Areal distribution of 129I in west cumbrian solis

¹²⁹I has been released during operations at the BNFL nuclear fuel reprocessing plant at Sellafield in west Cumbria over the past thirty years with about 95% being discharged into the sea and 5% into the atmosphere. Soil samples have been taken within a 40 km radius of Sellafield to determine the extent to which the ¹²⁹I is deposited in the immediate vicinity of the plant. The ¹²⁹I content has been determined by a sensitive neutron activation technique and levels in soil were found to be elevated above global levels in all samples. The areal distribution of ¹²⁹I was consistent with direct deposition following release to the atmosphere from Sellafield and the relationship between ¹²⁹I activity and the distance from Sellafield was of a form predicted by atmospheric dispersion models. The absence of any observable return of ¹²⁹I from the sea has implications for assessments of dose.     

LONGITUDINAL AND SEASONAL WATER CHEMISTRY VARIATIONS IN A NORTHERN APPALACHIAN STREAM1

ABSTRACT: Quaker Run, a fourth order stream located in southwestern New York State, exhibits a highly unusual chemical gradient along its upper reaches. Weekly water samples showed an increase in the mean annual pH from 5.07 to 7.01 along a stretch of only 2.2 km. Mean alkalinity, calcium, magnesium, sodium, potassium, nitrate-nitrite-nitrogen, silica, and conductivity also increased appreciably over this distance. The study area receives some of the most highly acidic atmospheric deposition in the United States. Minimal buffering of these acidic inputs in the extreme upper watershed, and an abrupt downstream increase in buffering associated with changes in soil type, apparently produce the observed streamwater chemistry gradient. In contrast, a comparison between 11 midstream, downstream, and tributary sites showed relatively little variation in streamwater chemistry. In addition to the pronounced longitudinal chemistry changes along the upper portion of the stream, pronounced temporal chemistry variations were also observed at all sampling sites. High flow during snowmelt and heavy rains produced more dilute, acidic conditions, while streamwater pH and dissolved base cations were generally highest during low flow. Much of this temporal variation in streamwater chemistry is attributed to seasonal variation in residence times of soil water.     

Failure to detect fetal obstructive uropathy by second trimester ultrasound

The prenatal diagnosis, management and outcome of an hereditary obstructive uropathy is presented. Serial ultrasonic assessment of the fetal urinary tract was carried out from the early second trimester onward. Slight bilateral hydronephrosis as a first sign of obstructive uropathy was only established as late as 30 weeks of gestation. On the basis of weekly ultrasound scans, a conservative approach was adopted. In view of fetal maturity, labour was induced at 36 weeks resulting in the vaginal delivery of a male infant with moderate bilateral hydronephrosis. Neonatally, anuria developed due to bilateral obstruction of the ureters as a result of increasing bladder wall hypertrophy due to urethral valves. A bilateral uretero-cutaneostomy was carried out. The infant so far develops normally, and renal function is normal for age. Women at risk for fetal obstructive uropathy should have ultrasonic monitoring throughout pregnancy.     

Goitre and environmental iodine deficiency in the UK — Derbyshire: A review

Endemic goitre was prevalent in the population of Derbyshire in the UK for many centuries until it declined from the 1930s. A contemporary medical survey showed that endemicity of goitre was particularly higher in the Carboniferous limestone areas of the Derbyshire-Peak District. Unlike classical goitrous areas of the world, where the distribution of goitre has been found to be related to the iodine content in the environment, there is no such relationship reported for the Derbyshire-Peak District area. The present study reviews the presence of endemic goitre in this area with reference to iodine in different environmental media using past and present data. In comparison with the world average values, the iodine contents in the soil and sediment in the Peak District are not deficient, but compared to England, Wales and Scotland averages, these levels are low. As no information on the mobility and bioavailability of iodine of this area is available, a cautious approach is necessary before any assumption is made on the aetiology of endemic goitre. The study also discusses some hypotheses relating to the possible cause of endemic goitre in the limestone areas. Further research needs are suggested depending on the land use and geochemistry of the Peak District to determine the underlying causes of the former endemic goitre in this area.     

Coefficient of variation of sea surface temperature (SST) as an indicator of coral bleaching

Coral bleaching has become a major problem on reefs around the world in recent decades. It is believed that mean temperature alone is the primary force driving this ecological phenomenon. We propose that variance in temperature in the short term is just as important as the mean. Thirty years of daily sea surface temperature (SST) data have been collected by the University of Puerto Rico at Mayaguez Marine Laboratory in La Parguera, PR. These data were collated and analyzed initially (by Amos Winter) for their relationship to coral bleaching in this area. We found that the data fell into three categories: high mean temperatures associated with severe bleaching, cooler mean temperatures associated with no bleaching, and years of high SSTs but with no coral bleaching. Here, we examined the relationship between mean temperature during those months in which bleaching occurred, temperature variance (as measured by standard deviation), and coefficient of variation (CV; i.e., SD standardized by the mean). We also derived a critical threshold temperature and level of resolution in time for calculating these statistics to clearly describe the circumstances of bleaching versus non-bleaching events, particularly at marginal bleaching temperatures. These characteristics were compared for the four warmest months of the year (July–October) for four warm bleaching years (1969, 1987, 1990, and 1995), four cool non-bleaching years (1984, 1985, 1986, and 1988), and two warm non-bleaching years (1994 and 2000). No relationship was found between the mean SST and SD in terms of predicting bleaching. The two primary statistics which, in concert, did indicate bleaching, however, were the short-term, biweekly mean temperature and its the associated CV. Bleaching occurs in association with both high temperatures and a high CV. The CV becomes a critical determinant of bleaching only when temperatures are ∼29.1–29.8°C. The warm, non-bleaching years were generally characterized by a CV of < 1.9 and a temperature range between 28.5 and 29.9°C. We conclude that increased mean SSTs alone are not sufficient to induce coral bleaching; a high variance in SST at marginal, lower bleaching temperatures can induce bleaching, and likewise, a low variance of such will not induce bleaching. This variance is most clearly described by the CV.     

Evolution of Organic Analytical Methods in Environmental Forensic Chemistry

Over the past few decades the development of environmental regulations, advances in analytical chemistry and other scientific disciplines, and increased rigor in quality control procedures have created a new discipline, environmental forensics. The need for analytical methods that determine qualitatively and quantitatively organic compounds in the environment, especially in drinking waters, was recognized in the early 1950s. These methods were developed gradually by the early 1960s. The important tools of gas chromatography and mass spectroscopy that evolved in the 1970s provided the early environmental forensic chemist for the first time with the ability to produce scientifically sound data that was admissible in court. By the 1990s, multivariate statistical techniques became available and accepted, including principal component analysis (PCA) and polytopic vector analysis (PVA). These techniques, coupled with the advancing analytical methods, have enabled forensic investigator tools to evaluate and demonstrate unique attributes of a set of data. Analyses of marker compounds, PCBs, PCDD/Fs and petroleum hydrocarbons are all shown to be potentially valuable in deciphering the source and fate of contamination. This paper shows how advancements in environmental analytical chemistry provide the forensic chemist with tools to assess the source(s) of site contamination.     

Elevated atmospheric ozone increases concentration of insecticidal Bacillus thuringiensis (Bt) Cry1Ac protein in Bt Brassica napus and reduces feeding of a Bt target herbivore on the non-transgenic parent

Sustained cultivation of Bacillus thuringiensis (Bt) transgenic crops requires stable transgene expression under variable abiotic conditions. We studied the interactions of Bt toxin production and chronic ozone exposure in Bt cry1Ac-transgenic oilseed rape and found that the insect resistance trait is robust under ozone elevations. Bt Cry1Ac concentrations were higher in the leaves of Bt oilseed rape grown under elevated ozone compared to control treatment, measured either per leaf fresh weight or per total soluble protein of leaves. The mean relative growth rate of a Bt target herbivore, Plutella xylostella L. larvae was negative on Bt plants in all ozone treatments. On the non-transgenic plants, larval feeding damage was reduced under elevated ozone. Our results indicate the need for monitoring fluctuations in Bt toxin concentrations to reveal the potential of ozone exposure for altering dosing of Bt proteins to target and non-target herbivores in field environments experiencing increasing ozone pollution.