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C Neal

Publications and source records attributed to C Neal.

At least 37 records · Page 2Linked to original sources

Association of the cyclin-dependent kinases and 14-3-3 sigma negatively regulates cell cycle progression.

14-3-3 sigma, implicated in cell cycle arrest by p53, was cloned by expression cloning through cyclin-dependent kinase 2 (CDK2) association. 14-3-3 sigma shares cyclin-CDK2 binding motifs with different cell cycle regulators, including p107, p130, p21(CIP1), p27(KIP1), and p57(KIP2), and is associated with cyclin.CDK complexes in vitro and in vivo. Overexpression of 14-3-3 sigma obstructs cell cycle entry by inhibiting cyclin-CDK activity in many breast cancer cell lines. Overexpression of 14-3-3 sigma can also inhibit cell proliferation and prevent anchorage-independent growth of these cell lines. These findings define 14-3-3 sigma as a negative regulator of the cell cycle progression and suggest that it has an important function in preventing breast tumor cell growth.

14-3-3 Proteins↗

Conclusions to the special issue of Science of the Total Environment concerning 'The water quality of UK rivers entering the North Sea'.

This paper presents an overview of the water quality functioning of eastern UK rivers draining into the North Sea. It summarises the results of three special issues of Science of the Total Environment and related work and complements a companion bibliography (Neal and Turner, 2000, this volume). The rivers are described in straightforward broad terms, and the reader is guided via the bibliography to the special volumes for the detailed findings. The water quality is shown to be highly variable over space and time. The changes over the past 300 years reflect first the transition from a rural society to the major impact of the industrial revolution and subsequently to one of the worlds' most successful environmental cleanups. The present water quality reflects the relative impacts of diffuse agricultural sources, urban and industrial point source discharges together with background inputs associated with geology: all these can be modified by within-river processes associated with physical mixing, biology and inorganic reactions. The work is set within the context of water quality, modelling and flux outputs to the North Sea and contemporary and future environmental research and management needs. A range of environmental impact studies is included. The detailed information is now available on a major and easily accessible database.

Agriculture↗

A summary of river water quality data collected within the Land-Ocean Interaction Study: core data for eastern UK rivers draining to the North Sea

A numerical summary of the water quality of rivers draining into the North Sea from the eastern UK is presented using core information collected within the Land-Ocean Interaction Study (LOIS) and a companion study by the Institute of Hydrology. The analysis is based on weekly monitoring for periods from 1993 to 1999 for major, minor, nutrient, trace and other water quality determinand chemistry. The data cover rivers ranging from the rural Tweed in southeastern Scotland, to the urban and industrially impacted Wear and Humber rivers in the north and central England and two agriculturally impacted rivers in the south of England (Great Ouse and Thames). Within the analysis, monthly averaged concentrations are plotted to show the seasonality. The summary provides specific information on the water quality of UK rivers which is of use in developing European and global initiatives for assessing pollutant inputs to estuarine, coastal and open-sea environments.

Journal Article↗

The water quality of the River Thames at a rural site downstream of Oxford

Water quality information is presented for the River Thames 34 km downstream of the market town of Oxford in Oxfordshire to provide an overview of the hydrochemical functioning of a major agriculturally impacted river entering the North Sea. The data, which cover the period from the spring of 1997 to the spring of 1999, relate to three types of data. These types are: (1) weekly spot sampling for determination of major, minor and trace elements, pH, alkalinity and herbicides; (2) tri-weekly spot sampling for pH, alkalinity and dissolved silicon; and (3) continuous measurements of pH and dissolved oxygen. Calcium and bicarbonate provide, respectively, the dominant cation and anion in solution and their compositions remain relatively constant through time, irrespective of flow levels. In contrast, many determinands show seasonally related fluctuations. Concentrations for most of the major anions, sodium, potassium as well as soluble reactive phosphorus and several soluble trace elements such as boron, antimony, arsenic and molybdenum decrease as flow increases. A reverse pattern is observed for nitrate, some herbicides and trace elements associated with particulate phases: concentrations increase with increasing flow. These patterns reflect the influence of: (1) a calcium carbonate rich groundwater system which provides the main stream flow component; (2) dilution of point source pollutant inputs associated with sewage and possibly light industry at high flows for several major, nutrient and trace elements; (3) enhanced nitrate and herbicide runoff from agricultural land at high flows; (4) enhanced microparticulate trace metal levels associated with increased suspended sediment loads at high flows; and (5) biological processes which affect pH, dissolved silicon, dissolved carbon dioxide and dissolved oxygen levels. An examination of soluble reactive phosphorus (SRP) and boron relationships reveals a reduction in concentrations for SRP associated possibly with phosphorus removal from a major sewage treatment works on an upstream tributary of the Thames, the Thame.

Journal Article↗

The water quality of a tributary of the Thames, the Pang, southern England.

The water quality of a tributary of the Thames, the Pang, draining a rural part of the Thames basin is described and related to the influences of inputs from farming activity and groundwater from the underlying chalk aquifer as modified by biological within-stream processes. The groundwater inputs ensures that the waters are calcium and bicarbonate bearing and have relatively uniform concentrations. Agricultural inputs result in enhanced levels of nutrients, nitrate and soluble reactive phosphorus (SRP) in particular. For nitrate, the concentrations are higher during the winter months due to increased surface runoff. In contrast, SRP shows a more erratic behaviour with higher concentrations occurring during the early storm hydrograph rise following summer baseflow recession. Within the stream, biological activity results in: (a) marked diurnal fluctuations in the dissolved levels of carbon dioxide and oxygen; (b) a strong seasonal pattern in chlorophyll a levels; and (c) dissolved silica concentration reductions during the early spring period. Carbon dioxide levels are particularly high in the groundwater (typically approximately 60 times the atmospheric value) as observed at a spring discharge. However, within the stream, considerable degassing occurs although values remain an order of magnitude above atmospheric pressure. The findings are discussed in the context of the water quality functioning of agriculturally and sewage impacted southern eastern UK rivers. For example, the work shows that unlike for riverine systems with point sewage discharges or limited groundwater storage, there is a very poor link between chemical concentrations and flow even for components such as SRP and boron which are often connected to sewage discharges.

Agriculture↗

The water quality of the River Kennet: initial observations on a lowland chalk stream impacted by sewage inputs and phosphorus remediation.

The water quality of seven sites on the upper reaches of the River Kennet round the market town of Marlborough is described and related to the introduction of phosphorus treatment of effluent from Marlborough sewage treatment works (STW). The River Kennet is mainly groundwater-fed from a Cretaceous chalk aquifer and hence the river water is calcium- and bicarbonate-bearing and has a relatively constant composition of many major water quality determinants. In-stream biological activity gives rise to marked diurnal fluctuations in pH (of approx. 0.8 units). Dissolved carbon dioxide and dissolved oxygen also show marked diurnal fluctuations. Dissolved carbon dioxide varies from approximately 10 to 70 times atmospheric pressure, indicating net release of carbon dioxide and the dominance of heterotrophic (respiratory) processes over autotrophic processes (photosynthesis). Much of the excess carbon dioxide is probably associated with carbon dioxide laden groundwater inputs and the relatively short within-stream residence times ensures only limited degassing to the atmosphere. Diurnal fluctuations in dissolved oxygen vary from approximately 20% to 200% saturation. For both dissolved carbon dioxide and dissolved oxygen, the amplitude of fluctuations is much lower during the winter period, when biological activity is at its lowest. The concentrations of soluble reactive phosphorus (SRP), total phosphorus (TP) and boron increase markedly just downstream of the sewage works as a result of this point source input. These concentrations slowly decline further downstream as additional groundwater inputs dilute the effluent further. The introduction of chemical treatment of sewage effluent for phosphorus reduction at Marlborough STW resulted in a marked decrease in within-river SRP and TP concentrations to levels approximately the same as those upstream of the STW. A comparison of SRP and boron concentrations reveals a reduction in in-stream SRP concentrations by approximately 75% following effluent treatment. In terms of within-river processes controlling in-stream phosphorus concentrations, previous studies have indicated that one potentially important mechanism within calcium bicarbonate bearing rivers may be related to co-precipitation of phosphorus with calcium carbonate (calcite). The present study shows that the waters are oversaturated with respect to calcium carbonate, that no equilibrium conditions exist and that phosphorus removal has led to undetectable changes in calcium carbonate oversaturation. Hence, it is concluded that the primary changes in phosphorus levels within the river is directly associated with changing point source contributions from the STW and physical dilution within the river. However (1) the results relate to only the first year of study and subsequent differences may become apparent and (2) reactions between the water column and plant and bottom sediment interfaces may be important in regulating phosphorus fluxes within the river. The results presented in this paper mark a pilot phase of a longer-term initiative and this paper provides a background setting. The paper discusses the longer-term objectives and important gaps in knowledge of the system that requires further address.

England↗

Temporal and small-scale spatial variations of dissolved oxygen in the Rivers Thames, Pang and Kennet, UK.

Small-scale spatial dissolved oxygen concentrations were measured on three rivers by taking a number of transects along a river reach. Temporal (diurnal) variations were measured by use of continuous (15-min) monitors located at the mid-transect of the spatial observations. Spatial variation of dissolved oxygen concentrations were found to be relatively small (approx. +/- 10% dissolved oxygen) and biologically insignificant compared to diurnal changes under conditions of high productivity (approx. +/- 60% dissolved oxygen). The diurnal curves were analysed in order to estimate values of reaeration, photosynthesis and respiration on a daily basis for almost 3 months using process-based analytical techniques (the Delta and Hornberger and Kelly methods). The River Kennet was shown to be the most productive river followed by the River Pang and then the River Thames. The patterns of reaeration, photosynthesis and respiration and the behaviour of the three rivers are discussed.

England↗

Phosphate measurement in natural waters: two examples of analytical problems associated with silica interference using phosphomolybdic acid methodologies

Assessment of phosphate species for bicarbonate-bearing lowland rivers of the Thames valley, England and acidic Welsh upland streams (the Plynlimon area, mid-Wales) reveal problems of silica interference when employing standard automated 'phosphomolybdic acid' colorimetric methodologies. The interference occurs under a combination of two conditions: (1) when the reagents and samples are heated to speed up the rate of formation of phosphomolybdic acid; and (2) when the strength of a sulfuric acid reagent is too low. While this paper alerts researchers to potential analytical problems with silica interference within phosphomolybdic acid methodologies to determine soluble reactive phosphorus (SRP) concentrations, it cannot detail whether or not there is a general problem. This lack of specificity occurs because there are a variety of phosphomolybdic acid methodologies available which vary in their reagent recipes and it is not clear which methods will or will not suffer from silica interference. Changing the sulfuric acid reagent strength by a factor of two overcame the problem, in this case, with regards to the determination of soluble reactive phosphorus. However, even here, the method may not be applicable to very high alkalinity waters owing to their potential for reducing the acidity of the analyte. With regard to total dissolved phosphorus (TDP) and total phosphorus (TP) measurements, the importance of undertaking the analysis under ambient conditions is clearly shown. There are many small variants on standard phosphomolybdate methods for determining SRP, TDP and TP in use and it is not always clear which methods will or will not show silica interference for particular water types. It is therefore recommended that individual laboratories check their methodologies for silica interference using phosphate-free solutions with similar silica and alkalinity ranges for the waters being assayed.

Journal Article↗

The water quality of the River Wear, north-east England

A 1-year detailed study of water quality in the River Wear in combination with longer (decadal) term Environment Agency data (Harmonised Monitoring Scheme) show the influences of historic lead-zinc and coal mining and sewage inputs. The water quality for many determinands, such as sodium, chloride, boron, nitrate, and soluble reactive phosphorus, varies seasonally due to changing flow conditions. For most dissolved determinands, concentrations decrease with increasing flow in response to dilution of point and diffuse sources by rainfall. However, concentrations increase with increasing flow for dissolved organic carbon, aluminium, lead, iron, yttrium, and the lanthanides and actinides. This increase probably reflects two processes. Firstly, trace element-enriched runoff occurs from the acidic moorland areas of the catchment when it wets up. Secondly, at high flows, increased production of transition metals bearing microparticulate material occurs; these pass through conventional filters used to separate dissolved from particulate materials. For the particulate components, iron, manganese, aluminium, and some trace transition metals are present above the analytical detection limits and concentrations increase with increasing flow in response to increasing suspended sediment levels. However, particulate metal concentrations are relatively low for the Wear compared to the other eastern UK rivers, even though historic lead-zinc mining activity in the upper portions of the Wear catchment has led to extensive spoil contamination of the land. This feature probably reflects the lack of a significant flood plain area, where trace contaminants can accumulate within the sediments. The importance of inputs of pumped water from former coalmines is highlighted; increased manganese and dissolved carbon dioxide concentrations and reduced pH result. Examination of the Harmonised Monitoring Scheme data indicate no clear long-term changes in water quality for all but one determinand, although analysis is hampered by changes in sampling frequency for all determinands and changes in detection limits for certain trace metals. The only clear long-term change is a reduction in the micro-organic insecticide, aldrin. Nonetheless, the long-term data, when plotted as a function of month, follow the same pattern as the LOIS data. For aldrin, the higher values during the early period of record occurred in the latter half of each year, presumably as a consequence of seasonal application and enhanced leaching during the autumn.

Journal Article↗

River water quality in the Humber catchment: an introduction using GIS-based mapping and analysis

The regional water quality of the Humber catchment was mapped for key inorganic chemical determinands using a GIS system and an extensive Environment Agency and LOIS monitoring database. The resultant maps revealed the major factors affecting the general characteristics of regional water quality. Sewage inputs from industrial and domestic sources account for the high concentration of many determinands in urban areas. The concentrations of particulate components increase in tidal zones because of sediment trapping and tidal re-suspension effects. Some determinands also exhibit localized high concentrations related to coal mine drainage, soil pollution caused by past ore mining, bedrock geology, the agricultural use of fertilizers and the ingression of seawater into the estuary.

Journal Article↗

Pollution regimes and variability in river water quality across the Humber catchment: interrogation and mapping of an extensive and highly heterogeneous spatial dataset

Water quality inter-relationships based on an extensive Environment Agency database are used to identify seven key types of clean and polluted riverine environments within the Humber catchment. These types were selected on the basis of linear separations between average concentrations of ammonium, chloride, dissolved nickel and chromium and acid-available particulate nickel and chromium. However, a more detailed analysis of determinand and flow relationships at each type locality revealed complex patterns due to the highly variable nature of pollutant sources at the local scale. The information presented contrasts systems at a larger scale, where simpler integrated features are observed, and which can be represented by two-component mixing models. Scale and hydrology seem to be important features in determining the simplicity or complexity of determinand inter-relationships, and the implications of these findings are discussed.

Journal Article↗

Riverine inputs of major ions and trace elements to the tidal reaches of the River Tweed, UK.

This paper examines spatial and temporal variability in freshwater inputs of trace elements and major ions to the tidal reaches of the River Tweed. The relationships between concentrations of major ions and trace elements (in dissolved and acid-available particulate forms) and flow are examined, and a simple two-component endmember mixing analysis performed to link river water chemistry to catchment sources, and to identify whether within-river processes modify concentrations to produce non-conservative behaviour. The results indicate that most dissolved major ions and trace elements behave conservatively in the lower reaches of the River Tweed, the variability in concentrations being dominated by hydrology and the existence of different high-flow and low-flow endmember runoff chemistries. This suggests that the variability in concentration of most dissolved trace elements and major ions in the lower Tweed can be modelled using simple mixing relationships. However, the relationships between pH, Ca, Mg and Gran alkalinity show pronounced non-conservative behaviour, indicating the importance of understanding within-river process for modelling these determinants. The non-conservative behaviour identified is related to biological controls and the resultant diurnal variations in pH which promote daytime removal of Ca from solution by precipitation of calcium carbonate (and corresponding removal of Mg by co-precipitation) during extreme low-flow conditions and algal blooms during the summer.

Eutrophication↗

Patterns in trace element chemistry in the freshwater tidal reaches of the River Trent

The major, minor and trace element chemistries at two freshwater tidal sites on the River Trent are described and compared with the non-tidal river, to demonstrate the variability in chemical processes in a major chemically and hydrologically active part of the river system, which is often overlooked in freshwater hydrochemical studies. The study shows a chemical gradient along which concentrations increase downstream for suspended sediments and acid-available particulate (AAP; > 0.45 microm) trace element fractions and also the 'dissolved' (< 0.45 microm) fractions of those trace elements with low-solubility phases. The study highlights the importance of tidally induced suspended-sediment dynamics and the generation of microparticulates for trace element transport within the tidal reaches. The microparticulate and particulate fractions are associated with both anthropogenic and lithogenous sources, and the concentrations of these two fractions co-vary according to a two-component mixing model involving riverine and tidal endmembers, with the tidal endmember exhibiting a strong lithogenous component. In many cases the AAP trace element concentrations are highly linearly correlated. At the downstream tidal site, suspended sediment concentrations were particularly high and ranged from 44 to over 24,000 mg/l as a result of tidally induced sediment mobilisation. As a consequence of this, particulate metal concentrations are especially high, and here, for the first time within the east coast studies of UK rivers, particulate fractions were measurable for trace elements such as boron and molybdenum, previously reported above detection limits only in dissolved form. It is demonstrated that the microparticulate components are not simply related to suspended sediment concentrations or to the bulk composition of the AAP fraction. Rather, microparticulate generation is related to a more complex pattern, probably linked to hydrodynamic factors involving sediment resuspension and microparticulate transport mechanisms.

Journal Article↗

The water quality of the Great Ouse

The results of a 1-year detailed water quality study of the Great Ouse are presented. Being recharged to an important degree from groundwater sources within the carbonate bearing bedrock, the waters are enriched in base cations and they are of relatively high alkalinity (approx. 4000 microEq./l) and pH (approximately 8). Many chemical constituents such as sodium, chloride, boron, nitrate and soluble reactive phosphorus vary over time in response to changing flow conditions. For most determinands, concentrations decrease with increasing flow in response to dilution of point and groundwater sources by rainfall. However, for barium and nitrate, concentrations increase with flow and this is indicative of increased runoff from the agriculturally impacted soils. While this feature is certainly expected for nitrate due to fertiliser application, the pattern for barium is at face value unexpected as it would normally be expected to behave like other divalent base cations such as calcium, coming from aquifer leaching. However, it seems that agricultural disturbance of the land can also lead to enhanced runoff: a feature now becoming apparent in several UK studies. The concentrations of micro-organic herbicides vary over time in response to the different times of application and only isoproturon shows a clear response to varying flow conditions. With regards to biological processes, this is manifest by changes in pH, dissolved carbon dioxide and silica. At most times of the year the waters are oversaturated with respect to atmospheric CO2 (EpCO2) by a factor of approximately 6 and at these times pH is approximately 7.7 and silica concentrations are approximately 4 mg-Si/l. However, in the early spring period pH increases to values over 8, EpCO2 declines to about the atmospheric levels and silica declines to approximately 1 mg-Si/l. This change probably reflects the dynamic diatom blooms and decays common in this river.

Journal Article↗

The water quality of the River Trent: from the lower non-tidal reaches to the freshwater tidal zone

The water quality of a major river system, the River Trent, which flows into the Humber estuary and drains large centres of population and industry in central England, is examined in terms of trace element, nutrient, major-ion, suspended sediment and carbon concentrations and set within the context of the transition from non-tidal to the tidal freshwater reaches. Detailed investigation of the water quality variability in the non-tidal river Trent has revealed mainly simple patterns in dissolved chemical concentrations, controlled largely by hydrology and the mixing of baseflow and stormflow endmember chemistries. However, silicon, carbon and nitrate show much more complex behaviour, as concentrations of these chemical determinands are regulated by in-stream biological processes. Major increases in concentrations of suspended solids and acid-available particulate (AAP) trace elements are shown to be linked to tidal mobilization of sediment and the location of the 'turbidity maximum'. Reductions in the concentrations of AAP trace elements per gram of suspended sediment suggest the mobilization of a different sediment type with a lower trace element content, which may result from: (i) a secondary sediment source; or (ii) mobilization of coarser-grained sediment under the stronger tidal hydrodynamic forces. Increased correlations for AAP-trace element interrelationships downstream suggest increasing simplicity of mixing relationships.

Journal Article↗

A bibliography for the conclusions to the special issue of Science of the Total Environment concerning 'The water quality of UK rivers entering the North Sea'. Sci. Tot. Environ., this volume.

In this document, a bibliography for the conclusions to the special issue of Science of the Total Environment concerning 'The water quality of UK rivers entering the North Sea'. Sci. Tot. Environ., this volume, is presented. It comprises a list of the papers presented in five special issues in learned journals, three in Science of the Total Environment (this volume and volumes 194/195, 1997 and 210/211, 1998) as well as Hydrological Processes (1999, vol 13: Special Issue, River Basin Sediment Dynamics, eds. Anderson, M.G., Peters, N.E. and Walling, D.E.) and Marine Pollution Bulletin [1999, vol 37(3-7) Special Issue: Flux of Materials between Rivers and Coastal Waters, eds. Stebbing, A.R.D., Huntley, D. and Leeks, G.J.L.]. The bibliography comprises six main sections with subsections for specific water quality issues. These are as follows: Section 1 deals with the introduction to LOIS and contained in this section is background material over the nature of the programme, the study area, remit, water quality issues and international context. Section 2 provides the main meat to the bibliography and it splits into Section 2.1 historical and Section 2.2 current water quality issues. Within Section 2.2 there are subsections dealing with specific current aspects of water quality (Section 2.2.1, major ions; Section 2.2.2, pH, dissolved carbon dioxide and dissolved oxygen; Section 2.2.3 nutrients; Section 2.2.4, trace elements; Section 2.2.5 micro-organics; Section 2.2.6 sediments; Section 2.2.7 biology). Section 3 deals with hydrology and climate variability, Section 4, modelling, Section 5 load estimation and Section 6 conclusions. A full listing of the LOIS programme is available from the LOIS programme office, CCMS, Plymouth Laboratory, Prospect Place, West Hoe, Plymouth, PL1 3DH, UK (e-mail lois@ccms.ac.uk).

Carbon↗

Frequency of BRCA1/BRCA2 mutations in a population-based sample of young breast carcinoma cases.

BACKGROUND: There is a clear and growing need for data regarding BRCA1 and BRCA2 mutation frequencies among breast carcinoma cases not specifically ascertained on the basis of extreme family history profiles. Toward this end, the authors previously reported results with regard to BRCA1 in breast carcinoma patients drawn from a population-based study. In the current study the authors present new findings concerning BRCA2 mutation frequency in this same population, as well as summary data regarding the combined contribution of these two genes. METHODS: Subjects were drawn from two population-based, case-control studies of breast carcinoma in young women conducted in western Washington State and focused on 1) women diagnosed with breast carcinoma before age 35 years (n = 203); and 2) women with a first-degree family history of breast carcinoma who were diagnosed before age 45 years (n = 225). Similarities and differences between BRCA2 carriers and BRCA1 carriers were analyzed in terms of age at diagnosis, family history status, and disease features. RESULTS: Of cases diagnosed before age 35 years, all of whom were unselected for family history, 9.4% carried germline mutations (3.4% for BRCA2 and 5.9% for BRCA1). Of cases diagnosed before age 45 years who had a first-degree family history of breast carcinoma, 12.0% carried germline mutations (4.9% for BRCA2 and 7.1% for BRCA1). Increased frequencies of mutations were observed in cases with a personal or family history of early age at diagnosis and in those with four or more family members affected with breast carcinoma. BRCA2 mutations were less common than BRCA1 mutations in families with any history of ovarian carcinoma. CONCLUSIONS: Overall, given current constraints on health care resources, these data suggest that screening for germline mutations in these breast carcinoma susceptibility genes may have the greatest impact on overall health care if it is prioritized toward high and moderate risk populations.

Adult↗