Discrimination of marine algal taxonomic groups based on fluorescence excitation emission matrix, parallel factor analysis and CHEMTAX

An in vivo three-dimensional fluorescence method for the determination of algae community structure was developed by parallel factor analysis （PARAFAC） and CHEMTAX. The PARAFAC model was applied to fluo-rescence excitation-emission matrix （EEM） of 60 algae species belonging to five divisions and 11 fluorescent components were identified according to the residual sum of squares and specificity of the composition profiles of fluorescent. By the 11 fluorescent components, the algae species at different growth stages were classified correctly at the division level using Bayesian discriminant analysis （BDA）. Then the reference fluo-rescent component ratio matrix was constructed for CHEMTAX, and the EEM-PARAFAC-CHEMTAX method was developed to differentiate algae taxonomic groups. The correct discrimination ratios （CDRs） when the fluorometric method was used for single-species samples were 100% at the division level, except for Bacil-lariophyta with a CDR of 95.6%. The CDRs for the mixtures were above 94.0% for the dominant algae species and above 87.0% for the subdominant algae species. However, the CDRs of the subdominant algae species were too low to be unreliable when the relative abundance estimated was less than 15.0%. The fluorometric method was tested using the samples from the Jiaozhou Bay and the mesocosm experiments in the Xiaomai Island Bay in August 2007. The discrimination results of the dominant algae groups agreed with microscopy cell counts, as well as the subdominant algae groups of which the estimated relative abundance was above 15.0%. This technique would be of great aid when low-cost and rapid analysis is needed for samples in a large batch. The fluorometric technique has the ability to correctly identify dominant species with proper abundance both in vivo and in situ.

Characterization of dissolved organic matter in urban sewage using excitation emission matrix fluorescence spectroscopy and parallel factor analysis

Wastewater dissolved organic matter （DOM） from different processing stages of a sewage treatment plant in Xiamen was characterized using fluorescence and absorption spectroscopy. Parallel factor analysis modeling of excitation-emission matrix spectra revealed five fluorescent components occurring in sewage DOM： one protein-like （C1）, three humic-like （C2, C4 and C5） and one xenobiotic-like （C3） components. During the aerated grit chamber and primary sedimentation tank stage, there was only a slight decrease in fluorescence intensity and the absorption coefficient at 350 nm （a 350 ）. During the second aeration stage, high concentration of protein-like and short-wavelength-excited humic-like components were significantly degraded accompanied by significant loss of DOC （80%） and a 350 （30%）, indicating that C1 and C2 were the dominant constituents of sewage DOM. As a result, long-wavelength- excited C4 and C5 became the dominant humic-like components and the DOM molecular size inferred from the variation of spectral slope S （300–650 nm） and specific absorption （a 280 /DOC） increased. Combination use of F max of C1 and the ratio of C1/C5, or a 350 may provide a quantitative indication for the relative amount of raw or treated sewage in aquatic environment.

Simulated photo-degradation of dissolved organic matter in lakes revealed by three-dimensional excitation-emission matrix with regional integration and parallel factor analysis

Simulated photo-degradation of fluorescent dissolved organic matter(FDOM) in Lake Baihua(BH) and Lake Hongfeng(HF) was investigated with three-dimensional excitationemission matrix(3 DEEM) fluorescence combined with the fluorescence regional integration(FRI),parallel factor(PARAFAC) analysis,and multi-order kinetic models.In the FRI analysis,fulvic-like and humic-like materials were the main constituents for both BH-FDOM and HF-FDOM.Four individual components were identified by use of PARAFAC analysis as humic-like components(C1),fulvic-like components(C2),protein-like components(C3) and unidentified components(C4).The maximum 3 DEEM fluorescence intensity of PARAFAC components C1-C3 decreased by about 60%,70% and 90%,respectively after photo-degradation.The multi-order kinetic model was acceptable to represent the photo-degradation of FDOM with correlation coefficient(Radj2)(0.963-0.998).The photo-degradation rate constants(kn) showed differences of three orders of magnitude,from 1.09 × 10-6 to 4.02 × 10-4 min-1,and half-life of multi-order model(T1/2n)ranged from 5.26 to 64.01 min.The decreased values of fluorescence index(FI) and biogenic index(BI),the fact that of percent fluorescence response parameter of Region I(PⅠ,n) showed the greatest change ratio,followed by percent fluorescence response parameter of Region II(PⅡ,n,while the largest decrease ratio was found for C3 components,and the lowest T1/2n was observed for C3,indicated preferential degradation of protein-like materials/components derived from biological sources during photodegradation.This research on the degradation of FDOM by 3 DEEM/FRI-PARAFAC would be beneficial to understanding the photo-degradation of FD OM in natural environments and accurately predicting the environmental behaviors of contaminants in the presence of FDOM.

Joint frequency,2-D DOA,and polarization estimation using parallel factor analysis

This paper proposes a new algorithm for joint frequency, two-dimensional （2-D） directions-of-arrival （DOA）, and polarization estimation using parallel factor （PARAFAC） analysis model and cumulant. The proposed algorithm designs a new array configuration, and extends the PARAFAC analysis model from the common data-domain and subspace-domain to the cumulant one, and forms three-way arrays by using the three cumulant matrices obtained from the properly chosen dipole outputs, and analyzes the uniqueness of low-rank decomposition of the three-way arrays, and then jointly estimates the source parameters via the low-rank decomposition of the constructed PARAFAC model. In comparison with the conventional methods, the proposed method alleviates the aperture loss, and avoids pairing parameter. Finally, the simulation results are presented to validate the performance of the proposed method.

Fast parallel factor decomposition technique for coherently distributed source localization

This paper links parallel factor（PARAFAC） analysis to the problem of nominal direction-of-arrival（DOA） estimation for coherently distributed（CD） sources and proposes a fast PARAFACbased algorithm by establishing the trilinear PARAFAC model.Relying on the uniqueness of the low-rank three-way array decomposition and the trilinear alternating least squares regression, the proposed algorithm achieves nominal DOA estimation and outperforms the conventional estimation of signal parameter via rotational technique CD（ESPRIT-CD） and propagator method CD（PM-CD）methods in terms of estimation accuracy. Furthermore, by means of the initialization via the propagator method, this paper accelerates the convergence procedure of the proposed algorithm with no estimation performance degradation. In addition, the proposed algorithm can be directly applied to the multiple-source scenario,where sources have different angular distribution shapes. Numerical simulation results corroborate the effectiveness and superiority of the proposed fast PARAFAC-based algorithm.

Impact of transparent exopolymer particles on the dynamics of dissolved organic carbon in the Amundsen Sea,Antarctica

The Southern Ocean is an important carbon sink pool and plays a critical role in the global carbon cycling.The Amundsen Sea was reported to be highly productive in inshore area in the Southern Ocean.In order to investigate the influence of transparent exopolymer particles(TEP)on the behavior of dissolved organic carbon(DOC)in this region,a comprehensive study was conducted,encompassing both open water areas and highly productive polynyas.It was found that microbial heterotrophic metabolism is the primary process responsible for the production of humic-like fluorescent components in the open ocean.The relationship between apparent oxygen utilization and the two humic-like components can be accurately described by a power-law function,with a conversion rate consistent with that observed globally.The presence of TEP was found to have little impact on this process.Additionally,the study revealed the accumulation of DOC at the sea surface in the Amundsen Sea Polynya,suggesting that TEP may play a critical role in this phenomenon.These findings contribute to a deeper understanding of the dynamics and surface accumulation of DOC in the Amundsen Sea Polynya,and provide valuable insights into the carbon cycle in this region.

Characteristics of dissolved organic matter in lakes with different eutrophic levels in southeastern Hubei Province,China

Dissolved organic matter(DOM)plays a crucial role in both the carbon cycle and geochemical cycles of other nutrient elements,which is of importance to the management and protection of the aquatic environments.To achieve a more comprehensive understanding the characteristics of DOM in the Changjiang(Yangtze)River basin,water samples from four natural lakes(Xiandao,Baoan,Daye,and Qingshan)in southeastern Hubei Province in China with different eutrophication levels were collected and analyzed.The optical characteristics were analyzed using ultraviolet-visible spectrophotometry and excitation-emission matrix spectroscopy coupled with parallel factor analysis.The results show that:(1)two humic-like components(C1 and C2)and two protein-like substances(C3 and C4)of DOM were identified in all waterbodies;(2)C3 originated primarily from the degradation of microalgae and contributed substantially to humic-like components during transformation.C4 was widely present in the Changjiang River basin and its formation was related to microbial activity,rather than algal blooms or seasons.Influenced by the water mixing,the protein-like components were more likely to be transformed by microorganism,whereas humic-like components were more easily to be photobleached;(3)the concentration of DOM and the fluorescence intensity of humic-like components gradually increased with rising lake eutrophication levels.With respect to protein-like components,only C3 showed changes along the eutrophication gradients;(4)DOM showed a high affinity with permanganate index(COD Mn)and chlorophyll a(chl a)while the relationship was variable with phosphorus.This study helps us systematically understand the DOM characteristics,microbial activities,and pollutant transformation in the Changjiang River basin and provides reference to the ecological restoration of aquatic environments.

Optical properties of estuarine dissolved organic matter isolated using cross-flow ultrafiltration

Dissolved organic matter （DOM） from freshwater, mid-salinity, and seawater endmember samples in the Jiulong River Estuary, China were fractionated using cross-flow ultrafiltration with a 10-kDa membrane. The colloidal organic matter （COM; 10 kDa-0.22 pm） retentate, low molecular weight （LMW） DOM （〈10 kDa） permeate, and bulk samples were analyzed using absorption spectroscopy and three-dimensional fluorescence excitation-emission-matrix spectroscopy. The UV-visible spectra of COM were very similar to those obtained for permeate and bulk samples, decreasing monotonically with increasing wavelength. Most of the chromophoric DOM （CDOM, expressed as the absorption coefficient a355） occurred in the LMW fraction, while the percentage of CDOM in the colloidal fraction was substantially higher in the freshwater endmembet （13.4% of the total） than in the seawater endmember （6.8%）. The bulk CDOM showed a conservative mixing behavior in the estuary, while there was removal of the COM fraction and a concurrent addition of the permeate fraction in the mid-salinity sample, implying that part of the colloidal CDOM was transformed into LMW CDOM. Two humic-like components （CI： 〈250, 325/402 nm; and C2： 265, 360/458 nm） and one protein-like component （C3：275/334 nm） were identified using parallel factor analysis. The contributions of the C1, C2, and C3 components of the COM fraction to the bulk sample were 2.5%-8.7%, 4.8%-12.6%, and 7.4%-14.7%, respectively, revealing that fluorescent DOM occurred mainly in the LMW fraction in the Jiulong River Estuary. The C1 and C2 components in the retentate and permeate samples showed conservative mixing behavior, but the intensity ratio of C2/C1 was higher in the retentate than in the permeate fractions for all salinity samples, showing that the humic component was more enriched in the COM than the fulvic component. The intensity ratio of C3/（C 1 ＋C2） was much higher in the retentate than in the permeate fraction for mid-salinity and seawater samples, revealing that the protein-like component was relatively more enriched in COM than the humic-like component. The contribution of the protein-like component （C3） to the total fluorescence in the retentate increased from 14% in the freshwater endmember to 72% for the seawater endmember samples, clearly indicating the variation of dominance by the humic-like component compared to the protein-like component during the estuarine mixing process of COM.

Investigation of seasonal variability of CDOM fluorescence in the southern Changjiang River Estuary by EEM-PARAFAC

The southern Changjiang River Estuary has attracted considerable attention from marine scientists because it is a highly biologically active area and is biogeochemically significant. Moreover, land-ocean interactions strongly impact the estuary, and harmful algal blooms （HABs） frequently occur in the area. In October 2010 and May 2011, water samples of chromophoric dissolved organic matter （CDOM） were collected from the southern Changjiang River Estuary. Parallel factor analysis （PARAFAC） was used to assess the samples＇ CDOM composition using excitation-emission matrix （EEM） spectroscopy. Four components were identified： three were humic-like （C1, C2 and C3） and one was protein-like （C4）. Analysis based on spatial and seasonal distributions, as well as relationships with salinity, Chl a and apparent oxygen utilization （AOU）, revealed that terrestrial inputs had the most significant effect on the three humic-like Components C1, C2 and C3 in autumn. In spring, microbial processes and phytoplankton blooms were also important factors that impacted the three components. The protein-like Component C4 had autochthonous and allochthonous origins and likely represented a biologically labile component. CDOM in the southern Changjiang River Estuary was mostly affected by terrestrial inputs. Microbial processes and phytoplankton blooms were also important sources of CDOM, especially in spring. The fluorescence intensities of the four components were significantly higher in spring than in autumn. On average, C1, C2, C3, C4 and the total fluorescence intensity （TFI） in the surface, middle and bottom layers increased by 123%-242%, 105%-195%, 167%-665%, 483%-567% and 184%-245% in spring than in autumn, respectively. This finding corresponded with a Chl a concentration that was 16-20 times higher in spring than in autumn and an AOU that was two to four times lower in spring than in autumn. The humification index （HIX） was lower in spring that in autumn, and the fluorescence index （FI） was higher in spring than in autumn. This result indicated that the CDOM was labile and the biological activity was intense in spring.

Determination of captopril in pharmaceutical preparation and biological fluids using two- and three-way chemometrics methods

Spectrophotometric method has been developed for the direct quantitative determination of captopril in pharmaceutical preparation and biological fluids （human plasma and urine） samples. The method was accomplished based on parallel factor analysis （PARAFAC） and partial least squares （PLS）. The study was carried out in the pH range from 2.0 to 12.8 and with a concentration from 0.70 to 61.50μg mL^-1 of captopril. Multivariate calibration models such as PLS at various pH and PARAFAC were elaborated from ultraviolet spectra deconvolution and captopril determination. The best models for this system were obtained with PARAFAC and PLS at pH 2.0. The applications of the method for determination of real samples were evaluated by analysis of captopril in pharmaceutical preparations and biological fluids with satisfactory results. The accuracy of the method, evaluated through the RMSEE was 0.5801 for captopril with best calibration curve by PARAFAC and 0.6168 for captopril with PLS at pH 2.0 model.

Chemical composition and Pb(II)binding of dissolved organic matter in a hypersaline lake in China

Dissolved organic matter(DOM)plays a vital role in promoting carbon and nutrient cycling.It is a food source for organisms and controls the migration and transformation of trace metals and other contaminants in aquatic systems.The contributions of aquatic DOM to the environment and ecology of a system are closely related to its abundance and chemical structure.In this study,the chemical composition and binding properties of DOM in a hypersaline lake watershed were investigated for the fi rst time using dissolved organic carbon(DOC)analysis,absorption spectroscopy,Fourier transform infrared spectroscopy,pyrolysis-GC-MS(Py-GC-MS),and fl uorescence parallel factor(PARAFAC)analysis combined with Pb(II)titration techniques.The results showed that DOM from the tributaries that fl owed into the lake had a lower DOC content,higher molecular weight,and higher specifi c UV absorbance than the DOM in lake water.Protein-like fl uorophores were mainly found in tributary and lake surface water DOM(LSDOM)and humic-like substances were abundant in lake groundwater DOM(LGDOM).Using this multi-methodological approach,we found that the DOM from the hypersaline lake watershed was mainly from microbial origins,and consisted of aromatics,carbohydrates,and aliphatics.The results from quantitative analysis showed that DOM from the infl owing tributaries contained more aromatics,lower carbohydrates,and lower aliphatics than DOM in the lake.Monocyclic aromatic hydrocarbons and carbohydrates were more abundant in LSDOM than LGDOM.The results from the Pb(II)titration technique coupled with PARAFAC analysis suggested that PARAFAC-derived components had relatively low condition stability constants(log K_(M)<2).Of the two types of lake DOM,the LGDOM had a higher Pb(II)binding potential than the LSDOM.From this study we have improved our understanding of how DOM within a hypersaline lake watershed varies in its composition and potential to bind with metals.

Optical Characteristics of Chromophoric Dissolved Organic Matter(CDOM)in Upstream and Downstream Lakes of Taihu Lake Basin:New Insights for Water Environmental Management

Chromophoric dissolved organic matter(CDOM)is a key component of organic matter that contributes to the ecological functioning of lakes.The lakes in Taihu Lake Basin play an important role in maintaining regional ecological stabilities;however,the optical characteristics of the CDOM in the upstream and downstream lakes in this basin have not yet been systematically studied.Here,the optical characteristics of CDOM in ten lakes of upstream and downstream of the Taihu Lake Basin were studied using UV-Visible and excitation-emission matrix spectroscopies.Three different fluorophores consisting of two humic-like components(C1,C2)and one protein-like component(C3)were identified by parallel factor analysis.Soil or surface erosion was responsible for the higher abund-ance of C1 in the upstream lakes,and increased biological activities accounted for the higher abundance of C3 in the downstream lakes.Rainfall erosion in the wet season led to an increase in CDOM.We also found that the photodegradation and flocculation degree,which played a significant role in reducing CDOM,were higher in downstream lakes than in upstream lakes.Optical analysis of CDOM provides a promising method for monitoring water qualities(e.g.,total phosphorus and potassium permanganate index)in each lake.Re-ductions in soil or surface erosion in the upstream are needed to improve water quality.

Rapid quantification of acid value in frying oil using iron tetraphenylporphyrin fluorescent sensor coupled with density functional theory and multivariate analysis

A metalloporphyrin-based fluorescent sensor was developed to determine the acid value in frying oil.The electronic and structural performances of iron tetraphenylporphyrin(FeTPP)were theoretically investigated using time-dependent density functional theory and density functional theory at the B3LYP/LANL2DZ level.The quantified FeTPP-based fluorescent sensor results revealed its excellent performance in discriminating different analytes.In the present work,the acid value of palm olein was determined after every single frying cycle.A total of 10 frying cycles were conducted each day for 10 consecutive days.The FeTPP-based fluorescent sensor was used to quantify the acid value,and the results were compared with the chemical data obtained by conventional titration method.The synchronous fluorescence spectrum for each sample was recorded.Parallel factor analysis was used to decompose the three-dimensional spectrum data.Then,the support vector regression(SVR),partial least squares,and back-propagation artificial neural network methods were applied to build the regression models.After the comparison of the constructed models,the SVR models exhibited the highest correlation coefficients among all models,with 0.9748 and 0.9276 for the training and test sets,respectively.The findings suggested the potential of FeTPP-based fluorescent sensor in rapid monitoring of frying oil quality and perhaps also in other foods with higher oil contents.

A chemometric analysis on the fluorescent dissolved organic matter in a full-scale sequencing batch reactor for municipal wastewater treatment

Rapid monitoring of water quality is crucial to the operation of municipal wastewater treatment plants （WWTPs）. Fluorescence excitation-emission matrix （EEM） in combination with parallel lhctor analysis （PARAFAC） has been used as a powerful tool for the characterization of dissolved organic matter （DOM） in WWTPs. However, a recent work has revealed the drawback of PARAFAC analysis, i.e., overestimating the component number. A novel method, parallel lhctor framework-clustering analysis （PFFCA）,＂has been cleveloped in our earlier work to resolve this drawback of PARAFAC. In the present work, both PARAFAC and PFFCA were used to analyze the EEMs of water samples from a full-scale WWTP from a practical application point of view. The component number and goodness-of- fit from these two methods were compared and the relationship between the relative score change of component and the actual concentration was investigated to evaluate the estimation error introduced by 9 both methods. PFFCA score and actual concentration exhibited a higher correlation coefficient （R- = 0.870） compared with PARAFAC （R2〈 0.771）, indicating that PFFCA provided a more accurate relative change estimation than PARAFAC. The results suggest that use of PARAFAC may cause confusion in selecting the component number, while EEM-PFFCA is a more reliable alternative approach for monitoring water quality in WWTPs.

Comparison of UV-based advanced oxidation processes for the removal of different fractions of NOM from drinking water

This study examined the effectiveness for degradation of hydrophobic (HPO),transphilic(TPI) and hydrophilic (HPI) fractions of natural organic matter (NOM) during UV/H_(2)O_(2),UV/TiO_(2)and UV/K2S2O8(UV/PS) advanced oxidation processes (AOPs).The changing characteristics of NOM were evaluated by dissolved organic carbon (DOC),the specific UV absorbance (SUVA),trihalomethanes formation potential (THMFP),organic halogen adsorbable on activated carbon formation potential (AOXFP) and parallel factor analysis of excitation–emission matrices (PARAFAC-EEMs).In the three UV-based AOPs,HPI fraction with low molecular weight and aromaticity was more likely to degradate than HPO and TPI,and the removal efficiency of SUVA for HPO was much higher than TPI and HPI fraction.In terms of the specific THMFP of HPO,TPI and HPI,a reduction was achieved in the UV/H_(2)O_(2)process,and the higest removal rate even reached to 83%.UV/TiO_(2)and UV/PS processes can only decrease the specific THMFP of HPI.The specific AOXFP of HPO,TPI and HPI fractions were all able to be degraded by the three UV-based AOPs,and HPO content is more susceptible to decompose than TPI and HPI content.UV/H_(2)O_(2)was found to be the most effective treatment for the removal of THMFP and AOXFP under given conditions.C1 (microbial or marine derived humic-like substances),C_(2) (terrestrially derived humic-like substances)and C_(3) (tryptophan-like proteins) fluorescent components of HPO fraction were fairly labile across the UV-based AOPs treatment.C_(3) of each fraction of NOM was the most resistant to degrade upon the UV-based AOPs.Results from this study may provide the prediction about the consequence of UV-based AOPs for the degradation of different fractions of NOM with varied characteristics.

Simultaneous degradation of sulfadiazine and dissolved organic matter based on low-impact development facilities

Sulfadiazine(SD)is a common antibiotic administered to treat bacterial infections in livestock,and its fate andmigration are greatly affected by dissolved organicmatter(DOM).The soil infiltration system[a typical low-impact development(LID)facility]can significantly alterDOMproperties during runoff pollution,thus affecting the complexation of SDwithDOM.Here,the binding characteristics of different DOM components and SD in the soil infiltration system were explored using spectroscopic techniques(excitation–emission matrices,parallel factor analysis,and synchronous fluorescence spectroscopy).Combined with the weakening of DOM fluorescence intensity and 78.63%reduction in mean SD concentration following treatment,synchronous degradation may have occurred.The binding sequence of SD and DOM fluorophores was further explored using two-dimensional correlation spectroscopy.Effluent DOM showed greater sensitivity to SD and more binding sites than influent DOM.Moreover,hydrophobic protein-like substances exhibited higher log K_(M) values than other fluorescent components,indicating that protein-like components play significant roles in SD complexation.The soil percolation system improved the complexation stability and binding sequence of fulvic-like substances.Thus,SD–DOM can be intercepted and degraded using LID facilities to reduce the risk of SD in aquatic environments.

Growth and photosynthesis responses of Phaeodactylum tricornutum to dissolved organic matter from salt marsh plant and sediment

The effects of allochthonous dissolved organic matter （DOM） on the growth and photosynthesis of Phaeodactylum tricornutum were investigated. P. tricornutum incubated in f/2 medium was exposed to DOM additives, which were extracted from the plant and sediment samples of a salt marsh in North Branch of the Yangtze estuary, China. During 12 days incubation, the chlorophyll fluorescence parameters of P. tricornutum were measured by a Phyto-PAM phytoplankton analyzer. Spectral properties of DOM in algae filtrates were also observed. The concentrations of chlorophyll a, active chlorophyll a, and the maximum quantum yield of photosystem II significantly decreased after four days of incubation, suggesting that the growth and photosynthetic efficiency of P. tricornutum were inhibited. After adding sediment-DOM extract, both a 250 /a 365 （the ratio of the absorption coefficients at 250 and 365 nm） and S values （spectral slope coefficients） of algae filtrates declined in the first two days, which demonstrated a loss of low molecular weight DOM. Parallel factor analysis of fluorescence spectra of DOM in algae filtrates revealed that DOM could be classified into two humic-like and two protein-like components. The fluorescence intensity of tyrosine-like component originating from algae increased significantly during incubation. This study supports the hypothesis that allochthonous DOM derived from salt marsh plant and sediment have a strong influence on the adjacent aquatic ecosystems.

Passive localization of 3-D near-field sources in coexisted multiplicative noise and additive noise

By exploiting thvorable characteristics of a uniIbrm cross-array, a passive localization algorithm of narrowband sources in the spherical coordinates （azimuth, elevation and range） is proposed. Based on the properly chosen sensor outputs, we compute the third-order cyclic moment matrices, and exploit a pre-calibration technique to eliminate multiplicative noise. Then, we construct a parallel factor （PARAFAC） model, and adopt trilinear altemating least squares regression （TALS） to estimate three-dimensional （3-D） near-field parameters. The investigated algorithm is efficient in the sense that it can eliminate multiplicative noise and additive noise, provide the improved estimation accuracy, as well as avoid the parameter-pairing procedure. Simulation results are carried out to demonstrate the performance of the proposed algorithm.

Identification of sources,characteristics and photochemical transformations of dissolved organic matter with EEM-PARAFAC in the Wei River of China

Dissolved organic matter(DOM)in rivers is a critical regulator of the cycling and toxicity of pollutants and the behavior of DOM is a key indicator for the health of the environment.We investigated the sources and characteristics of DOM in surface water and sediment samples of the Wei River,China.Dissolved organic carbon(DOC)concentration and ultraviolet absorbance at 254 nm(UV254)increased in the surface water and were decreased in the sediment downstream,indicating that the source of DOM in the water differed from the sediment.Parallel factor(PARAFAC)analysis of the excitation-emission matrices(EEM)revealed the presence of terrestrial humus-like,microbial humus-like and tryptophan-like proteins in the surface water,whereas the sediment contained UVA humic-like,UVC humic-like and fulvic-like in the sediment.The DOM in the surface water and sediment were mainly derived from microbial metabolic activity and the surrounding soil.Surface water DOM displayed greater photodegradation potential than sediment DOM.PARAFAC analysis indicated that the terrestrial humic-like substance in the water and the fulvic-like component in the sediment decomposed more rapidly.These data describe the characteristics of DOM in the Wei River and are crucial to understanding the fluctuations in environmental patterns.

Identifying the major fluorescent components responsible for ultrafiltration membrane fouling in different water sources

Three-dimensional fluorescence excitation–emission matrix（EEM） coupled with parallel factor analysis（PARAFAC） was performed for a total of 18 water samples taken from three water sources（two lakes and one wastewater treatment plant（WWTP） secondary effluent）,with the purpose of identifying the major ultrafiltration（UF） membrane foulants in different water sources. Three fluorescent components（C1, C2 and C3） were identified,which represented terrestrially derived humic-like substances（C1）, microbially derived humic-like substances（C2）, and protein-like substances（C3）. The correlations between the different fluorescent components and UF membrane fouling were analyzed. It was shown that for the WWTP secondary effluent, all three components（C1, C2 and C3） made a considerable contribution to the irreversible and total fouling of the UF membrane.However, for the two lakes, only the C3 exhibited a strong correlation with membrane fouling, indicating that the protein-like substances were the major membrane foulants in the lake waters. Significant attachment of C1, C2 and C3 to the UF membrane was also confirmed by mass balance analyses for the WWTP secondary effluent; while the attachment of C1 and C2 was shown to be negligible for the two lakes. The results may provide basic formation for developing suitable fouling control strategies for sustainable UF processes.