Coupled steroid and phosphorus leaching from cattle slurry at lysimeter scale

Water quality degradation can be caused by excessive agricultural nutrient transfers from fertilised soils exposed to wet weather. Mitigation measures within the EU Nitrates Directive aim to reduce this pressure by including ‘closed’ fertiliser spreading periods during wet months. For organic fertilisers such as slurry and manure, this closed period requires sufficient on-farm winter storage and good weather conditions to relieve storage at the end of the period. Therefore, robust scientific evidence is needed to support the measure. Incidental nutrient transfers of recently applied organic fertilisers in wet weather can also be complicated by synchronous transfers from residual soil stores and tracing is required for risk assessments. The combination of nutrient monitoring and biomarker analyses may aid this and one such biomarker suite is faecal steroids. Accordingly, this study investigated the persistence of steroids and their association with phosphorus during leaching episodes. The focus was on the coupled behaviour of steroids and total phosphorus (TP) concentrations in sub-surface hydrological pathways. Cattle slurry was applied to monolith lysimeters either side of a closed period and concentrations of both steroids and TP were monitored in the leachate. The study showed no significant effect of the treatment (average p = 0.17), though tracer concentrations did significantly change over time (average p = 0.001). While the steroidal concentration ratio was validated for herbivorous faecal pollution in the leachate, there was a weak positive correlation between the steroids and TP. Further investigation at more natural scales (hillslope/catchment) is required to confirm tracer behaviours/correlations and to compliment this sub-surface pathway study

Linking Hydro-Geophysics and Remote Sensing Technology for Sustainable Water and Agricultural Catchment Management

PosterThe acquisition of sub-surface data for agricultural purposes is traditionally achieved by in situ point sampling in the top 2m over limited target areas (farm scale ~ km2) and time periods. This approach is inadequate for integrated regional (water catchment ~ 100 km2) scale management strategies which require an understanding of processes varying over decadal time scales in the transition zone (~ 10’s m) from surface to bedrock. With global food demand expected to increase by 100% by 2050, there are worldwide concerns that achievement of production targets will be at the expense of water quality. In order to overcome the limitations of the traditional approach, this research programme will combine airborne and ground geophysics with remote sensing technologies to access hydrogeological and soil structure information on Irish Soils at multiple spatial scales. It will address this problem in the context of providing tools for the sustainable management of agricultural intensification envisioned in Food Harvest 2020 and Food Wise 2025 and considering the EU Habitats and Water Framework Directives (WFD), Clean Air Policy and Soil Thematic Strategies. The work will use existing ground based geophysical and hydrogeological data from Teagasc Agricultural Catchment Programme (ACP) and Heavy Soil sites co-located ground and airborne electromagnetic data. Neural Networks training and Machine learning approaches will supplement traditional geophysical workflows. Work will then focus on upscaling results from ACP to WFD catchment scale. This upscaling will require modification of traditional satellite remote sensing conceptual frameworks to analyse heterogeneous, multi-temporal data streams

Comparing Extraction Methods for Biomarker Steroid Characterisation from Soil and Slurry

Clean water is a precious resource, and policies/programmes are implemented worldwide to protect and/or improve water quality. Faecal pollution can be a key contributor to water quality decline causing eutrophication through nutrient enrichment and pathogenic contamination. The robust sourcing of faecal pollutants is important to be able to target the appropriate sector and to engage managers. Biomarker technology has the potential for source confirmation, by using, for example the biomarker suite of steroids. Steroids have been used in the differentiation of human and animal faeces; however, there is no unequivocal extraction technique. Some of the methods used include (i) Soxhlet extraction, (ii) Bligh and Dyer (BD) extraction, and (iii) accelerated solvent extraction (ASE). The less costly and time intensive technique of ASE is particularly attractive, but a current research gap concerns further comparisons regarding ASE lipid extraction from soils/slurries compared with the more traditional Soxhlet and BD extractions. Accordingly, a randomised complete block experiment was implemented to assess differences between the three extraction methods, differences between the different sample types, and the interactions between these two factors. Following GC-MS, it was found that there was no significant difference between the results of the steroid extraction methods, regardless of the type of sample used, for the quantity of each steroid extracted. It was concluded that ASE could be used confidently instead of the more established steroid extraction methods, thereby delivering time and cost savings

Using a multi-dimensional approach for catchment scale herbicide pollution assessments

peer-reviewedWorldwide herbicide use in agriculture, whilst safeguarding yields also presents water quality issues. Controlling factors in agricultural catchments include both static and dynamic parameters. The present study investigated the occurrence of herbicides in streams and groundwater in two meso-scale catchments with contrasting flow controls and agricultural landuse (grassland and arable land). Using a multi-dimensional approach, streams were monitored from November 2018 to November 2019 using Chemcatcher® passive sampling devices and groundwater was sampled in 95 private drinking water wells. The concentrations of herbicides were larger in the stream of the Grassland catchment (8.9–472.6 ng L−1) dominated by poorly drained soils than in the Arable catchment (0.9–169.1 ng L−1) dominated by well-drained soils. Incidental losses of herbicides during time of application and low flows in summer caused concentrations of MCPA, Fluroxypyr, Trichlorpyr, Clopyralid and Mecoprop to exceeded the European Union (EU) drinking water standard due to a lack of dilution. Herbicides were present in the stream throughout the year and the total mass load was higher in winter flows, suggesting a persistence of primary chemical residues in soil and sub-surface environments and restricted degradation. Losses of herbicides to the streams were source limited and influenced by hydrological conditions. Herbicides were detected in 38% of surveyed drinking water wells. While most areas had concentrations below the EU drinking water standard some areas with well-drained soils in the Grassland catchment, had concentrations exceeding recommendations. Individual wells had concentrations of Clopyralid (619 ng L−1) and Trichlorpyr (650 ng L−1). Despite the study areas not usually associated with herbicide pollution, and annual mass loads being comparatively low, many herbicides were present in both surface and groundwater, sometimes above the recommendations for drinking water. This whole catchment assessment provides a basis to develop collaborative measures to mitigate pollution of water by herbicides.Horizon 2020 Framework Programm

Groundwater nitrate reduction versus dissolved gas production: A tale of two catchments

peer-reviewedAt the catchment scale, a complex mosaic of environmental, hydrogeological and physicochemical characteristics combine to regulate the distribution of groundwater and stream nitrate (NO3−). The efficiency of NO3− removal (via denitrification) versus the ratio of accumulated reaction products, dinitrogen (excess N2) & nitrous oxide (N2O), remains poorly understood. Groundwater was investigated in two well drained agricultural catchments (10 km2) in Ireland with contrasting subsurface lithologies (sandstone vs. slate) and landuse. Denitrification capacity was assessed by measuring concentration and distribution patterns of nitrogen (N) species, aquifer hydrogeochemistry, stable isotope signatures and aquifer hydraulic properties. A hierarchy of scale whereby physical factors including agronomy, water table elevation and permeability determined the hydrogeochemical signature of the aquifers was observed. This hydrogeochemical signature acted as the dominant control on denitrification reaction progress. High permeability, aerobic conditions and a lack of bacterial energy sources in the slate catchment resulted in low denitrification reaction progress (0–32%), high NO3− and comparatively low N2O emission factors (EF5g1). In the sandstone catchment denitrification progress ranged from 4 to 94% and was highly dependent on permeability, water table elevation, dissolved oxygen concentration solid phase bacterial energy sources. Denitrification of NO3 − to N2 occurred in anaerobic conditions, while at intermediate dissolved oxygen; N2O was the dominant reaction product. EF5g1 (mean: 0.0018) in the denitrifying sandstone catchment was 32% less than the IPCC default. The denitrification observations across catchments were supported by stable isotope signatures. Stream NO3− occurrence was 32% lower in the sandstone catchment even though N loading was substantially higher than the slate catchment.Teagasc Walsh Fellowship Programm