Biomedical subjects

A P Rowland

Publications and source records attributed to A P Rowland.

5 recordsLinked to original sources

PubMed2001

Organic nitrogen in precipitation: real problem or sampling artefact?

Published observations of organic nitrogen (N) compounds in precipitation go back almost a century. Several different methods have been used to measure both the total and ionic concentrations of N. There is therefore some uncertainty as to whether reported "organic N" is real, or simply the result of uncertainties in chemical analyses or inadequate sampling methods. We found that the materials from which the collector was made (polypropylene, steel, or glass) had no significant effect on the composition of dissolved organic N (DON). The use of a biocide was found to be very important during sampling and storage of samples before analysis. We set up a network of seven collectors across the U.K., from the Cairngorms to Dorset, all operating to the same protocol, and including a biocide. Samples were analysed centrally, using proven methods. Over 6 months, organic N contributed about 20% to the total N in U.K. precipitation, but with a large variation across the country. This means that current estimates of wet deposited N to the U.K., which are based only on the ammonium and nitrate concentrations, are too small. Organic N is not an artefact, but a real problem that needs to be addressed.

Air Pollutants↗

PubMed2000

Effects of beach sand properties, temperature and rainfall on the degradation rates of oil in buried oil/beach sand mixtures.

Lysimeters located outdoors have been used to evaluate the decomposition of buried oily beach sand waste (OBS) prepared using Forties light crude oil and sand from different locations around the British coast. The OBS (5% oil by weight) was buried as a 12-cm layer over dune pasture sub-sand and overlain by 20 cm of dune pasture topsoil. Decomposition rates of oil residues averaged 2300 kg ha(-1) in the first year and the pattern of oil decomposition may be represented by a power curve. Oil decomposition was strongly related to the temperature in the OBS layer, but was also significantly affected by rainfall in the previous 12 h. The CO(2) flux at the surface of the treatment lysimeters followed the relationship [log(10) CO(2) (mg C m(-2) h(-1))=0.93+0.058x OBS temp. (degrees C)-0.042x12 h rain (mm)]. There was considerable variation in the rate of oil decomposition in sands collected from different sites. Sand from Askernish supported most microbial activity whilst sand from Tain was relatively inactive. The decomposition process appeared to cease when the sand became saturated with water, i.e. temporarily anaerobic. However, decomposition recommenced when the soil dried out. The fastest rate of decomposition occurred in sand from one of the two sites predicted to have high populations of hydrocarbon-degrading bacteria. Larger particle size and higher Ca content may also be significant factors governing the rate of decomposition.

Journal Article↗

PubMed1998

The dynamics of dissolved nitrogen in a blanket peat dominated catchment.

Precipitation, soil solution and drainage water were collected from a blanket peat catchment at Moor House National Nature Reserve in the Northern Pennine Uplands, UK, an area of moderately high N deposition. Two tributaries of the main stream were also sampled. Between 1993 and 1995 samples were analysed for NH4+ and NO3- and for part of the period for organic N. Inputs of N in precipitation exceeded outputs in stream water. Organic N represented a small proportion of N inputs while inputs of inorganic N averaged 10.2 kg ha(-1) a(-1). Soil solution from 10 cm depth in the peat was dominated by organic N whereas at 50 cm NH4+ slightly exceeded organic N. NO3- was rarely detected at either depth except during a period of exceptionally warm and dry weather in 1995. Output fluxes in stream water of organic N (5.7 to 6.5 kg ha(-1) a(-1)) were much greater than those of inorganic N (0.6 to 2.2 kg ha(-1) a(-1)). Inorganic N in streams was predominantly NO3- except in the smallest stream which had the largest concentrations of NH4+. This suggests that N transformations, particularly nitrification, may be taking place in the mineral soils adjacent to the streams or within the stream channel of the larger catchment.

Journal Article↗

PubMed1997

Applications of anion chromatography in terrestrial environmental research.

Ion chromatography can be applied to characterise single samples for a wide range of ionic species, at elevated or trace concentrations, or with automation may be used to determine many of the common ions on several thousand samples per year. It has been applied to a wide range of sample types of environmental interest. Examples of applications are given for the common sample types, i.e. atmospheric gases and particulates, water, biological materials and soil. The recent literature in the field of anion chromatography, as applied to environmental research, is reviewed (102 references). Suppressed and non-suppressed systems are covered, as are comparisons with other methods of analysis. Development of sample preparation methods, stationary and mobile phases, detection systems and techniques are also discussed.

Chromatography, Ion Exchange↗

PubMed1993

Dissolved inorganic nitrogen budget for a forested catchment at Beddgelert, North Wales.

An input-output budget for dissolved inorganic-N in a small forested catchment in North Wales is presented. From 1982 to 1990, bulk precipitation inputs averaged 10.3 kg ha(-1) year(-1), whereas throughfall inputs in 1983-1984 were 20.3 kg ha(-1) year(-1). Streamwater outputs were consistently larger than bulk precipitation inputs, averaging 14.6 kg ha(-1) year(-1). Inorganic-N in the forest stream was predominantly nitrate and concentrations were substantially higher than in a nearby moorland stream. Both streams showed seasonal trends in nitrate concentration, with highest concentrations occurring in summer in the forest stream but in winter in the moorland stream. Nitrate concentration in the forest stream increased with increasing soil temperature up to approximately 7 degrees C and decreased at higher temperatures. Nitrification is thought to be responsible for nitrate production at temperatures both below and above 7 degrees C, but root uptake becomes significant only at the higher temperatures. In the forest, dry deposition and cloudwater inputs of inorganic-N are responsible for increased nitrogen fluxes in throughfall compared with wet deposition. Mineralization and nitrification in excess of plant needs causes the organic soil horizons to act as a net source of dissolved inorganic-N. Nitrogen transformations in the soil lead to soil acidification at a rate of 1.0 keq ha(-1) year(-1).

Journal Article↗