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At least 559 records · Page 31Linked to original sources
USGS2013

Constructing a reference tephrochronology for Augustine Volcano, Alaska

Augustine Volcano is the most historically active volcano in Alaska's populous Cook Inlet region. Past on-island work on pre-historic tephra deposits mainly focused on using tephra layers as markers to help distinguish among prevalent debris-avalanche deposits on the island (Waitt and Beget, 2009, USGS Prof Paper 1762), or as source material for petrogenetic studies. No comprehensive reference study of tephra fall from Augustine Volcano previously existed. Numerous workers have identified Holocene-age tephra layers in the region surrounding Augustine Island, but without well-characterized reference deposits, correlation back to the source volcano is difficult. The purpose of this detailed tephra study is to provide a record of eruption frequency and magnitude, as well as to elucidate physical and chemical characteristics for use as reference standards for comparison with regionally distributed Augustine tephra layers. Whole rock major- and trace-element geochemistry, deposit componentry, and field context are used to correlate tephra units on the island where deposits are coarse grained. Major-element glass geochemistry was collected for use in correlating to unknown regional tephra. Due to the small size of the volcanic island (9 by 11 km in diameter) and frequent eruptive activity, on-island exposures of tephra deposits older than a couple thousand years are sparse, and the lettered Tephras B, M, C, H, I, and G of Waitt and Beget (2009) range in age from 370-2200 yrs B.P. There are, however, a few exposures on the south side of the volcano, within about 2 km of the vent, where stratigraphic sections that extend back to the late Pleistocene glaciation include coarse pumice-fall deposits. We have linked the letter-named tephras from the coast to these higher exposures on the south side using physical and chemical characteristics of the deposits. In addition, these exposures preserve at least 5 older major post-glacial eruptions of Augustine. These ultra-proximal sites, along with an off-island section 20 km to the west, provide the first continuous tephrochronology for Augustine that extends from the earliest to latest Holocene. Because examined pumice-fall exposures are limited to a narrow azimuth on the south side of the volcano, the on-island record is likely an incomplete catalog of major eruptions. It is possible however, that the coarse-grained near vent exposures (within 2 km) represent large eruptions that blanketed the entire island in tephra and are representative of the entire Holocene record. The major Holocene tephra units exposed on-island are composed of coarse-grained (cm-scale) pumice ranging in color from white to cream (variably oxidized), and light to medium gray as well as banded varieties. Accidental lithic assembles are highly variable and often unique for individual eruptions. Pumices range from 60-66 wt % SiO2 in whole-rock composition and are distinguishable using trace and minor element abundances and field context. Glass geochemistry is often distinguishable between tephras, but more overlap exists among deposits and presents challenges for correlating to regional tephras.

Alaska↗
USGS2017

A newly identified role of the deciduous forest floor in the timing of green‐up

Plant phenology studies rarely consider controlling factors other than air temperature. We evaluate here the potential significance of physical and chemical properties of soil (edaphic factors) as additional important controls on phenology. More specifically, we investigate causal connections between satellite‐observed green‐up dates of small forest watersheds and soil properties in the Adirondack Mountains of New York, USA. Contrary to the findings of previous studies, where edaphic controls of spring phenology were found to be marginal, our analyses show that at least three factors manifest themselves as significant controls of seasonal patterns of variation in vegetated land surfaces observed from remote sensing: (1) thickness of the forest floor, (2) concentration of exchangeable soil potassium, and (3) soil acidity. For example, a thick forest floor appears to delay the onset of green‐up. Watersheds with elevated concentrations of potassium are associated with early surface greening. We also found that trees growing in strongly acidified watersheds demonstrate delayed green‐up dates. Overall, our work demonstrates that, at the scale of small forest watersheds, edaphic factors can explain a significant percentage of the observed spatial variation in land surface phenology that is comparable to the percentage that can be explained by climatic and landscape factors. We conclude that physical and chemical properties of forest soil play important roles in forest ecosystems as modulators of climatic drivers controlling the rate of spring soil warming and the transition of trees out of winter dormancy.

New York↗
USGS2012

Groundwater, surface-water, and water-chemistry data from C-aquifer monitoring program, northeastern Arizona, 2005-11

The C aquifer is a regionally extensive multiple-aquifer system supplying water for municipal, agricultural, and industrial use in northeastern Arizona, northwestern New Mexico, and southeastern Utah. An increase in groundwater withdrawals from the C aquifer coupled with ongoing drought conditions in the study area increase the potential for drawdown within the aquifer. A decrease in the water table and potentiometric surface of C aquifer is illustrated locally by the drying up of Obed Meadows, a natural peat deposit, and Hugo Meadows, a natural wetland, both south of Joseph City, Arizona. Continual increase in water use from the C aquifer, including a planned increase in pumpage by the City of Flagstaff, is justification for continued monitoring of the C-aquifer system in order to quantify physical and chemical responses to pumping stresses. Fifteen of the 35 C-aquifer wells analyzed had water-level data sufficient for percentage difference calculation for 2005–11. Change in water level as a percentage of the initial water-level measurement for these 15 wells ranged from about -0.2 to about -0.5 percent. For historical water-level data, changes in water levels were greatest around pumping centers, as indicated by a -97.0 feet (percentage difference of -16.5 percent) change over the period of record (1962–2005) for the Lake Mary 1 Well near Flagstaff, Arizona. In more rural areas of the C aquifer, water levels showed less change for both the temporal focus of this report (2005–11) and for historical values. Continuous records of surface-water discharge from 2005 to 2007 for three discontinued streamflow-gaging stations (Clear Creek near Winslow, AZ, 09399000; Clear Creek below McHood Lake near Winslow, AZ, 09399100; and Chevelon Creek near Winslow, AZ, 09398000) were tabulated. For the period of record, Clear Creek near Winslow, AZ, and Chevelon Creek near Winslow, AZ, showed seasonal discharge distributions indicative of natural streams in the southwestern United States. Clear Creek below McHood Lake near Winslow, AZ, showed discharge distribution indicative of perennial spring flow with little variation annually. Physical and chemical data collected during four baseflow investigations (summer 2005, summer 2006, summer 2008, and winter 2010) conducted on Clear Creek, Chevelon Creek, and a portion of the Little Colorado River were compiled and analyzed. Data from 7 sampling sites established on the Little Colorado River, 11 sites along Chevelon Creek, and 14 sites along Clear Creek were included. For the four baseflow investigations presented, a 2,000–3,000 microsiemens per centimeter increase in specific conductance was measured in Chevelon Creek from near its headwaters to the confluence with the Little Colorado River because of the contribution of highly conductive spring discharge. Clear Creek showed a less consistent pattern of increase in specific conductance with distance, but still exhibited changes on the order of 5,000 microsiemens per centimeter over just a few river miles. Water-chemistry data for selected wells and baseflow investigations sites are presented. No well samples analyzed exceeded the U.S. Environmental Protection Agency Maximum Contaminant Level standards for drinking water, but several samples exceeded Secondary Maximum Contaminant Level standards for chloride, fluoride, sulfate, iron, and total dissolved solids.

Arizona↗
USGS1998

Occurrence and distribution of dissolved pesticides in the San Joaquin River basin, California

The effects of pesticide application, hydrology, and chemical and physical properties on the occurrence of pesticides in surface water in the San Joaquin River Basin, California, were examined. The study of pesticide occurrence in the highly agricultural San Joaquin?Tulare Basins is part of the National Water-Quality Assessment Program of the U.S. Geological Survey. One hundred forty-three water samples were collected throughout 1993 from sites on the San Joaquin River and three of its tributaries: Orestimba Creek, Salt Slough, and the Merced River. Of the 83 pesticides selected for analysis in this study, 49 different compounds were detected in samples from the four sites and ranged in concentration from less than the detection limit to 20 micrograms per liter. All but one sample contained at least one pesticide, and more than 50 percent of the samples contained seven or more pesticides. Six compounds were detected in more than 50 percent of the samples: four herbicides (dacthal, EPTC, metolachlor, and simazine) and two insecticides (chlorpyrifos and diazinon). None of the measured concentrations exceeded U.S. Environmental Protection Agency drinking water criteria, and many of the measured concentrations were very low. The concentrations of seven pesticides exceeded criteria for the protection of freshwater aquatic life: azinphos-methyl, carbaryl, chlorpyrifos, diazinon, diuron, malathion, and trifluralin. Overall, some criteria for protection of aquatic life were exceeded in a total of 97 samples. Factors affecting the spatial patterns of occurrence of the pesticides in the different subbasins included the pattern of application and hydrology. Seventy percent of pesticides with known application were detected. Overall, 40 different pesticides were detected in Orestimba Creek, 33 in Salt Slough, and 26 in the Merced River. Samples from the Merced River had a relatively low number of detections, despite the high number (35) of pesticides applied, owing to the generally low percentage of irrigation return flow and contribution of pesticide-free streamflow from reservoir releases. Irrigation return flows in the Orestimba Creek and Salt Slough subbasins generally contained more pesticides at higher concentrations. In addition, the distribution of seven pesticides (alachlor, cyanazine, dacthal, fonofos, molinate, napropamide, and trifluralin) in the subbasins showed a direct spatial correspondence between occurrence and application rates. Temporal patterns of occurrence also were affected by patterns of application and hydrology. Most pesticides showed a clear correspondence between the times of their application and their occurrence. Fourteen pesticides had maximum application and concentrations during the summer irrigation season. However, several pesticides exhibited maximum concentrations during winter storms, although maximum application occurred at some other time of year?the result of differences in precipitation and streamflow between seasons. In some subbasins, precipitation runoff was more effective than irrigation return flows at transporting pesticides from the site of application to the stream. Also, during autumn, when there was neither precipitation nor irrigation, the transport of pesticides to streams was limited. The effect of chemical and physical properties on the occurrence of pesticides was examined for the San Joaquin River Basin as a whole. The runoff potential of each pesticide, calculated from the solubility, water-soil organic carbon partition coefficient Koc, and hydrolysis half-life, is generally consistent with the frequency of detection of pesticides in surface water in relation to the amount applied. These three properties each were generally, and weakly, correlated with the relative load of the pesticides in surface water. Pesticide occurrence and concentrations at the mouth of the basin (the San Joaquin River near Vernalis) was compared with pesticide occurrence and concentration in the three

Water-Resources Investigations Report↗
USGS2006

The prediction of aquatic sediment-associated trace element concentration using selected geochemical factors

Multiple linear regression models calculated from readily obtainable chemical and physical parameters can explain a high percentage (70 per cent or greater) of observed sediment-trace element variance for Cu, Zn, Pb, Cr, Ni, Co, As, Sb, Se, and Hg in a widely divergent suite of 61 sediment samples. The independent variables used in the models may be single parameters, principal component scores, or principal component scores combined with their cross-products. The most useful type of variable must be determined on a case-by-case basis. The independent variables (geochemical parameters) incorporated in the models calculated during this study probably are applicable to many aquatic sediments; albeit, use of a larger data set (>61) could alter the magnitude of the calculated coefficients. The geochemical parameters included in the models were of a physical (e.g. grain size, surface area) and a chemical (e.g. organic matter, amorphous iron oxides) nature. Comparison between actual and predicted trace element concentrations obtained from the models may provide a means of defining ‘average’ sediment-trace element concentrations. In this context, the models may also help identify either naturally or anthropogenically impacted sites for additional study.

Hydrological Processes↗
USGS2018

Exclusion of small mammals and lagomorphs invasion interact with human-trampling to drive changes in topsoil microbial community structure and function in semiarid Chile

Species losses and additions can disrupt the relationship between resident species and the structure and functioning of ecosystems. Persistent human-trampling, on the other hand, can have similar effects through the disruption of biocrusts on surface soils of semiarid systems, affecting soil stability and fixation of carbon and nitrogen. Here, we tested the interactive and synergistic impacts of the exclusion of native mammalian herbivores and the effects of introduced lagomorphs in a semiarid thorn scrub ecosystem, where soils were subjected to two different trampling intensities (i.e., trampled and non-trampled). We postulated that because of their differential habitat use and fossorial activities, with respect to native small mammals, lagomorphs would have strong negative effects on soil structure, biocrust cover, and biocrust bacterial community structure. Our expectations were that changes in biocrust cover in response to trampling where native mammals were excluded, but exotic lagomorphs were present, will spread their impacts on soil chemical and physical features. To test our hypotheses, we measured changes in soil biogeochemical properties in four experimental plots where lagomorphs (L)/small mammals (SM) were experimentally manipulated to exclude them from the plots (−), or let them be present (+). The experimental combinations monitored were: -L/+SM, -L/-SM, +L/+SM, and +L/-SM. Results showed that human-trampling disturbance interacted with the loss of native small mammals and the presence of non-native lagomorphs to cause large changes on biological (i.e., biocrust cover, bacterial and nifH genes abundance), physical (i.e., soil moisture and soil stability) and chemical (i.e., TC and TN) soil features. The relative impacts of trampling disturbance on biological and physicochemical features were strongly influenced by the presence of non-native lagomorphs. For example, larger decreases in biocrust cover and bacterial abundance were observed in treatments without lagomorphs (-L/+SM; -L/-SM). In turn, losses of biocrust cover, in addition to trampling, determined decreases in soil stability in all treatments. These results suggest that non-native lagomorphs surpass the effects of the loss of native small mammals in reducing soil quality and productivity. Therefore, human-trampling has the potential to convert low disturbed soils, as those observed in non-trampled soils in treatments -L/+SM, -L/-SM into poor soils with low biocrusts cover and concomitant low stability, as observed in +L/+SM; +L/-SM treatments. These findings agree with previous observations that different components of global change act in synergic ways in fragile, water-limited environments. Because biological invasions and soil surface disturbance are becoming widespread in dryland regions globally, understanding the long-term consequences of these interactions is essential.

Fray Jorge National Park↗
USGS2002

Chemical attributes of some clouds amid a forest ecosystem's trees

Simultaneous physical and chemical characteristics of clouds amid and above the trees of a montane forest, located about 3.3 km southwest of Mt. Mitchell, NC, were collected between 13 and 22 June 1993. This paper summarizes the chemical characteristics of the cloud droplets amid the trees. The ionic composition and pH of the analyzed amid-canopy cloud water samples are generally consistent with those of previous above-canopy cloud water samples obtained at this site. Magnesium, sodium, and calcium are highly correlated to each other amid the canopy as compared to above the canopy. Above-canopy and amid-canopy cloud-only episodes, with concurrent event-averaged cloud water pH values at or below 3.1, generally contain more magnesium, sodium, and calcium in the amid-canopy cloud water samples compared to concurrent above-canopy cloud water samples. The observed chemical differences between the amid-canopy cloud and the above-canopy cloud suggest an unhealthier environment for the tree canopy when the cloud water traversing this site has a pH value at or below 3.1. The predominant ion deposition fluxes were calculated to provide preliminary data for studies designed to explicitly quantify how the chemical composition of cloud water affects tree health.

Atmospheric Research↗
USGS2015

Physical abrasion of mafic minerals and basalt grains: application to Martian aeolian deposits

Sediment maturity, or the mineralogical and physical characterization of sediment deposits, has been used to locate sediment source, transport medium and distance, weathering processes, and paleoenvironments on Earth. Mature terrestrial sands are dominated by quartz, which is abundant in source lithologies on Earth and is physically and chemically stable under a wide range of conditions. Immature sands, such as those rich in feldspars or mafic minerals, are composed of grains that are easily physically weathered and highly susceptible to chemical weathering. On Mars, which is predominately mafic in composition, terrestrial standards of sediment maturity are not applicable. In addition, the martian climate today is cold, dry and sediments are likely to be heavily influenced by physical weathering rather than chemical weathering. Due to these large differences in weathering processes and composition, martian sediments require an alternate maturity index. Abrason tests have been conducted on a variety of mafic materials and results suggest that mature martian sediments may be composed of well sorted, well rounded, spherical basalt grains. In addition, any volcanic glass present is likely to persist in a mechanical weathering environment while chemically altered products are likely to be winnowed away. A modified sediment maturity index is proposed that can be used in future studies to constrain sediment source, paleoclimate, mechanisms for sediment production, and surface evolution. This maturity index may also provide details about erosional and sediment transport systems and preservation processes of layered deposits.

Icarus↗
USGS1986

Water-quality data for the ground-water network in eastern Broward County, Florida, 1983-84

During 1983-84, ground water from 63 wells located at 31 sites throughout, eastern Broward County, Florida, was sampled and analyzed to determine baseline water-quality conditions. The physical and chemical parameters analyzed included field measurements (pH and temperature), physical characteristics (color, turbidity, and specific conductance), major inorganic ions, nutrients (nitrogen, phosphorus, and carbon), selected trace metals, and total phenolic compounds. Ground-water samples were collected at the end of the dry season (April), during rising water levels (June and July), and during yearly peak water levels (September and October). These data are tabulated, by well, in this report.

Florida↗
USGS2002

Parameterizing the equilibrium distribution of chemicals between the dissolved, solid particulate matter, and colloidal matter compartments in aqueous systems

The manner in which a chemical material partitions among the dissolved (D), participate (P), and colloidal (C) phases affects both its chemical and physical behavior in the aquatic environment. The fractions of the chemical that are present in each of these three phases will be determined by the values of two simple parameters, KpSp/??w and KcSc/??w. The variables Kp and Kc are the particle/water and colloid/water partition constants (mL/g), respectively, Sp and Sc are the volume concentrations of particulate and colloidal material (mg/L), respectively, and ??w is the fractional volume of the system that is aqueous. This parameterization allows a rapid overview of how partitioning (1) changes as a function of chemical partitioning properties and water type, (2) affects apparent partition constants (i.e., Kpapp values) computed between the particulate phase and the remainder of the system, and (3) causes Kpapp values to become independent of chemical properties at high values of KcSc/??w. ?? 1991 American Chemical Society.

Environmental Science & Technology↗
USGS2014

Extending the turbidity record: making additional use of continuous data from turbidity, acoustic-Doppler, and laser diffraction instruments and suspended-sediment samples in the Colorado River in Grand Canyon

Turbidity is a measure of the scattering and absorption of light in water, which in rivers is primarily caused by particles, usually sediment, suspended in the water. Turbidity varies significantly with differences in the design of the instrument measuring turbidity, a point that is illustrated in this study by side-by-side comparisons of two different models of instruments. Turbidity also varies with changes in the physical parameters of the particles in the water, such as concentration, grain size, grain shape, and color. A turbidity instrument that is commonly used for continuous monitoring of rivers has a light source in the near-infrared range (860±30 nanometers) and a detector oriented 90 degrees from the incident light path. This type of optical turbidity instrument has a limited measurement range (depending on pathlength) that is unable to capture the high turbidity levels of rivers that carry high suspended-sediment loads. The Colorado River in Grand Canyon is one such river, in which approximately 60 percent of the range in suspended-sediment concentration during the study period had unmeasurable turbidity using this type of optical instrument. Although some optical turbidimeters using backscatter or other techniques can measure higher concentrations of suspended sediment than the models used in this study, the maximum turbidity measurable using these other turbidimeters may still be exceeded in conditions of especially high concentrations of suspended silt and clay. In Grand Canyon, the existing optical turbidity instruments remain in use in part to provide consistency over time as new techniques are investigated. As a result, during these periods of high suspended-sediment concentration, turbidity values that could not be measured with the optical turbidity instruments were instead estimated from concurrent acoustic attenuation data collected using side-looking acoustic-Doppler profiler (ADP) instruments. Extending the turbidity record to the full range of sediment concentrations in the study area using data from the ADP instruments is particularly useful for biological studies. In Grand Canyon, turbidity has been correlated with food availability for aquatic organisms (gross primary production) as well as with fish behavior specific to predator-prey interactions. On the basis of the complete “extended” turbidity record and the relation between suspended-sediment concentration and turbidity, levels were higher before the construction of Glen Canyon Dam by a factor of approximately 2,000 at the Lees Ferry monitoring station (15 miles downstream from the dam) and by a factor of approximately 20 at the monitoring station 87 miles downstream from Lees Ferry (102 miles downstream from the dam). A comparison of turbidity data with data from Laser In-Situ Scattering and Transmissometry (LISST) laser-diffraction instruments, suspended-sediment concentration data, and ADP data shows the influence of the physical properties of suspended sediment. Apparent outliers in relations between turbidity, ADP, and suspended-sediment data during two events within the study period, a 2007 tributary flood from a watershed altered by a recent wildfire and a 2008 experimental controlled-flood release from Glen Canyon Dam, are explained in part by atypical grain sizes, shapes, densities, colors, and (or) clay mineral assemblages of suspended sediment occurring in the Colorado River during these two events. These analyses demonstrate the value of using multiple data-collection strategies for turbidity and sediment-transport studies and of continuous monitoring for capturing the full range and duration of turbidity and sediment-transport conditions, identifying the provenance of the sediment causing turbidity, and detecting physical and chemical processes that may be important for management of critical physical and biological resources.

Arizona↗
USGS2017

Rock-weathering rates as functions of time

The scarcity of documented numerical relations between rock weathering and time has led to a common assumption that rates of weathering are linear. This assumption has been strengthened by studies that have calculated long-term average rates. However, little theoretical or empirical evidence exists to support linear rates for most chemical-weathering processes, with the exception of congruent dissolution processes. The few previous studies of rock-weathering rates that contain quantitative documentation of the relation between chemical weathering and time suggest that the rates of most weathering processes decrease with time. Recent studies of weathering rinds on basaltic and andesitic stones in glacial deposits in the western United States also clearly demonstrate that rock-weathering processes slow with time. Some weathering processes appear to conform to exponential functions of time, such as the square-root time function for hydration of volcanic glass, which conforms to the theoretical predictions of diffusion kinetics. However, weathering of mineralogically heterogeneous rocks involves complex physical and chemical processes that generally can be expressed only empirically, commonly by way of logarithmic time functions. Incongruent dissolution and other weathering processes produce residues, which are commonly used as measures of weathering. These residues appear to slow movement of water to unaltered material and impede chemical transport away from it. If weathering residues impede weathering processes then rates of weathering and rates of residue production are inversely proportional to some function of the residue thickness. This results in simple mathematical analogs for weathering that imply nonlinear time functions. The rate of weathering becomes constant only when an equilibrium thickness of the residue is reached. Because weathering residues are relatively stable chemically, and because physical removal of residues below the ground surface is slight, many weathering features require considerable time to reach constant rates of change. For weathering rinds on volcanic stones in the western United States, this time is at least 0.5 my.

Quaternary Research↗
USGS1999

Geochemical heterogeneity of a gasoline-contaminated aquifer

The scale of biogeochemical reactions was studied in a physically and chemically heterogeneous surficial Coastal Plain aquifer contaminated by a gasoline spill. The physical heterogeneity of the aquifer is manifested in two hydrologic units, a shallow local aquifer of perched water and a regional sandy aquifer. Over the studied vertical interval of 21.3 ft (6.5 m), concentrations of reactive species varied by orders of magnitude, and the impact of biodegradation was expressed to widely varying degrees. A thin (3 ft thick) section of the perched-water zone was the most contaminated; total aromatic hydrocarbons were as high as 19.4 mg/l. Hydrocarbons were degraded by microbially mediated reactions that varied over short vertical distances and time. Anaerobic processes dominated within the low-permeability clay unit, whereas in the more permeable sandy layers nitrate reduction and aerobic degradation occurred. Hydrocarbons were more persistent over time in the low-permeability layer due to the limited availability of electron acceptors for degradation. The microbial degradation of hydrocarbons was linked to sulfate and iron reduction in the clay unit and led to alterations in the aquifer solids; electron microscopy revealed the presence of FeS minerals encrusting primary aquifer grains. High concentrations of Fe 2+ in groundwater, up to 34.5 mg/l, persist in kinetic disequilibrium in the presence of elevated H 2 S levels of 1.0 mg/l. Assessment of aquifer heterogeneities and groundwater contamination was possible due to sample discrimination at a scale of approximately 2 ft (∼0.6 m), a much finer resolution than is attempted in many remedial investigations of polluted aquifers. The information obtained in this type of study is essential to the development of models capable of estimating the fate of hydrocarbons at a site scale.

Journal of Contaminant Hydrology↗
USGS1996

Ground-Water Quality in the Caguas-Juncos Valley, Puerto Rico, April to October 1990

Ground water from 48 wells and 1 spring in the Caguas-Juncos Valley was sampled and analyzed for major ions, nutrients, trace metals, and volatile synthetic organic chemicals from April to October 1990. This report presents the results of physical and chemical analyses made on these water samples. Dissolved-solids concentrations exceeded 500 milligrams per liter in 28 percent of the samples. Concentrations of trace metals were below the maximum contaminant levels set by Federal and Commonwealth agencies. Volatile synthetic organic chemicals were detected in water from five wells, four of which were located in urban and industrial areas. Concentrations of benzene, ethylbenzene, toluene, and xylene detected in samples from one observation well exceeded the maximum contaminant levels set be Federal and Commonwealth agencies.

Open-File Report↗
USGS1973

Water resources data for Arizona, water year 1972

Water resources data for the 1972 water year for Arizona include records of data for the chemical and physical characteristics of surface water. Data on the quality of surface water (chemical, temperature, and sediment) were collected from designated sampling sites at predetermined intervals, such as once daily, weekly, monthly, or less frequently; at some sites, data were collected continuously by means of automatic recording devices . Records are given for 77 sampling stations, of which 46 are continuous record stations, 8 are partial-record stations, and 23 are miscellaneous sampling stations. Locations of surface water-quality stations are shown in figures 1 and 2. A few pertinent stations in bordering States are also included. The records were collected by the Water Resources Division of the U.S. Geological Survey under the direction of H. M. Babcock, district chief. These data represent that portion of the National Water Data System collected bythe U.S. Geological Survey and cooperating State and Federal agencies in Arizona. The Geological Survey has published records of chemical quality, water temperatures, and sediment since 1941 in an annual s eries of water-supply papers entitled, ''Quality of Surface Waters of the United States." Beginning with the 1964 water year, water - quality records have been released by the Geological Survey in annual reports on a State boundary basis. These reports are for limited distribution and are designed primarily for rapid release of data shortly after the end of the water year. These records will be published later in Geological Survey water-supply papers.

Arizona↗
USGS1974

Water resources data for Arizona, water year 1973: Part 2. Water quality records

Water resources data for the 1973 water year for Arizona include records of data for the chemical and physical characteristics of surface water. Data on the quality of surface water (chemical, temperature, and sediment) were collected from designated sampling sites at predetermined intervals, such as once daily, weekly, monthly, or less frequently; at some sites, data were collected continuously by means of automatic recording devices. Records are given for 81 sampling stations, of which 48 are continuous record stations, 6 are partial-record stations, and 27 are miscellaneous sampling stations. Locations of surface water-quality stations are shown in figures 1 and 2. A few pertinent stations in bordering States are also included. The records were collected by the Water Resources Division of the U.S. Geological Survey under the direction of H. M. Babcock, district chief. These data represent that portion of the National Water Data System collected by the U. S. Geological Survey and cooperating State and Federal agencies in Arizona. The Geological Survey has published records of chemical quality, water temperatures, and sediment since 1941 in an annual series of water-supply papers entitled, "Quality of Surface Waters of the United States." Beginning with the 1964 water year, water-quality records have been released by the Geological Survey in annual reports on a State boundary basis. These reports are for limited distribution and are designed primarily for rapid release of data shortly after the end of the water year. These records will be published later in Geological Survey water-supply papers.

Arizona↗
USGS1972

Water resources data for Idaho, water year 1971: Part 2. Water quality records

Water resources data for the 1971 water year for Idaho include records of data for the chemical and physical characteristics of surface water. Data on the quality of surface water (chemical, temperature, and sediment) were collected from designated sampling sites at predetermined intervals such as once daily, weekly, monthly or less frequently, and at some sites data were recorded on punched paper tape at 15-minute intervals. Locations of surface water-quality stations are shown in figure 1. A few pertinent stations in bordering States are also included. The records were collected by the Water Resources Division of the U.S. Geological Survey under the direction of H. K. Hall, district chief. These data represent that portion of the National Water Data System collected by the U.S. Geological Survey and cooperating State and Federal agencies in Idaho.

Idaho↗