Nitrogen removal in a small constructed wetland: an isotope mass balance approach.

The nitrogen (N) removal potential of constructed wetlands is increasingly used to lower the N load from agricultural nonpoint sources to inland and coastal waters. To determine the removal efficiency and key factors limiting wetland N removal, N fluxes were studied in a small constructed wetland in Central Switzerland. With an isotope mass balance approach integrating the natural isotope signature of nitrate (NO3-, ammonium (NH4+), and particulate nitrogen (PN), the N transformations such as assimilation, mineralization, nitrification, and denitrification were quantified. On average, the wetland removed 45 g m(-2) yr(-1) N during the studied 2.5 years, corresponding to a removal efficiency of 27%. Denitrification contributed 94% to the N removal, while only 6% of the removed N accumulated in the sediments. Denitrification was most efficient during periods with an oxic water column overlying anoxic sediments, as NH4+ released during mineralization of sediment organic matter was completely nitrified and subsequently denitrified at the sediment-water interface. During water column anoxia, NH4+ accumulated in the water and fueled assimilation by duckweed and internal recycling. The NO3-N isotope signature in the wetland mainly reflected the mineralization of sediment organic matter and subsequent nitrification, while denitrification at the sediment-water interface produced no fractionation.

Phosphorus retention in small constructed wetlands treating agricultural drainage water.

The construction of artificial wetlands has become a measure increasingly applied to reduce nonpoint-source (NPS) pollution and to contribute to the restoration of eutrophic lakes and coastal waters. In a 2-yr study monitoring fluxes of particulate and dissolved phosphorus (P) in a small artificial wetland for the treatment of agricultural drainage water in Central Switzerland, water residence time was identified as the main factor controlling P retention in the system. Since most of the annual P load (62% as dissolved reactive phosphorus, DRP) was related to high discharge events, it was not average but minimum water residence time during flood events that determined the wetland's P retention. In agreement with a continuous stirred tank reactor (CSTR) model, our investigations suggest a minimum water residence time of 7 d to retain at least 50% of the bioavailable P. The investigated wetland retained only 2% of the bioavailable P, since the water residence time was shorter than 7 d during 61% of time in both years. Settling of phytoplankton rather than DRP uptake into phytoplankton limited the retention of bioavailable P. The overall retention efficiency of 23% total phosphorus (TP), corresponding to a surface related retention of 1.1 g P m(-2) yr(-1), was due to the efficient trapping of pedogenic particles.

On-site simultaneous determination of anions and cations in drainage water using a flow injection-capillary electrophoresis system with contactless conductivity detection.

Drainage water diverted from a farm pasture, which was heavily loaded with manure, was monitored during a rain event. Concurrent anion and cation determinations at intervals of 10 min could be achieved with a new capillary electrophoresis system employing dual injection at opposite ends of the separation capillary. The flow injection approach enabled automation of the sampling process. Interruption of the separation voltage was not necessary. Contactless conductivity detection with an electrolyte solution optimized for the purpose allowed the facile simultaneous detection of the inorganic ions Cl(-), NO(3)(-), SO(4)(2-), HPO(4)(2-), NO(2)(-), NH(4)(+), K(+), Ca(2+), Na(+) and Mg(2+) and the acquisition of temporal concentration profiles of these species. The detection limits achieved were between 20 and 200 [micro sign]g l(-1) for all ions and the repeatability of peak areas and peak heights was better than 1%. The quantitative results were verified by analysing individual samples later in the laboratory with photometry and ion chromatography and the average deviations were found to be between 4 and 12%. This contribution presents a further step in the development of capillary electrophoresis towards a fully automated, low maintenance field method.

High temporal resolution monitoring of inorganic nitrogen load in drainage waters.

Nitrate (NO3-), ammonium (NH4+) and pH were monitored with a novel flow cell equipped with ion-selective electrodes (ISEs) in a drainage pipe during one year. The high temporal resolution of the measurements (six measurements per hour) allowed the detection of diurnal oscillations in pH, NO3- and NH4+ concentrations, the relation of variations in concentrations to discharge rates changing during rain events, understanding of the processes resulting in such variations and tracing of unpredictable manure spills. Annual loads estimated from random samples collected every second day tended to underestimate the "true" loads calculated from quasi-continuous electrode measurements by 550% for NH4+ and 22% for NO3-.