QUANTIFICATION OF THE WATER BUDGET AND NUTRIENT LOADING IN A SMALL PEATLAND1

ABSTRACT: Few water budgets exist for specific types of wetlands such as peatlands, even though such information provides the basis from which to investigate linkages between wetlands and upland ecosystems. In this study, we first determined the water budget and then estimated nutrient loading from an upland farm field into a 1.5 ha, kettle-block peatland. The wetland contains highly anisotropic peat and has no distinct, active layer of groundwater flow. We estimated the depth of the active layer using Fick's law of diffusion and quantified groundwater flow using a chemical mass balance model. Evapotranspiration was determined using MORECS, a semi-physical model based on the Penman-Monteith approach. Precipitation and surface outflow were measured using physical means. Groundwater provided the major inflow, 84 percent (44,418 m³) in 1993 and 88 percent (68,311 m³) in 1994. Surface outflow represented 54 percent (28,763 m³) of total outflows in 1993 and 48 percent (37,078 m³) in 1994. A comparison of several published water budgets for wetlands and lakes showed that error estimates for hydrologic components in this study are well within the range of error estimates calculated in other studies. Groundwater inflow estimates and nutrient concentrations of three springs were used to estimate agricultural nutrient loading to the site. During the study period, nutrient loading into the peatland via groundwater discharge averaged 24.74 kg K ha^-1, 1.83 kg total inorganic P ha^d, and 21.81 kg NO₃-N ha^-1.     

Isochromosome 5p mosaicism at prenatal diagnosis: observations and outcomes in six cases at chorionic villus sampling and one at amniocentesis

We present six cases of 47,+i(5p)/46 mosaicism diagnosed at chorionic villus sampling (CVS), this being the first prospective series to be reported. The clinical indication in each was advanced maternal age. Further prenatal studies in four (amniocentesis, plus fetal blood sampling in one) did not show the isochromosome. In one case, subsequent amniocentesis showed 1/48 in situ colonies with the isochromosome, but fetal blood was karyotypically normal. These five pregnancies resulted in phenotypically normal livebirths; further normal follow-up reports (from age 4 months through 4 years) are noted in four of these. Analysis of placental tissue in one case confirmed the presence of the i(5p) mosaicism. In the remaining case, in which 100% of CVS cultured cells had the i(5p), the pregnancy was terminated. Fetal skin fibroblasts did not show the i(5p). Thus, in none of these six cases was true fetal mosaicism detected, nor an abnormal phenotype noted. We suggest that a 47,+i(5p)/46 karyotype, detected at CVS, may frequently reflect confined placental mosaicism. In addition, we report a case of the primary diagnosis of 47,+i(5p)/46 mosaicism at amniocentesis. The infant appeared normal at birth, but a brain malformation was subsequently identified. Copyright © 2002 John Wiley & Sons, Ltd.