Regionalization of Landscape Pattern Indices Using Multivariate Cluster Analysis

Regionalization, or the grouping of objects in space, is a useful tool for organizing, visualizing, and synthesizing the information contained in multivariate spatial data. Landscape pattern indices can be used to quantify the spatial pattern (composition and configuration) of land cover features. Observable patterns can be linked to underlying processes affecting the generation of landscape patterns (e.g., forest harvesting). The objective of this research is to develop an approach for investigating the spatial distribution of forest pattern across a study area where forest harvesting, other anthropogenic activities, and topography, are all influencing forest pattern. We generate spatial pattern regions (SPR) that describe forest pattern with a regionalization approach. Analysis is performed using a 2006 land cover dataset covering the Prince George and Quesnel Forest Districts, 5.5 million ha of primarily forested land base situated within the interior plateau of British Columbia, Canada. Multivariate cluster analysis (with the CLARA algorithm) is used to group landscape objects containing forest pattern information into SPR. Of the six generated SPR, the second cluster (SPR2) is the most prevalent covering 22% of the study area. On average, landscapes in SPR2 are comprised of 55.5% forest cover, and contain the highest number of patches, and forest/non-forest joins, indicating highly fragmented landscapes. Regionalization of landscape pattern metrics provides a useful approach for examining the spatial distribution of forest pattern. Where forest patterns are associated with positive or negative environmental conditions, SPR can be used to identify similar regions for conservation or management activities.     

First Step for an Ecological Risk Assessment to Evaluate the Impact of Diffuse Pollution in Lake Vela (Portugal)

Lake Vela, located in the Portuguese littoral-centre, is a temperate shallow lake exhibiting a high trophic status. This aquatic ecosystem has been potentially exposed to contamination generated by agricultural and livestock activities held in their drainage basin, which seriously compromise their health. This work summarizes some background information and presents the problem formulation step of the ERA. Therefore, it evaluates the characteristics of the stressor(s), describes the ecological system and receptors and suggests a conceptual model, which predicts the potential exposure pathways, relating suspected sources to the defined endpoints. This introductory step also described an analysis plan on the entire study, which includes a delineation of the assessment design, data needs, measures, and methods for conducting the analysis phase of the risk assessment process.     

Contamination Levels and Preliminary Assessment of the Technical Feasibility of Employing Natural Attenuation in 5 Priority Areas of Presidente Bernardes Refinery in Cubatão, São Paulo, Brazil

Five priority areas of potential impact by contaminants (API) were investigated at the Presidente Bernardes Refinery in Cubatão, São Paulo, Brazil with the following aims: (i) to identify both organic and inorganic contaminants present in soil and groundwater; (ii) to define the environmental conditions relevant for microbial activity at the site and (iii) to evaluate the feasibility of employing natural attenuation for treatment of the hydrocarbon contamination. One area (API 1) was an uncontrolled landfill, where waste materials from the refinery were deposited between 1954 and 1986, and four areas (API 4, 5, 7 and 11) were located in the operational section of the refinery. Soil contamination by regulated BTEX compounds (benzene, toluene, total xylenes) was restricted to two samples from API 1. Nonregulated ethylbenzene was detected in one soil sample from API 4, one from API 5 and two from API 1. No soil contained regulated PAH above threshold levels. Several nonregulated PAHs were found in 6 soil samples from API 1, 3 soil samples from API 4 and 1 soil sample from API 5. Site soils contained very high aluminium concentrations, but metal contamination was restricted to one soil sample from API 1, which contained nickel above threshold limits. BTEX contamination of groundwater was due mostly to benzene. Of the 17 PAH molecules tested, only naphthalene and 2-methylnaphthalene occurred in groundwater. The sum of total BTEX and total PAH exceeded 200 μg/L in only a few monitoring wells in API 4, 5 and 11 and was always below 2.640 μg/L. Be, Cd, Cr, Cu, Hg, Ni, Se, Ag, Tl and Zn were not detected in groundwater, which was contaminated in a few locations by aluminium (mostly below 1 mg/L), lead (<0.066 mg/L) and arsenic (<0.056 mg/L). S, K, Ca, Mg and Fe were present in groundwater in excess of physiological requirements for microbial growth, but low concentrations of N and P could become growth limiting. However, BTEX were efficiently degraded in saturated and unsaturated zone microcosms and nutrient amendments did not stimulate biodegradation rates measurably. The inorganic carbon pool in groundwater was up to one order of magnitude larger than the organic carbon pool. Total inorganic carbon (TIC) in API groundwater exceeded TIC of clean groundwater by factors of 2 (API 4), 6 (API 5, 7 and 11) or 10 (API 1). Most of the inorganic carbon incorporated into groundwater beneath the refinery originated from biodegradation in the unsaturated soil, which contained a microbiota (10⁶ cells/g on average) capable of growth with most of the pure (benzene, toluene, ethylbenzene and xylene) and mixed hydrocarbons tested (diesel oil, gasoline, naphtha, condensate, aromatic residue and fuel oil). A viscous hydrocarbon paste uncovered in API 1 was insoluble in water but dissolved in dichloromethane. Many organic components of this paste were biodegradable as evidenced by weight reduction of the hydrocarbon paste and by the growth of suspended and attached biomass in saturated zone microcosms, where the paste was the only carbon source. This study indicates that monitored natural attenuation may be a technically feasible and efficient means for plume control in API 1, 4 and 5, provided the plumes in API 4 and 5 are not expanding. This technique is not suitable for contaminant reduction in API 11.     

Twenty-year inter-annual trends and seasonal variations in precipitation and stream water chemistry at the Bear Brook Watershed in Maine, USA

Mean annual concentration of ${\textrm{SO}}_{4}^{2-}$ in wet-only deposition has decreased between 1988 and 2006 at the paired watershed study at Bear Brook Watershed in Maine, USA (BBWM) due to substantially decreased emissions of SO₂. Emissions of NO_x have not changed substantially, but deposition has declined slightly at BBWM. Base cations, ${\textrm{NH}}_{4}^{+}$ , and Cl^??? concentrations were largely unchanged, with small irregular changes of <1 μeq L^???1 per year from 1988 to 2006. Precipitation chemistry, hydrology, vegetation, and temperature drive seasonal stream chemistry. Low flow periods were typical in June–October, with relatively greater contributions of deeper flow solutions with higher pH; higher concentrations of acid-neutralizing capacity, Si, and non-marine Na; and low concentrations of inorganic Al. High flow periods during November–May were typically dominated by solutions following shallow flow paths, which were characterized by lower pH and higher Al and DOC concentrations. Biological activity strongly controlled ${\textrm{NO}}_{3}^{-}$ and K^?+?. They were depressed during the growing season and elevated in the fall. Since 1987, East Bear Brook (EB), the reference stream, has been slowly responding to reduced but still elevated acid deposition. Calcium and Mg have declined fairly steadily and faster than ${\textrm{SO}}_{4}^{2-}$ , with consequent acidification (lower pH and higher inorganic Al). Eighteen years of experimental treatment with (NH₄)₂SO₄ enhanced acidification of West Bear Brook’s (WB) watershed. Despite the manipulation, ${\textrm{NH}}_{4}^{+}$ concentration remained below detection limits at WB, while leaching of ${\textrm{NO}}_{3}^{-}$ increased. The seasonal pattern for ${\textrm{NO}}_{3}^{-}$ concentrations in WB, however, remained similar to EB. Mean monthly concentrations of ${\textrm{SO}}_{4}^{2-}$ have increased in WB since 1989, initially only during periods of high flow, but gradually also during base flow. Increases in mean monthly concentrations of Ca^2?+?, Mg^2?+?, and K^?+? due to the manipulation occurred from 1989 until about 1995, during the depletion of base cations in shallow flow paths in WB. Progressive depletion of Ca and Mg at greater soil depth occurred, causing stream concentrations to decline to pre-manipulation values. Mean monthly Si concentrations did not change in EB or WB, suggesting that the manipulation had no effect on mineral weathering rates. DOC concentrations in both streams did not exhibit inter- or intra-annual trends.     

Radioactive fallout in the United States due to the Fukushima nuclear plant accident

The release of radioactivity into the atmosphere from the damaged Fukushima Daiichi nuclear power plant started on March 12th, 2011. Among the various radionuclides released, iodine -131 ((131)I) and cesium isotopes ((137)Cs and (134)Cs) were transported across the Pacific Ocean and reached the United States on 17-18 March 2011. Consequently, an elevated level of fission products (131)I, (132)I, (132)Te, (134)Cs and (137)Cs were detected in air, water, and milk samples collected across the United States between March 17 and April 4, 2011. The continuous monitoring of activities over a period of 25 days and spatial variations across more than 100 sampling locations in the United States made it possible to characterize the contaminated air masses. For the entire period, the highest detected activity values ranged from less than 1 m Bq m(-3) to 31 m Bq m(-3) for the particulate (131)I, and up to 96 m Bq m(-3) for the gaseous (131)I fraction.     

Song length variation serves multiple functions in the white-crowned sparrow

A wide variety of hypotheses has been proposed to explain the structural diversity in bird song repertoires. Song diversity is frequently described in terms of song “types” or within-type “variants.” Male Puget Sound white-crowned sparrows, Zonotrichia leucophrys pugetensis, produce variants of their single adult song type by altering the number of repetitions of syllables in the terminal trill. We tested whether variation in trill length correlated with distance to the receiver and with signaling context as predicted by the eavesdropping avoidance hypothesis and the strategic signaling hypothesis. In accordance with the eavesdropping avoidance hypothesis, males sang variants with shorter trills, and sang quieter and less frequently when near their mate during the incubation phase than during spontaneous singing while unpaired. Males also sang variants with short trills, but at a high rate and variable amplitude when within 10 m of an opponent during close male–male territorial interactions. In agreement with the strategic signaling hypothesis, males decreased trill length immediately before chasing an opponent, but did not change length consistently prior to flight. We conclude that the occurrence of short quiet songs sung near the mate agrees with predictions of the eavesdropping avoidance hypothesis, while short songs sung near other males are best explained by the strategic signaling hypothesis. Trill length variation may be a conventional signal of aggressive intentions in male–male contests stabilized by receiver-imposed retaliation costs.     

Mercury photoreduction and photooxidation in lakes: Effects of filtration and dissolved organic carbon concentration

Mercury is a globally distributed, environmental contaminant. Quantifying the retention and loss of mercury is integral for predicting mercury-sensitive ecosystems. There is little information on how dissolved organic carbon(DOC) concentrations and particulates affect mercury photoreaction kinetics in freshwater lakes. To address this knowledge gap,samples were collected from ten lakes in Kejimkujik National Park, Nova Scotia(DOC: 2.6–15.4 mg/L). Filtered(0.2 μm) and unfiltered samples were analysed for gross photoreduction, gross photooxidation, and net reduction rates of mercury using pseudo first-order curves. Unfiltered samples had higher concentrations(p = 0.04) of photoreducible divalent mercury(Hg(II)RED)(mean of 754 ± 253 pg/L) than filtered samples(mean of 482 ± 206 pg/L);however, gross photoreduction and photooxidation rate constants were not significantly different in filtered or unfiltered samples in early summer. DOC was not significantly related to gross photoreduction rate constants in filtered(R~2= 0.43; p = 0.08) and unfiltered(R~2= 0.02; p = 0.71) samples; DOC was also not significantly related to gross photooxidation rate constants in filtered or unfiltered samples. However, DOC was significantly negatively related with Hg(Ⅱ)_(RED) in unfiltered(R2= 0.53; p = 0.04), but not in filtered samples(R~2= 0.04;p = 0.60). These trends indicate that DOC is a factor in determining dissolved mercury photoreduction rates and particles partially control available Hg(Ⅱ)_(RED) in lake water. This research also demonstrates that within these lakes gross photoreduction and photooxidation processes are close to being in balance. Changes to catchment inputs of particulate matter and DOC may alter mercury retention in these lakes and could partially explain observed increases of mercury accumulation in biota.     

Development of Emission Factors for Polyamide Processing

ABSTRACT

Emission factors for selected volatile organic compounds (VOCs) and particulate material were developed during processing of commercial grades of polyamide 6, polyamide 66, and polyamide 66/6 resins. A small commercial-type extruder was used, and melt temperatures ranged from 475 to 550 °F. An emission factor was calculated for each substance measured and is reported as pounds released to the atmosphere per million pounds of polymer resin processed. Scaled to production volumes, these emission factors can be used by processors to estimate emission quantities from similar polyamide extrusion operations.     

automated data handling for small authorities

The body of information presented in this paper is directed to administrators of smaller authorities—defined, arbitrarily, as those with small staff and not embracing large metropolitan areas. As their activities increase, viable programs are likely to produce prodigious quantities of data, necessitating the use of modern computers for most efficient analysis.

Remote links with high-speed time sharing computers provide a means for smaller authorities to satisfy this need. The capabilities of a large computer can be brought into the local office to handle (a) administrative and enforcement problems, (b) technical data analysis, and (c) instructional needs.

A data handling system being developed for use by the Northwest Air Pollution Authority is described, together with an examination of its potential utility to the Authority as its activities increase.