Chih-Feng Chen

Assessment of toxicity of polycyclic aromatic hydrocarbons in sediments of Kaohsiung Harbor, Taiwan

Polycyclic aromatic hydrocarbon (PAH) contamination and toxicity levels in the surface sediments of Kaohsiung Harbor, Taiwan were evaluated using sediment quality guidelines (SQGs) and toxic equivalent factors. Eighty surface sediment samples were collected from twenty locations in Kaohsiung Harbor for PAH analysis using gas chromatography/mass spectrometry (GC/MS). Concentrations of total PAHs varies from 34.0 to 16,700 ng/g with a mean concentration of 1490±2689 ng/g. The spatial distribution of PAHs reveals that PAH concentration is relatively higher in the river mouth regions, especially in the Salt River mouth where it gradually diminishes toward the harbor region. Distributions of PAHs, during both the wet and dry seasons, show that PAHs are more easily disbursed in the receiving sea water thereby leading to a wider range of chemical distribution. Hence, most of the chemicals accumulate in the harbor water channel. Diagnostic ratios show that the possible source of PAHs in the southern industrial area of the harbor could be coal combustion while in the other zones it could be petroleum combustion and/or a mixed sources. The toxic equivalent concentrations (TEQ(carc)) of PAHs varied from 3.9 to 1970 ng TEQ/g. The higher total TEQ(carc) values were found in the southern industrial area of the harbor. As compared with US sediment quality guidelines, the observed levels of PAHs in the industrial zone exceeded the effects range low (ERL), which will eventually cause acute biological damage. Based on the analyses using the SQGs, surface sediments from Kaohsiung Harbor were moderately contaminated and most samples have a low probability of toxicity pollution, except for the Salt River mouth situated in the south Kaohsiung Harbor area. This area has a medium to high probability of toxicity pollution.

Assessing of natural attenuation and intrinsic bioremediation rates at a petroleum-hydrocarbon spill site: laboratory and field studies.

Natural attenuation is a passive remedial approach that depends upon natural processes to degrade and dissipate contaminants in soil and groundwater. Intrinsic bioremediation is believed to be the major process among the natural attenuation mechanisms that account for the reduction of contaminant concentrations. In this study, a mass flux approach was used to calculate the contaminant mass reduction at a petroleum-hydrocarbon spill site. The mass flux technique is a simplified mass balance procedure, which is accomplished using the differences in total contaminant mass flux across two cross sections of the contaminant plume. The mass flux calculation results show that up to 86% of the dissolved total benzene, toluene, ethylbenzene, and xylene (BTEX) isomers removal was observed via natural attenuation at this site. Evidence for the occurrence of natural attenuation was the decreased contaminant mass flux through the plume cross sections along the transport path and limited spreading of the BTEX plume. Evi...

Distribution of Phthalate Esters in Sediments of Kaohsiung Harbor, Taiwan

The major objectives of this research are to study the species and concentration of phthalate esters (PAEs), an organic endocrine disruptor, in the sediments of Kaohsiung Harbor, Taiwan. Twenty monitoring stations were installed in the waterways of Kaohsiung Harbor to collect sediment samples for analyzing six species of PAEs. Results of laboratory analyses show that concentrations of ΣPAE6 in the harbor sediment are between 0.40 and 34.8 mg/kg with an average of 5.02 mg/kg. Among all chemicals, di-(2-ethylhexyl) phthalate (DEHP) is the major species that constitutes 92% of all chemicals found in the sediment. Where the spatial distribution of the chemicals is concerned, all rivers (i.e., Love River, Canon River, and Salt River) show the highest concentrations near the mouth where they discharge into the harbor. This indicates that major sources of pollution originate from the upstream municipal and industrial wastewater discharges. Distributions of PAEs during both wet and dry seasons show that PAEs are more easily disbursed in the receiving sea water, leading to a wider range of chemical distribution, and hence most of the chemicals are accumulated in the harbor water channel. The assessment of ecological toxicity indicates that concentrations of the 88% DEHP found in the sediment are higher than environmental risk limits (ERLs), implying that the Kaohsiung Harbor sediments pose potential risks to the local ecological system. Hence, an effective PAE management and control strategy must be developed and implemented in order to improve the harbor sediment quality, and keep the harbor ecological environment free from the interference of chemicals that interrupt endocrine hormones.

Age and growth of albacore Thunnus alalunga in the North Pacific Ocean.

The age and growth of North Pacific albacore Thunnus alalunga were investigated using obliquely sectioned sagittal otoliths from samples of 126 females and 148 males. Otolith edge analysis indicated that the identified annulus in a sagittal otolith is primarily formed during the period from September to February. The assessments of the fish age at first annulus formation indicated that the first annulus represents an age of <1 year. This study presents an age estimate (0·75 years) for the formation of the first annulus. The oldest fish ages observed in this study were 10 years for females and 14 years for males. The von Bertalanffy growth parameters of females estimated were L(∞) = 103·5 cm in fork length (L(F) ), K = 0·340 year(-1) and t(0) = -0·53 years, and the parameters of males were L(∞) = 114·0 cm, K = 0·253 year(-1) and t(0) = -1·01 years. Sexual size dimorphism between males and females seemed to occur after reaching sexual maturity. The coefficients of the power function for expressing the L(F) -mass relationship obtained from sex-pooled data were a = 2·964 × 10(-5) and b = 2·928.

Vertical profile, contamination assessment, and source apportionment of heavy metals in sediment cores of Kaohsiung Harbor, Taiwan

Six sediment cores collected at the Kaohsiung Harbor of Taiwan were analyzed to evaluate their vertical profiles, enrichments, accumulations, and source apportionments of heavy metals. This was performed to investigate any potential ecological risks posed by heavy metals. Results indicated that the mean heavy metal content (mg kg-1) in the six sediment cores was as follows: Hg (0.4-6.4), Cd (<0.05-2.4), Cr (18-820), Cu (16-760), Pb (31-140), and Zn (76-1900). The patterns of heavy metal content in the sediment cores differed substantially among the four river mouths. However, the vertical profiles of metals were relatively stable, indicating that wastewater has the constant characteristics and has been discharged into the rivers for a long period of time. Results of pollution assessment of enrichment factor, geo-accumulation index, and pollution load index revealed that river mouths experience severe enrichment, strong accumulation, and high contamination from the primary heavy metals. It was not consistent in the assessment results of mean effect range median quotient, potential ecological risk index, and total toxic unit method. Potential ecological risks caused by Hg in the sediments at Canon River and Love River mouths on aquatic organisms were extremely high. The estimates derived from the receptor modeling of multiple linear regression of the absolute principal component scores indicated that the contributions of the composite heavy metals derived from the Canon River and the Love River on the potential toxicity and risks to the water environment of Kaohsiung Harbor were highest, followed by those derived from Salt River and Jen-Gen River.

Vertical profile, sources, and equivalent toxicity of polycyclic aromatic hydrocarbons in sediment cores from the river mouths of Kaohsiung Harbor, Taiwan

Six sediment cores collected at four contaminated river mouths and two harbor entrances in Kaohsiung Harbor (Taiwan) were analyzed to evaluate the sources and potential toxicity of polycyclic aromatic hydrocarbons (PAHs). PAHs presented the wide variations ranging from 369±656 to 33,772±14,378 ng g(-1) at the six sampling sites. The composition of PAHs presented a uniform profile reflecting the importance of atmospheric input from vehicle exhausts or coal combustion in the river mouths. PAHs diagnostic ratios indicated a stronger influence of coal combustion in the Salt River mouth and the prevalence of petroleum combustion and mixed sources in the other rivers and harbor entrances. PAHs toxicity assessment using the mean effect range-median quotient (m-ERM-q: 0.011-1.804), benzo[a]pyrene-toxicity equivalent (TEQ(carc): 22-2819 ng TEQ g(-1)), and dioxin-toxicity equivalent (TEQ(fish): 37-5129 pg TEQ g(-1)) identified the Salt River mouth near the industrial area of the harbor as the most affected area.

Metal Speciation and Contamination in Dredged Harbor Sediments from Kaohsiung Harbor, Taiwan

The status of metal speciation and contamination of sediments in Kaohsiung Harbor, Taiwan, was evaluated by a five-step sequential extraction procedure (exchangeable, carbonate, Fe–Mn oxides, organic matter, and residual). Eleven dredged sediment samples from various locations in the harbor were characterized in terms of heavy metals, grain size, and total organic carbons. Results showed that Hg, Pb, Cd, Cr, Cu, Zn, Ni, and Mn had different species composition patterns. The degree of sediment contamination was determined for an individual contamination factor (ICF) and a global contamination factor (GCF); results showed that Kaohsiung Harbor had a high potential risk for Pb, Cd, Cr, and Cu. Based on GCF values, the results showed that those stations, located in the vicinity of the river mouth, fish port, and industrial sites, contributed high potential risk to Kaohsiung Harbor. The potential risk of heavy metals to the environment was assessed for risk using the risk assessment code (RAC) and results showed that Pb, Cd, Zn, and Mn generally created a medium to high risk, and Hg, Cr, Cu, and Ni generally created a low to medium risk.

Removal of polycyclic aromatic hydrocarbons from sediments using sodium persulfate activated by temperature and nanoscale zero-valent iron

The oxidation of 16 polycyclic aromatic hydrocarbons (PAHs) compounds in sediments by sodium persulfate (Na2S2O8) simultaneously activated by temperature and nano zero-valent iron (nZVI) as the source of catalytic ferrous iron was investigated. The effect of various controlling factors, including S2O82− (0.017–170 g/L), nZVI (0.01–1 g/L), and temperature (50–70 °C) were performed. The efficiency to remove PAHs was 10.7–39.1% for unactivated persulfate. The treated sample had over 50% of the persulfate still remaining from an initial persulfate dose of 170 g/L, whereas less than 1% of the persulfate remained from an initial persulfate dose of 0.017, 0.17, and 1.7 g/L. Adequate persulfate (170 g/L) must be present because it is the source of the sulfate radicals responsible for the degradation of PAHs. Results indicated that increasing temperature and the addition of nZVI into a persulfate-slurry system could enhance the persulfate oxidation process. The best removal efficiency (90%) was achieved after 24 hr while adding nZVI (0.01 g/L) to persulfate (170 g/L) at temperature of 70 °C. The results suggested that nZVI assisted persulfate oxidation without elevating temperature may be a suitable and economic alternative for the ex situ treatment of PAH-contaminated sediments. Implications: Nano zero-valent iron (nZVI) has been successfully applied to transform/degrade contaminants in soils and water. Additionally, nZVI has been used as a catalyst to activate persulfate for the treatment of various contaminants. In this study, with the support of temperature, nZVI-persulfate oxidation system for treatment of PAH-contaminated sediments was improved significantly and the treated sediment could meet remediation goals.

Distribution and contamination status of chromium in surface sediments of northern Kaohsiung Harbor, Taiwan.

The distribution, enrichment, accumulation, and potential ecological risk of chromium (Cr) in the surface sediments of northern Kaohsiung Harbor, Taiwan, China were investigated. Sediment samples from ten locations located between the river mouths and harbor entrance of northern Kaohsiung Harbor were collected quarterly in 2011 and characterized for Cr, aluminum, water content, organic matter, total nitrogen, total phosphorous, total grease, and grain size. Results showed that the Cr concentrations varied from 27.0 to 361.9 mg/kg with an average of (113.5 +/- 87.0) mg/kg. High Cr concentration was observed near the Jen-Gen River mouth. The mean Cr concentration was high at 255.5 mg/kg, which was at least 2 to 7 times than that of other sites. This might imply significant Cr contribution from upstream receiving tanneries wastewater into the Jen-Gen River. The spatial distribution of Cr reveals relatively high in the river mouth region, especially in Jen-Gen River, and gradually diminishes toward the harbor entrance region. This indicates that the major sources of Cr pollution from upstream industrial and municipal wastewaters discharged along the river bank; and Cr may drift with sea current and be dispersed into open sea. Moreover, Cr concentrations correlated closely to the physical-chemical properties of the sediments, which suggested the influence of industrial and municipal wastewaters discharged from the neighboring industrial parks and river basins. Results from the enrichment factor and geo-accumulation index analyses imply that the Jen-Gen River sediments can be characterized as moderate enrichment and none to medium accumulation of Cr, respectively. However, results of potential ecological risk index indicate that the sediment has low ecological potential risk. The results can provide valuable information to developing future strategies for the management of river mouth and harbor.

Platinum particles supported on mesoporous carbons: fabrication and electrocatalytic performance in methanol-tolerant oxygen-reduction reactions

In this report, we describe the preparation and electrochemical characterization of a Pt electrocatalyst, which was synthesized from hexachloroplatinic acid, using the incipient wetness impregnation method. This carbon mesoporous materials (Pt-CMMs) electrocatalyst was used for catalyzing the oxidation of methanol and its oxygen-reduction reaction. The electrocatalytic oxidation of methanol was studied using linear-sweep voltammograms (LSV), polarization and chronoamperometric measurements. Phase characterizations and morphological analyses were performed using 3D excitation-emission fluorescent matrix (EEFM) spectroscopy, UV-Vis absorption measurements, and X-ray diffraction (XRD) and environmental scanning electron microscopy (ESEM) techniques; the ESEM system was equipped with an energy-dispersive spectrometer (EDS). The oxidation capacity measured using a LSV might explain the high activity exhibited by the Pt-CMM electrocatalysts in methanol-tolerant oxygen reduction, and the results demonstrated that the potential and current density of the main reaction peak of the Pt-CMMs electrocatalyst changed during the reaction. Moreover, EEFM spectroscopy and XRD were determined to be appropriate and effective methods for characterizing Pt clusters that enhance their intrinsic emission from Pt-CMMs electrocatalysts in electrocatalytic-treatment systems. Furthermore, the ESEM-EDS results showed that fresh Pt nanoparticles were highly dispersed on CMMs and featured a 20 nm diameter and a narrow particle-size distribution.