A dual-porosity model for nitrogen leaching from a watershed/Un modèle à double porosité pour le lessivage de l’azote d’un bassin versant

Abstract

Abstract The MASONW (MACRO + SOILN + Watershed) model describing nitrogen leaching in watersheds was developed and tested. The model is based on the MACRO and SOILN models. The dual-porosity model MACRO simulates water flow on the field scale. The SOILN model describes turnover and leaching of nitrogen. Two main features of a watershed have been added into these two models: (a) the existence of a river system, and (b) variable thickness of the aeration zone within a watershed. Good agreement between the output of the MASONW model and observed data for water discharge and nitrate concentrations were achieved in the Odense watershed (496 km²) in Denmark.     

Stream nitrate uptake and transient storage over a gradient of geomorphic complexity,north‐central Colorado,USA

The understanding of nutrient uptake in streams is impeded by a limited understanding of how geomorphic setting and flow regime interact with biogeochemical processing. This study investigated these interactions as they relate to transient storage and nitrate uptake in small agricultural and urban streams. Sites were selected across a gradient of channel conditions and management modifications and included three 180‐m long geomorphically distinct reaches on each of two streams in north‐central Colorado. The agricultural stream has been subject to historically variable cattle‐grazing practices, and the urban stream exhibits various levels of stabilisation and planform alteration. Reach‐scale geomorphic complexity was characterised using highly detailed surveys of channel morphology, substrate, hydraulics and habitat units. Breakthrough‐curve modelling of conservative bromide (Br^?) and nonconservative nitrate (NO₃^?) tracer injections characterised transient storage and nitrate uptake along each reach. Longitudinal roughness and flow depth were positively associated with transient storage, which was related to nitrate uptake, thus underscoring the importance of geomorphic influences on stream biogeochemical processes. In addition, changes in geomorphic characteristics due to temporal discharge variation led to complex responses in nitrate uptake. Copyright © 2011 John Wiley & Sons, Ltd.     

Dynamic evolution of nutrient discharge under stormflow and baseflow conditions in a coastal agricultural watershed in Ishigaki Island,Okinawa, Japan

Excessive terrestrial nutrient loadings adversely impact coral reefs by primarily enhancing growth of macroalgae, potentially leading to a phase‐shift phenomenon. Hydrological processes and other spatial and temporal factors affecting nutrient discharge must be examined to be able to formulate effective measures for reducing nutrient export to adjacent reefs. During storm events and baseflow periods, water samples were obtained from the tropical Todoroki River, which drains an intensively agricultural watershed into Shiraho coral reef. In situ nutrient analyzers were deployed for 6 months to hourly measure dissolved nutrient (NO₃⁻‐N and PO₄³⁻‐P) concentrations. Total phosphorus (TP) and suspended solid concentration (TSS) were increased by higher rainfall intensity (r = 0·94, p < 0·01) and river discharge Q (r = 0·88, p < 0·01). In contrast, NO₃⁻‐N concentration tends to decrease drastically (e.g. from 3 to 1 mg l⁻¹) during flood events. When base flow starts to dominate afterwards, NO₃⁻‐N manifested an increasing trend, but decreases when baseflow discharge becomes low. This counter‐clockwise hysteresis for NO₃⁻‐N highlights the significant influence of groundwater discharge. N delivery can therefore be considered a persistent process compared to sediment and P discharge, which are highly episodic in nature. Based on GIS analysis, nutrient concentration along the Todoroki River was largely affected by the percentage of sugarcane/bare areas and bedrock type. The spatial distribution of N concentration in the river reflects the considerable influence of subsurface geology—higher N levels in limestone‐dominated areas. P concentrations were directly related to the total length of artificial drainage, which enhances sediment transport. The use of high‐resolution monitoring data coupled with GIS‐based spatial analysis therefore enabled the clarification of control factors and the difference in the spatio‐temporal discharge characteristics between N and P. Thus, although erosion‐reduction schemes would reduce P discharge, other approaches (e.g. minimize fertilizer) are needed to reduce N discharge. Copyright © 2010 John Wiley & Sons, Ltd.     

The role of vibrationally excited nitrogen in the ionosphere

Theoretical and experimental aspects of the production, transformation, diffusion and loss of N₂ in the upper atmosphere are considered. The N₂-CO₂ near-resonant system in theD andE regions is taken into account. We describe our understanding of the methods necessary to find the vibrational populations of N₂ and CO₂ (asymmetric mode of CO₂). The calculations of the vibrational temperatures in theD, E, andF regions for the mid-latitude ionosphere and an aurora are presented. The connection between the excited species and the 4.26-m radiation intensities is considered. The models for the rate coefficient of the reaction of O⁺ with N₂ and the electron density decrease resulting from N₂ in the F region are discussed.     

Phosphorus and nitrogen limitation of algal biomass across trophic gradients

Regression results based on data from 46 northern temperate lakes show that total phosphorus (TP) is the best predictor for phytoplankton (as chl-a) at lower trophic levels, TP < 200 mg · m^–3. A regression including both TP and TN as regressors is the best predictor for lakes with TP > 200 mg · m^–3. However, the good correlation is probably due to a high correlation between lake average chl-a (all years observed) and lake average TP and TN. Within single hypereutrophic lakes, TN alone is the best predictor. It was not possible to identify a medium trophic domain where TN and TP in combination was the best predictor for chl-a. The ratio TN:TP in the water decreases from about 40 to about 5 with increasing trophic level. Optimum TN:TP ratio for algal species with high abundance during late summer and autumn reflects this decreasing ratio, but within a lesser range, i.e., 20 to 5. In contrast, TN:TP ratios for species abundant during the early vernal period showed no, or an inverse, relation to the TN:TP ratio of the water.     

Historical changes in sediments of Pyramid Lake,Nevada, USA: consequences of changes in the water balance of a terminal desert lake

Sediment cores from the shallow and deep basins of Pyramid Lake, Nevada, revealed variations in composition with depth reflecting changes in lake level, river inflow, and lake productivity. Recent sediments from the period of historical record indicate: (1) CaCO₃ and organic content of sediment in the shallow basin decrease at lower lake level, (2) CaCO₃ content of deep basin sediments increases when lake level decreases rapidly, and (3) the inorganic P content of sediments increases with decreasing lake volume. Variations in sediment composition also indicate several periods for which productivity in Pyramid Lake may have been elevated over the past 1000 years. Our data provide strong evidence for increased productivity during the first half of the 20th Century, although the typical pattern for cultural eutrophication was not observed. The organic content of sediments also suggests periods of increased productivity in the lake prior to the discovery and development of the region by white settlers. Indeed, a broad peak in organic fractions during the 1800's originates as an increase starting around 1600. However, periods of changing organic content of sediments also correspond to periods when inflow to the lake was probably at extremes (e.g. drought or flood) indicating that fluctuations in river inflow may be an important factor affecting sediment composition in Pyramid Lake.     

Nitrogen and sulfur species in Antarctic aerosols at Mawson,Palmer Station,and Marsh (King George Island)

High volume bulk aerosol samples were collected continuously at three Antarctic sites: Mawson (67.60° S, 62.50° E) from 20 February 1987 to 6 January 1992; Palmer Station (64.77° S, 64.06° W) from 3 April 1990 to 15 June 1991; and Marsh (62.18° S, 58.30° W) from 28 March 1990, to 1 May 1991. All samples were analyzed for Na⁺, SO ₄ ^2– , NO ₃ ^– , methanesulfonate (MSA), NH ₄ ⁺ ,²¹⁰Pb, and⁷Be. At Mawson for which we have a multiple year data set, the annual mean concentration of each species sometimes vary significantly from one year to the next: Na⁺, 68–151 ng m^–3; NO ₃ ^– , 25–30 ng m^–3; nss SO ₄ ^2– , 81–97 ng m^–3; MSA, 19–28 ng m^–3; NH ₄ ⁺ , 16–21 ng m^–3;²¹⁰Pb, 0.75–0.86 fCi m^–3. Results from multiple variable regression of non-sea-salt (nss) SO ₄ ^2– with MSA and NO ₃ ^– as the independent variables indicates that, at Mawson, the nss SO ₄ ^2– /MSA ratio resulting from the oxidation of dimethylsulfide (DMS) is 2.80±0.13, about 13% lower than our earlier estimate (3.22) that was based on 2.5 years of data. A similar analysis indicates that the ratio at Palmer is about 40% lower, 1.71±0.10, and more comparable to previous results over the southern oceans. These results when combined with previously published data suggest that the differences in the ratio may reflect a more rapid loss of MSA relative to nss SO ₄ ^2– during transport over Antarctica from the oceanic source region. The mean²¹⁰Pb concentrations at Palmer and Marsh and the mean NO ₃ ^– concentration at Palmer are about a factor of two lower than those at Mawson. The²¹⁰Pb distributions are consistent with a²¹⁰Pb minimum in the marine boundary layer in the region of 40°–60° S. These features and the similar seasonalities of NO ₃ ^– and²¹⁰Pb at Mawson support the conclusion that the primary source regions for NO ₃ ^– are continental. In contrast, the mean concentrations of MSA, nss SO ₄ ^2– , and NH ₄ ⁺ at Palmer are all higher than those at Mawson: MSA by a factor of 2; nss SO ₄ ^2– by 10%; and NH ₄ ⁺ by more than 50%. However, the factor differences exhibit substantial seasonal variability; the largest differences generally occur during the austral summer when the concentrations of most of the species are highest. NH ₄ ⁺ /(nss SO ₄ ^2– +MSA) equivalent ratios indicate that NH₃ neutralizes about 60% of the sulfur acids during December at both Mawson and Palmer, but only about 30% at Mawson during February and March.     

Amino acid nitrogen in atmospheric aerosols: Occurrence,sources and photochemical modification

The presence of amino acids in atmospheric precipitation and aerosols has been noted for many years, yet relatively little is known about these or other nitrogen containing organic compounds in the atmosphere. Marine and continental rainwater analyses indicate that atmospheric aerosols, and subsequently atmospheric precipitation, may contain substantial levels of free and combined amino acids. The most likely source of amino N in the remote marine atmosphere appears to be the injection of proteinaceous material through the action of bursting bubbles at the sea-air interface or the long range transport from terrestrial sources. The capacity of these substrates to undergo photooxidation and photodegradation in the atmosphere to simpler species, such as ammonium ions, carboxylic acids, and for the S containing amino acids, oxidized forms of sulfur, has received little attention from atmospheric chemists. The photochemistry of covalently bound amino groups, particularly as found in peptides and amino acids, is discussed here with the purpose of summarizing what is known of their occurrence and their possible importance to atmospheric chemistry.     

A photoelectric detector for the measurement of photolysis frequencies of ozone and other atmospheric molecules

Photoelectric detectors for the measurement of photolysis frequencies of different trace gases in the atmosphere are described. They exhibit uniform response characteristics over one hemisphere (2 sr) and wavelength characteristics closely matched to those of the photolysis frequencies J _O1D, J _NO2, and J _NO3, respectively. Absolute calibration of the J _O1D detector was performed by chemical actinometry with an accuracy of ±16 percent. Simultaneous measurements of J _NO2 and J _O1D are presented.     

Aspects of the cycle of inorganic nitrogen compounds in the tropical rain forest of the Ivory Coast

A partial balance of mineral N is given for the basins of two coastal rivers in a forest zone in the Ivory Coast. The dry and wet depositions on the basin surfaces is given for particulate matter (NO₃ ^–, NH₄ ⁺). The quantity of mineral N washed away in the rivers is evaluated. The losses from leaching of the soils by rainwater are about 0.33 to 1.0% of the atmospheric depositions for NH₄ ⁺–N and 2.2 to 5.8% for NO₃ ^––N. The yearly atmospheric input of N compounds to the ecosystem, about 1.4 g N m^–2 y^–1, is at least 14% of mineral N formed in the soils and is therefore quite significant.