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The Boller Review, 2018 Introduction Evolution of Groundwater Quality and Source Tracking of Nitrate Contamination in the Seymour Aquifer of Texas Caitlin Payblas - Environmental Science, School of Geology, Energy and the Environment Faculty Advisors: Dr. Omar Harvey and Tamie Morgan, SGEE The graph on the right shows extrapolated averaged Cl - and NO 3 -N at sampled locations Confirms covariation between Cl - and NO 3 -N in the aquifer. Nitrate nitrogen (NO 3 -N) contamination of groundwater in the Seymour Aquifer has been documented since pre-1960. Concentrations as high as 35 mg/L NO 3 -N have been reported (3.5 times the EPA allowable standard for drinking water). While most water from the Seymour Aquifer is used for agricultural irrigation, a portion is still used for domestic purposes and poses potential risk to human health. The specific source of NO 3 -N contamination is still debated My research combined chemical and geospatial analysis with specific objectives: 1) Assessing the evolution of groundwater in the Seymour Aquifer since pre-1960 and after Groundwater quality data from the Texas Water Development Board was used in conjunction with geospatial and chemical analysis to identify changes in the groundwater quality over time. Empirical Bayesian kriging (EBK) analysis was used to interpolate chloride (Cl - ) and NO 3 -N across the study area pre-1960 (pre-heavy fertilizer use) and thereafter. 2) Determining the most likely source(s) of NO 3 -N in sampled wells. 14 groundwater samples were collected in Spring 2017 (3/18/17) and Fall 2017 (9/14/17) from selected domestic and irrigation wells δ 15 N and δ 18 O stable isotopic signatures of the samples were evaluated as a means of isolating NO 3 -N source as fertilizer/rain, soil or septic/manure in origin. Based on isotopic signatures, two possible scenarios exists for NO 3 -N in sampled wells: NO 3 -N existed as soil N and then transformed via partial denitrification into septic nitrogen or There are two separate sources, septic and Soil N decline of septic NO 3 -N may have resulted from the 1972 Clean Water Act? Fertilizer use didn’t drop while NO 3 -N did in decades post-1975possibly due to better agricultural management? Three possible sources of NO 3 -N contamination were considered in this study geology of the aquifer (natural salt accumulation from water confined in patches of Quaternary-age alluvium) contribution of nitrate from sewage and agricultural fertilizers (cotton, wheat, peanuts) historical land use change of the area above the aquifer (leguminous nitrogen-fixing mesquite cleared in the 1930’s for agriculture) mg/L <300 300 – 600 600 – 900 900 – 1,200 >1,200 mg/L <10 10 – 20 20 – 30 30 – 40 >40 Cl - and NO 3 -N Evolution 0 5 10 15 20 25 30 0 50 100 150 200 250 300 350 400 450 500 pre-1960 1966 1976 1986 2017 NO 3 -N (mg/L) Cl - (mg/L) Year Sampled Well Sites Predicted Data Chloride (Cl-) Nitrate (NO3-N) Map on left shows the locations for the 14 wells sampled in 2017 - overlaid onto 1986-1997 groundwater composition map. NO3-N = 10 mg/L Cl - and NO 3 -N behavior is concomitant and changes are likely being driven by the same phenomenon. NO 3 -N is potentially coming from soil-N with partial denitrification and or a septic/manure source. Further research will include increasing sample size (from n=14 to n = 30) to provide a better view of present aquifer contamination and conducting more detailed isotopic analysis methods to differentiate between origins of NO 3 -N as soil N and sewage N “Groundwater Database (GWDB) Reports.” Groundwater Data | Texas Water Development Board, Texas Water Development Board, www.twdb.texas.gov/groundwater/data/gwdbrpt.asp . “Texas Natural Resources Information System.” TNRIS - Texas Natural Resources Information System, tnris.org/. Acknowledgements: Dale Carrol and well owners. UC Davis Stable Isotope Facility; Stephen F. Austin Soil, Plant, and Water Analysis Lab Chloride, Cl - Nitrate, NO 3 -N References and Acknowledgements Conclusions and Further Research Research Findings (continued) Research Findings Research Approach Isotopic Analysis of Sampled Wells Stiff diagrams represent average groundwater composition across the aquifer Averaged groundwater composition was graphed over the past six decades to determine which component (if any) drove overall chemical change From stiff diagrams, chloride was the main component driving overall changes in groundwater Partial Nitrification Ammonia Volatilization Domestic Wells Irrigation Wells Groundwater Cl - and NO 3 -N changed more in the northern and southern portions of the aquifer. Widespread NO 3 -N contamination pre-1960 to 1997 with trends suggesting co-variation in Cl - and NO 3 -N

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Page 1: Evolution of Groundwater Quality and Source Tracking of

The Boller Review, 2018

Introduction

Evolution of Groundwater Quality and Source Tracking of Nitrate Contamination in the Seymour Aquifer of Texas

Caitlin Payblas - Environmental Science, School of Geology, Energy and the Environment Faculty Advisors: Dr. Omar Harvey and Tamie Morgan, SGEE

The graph on the right shows extrapolated averaged Cl- and NO3-N at sampled locations

Confirms covariationbetween Cl- and NO3-N in the aquifer.

Nitrate nitrogen (NO3-N) contamination of groundwater in the Seymour Aquifer has been documented since pre-1960.

Concentrations as high as 35 mg/L NO3-N have been reported (3.5 times the EPA allowable standard for drinking water).

While most water from the Seymour Aquifer is used for agricultural irrigation, a portion is still used for domestic purposes and poses potential risk to human health.

The specific source of NO3-N contamination is stilldebated

My research combined chemical and geospatial analysis with specific objectives:

1) Assessing the evolution of groundwater in the Seymour Aquifer since pre-1960 and after Groundwater quality data from the Texas Water

Development Board was used in conjunction with geospatial and chemical analysis to identify changes in the groundwater quality over time.

Empirical Bayesian kriging (EBK) analysis was used to interpolate chloride (Cl-) and NO3-N across the study area pre-1960 (pre-heavy fertilizer use) and thereafter.

2) Determining the most likely source(s) of NO3-N in sampled wells. 14 groundwater samples were collected in

Spring 2017 (3/18/17) and Fall 2017 (9/14/17) from selected domestic and irrigation wells

δ15N and δ18O stable isotopic signatures of thesamples were evaluated as a means of isolating NO3-N source as fertilizer/rain, soil or septic/manure in origin.

Based on isotopic signatures, two possible scenarios exists for NO3-N in sampled wells:

NO3-N existed as soil N and then transformed via partial denitrification into septic nitrogen or

There are two separate sources, septic and Soil N decline of septic NO3-N may have resulted from the 1972 Clean

Water Act? Fertilizer use didn’t drop while NO3-N did in decades post-1975—

possibly due to better agricultural management?

Three possible sources of NO3-N contamination were considered in this study

geology of the aquifer (natural salt accumulation from water confined in patches of Quaternary-age alluvium)

contribution of nitrate from sewage and agricultural fertilizers (cotton, wheat, peanuts)

historical land use change of the area above the aquifer (leguminous nitrogen-fixing mesquite cleared in the 1930’s for agriculture)

Cl-mg/L

<300

300 – 600

600 – 900

900 – 1,200

>1,200

NO3-Nmg/L

<10

10 – 20

20 – 30

30 – 40

>40

Cl- and NO3-N Evolution

0

5

10

15

20

25

30

0

50

100

150

200

250

300

350

400

450

500

pre-1960 1966 1976 1986 2017

NO3-N

(mg/

L)

Cl- (

mg/

L)

Year

Sampled Well Sites Predicted Data

Chloride (Cl-) Nitrate (NO3-N)

Map on left shows the locations for the 14 wells sampled in 2017 -overlaid onto 1986-1997 groundwater composition map.

NO3-N = 10 mg/L

Cl- and NO3-N behavior is concomitant and changes are likely being driven by the same phenomenon.

NO3-N is potentially coming from soil-N with partial denitrification and or a septic/manure source.

Further research will include increasing sample size (from n=14 to n = 30) to provide a better view of present aquifer contamination and conducting more detailed isotopic analysis methods to differentiate between origins of NO3-N as soil N and sewage N

“Groundwater Database (GWDB) Reports.” Groundwater Data | Texas Water Development Board, Texas Water Development Board, www.twdb.texas.gov/groundwater/data/gwdbrpt.asp.“Texas Natural Resources Information System.” TNRIS - Texas Natural Resources Information System, tnris.org/. Acknowledgements: Dale Carrol and well owners. UC Davis Stable Isotope Facility; Stephen F. Austin Soil, Plant, and Water Analysis Lab

Chloride, Cl- Nitrate, NO3-N

References and Acknowledgements

Conclusions and Further Research

Research Findings (continued)Research Findings

Research Approach

Isotopic Analysis of Sampled Wells

Stiff diagrams represent average groundwater composition across the aquifer

Averaged groundwater composition was graphed over the past six decades to determine which component (if any) drove overall chemical change

From stiff diagrams, chloride was the main component driving overall changes in groundwater

Partial Nitrification

Ammonia Volatilization

Domestic Wells Irrigation Wells

Groundwater Cl- and NO3-Nchanged more in the northern and southern portions of the aquifer.

Widespread NO3-N contamination pre-1960 to 1997 with trends suggesting co-variation in Cl- and NO3-N