Shifts in the composition of nitrogen deposition in the conterminous United States are discernable in stream chemistry.

Across the conterminous United States (U.S.), the composition of atmospheric nitrogen (N) deposition is changing spatially and temporally. Previously, deposition was dominated by oxidized N, but now reduced N (ammonia [NH3] + ammonium [NH4+]) is equivalent to oxidized N when deposition is averaged across the entire nation and, in some areas, reduced N dominates deposition. To evaluate if there are effects of this change on stream chemistry at the national scale, estimates of N deposition form (oxidized or reduced) from the National Atmospheric Deposition Program Total Deposition data were coupled with stream measurements from the U.S. Environmental Protection Agency (EPA) National Rivers and Streams Assessments (three stream surveys between 2000 and 2014). A recent fine-scaled N input inventory was used to identify watersheds (<1000 km2) where atmospheric deposition is the largest N source (n = 1906). Within these more atmospherically-influenced watersheds there was a clear temporal shift from a greater proportion of sites dominated by oxidized N deposition to a greater proportion of sites dominated by reduced forms of N deposition. We found a significant positive correlation between oxidized N deposition and stream NO3- concentrations, whereas the correlation between reduced N deposition and stream NO3- concentrations were significant but weaker. Sites dominated by atmospheric inputs of reduced N forms had higher stream total organic N and total N despite lower total N deposition on average. This higher stream concentration of total N is mainly driven by the higher concentration of total organic N, suggesting an interaction between elevated reduced N in deposition and living components of the ecosystem or soil organic matter dynamics. Regardless of the proportion of reduced to oxidized N forms in deposition, stream NH4+ concentrations were generally low, suggesting that N deposited in a reduced form is rapidly immobilized, nitrified and/or assimilated by watershed processes.

Mechanisms of nitrogen deposition effects on temperate forest lichens and trees.

We review the mechanisms of deleterious nitrogen (N) deposition impacts on temperate forests, with a particular focus on trees and lichens. Elevated anthropogenic N deposition to forests has varied effects on individual organisms depending on characteristics both of the N inputs (form, timing, amount) and of the organisms (ecology, physiology) involved. Improved mechanistic knowledge of these effects can aid in developing robust predictions of how organisms respond to either increases or decreases in N deposition. Rising N levels affect forests in micro- and macroscopic ways from physiological responses at the cellular, tissue, and organism levels to influencing individual species and entire communities and ecosystems. A synthesis of these processes forms the basis for the overarching themes of this paper, which focuses on N effects at different levels of biological organization in temperate forests. For lichens, the mechanisms of direct effects of N are relatively well known at cellular, organismal, and community levels, though interactions of N with other stressors merit further research. For trees, effects of N deposition are better understood for N as an acidifying agent than as a nutrient; in both cases, the impacts can reflect direct effects on short time scales and indirect effects mediated through long-term soil and belowground changes. There are many gaps on fundamental N use and cycling in ecosystems, and we highlight the most critical gaps for understanding potential deleterious effects of N deposition. For lichens, these gaps include both how N affects specific metabolic pathways and how N is metabolized. For trees, these gaps include understanding the direct effects of N deposition onto forest canopies, the sensitivity of different tree species and mycorrhizal symbionts to N, the influence of soil properties, and the reversibility of N and acidification effects on plants and soils. Continued study of how these N response mechanisms interact with one another, and with other dimensions of global change, remains essential for predicting ongoing changes in lichen and tree populations across North American temperate forests.

How inhibiting nitrification affects nitrogen cycle and reduces environmental impacts of anthropogenic nitrogen input.

Anthropogenic activities, and in particular the use of synthetic nitrogen (N) fertilizer, have doubled global annual reactive N inputs in the past 50-100 years, causing deleterious effects on the environment through increased N leaching and nitrous oxide (N2 O) and ammonia (NH3 ) emissions. Leaching and gaseous losses of N are greatly controlled by the net rate of microbial nitrification. Extensive experiments have been conducted to develop ways to inhibit this process through use of nitrification inhibitors (NI) in combination with fertilizers. Yet, no study has comprehensively assessed how inhibiting nitrification affects both hydrologic and gaseous losses of N and plant nitrogen use efficiency. We synthesized the results of 62 NI field studies and evaluated how NI application altered N cycle and ecosystem services in N-enriched systems. Our results showed that inhibiting nitrification by NI application increased NH3 emission (mean: 20%, 95% confidential interval: 33-67%), but reduced dissolved inorganic N leaching (-48%, -56% to -38%), N2 O emission (-44%, -48% to -39%) and NO emission (-24%, -38% to -8%). This amounted to a net reduction of 16.5% in the total N release to the environment. Inhibiting nitrification also increased plant N recovery (58%, 34-93%) and productivity of grain (9%, 6-13%), straw (15%, 12-18%), vegetable (5%, 0-10%) and pasture hay (14%, 8-20%). The cost and benefit analysis showed that the economic benefit of reducing N's environmental impacts offsets the cost of NI application. Applying NI along with N fertilizer could bring additional revenues of $163 ha(-1)  yr(-1) for a maize farm, equivalent to 8.95% increase in revenues. Our findings showed that NIs could create a win-win scenario that reduces the negative impact of N leaching and greenhouse gas production, while increases the agricultural output. However, NI's potential negative impacts, such as increase in NH3 emission and the risk of NI contamination, should be fully considered before large-scale application.

Climate change impacts of US reactive nitrogen.

Fossil fuel combustion and fertilizer application in the United States have substantially altered the nitrogen cycle, with serious effects on climate change. The climate effects can be short-lived, by impacting the chemistry of the atmosphere, or long-lived, by altering ecosystem greenhouse gas fluxes. Here we develop a coherent framework for assessing the climate change impacts of US reactive nitrogen emissions, including oxides of nitrogen, ammonia, and nitrous oxide (N(2)O). We use the global temperature potential (GTP), calculated at 20 and 100 y, in units of CO(2) equivalents (CO(2)e), as a common metric. The largest cooling effects are due to combustion sources of oxides of nitrogen altering tropospheric ozone and methane concentrations and enhancing carbon sequestration in forests. The combined cooling effects are estimated at -290 to -510 Tg CO(2)e on a GTP(20) basis. However, these effects are largely short-lived. On a GTP(100) basis, combustion contributes just -16 to -95 Tg CO(2)e. Agriculture contributes to warming on both the 20-y and 100-y timescales, primarily through N(2)O emissions from soils. Under current conditions, these warming and cooling effects partially offset each other. However, recent trends show decreasing emissions from combustion sources. To prevent warming from US reactive nitrogen, reductions in agricultural N(2)O emissions are needed. Substantial progress toward this goal is possible using current technology. Without such actions, even greater CO(2) emission reductions will be required to avoid dangerous climate change.

Ecosystem services altered by human changes in the nitrogen cycle: a new perspective for US decision making.

Human alteration of the nitrogen (N) cycle has produced benefits for health and well-being, but excess N has altered many ecosystems and degraded air and water quality. US regulations mandate protection of the environment in terms that directly connect to ecosystem services. Here, we review the science quantifying effects of N on key ecosystem services, and compare the costs of N-related impacts or mitigation using the metric of cost per unit of N. Damage costs to the provision of clean air, reflected by impaired human respiratory health, are well characterized and fairly high (e.g. costs of ozone and particulate damages of $28 per kg NO(x)-N). Damage to services associated with productivity, biodiversity, recreation and clean water are less certain and although generally lower, these costs are quite variable (<$2.2-56 per kg N). In the current Chesapeake Bay restoration effort, for example, the collection of available damage costs clearly exceeds the projected abatement costs to reduce N loads to the Bay ($8-15 per kg N). Explicit consideration and accounting of effects on multiple ecosystem services provides decision-makers an integrated view of N sources, damages and abatement costs to address the significant challenges associated with reducing N pollution.

A global perspective on belowground carbon dynamics under nitrogen enrichment.

Nitrogen (N) effects on ecosystem carbon (C) budgets are critical to understand as C sequestration is considered as a mechanism to offset anthropogenic CO(2) emissions. Interactions between aboveground C and N cycling are more clearly characterized than belowground processes. Through synthesizing data from multiple terrestrial ecosystems, we quantified the responses of belowground C cycling under N addition. We found that N addition increased litter input from aboveground (+20%) but not from fine root. N addition inhibited microbial activity as indicated by a reduction in microbial respiration (-8%) and microbial biomass carbon (-20%). Although soil respiration was not altered by N addition, dissolved organic carbon concentration was increased by 18%, suggesting C leaching loss may increase. N addition increased the C content of the organic layer (+17%) but not the mineral soil layer. Overall, our meta-analysis indicates that N addition will increase short term belowground C storage by increasing C content of organic layer. However, it is difficult to predict the response of long term C sequestration since there is no significant change in mineral soil C content.

A review of nitrogen enrichment effects on three biogenic GHGs: the CO2 sink may be largely offset by stimulated N2O and CH4 emission.

Anthropogenic nitrogen (N) enrichment of ecosystems, mainly from fuel combustion and fertilizer application, alters biogeochemical cycling of ecosystems in a way that leads to altered flux of biogenic greenhouse gases (GHGs). Our meta-analysis of 313 observations across 109 studies evaluated the effect of N addition on the flux of three major GHGs: CO(2), CH(4) and N(2)O. The objective was to quantitatively synthesize data from agricultural and non-agricultural terrestrial ecosystems across the globe and examine whether factors, such as ecosystem type, N addition level and chemical form of N addition influence the direction and magnitude of GHG fluxes. Results indicate that N addition increased ecosystem carbon content of forests by 6%, marginally increased soil organic carbon of agricultural systems by 2%, but had no significant effect on net ecosystem CO(2) exchange for non-forest natural ecosystems. Across all ecosystems, N addition increased CH(4) emission by 97%, reduced CH(4) uptake by 38% and increased N(2)O emission by 216%. The net effect of N on the global GHG budget is calculated and this topic is reviewed. Most often N addition is considered to increase forest C sequestration without consideration of N stimulation of GHG production in other ecosystems. However, our study indicated that although N addition increased the global terrestrial C sink, the CO(2) reduction could be largely offset (53-76%) by N stimulation of global CH(4) and N(2)O emission from multiple ecosystems.

Linking marine resources to ecotonal shifts of water uptake by terrestrial dune vegetation.

As evidence mounts that sea levels are rising, it becomes increasingly important to understand the role of ocean water within terrestrial ecosystem dynamics. Coastal sand dunes are ecosystems that occur on the interface of land and sea. They are classic ecotones characterized by zonal distribution of vegetation in response to strong gradients of environmental factors from the ocean to the inland. Despite the proximity of the dune ecosystem to the ocean, it is generally assumed that all vegetation utilizes only freshwater and that water sources do not change across the ecotone. Evidence of ocean water uptake by vegetation would redefine the traditional interpretation of plant-water relations in the dune ecosystem and offer new ideas for assessing maritime influences on function and spatial distribution of plants across the dune. The purpose of this study was to identify sources of water (ocean, ground, and rain) taken up by vegetation using isotopic analysis of stem water and to evaluate water uptake patterns at the community level based on the distribution and assemblage of species. Three coastal dune systems located in southern Florida, USA, and the Bahamian bank/platform system were investigated. Plant distributions across the dune were zonal for 61-94% of the 18 most abundant species at each site. Species with their highest frequency on the fore dune (nearest the ocean) indicate ocean water uptake as evidenced by delta 18O values of stem water. In contrast, species most frequent in the back dune show no evidence of ocean water uptake. Analysis of species not grouped by frequency, but instead sampled along a transect from the ocean toward the inland, indicates that individuals from the vegetation assemblage closest to the ocean had a mixed water-harvesting strategy characterized by plants that may utilize ocean, ground-, and/or rainwater. In contrast, the inland vegetation relies mostly on rainwater. Our results show evidence supporting ocean water use by dune vegetation and demonstrate an exciting relationship between seawater and ecotonal shifts in plant function of a terrestrial ecosystem.

Heterogeneous reflected light influences asymmetry in leaf anatomy and gas exchange.

Soil and vegetative groundcovers reflect light heterogeneously in habitats lacking a continuous overhead canopy, however the effects of reflected light on vegetation in these habitats has received little attention. We test the hypothesis that reflected light flux affects leaf optical properties, anatomy, and photosynthesis of Ipomoea pes-caprae (Convolvulacae), a common sand dune vine with functionally symmetric leaves, by comparing leaves growing over patches of high and low reflected light flux. Patches of high reflected light were found directly over sand and reflected 26.0 ± 0.9% (mean ± 1 SE) of incident photosynthetically active radiation (PAR) while patches of low reflected light were found over vegetation and reflected 6.1 ± 0.7% of incident PAR. Using a novel in situ method to simultaneously illuminate and measure gas exchange of one leaf surface at a time, we show that abaxial surface photosynthetic maxima and palisade parenchyma in sand patches were, respectively, 2.6 times greater and 20% thicker than those found over vegetation patches. Our results suggest that reflected light strongly influences leaf anatomy and gas exchange of I. pes-caprae, demonstrating that reflected light can be an important component of the light environment for vegetation of habitats characterized by high-albedo substrates.