ALGAE IN THE SPOON RIVER,ILLINOIS 1971–19721

ABSTRACT: As a part of a water quality survey of the Spoon River, Illinois, algal genera were identified and their densities were enumerated. Weekly samples were collected at five stations starting on June 1, 1971. This report presents the first year's results. Algal densities for each station were found to be distributed geometrically normal. Total algal densities increased as water progressed downstream. Although water temperature has been observed to be an important factor affecting the density and the composition of algae in streams, attempts to correlate algal densities with temperatures for the Spoon River were not fruitful. Correlations of algal densities with dissolved oxygen, flow, and coliform densities also could not be made. The dominant genera observed were Cyclotella, Navicula, Scenedesmus, and Euglena. On the average diatoms accounted for 87% of all algae counts. The average diversity indices varied about 1.0 to 1.5 for five stations. There did not appear to be any advantage in the use of diversity index over that of algal density and genera richness in characterizing algae in the Spoon River.     

DETERMINATION OF CATION-EXCHANGE CAPACITY OF SUSPENDED SEDIMENT1

ABSTRACT: A procedure for determining cation-exchange capacity of river suspended sediment is described. Water samples for suspended sediment analyses were obtained from the Spoon River in Illinois. The procedure involves two substitution steps to convert all exchange sites to potassium, five washing steps to remove the excess cation, and two replacement steps using barium. The replaced potassium was determined with an atomic absorption spectrophotometer. Reproducibility is excellent; and the procedure is applicable to a wide range of suspended sediment concentration.     

CLIMATE VARIABILITY AND FLOOD FREQUENCY ESTIMATION FOR THE UPPER MISSISSIPPI AND LOWER MISSOURI RIVERS1

ABSTRACT: This paper considers the distribution of flood flows in the Upper Mississippi, Lower Missouri, and Illinois Rivers and their relationship to climatic indices. Global climate patterns including El Niño/Southern Oscillation, the Pacific Decadal Oscillation, and the North Atlantic Oscillation explained very little of the variations in flow peaks. However, large and statistically significant upward trends were found in many gauge records along the Upper Mississippi and Missouri Rivers: at Hermann on the Missouri River above the confluence with the Mississippi (p = 2 percent), at Hannibal on the Mississippi River (p < 0.1 percent), at Meredosia on the Illinois River (p = 0.7 percent), and at St. Louis on the Mississippi below the confluence of all three rivers (p = 1 percent). This challenges the traditional assumption that flood series are independent and identically distributed random variables and suggests that flood risk changes over time.     

Phosphorus transport pathways to streams in tile-drained agricultural watersheds

Agriculture is a major nonpoint source of phosphorus (P) in the Midwest, but how surface runoff and tile drainage interact to affect temporal concentrations and fluxes of both dissolved and particulate P remains unclear. Our objective was to determine the dominant form of P in streams (dissolved or particulate) and identify the mode of transport of this P from fields to streams in tile-drained agricultural watersheds. We measured dissolved reactive P (DRP) and total P (TP) concentrations and loads in stream and tile water in the upper reaches of three watersheds in east-central Illinois (Embarras River, Lake Fork of the Kaskaskia River, and Big Ditch of the Sangamon River). For all 16 water year by watershed combinations examined, annual flow-weighted mean TP concentrations were >0.1 mg L(-1), and seven water year by watershed combinations exceeded 0.2 mg L(-1). Concentrations of DRP and particulate P (PP) increased with stream discharge; however, particulate P was the dominant form during overland runoff events, which greatly affected annual TP loads. Concentrations of DRP and PP in tiles increased with discharge, indicating tiles were a source of P to streams. Across watersheds, the greatest DRP concentrations (as high as 1.25 mg L(-1)) were associated with a precipitation event that followed widespread application of P fertilizer on frozen soils. Although eliminating this practice would reduce the potential for overland runoff of P, soil erosion and tile drainage would continue to be important transport pathways of P to streams in east-central Illinois.     

环境因子对长江宜宾段底泥吸附磷的影响

本文主要研究模拟长江底泥对富营养化水体磷的吸附,分析环境因子对底泥吸附磷的影响。结果显示：（1）在25℃时,底泥对磷的吸附在碱性条件时的吸附速率小于酸性和中性条件,中性条件下的吸附速率最大;（2）在控制上覆水温度时,温度越高底泥对磷的吸附量越小,20℃时底泥的吸附量是30℃吸附量的1.5倍;（3）上覆水中溶解氧的浓度越高,吸附速率越高。     

农作物废料对海洋溢油吸附研究

根据海上围油栏围油原理,使用小型围油设备模拟出在围油栏除油后海上剩余溢油的质量M。收集稻壳、小米壳、小麦壳3种农作物废料作为吸油材料,室温下分别测出3种吸油材料对质量为M的溢油的饱和吸附时间。在吸附平衡的条件下,利用紫外分光光度计分别测出3种吸油材料吸附海水表面M质量溢油后的平衡吸附浓度ce。根据物理吸附理论,由平衡吸附浓度ce和平衡吸附量qe分别得出3种材料的Freundlich吸附等温式,从Freundlich吸附等温式比较了3种农作物废料的吸油性能。结果表明:稻壳的吸油性能最佳。     

Spatial and Temporal Variations in Phosphorus Loads in the Illinois River Basin,Illinois USA

Total phosphorus (TP) loads in many rivers in the north-central United States have increased, including the Illinois River at Valley City, Illinois, USA, which increased 39% from the periods 1989–1996 to 2015–2019 despite efforts to reduce loads from point and nonpoint sources. Here, we quantify long-term variations in phosphorus (P) loads in the Illinois River and its tributaries and identify factors that may be causing the variations. We calculated river loads of dissolved (DP) and particulate P (PP), total and volatile suspended solids (TSS and VSS), and other potentially related constituents at 41 locations. DP loads generally increased and PP and TSS loads generally decreased from 1989–1996 to 2015–2019. During 1989–1996, P accumulated in the lower basin between Marseilles and Valley City (excluding monitored tributaries). This portion of the basin is very flat and accumulates sediment. During 2015–2019, this section shifted from being a net sink to being a net source of P, accounting for 78% of the increased TP load at Valley City. We present evidence supporting several mechanisms that could have caused this shift: increased DP and chloride loads, reduced sulfate and nitrate concentrations influencing ionic strength and redox potential in the sediments, and increased VSS loads at Valley City possibly indicating greater algal production and contributing to hypoxia in lower river sediments. Additional research is needed to quantify the relative importance of these mechanisms.     

Temporal and spatial distributions of sediment total organic carbon in an estuary river

Understanding temporal and spatial distributions of naturally occurring total organic carbon (TOC) in sediments is critical because TOC is an important feature of surface water quality. This study investigated temporal and spatial distributions of sediment TOC and its relationships to sediment contaminants in the Cedar and Ortega Rivers, Florida, USA, using three-dimensional kriging analysis and field measurement. Analysis of field data showed that large temporal changes in sediment TOC concentrations occurred in the rivers, which reflected changes in the characteristics and magnitude of inputs into the rivers during approximately the last 100 yr. The average concentration of TOC in sediments from the Cedar and Ortega Rivers was 12.7% with a maximum of 22.6% and a minimum of 2.3%. In general, more TOC accumulated at the upper 1.0 m of the sediment in the southern part of the Ortega River although the TOC sedimentation varied with locations and depths. In contrast, high concentrations of sediment contaminants, that is, total polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyls (PCBs), were found in sediments from the Cedar River. There was no correlation between TOC and PAHs or PCBs in these river sediments. This finding is in contradiction to some other studies which reported that the sorption of hydrocarbons is highly related to the organic matter content of sediments. This discrepancy occurred because of the differences in TOC and hydrocarbon source input locations. It was found that more TOC loaded into the southern part of the Ortega River, while almost all of the hydrocarbons entered into the Cedar River. This study suggested that the locations of their input sources as well as the land use patterns should also be considered when relating hydrocarbons to sediment TOC.     

GEOCHEMICAL CHARACTERIZATION OF STREAMBED SEDIMENT IN THE UPPER ILLINOIS RWER BASIN1

ABSTRACT: Geochemistry of fine-fraction streambed sediments collected from the upper illinois River basin was surveyed in the fall of 1987 as part of the U.S. Geological Survey National Water-Quality Assessment pilot projects. The survey included 567 samples analyzed for 46 elements. Three distinctive distribution patterns were found for seven U.S. Environmental Protection Agency priority pollutants surveyed, as well as for boron and phosphorus: (1) enrichment of elements in the Chicago urban area and in streams draining the urban area relative to rural areas, (2) enrichment in main stems relative to tributaries, and (3) enrichment in low-order streams at high-population-density sites relative to low-population-density sites. Significant differences in background concentrations, as measured by samples from low-order streams, were observed among five subbasins in the study area. Uncertain geochemical correspondence between low-order, background sites and high-order, generally metal enriched sites prevented determination of background levels that would be appropriate for high-order sites. The within-sample ratio of enriched elements was variable within the Chicago area but was constant in the Illinois River downstream from Chicago. Element ratios imply a composite fine-fraction sediment in the Illinois River of 35–40 percent Des Plaines River origin and 60–65 percent Kankakee River origin.     

Possible Utilization of Silica Gel Sludge for the Removal of Phenol from Aqueous Solutions: Laboratory Studies

This paper discusses the adsorption capacity of silica gel sludge for phenol removal from aqueous solution. Kinetic experiments showed that phenol adsorption was completed after 2 h. Adsorption isotherms were measured for phenol from aqueous solution onto silica gel sludge under various pHs and temperatures. Results showed that the adsorption capacities for phenol was increased as pH decreased from 6.5 to 2. Temperature also was found to affect the adsorption isotherm. As temperature increases from 30 to 50°C, the adsorption capacity increases. The adsorption equilibrium of phenol on silica gel sludge was described by the linear Freundlich and Langmuir models. Furthermore, results showed that the isotherm parameters fit both linearized Langmuir and Freundlich adsorption isotherms. The Freundlich and Langmuir parameters at optimum pH was found as K _f=2.89, 1/n=0.23 and K _d=22.0, q _m=7.98, respectively. Whereas, for those at optimum temperature it was observed as K _f=2.87, 1/n=0.16 and K _d=20.93, q _m=7.91, respectively.     

分子印迹硅纳米改性氧化石墨烯复合材料的制备及其对双酚A的吸附研究

制备了分子印迹硅纳米-氧化石墨烯复合吸附材料,并研究了复合材料对双酚A(Bisphenol A,BPA)的吸附性能.实验结果表明:复合吸附材料对BPA的吸附在35min内达到吸附平衡,Langmuir等温线模型得出最大吸附容量约为338.3mg/g;相对于BPA的结构类似物,对BPA具有良好的选择吸附性能;在溶液pH接...     

Disturbance and recovery of large floodplain rivers

Disturbance in a river-floodplain system is defined as an unpredictable event that disrupts structure or function at the ecosystem, community, or population level. Disturbance can result in species replacements or losses, or shifts of ecosystems from one persistent condition to another. A disturbance can be a discrete event or a graded change in a controlling factor that eventually exceeds a critical threshold. The annual flood is the major driving variable that facilitates lateral exchanges of nutrients, organic matter, and organisms. The annual flood is not normally considered a disturbance unless its timing or magnitude is “atypical.” The record flood of 1973 had little effect on the biota at a long-term study site on the Mississippi River, but the absence of a flood during the 1976–1977 Midwestern drought caused short- and long-term changes. Body burdens of contaminants increased temporarily in key species, because of increased concentration resulting from reduced dilution. Reduced runoff and sediment input improved light penetration and increased the depth at which aquatic macrophytes could grow. Developing plant beds exerted a high degree of biotic control and were able to persist, despite the resumption of normal floods and turbidity in subsequent years. In contrast to the discrete event that disturbed the Mississippi River, a major confluent, the Illinois River, has been degraded by a gradual increase in sediment input and sediment resuspension. From 1958 to 1961 formerly productive backwaters and lakes along a 320-km reach of the Illinois River changed from clear, vegetated areas to turbid, barren basins. The change to a system largely controlled by abiotic factors was rapid and the degraded condition persists. Traditional approaches to experimental design are poorly suited for detecting control mechanisms and for determining the critical thresholds in large river-floodplains. Large river-floodplain systems cannot be manipulated or sampled as easily as small streams, and greater use should be made of man-made or natural disturbances and environmental restoration as opportunistic experiments to measure thresholds and monitor the recovery process. Coauthors are listed in alphabetical order.     

不同物质对垃圾渗滤液中腐殖酸的吸附研究

垃圾渗滤液是一种有毒有害的高浓度有机废水,其中含大量腐殖酸。腐殖酸具有离子交换能力、吸附能力和脱除杂质能力,因此在很多方面有实用价值。活性碳、土壤、堆肥对废水中的有机物有一定的吸附能力。本文采用正交设计的方法,研究了活性碳、土壤、堆肥在不同温度,液／固,腐殖酸初始浓度的条件下对垃圾渗滤液中腐殖酸的吸附效果。实验结果表明：四种实验因素对吸附剂的吸附能力的影响程度为：吸附剂类型〉腐殖酸的初始浓度〉吸附反应温度〉液固比。在温度为25℃,液固比为50／0．5（mL/g）,腐殖酸初始浓度为41．99（mg／L）,吸附剂类型为活性碳时,腐殖酸吸附量最大,为40．86mg。同时分析了响应指标随因素的变化趋势。     

Spatial distribution of DDT in sediments from estuarine rivers of central Florida

Sediments may act as both a carrier for and a potential source of contaminants such as toxic organics in aquatic environments. This study investigated the spatial distribution of the pesticide DDT [1,1, 1-trichloro-2,2-bis(p-chlorophenyl)ethane] in sediments from the Cedar and Ortega Rivers located in the lower St. Johns River basin, Florida, USA, using field measurements and three-dimensional kriging analysis. High DDT concentrations were found near the junction of the Cedar and Ortega Rivers and at the north end of the Ortega River in the upper 0.5 m of the sediments, indicating that the sediment was enriched with DDT in the top layer although use of this chlorinated compound was banned in 1972. Further study revealed that the influence of sediment grain size or texture on DDT contamination was negligible in this river system and no linear correlations existed among DDT and its metabolites such as DDD [1,1-dichloro-2,2-bis(p-chlorophenyl)ethane] and DDE [1,1-dichloro-2,2-bis(p-chlorophenyl)ethylene]. Comparison of three-dimensional distribution of DDT content to the Florida sediment quality assessment guideline or probable effect level (PEL) showed several "hot spots" in the Ortega River sediments, where DDT contents exceeded the PEL value of 4.78 microg kg(-1). Such contamination may pose a significant hazard to aquatic life.     

Removal of basic dye (Astrazon Blue FGRL) using macroalga Caulerpa lentillifera

The macroalga Caulerpa lentillifera was found to have adsorption capacity for a basic dye, Astrazon Blue FGRL. For the whole range of concentrations employed in this work (20-1280 mgl(-1)), the adsorption reached equilibrium within the first hour. The kinetic data corresponded well with the pseudo second-order kinetic model where the rate constants decreased as initial dye concentrations increased. At low dye concentrations (20-80 mgl(-1)), an increase in the adsorbent dosage resulted in a higher removal percentage of the dye, but a lower amount of dye adsorbed per unit mass (q). The adsorption isotherm followed both the Langmuir and Freundlich models within the temperature range employed in this work (18-70 degrees C). The highest maximum adsorption capacity (q(m)) was obtained at 50 degrees C. The enthalpy of adsorption was estimated at 14.87 kJmol(-1) suggesting a chemical adsorption mechanism.     

Phosphorus concentrations, loads, and sources within the Illinois River drainage area, northwest Arkansas, 1997-2008

In the Ozark Highlands and across the United States, effluent phosphorus (P) sources often have a profound impact on water column concentrations and riverine transport. This study evaluated (i) annual P loads at the Illinois River at Arkansas Highway 59 from calendar year 1997 through 2008, (ii) the relative contribution of effluent P sources to annual riverine P transport, (iii) longitudinal gradients in water column P concentrations downstream from several wastewater treatment plant effluent discharges, and (iv) changes in monthly P loads over the last decade. This study showed that annual P loads have ranged from 64,000 kg to over 426,000 kg and that P transport was positively correlated to hydrology (i.e., the amount of water delivered downstream). The relative contribution of P inputs from municipal facilities has decreased from 40% of the annual P load at the Illinois River at Arkansas Highway 59 to < 15% in recent years. Elevated P concentrations during base flow conditions were traced 45 river km upstream to one municipal effluent discharge, but all effluent discharges influenced P concentrations in the receiving streams. Most important, flow-adjusted monthly P loads showed two distinct trends over time. Flow-adjusted loads significantly increased from 1997 through 2002 and significantly decreased from 2002 through 2008. The concentrations and transport of P within the Illinois River drainage area are significantly decreasing from all the watershed management changes that have occurred, and monitoring should continue to determine if this decrease continues at the same rate over the next several years.     

Removal of phenol from aqueous solutions by adsorption

Experiments have been conducted to examine the liquid-phase adsorption of phenol from water by silica gel, HiSiv 3000, activated alumina, activated carbon, Filtrasorb-400, and HiSiv 1000. Experiments were carried out for the analysis of adsorption equilibrium capacities and kinetics. The adsorption isotherm model of the Langmuir-Freundlich type was the best to describe adsorption equilibrium data for phenol for the adsorbents studied. Results of kinetic experiments indicated that HiSiv 1000 had the highest rate of adsorption among the adsorbents studied and therefore more detailed studies were carried out with this adsorbent. The influence of particle size, temperature, and thermal regeneration on adsorption of phenol by HiSiv 1000 was evaluated. From particle size experiments it appeared that adsorption capacity of HiSiv 1000 did not change by changing the particle size, but the rate of adsorption decreased considerably by increasing the particle size. The effect of temperature on adsorption was studied by determining equilibrium isotherms for HiSiv 1000 at 25, 40, and 55 degrees C. The results showed that adsorption capacity decreased with increasing temperature. Thermal regeneration of HiSiv 1000 was performed at 360 degrees C. It was observed that adsorption capacity of HiSiv 1000 did not change after 14 regeneration cycles. Equilibrium experiments showed that the adsorption capacities of activated carbon and Filtrasorb-400 were several times higher than that of HiSiv 1000.     

CENTRAL NEBRASKA RIVER BASINS,NEBRASKA1

ABSTRACT: The Central Nebraska Basins (NAWQA) study unit includes the Platte River and two major tributaries, the Loup and Elkhorn Rivers. Platte River flows are variable in the western part of the study unit because of diversions, but the Loup and Elkhorn Rivers originate in an area of dune sand covered by grassland that generates consistent base flows. More frequent runoff in the eastern part of the study unit also sustains stream flow. Ground water in the study unit has no regional confining units and the system is a water table aquifer throughout. Macroinvertebrate and fish taxa at biological sampling sites in the state were related to stream flow. One of the four wetland complexes identified in the study unit includes habitat for threatened and endangered bird species. The study unit is an agricultural area that includes row crops, both irrigated and nonirrigated in the eastern and southern parts, and rangeland in the Sand Hills of the western part. A water quality assessment will be based on the differences in environmental setting in each of four subunits within the study unit.]     

XDA-1型大孔吸附树脂对水中氯仿的吸附性能

研究了XDA-1型大孔吸附树脂对用自来水配制的低浓度溶液中氯仿的动态吸附能力,以及浓度、流速、温度和pH等因素对吸附过程的影响.结果显示,采用XDA-1大孔树脂吸附水中的氯仿,其吸附效率可达99%以上,泄漏点前的吸附量为160mg/ml.采用热空气热解吸方式回收氯仿,回收率达85%,为含氯仿工业废水的处理提出一种新的处理工艺.     

Experimental investigation of adsorption capacity of anthill in the removal of heavy metals from aqueous solution

In the present work, the adsorption capacity of anthill was investigated as a low‐cost adsorbent to remove the heavy metal ions, lead (II) ion (Pb²⁺), and zinc (II) ion (Zn²⁺) from an aqueous solution. The equilibrium adsorption isotherms of the heavy metal ions were investigated under batch process. For the study we examined the effect of the solution's pH and the initial cations concentrations on the adsorption process under a fixed contact time and temperature. The anthill sample was characterized using a scanning electron microscope (SEM), X‐ray fluorescence (XRF), and Fourier transform infrared (FTIR) techniques. From the SEM analysis, structural change in the adsorbent was a result of heavy metals adsorption. Based on the XRF analysis, the main composition of the anthill sample was silica (SiO₂), alumina (Al₂O₃), and zirconia (ZrO₂). The change in the peaks of the spectra before and after adsorption indicated that there was active participation of surface functional groups during the adsorption process. The experimental data obtained were analyzed using 2‐ and 3‐parameter isotherm models. The isotherm data fitted very well to the 3‐parameter Radke–Prausnitz model. It was noted that Pb²⁺ and Zn²⁺ can be effectively removed from aqueous solution using anthill as an adsorbent.