Other Organic Wastewater Contaminants
in U.S. Streams, 1999-2000:
A National Reconnaissance
Environ. Sci. Technol.,36 (6),1202-1211, Mar02
Dana W. Kolpin* U.S. Geological Survey, 400 S. Clinton Street, Box 1230, Iowa City, Iowa 52244
Edward T. Furlong U.S. Geological Survey, Box 25046, MS 407, Denver, Colorado 80225-0046
Michael T. Meyer U.S. Geological Survey, 4500 SW 40th Avenue, Ocala, Florida 34474
E. Michael Thurman U.S. Geological Survey, 4821 Quail Crest Place, Lawrence, Kansas 66049
Steven D. Zaugg U.S. Geological Survey, Box 25046, MS 407, Denver, Colorado 80225-0046
Larry B. Barber U.S. Geological Survey, 3215 Marine Street, Boulder, Colorado 80303
Herbert T. Buxton U.S. Geological Survey, 810 Bear Tavern Road, West Trenton, New Jersey 08628
Received for review June 12, 2001
Revised manuscript received November 26, 2001
Accepted December 12, 2001
To provide the first nationwide reconnaissance of the occurrence of pharmaceuticals, hormones, and other organic wastewater contaminants (OWCs) in water resources, the U.S. Geological Survey used five newly developed analytical methods to measure concentrations of 95 OWCs in water samples from a network of 139 streams across 30 states during 1999 and 2000. The selection of sampling sites was biased toward streams susceptible to contamination (i.e. downstream of intense urbanization and livestock production). OWCs were prevalent during this study, being found in 80% of the streams sampled. The compounds detected represent a wide range of residential, industrial, and agricultural origins and uses with 82 of the 95 OWCs being found during this study. The most frequently detected compounds were coprostanol (fecal steroid), cholesterol (plant and animal steroid), N,N-diethyltoluamide (insect repellant), caffeine (stimulant), triclosan (antimicrobial disinfectant), tri(2-chloroethyl)phosphate (fire retardant), and 4-nonylphenol (nonionic detergent metabolite). Measured concentrations for this study were generally low and rarely exceeded drinking-water guidelines, drinking-water health advisories, or aquatic-life criteria. Many compounds, however, do not have such guidelines established. The detection of multiple OWCs was common for this study, with a median of seven and as many as 38 OWCs being found in a given water sample. Little is known about the potential interactive effects (such as synergistic or antagonistic toxicity) that may occur from complex mixtures of OWCs in the environment. In addition, results of this study demonstrate the importance of obtaining data on metabolites to fully understand not only the fate and transport of OWCs in the hydrologic system but also their ultimate overall effect on human health and the environment.
The continued exponential growth in human population has created a corresponding increase in the demand for the Earth's limited supply of freshwater. Thus, protecting the integrity of our water resources is one of the most essential environmental issues of the 21st century. Recent decades have brought increasing concerns for potential adverse human and ecological health effects resulting from the production, use, and disposal of numerous chemicals that offer improvements in industry, agriculture, medical treatment, and even common household conveniences (1). Research has shown that many such compounds can enter the environment, disperse, and persist to a greater extent than first anticipated. Some compounds, such as pesticides, are intentionally released in measured applications. Others, such as industrial byproducts, are released through regulated and unregulated industrial discharges to water and air resources. Household chemicals, pharmaceuticals, and other consumables as well as biogenic hormones are released directly to the environment after passing through wastewater treatment processes (via wastewater treatment plants, or domestic septic systems), which often are not designed to remove them from the effluent (2). Veterinary pharmaceuticals used in animal feeding operations may be released to the environment with animal wastes through overflow or leakage from storage structures or land application (3). As a result, there are a wide variety of transport pathways for many different chemicals to enter and persist in environmental waters.
Surprisingly, little is known about the extent of environmental occurrence, transport, and ultimate fate of many synthetic organic chemicals after their intended use, particularly hormonally active chemicals (4), personal care products, and pharmaceuticals that are designed to stimulate a physiological response in humans, plants, and animals (1, 5). One reason for this general lack of data is that, until recently, there have been few analytical methods capable of detecting these compounds at low concentrations which might be expected in the environment (6). Potential concerns from the environmental presence of these compounds include abnormal physiological processes and reproductive impairment (7-12), increased incidences of cancer (13), the development of antibiotic-resistant bacteria (14-17), and the potential increased toxicity of chemical mixtures (18). For many substances, the potential effects on humans and aquatic ecosystems are not clearly understood (1, 2, 19)
The primary objective of this study is to provide the first nationwide reconnaissance of the occurrence of a broad suite of 95 organic wastewater contaminants (OWCs), including many compounds of emerging environmental concern, in streams across the United States. These OWCs are potentially associated with human, industrial, and agricultural wastewaters and include antibiotics, other prescription drugs, nonprescription drugs, steroids, reproductive hormones, personal care products, products of oil use and combustion, and other extensively used chemicals. The target OWCs were selected because they are expected to enter the environment through common wastewater pathways, are used in significant quantities, may have human or environmental health implications, are representative or potential indicators of certain classes of compounds or sources, and/or can be accurately measured in environmental samples using avail able technologies. Although these 95 OWCs are just a small subset of compounds being used by society, they represent a starting point for this investigation examining the transport of OWCs to water resources of the United States.
This paper describes the analytical results available from 139 streams sampled during 1999-2000 (Figure 1). The results are intended to determine if OWCs are entering U.S. streams and to estimate the extent of their co-occurrence in susceptible waters. In addition, this study provides a focal point for the development and testing of new laboratory methods for measuring OWCs in environmental samples at trace levels, an interpretive context for future assessments of OWCs, and a means for establishing research priorities and future monitoring strategies. More complete interpretations, including an evaluation of the role of potential sources of contamination, will follow in subsequent papers.
|Figure 1 Location of 139 stream sampling sites.|
Site Selection and Sampling
Little data were available on the occurrence of most of the targeted OWCs in U.S. streams at the onset of this investigation. Therefore, the selection of sampling sites primarily focused on areas considered susceptible to contamination from human, industrial, and agricultural wastewater. The 139 stream sites sampled during 1999-2000 (Figure 1) represent a wide range of geography, hydrogeology, land use, climate, and basin size. Specific information on the individual sampling sites is provided elsewhere (20).
All samples were collected by U.S. Geological Survey personnel using consistent protocols and procedures designed to obtain a sample representative of the streamwaters using standard depth and width integrating techniques (21). At each site, a composite water sample was collected from about 4-6 vertical profiles which was split into appropriate containers for shipment to the participating laboratories. For those bottles requiring filtration, water was passed through a 0.7 µm, baked, glass-fiber filter in the field where possible, or else filtration was conducted in the laboratory. Water samples for each chemical analysis were stored in precleaned-amber, glass bottles and collected in duplicate. The duplicate samples were used for backup purposes (in case of breakage of the primary sample) and for laboratory replicates. Following collection, samples were immediately chilled and sent to the laboratory. To minimize contamination of samples, use of personal care items (i.e. insect repellents, colognes, perfumes), caffeinated products, and tobacco were discouraged during sample collection and processing.
Each stream site was sampled once during the 1999-2000 study period. Samples collected in 1999 were analyzed for a subset of the OWCs based on the watershed land-use characteristics. Samples collected in 2000 were analyzed for the complete suite of OWCs. The analytical results for each stream sample are available elsewhere (20).
To determine the environmental extent of 95 OWCs (Table 1) in susceptible streams, five separate analytical methods were used. Each method was developed independently in different laboratories, with somewhat different data objectives, such as identifying hormones versus identifying antibiotics. As a result of these differing objectives, varying approaches were used in the development of the five analytical methods. For example, select methods (Methods 1-3 below) used filtered water for solid-phase extraction (SPE) with liquid chromatography/mass spectrometry positive-ion electrospray (LC/MS-ESI(+)) analysis, while others (Methods 4 and 5 below) used whole-water continuous liquid-liquid extraction (CLLE) with capillary gas chromatography/mass spectrometry (GC/MS) analysis.
All methods use selected ion monitoring (SIM) for improved sensitivity, thus, only the target compounds were reported with no attempt to report data for nontarget compounds. Target compounds within each method were selected from the large number of chemical possibilities based upon usage, toxicity, potential hormonal activity, and persistence in the environment. Some compounds that fit the above criteria, however, could not be included (such as amoxicillin, roxarsone, polybrominated diphenyl ethers) because they were either incompatible with the corresponding method or reference standards were not available. Positive identification of a compound required elution within the expected retention time window. In addition, the sample spectra and ion abundance ratios were required to match that of the reference standard compounds. The base-peak ion was used for quantitation, and, if possible, two qualifier ions were used for confirmation. After qualitative criteria were met, compound concentrations were calculated from 5 to 8 point calibration curves (generally from 0.01 to 10.0 µg/L) using internal standard quantitation. Methods 1 and 2 process calibration standards through the extraction procedure, which generally corrects concentrations for method losses but not matrix effects. Methods 3-5 do not extract calibration standards, thus the reported concentrations are not corrected for method losses. Reporting levels (RLs) were determined for each method by either an evaluation of instrument response, calculation of limit of detection, or from a previously published procedure. RLs were adjusted based on experience with the compounds in each method, known interferences, or known recovery problems.
The following descriptions are intended to provide a brief overview of the five analytical methods used for this study. More comprehensive method descriptions are provided elsewhere (26-28) or will be available in subsequent publications.
Method 1. This method targets 21 antibiotic compounds (Table 1) in 500-mL filtered water samples using modifications from previously described methods (26, 29). The antibiotics were extracted and analyzed by tandem SPE and single quadrapole, LC/MS-ESI(+) using SIM. To prevent the tetracycline antibiotics from complexing with Ca2+ and Mg2+ ions and residual metals on the SPE cartridges, 0.5 mg of disodium ethylenediaminetetraacetate (Na2EDTA; C10H14O8Na2N2-H2O) was added to each water sample. Sample pH was adjusted to 3 using concentrated H2SO4. The tandem SPE included an Oasis Hydrophilic-Lipophilic-Balance (HLB) cartridge (60 mg) followed by a mixed mode, HLB-cation exchange (MCX) cartridge (60 mg) (Waters Inc., Milford, MA). The HLB and MCX cartridges were conditioned with ultrapure H2O, CH3OH, and CH3OH with 5% NH4OH. The HLB cartridge was attached to the top of the MCX cartridge, and the sample was passed through the SPE cartridges using a vacuum extraction manifold. The cartridges were eluted with CH3OH, and the MCX cartridge was eluted separately using CH3OH with 5% NH4OH. The eluate was spiked with 500 ng of 13C6-sulfamethazine (internal standard), vortexed, and evaporated to 20 µL using N2 and a water bath of 55° C. Three hundred µL of 20 mM of NH4C2H3OO (pH 5.7) was added to sample eluate, vortexed, transferred to a glass chromatography vial, and frozen until analysis. Samples were extracted as a set of 11 environmental samples, one duplicate sample, two fortified ultrapure water spikes (check standards), and two ultrapure water blanks.
Method 2. This method targets eight antibiotic compounds (Table 1) in filtered water samples. Complete details of this method have been described previously (26). The antibiotics were extracted and analyzed using SPE and SIM LC/MS-ESI(+). Samples were prepared for extraction by adding 13C6-sulfamethazine and meclocycline as surrogate standards, Na2EDTA, and H2SO4. Target compounds were extracted using 60-mg HLB cartridges preconditioned with CH3OH, NHCl, and distilled H2O. Target compounds were eluted with CH3OH into a test tube containing the internal standard, simatone. The extracts were then concentrated under N2 to approximately 50 µL, and mobile phase A (10 mM NH4H2O2 in 90/10 water/CH3OH with 0.3% CH2O2) was added. The resulting solutions were transferred to amber autosampler vials to prevent photodegradation of tetracyclines (30). Mobile phase conditions are described in detail elsewhere (26).
For each compound, the proton adduct of the molecular ion (M + H)+ and at least one confirming ion were acquired using LC/MS-ESI(+). All mass spectral conditions are described in detail elsewhere (26). Quantitation was based on the ratio of the base peak ion (M + H)+ of the analyte to the base peak of the internal standard. Standard addition was used for quantitation where each sample was analyzed with and without the addition of a 0.5 µg/L spike to correct for suppression of the electrospray signal.
Method 3. This method targets 21 human prescription and nonprescription drugs and their select metabolites (Table 1) in filtered water samples. Compounds were extracted from1 L water samples using SPE cartridges that contain 0.5 g of HLB (flow rate of 15 mL/min). After extraction, the adsorbed compounds were eluted with CH3OH followed by CH3OH acidified with C2HCl3O2. The two fractions were reduced under N2 to near dryness and then combined and brought to a final volume of 1 mL in 10% C2H3N:90% H2O buffered with NH4H2O2/CH2O2.
Compounds were separated and measured by high-performance liquid chromatography (HPLC) using a polar (neutral silanol) reverse-phase octylsilane (C8) HPLC column (Metasil Basic 3 µm, 150 × 2.0 mm; Metachem Technologies). The compounds were eluted with a binary gradient of mobile phase A (aqueous NH4H2O2/CH2O2 buffer; 10 mM, pH 3.7) and mobile phase B (100% C2H3N).
Method 4. This method (27, 28) targets 46 OWCs (Table 1) in unfiltered water. One-liter whole-water samples were extracted using CLLE with CH2Cl2. Distilled solvent was recycled through a microdroplet dispersing frit to improve extraction efficiency. Samples were extracted for 3 h at ambient pH and for an additional 3 h at pH 2. The extract was concentrated under N2 to 1 mL and analyzed by capillary-column GC/MS. Available standards for the 4-nonylphenol compounds were composed of multiple isomers, and thus, laboratory standards for these compounds as well as octylphenol ethoxylates were prepared from technical mixtures.
Method 5. This method (28) targets 14 steroid compounds including several biogenic and synthetic reproductive hormones (Table 1). The CLLE extracts from the previously analyzed samples of Method 4 were derivatized and reanalyzed. Analysis of steroid and hormone compounds by GC/MS is enhanced by derivatization to deactivate the hydroxyl and keto functional groups. The technique used in this study is the formation of trimethylsilyl (TMS) ethers of the hydroxyl groups and oximes of the keto groups. Samples were stored in a silanizing reagent to prevent hydrolysis of the derivatives back to the free compound. Surrogate standards (d4estradiol and d7cholesterol) were added to the samples prior to derivatization to evaluate method performance. After derivatization, the samples were analyzed by GC/MS.
Quality Assurance Protocol. At least one fortified laboratory spike and one laboratory blank was analyzed with each set of 10-16 environmental samples. Most methods had surrogate compounds added to samples prior to extraction to monitor method performance. A summary of recoveries for target compounds and surrogate compounds in environmental samples (Table 2) indicates the general proficiency of the methods. The RL (Table 1) is equivalent to the lowest concentration standard that could be reliably quantitated. The compound concentrations reported below the RL or the lowest calibration standard were estimated as indicated in Figure 2. The concentration of compounds with <60% recovery, routinely detected in laboratory blanks, or prepared with technical grade mixtures, was also considered estimated (Table 1).
|Figure 2 Measured concentrations for the 30 most frequently detected organic wastewater contaminants. Boxplots show concentration distribution truncated at the reporting level. Estimated values below the reporting level are shown. Estimated maximum values for coprostanol and cholesterol obtained from Method 5 (Table 1) are not shown. The analytical method number is provided (in parentheses) at the end of each compound name. An explanation of a boxplot is provided in Figure 3.|
The laboratory blanks were used to assess potential sample contamination. Blank contamination was not subtracted from environmental results. However, environmental concentrations within twice the values observed in the set blank were reported as less than the RL.
A field quality assurance protocol was used to determine the effect, if any, of field equipment and procedures on the concentrations of OWCs in water samples. Field blanks, made from laboratory-grade organic free water, were submitted for about 5% of the sites and analyzed for all of the 95 OWCs. Field blanks were subject to the same sample processing, handling, and equipment as the stream samples. To date, one field blank had a detection of coprostanol and testosterone, one field blank had a detection of naphthalene and tri(dichlorisopropyl)phosphate, and one field blank had a detection of naphthalene, 4-nonylphenol, phenol, 4-tert-octylphenol monoethoxylate, and ethanol,2-butoxy-phosphate. Most of these detections were near their respective RLs verifying the general effectiveness of the sampling protocols used for this study. In addition all field blanks had low level concentrations of cholesterol being measured using Method 5 (median concentration = 0.09 µg/L) documenting its ubiquitous nature in the environment. Cholesterol concentrations from 0.005 to 0.18 µg/L obtained through Method 5 were set to less than the RL.
Compounds that were measured by more than one analytical method (Table 1; Figure 3) also were used to evaluate the results for this study. The presence or absence of these compounds were confirmed in 100% of the determinations for sulfamerazine, and sulfathiazole; 98.8% for oxytetracycline, sulfadimethoxine, sulfamethazine, and tetracycline; 98.6% for cholesterol and coprostanol; 97.6% for chlortetracyline; 95.7% for 17ß-estradiol; 94.4% for cotinine; 94.0% for trimethoprim; 89.1% for sulfamethoxazole; 86.4% for codeine; and 83.3% for caffeine. The comparisons for codeine, caffeine, and cotinine may have been affected by the differing extractions (SPE versus CLLE) as well as differing types of sample (filtered versus whole water).
|Figure 3 Comparison of concentrations of select compounds that were measured using two different methods with significantly different reporting levels. Boxplots show concentration distribution truncated at the reporting level. Estimated values below the reporting level are shown. Estimated maximum values for chloesterol and coprostanol obtained from Method 5 (Table 1) are not shown. The analytical method number is provided (in parentheses) at the end of each compound name.|
An interlaboratory comparison of Methods 1 and 3 was conducted using two reagent water blanks and 24 reagent water spikes prepared at concentrations ranging from 0.5 to 1.1 µg/L for two frequently detected antibiotics (sulfamethoxazole and trimethoprim). The results demonstrated that both methods are accurately confirming the presence of sulfamethoxazole and trimethoprim in water, with the measured concentrations being within a factor of 3 or better of the actual concentrations for these compounds. No false positives or false negatives occurred for this experiment.
Results and Discussion
One or more OWCs were found in 80% of the 139 streams sampled for this study. The high overall frequency of detection for the OWCs is likely influenced by the design of this study, which placed a focus on stream sites that were generally considered susceptible to contamination (i.e. downstream of intense urbanization and livestock production). In addi tion, select OWCs (such as cholesterol) can also be derived from nonanthropogenic sources. Furthermore, some of the OWCs were selected because previous research (28) identified them as prevalent in the environment. Thus, the results of this study should not be considered representative of all streams in the United States. A previous investigation of streams downstream of German municipal sewage treatment plants also found a high occurrence of OWCs (31).
A large number of OWCs (82 out of 95) were detected at least once during this study (Table 1). Only eight antibiotics and five other prescription drugs were not detected in the samples analyzed (Table 1). Measured concentrations were generally low (median detectable concentrations generally <1 µg/L, Table 1), with few compounds exceeding drinking-water guidelines, health advisories, or aquatic-life criteria (Table 1). The concentration of benzo[a]pyrene exceeded its maximum contaminant level (MCL) of 0.2 µg/L at one site and bis(2-ethylhexyl)phthalate concentrations exceeded its MCL of 6.0 µg/L at five sites. In addition, aquatic-life criteria were exceeded for chlorpyrifos (Table 1) at a single site. However, many of the 95 OWCs do not have such guidelines or criteria determined (Table 1). In fact, much is yet to be known about the potential toxicological effects of many of the OWCs under investigation (1). For many OWCs, acute effects to aquatic biota appear limited because of the low concentrations generally occurring in the environment (24, 32-34). More subtle, chronic effects from low-level environmental exposure to select OWCs appear to be of much greater concern (1). Such chronic effects have been documented in the literature (34-38). In addition, because antibiotics are specifically designed to reduce bacterial populations in animals, even low-level concentrations in the environment could increase the rate at which pathogenic bacteria develop resistance to these compounds (15-17, 39).
The 30 most frequently detected compounds represent a wide variety of uses and origins including residential, industrial, and agricultural sources (Figure 2, Table 1). Only about 5% of the concentrations for these compounds exceeded 1 µg/L. Over 60% of these higher concentrations were derived from cholesterol and three detergent metabolites (4-nonyphenol, 4-nonylphenol monoethoxylate, and 4-nonylphenol diethoxylate). The frequent detection of cotinine, 1,7-dimethylxanthine, erythromycin-H2O, and other OWC metabolites demonstrate the importance of obtaining data on degradates to fully understand the fate and transport of OWCs in the hydrologic system. In addition, their presence suggests that to accurately determine the overall effect on human and environmental health (such as pathogen resistance and genotoxicity) from OWCs, their degradates should also be considered. The presence of the parent compound and/or their select metabolites in water resources has previously been documented for OWCs (40, 41) as well as other classes of chemicals such as pesticides (42, 43).
Many of the most frequently detected compounds (Figure 2) were measured in unfiltered samples using Method 4. Thus, their frequencies of detection may be somewhat higher because concentrations being measured include both the dissolved and particulate phases, whereas concentrations measured by Methods 1-3 include just the dissolved phase. For example, about 90% of the coprostanol discharged from sewage effluents has been shown to be associated with particulate matter (44). Thus, the concentration and frequency of detection for select compounds would likely have been reduced if sample filtration had taken place.
Variations in RL also influence the frequency of OWC detection (Figure 2). For example, the detection of 4-nonylphenol would likely have been much greater if an order of magnitude lower RL (similar to other OWCs) could have been achieved. The effect of RL on frequencies of detection is more clearly demonstrated by comparison of concentrations of select compounds that were measured using multiple analytical methods (Figure 3). As expected, the frequency of detection for a given compound was higher with the lower RL. The only exception being caffeine, where filtration of Method 3 may have reduced caffeine concentrations compared to that of the unfiltered Method 4. Figures 2 and 3 also demonstrate the importance of estimated values (45) below the RL. Clearly the numerous estimated concentrations illustrate that the current RLs are not low enough to accurately characterize the total range of OWC concentrations in the stream samples and that the frequencies of detection for this study are conservative.
To obtain a broader view of the results for this study, the 95 OWCs were divided into 15 groups based on their general uses and/or origins. The data show two environmental determinations: frequency of detection (Figure 4A) and percent of total measured concentration (Figure 4B) for each group of compounds. These two views show a vastly different representation of the data. In relation to frequency of detection, there were a number of groups that were frequently detected, with seven of the 15 groups being found in over 60% of the stream samples (Figure 4A). However, three groups (detergent metabolites, plasticizers, and steroids) contributed almost 80% of the total measured concentration (Figure 4B).
|Figure 4 Frequency of detection of organic wastewater contaminants by general use category (4A), and percent of total measured concentration of organic wastewater contaminants by general use category (4B). Number of compounds in each category shown above bar.|
For those groups of compounds that have received recent public attention-namely antibiotics, nonprescription drugs, other prescription drugs, and reproductive hormones (1, 2, 10)-nonprescription drugs were found with greatest frequency (Figure 4A). Antibiotics, other prescription drugs, and reproductive hormones were found at relatively similar frequencies of detection. The greater frequency of detection for nonprescription drugs may be at least partially derived from their suspected greater annual use compared to these other groups of compounds. When toxicity is considered, measured concentrations of reproductive hormones may have greater implications for health of aquatic organisms than measured concentrations of nonprescription drugs. Previous research has shown that even low-level exposure (<0.001 µg/L) to select hormones can illicit deleterious effects in aquatic species (7, 46, 47).
Mixtures of various OWCs were prevalent during this study, with most (75%) of the streams sampled having more than one OWC identified. In fact, a median of seven OWCs were detected in these streams, with as many as 38 compounds found in a given streamwater sample (Figure 5). Because only a subset of the 95 OWCs were measured at most sites collected during the first year of study, it is suspected that the median number of OWCs for this study is likely underestimated. Although individual compounds were generally detected at low-levels, total concentrations of the OWCs commonly exceeded 1 µg/L (Figure 5). In addition, 33 of the 95 target OWCs are known or suspected to exhibit at least weak hormonal activity with the potential to disrupt normal endocrine function (4, 7, 8, 10, 12, 22, 36, 37, 48-50), all of which were detected in at least one stream sample during this study (Table 1). The maximum total concentration of hormonally active compounds was 57.3 µg/L. Aquatic species exposed to estrogenic compounds have been shown to alter normal hormonal levels (7, 48, 51). Thus, the results of this study suggest that additional research on the toxicity of the target compounds should include not only the individual OWCs but also mixtures of these compounds. The prevalence of multiple compounds in water resources has been previously documented for other contaminants (52, 53). In addition, research has shown that select chemical combinations can exhibit additive or synergistic toxic effects (54-56), with even compounds of different modes of action having interactive toxicological effects (57).
Relation between total concentration (summation from all detections) and number of organic wastewater contaminants found per water sample (Spearman's rank correlation coefficient = 0.94, P < 0.001).
The results of this study document that detectable quantities of OWCs occur in U.S. streams at the national scale. This implies that many such compounds survive wastewater treatment (1, 6, 58) and biodegradation (59). Future research will be needed to identify those factors (i.e. high use and chemical persistence) that are most important in determining the occurrence and concentration of OWCs in water resources.
Although previous research has also shown that antibiotics (60), other prescription drugs (1, 2, 19, 61-63), and nonprescription drugs (1, 40, 62, 64) can be present in streams, this study is the first to examine their occurrence in a wide variety of hydrogeologic, climatic, and land-use settings across the United States. Much is yet to be learned pertaining to the effects (particularly those chronic in nature) on humans, plants, and animals exposed to low-level concentrations of pharmaceuticals and other OWCs. Furthermore, little is known about the potential interactive effects (synergistic or antagonistic toxicity) that may occur from complex mixtures of these compounds in the environment. Finally, additional research also needs to be focused on those OWCs not frequently detected in this stream sampling. Select OWCs may be hydrophobic and thus may be more likely to be present in stream sediments than in streamwater (65, 66). For example, the low frequency of detection for the tetracycline (chlortetracycline, doxycycline, oxytetracycline, tetracycline) and quinolone (ciprofloxacin, enrofloxacin, norfloxacin, sarafloxacin) antibiotics is not unexpected given their apparent affinity for sorption to sediment (66). In addition, select OWCs may be degrading into new, more persistent compounds that could be transported into the environment instead of (or in addition to) their associated parent compound.
The authors wish to acknowledge the USGS scientists and field technicians who provided essential assistance to this project by identifying candidate stream sites across the United States and in collecting and processing stream samples. In addition, the authors thank Michele Lindsey, Jeff Cahill, and Greg Brown for their important contributions to developing the analytical methods being used. The authors also acknowledge Steffanie Keefe for her efforts in compiling the existing ecotoxicological data, Jessica Hopple for her as sistance in generating select figures for this paper, and Kymm Barnes for her assistance in compiling the water-quality data for this study. This project was supported by the U.S. Geological Survey, Toxic Substances Hydrology Program. The use of trade, firm, or brand names in this paper is for identification purposes only and does not constitute endorsement by the U.S. Geological Survey.
* Corresponding author phone: (319)358-3614; fax: (319)358-3606; e-mail: firstname.lastname@example.org .
1. Daughton, C. G.; Ternes, T. A. Environ. Health Perspect. 1999, 107 (Supplement 6), 907-938.
2. Halling-Sorensen, B.; Nielson, S. N.; Lanzky, P. F.; Ingerslev, F.; Holten Lutzhoft, J.; Jorgensen, S. E. Chemosphere 1998, 35, 357-393.
3. Meyer, M. T.; Bumgarner, J. E.; Varns, J. L.; Daughtridge, J. V.; Thurman, E. M.; Hostetler, K. A. Sci. Total Environ. 2000, 248, 181-187.
4. National Research Council. Hormonally active agents in the environment; National Academy Press: Washington, DC, 1999; 430 pp.
5. Jorgensen, S. E.; Halling-Sorensen, B. Chemosphere 2000, 40, 691-699.
6. Sedlak, D. L.; Gray, J. L.; Pinkston, K. E. Envrion. Sci. Technol. 2000, 34, 509A-515A.
7. Purdom, C. E.; Hardiman, P. A.; Bye, V. J.; Eno, N. C.; Tyler, C. R.; Sumpter, J. P. Chem. Ecol. 1994, 8, 275-285.
8. White, R.; Jobling, S.; Hoare, S. A.; Sumpter, J. P.; Parker, M. G. Endocrinology 1994, 135, 175-182.
9. Sharpe, R. M.; Skakkebaek, N. E. Lancet 1993, 341, 1392-1395.[Medline]
10. Panter, G. H.; Thompson, R. S.; Sumpter, J. P. Environ. Sci. Technol. 2000, 34, 2756-2760.
11. Harrison, P. T. C.; Holmes, P.; Humfrey, C. D. N. Sci. Total Environ. 1997, 205, 97-106.
12. Jobling, S.; Nolan, M.; Tyler, C. R.; Brighty, G.; Sumpter, J. P. Environ. Sci. Technol. 1998, 32, 2498-2506.
13. Davis, D. L.; Bradlow, H. L. Sci. Am. 1995, 273, 166-172.
14. DuPont, H. L.; Steele, J. H. Rev. Infect. Dis. 1987, 9, 447-460.
15. Gilliver, M. A.; Bennett, M.; Begon, M.; Hazel, S. M.; Hart, C. A. Nature 1999, 401, 233-234.
16. Khachatourians, G. G. Can. Med. Assoc. J. 1998, 159, 1129-1136.
17. Smith, K. E.; Besser, J. M.; Hedberg, C. W.; Leano, F. T.; Bender, J. B.; Wicklund, J. H.; Johnson, B. P.; Moore, K. A.; Osterholm, M. T. N. Engl. J. Med. 1999, 340, 1525-1532.
18. Sumpter, J. P.; Jobling, S. Environ. Health Perspect. 1995, 103, 174-178.
19. Ayscough, N. J.; Fawell, J.; Franklin, G.; Young, W. Review of human pharmaceuticals in the environment; Environment Agency, R&D Technical Report P390; 2000.
21. Shelton, L. R. Open-File Rep., U.S. Geol. Surv. 1994, No. 94-455.
22. Foran, C. M.; Bennett, E. R.; Benson, W. H. Mar. Environ. Res. 2000, 50, 153-156.
23. U.S. Environmental Protection Agency. U.S. EPA No. 822-B-00-001; U.S. Government Printing Office; Washington, DC, 2000.
24. U.S. Environmental Protection Agency Ecotoxicology database. http://www.epa.gov/medecotx/quicksearch.htm. (accessed May 2001).
25. U.S. Environmental Protection Agency. Guidelines establishing test procedures for the analysis of pollutants (App. B to Part 136, Definition and procedure for the determination of the method detection limit) U.S. Code of Federal Regulations, Title 40, revised as of July 1, 1992.
26. Lindsey, M. E.; Meyer, M.; Thurman, E. M. Anal. Chem. 2001, 73, 4640-4646.
27. Brown, G. K.; Zaugg, S. D.; Barber, L. B. Water-Resour. Invest. Rep.-U.S. Geol Surv. 1999, No. 99-4018B, pp 431-435.
28. Barber, L. B.; Brown, G. K.; Zaugg, S. D. In Analysis of Environmental Endocrine Disruptors; Keith, L. H., Jones-Lepp, T. L., Needham, L. L., Eds.; ACS Symposium Series 747; American Chemical Society: Washington, DC, 2000; pp 97-123.
29. Hirsch, R.; Ternes, T. A.; Haberer, K.; Mehlich, A.; Ballwanz, F.; Kratz, K. L. J. Chromatogr. A 1998, 815, 213-223.
30. Mitscher, L. A. The Chemistry of the Tetracycline Antibiotics; Marcel Dekker: New York, Basel, 1978.
31. Heberer, T.; Schmidt-Baumler, K.; Stan, H. J. Acta Hydrochim. Hydrobiol. 1998, 26, 272-278.
32. Baguer, A. J.; Jensen, J.; Krogh, P. H. Chemosphere 2000, 40, 751-757.
33. Lutzhoft, H. C.; Halling-Sorensen, B.; Jorgensen, S. E. Arch. Environ. Contam. Toxicol. 1999, 36, 1-6.
34. Wollenberger, L.; Halling-Sorensen, B.; Kusk, K. O. Chemosphere 2000, 40, 723-730.
35. Hartmann, A.; Golet, E. M.; Gartiser, S.; Alder, A. C.; Koller, T.; Widmer, R. M. Arch. Environ. Contam. Toxicol. 1999, 36, 115-119.
36. Fong, P. P. Biol. Bull. 1998, 194, 143-149.
37. Sohoni, P.; Tyler, C. R.; Hurd, K.; Caunter, J.; Hetheridge, M.; Williams, T.; Woods, C.; Evans, M.; Toy, R.; Gargas, M.; Sumpter, J. P. Environ. Sci. Technol. 2001, 35, 2917-2925.
38. Harris, C. A.; Santos, E. M.; Janbakhsh, A.; Pottinger, T. G.; Tyler, C. R.; Sumpter, J. P. Environ. Sci. Technol. 2001, 35, 2909-2916.
39. Chee-Sanford, J. C.; Aminov, R. I.; Krapac, I. J.; Garrigues-Jeanjean, N.; Mackie, R. I. Appl. Environ. Microbiol. 2001, 67, 1949-1502.
40. Buser, H.-R.; Poiger, T.; Muller, M. D. Environ. Sci. Technol. 1998, 32, 3449-3456.
41. Buser, H.-R.; Poiger, T.; Muller, M. D. Environ. Sci. Technol. 1999, 33, 2529-2535.
42. Kolpin, D. W.; Thurman, E. M.; Linhart, S. M. Sci. Total Environ. 2000, 248, 115-122.[Medline]
43. Clark, G. M.; Goolsby, D. A. Sci. Total Environ. 2000, 248, 101-113.
44. Venkatesan, M. I.; Kaplan, I. R. Environ. Sci. Technol. 1990, 24, 208-213.
45. Childress, C. J. O.; Foreman, W. T.; Connor B. F.; Maloney, T. J. Open-File Rep.-U.S. Geol. Surv. 1999, No. 99-193.
46. Baronti, C.; Curini, R.; D'Ascenzo, G.; Di Corcia, A.; Gentili, A.; Samperi, R. Environ. Sci. Technol. 2000, 34, 5059-5066.
47. Routledge, E. J.; Sheahan, D.; Desbrow, C.; Sumpter, J. P.; Waldock, M. Environ. Sci. Technol. 1998, 32, 1559-1565.
48. Lye, C. M.; Frid, C. L. J.; Gill, M. E.; Cooper, D. W.; Jones, D. M. Environ. Sci. Technol. 1999, 33, 1009-1014.
49. Swann, J. M.; Schultz, T. W.; Kennedy, J. R. Arch. Environ. Contam. Toxicol. 1996, 30, 188-194.
50. Keith, T. L.; Snyder, S. A.; Naylor, C. G.; Staples, C. A.; Sumer, C.; Kannan, K.; Giesy, J. P. Environ. Sci. Technol. 2001, 35, 10-13.
51. Folmar, L. C.; Denslow, N. D.; Kroll, K.; Orlando, E. F.; Enblom, J.; Marcino, J.; Metcalfe, C.; Guillette, L. J., Jr. Arch. Environ. Contam. Toxicol. 2001, 40, 392-398.
52. Kolpin, D. W.; Barbash, J. E.; Gilliom, R. J. Ground Water 2000, 38, 858-863.
53. Stackelberg, P. E.; Kauffman, L. J.; Ayers, M. A.; Baehr, A. L. Environ. Toxicol. Chem. 2001, 20, 853-865.
54. Marinovich, M.; Ghilardi, F.; Galli, C. L. Toxicology 1996, 108, 201-206.
55. Thompson, H. M. Ecotoxicology 1996, 5, 59-81.
56. Thorpe, K. L.; Hutchinson, T. H.; Hetheridge, M. J.; Scholze, M.; Sumpter, J. P.; Tyler, C. R. Environ. Sci. Technol. 2001, 35, 2476-2481.
57. Porter, W. P.; Jaeger, J. W.; Carlson, I. H. Toxicol. Ind. Health 1999, 15, 133-150.
58. Kuch, H. M.; Ballschmiter, K. Environ. Sci. Technol. 2001, 35, 3201-3206.
59. Al-Ahmad, A.; Daschner, F. D.; Kummerer, K. Arch. Environ. Contam. Toxicol. 1999, 37, 158-153.
60. Hirsch, R.; Ternes, T.; Haberer, K.; Kratz, K. Sci. Total Environ. 1999, 225, 109-118.
61. Koenig, B. G.; Metcalfe, C. D.; Ternes, T.; Hirsch, R. SETAC Proceedings 2000, 76.
62. Stumpf, M.; Ternes, T. A.; Wilken, R.; Rodriques, S. V.; Baumann, W. Sci. Total Environ. 1999, 225, 135-141.
63. Ternes, T. A. Water Res. 1998, 32, 3245-3260.
64. Seiler, R. L.; Zaugg, S. D.; Thomas, J. M.; Howcroft, D. L. Ground Water 1999, 37, 405-410.
65. Heberer, T. J. Hydrol. 2002 (in press).
Table 1. Summary of Analytical Results of Streams Sampled for 95 Organic Wastewater Contaminantsi
Veterinary and Human Antibiotics . lowest LC50 for the most sensitive indicator species chemical RL freq max med MCL or HAL (µg/L)/no. of aquatic studies (method) CASRN/N (g/L) (%) (g/L) (g/L) use (23)(g/L) idenified (24) carbodox(1) 6804-07-5/104 0.10 0 ND ND antibiotic - -/1 chlortetracycline(1) 57-62-5/115 0.05 0 ND ND antibiotic - 88000a/3 chlortetracycline(2) 57-62-5/84 0.10 2.4 0.69 0.42 antibiotic - 88000a/3 ciprofloxacin(1) 85721-33-1/115 0.02 2.6 0.03 0.02 antibiotic - -/0 doxycycline(1) 564-25-0/115 0.1 0 ND ND antibiotic - -/0 enrofloxacin(1) 93106-60-6/115 0.02 0 ND ND antibiotic - 40b/29 erythromycin-H2O(1) 114-07-8/104 0.05 21.5 1.7 0.1 erythromycin - 665000b/35 metabolite lincomycin(1) 154-21-2/104 0.05 19.2 0.73 0.06 antibiotic - -/0 norfloxacin(1) 70458-96-7/115 0.02 0.9 0.12 0.12 antibiotic - -/6 oxytetracycline(1) 79-57-2/115 0.1 0 ND ND antibiotic - 102000a/46 oxytetracycline(2) 79-57-2/84 0.10 1.2 0.34 0.34 antibiotic - 102000a/46 roxithromycin(1)80214-83-1/104 0.03 4.8 0.18 0.05 antibiotic - -/0 sarafloxacin(1) 98105-99-8/115 0.02 0 ND ND antibiotic - -/0 sulfachloropyridazine(2) 80-32-0/84 0.05 0 ND ND antibiotic - -/0 sulfadimethoxine(1) 122-11-2/104 0.05 0 ND ND antibiotic - -/5 sulfadimethoxine(2) 122-11-2/84 0.05 1.2 0.06 0.06 antibiotic - -/5 sulfamerazine(1)127-79-7/104 0.05 0 ND ND antibiotic - 100000c/17 sulfamerazine(2)127-79-7/84 0.05 0 ND ND antibiotic - 100000c/17 sulfamethazine(1) 57-68-1/104 0.05 4.8 0.12 0.02 antibiotic - 100000c/17 sulfamethazine(2) 57-68-1/84 0.05 1.2 0.22 0.22 antibiotic - 100000c/17 sulfamethizole(1) 144-82-1/104 0.05 1.0 0.13 0.13 antibiotic - -/0 sulfamethoxazole(1) 723-46-6/104 0.05 12.5 1.9 0.15 antibiotic - -/0 sulfamethoxazole(3) 723-46-6/84 0.023 19.0 0.52 0.066 antibiotic - -/0 sulfathiazole(1)72-14-0/104 0.10 0 ND ND antibiotic - -/0 sulfathiazole(2)72-14-0/84 0.05 0 ND ND antibiotic - -/0 tetracycline(1) 60-54-8/115 0.05 0 ND ND antibiotic - 550000b/3 tetracycline(2) 60-54-8/84 0.10 1.2 0.11 0.11 antibiotic - 550000b/3 trimethoprim(1) 738-70-5/104 0.03 12.5 0.71 0.15 antibiotic - 3000c/4 trimethoprim(3) 738-70-5/84 0.014 27.4 0.30 0.013 antibiotic - 3000c/4 tylosin(1) 1401-69-0/104 0.05 13.5 0.28 0.04 antibiotic - -/0 virginiamycin(1)21411-53-0/104 0.10 0 ND ND antibiotic - -/0 Prescription Drugs . albuterol(salbutamol)(3) 18559-94-9/84 0.029 0 ND ND antiasthmatic - -/0 cimetidine(3) 51481-61-9/84 0.007 9.5 0.58d 0.074d antacid - -/0 codeine(3) 76-57-3/46 0.24 6.5 0.019 0.012 analgesic - -/0 codeine(4) 76-57-3/85 0.1 10.6 1.0d 0.2d analgesic - -/0 dehydronifedipine(3) 67035-22-7/84 0.01 14.3 0.03 0.012 antianginal - -/0 digoxin(3) 20830-75-5/46 0.26 0 NDd NDd cardiac - 10000000a/24 stimulant digoxigenin(3) 1672-46-4/84 0.008 0 ND ND digoxin - -/0 metabolite diltiazem(3) 42399-41-7/84 0.012 13.1 0.049 0.021 antihypertensive - -/0 enalaprilat(3) 76420-72-9/84 0.15 1.2 0.046d 0.046d enalapril maleate - -/0 (antihypertensive) metabolite fluoxetine(3) 54910-89-3/84 0.018 1.2 0.012d 0.012d antidepressant - -/0 gemfibrozil(3) 25812-30-0/84 0.015 3.6 0.79 0.048 antihyperlipidemic - -/0 metformin(3) 657-24-9/84 0.003 4.8 0.15d 0.11d antidiabetic - -/0 paroxetine metabolite(3) -/84 0.26 0 NDd NDd paroxetine - -/0 (antidepressant) metabolite ranitidine(3) 66357-35-5/84 0.01 1.2 0.01d 0.01d antacid - -/0 warfarin(3) 81-81-2/84 0.001 0 ND ND anticoagulant - 16000c/33 Nonprescription Drugs acetaminophen(3)103-90-2/84 0.009 23.8 10 0.11 antipyretic - 6000a/14 caffeine(3) 58-08-2/84 0.014 61.9 6.0 0.081 stimulant - 40000e/77 caffeine(4) 58-08-2/85 0.08 70.6 5.7 0.1 stimulant - 40000e/ 77 cotinine(3) 486-56-6/84 0.023 38.1 0.90 0.024 nicotine - -/0 metabolite cotinine(4) 486-56-6/54 0.04 31.5 0.57 0.05 nicotine - -/0 metabolite 1,7-dimethylxanthine(3) 611-59-6/84 0.018 28.6 3.1d 0.11d caffeine - -/0 metabolite ibuprofen(3) 15687-27-1/84 0.018 9.5 1.0 0.20 antiinflammatory - -/0 Other Wastewater-Related Compounds . lowest LC50 for the most sensitive indicator species chemical RL freq max med MCL or HAL (µg/L)/no. of aquatic studies (method) CASRN/N (g/L) (%) (g/L) (g/L) use (23)(g/L) idenified (24) 1,4-dichlorobenzene(4) 106-46-7/85 0.03 25.9 4.3 0.09 deodorizer 75 1100c/190 2,6-di-tert-butylphenol(4) 128-39-2/85 0.08 3.5 0.11d 0.06d antioxidant - -/2 2,6-di-tert-butyl-1,4-benzoquinone(4) 719-22-2/85 0.10 9.4 0.46 0.13 antioxidant - -/0 5-methyl-1H-benzotriazole(4) 136-85-6/54 0.10 31.5 2.4 0.39 antiocorrosive - -/0 acetophenone(4) 98-86-2/85 0.15 9.4 0.41 0.15 fragrance - 155000e/21 anthracene(4) 120-12-7/85 0.05 4.7 0.11 0.07 PAH - 5.4e/188 benzo[a]pyrene(4) 50-32-8/85 0.05 9.4 0.24 0.04 PAH 0.2 1.5a/428 3-tert-butyl-4-hydroxy anisole(4) 25013-16-5/85 0.12 2.4 0.2d 0.1d antioxidant - 870c/14 butylated hydroxy toluene(4) 128-37-0/85 0.08 2.4 0.1d 0.1d antioxidant - 1440a/15
bis(2-ethylhexyl)adipate(4) 103-23-1/85 2.0 3.5 10f 3f plasticizer 400 480a/9 bis(2-ethylhexyl)phthalate(4) 117-81-7/85 2.5 10.6 20f 7f plasticizer 6 7500a/309 bisphenol A(4) 80-05-7/85 0.09 41.2 12 0.14 plasticizer - 3600e/26 carbaryl (4) 63-25-2/85 0.06 16.5 0.1d 0.04d insecticide 700 0.4a/1541 cis-chlordane(4)5103-71-9/85 0.04 4.7 0.1 0.02 insecticide 2 7.4b/28 chlorpyrifos(4) 2921-88-2/85 0.02 15.3 0.31 0.06 insecticide 20 0.1a/1794 diazinon(4) 333-41-5/85 0.03 25.9 0.35 0.07 insecticide 0.6 0.56a/1040 dieldrin(4) 60-57-1/85 0.08 4.7 0.21 0.18 insecticide 0.2 2.6c/1540 diethylphthalate(4) 84-66-2/54 0.25 11.1 0.42 0.2 plasticizer - 12000c/129 ethanol,2-butoxy-phosphate(4) 78-51-3/85 0.2 45.9 6.7 0.51 plasticizer - 10400e/7 fluoranthene(4) 206-44-0/85 0.03 29.4 1.2 0.04 PAH - 74e/216 lindane(4) 58-89-9/85 0.05 5.9 0.11 0.02 insecticide 0.2 30c/1979 methyl parathion4) 298-00-0/85 0.06 1.2 0.01 0.01 insecticide 2 12a/888 4-methyl phenol(4) 106-44-5/85 0.04 24.7 0.54 0.05 disinfectant - 1400a/74 naphthalene(4) 91-20-3/85 0.02 16.5 0.08 0.02 PAH 20 910c/519 N,N-diethyltoluamide(4) 134-62-3/54 0.04 74.1 1.1 0.06 insect repellant - 71250c/9 4-nonylphenol(4)251-545-23/85 0.50 50.6 40g 0.8g nonionic detergent - 130e/135 metabolite 4-nonylphenol monoethoxylate(4) -/85 1.0 45.9 20g 1g nonionic detergent 14450a/4 metabolite 4-nonylphenol diethoxylate(4) -/85 1.1 36.5 9g 1g nonionic detergent - 5500a/6 metabolite 4-octylphenol monoethoxylate(4) -/85 0.1 43.5 2g 0.2g nonionic detergent - -/0 metabolite 4-octylphenol diethoxylate(4) -/85 0.2 23.5 1g 0.1g nonionic detergent - -/0 metabolite phenanthrene(4) 85-01-8/85 0.06 11.8 0.53 0.04 PAH - 590a/192 phenol(4) 108-95-2/85 0.25 8.2 1.3f 0.7f disinfectant 400 4000c/2085 phthalic anhydride(4) 85-44-9/85 0.25 17.6 1f 0.7f plastic - 40400c/5 manufacturing pyrene(4) 129-00-0/85 0.03 28.2 0.84 0.05 PAH - 90.9a/112 tetrachloroethylene(4) 127-18-4/85 0.03 23.5 0.70d 0.07d solvent, 5 4680c/147 degreaser triclosan(4) 3380-34-5/85 0.05 57.6 2.3 0.14 antimicrobial - 180e/3 disinfectant tri(2-chloroethyl)phosphate(4) 115-96-8/85 0.04 57.6 0.54 0.1 fire retardant - 66000b/8 tri(dichlorisopropyl)phosphate(4) 13674-87-8/85 0.1 12.9 0.16 0.1 fire retardant - 3600b/9 triphenyl phosphate(4) 115-86-6/85 0.1 14.1 0.22 0.04 plasticizer - 280c/66 Steroids and Hormones . cis-androsterone(5) 53-41-8/70 0.005 14.3 0.214 0.017 urinary steroid - -/0 cholesterol(4) 57-88-5/85 1.5 55.3 10d 1d plant/animal - -/0 steroid cholesterol(5) 57-88-5/70 0.005 84.3 60h 0.83 plant/animal - -/0 steroid coprostanol(4) 360-68-9/85 0.6 35.3 9.8d 0.70d fecal steroid - -/0 coprostanol(5) 360-68-9/70 0.005 85.7 150h 0.088 fecal steroid - -/0 equilenin(5) 517-09-9/70 0.005 2.8 0.278 0.14 estrogen - -/0 replacement equilin(5) 474-86-2/70 0.005 1.4 0.147 0.147 estrogen - -/0 replacement 17-ethynyl estradiol(5) 57-63-6/70 0.005 15.7 0.831 0.073 ovulation - -/22 inhibitor 17-estradiol(5) 57-91-0/70 0.005 5.7 0.074 0.03 reproductive - -/0 hormone 17-estradiol(4) 50-28-2/85 0.5 10.6 0.2d 0.16d reproductive - -/0 hormone 17-estradiol(5) 50-28-2/70 0.005 10.0 0.093 0.009 reproductive - -/0 hormone estriol(5) 50-27-1/70 0.005 21.4 0.051 0.019 reproductive - -/0 hormone estrone(5) 53-16-7/70 0.005 7.1 0.112 0.027 reproductive - -/11 hormone mestranol(5) 72-33-3/70 0.005 10.0 0.407 0.074 ovulation - -/0 inhibitor 19-norethisterone(5) 68-22-4/70 0.005 12.8 0.872 0.048 ovulation - -/0 inhibitor progesterone(5) 57-83-0/70 0.005 4.3 0.199 0.11 reproductive - -/0 hormone stigmastanol(4) 19466-47-8/54 2.0 5.6 4d 2d plant steroid - -/0 testosterone(5) 58-22-0/70 0.005 2.8 0.214 0.116 reproductive - -/4 hormone a Daphnia magna (water flea) - 48 h exposure LC50. b Other species and variable conditions. c Oncorhynchus mykiss (rainbow trout) - 96 h exposure LC50. d Concentration estimated - average recovery <60%. e Pimephales promelas (fathead minnow) - 96 h exposure LC50. f Concentration estimated - compound routinely detected in laboratory blanks. g Concentration estimated - reference standard prepared from a technical mixture. h Concentration estimated - value greater than highest point on calibration curve. i Compounds suspected of being hormonally active are in bold (4, 22). CASRN, Chemical Abstracts Service Registry Number; N, number of samples; RL, reporting level; freq, frequency of detection; max, maximum concentration; med, median detectable concentration; MCL, maximum contaminant level; HAL, health advisory level; LC50, lethal concentration with 50% mortality; ND, not detected; -, not available; PAH, polycyclic aromatic hydrocarbon.
Table 2. Summary of Quality Assurance/Quality Control Results for Target and Surrogate Compoundsb
spike concn mean % compound (µg/L) recovery %RSD Method 1 target compounds 1.0 99.0 12.1 Method 2 target compounds 1.0 97.5 12.2 13C6-sulfamethazine 1.0 80.0 20.0 meclocycline 1.0 80.0 20.0 Method 3 target compounds 0.5 85.1 11.6 C13-phenacetin 1.0 96.8 14.0 Method 4 target compounds 1.0 81.0 11.0 d21-BHT 2.0 63.0 25.0 n-nonylphenol 2.0 83.0 20.0 Method 5 target compounds NA NA NA d4-estradiola 0.047 128.8 42.0 d3-testosteronea 0.051 148.5 47.3 d7-cholesterola 0.053 116.9 55.9 a Surrogate standard added after CCLE extraction but prior to derivitization. b RSD, relative standard deviation; NA, not currently available.
If you have come to this page from an outside location click here to get back to mindfully.org