Diel and seasonal methane flux across water–air interface of a subtropic eutrophic pond

Abstract

Methane, which is an important greenhouse gas, has received less attention regarding its flux in ponds. Small ponds, whose area only occupies approximately 8.6%, comprise the bulk of CH₄ efflux from lakes and ponds on a global scale. However, temporal and spatial variability, as well as consequences of CH4 fluxes from ponds, remains unknown. The aim of this study was to examine using 4 field experiments diel methane (CH₄) fluxes from a subtropic eutrophic pond in different seasons. For the eutrophic pond, the mean CH₄ efflux for all seasons was 1.772?mg/m²/h, and CH₄ emissions in summer were approximately three-fold higher than total of winter, spring, and autumn. Methane diffusive emissions were positively correlated with water temperature, dissolved oxygen (DO) and air temperature but negatively related to pH and to the difference between water temperature and air temperature. The diel diffusive CH₄ flux among different seasons varied significantly. The CH₄ bubble flux did not differ markedly in winter, spring and autumn, but the quantity in summer was significantly different from all other seasons. Bubble is the main pathway for CH₄ emissions. The CH₄ ebullition flux accounts for 66, 71, 97 and 98% of the total in winter, spring, summer and autumn, respectively. On an annual scale, the CH₄ ebullition flux accounts for 77% of the total fluxes (diffusive?+?ebullitive). Our results show that further investigations need to be carried out to probe temporal variability of CH₄ fluxes in ponds located in different climate zones for better understanding of the global carbon budget, which is critical to predict future climate changes.     

Inductively coupled plasma‐atomic emission spectroscopy in air and water pollution analysis†

The inductively coupled plasma (ICP), when employed as an excitation source in optical atomic emission spec.troscopy (AES), is finding widespread utilization for single and multielement inorganic trace analysis of pollutants. The recent availability of commercial ICP‐AES instrument systems has stimulated applications for the determination of metals and metalloids in diverse materials ranging from air particulates and fly ash to industrial effluents, sewage, and hard, soft, and saline waters.

The capabilities and limitations of ICP‐AES for applications in air and water pollution analysis are reviewed, and a number of recent examples presented.     

Aqueous high‐temperature chemistry of arsenic‐containing compounds in water at 300°C

Arsenic compounds, and especially organo‐arsenic derivatives, are highly toxic and many have been manufactured as chemical warfare agents. This study was designed to provide background information relevant to the potential application of aquathermolysis techniques for the detoxification of such potent military warfare agents. Six arsenic‐containing compounds with structural features which mimic known agents were studied in neutral superheated water: 4‐aminophenylarsine oxide, 4‐arsanilic acid, 4‐nitrophenylarsonic acid, 5, 10‐dihydro‐10‐ethylphenarsazine, tetraphenylarsonium chloride hydrate, and (3‐cyanopropyl)dimethyl(2‐phenethyl)arsonium bromide. Most of these compounds were moderately susceptible to hydrolysis for 1h at 300°C. o‐ and p‐Aminosubsituted arsenic compounds were more reactive than compounds with an electron‐withdrawing group substituent. Aromatic C—As bonds were more resistant to cleavage than aliphatic C—As bonds.     

Concentrations of polychlorinated dibenzo‐p‐dioxins and dibenzofurans in outdoor air of North‐Rhine‐Westphalia,Germany

Measurements of polychlorinated dibenzo‐p‐dioxins (PCDD) and dibenzofurans (PCDF) in outdoor air of North‐Rhine‐Westphalia were carried out. Fifty‐six samples were taken at different sites in areas of different land use and emission structures. A special filter system allowed analysis of the gas and particle phases separately. It was found that higher chlorinated PCDD/PCDF (7 or 8 chlorine atoms) are collected on glass fiber filter and lower chlorinated PCDD/PCDF (tetra‐ and penta‐CDD/CDF) are absorbed on polyurethane foam. The following isomers were determined: OCDD, OCDF and 11 isomers with chlorine substitution in 2,3,7,8‐position as well as the sum of TCDD, PeCDD, HxCDD, HpCDD, TCDF, PeCDF, HxCDF, HpCDF and the sum of PCDD (4–8) and PCDF (4–8). No 2,3,7,8‐TCDD could be detected but 2,3,7,8‐TCDF was found at 15 sites. Mean concentration in the Rhine‐Ruhr‐District for the sum of PCDD (4–8) and PCDF (4–8) was 3.2pg/m³ and 5.5pg/m³ respectively. Detection limit for TCDD and PCDD/PCDF (5–8) was 0.1–0.2 pg/m³ and 0.005–0.015 pg/m³ respectively. There is no significant indication that 2,3,7,8‐chlorinated isomers of PCDD/PCDF are predominantly decomposed by photochemical reactions in outdoor air.     

Input and fate of anthropogenic estrogens and gadolinium in surface water and␣sewage plants in the hydrological basin of Prague (Czech Republic)

The concentration of the estrogens 17β-estradiol, estriol, estrone, 17α-ethinylestradiol, mestranol and norethisterone and of the anthropogenic gadolinium (Gd_ant) has been determined in the creeks and rivers, sewage treatment plants and water works of the city of Prague. The rapid degradation of estrogens in surface water allows the estrogen concentration gradient to be used as a very precise and sensitive guideline by which to pin-point sewage leaks into surface run-off water. The rather conservative behavior of Gd_ant in surface and ground water documents in the present case the presence of sewage water in the surface water cycle.     

Diffusional mass transfer coefficient at the water–sediment interface for wind-induced flow in very shallow lagoons

Very shallow lagoons that are a few centimeters deep are common in the arid Andes of Northern Chile, Argentina, Bolivia and Perú. The dynamics of these lagoons are dominated by the water–sediment interface (WSI) and strong afternoon winds. Although many studies have examined the diffusional mass transfer coefficients (k _t ) of open channel flows, estimates for wind-induced flows are still unknown. The aim of this article is to propose and validate an analytical expression for computing k _t at the WSI for wind-induced flow. The laboratory measurements were conducted in a wind tunnel with a water tank of variable depth located at its downwind end. Natural muddy sediments were placed in the middle of the tank so that the dissolved oxygen (DO) was consumed in the sediments. The diffusional mass transfer coefficient that characterizes the DO uptake in the sediment was obtained from DO micro-profiles measured with an OX-25 Unisense microelectrode. Water velocity profiles were measured with a 2D side-view Sontek acoustic doppler velocimetry (ADV), and the wind shear velocity was computed based on wind velocity profiles that were measured with an Extech hot-wire anemometer. A total of 16 experiments were conducted with different water depths and wind shear stresses. The constants required by the model were determined from these experiments, and the analytical expression was successfully validated by the laboratory observations. The analytical expression obtained for computing k _t was also validated with field observations that were conducted in October, 2012, in Salar del Huasco, Northern Chile (20.274° S, 68.883° W, 3800 m above sea level). The comparison between the observed and predicted values of k _t provides a determination coefficient of r ² = 0.48 and a p value < 0.01. The results show that the value of k _t for wind-induced flow is proportional to the wind shear velocity and the inverse of the Reynolds number of the wind-induced current.     

Transport of metanil yellow in the rat plasma and interaction of its metabolite,p‐aminodiphenylamine with serum proteins

Binding affinity of metanil yellow and its breakdown product p‐aminodiphenylamine to serum proteins has been studied employing chromatographic separation on Sephadex G‐200 and by paper and polyacrylamide gel electrophoresis. Metanil yellow has more affinity towards albumin than to globulins. The complexing is presumably through electrostatic forces. p‐Aminodiphenylamine on the other hand, preferably binds to globulin fractions of serum protein. However, a stable binding with BSA alone was also observed. The binding was quite stable and was accompanied by a shift in absorbance from 430 nm to 500 nm. Aspartic acid moiety of protein was found to be one of the units involved in the binding of p‐ADPA to proteins.     

Effects of bedform migration on nutrient fluxes at the sediment–water interface: a theoretical analysis

Environmental Fluid Mechanics - Nutrient fluxes at the sediment–water interface are essential for water quality and aquatic ecosystems. In this study, a unified expression for the sediment...     

Body and resource size at the land–sea interface

Body size in animals varies with many parameters, amongst them taxonomic affiliation, lifestyle and ambient environment oxygen levels. Size has considerable implication to possibilities for animals; for example, parasites need to be small and top predators large. Body size and resource requirements (shell size) were investigated across the land–sea interface in hermit crabs (Crustacea: Malacostraca: Decapoda) and snails (Mollusca: Gastropoda: Prosobranchia). These are two of the few taxa to occur in the sea, on the shore and on land as residents. Both taxa are also appropriate for such an analysis as they are abundant, speciose, cohabit the same environments and are linked—gastropod shells are a critical resource to hermit crabs. Both the maximum and mean sizes of hermit crab species showed parabolic relationships with shore height, decreasing from the sublittoral and supralittoral to the eulittoral. Average maximum size of gastropods exhibited a similar intertidal minimum although variability was high. It is suggested that this pattern is robust: not only did two distantly related taxa show the same pattern, but neither region nor site contributed significantly to total variability. The mass of resources (gastropod shells) used by hermit crabs, however, showed a converse pattern. The smallest shells (relative to hermit crab body size) were used in the sublittoral and supralittoral. Response to environmental stress and predation pressure are offered as two alternate theories to explain the observed body dwarfism and resource gigantism in the intertidal zone.Communicated by J.P. Thorpe, Port Erin     

Abundance and variability of microorganisms and transparent exopolymer particles across the ice–water interface of melting first-year sea ice in the Laptev Sea (Arctic)

The distribution and abundance of transparent exopolymer particles (TEP) was determined in and below pack ice of the Laptev Sea from July to September 1995. Samples were collected from the lowermost 10 cm of ice floes and at 10 cm below the ice–water interface. Abundance of bacteria, protists and TEP was determined, and the sea ice–water boundary layer was characterized using temperature, salinity and molecular viscous shear stress. TEP, with a distinct size distribution signal, were found in highest concentrations inside the sea ice, ranging from not detectable to 16 cm² l⁻¹ (median: 2.9 cm² l⁻¹). In the water, concentrations were one order of magnitude lower, ranged from below detection to 2.7 cm² l⁻¹ (median: 0.2 cm² l⁻¹) and decreased after the middle of August, whereas abundances of autotrophic flagellates (AF), diatoms, heterotrophic flagellates (HF) and ciliates increased. The abundance of TEP decreased with its size in all samples following a power law relationship. The relation of TEP to the microbial community differed between the sea ice and water, being positively correlated with bacteria and diatoms in the ice and negatively correlated with HF in the sea water. The presence of a pycnocline significantly influenced the abundance of organisms, diatom composition and TEP concentrations. Pennate diatoms dominated by Nitzschia frigida were most abundant inside the ice. Though bacteria have the potential to produce exopolymeric substances (EPS), the results of this study indicate that the majority of TEP at the ice–water interface in first-year Arctic summer pack ice are produced by diatoms. Received: 19 August 1999 / Accepted: 4 July 2000     

Effects of the Ellagic acid on the N‐Acetyltransferase activity and Acetylation of 2‐aminofluorene in the rat

The effects of the ellagic acid on the in vitro and in vivo acetylation of 2‐aminofluorene were investigated in male Sprague‐Dawley rats. For in vitro examination, cytosols with or without ellagic acid co‐treatment showed different percentage of 2‐aminofluorene acetylation. For in vivo examination, pre‐treatment of male rats with ellagic acid (10 mg/kg) 24h prior to the administration of 2‐aminofluorene (50 mg/kg) resulted in a 26% and 29%, respectively, decrease in the urinary and fecal recovery of N‐acetyl‐2‐aminofluorene, and a 37% decrease in the metabolic clearance of 2‐aminofluorene to N‐acetyl‐2‐aminofluorene. This is the first demonstration that ellagic acid decrease the N‐acetylation of carcinogens in vitro and in vivo.     

Sorption‐desorption kinetics of some organochlorine insecticides in silt‐water suspensions

Kinetic (batch) sorption and desorption experiments for some organochlorine insecticides in silt‐water suspensions are described. The effect of possible experimental artifacts on the results is examined. The influence of the silt/water ratio on the linear sorption coefficient and on the “nonextractable”; solute fraction is determined. The sorption process is described in terms of some kinetic models.     

Total phosphorus concentrations in surface water of typical agro- and forest ecosystems in China, 2004–2010

The concentrations of total phosphorus （TP） from 83 surface water sampling sites in 29 of the Chinese Ecosystem Research Network （CERN） monitored ecosystems, representing typical agro- and forest ecosystems, were assessed using monitoring data collected between 2004 and 2010 from still and flowing surface water. Results showed that, TP concentrations were significantly higher in agro-ecosystems than those in forest ecosystems both for still and flowing surface water. For agro- ecosystems, TP concentrations in the southern area were significantly higher than those in the northern and north- western areas for both still and flowing surface water, however no distinct spatial pattern was observed for forest ecosystems. In general, the median values of TP within agro- and forest ecosystems did not exceed the Class V guideline for still （0.2mg.L-1） or flowing （0.4mg.L-1） surface water, however, surface water at some agro- ecosystem sampling sites was frequently polluted by TE Elevated concentrations were mainly found in still surface water at the Changshu, Fukang, Linze and Naiman monitored ecosystems, where exceedance （〉 0.2 mg.L-1） frequencies varied from 43% to 78%. For flowing water, elevated TP concentrations were found at the Hailun, Changshu and Shapotou monitored ecosystems, where exceedance （〉 0.4 mg. L-1） frequencies varied from 29% to 100%. Irrational fertilization, frequent irrigation and livestock manure input might be the main contributors of high TP concentrations in these areas, and reduced fertilizer applications, improvements in irrigation practices and centralized treatment of animal waste are necessary to control P loss in these TP vulnerable zones.     

Long‐term desorption kinetics of Cu2+from biosorbent in water and seawater

A long‐term study of the desorption kinetics of Cu²⁺from biosorbent materials in water and seawater environments was carried out. The biosorbents were un‐treated and pre‐treated biomass of marine alga Durvillaea potatorum.The pre‐treatment of the biomass was carried out with calcium chloride (CaCl₂) solution followed by thermal treatment. The biosorbents were loaded with Cu²⁺in batch adsorption experiments and the desorption kinetics were measured in water and seawater in static batch desorption experiments for a period over 10 months. The physical and structure characteristics of the biosorbents were also examined under a microscope. The un‐treated biosorbent structure completely broke down in 2 and 1 months in water and seawater environments, respectively. The pre‐treatment procedure applied improved the biosorbent stability and its long term desorption rate was extremely low.     

Determination of phenol,cresols and xylenols in workplace air using XAD‐2 sorbent cartridges

A method for sampling and analysis of phenolic compounds in workplace atmospheres using Amberlite XAD‐2 sorbent tubes has been laboratory and field tested. After extraction of the adsorbed phenols with methylene chloride, the concentrated extract was analyzed by capillary column gas chromatography coupled with a flame ionization detector or a mass spectrometer. For a 3L air sample, the method has a detection limit for phenol, cresols, alkyl‐substituted phenols and xylenols of 0.3 mg/m³ using gas chromatography with flame ionization detection (GC/FID) analysis and 0.07 mg/m³ using gas chromatography mass spectroscopy/selected ion monitoring GC‐MS/SIM. Evaluation tests conducted in the laboratory indicated recoveries >85% for a wide range of phenols, cresols, xylenols and other alkyl‐substituted phenols and resorcinol. Sampling conditions were established to ensure that no breakthrough occurred for a predetermined sample volume of three (3) liters even in humid atmospheres. Stability tests indicated that for storage of up to 2 weeks at 4°C, only resorcinol showed a significant reduction in sample recovery. The proposed method and NIOSH Method 3502 were compared for the determination of phenol concentrations in air samples collected at a plant processing phenolic resins. Phenol was positively identified in the XAD sample using GC‐MS/SIM and was detected at concentrations of 40–50% of the total phenols detected using NIOSH Method 3502. This difference is attributed to the airborne paniculate matter which is known to contain bisphenols that will contribute to the total phenolic content sampled in Method 3502, but not on the XAD sample.     

Shared ways of thinking in Brazil about the science–practice interface in ecology and conservation

The debate in the literature on the science–practice interface suggests a diversity of opinions on how to link science and practice to improve conservation. Understanding this diversity is key to addressing unequal power relations, avoiding the consideration of only dominant views, and identifying strategies to link science and practice. In turn, linking science and practice should promote conservation decisions that are socially robust and scientifically informed. To identify and describe the viewpoints of scientists and decision makers on how the science–practice interface should work in order to improve conservation decisions, we interviewed Brazilian scientists (ecologists and conservation scientists, n = 11) and decision makers (n = 11). We used Q methodology and asked participants to rank their agreement with 48 statements on how the science–practice interface should work in order to improve conservation decisions. We used principal component analysis to identify shared viewpoints. The predominant viewpoint, shared by scientists and decision makers, was characterized by valuing the integration of scientific and strategic knowledge to address environmental problems. The second viewpoint, held mostly by decision makers, was distinguished by assigning great importance to science in the decision-making process and calling for problem-relevant research. The third viewpoint, shared only by scientists, was characterized by an unwillingness to collaborate and a perception of scientists as producers of knowledge that may help decision makers. Most participants agreed organizations should promote collaboration and that actors and knowledge from both science and practice are relevant. Disagreements concerned specific roles assigned to actors, willingness to collaborate, and organizational and institutional arrangements considered effective to link science and practice. Our results suggest there is ample room for collaborations and that impediments lie mainly in existing organizations and formal institutional arrangements rather than in negative attitudes between scientists and decision makers.     

Photodegradation of pesticides .1. Photolysis rates and half‐life of acylanilides and their major metabolites in water

The photolysis in water solution of three fungicides (Metalaxyl, Benalaxyl, and Furalaxyl) was studied under artificial light. At λ = 254 Benalaxyl and Furalaxyl underwent fast degradation with rearrangement reactions less complex than those of Metalaxyl. Under A = 254–290 the photolysis was very fast and Benalaxyl and Furalaxyl show a common behaviour. This was found to be a kinetic consecutive process leading, at first, to N‐2,6‐xylyl‐D,L‐alaninate (II), which was degraded to 2,6‐dimethylaniline (IV). This amine gives unknown products. Metalaxyl underwent a parallel/consecutive photodegradtion to give (II) and N‐(methoxyacetyl)‐2,6‐dimethylaniline (VI). While (II) was easily converted to (IV) as earlier, (VI) was more stable to photolysis. Under λ > 290 all the fungicides shown very slow degradation with pseudo first order rate constants. The photoproducts were degraded faster than the parent compounds by factors from 13 to 1800. The presence of photosensitizer in water (humic acids or acetone) resulted in total decomposition of fungicides and of their photoproducts.     

The occurrence of disinfection by‐products in Taiwan drinking water

In this study, samples were taken from six conventional water treatment plants for disinfection by‐products analysis. Results from the analysis revealed that trihalomethanes (THMs) concentrations in all samples were below regulatory levels (100 μg/L). Although the national standard for haloacetic acids (HAA5) has not yet been promulgated in Taiwan, samples from two water plants contained HAA5 concentrations exceeding the USEPA limit (MCL of HAA5 of Stage 1, 60 μg/L). THMs and HAA5 were found to be the major disinfection by‐products in all water treatment plants. It was noted that the concentration of HAA5 in most samples was higher than that of the trihalomathanes. However, the formation potential of THM (THMFP) was found to be higher than that of HAA (HAAFP). Good correlation also was found between THMFP (or THMFP) and HAA5 (or THMs). In evaluating the performance of the treatment processes, it was found that conventional water treatment processes followed by activated carbon were effective in removing disinfection by‐products (DBPs) from source water with pre‐ozonation. The treatment processes were at their optimum performance in removing contaminants when O₃/TOC₀ was held at 0.75.     

Turbulent air–water flows in hydraulic structures: dynamic similarity and scale effects

In hydraulic structures, free-surface aeration is commonly observed: i.e., the white waters. The air bubble entrainment may be localised (hydraulic jumps, plunging jets) or continuous along an interface (water jets, chutes). Despite recent advances, there are some basic concerns about the extrapolation of laboratory results to large size prototype structures. Herein the basic air bubble entrainment processes are reviewed and the relevant dynamic similarities are discussed. Traditionally, physical studies are conducted using a Froude similitude which implies drastically smaller laboratory Reynolds numbers than in the corresponding prototype flows. Basic dimensional analyses are developed for both singular and interfacial aeration processes. The results are discussed in the light of systematic investigations and they show that the notion of scale effects is closely linked with the selection of relevant characteristic air–water flow properties. Recent studies of local air–water flow properties highlight that turbulence levels, entrained bubble sizes and interfacial areas are improperly scaled based upon a Froude similitude even in large-size models operating with the so defined Reynolds numbers ρ _w × q _w/μ _w up to 5 E+5. In laboratory models, the dimensionless turbulence levels, air–water interfacial areas and mass transfer rates are drastically underestimated.     

Differential effects of increased corticosterone on behavior at the nest and reproductive output of chick-rearing Adélie penguins

Glucocorticoid hormones (GCs) are important mediators of physiological and behavioral responses to stress. While many studies have evaluated the environmental, behavioral, or physiological correlates of GCs and their effects on reproductive performances, further work is needed to clarify the relationship between GCs and fitness. Assessing the effects of increased GC levels on specific behaviors of breeding animals should improve our understanding of how GCs affect parental care. In this experimental study, we measured the effects of an experimental increase in corticosterone (CORT, the main avian GC) levels on the behavior of free-living male Adélie penguins (Pygoscelis adeliae) within the colony, their reproductive output, and the indirect consequences of both on the behavior of their partners. We show that increased CORT levels in males decreased their foraging time at sea while increased their attendance at the nest, although their attentiveness toward the nest itself decreased. In addition, treated males spent more time on comfort behaviors (e.g., preening), vocalizing, and engaging in positive social interactions relative to controls. Treatment further affected the behavior of their partners, but not chick begging and feeding rates. Penguins with increased CORT levels also exhibited decreased reproductive output. Previous studies of Adélie penguins in different life history stages and environmental conditions suggest that the consequences of CORT treatment on reproductive performance are context-dependent. In addition to the potential delay in the effects of increased CORT levels on reproduction, this context dependence should be taken into account when studying the behavior of free-living animals in relation to stress-inducing situations.