)是大气氮氧化物之一,是大气气溶胶颗粒形成的主要成分,降低大气NO₂浓度可减轻空气中的雾霾.大气NO₂通过干沉降和湿沉降两种方式降落到植物叶片.植物吸收NO₂后主要通过两种代谢途径来降低空气中NO₂浓度: 一是主要在细胞质和叶绿体中利用还原酶的氮代谢途径,二是在质外体和细胞质中的歧化反应.植物吸收NO₂干扰了植物正常的生长和生理代谢,包括: 植物营养和生殖生长,植物体内硝酸还原酶(NaR)活性、亚硝酸还原酶(NiR)活性、氮素吸收、光合等生理代谢过程.对目前国内外有关大气NO₂影响植物生长与代谢的研究进展进行了综述,并对植物吸收NO₂的生理及分子机制的未来研究方向进行了展望.     

氮硅添加对青藏高原高寒草甸土壤氮矿化的影响

为了解全球气候变化背景下氮沉降对土壤氮矿化的影响及硅添加对土壤氮矿化的促进作用, 该试验设置不同浓度的氮肥单独添加(0、20、40、60 g·m ^-2, 分别为对照CK、N20、N40、N60)以及与硅肥配施(硅酸4 g·m ^-2, Si4), 测定不同处理下0-20、20-40、40-60 cm土层土壤硝态氮含量、铵态氮含量、净硝化速率、净氨化速率以及净矿化速率。结果显示: (1)单独添加氮肥, 各土层土壤硝态氮和铵态氮含量均随处理浓度的增加而增加, 0-20 cm土层N20、N40、N60处理下土壤硝态氮和铵态氮分别较CK增加63.48%、126.04%、247.03%和80.66%、152.52%、244.56%; 随着土层深度增加, 土壤硝态氮、铵态氮含量均有下降, 20-40、40-60 cm土层较0-20 cm土层硝态氮含量分别平均减少53.90%、76.05%, 铵态氮含量分别平均减少48.62%、68.23%。(2)土壤净硝化速率、净氨化速率及净矿化速率随着氮肥浓度增加均呈上升趋势。相同氮肥添加浓度下, 土壤净硝化速率、净氨化速率和净矿化速率随着土层深度增加逐渐下降(除CK外)。(3)与单独添加氮肥比较, 氮硅肥配施, 土壤氮含量有显著提高, 在0-20 cm土层硝态氮和铵态氮较CK分别增加98.78%、192.62%、330.16%和99.96%、195.82%、306.32%, 20-40、40-60 cm土层也有类似趋势。同时, 氮硅配施促进了土壤氮矿化行为, 在0-20 cm土层, N60Si4处理下的土壤净硝化速率、净氨化速率较单独施氮时分别增加35.88%、27.41%。以上结果表明, 与单独氮肥添加相比, 氮硅配施不但能提高土壤氮含量, 而且能促进土壤氮的矿化作用, 对大气氮沉降有一定的缓解作用。     

黄土丘陵区植被恢复对土壤可溶性氮组分的影响

为探究黄土丘陵地区人工植被恢复对土壤氮素养分累积与有效性的影响,研究分析了植被恢复15年刺槐、柠条、刺槐侧柏混交、刺槐山桃混交以及荒草地土壤可溶性氮组分含量及其垂直分布特征。结果表明,与耕地相比,植被恢复显著提高了0—30 cm土壤可溶性氮组分含量,这也使0—30 cm土壤可溶性氮组分密度显著增加,可溶性有机氮密度增幅表现为柠条(262.2%)刺槐(232.8%)刺槐山桃混交、刺槐侧柏混交(34.5%)荒草地(-21.5%),硝态氮密度整体表现为柠条刺槐刺槐山桃混交荒草地刺槐侧柏混交,增幅为7.9%—182.8%,铵态氮密度以刺槐山桃混交增幅最大(110.3%),荒草地最小为2.6%。可溶性有机氮、硝态氮占全氮的比例以刺槐最高,分别提升了2.4倍和0.6倍,铵态氮占全氮的比例以刺槐山桃混交最高,提升了1.0倍。可溶性氮组分受微生物量碳氮的影响大于有机质和全氮,微生物量氮与可溶性氮组分的相关性优于微生物量碳,硝态氮对土壤有机质、全氮和微生物量碳氮的变化最为敏感。综上,植被恢复能够提高土壤可溶性氮组分含量、密度及其占全氮比例,增加土壤氮的有效性,以刺槐、柠条提升效果最好。     

陕西果园主要分布区氮素投入特点及氮负荷风险分析

为了研究果园氮素投入特点及分析氮素负荷特征,加强果园氮素管理、指导果农科学合理施肥。以陕西省果园主要分布区土壤氮素分析、农户投入调查等统计数据为基础,采用盈余法从果树种类和区域角度分析果园生产体系中的氮素输入输出特点及氮素盈余状况。结果表明,陕西果园主要分布区平均化肥氮投入量927.2 kg/hm2,主要来源于尿素和复合肥,其中尿素占调查样本量的40%以上;通过有机肥投入的氮仅为139.4 kg/hm2。94.8%的果园氮素处于盈余,总体平均盈余量为876.3 kg/hm2,其中氮盈余量超过500 kg/hm2的样本占57.5%,盈余量超过1 000 kg/hm2的样本亦占了27.3%。不同果园相比,猕猴桃园氮素投入及盈余量最高,分别为1 432.9、1 186.9 kg/hm2。不同区域果园比较,土壤氮环境负荷以关中灌区果园较高,达1046.1kg/hm2。果园氮素施用与养分盈余量之间存在极显著的正相关。陕西果园氮素的高量投入给土壤环境带来较大的氮素负荷,这对土壤环境和周围水体造成很大威胁。     

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.