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Article

Temporal Dynamics and Influential Factors of Taste and Odor Compounds in the Eastern Drinking Water Source of Chaohu Lake, China: A Comparative Analysis of Global Freshwaters

1
CAS Key Laboratory of Marine Ecology and Environmental Sciences, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China
2
State Key Laboratory of Lake Science and Environment, Nanjing Institute of Geography and Limnology, Chinese Academy of Sciences, Nanjing 210008, China
3
Changzhou Academy of Environmental Science, Changzhou 213022, China
*
Authors to whom correspondence should be addressed.
Toxins 2024, 16(6), 264; https://doi.org/10.3390/toxins16060264
Submission received: 11 May 2024 / Revised: 31 May 2024 / Accepted: 4 June 2024 / Published: 9 June 2024
(This article belongs to the Special Issue Monitoring and Management of Algal and Cyanobacterial Blooms)

Abstract

:
The escalating proliferation of cyanobacteria poses significant taste and odor (T/O) challenges, impacting freshwater ecosystems, public health, and water treatment costs. We examined monthly variations in four T/O compounds from September 2011 to August 2012 in Chaohu Lake’s eastern drinking water source (DECL). More importantly, we compared the reported T/O occurrence and the related factors in freshwater bodies worldwide. The assessment of T/O issues indicated a severe and widespread problem, with many cases surpassing odor threshold values. Remarkably, China reported the highest frequency and severity of odor-related problems. A temporal analysis revealed variations in odor occurrences within the same water body across different years, emphasizing the need to consider high values in all seasons for water safety. Globally, T/O issues were widespread, demanding attention to variations within the same water body and across different layers. Algae were crucial contributors to odor compounds, necessitating targeted interventions due to diverse odorant sources and properties. A correlation analysis alone lacked definitive answers, emphasizing the essential role of further validation, such as algae isolation. Nutrients are likely to have influenced the T/O, as GSM and MIB correlated positively with nitrate and ammonia nitrogen in DECL, resulting in proposed control recommendations. This study offers recommendations for freshwater ecosystem management and serves as a foundation for future research and management strategies to address T/O challenges.
Key Contribution: A comprehensive comparative analysis and discourse were undertaken on documented T/O incidents and their associated determinants in freshwater environments globally.

1. Introduction

Over the past few decades, the frequency and intensity of harmful cyanobacterial blooms in freshwater environments worldwide have increased, primarily due to eutrophication and global warming [1,2,3,4,5]. In addition to their association with oxygen depletion and the production of cyanotoxins, cyanobacteria are linked to taste and odor (T/O) compounds [6,7,8,9,10,11,12]. Undesirable tastes and odors have been observed to manifest genotoxic and estrogenic effects on fish hepatocytes, thereby posing potential risks to human health through the consumption of aquatic products [13]. Furthermore, the presence of T/O compounds has prompted a series of public grievances, particularly concerning the acceptability of surface waters for recreational purposes and the quality and safety of drinking water [10,11,14,15]. The occurrence of T/O events in freshwater ecosystems has evolved into a global water issue, with numerous instances documented in studies conducted across China, Japan, Korea, North America, and Europe, thereby underscoring the widespread significance of this concern [16,17,18,19,20,21,22,23].
Two bicyclic terpenoid compounds, namely, geosmin (trans-1,10-dimethyl-trans-9-decalol, GSM) and 2-methylisoborneol (1,2,7,7-tetramethyl-exo-bicycloheptan-2-ol, MIB), which are renowned for their earthy and musty odors, represent the most frequently identified T/O substances in freshwater bodies globally [24,25,26,27,28,29]. Additional investigations have been conducted on alternative T/O compounds associated with cyanobacterial blooms, such as β-cyclocitral (CYC) and β-ionone (ION). These compounds, stemming from the degradation of β-carotene, exhibit distinctive odors reminiscent of wood, violets, tobacco, and flowers and have been scrutinized in certain water sources [30,31,32]. The simultaneous presence of multiple T/O compounds introduces complexity to water quality management and constitutes a significant concern in the context of natural and drinking water in several countries, including China [11,12,22,33,34,35].
Given the generally minuscule odor threshold concentrations (OTCs) of T/O compounds, specifically, 4, 15, 19.3, and 7 ng·L−1 for GSM, MIB, CYC, and ION, respectively [36], these compounds can be perceptible to humans at trace levels. Notably, China has incorporated GSM and MIB into their drinking water quality standards, establishing current standard values for both compounds at 10 ng·L−1 [37]. The resilience of these compounds to oxidation posed a substantial challenge for aquaculture and drinking water facilities in terms of effective monitoring and control [38,39]. The adoption of advanced treatment methods or a multifaceted approach to eradicate T/O compounds imposes significant financial burdens on water utilities. Therefore, formulating a strategy to prevent the generation of T/O compounds in source water is imperative. As a result, a nuanced comprehension of the foundational information concerning odorants and their interrelation with environmental conditions became imperative for the control and management of odor sources. Furthermore, in the pursuit of eradicating T/O compounds from freshwater systems, it is paramount to discern the temporal and spatial patterns of variation and pinpoint the pivotal factors that contribute to the emergence of odorous manifestations.
The dynamics and influencing factors of T/O compounds in aquatic systems have been extensively investigated [16,21,24,40,41,42,43,44,45]. The occurrence of T/O compounds in water bodies has been associated with diverse biotic and abiotic parameters, encompassing the phytoplankton community, water temperature, pH, and nutrient concentrations and/or ratios, etc. [22,28,42,44,46,47,48,49,50,51]. These studies provided valuable insights for a more nuanced comprehension of the origins and impacts of odors in aquatic environments. However, the relationships between T/O compounds and environmental factors are intricate. Moreover, numerous ambiguous ecological interactions between cyanobacteria and other organisms contribute to a substantial disparity observed among various water bodies. It would prove advantageous if the presence of odorants could be correlated with monitored environmental parameters, as such associations could potentially serve to estimate the presence of these T/O compounds in water.
Chaohu Lake (30°25′–31°43′ N, 117°16′–117°51′ E), positioned in the central region of Anhui Province, stands as the fifth-largest freshwater lake in China. Functioning as a pivotal regional fishery and tourism resource, it simultaneously serves as a critical potable water reservoir for approximately one million residents [52]. Nonetheless, it is also a recipient of domestic sewage and industrial effluents originating from the surrounding urban and rural areas. In the late 1980s, the exchange rate with the Yangtze River decelerated due to the establishment of the Chaohu Lake Gate, leading to an upsurge in nutrient inputs resulting from rapid agricultural intensification and industrial development in the basin [53]. Consequently, Chaohu Lake has been grappling with eutrophication since the 1980s [52]. Despite its eutrophic status, Chaohu Lake retains its pivotal role as a strategic water reserve due to its substantial storage capacity. However, specific areas within Chaohu Lake accumulate a notable quantity of cyanobacteria, and the issue of distinct odors has adversely impacted water quality, necessitating further investigation.
For the early detection of T/O incidents to effectively manage the drinking water sources and their respective treatment facilities in Chaohu Lake, this study aimed to (1) investigate the monthly dynamics of dissolved and particulate compounds from four typical T/O (GSM, MIB, CYC, and ION), (2) identify cyanobacteria in the eastern drinking water source of Chaohu Lake, (3) estimate the water quality variables influencing T/O contents, and (4) conduct a comprehensive comparative analysis and discussion of documented T/O incidents and their associated determinants in freshwater environments globally.

2. Results and Discussion

2.1. Seasonal Variations of the Dissolved and Particulate T/O Compounds in the Eastern Drinking Water Source of Chaohu Lake

In the eastern drinking water source of Chaohu Lake, the concentrations of dissolved and particulate T/O compounds displayed intricate seasonal variations (Figure 1). Geosmin exhibited its highest concentration in March (39.7 ± 10.6 ng·L−1), with particulate concentrations consistently below 2 ng·L−1. The concentrations of MIB were notably elevated from May to October, peaking at 180.5 ng·L−1 in July 2012. The maximum concentration of MIB in both the dissolved and particulate forms was recorded at 164.0 ng·L−1 (July 2012) and 20.7 ng·L−1 (June 2012), respectively. The average values for the total concentration of CYC in the investigated drinking water source exhibited three peaks in January 2012 (105.6 ng·L−1), March (53.5 ng·L−1), and June (54.0 ng·L−1), respectively, with both the dissolved and particle concentrations reaching their zenith in January 2012. Two distinct peaks in the total concentrations of ION were evident in December (53.3 ng·L−1) and June 2012 (136.6 ng·L−1), respectively. Although there is a limited body of literature specifically investigating T/O compounds in Chaohu Lake, it is evident that T/O issues are pronounced in this lake. This is manifested both by the reported maximum concentrations of four T/O compounds, with respective values of 1300 (GSM), 180.5 (MIB), 800 (ION), and 8300 ng·L−1, and the presence of significant olfactory problems in both the eastern and western regions of the lake (Refs. [11,22,33,42] and this study). The seasonal variations in the concentrations of T/O compounds within the eastern drinking water source of Chaohu Lake might be attributed to meteorological conditions, water temperature fluctuations, and biological activities [44,54].
Concerning the distribution between the dissolved and particulate forms, varied patterns were evident among different T/O compounds (Figure 1). Specifically, the four examined T/O compounds exhibited distribution patterns ranging from 11% to 91% outside cellular structures throughout the year, except for December, when no dissolved substance was detected. More than 79% of both GSM and MIB were found in the dissolved form, except for December, when the proportions were 0% for the former and 5% for the latter in June. Over the entire year, the average proportion of particulate CYC was 45%, comprising approximately 20% from September to November, 4–35% from February to May, and 62–100% in the remaining months. The majority of ION was observed within cellular structures, with an average particulate ratio of 71% throughout the year. Exceptions included 11–25% in April, September, and October and 59–78% in March, July, and August, with concentrations reaching 97–100% in the remaining months. Overall, GSM and MIB predominantly existed in dissolved form, while CYC and ION exhibited notable variations in their distribution between dissolved and particulate forms.
The aggregate concentrations of the four T/O compounds, encompassing both dissolved and particulate fractions, within the three designated sampling sites exhibited a range of 8.9–292.6 ng·L−1 (Figure 1). The concentrations of dissolved GSM, MIB, CYC, and ION surpassed their respective OTCs [36] in 75%, 42%, 25%, and 33% of the months, respectively. In terms of the overall concentrations, the proportions of GSM and MIB exceeding OTCs remained relatively constant, while those of CYC and ION increased to 75% and 100%, respectively. Hence, the concentrations of dissolved GSM, MIB, CYC, and ION surpassed their respective odor threshold concentrations in certain months, potentially impacting the perception and acceptability of water quality. The proportion of particulate forms, particularly observed in CYC and ION, demonstrated relatively higher proportions during specific months, indicating an inclination of these compounds to associate with particulate matter, possibly linked to biological activities in the water or organic matter in the sediment.

2.2. Factors Influencing the T/O Compound Variation in the Eastern Drinking Water Source of Chaohu Lake

Correlation coefficients were employed to assess the impact of biological, physicochemical, and organic indices on the temporal variability of T/O compounds in the eastern drinking water source of Chaohu Lake (Table 1). Notably, all four T/O compounds showed no significant correlation with cyanobacterial densities and Chl-a concentrations, suggesting independence from overall cyanobacterial abundance. However, specific associations emerged; MIB correlated positively with Microcystis spp., and ION showed a positive relationship with Dolichospermum spp. Both GSM and MIB displayed significant inverse correlations with Dolichospermum spp., indicating a nuanced interaction. In terms of physicochemical indices, MIB inversely correlated with dissolved oxygen and positively correlated with temperature, pH, and conductivity, suggesting sensitivity to these parameters. GSM exhibited a positive association with conductivity. Nutrient-wise, GSM and MIB correlated positively with nitrate and ammonia nitrogen, respectively, while ION had a negative correlation with total phosphorus, indicating nutrient influence. Regarding organic indices, MIB correlated positively with the potassium permanganate index and dissolved organic carbon, linking its concentration to water’s organic content.
The utilization of redundancy analysis systematically identified key environmental factors influencing the seasonal fluctuations of both dissolved and particulate T/O compounds. Among the fifteen examined variables, five, namely the densities of Microcystis spp. and Dolichospermum spp., water temperature, pH, and nitrate, significantly contributed to the variance of T/O compounds (p < 0.05) (Figure 2). The outcomes indicated a positive correlation between dissolved MIB and ION, both of which exhibited high associations with the cell density of Microcystis spp. and water temperature. Additionally, a positive correlation emerged between dissolved GSM and CYC, with the former positively and the latter negatively correlated with nitrate and pH, respectively. Moreover, particulate GSM and ION, along with particulate MIB and CYC, exhibited positive interrelations. All these particulate compounds were positively correlated with pH and the concentrations of Dolichospermum spp.

2.3. Relationships among T/O Compounds and Algal Toxins in the Eastern Drinking Water Source of Chaohu Lake

Considering the frequent co-occurrence of T/O compounds with algal toxins in eutrophic lakes experiencing cyanobacterial blooms [11,55], our investigation delved into the interrelationships among four T/O compounds and three prevalent microcystin (MC) variants, namely MC-LR, MC-RR, and MC-YR (Table 2). Positive correlations were observed among the three T/O compounds—GSM, CYC, and ION—suggesting a potential co-occurrence or similar influencing factors for these compounds. However, it is noteworthy that an inverse association was identified between GSM and MC-YR, indicating a contrasting relationship between these specific T/O and MC variants. Interestingly, no significant correlations were found between the other microcystin variants (MC-LR and MC-RR) and the examined T/O compounds. This suggests a complex and nuanced relationship between T/O compounds and specific microcystin variants, with potential variations in their production or dynamics. These findings contribute to our understanding of the interactions between T/O compounds and microcystins in eutrophic lakes during cyanobacterial blooms. The absence of correlations with certain microcystin variants suggests distinct regulatory mechanisms or factors influencing their dynamics.

2.4. Characteristics of the T/O Compounds in Freshwaters of the World

2.4.1. Spatiotemporal Distribution of T/O Compounds in Freshwater Sources Worldwide

We compiled a review of the literature spanning from 1986 to 2023 that documented the presence of typical cyanobacteria-derived T/O compounds, namely GSM, MIB, CYC, and ION, in freshwater bodies worldwide (Table 3). The findings revealed prevalent T/O issues in raw water sourced from drinking water treatment plants, lakes, reservoirs, rivers, aqueducts, and fishponds, with manifestations reported in diverse regions, including China, Egypt, Germany, Italy, Japan, Korea, Spain, Switzerland, Thailand, the United States of America, and North America. These freshwater bodies exhibited variability in T/O types, concentrations, and the months of maximum occurrence.
GSM and MIB are two of the most prominent musty/earthy compounds detected in natural water systems, exhibiting significant concentrations that pose potential risks. GSM concentrations have reached alarmingly high levels, with a record of 7200 ng·L−1 reported in the YH Reservoir in Hebei Province, China, in July 2007 [26]. Similarly, MIB concentrations peaked at 5302.7 ng·L−1 in fishponds in Tianjin, China, in July 2006 [70]. The documented concentrations of GSM and MIB in 91% and 81% of the 67 and 64 studies, respectively, surpassed their respective OTCs of 4 and 15 ng·L−1. This indicates the widespread occurrence of these compounds and their potential impact on water quality.
In China, GSM concentrations have reached noteworthy peaks, including 1300 ng·L−1 in Chaohu Lake in August 2012 [33], 2711.5 ng·L−1 in Xionghe Lake in July 2007, 826.7 ng·L−1 in the same lake in November 2007 [66], and the aforementioned 7200 ng·L−1 in the YH Reservoir. Additionally, GSM concentrations exceeding 600 ng·L−1 have been documented in various countries, such as Germany, Japan, Korea, and the USA. MIB concentrations have also been reported at high levels in China, with Chaohu Lake recording a maximum concentration of 180.5 ng·L−1 in August 2012 [11]. Many other water bodies in China, including Dianchi Lake, Donghu Lake, Taihu Lake, Xionghe Reservoir, and a landscape lake in Beijing, have exhibited MIB values over 20 times the OTC. For example, MIB concentrations reached 450 ng·L−1 in Dianchi Lake in July 2003 [46], 317 ng·L−1 in Donghu Lake in January 1996 [56], 325 ng·L−1 in Taihu Lake in September 2009 [23], and 5302.7 ng·L−1 in a fishpond in July 2006 [70]. In other countries and regions, MIB concentrations generally ranged from 0 to 289 ng·L−1, except for Japan, where a concentration of 1400 ng·L−1 was reported [78]. These high concentrations of GSM and MIB not only indicate potential risks to water quality but also suggest the need for continued monitoring and management efforts to mitigate their impacts on drinking water supplies and aquatic ecosystems.
In contrast, both CYC and ION were reported in only 15 studies, encompassing seven water bodies (Table 3). Regarding CYC, it is noteworthy that in seven Chinese reservoirs [21] and the Llobregat River in Spain [81], CYC was not detected. However, the recorded peak values exceeded the OTC of 19.3 ng·L−1 in 14 publications, spanning seven water bodies. Specifically, in China, Eastern Chaohu Lake, a drinking water source, recorded concentrations as high as 800 ng·L−1 in August 2012 [33]. Western Chaohu Lake had a concentration of 105.6 ng·L−1 in January 2012 [11], while Eastern Chaohu Lake again reached 714.8 ng·L−1 in September 2013 [42]. Elevated concentrations were also reported in other Chinese lakes, including Dianchi Lake (450 ng·L−1 in September 2003 [46]), Taihu Lake (2080 ng·L−1 in September 2009 [23]), and landscape lakes in Beijing, reaching a remarkable 6000 ng·L−1 in May 2016 [45,69]. In different geographical regions, CYC has also been detected. For instance, Bao et al. (1997) reported concentrations ranging from 0 to 57 ng·L−1 in the Arno River in Japan in May 1995 [34], while Young et al. (1999) found 133 ng·L−1 in Winnebago Lake in the USA in August 1996 [40]. These findings highlight the widespread occurrence of CYC and the potential need for further investigation and monitoring in diverse aquatic systems.
Regarding ION, the reported maximum concentrations in 14 publications, inclusive of the current study, exceeded the odor threshold concentration (OTC) of 7 ng·L−1. Notably, ION was not detected in seven significant reservoirs located in eastern China, as reported by Wu et al. (2021b) [21], and concentrations in the Arno River in Italy ranged from 0 to 7 ng·L−1, as documented by Bao et al. (1997) [34]. Among the various water bodies studied, Chaohu Lake and Taihu Lake stand out as having been extensively investigated. Chaohu Lake recorded a peak concentration of 8300 ng·L−1 in December 2012 [33], while Taihu Lake exhibited a peak concentration of 1976.4 ng·L−1 in September 2017 [22]. These high concentrations indicate potential environmental concerns in these regions. In addition to Chaohu and Taihu lakes, other Chinese water bodies also showed elevated ION concentrations. For instance, Dianchi Lake recorded 570 ng·L−1 in September 2003 [46], Songhua Lake reached 8.9 ng·L−1 in September 2017 [22], and the main canal of the Middle Route of the South-to-North Water Diversion Project had concentrations with ranges of 11.973 ± 20.643 ng·L−1 between September 2018 and August 2019 [71]. Further, the Liangxi River had a concentration of 350 ng·L−1 in September 2018 [51], and raw water from a Chinese city registered a concentration of 358 ng·L−1 [26]. In contrast, limited data are available for ION concentrations in water bodies outside of China. This suggests that further research and monitoring efforts are needed to comprehensively understand the occurrence and impact of ION in global aquatic systems.

2.4.2. Implications of Spatiotemporal Distribution of T/O Compounds for Management

Overall, numerous countries or regions worldwide grapple with profoundly severe T/O problems in their aquatic ecosystems. China has garnered extensive research attention due to its pronounced T/O challenges, which stand out as the most severe among studied regions. These challenges manifest not only in widespread distribution across diverse water bodies (e.g., lakes, reservoirs, rivers, canals, fishponds, and raw water from drinking water treatment plants) but also in the heightened concentrations of odoriferous substances they entail (see references in Table 3). The highest concentrations of these four T/O substances have been consistently reported in China. Furthermore, most documented water bodies exhibit maximum concentrations surpassing their corresponding OTCs. In other countries, there has been a relatively extensive amount of research on GSM and MIB. However, there has been comparatively less research on CYC and ION. Considering that the concentrations of both CYC and ION can reach 6000 and 8300 ng·L−1, respectively, in the field [33,45,69], it is advisable to include them in the scope of detection, as well (Table 4).
From the perspective of the temporal distribution of T/O compounds, most peak concentrations occur during the summer and autumn seasons. In terms of management and monitoring, it is crucial to recognize that many studies do not provide year-round coverage and tend to favor observations during these two seasons. Notably, certain T/O compounds in specific water bodies exhibit peak concentrations in other seasons, which recommended involving winter data in future predictions models ([96] and this study). Moreover, studies also emphasized the temporal variability of odor occurrences within the same water body across different years, which could be attributed to various factors, including environmental conditions, biological dynamics, water mixing patterns, and anthropogenic influences [11,22,23,33,35,42,64,65]. A comprehensive understanding of the temporal dynamics of odor events was crucial in developing water quality management and treatment strategies, facilitating the recognition of patterns and trends, and furnishing essential information for the establishment of early warning systems.
The spatial distribution of odorants reveals that odor issues were widespread in water bodies globally, with different water systems exhibiting diverse odorant scenarios. This variability could be attributed to factors such as nutrient concentration, sources, and geographical conditions. In China, lakes with severe eutrophication, such as Chaohu and Taihu Lake, experienced prominent odor problems. Among all the lakes in China, Taihu Lake stood out for its more severe T/O issues and increased attention, likely due to the warmer temperatures and well-developed economy in the surrounding areas [22]. Similarly, situated in the central part of China, Chaohu Lake is a vital managed water body grappling with significant eutrophication, demanding heightened attention. However, there is a noticeable dearth of literature addressing taste and odor occurrences in Chaohu Lake, highlighting the need for further research. For the same water body, such as Lake Taihu, variations in odor compounds among different regions exist. Deng et al. (2019) unveiled spatial disparities in nutrients and T/O compounds between blooming and non-blooming areas [64]. Elevated concentrations of compounds like CYC and ION in blooming areas contrasted with lower levels in non-blooming areas. Considering both the biological and non-biological factors in lake management facilitated the development of effective odor control strategies, thereby contributing to water quality management and ecological balance. Additionally, attention should be directed toward the distribution of odor compounds in different water layers. Research on Lake Zürich illuminated the significant seasonal dynamics of odorant concentrations influenced by lake stratification [86]. Internal factors, such as temperature gradients and nutrient distribution, led to distinct odorant concentrations across various water layers. Managing water extraction necessitated addressing odorant variability in specific lake layers, thereby influencing water quality at extraction points. Recognizing the importance of considering seasonal variations and lake stratification was crucial in water resource management for predicting and controlling odorant distribution, ensuring stable and safe water quality at intake points.

2.5. Sources and Influencing Factors of T/O Compounds in Freshwater Bodies of the World

Comprehending the sources and determining factors of T/O compounds is pivotal for preempting T/O challenges and laying the groundwork for their management. The variability in T/O compounds is shaped by a confluence of biological, physical, and chemical indicators (Table 4).

2.5.1. Biotic Factors

To address odor issues in water bodies, it is crucial to study their sources and primary influencing factors. Typically, studies explored the relationship between biological factors and the concentration of odor substances to identify their producers. Biotic factors were generally assessed by examining the biomass or density of total cyanobacteria, specific genera and/or species, and various indices, including Chl-a, phycocyanin, and genes associated with T/O compounds synthesis.
The concentrations of GSM in various water bodies exhibit diverse correlations with Chl-a and other factors. Several studies have found positive correlations between GSM concentrations and Chl-a. For instance, Ma et al. (2013) observed this positive correlation in Taihu Lake, China [23], while Wu et al. (2021b) reported a similar trend in seven important reservoirs in eastern China [21]. Additionally, Smith et al. (2002) noted a positive correlation in Cheney Reservoir in the United States. However, contrasting results have been observed in other water bodies [14]. In the current study, no significant correlation was found between GSM concentrations and Chl-a in DECL. Similarly, Zhang et al. (2019) reported no significant correlation in Chaohu Lake and Songhua Lake in China, as well as in Taihu Lake, also in China [22]. Li et al. (2007) found no correlation in Dianchi Lake in China [46], Jahnichen et al. (2011) found no correlation in Wahnbach Reservoir in Germany [16], and Bruder et al. (2014) found no correlation in Eagle Creek Reservoir in the United States [49].
Similar variability was observed for the correlation between cyanobacteria and GSM concentrations. Positive correlations were found in some water bodies (e.g., Phayao Lake in Thailand [87], Bukhan River and Namhan River in South Korea [18], and Paldang Lake in Korea [15]), while in others (DECL (this study), Dianchi Lake in China [46], and Eagle Creek Reservoir in the US [49]), there was no apparent relationship between cyanobacteria and GSM. Notably, specific types of cyanobacteria, such as Microcystis, Dolichospermum, and Pseudoanabaena, have been extensively researched in relation to GSM. Positive correlations between GSM and Microcystis were observed in various water bodies, including Taihu Lake in China [23], California Aqueduct in the US [24], Bukhan River and Namhan River in South Korea [18], and Lake Winnebago in the US [40]. Moreover, in specific lakes, such as Western Chaohu Lake [42] and Dianchi Lake in China [46], Paldang Lake in Korea [82], Bukhan River and Namhan River in South Korea [18], raw water from drinking water treatment plants in Japan [78], and Diamond Valley Lake in the US [25], GSM showed positive correlations with Dolichospermum, while in others (Taihu Lake in China [65], nine sampling sites along the main canal of the Middle Route of South-to-North Water Diversion Project in China [71], San Vicente Reservoir [93] and Lake Skinner in the US [93], and Lake Y in Japan [80]), it exhibited a positive correlation with Pseudoanabaena. However, it is crucial to note that some studies report scenarios in which no correlation was observed. Furthermore, positive correlations between GSM and other factors, such as Merismopedia (Namhan River in South Korea [18]), Phormidium (Lake Kasumigaura in Japan [9]), Planktothrix (Eagle Creek Reservoir in the US [28]), Cylindrospermopsis raciborskii (Eagle Creek Reservoir in the US [49]), and Coelosphaerium (Lake Shinji in Japan [77]), have been reported in certain studies.
For MIB, its relationship with various factors mirrors that of GSM, displaying positive or non-correlative associations with Chl-a, cyanobacteria, Microcystis, Pseudoanabaena, Oscillatoria, Planktothrix, and diatoms. In certain studies, positive correlations have been established with phycocyanin in specific regions (seven important reservoirs in eastern China [21]), while no correlation was found with Dolichospermum (Dianchi Lake [46] and Lake Yangcheng in China [47]), or a negative correlation was reported (DECL (this study)). MIB exhibited no correlation with Merismopedia in certain contexts (Lake Yangcheng in China [47]). However, positive correlations have been reported with Phormidium in various water bodies (Huangpu River [58], Lake Yangcheng in China [47], raw water from drinking water treatment plants [78], and Lake Kasumigaura [9] and Lake Kasumigaura in Japan [17]), and a positive correlation has been observed with Lyngbya in a specific study (California Aqueduct in the US [24]).
In comparison, there has been relatively less extensive research on CYC and ION. Studies such as Taihu Lake [23,64] and Dianchi Lake in China [46] have shown a positive correlation between Chl-a and both CYC and ION. Additionally, in Liangxi River [51] and 13 eutrophic lakes in China [48], there was a positive association between Chl-a and CYC. However, in certain locations, including DECL (this study) and nine sampling sites along the main canal of the Middle Route of South-to-North Water Diversion Project in China [71], CYC did not exhibit a correlation with Chl-a. Similarly, in DECL (this study), Chaohu Lake [22], Songhua Lake [22], Taihu Lake [22], and nine sampling sites along the main canal of the Middle Route of South-to-North Water Diversion Project in China [71], ION was not correlated with Chl-a. Concerning cyanobacteria, a positive correlation with both CYC and ION was observed in Dianchi Lake in China [46], while in DECL (this study), there was no association. Specifically for Microcystis, studies such as seven landscape lakes in Beijing [45,69], Taihu Lake [23,64], Western Chaohu Lake [42], Eastern Chaohu Lake [33] and Dianchi Lake in China [46], and Lake Winnebago in the US [40] have shown a positive correlation between CYC and Microcystis, and ION was positively correlated with CYC in Taihu Lake [23,64] and Dianchi Lake in China [46]. However, in DECL (this study), both CYC and ION were unrelated to Microcystis. Furthermore, CYC and Dolichospermum exhibited no significant correlation, whereas ION demonstrated a positive correlation with Dolichospermum in this study. In Taihu Lake of China, both CYC and ION were unrelated to Oscillatoria [64].
It is worth noting that both GSM and MIB are often produced by bacteria. Therefore, some studies have explored their relationship with bacteria. For instance, in Phayao Lake in Thailand [87], Lake Kasumigaura in Japan [17], and Paldang Lake in Korea [82]), GSM exhibited a positive correlation with actinomycetes. It is noteworthy to mention that alternative findings have been reported by Lee et al. (2020) in the context of Paldang Lake in Korea [15], where the sampling period ranged from June to September 2021, as reported by Park et al. (2016) [82]. In this study, there was no discernible association observed between GSM and actinomycetes. In Eagle Creek Reservoir in the US [29], GSM was positively correlated with α-Proteobacteria. MIB showed a positive correlation with actinomycetes in Eagle Creek Reservoir in the US [28] and fishponds in China [70], while in Eagle Creek Reservoir in the US, MIB displayed a positive correlation with Flavobacterium [29].
A positive correlation between the copy number of the synthesis gene and T/O compounds has been identified in various studies, including those conducted in Paldang Lake in Korea [84], Qingcaosha Reservoir [61], and Lushui Reservoir in China [59]. Consequently, Cao et al. (2023) [62] proposed that the abundance of the MIB synthesis gene (mic) in both the DNA and RNA forms could serve as valuable parameters for early warning systems associated with MIB production.
The comprehensive findings revealed significant positive correlations among Chl-a, phycocyanin, cyanobacteria (Microcystis, Dolichospermum, Merismopedia, Oscillatoria, Phormidium, Planktothrix, Pseudanabaena, Cylindrospermopsis, Coelosphaerium, and Lyngbya), diatoms, and certain T/O compounds (Table 4). These identified biotic factors were implicated in the potential generation of T/O compounds in natural water bodies affected by algal blooms. As in some eutrophic lakes, cyanobacteria and T/O compounds, such as MIB and GSM, exhibited a significant positive correlation with Chl-a. This underscored that the nutritional status, particularly Chl-a, served as an excellent indicator for T/O compounds [14,97]. As a result, certain national regulatory authorities established Chl-a concentration standards to anticipate the occurrence of T/O issues in lakes [98]. However, other microorganisms, such as actinomycetes, Flavobacterium, and α-Proteobacteria, were also observed to be positively related to GSM or MIB, implying a possible source of T/O compounds [29]. In this case, the above biological indicators showed no apparent correlation with odorants, even in the same lake with different investigation periods or regions. There were also few articles reporting a positive correlation between phycocyanin and the synthesis gene with MIB, which has opened a new avenue for T/O exploration. However, relying solely on correlation analysis to trace the source may lead to misjudgments; therefore, further analysis, such as isolating and establishing cultures for direct determination, is essential to identify the exact algae species responsible for the production.

2.5.2. Physical Factors

The occurrence of T/O compounds in water bodies exhibited a nuanced relationship with various physical indicators, as evidenced by diverse findings in multiple studies (Table 4). Temperature, a key factor, was shown to have both positive and negative correlations with the four T/O compounds. While positive correlations were observed in studies like Lake Taihu (for GSM, CYC, and particle-bound MIB and ION [64]) and seven important reservoirs in eastern China [21], instances of negative correlations, notably in Eagle Creek Reservoir [49] and Lake Taihu (for dissolved MIB [64]), challenged the generalization of these associations. Dissolved oxygen further complicated the picture, with instances of positive and negative correlations with T/O compounds across different studies, emphasizing the multifaceted nature of the interactions. Conductivity, water depth, turbidity, and total dissolved solids contributed additional dimensions to the complexity. For example, positive correlations between GSM and MIB with conductivity in a Chinese lake (DECL, this study) differed from findings in Eagle Creek Reservoir [49] and Feng-Shen Reservoir [57]. The negative correlation between MIB and water depth in East Taihu Lake introduced further variability [50]. The lack of correlation between GSM and turbidity in Paldang Lake underscored the site-specific nature of these relationships [15]. The inclusion of oxidation-reduction potential as a contributing factor in Eagle Creek Reservoir highlighted the need for a comprehensive understanding of redox conditions in T/O dynamics [49].
For other physical indicators, in DECL in China, GSM and MIB exhibit a positive correlation with conductivity (this study). Conversely, in Eagle Creek Reservoir in the US [49] and Feng-Shen Reservoir [57], GSM and MIB show no correlation with conductivity. Moreover, in DECL in China, CYC and ION are unrelated to conductivity. In Taihu Lake, MIB was negatively correlated with water depth [50]. In Paldang Lake in Korea, GSM was unrelated to turbidity [15]. Furthermore, in Eagle Creek Reservoir in the US, GSM and MIB displayed a positive correlation with total dissolved solids and showed no correlation with oxidation-reduction potential [49]. The intricate interplay between T/O compounds and physical indicators emphasized the importance of context-specific studies, recognizing the site-specific nature of these interactions for effective water quality management and odor control strategies.

2.5.3. Nutrients

The relationships between T/O compounds and various nitrogen forms have been investigated across multiple studies. Although positive correlations have been identified in specific instances, such as the association between GSM and total nitrogen in seven important reservoirs in eastern China [21] and the correlations of MIB, CYC, and ION with total nitrogen in East Taihu Lake, China [44], as well as ION with total nitrogen in Liangxi River, China [51], the majority of studies conducted by Bruder et al. (2014) [49], Shi et al. (2023) [50], Yu et al. (2019) [44] and Zhang et al. (2019) [22], as well as the present investigation did not observe significant correlations. Furthermore, variations have been noted in the relationships with nitrate and ammonia nitrogen among different compounds across various studies. Specifically, for nitrate, GSM exhibited a positive correlation with it in DECL (this study), Songhua Lake [22], and Liangxi River in China [51], while no correlation was observed in Taihu Lake in China [22,44] or Eagle Creek Reservoir in the US [49].
MIB exhibited a positive correlation with nitrate in nine sampling sites along the main canal of the Middle Route of the South-to-North Water Diversion Project in China [71]. Conversely, no significant correlation was discerned in DECL (this study), Songhua Lake [22], Chaohu Lake [22], Taihu Lake in China [22], and Eagle Creek Reservoir in the US [49]. Similarly, CYC demonstrated a positive correlation with nitrate in the specified sampling sites [71], while no significant correlation was evident in the present study. In the case of ION, it displayed a positive correlation with nitrate in Songhua Lake [22] and nine sampling sites along the main canal of the Middle Route of the South-to-North Water Diversion Project in China [71]. Conversely, a negative correlation was observed in East Taihu Lake [44], and no significant correlation was found in DECL (this study), Chaohu Lake [22], or Taihu Lake in China [22]. Examining ammonia nitrogen, GSM demonstrated a positive correlation with it in Songhua Lake [22], while no significant correlation was observed in DECL (this study), Chaohu Lake [22] and Taihu Lake in China [22,44], or Eagle Creek Reservoir in the US [49]. MIB showed a positive correlation with ammonia nitrogen in DECL in China (this study) and Eagle Creek Reservoir in the US [49], a negative correlation in seven landscape lakes in Beijing [45,69], and no significant correlation in Songhua Lake, Chaohu Lake, Taihu Lake [22], and Feng-Shen Reservoir in China [57]. In this study, CYC was unrelated to ammonia nitrogen. Furthermore, ION exhibited a positive correlation with ammonia nitrogen in Songhua Lake [22] and Liangxi River in China [51], while no significant correlation was noted in DECL (this study), Chaohu Lake, or Taihu Lake in China [22]. Bruder et al. (2014) also investigated total Kjeldahl nitrogen, finding a positive correlation with GSM in Eagle Creek Reservoir in the US and no correlation with MIB [49].
In the investigation of odorants and total phosphorus, there was a lack of research on a positive correlation between GSM and total phosphorus. Conversely, in Chaohu Lake, GSM exhibited a negative correlation with total phosphorus [22]. In subsequent studies, namely, in DECL (this study), Taihu Lake in China [22,44], and Eagle Creek Reservoir in the US [49], no correlation was observed between GSM and total phosphorus. However, MIB showed a positive correlation with total phosphorus in Taihu Lake in China [23,50] and Eagle Creek Reservoir in the US [49] and a negative correlation in Lake Yangcheng, China [47]. In DECL (this study), Songhua Lake [22], Chaohu Lake [22], and Taihu Lake in China [22], MIB was unrelated to total phosphorus. CYC exhibited a positive correlation with total phosphorus in Western Chaohu Lake [42], Taihu Lake [23], and 13 eutrophic lakes in China [48] and was unrelated in DECL in China (this study). ION was positively correlated with total phosphorus in Western Chaohu Lake [42] and Taihu Lake in China [23], negatively correlated in DECL (this study) and Chaohu Lake [22], and unrelated in Songhua Lake [22] and Taihu Lake in China [22]. Regarding other forms of phosphorus, dissolved inorganic phosphorus was negatively correlated with GSM in Chaohu Lake, China [22]. Dissolved inorganic phosphorus and dissolved organic phosphorus were unrelated to GSM in Songhua Lake, and unrelated to MIB and ION in Songhua Lake and Chaohu Lake, China [22]. Concerning orthophosphate, GSM was positively correlated with it in Western Chaohu Lake, China [42], MIB was negatively correlated with it in seven landscape lakes in Beijing [45,69], and no correlation was found with the four odorants in DECL in China (this study). Furthermore, research explored the relationship between the N/P ratio and odorants. The N/P ratio was positively correlated with all four odorants in East Taihu Lake, China [44], and negatively correlated in Liangxi River [51], where MIB showed no correlation with the N/P ratio in Lake Yangcheng, China [47].
These comprehensive investigations delved into the intricate relationships between T/O compounds and various nitrogen and phosphorus forms in diverse water bodies (see references in Table 4). While specific instances illustrated positive correlations, such as the association between GSM and total nitrogen in certain Chinese reservoirs, the overall findings revealed considerable variability across studies. MIB, CYC, and ION exhibited diverse correlations with total nitrogen, emphasizing the complex nature of these interactions. Studies further unveiled nuanced relationships with nitrate and ammonia nitrogen, showcasing positive, negative, or non-significant correlations among different T/O compounds in different locations. Regarding phosphorus forms, the investigation uncovered intricate associations between T/O compounds and total phosphorus, with varying correlations observed for GSM, MIB, CYC, and ION across different water bodies. Additional exploration into other phosphorus forms and the nitrogen-to-phosphorus ratio highlighted the complexity of these relationships, displaying diverse trends in different contexts. The observed variability underscores the need for a contextual and location-specific approach to studying these relationships. Further research is essential to unravel the complexities and refine our comprehension of the factors influencing T/O compounds in aquatic ecosystems.

2.5.4. Organic Matter

In various investigations, the association between odorants and organic matter has been examined using the following four primary indicators: UV254, specific UV absorbance (SUVA), potassium permanganate index (COD), and dissolved organic carbon (DOC). According to the research conducted by Zhang et al. (2019), it was observed that GSM and ION exhibit a negative correlation with UV254 in Songhua Lake, China [22]. However, in Chaohu Lake, China, GSM, MIB, and ION were found to be unrelated to UV254 [22]. Moreover, MIB demonstrated no correlation with UV254 in Songhua Lake [22]. Concerning SUVA, GSM was found to have no correlation with it in both Songhua Lake and Chaohu Lake [22]. On the other hand, MIB showed a positive correlation with SUVA in seven landscape lakes in Beijing [45,69] but no correlation in Songhua Lake, Chaohu Lake, or Taihu Lake in China [22]. ION displayed no correlation with SUVA in either Songhua Lake or Chaohu Lake [22]. Moving on to COD, GSM exhibited a positive correlation with it in Yuqiao Reservoir [74], while MIB demonstrated a positive correlation with COD in DECL in China (this study) and Yuqiao Reservoir [74]. In DECL in China, GSM, CYC, and ION were found to be unrelated to COD (this study). In terms of DOC, GSM displayed a negative correlation with it in Chaohu Lake [22] but no correlation in DECL in China (this study), Songhua Lake, or Taihu Lake [22]. MIB exhibited a positive correlation with DOC in DECL in China (this study), but a negative correlation in Songhua Lake and Chaohu Lake [22]. CYC and ION were unrelated to DOC in DECL in China, and ION showed no correlation with DOC in either Songhua Lake or Taihu Lake [22].

2.5.5. Interrelationships among Metabolites

Regarding the interrelations among volatile organic compounds, both consistencies and variations were observed (Table 4). GSM demonstrated positive correlations with MIB in certain water bodies, such as Eagle Creek Reservoir in the US [49], Chaohu Lake [22], Lake Taihu [23], and East Taihu Lake in China [44] but exhibited a negative correlation in the DECL (this study). Additionally, GSM showed positive correlations with CYC and ION, presenting intricate associations in different aquatic environments.
The coexistence of odorants and toxins in aquatic environments represents a prevalent challenge encountered by numerous water systems; however, comprehensive research in this domain remains inadequate. The limited studies available found that GSM was negatively correlated with MC in DECL in China (this study). Conversely, in Eagle Creek Reservoir in the US [49], there was no discernible correlation between GSM and MC. Furthermore, in DECL in China (this study) and Eagle Creek Reservoir in the US [49], MIB demonstrated negative association with MC.

3. Conclusions

The comparative analysis of T/O occurrences in targeted lakes, considering various nutritional states and geographic locations, has proven to be an invaluable tool for early warning systems associated with algal blooms and T/O events. This study identified management solutions for recurrent off-flavor events, emphasizing the imperative to mitigate eutrophication in surrounding watersheds while acknowledging the potential impact of lake-wide mixing on off-flavor dynamics. Additionally, the research delved into the seasonal variation and complexity of odorant dynamics, highlighting disparities in concentration trends across lake regions and variations in intra- and extracellular concentrations of odorants. These intricacies posed challenges for regulatory and removal strategies, underscoring the importance of enhanced monitoring to comprehend concentration trends in water sources. Furthermore, the global impact of cyanobacterial outbreaks on lakes and reservoirs was acknowledged, resulting in odor-related issues affecting landscape ecology and drinking water safety. This study underscored the significance of fortifying research on the spatial and temporal variations of T/O compounds and their influencing factors to provide technical guidance for controlling cyanobacteria and ensuring the safety of drinking water. The results also provided insights into managing different ecotypes facing nuisance odorant problems, necessitating the development of methods to predict metabolite production for implementing appropriate water treatment procedures. A more profound understanding of the ecology of communities involved in T/O dynamics was deemed essential for establishing proactive management strategies based on key mechanisms driving T/O dynamics. Lastly, in shallow eutrophic lakes, this study recognized the complicated and dynamic environmental conditions, recommending the future consideration of environmental factors responsible for odorant removal processes, such as volatilization and hydrodynamic movement. The call for ongoing research efforts was emphasized, highlighting the necessity of advancing our understanding and developing targeted strategies for water quality management. Overall, these collective insights underscored the complexity of T/O dynamics in water bodies and emphasized the need for a comprehensive, interdisciplinary approach to effectively manage and mitigate associated issues.
Based on the research, the following recommendations were drawn: (1) Monitoring and Surveillance: Given the severe and widespread nature of T/O issues in freshwater ecosystems, especially in China, there is a need for continuous monitoring and surveillance of T/O compounds in drinking water sources. This should include monitoring for seasonal variations and across different water layers. (2) Seasonal Considerations: The temporal analysis revealed variations in odor occurrences within the same water body across different years, emphasizing the need to consider high T/O values in all seasons for water safety. This requires a seasonally adapted water quality management strategy. (3) Targeted Interventions: Since algae were identified as crucial contributors to odor compounds, targeted interventions are needed to control algae growth. This could include physical, chemical, or biological methods tailored to the specific water body and its environmental conditions. (4) Nutrient Management: Nutrients were likely to influence T/O issues, indicating the need for nutrient management strategies to reduce algae growth and subsequent T/O production. This could involve reducing nutrient inputs from agricultural runoff, industrial discharges, and urban wastewater. (5) Further Research and Validation: The correlation analysis alone was insufficient to provide definitive answers, emphasizing the need for further validation, such as algae isolation and analysis of odorant sources and properties. This will require more in-depth research to understand the mechanisms behind T/O production and identify effective control measures. (6) International Collaboration: Given the global nature of T/O issues, international collaboration and knowledge sharing are essential to develop comprehensive management strategies. This could involve sharing best practices, conducting joint research projects, and developing standardized monitoring and assessment protocols.

4. Material and Methods

4.1. Study Area Description and Hydrological Conditions of the Lake

With a surface area spanning 770 km2, a mean depth measuring 2.7 m, and a storage capacity reaching 2.1 billion m3, Chaohu Lake is a significant freshwater resource in the region. We selected the three primary drinking water intakes (117°50′15.13″ E/31°35′36.34″ N, 117°50′54.32″ E/31°35′24.82″ N, and 117°50′58.40″ E/31°35′32.30″ N, Figure 3) situated in the eastern sector of Chaohu Lake as the designated sampling sites, catering to a population exceeding 4 million consumers in the vicinity. Composite water samples were systematically collected monthly from September 2011 to August 2012, employing a 2.5 L sampler at 0.5 m intervals across the entire water column. Biological and physicochemical parameters and microcystins were analyzed parallel to the present work by Shang et al. (2015) and Shang et al. (2018) [11,52], with the minimum, maximum, and mean values detailed in Table 5.

4.2. Taste and Odor Compounds Analysis

4.2.1. Chemicals, Material and Standards

High-performance liquid chromatography (HPLC)-grade methanol and sodium chloride (NaCl) of ensured quality were procured from Merck (Darmstadt, Germany) and Sigma-Aldrich Chemical Co. (St. Louis, MO, USA), respectively. Headspace bottles were acquired from Anpel Company (Shanghai, China), while ultrapure water was sourced from a Milli-Q water purification system (Millipore, Billerica, MA, USA). All other reagents adhered to guaranteed reagent-grade standards. The standards for T/O compounds, specifically, GSM and MIB from Sigma-Aldrich Chemical Co. and CYC and ION from Adamas Reagent Co., Ltd. (Basel, Switzerland), were employed. A stock solution of 1 mg·L−1, comprising the four target T/O compounds in methanol, was securely stored in darkness at −20 °C and subsequently diluted into aqueous working standard solutions before utilization.

4.2.2. Sample Preparation and Analysis

The T/O compounds in samples were analyzed via solid-phase microextraction, combined with GC-MS, according to Watson et al. (2000) and Shang et al. (2018) [11,99]. In detail, one liter or more water samples were filtered immediately through a GF/C filter (Whatman, Dassel, Germany) at a low vacuum pressure. The dissolved fraction in water (80 mL) was transferred immediately into 125 mL headspace bottles with 25 g NaCl and a magnetic stir bar and measured using GC-MS in 12 h. Simultaneously, the particle-bound fraction retained on the filters was stored at −20 °C. For further extraction, the filters underwent three cycles of freeze-thawing and were then rinsed into a 125 mL vial with 80 mL of Milli-Q water. Subsequently, ultrasonication (JY92-2D, Xinzhi Co., Ningbo, China) was performed for 10 min in an ice bath. Enhanced recovery was achieved through the addition of NaCl and a magnetic stir bar. The T/O compound samples were stirred and extracted using a 2 cm-long CAR/DVB/PDMS fiber (Supelco, Inc., Bellefonte, PA, USA) at 65 °C for 30 min before injection into the GC-MS.
The T/O compounds, after extraction, underwent analysis utilizing an Agilent 6890 gas chromatograph interfaced with an Agilent 5973 mass spectrometer, equipped with a DB-5MS column (Agilent Technologies, Inc., Santa Clara, USA). The gas chromatography (GC) temperature program involved an initial holding phase at 60 °C for 2 min, followed by a gradual increase to 200 °C for 2 min at a rate of 8 °C/min, and subsequently elevated to 260 °C at a rate of 15 °C/min. Data analysis was executed in the selected ion monitoring mode. The identification of the targeted T/O compounds was accomplished through the comparison of retention times with established standards, alongside the verification of characteristic ions at m/z 112 and 126 for GSM, 107 and 95 for MIB, 137 and 152 for CYC, and m/z 177 and 91 for ION. The quantification of each analyte was carried out using the corresponding standard curve, with detection limits established at 0.2, 0.2, 0.5, and 0.4 ng·L−1 for GSM, MIB, CYC, and ION, respectively.

4.3. Literature Analysis

To acquire a comprehensive understanding, a literary analysis was undertaken to synthesize the exploration of T/O compounds in freshwater ecosystems globally, encompassing their concentrations and influencing factors. The database compilation involved meticulous keyword searches within the ISI Web of Science, encompassing 74 papers published from 1986 to 2023.

4.4. Statistical Analysis

The examination of concentrations for both dissolved and particulate T/O compounds was executed employing Origin 2018. A correlation analysis was conducted using the IBM Statistical Package for the Social Sciences Statistics 22. A redundancy analysis (RDA) was implemented through CANOCO 4.5 (Microcomputer Power, Ithaca, NY, USA) to ascertain the principal factors associated with T/O compounds [100].

Author Contributions

Conceptualization, L.S. and M.F.; methodology, L.S., F.K., X.X., and M.F.; software, L.S., F.K., and X.X.; validation, F.K. and X.X.; formal analysis, L.S., F.K., and X.X.; investigation, L.S., F.K., X.X., and M.F.; resources, L.S., X.X., M.F., and W.L.; data curation, L.S., X.X., M.F., and W.L.; writing—original draft preparation, L.S.; writing—review and editing, M.F. and W.L.; visualization, X.X. and W.L.; supervision, L.S. and M.F.; project administration, M.F. and W.L.; funding Acquisition, X.X. All authors have read and agreed to the published version of the manuscript.

Funding

This work was financially supported by the Yangtze River Ecological Environment Protection and Restoration Project (2022-LHYJ-02-0502-02-11).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

No datasets were generated or analyzed during the current study.

Conflicts of Interest

The authors declare that they have no competing interests.

References

  1. Plaas, H.E.; Paerl, H.W. Toxic cyanobacteria: A growing threat to water and air quality. Environ. Sci. Technol. 2021, 55, 44–64. [Google Scholar] [CrossRef]
  2. Glibert, P.; Elisa, B.; Michele, A.B.; Grant, C.P.; Mingjiang, Z. Global Ecology and Oceanography of Harmful Algal Blooms, 1st ed.; Springer Nature: Cham, Switzerland, 2018. [Google Scholar]
  3. O’Neil, J.M.; Davis, T.W.; Burford, M.A.; Gobler, C.J. The rise of harmful cyanobacteria blooms: The potential roles of eutrophication and climate change. Harmful Algae 2012, 14, 313–334. [Google Scholar] [CrossRef]
  4. Smith, V.H. Eutrophication of freshwater and coastal marine ecosystems—A global problem. Environ. Sci. Pollut. Res. 2003, 10, 126–139. [Google Scholar] [CrossRef]
  5. Huo, D.; Gan, N.; Geng, R.; Cao, Q.; Song, L.; Yu, G.; Li, R. Cyanobacterial blooms in China: Diversity, distribution, and cyanotoxins. Harmful Algae 2021, 109, 102106. [Google Scholar] [CrossRef]
  6. Li, H.; Gu, X.; Chen, H.; Mao, Z.; Shen, R.; Zeng, Q.; Ge, Y. Co-occurrence of multiple cyanotoxins and taste-and-odor compounds in the large eutrophic Lake Taihu, China: Dynamics, driving factors, and challenges for risk assessment. Environ. Pollut. 2022, 294, 118594. [Google Scholar] [CrossRef]
  7. Watson, S.B. Cyanobacterial and eukaryotic algal odour compounds: Signals or by-products? A review of their biological activity. Phycologia 2003, 42, 332–350. [Google Scholar] [CrossRef]
  8. Devi, A.; Chiu, Y.-T.; Hsueh, H.-T.; Lin, T.-F. Quantitative PCR based detection system for cyanobacterial geosmin/2-methylisoborneol (2-MIB) events in drinking water sources: Current status and challenges. Water Res. 2020, 188, 116478. [Google Scholar] [CrossRef]
  9. Sugiura, N.; Iwami, N.; Inamori, Y.; Nishimura, O.; Sudo, R. Significance of attached cyanobacteria relevant to the occurrence of musty odor in Lake Kasumigaura. Water Res. 1998, 32, 3549–3554. [Google Scholar] [CrossRef]
  10. Sun, D.L.; Yu, J.W.; Yang, M.; An, W.; Zhao, Y.Y.; Lu, N.; Yuan, S.G.; Zhang, D.Q. Occurrence of odor problems in drinking water of major cities across China. Front. Environ. Sci. Eng. 2014, 8, 411–416. [Google Scholar] [CrossRef]
  11. Shang, L.; Feng, M.; Xu, X.; Liu, F.; Ke, F.; Li, W. Co-occurrence of microcystins and taste-and-odor compounds in drinking water source and their removal in a full-scale drinking water treatment plant. Toxins 2018, 10, 26. [Google Scholar] [CrossRef]
  12. Manganelli, M.; Testai, E.; Tazart, Z.; Scardala, S.; Codd, G.A. Co-occurrence of taste and odor compounds and cyanotoxins in cyanobacterial blooms: Emerging risks to human health? Microorganisms 2023, 11, 872. [Google Scholar] [CrossRef]
  13. Gagné, F.; Ridal, J.; Blaise, C.; Brownlee, B. Toxicological effects of geosmin and 2-methylisoborneol on rainbow trout hepatocytes. Bull. Environ. Contam. Toxicol. 1999, 63, 174–180. [Google Scholar] [CrossRef]
  14. Smith, V.H.; Sieber-Denlinger, J.; deNoyelles, F.; Campbell, S.; Pan, S.; Randtke, S.J.; Blain, G.T.; Strasser, V.A. Managing taste and odor problems in a eutrophic drinking water reservoir. Lake Reserv. Manag. 2002, 18, 319–323. [Google Scholar] [CrossRef]
  15. Lee, J.E.; Youn, S.-J.; Byeon, M.; Yu, S.-J. Occurrence of cyanobacteria, actinomycetes, and geosmin in drinking water reservoir in Korea: A case study from an algal bloom in 2012. Water Supply 2020, 20, 1862–1870. [Google Scholar] [CrossRef]
  16. Jahnichen, S.; Jaschke, K.; Wieland, F.; Packroff, G.; Benndorf, J. Spatio-temporal distribution of cell-bound and dissolved geosmin in Wahnbach Reservoir: Causes and potential odour nuisances in raw water. Water Res. 2011, 45, 4973–4982. [Google Scholar] [CrossRef]
  17. Sugiura, N.; Nakano, K. Causative microorganisms for musty odor occurrence in the eutrophic Lake Kasumigaura. Hydrobiologia 2000, 434, 145–150. [Google Scholar] [CrossRef]
  18. Youn, S.J.; Kim, H.N.; Yu, S.J.; Byeon, M.S. Cyanobacterial occurrence and geosmin dynamics in Paldang Lake watershed, South Korea. Water Environ. J. 2020, 34, 634–643. [Google Scholar] [CrossRef]
  19. Watson, S.B.; Ridal, J. Periphyton: A primary source of widespread and severe taste and odour. Water Sci. Technol. 2004, 49, 33–39. [Google Scholar] [CrossRef]
  20. Harris, T.D.; Graham, J.L. Predicting cyanobacterial abundance, microcystin, and geosmin in a eutrophic drinking-water reservoir using a 14-year dataset. Lake Reserv. Manag. 2017, 33, 32–48. [Google Scholar] [CrossRef]
  21. Wu, T.; Zhu, G.; Zhu, M.; Xu, H.; Yang, J.; Zhao, X. Effects of algae proliferation and density current on the vertical distribution of odor compounds in drinking water reservoirs in summer. Environ. Pollut. 2021, 288, 117683. [Google Scholar] [CrossRef]
  22. Zhang, R.; Qi, F.; Liu, C.; Zhang, Y.; Wang, Y.; Song, Z.; Kumirska, J.; Sun, D. Cyanobacteria derived taste and odor characteristics in various lakes in China: Songhua Lake, Chaohu Lake and Taihu Lake. Ecotoxicol. Environ. Saf. 2019, 181, 499–507. [Google Scholar] [CrossRef]
  23. Ma, Z.M.; Xie, P.; Chen, J.; Niu, Y.; Tao, M.; Qi, M.; Zhang, W.; Deng, X.W. Microcystis blooms influencing volatile organic compounds concentrations in Lake Taihu. Fresenius Environ. Bull. 2013, 22, 95–102. [Google Scholar]
  24. Izaguirre, G.; Taylor, W.D. Geosmin and 2-methylisoborneol production in a major aqueduct system. Water Sci. Technol. 1995, 31, 41–48. [Google Scholar] [CrossRef]
  25. Izaguirre, G.; Taylor, W.D. Geosmin and MIB events in a new reservoir in southern California. Water Sci. Technol. 2007, 55, 9–14. [Google Scholar] [CrossRef]
  26. Yu, J.W.; Zhao, Y.M.; Yang, M.; Lin, T.F.; Guo, Z.H.; Gu, J.N.; Li, S.; Han, W. Occurrence of odour-causing compounds in different source waters of China. J. Water Supply Res. Technol.-Aqua 2009, 58, 587–594. [Google Scholar] [CrossRef]
  27. Olsen, B.K.; Chislock, M.F.; Wilson, A.E. Eutrophication mediates a common off-flavor compound, 2-methylisoborneol, in a drinking water reservoir. Water Res. 2016, 92, 228–234. [Google Scholar] [CrossRef]
  28. Clercin, N.A.; Druschel, G.K. Influence of environmental factors on the production of MIB and geosmin metabolites by bacteria in a eutrophic reservoir. Water Resour. Res. 2019, 55, 5413–5430. [Google Scholar] [CrossRef]
  29. Clercin, N.A.; Druschel, G.K.; Gray, M. Occurrences of 2-methylisoborneol and geosmin -degrading bacteria in a eutrophic reservoir and the role of cell-bound versus dissolved fractions. J. Environ. Manag. 2021, 297, 113304. [Google Scholar] [CrossRef]
  30. Du, S.; Xu, H.; Yang, M.; Pan, N.; Zheng, T.; Xu, C.; Li, Y.; Zuo, Z. Toxic mechanism of two cyanobacterial volatiles β-cyclocitral and β-ionone on the photosynthesis in duckweed by altering gene expression. Environ. Pollut. 2022, 308, 119711. [Google Scholar] [CrossRef]
  31. Jiittner, F. Characterization of Microcystis Strains by Alkyl Sulfides and β-Cyclocitral. Z. Für Naturforschung C 1984, 39, 867–871. [Google Scholar] [CrossRef]
  32. Watson, S.B.; Monis, P.; Baker, P.; Giglio, S. Biochemistry and genetics of taste- and odor-producing cyanobacteria. Harmful Algae 2016, 54, 112–127. [Google Scholar] [CrossRef]
  33. Jiang, Y.; Xie, P.; Nie, Y. Concentration and Bioaccumulation of Cyanobacterial Bioactive and Odorous Metabolites Occurred in a Large, Shallow Chinese Lake. Bull. Environ. Contam. Toxicol. 2014, 93, 643–648. [Google Scholar] [CrossRef]
  34. Bao, M.-L.; Barbieri, K.; Burrini, D.; Griffini, O.; Pantani, F. Determination of trace levels of taste and odor compounds in water by microextraction and gas chromatography-ion-trap detection-mass spectrometry. Water Res. 1997, 31, 1719–1727. [Google Scholar] [CrossRef]
  35. Qi, C.; Fang, J.; Wang, G.; Huang, H.; Wang, Z.; Si, Z.; Zhang, L. Characterization of odorants in contrasting ecotypes of Lake Taihu: Algae-dominated versus macrophyte-dominated zones. Environ. Sci. Pollut. Res. 2020, 27, 42221–42229. [Google Scholar] [CrossRef]
  36. Watson, S.B. Aquatic taste and odor: A primary signal of drinking-water integrity. J. Toxicol. Environ. Health-Part A-Curr. Issues 2004, 67, 1779–1795. [Google Scholar] [CrossRef]
  37. State Administration for Market Regulation, Standardization Administration of the People’s Republic of China. Standards for Drinking Water Quality; Standards Press of China: Beijing, China, 2022. Available online: https://std.samr.gov.cn/gb/search/gbDetailed?id=DAB6B92C0764FC96E05397BE0A0A5F84 (accessed on 3 January 2024). (In Chinese)
  38. Lin, T.F.; Wong, J.Y.; Kao, H.P. Correlation of musty odor and 2-MIB in two drinking water treatment plants in South Taiwan. Sci. Total Environ. 2002, 289, 225–235. [Google Scholar] [CrossRef]
  39. Jung, S.; Baek, K.; Yu, M. Treatment of taste and odor material by oxidation and adsorption. Water Sci. Technol. A J. Int. Assoc. Water Pollut. Res. 2004, 49, 289. [Google Scholar] [CrossRef]
  40. Young, C.C.; Suffet, I.H.; Crozes, G.; Bruchet, A. Identification of a woody-hay odor-causing compound in a drinking water supply. Water Sci. Technol. 1999, 40, 273–278. [Google Scholar] [CrossRef]
  41. Westerhoff, P.; Rodriguez-Hernandez, M.; Baker, L.; Sommerfeld, M. Seasonal occurrence and degradation of 2-methylisoborneol in water supply reservoirs. Water Res. 2005, 39, 4899–4912. [Google Scholar] [CrossRef]
  42. Jiang, Y.; Cheng, B.; Liu, M.X.; Nie, Y. Spatial and temporal variations of taste and odor compounds in surface water, overlying water and sediment of the western Lake Chaohu, China. Bull. Environ. Contam. Toxicol. 2016, 96, 186–191. [Google Scholar] [CrossRef]
  43. Wang, C.M.; Yu, J.W.; Guo, Q.Y.; Sun, D.L.; Su, M.; An, W.; Zhang, Y.; Yang, M. Occurrence of swampy/septic odor and possible odorants in source and finished drinking water of major cities across China. Environ. Pollut. 2019, 249, 305–310. [Google Scholar] [CrossRef]
  44. Yu, C.C.; Shi, C.F.; Ji, M.; Xu, X.G.; Zhang, Z.Q.; Ma, J.; Wang, G.X. Taste and odor compounds associated with aquatic plants in Taihu Lake: Distribution and producing potential. Environ. Sci. Pollut. Res. 2019, 26, 34510–34520. [Google Scholar] [CrossRef]
  45. Zhang, J.Z.; Zhang, H.X.; Li, L.W.; Wang, Q.; Yu, J.W.; Chen, Y.S. Microbial community analysis and correlation with 2-methylisoborneol occurrence in landscape lakes of Beijing. Environ. Res. 2020, 183, 109217. [Google Scholar] [CrossRef]
  46. Li, L.; Wan, N.; Gan, N.; Xia, B.D.; Song, L.R. Annual dynamics and origins of the odorous compounds in the pilot experimental area of Lake Dianchi, China. Water Sci. Technol. 2007, 55, 43–50. [Google Scholar] [CrossRef]
  47. Wu, A.; Wang, Y.; Friese, K.; Zhang, L.; Han, C.; Kang, D.; Shen, Q. Spatial and seasonal distribution of 2-methylisoborneol in a large eutrophic shallow lake, China. Water Air Soil Pollut. 2021, 232, 387. [Google Scholar] [CrossRef]
  48. Ren, R.; Deng, X.; Lu, W.; Xiao, R.; Ping, X.; Jun, C. Sediments are important in regulating the algae-derived off-flavor (?-cyclocitral) in eutrophic lakes. Sci. Total Environ. 2023, 875, 162536. [Google Scholar] [CrossRef]
  49. Bruder, S.; Babbar-Sebens, M.; Tedesco, L.; Soyeux, E. Use of fuzzy logic models for prediction of taste and odor compounds in algal bloom-affected inland water bodies. Environ. Monit. Assess. 2014, 186, 1525–1545. [Google Scholar] [CrossRef]
  50. Shi, X.; Huang, Q.; Shen, X.; Wu, J.; Nan, J.; Li, J.; Lu, H.; Yang, C. Distribution, driving forces, and risk assessment of 2-MIB and its producer in a drinking water source-oriented shallow lake. Environ. Sci. Pollut. Res. 2023, 30, 71194–71208. [Google Scholar] [CrossRef]
  51. Lv, C.; Shi, R.; Ji, M.; Liu, Q.; Ma, J.; Xu, X.; Wang, G. Distribution characteristics and influencing factors of odorants in urban rivers with high exogenous algae input. Environ. Chem. 2022, 41, 1579–1590. [Google Scholar]
  52. Shang, L.; Feng, M.; Liu, F.; Xu, X.; Ke, F.; Chen, X.; Li, W. The establishment of preliminary safety threshold values for cyanobacteria based on periodic variations in different microcystin congeners in Lake Chaohu, China. Environ. Sci. Process. Impacts 2015, 17, 728–739. [Google Scholar] [CrossRef]
  53. Chen, X.; Yang, X.; Dong, X.; Liu, E. Environmental changes in Chaohu Lake (southeast, China) since the mid 20th century: The interactive impacts of nutrients, hydrology and climate. Limnologica 2013, 43, 10–17. [Google Scholar] [CrossRef]
  54. Li, X.; Li, Y.; Li, G. A scientometric review of the research on the impacts of climate change on water quality during 1998–2018. Environ. Sci. Pollut. Res. 2020, 27, 14322–14341. [Google Scholar] [CrossRef]
  55. Graham, J.L.; Loftin, K.A.; Meyer, M.T.; Ziegler, A.C. Cyanotoxin mixtures and taste-and-odor compounds in cyanobacterial blooms from the Midwestern United States. Environ. Sci. Technol. 2010, 44, 7361–7368. [Google Scholar]
  56. Xu, Y.; Li, W.; Wu, W.; Zhang, Y. Study on aquaticd off-flavors in eutrophic Donghu Lake. Acta Ecol. Sin. 1999, 19, 212–216. [Google Scholar]
  57. Tung, S.C.; Lin, T.F.; Yang, F.C.; Liu, C.L. Seasonal change and correlation with environmental parameters for 2-MIB in Feng-Shen Reservoir, Taiwan. Environ. Monit. Assess. 2008, 145, 407–416. [Google Scholar] [CrossRef]
  58. Sun, D.L.; Yu, J.W.; An, W.; Yang, M.; Chen, G.G.; Zhang, S.J. Identification of causative compounds and microorganisms for musty odor occurrence in the Huangpu River, China. J. Environ. Sci. 2013, 25, 460–465. [Google Scholar] [CrossRef]
  59. Wang, Z.J.; Song, G.F.; Shao, J.H.; Tan, W.H.; Li, Y.G.; Li, R.H. Establishment and field applications of real-time PCR methods for the quantification of potential MIB-producing cyanobacteria in aquatic systems. J. Appl. Phycol. 2016, 28, 325–333. [Google Scholar] [CrossRef]
  60. Su, M.; Yu, J.W.; Zhang, J.Z.; Chen, H.; An, W.; Vogt, R.D.; Andersen, T.; Jia, D.M.; Wang, J.S.; Yang, M. MIB-producing cyanobacteria (Planktothrix sp.) in a drinking water reservoir: Distribution and odor producing potential. Water Res. 2015, 68, 444–453. [Google Scholar] [CrossRef]
  61. Huang, X.; Huang, Z.F.; Chen, X.P.; Zhang, D.; Zhou, J.Z.; Wang, X.Y.; Gao, N.Y. The predominant phytoplankton of Pseudoanabaena holding specific biosynthesis gene-derived occurrence of 2-MIB in a drinking water reservoir. Environ. Sci. Pollut. Res. 2018, 25, 19134–19142. [Google Scholar] [CrossRef]
  62. Cao, T.; Fang, J.; Jia, Z.; Zhu, Y.; Su, M.; Zhang, Q.; Song, Y.; Yu, J.; Yang, M. Early warning of MIB episode based on gene abundance and expression in drinking water reservoirs. Water Res. 2023, 231, 119667. [Google Scholar] [CrossRef]
  63. Rong, C.; Liu, D.P.; Li, Y.; Yang, K.; Han, X.B.; Yu, J.W.; Pan, B.L.; Zhang, J.S.; Yang, M. Source water odor in one reservoir in hot and humid areas of southern China: Occurrence, diagnosis and possible mitigation measures. Environ. Sci. Eur. 2018, 30. [Google Scholar] [CrossRef]
  64. Deng, X.; Qi, M.; Ren, R.; Liu, J.; Sun, X.; Xie, P.; Chen, J. The relationships between odors and environmental factors at bloom and non-bloom area in Lake Taihu, China. Chemosphere 2019, 218, 569–576. [Google Scholar] [CrossRef]
  65. Yang, C.; Shen, X.; Shi, X.; Cui, Z.; Nan, J.; Lu, H.; Li, J.; Huang, Q. Impact of submerged macrophytes on growth and 2-MIB release risk of Pseudanabaena sp.: From field monitoringa to cultural experiments. J. Hazard. Mater. 2023, 442, 130052. [Google Scholar] [CrossRef]
  66. Zhang, T.; Li, L.; Zuo, Y.; Zhou, Q.; Song, L. Biological origins and annual variations of earthy-musty off-flavours in the Xionghe Reservoir in China. Aqua 2010, 59, 243. [Google Scholar] [CrossRef]
  67. Zuo, Y.X.; Li, L.; Zhang, T.; Zheng, L.L.; Dai, G.Y.; Liu, L.M.; Song, L.R. Contribution of Streptomyces in sediment to earthy odor in the overlying water in Xionghe Reservoir, China. Water Res. 2010, 44, 6085–6094. [Google Scholar] [CrossRef]
  68. Lu, J.; Su, M.; Su, Y.; Wu, B.; Cao, T.; Fang, J.; Yu, J.; Zhang, H.; Yang, M. Driving forces for the growth of MIB-producing Planktothricoides raciborskii in a low-latitude reservoir. Water Res. 2022, 220, 118670. [Google Scholar] [CrossRef]
  69. Qiu, L. Oxidation of Odor Compound and Inactivation Efficiency of Two Kinds of Typical Cyanobacteria by Hydrogen Peroxide and Ozone. Master’s Thesis, Beijing University of Civil Engineering and Architecture, Beijing, China, 2017. [Google Scholar]
  70. Pan, Y.; Xu, L.; Cao, W.; Yin, S.; Wang, Z.; Zhou, Q. Actinomycetes and earthy-musty odorous compounds in brackish fishponds in Tianjin, China. Water Sci. Technol. A J. Int. Assoc. Water Pollut. Res. 2009, 59, 1185–1194. [Google Scholar] [CrossRef]
  71. Wang, Y.; Zhang, C.; Bi, Y.; Zhu, Y.; Song, G.; Wang, S.; Liang, J.; Mi, W. Spatio-temporal pattern of odorous compounds and its influencing factors in the canal of the midle-route of south-to-north water diversion project. Acta Hydrobiol. Sin. 2022, 46, 149–159. [Google Scholar]
  72. Luo, F.; Chen, H.; Wu, X.; Liu, L.; Chen, Y.; Wang, Z. Insights into the seasonal olfactory mechanism of geosmin in raw water of Huangpu River. Toxics 2022, 10, 485. [Google Scholar] [CrossRef]
  73. Lu, J.; Su, M.; Su, Y.; Fang, J.; Burch, M.; Cao, T.; Wu, B.; Yu, J.; Yang, M. MIB-derived odor management based upon hydraulic regulation in small drinking water reservoirs: Principle and application. Water Res. 2023, 244, 120485. [Google Scholar] [CrossRef]
  74. Qiu, P.; Zhang, Y.; Mi, W.; Song, G.; Bi, Y. Producers and drivers of odor compounds in a large drinking-water source. Front. Ecol. Evol. 2023, 11, 1216567. [Google Scholar] [CrossRef]
  75. Badawy, M.I.; Abou-Waly, H.F.; Ali, G.H. Excretion products of algae and their occurrence in Solar Lake. Taba, Egypt. Int. J. Environ. Health Res. 1999, 9, 233–243. [Google Scholar] [CrossRef]
  76. Henatsch, J.J.; Juttner, F. Production and degradation of geosmin in a stratified lake with anaerobic hypolimnion (Schleinsee). Fems Microbiol. Lett. 1986, 35, 135–139. [Google Scholar] [CrossRef]
  77. Godo, T.; Saki, Y.; Nojiri, Y.; Tsujitani, M.; Sugahara, S.; Hayashi, S.; Kamiya, H.; Ohtani, S.; Seike, Y. Geosmin-producing species of Coelosphaerium (Synechococcales, Cyanobacteria) in Lake Shinji, Japan. Sci. Rep. 2017, 7, 41928. [Google Scholar] [CrossRef]
  78. Kishida, N.; Sagehashi, M.; Takanashi, H.; Fujimoto, N.; Akiba, M. Nationwide survey of organism-related off-flavor problems in Japanese drinking water treatment plants (2010–2012). J. Water Supply Res. Technol.-Aqua 2015, 64, 832–838. [Google Scholar] [CrossRef]
  79. Akamatsu, Y.; Nakao, R.; Motozawa, H.; Furukawa, K.; Kurita, Y. Application of a quantitative PCR method for monitoring of geosmin-producing Anabaena spp. in a Japanese reservoir. Landsc. Ecol. Eng. 2023, 19, 87–93. [Google Scholar] [CrossRef]
  80. Boivin, S.; Hasegawa, E.; Yamaguchi, D.; Fujioka, T. The rapid counting method for 2-MIB-producing cyanobacteria (Pseudanabaena sp.) using fluorescence detection of phycocyanin pigments in algal cells. Environ. Sci.-Water Res. Technol. 2023, 9, 2561–2568. [Google Scholar] [CrossRef]
  81. Romero, J.; Ventura, F. Occurrence of geosmin and other odorous compounds of natural origin in surface and drinking waters. A case study. Int. J. Environ. Anal. Chem. 2000, 77, 243–254. [Google Scholar] [CrossRef]
  82. Park, T.J.; Yu, M.N.; Kim, H.S.; Cho, H.S.; Hwang, M.Y.; Yang, H.J.; Lee, J.C.; Lee, J.K.; Kim, S.J. Characteristics of actinomycetes producing geosmin in Paldang Lake, Korea. Desalination Water Treat. 2016, 57, 888–899. [Google Scholar] [CrossRef]
  83. Hwan, B.J.; Kim, H.N.; Kang, T.G.; Kim, B.-H.; Byeon, M.-S. Study of the cause of the generation of odor compounds (geosmin and 2-methylisoborneol) in the Han river system, the drinking water source, Republic of Korea. Water Supply 2023, 23, 1081–1093. [Google Scholar] [CrossRef]
  84. Lee, J.E.; Park, R.; Yu, M.; Byeon, M.; Kang, T. qPCR-based monitoring of 2-methylisoborneol/geosmin-producing cyanobacteria in drinking water reservoirs in South Korea. Microorganisms 2023, 11, 2332. [Google Scholar] [CrossRef]
  85. Shin, J.-K.; Park, Y.; Kim, N.-Y.; Hwang, S.-J. Downstream transport of geosmin based on harmful cyanobacterial outbreak upstream in a reservoir cascade. Int. J. Environ. Res. Public Health 2022, 19, 9294. [Google Scholar] [CrossRef]
  86. Durrer, M.; Zimmermann, U.; Juttner, F. Dissolved and particle-bound geosmin in a mesotrophic lake (Lake Zürich): Spatial and seasonal distribution and the effect of grazers. Water Res. 1999, 33, 3628–3636. [Google Scholar] [CrossRef]
  87. Suwanpakdee, S.; Gutierrez, R.; Pithakpol, S.; Jampeetong, A.; Pathom-aree, W.; Nomura, N.; Itayama, T.; Whangchai, N. Earthy-musty odour and off-flavour taints in Phayao Lake, Thailand. Chiang Mai J. Sci. 2016, 43, 1076–1085. [Google Scholar]
  88. Ridal, J.J.; Brownlee, B.; Lean, D.R.S. Occurrence of the odor compounds, 2-methylisoborneol and geosmin in eastern Lake Ontario and the upper St. Lawrence River. J. Great Lakes Res. 1999, 25, 198–204. [Google Scholar] [CrossRef]
  89. Ridal, J.J.; Brownlee, B.; Lean, D.R.S. Is Lake Ontario the source of taste and odor compounds to the Upper St. Lawrence River? J. Great Lakes Res. 2000, 26, 315–322. [Google Scholar] [CrossRef]
  90. Watson, S.B.; Chariton, M.; Rao, Y.R.; Howell, T.; Ridal, J.; Brownlee, B.; Marvin, C.; Millard, S. Off flavours in large waterbodies: Physics, chemistry and biology in synchrony. Water Sci. Technol. 2007, 55, 1–8. [Google Scholar] [CrossRef]
  91. Hooper, A.S.; Kille, P.; Watson, S.E.; Christofides, S.R.; Perkins, R.G. The importance of nutrient ratios in determining elevations in geosmin synthase (geoA) and 2-MIB cyclase (mic) resulting in taste and odour events. Water Res. 2023, 232, 119693. [Google Scholar] [CrossRef]
  92. Youngsteadt, N.W. Factors that influence phosphorus, filamentous cyanobacteria and odor in McDaniel Lake, a southwest Missouri water supply reservoir, 1983–2002. Lake Reserv. Manag. 2005, 21, 453–464. [Google Scholar] [CrossRef]
  93. Izaguirre, G.; Taylor, W.D.; Pasek, J. Off-flavor problems in two reservoirs, associated with planktonic Pseudanabaena species. Water Sci. Technol. 1999, 40, 85–90. [Google Scholar] [CrossRef]
  94. Harris, T.D.; Smith, V.H.; Graham, J.L.; Van de Waal, D.B.; Tedesco, L.P.; Clercin, N. Combined effects of nitrogen to phosphorus and nitrate to ammonia ratios on cyanobacterial metabolite concentrations in eutrophic Midwestern USA reservoirs. Inland Waters 2016, 6, 199–210. [Google Scholar] [CrossRef]
  95. Olsen, B.K.; Chislock, M.F.; Rebelein, A.; Wilson, A.E. Nutrient enrichment and vertical mixing mediate 2-methylisoborneol and geosmin concentrations in a drinking water reservoir. Water Sci. Technol.-Water Supply 2017, 17, 500–507. [Google Scholar] [CrossRef]
  96. Dzialowski, A.R.; Smith, V.H.; Huggins, D.G.; deNoyelles, F.; Lim, N.C.; Baker, D.S.; Beury, J.H. Development of predictive models for geosmin-related taste and odor in Kansas, USA, drinking water reservoirs. Water Res. 2009, 43, 2829–2840. [Google Scholar] [CrossRef]
  97. Downing, J.A.; Watson, S.B.; McCauley, E. Predicting cyanobacteria dominance in lakes. Can. J. Fish. Aquat. Sci. 2001, 58, 1905–1908. [Google Scholar] [CrossRef]
  98. Oklahoma Water Resources Board. Justification for Chlorophyll-a Criteria to Protect the Public and Private Water Supply Beneficial Use of Sensitive Water Supplies. Available online: http://www.owrb.ok.gov/quality/index.php (accessed on 3 January 2024).
  99. Watson, S.B.; Brownlee, B.; Satchwill, T.; Hargesheimer, E.E. Quantitative analysis of trace levels of geosmin and MIB in source and drinking water using headspace SPME. Water Res. 2000, 34, 2818–2828. [Google Scholar] [CrossRef]
  100. Braak, C.t.; Šmilauer, P. CANOCO reference manual and CanoDraw for Windows user’s guide: Software for canonical community ordination (version 4.5). In Section on Permutation Methods; Microcomputer Power: Ithaca, NY, USA, 2002. [Google Scholar]
Figure 1. Seasonal variations of dissolved and particulate geosmin (a), 2-methyl isoborneol (b), β-cyclocitral (c), and β-ionone (d) in the eastern drinking water source of Chaohu Lake. Dotted lines indicate the OTCs of 4, 15, 19.3, and 7 ng·L−1 for geosmin, MIB, β-cyclocitral, and β-ionone, respectively, Watson (2004); Error bars indicate the standard deviation of three sampling sites.
Figure 1. Seasonal variations of dissolved and particulate geosmin (a), 2-methyl isoborneol (b), β-cyclocitral (c), and β-ionone (d) in the eastern drinking water source of Chaohu Lake. Dotted lines indicate the OTCs of 4, 15, 19.3, and 7 ng·L−1 for geosmin, MIB, β-cyclocitral, and β-ionone, respectively, Watson (2004); Error bars indicate the standard deviation of three sampling sites.
Toxins 16 00264 g001
Figure 2. Redundancy analysis (RDA) biplots showed the concentrations of dissolved and particulate T/O compounds in relation to the density of Microcystis spp. (Mic) and Dolichospermum spp. (Dol) and the environmental factors, including water temperature (T), pH, dissolved oxygen, conductivity, TN, nitrate (NO3), nitrite, ammonia nitrogen, total phosphorus, and orthophosphate, in the eastern drinking water source of Chaohu Lake. d: dissolved T/O compounds; p: particulate T/O compounds.
Figure 2. Redundancy analysis (RDA) biplots showed the concentrations of dissolved and particulate T/O compounds in relation to the density of Microcystis spp. (Mic) and Dolichospermum spp. (Dol) and the environmental factors, including water temperature (T), pH, dissolved oxygen, conductivity, TN, nitrate (NO3), nitrite, ammonia nitrogen, total phosphorus, and orthophosphate, in the eastern drinking water source of Chaohu Lake. d: dissolved T/O compounds; p: particulate T/O compounds.
Toxins 16 00264 g002
Figure 3. Sampling sites in the eastern drinking water source of Chaohu Lake.
Figure 3. Sampling sites in the eastern drinking water source of Chaohu Lake.
Toxins 16 00264 g003
Table 1. Correlation coefficients between T/O compounds and phytoplankton and physicochemical parameters from September 2011 to August 2012 in the eastern drinking water source of Chaohu Lake.
Table 1. Correlation coefficients between T/O compounds and phytoplankton and physicochemical parameters from September 2011 to August 2012 in the eastern drinking water source of Chaohu Lake.
IndexesFactorsGeosmin2-Methyl Isoborneolβ-Cyclocitralβ-Ionone
BiologicalChlorophyll-a−0.1330.3000.2060.095
Cyanobacteria−0.2710.291−0.0130.052
Microcystis spp.−0.1870.505 **−0.039−0.121
Dolichospermum spp.−0.418 *−0.350 *−0.0870.387 *
PhysicalTemperature0.0400.722 **−0.066−0.132
pH0.2300.413 *0.2270.130
Dissolved oxygen0.004−0.762 **0.0690.253
Conductivity0.379 *0.788 **0.250−0.022
NutrientTotal nitrogen0.270−0.010−0.021−0.071
Nitrate0.404 *0.298−0.014−0.166
Ammonia nitrogen0.3220.372 *−0.025−0.247
Total phosphorus−0.0440.243−0.096−0.371 *
Orthophosphate−0.210−0.155−0.202−0.188
OrganicPotassium permanganate index0.2100.452 **0.287−0.030
Dissolved organic carbon0.0280.383 *0.0590.095
Note: Correlation significance is denoted with * p < 0.05 or ** p < 0.01.
Table 2. Correlation coefficients between concentrations of T/O compounds and microcystin congeners (MC-LR, MC-RR, and MC-YR) from September 2011 to August 2012 in the eastern drinking water source of Chaohu Lake.
Table 2. Correlation coefficients between concentrations of T/O compounds and microcystin congeners (MC-LR, MC-RR, and MC-YR) from September 2011 to August 2012 in the eastern drinking water source of Chaohu Lake.
Geosmin2-Methyl Isoborneolβ-Cyclocitralβ-IononeMC-LRMC-RRMC-YR
geosmin1
MIB0.2881
β-cyclocitral0.660 **0.2561
β-ionone0.408 *0.1690.654 **1
MC-LR−0.1830.2280.2390.0141
MC-RR−0.1360.2170.1570.0770.802 **1
MC-YR−0.368 *0.128−0.019−0.2650.817 **0.643 **1
Note: Correlation significance is denoted with * p < 0.05 or ** p < 0.01.
Table 3. Comparison of geosmin, 2-methyl isoborneol, β-cyclocitral, and β-ionone reported in different freshwater bodies of the world.
Table 3. Comparison of geosmin, 2-methyl isoborneol, β-cyclocitral, and β-ionone reported in different freshwater bodies of the world.
Country and RegionSampling SiteSampling TimeGeosmin (ng·L−1)2-Methyl Isoborneol (ng·L−1)β-Cyclocitral
(ng·L−1)
β-Ionone
(ng·L−1)
Reference
China Eastern Chaohu Lake August 2012, December 20120–1300 (August 2012)00–800
(August 2012)
0–8300 (December 2012)[33]
Drinking water intakes in the Eastern Chaohu LakeAugust 2011–August 20120.3–39.7
(March 2011)
0.1–180.5 (July 2012)11.3–105.6
(January 2012)
8.5–136.6
(June 2012)
This study, [11]
Western Chaohu LakeJuly 2013–December 20130–28.3
(December 2013)
0.4–1.8
(August 2013)
0.7–714.8
(September 2013)
0.2–11.2
(September 2013)
[42]
Chaohu LakeSeptember 20173.8–8.0 (September 2017)0.5–9.5 (September 2017) 9.4–28.0 (September 2017)[22]
Dianchi LakeJune 2003–May 20040–130
(October 2003)
0–450
(July 2003)
20–450
(September 2003)
40–570
(September 2003)
[46]
Donghu LakeMay 1995–April 19960–3.3
(June 1995)
10–317
(January 1996)
[56]
Feng-Shen ReservoirDecember 2000–July 2003 0–185
(July 2003)
[57]
Huangpu RiverJanuary 2009–December 2009 0–71
(August 2009)
[58]
Lushui ReservoirJuly 2010–November 20117.2–45.3 [59]
Miyun Reservoir2009–2012 0–195
(September 2010)
[60]
Qingcaosha ReservoirMay 2016–September 2016 0–7.3
(May 2016)
[61]
QCS Reservoir2021 0–99
(05/2021)
[62]
Shenzhen ReservoirOctober 28, 2016, May 8, 2017, 26/September 20171.2–4.2 (May 2017)0 [63]
Shiyan ReservoirOctober 28, 2016, May 8, 2017, 26/September 20171.7–8.0 (May 2017)22.1–52.9 (May 2017) [63]
Songhua LakeSeptember 20171.1–38.1 (September 2017)0.6–3.4 (September 2017) 1.1–8.9 (September 2017)[22]
East Taihu LakeSeptember 20174.7–16.8 (September 2017)13.1–32.7 (September 2017)15.0–37.24.4–13.8 (September 2017)[44]
August 2020–November 2021 0.5–1446
(August 2021)
[50]
Taihu LakeJanuary 2009–December 20090–4
(September 2009)
0–325
(September 2009)
5–2080
(September 2009)
32–573
(August 2009)
[23]
June 2009–May 20100.2–4
(June 2009)
2–152
(July 2009)
1–360
(July 2009)
2–80
(September 2009)
[64]
September 20170.3–1.2 (September 2017)0.2–1.0 (September 2017) 2.2–1976.4 (September 2017)[22]
2020 published1–2015–10022–5308–600[35]
11.7–1446 (August 2021) [65]
Xionghe ReservoirMay 2007–April 20080–2711.5
(July 2007)
0–378.4
(April 2008)
[66]
November 2007–October 20080–826.7
(November 2007)
0–148.1
(April 2008)
[67]
FH ReservoirJuly 2018–June 2019 3.0 ± 2.3–52.4 ± 8.4 (November 2019) [68]
Lake Yangcheng2018–2019 0.4–940.6
(August 2018)
[47]
Seven landscape lakes in BeijingMay 2016–September 2016 1–3509
(July 2016)
0–6000
(May 2016)
[45,69]
Seven important reservoirs in eastern ChinaAugust 201913.1118.3900[21]
RW from eight cities2005–20070–7200
(July 2007)
0–255
(September 2005)
0–358[26]
RW from rivers of DWTPsNovember 2019–March 20100–6.10–25.8 [10]
RW from lake/reservoir of DWTPsNovember 2019–March 20100–9.10–65.0 [10]
RW of 56 DWTPs in 31 major citiesJuly 2011–December 20110–5.50–104 [43]
FishpondsApril 2006–January 20070.3–12.1
(July 2006)
0.5–5302.7
(July 2006)
[70]
MRSNWDPSeptember 2018–August 2019
7.431 ± 9.63112.371 ± 12.80011.973 ± 20.643[71]
LWSPMarch 2016–December 20175.15–17.66 (Winter) [72]
Liangxi RiverSeptember 2018 3–1030–11918–23950–350[51]
Nanping Reservoir2017–2020 0–113 (August 2020) [73]
Zhuxiandong ReservoirMarch–Apirl 2021 51.7 ± 12.8 (Apirl 2021) [73]
Yuqiao Reservoir2018–20210–193
(August 2018)
0–938.30 [74]
13 eutrophic lakes in ChinaMay 2018–September 2019 0–49.05 (September 2019) [48]
EgyptSolar LakeMarch 1997, June 1997, July 1997, August 1997 [75]
GermanySchleinsee Lake1984,19850–180 (July 1984) [76]
Wahnbach ReservoirMay–October 2006–20090–600 (August)0 [16]
ItalyArno RiverMay 8, 199515–70 (May 1995)00–57 (May 1995)0–7 (May 1995)[34]
JapanLake KasumigauraSeptember 1989–October 19900–90
(September 1989)
0–150 (October 1990) [9]
1994–19970–560
(March 1995)
0–185
(April 1995)
[17]
Lake ShinjiSeptember 2009–October 20093–640
(October 2009)
[77]
RW of DWTPsOctober 2010–September 20120–5200–1400 [78]
A reservoir in Mie PrefectureDecember 10th, 20190–9.53 [79]
Lake Y in Nagasaki PrefectureMarch–July 2022<20–13 [80]
SpainLlobregat River1997–19995–20010–200 [81]
KoreaPaldang LakeJune 2012–September 2012
April 2017–November 2018
0–4384 (July 2012)
0–246 (August 2017)
2–31 (July 2020)
0–22 (July 2012)
0–280 (October 2017)
[15,82,83,84]
North Han River and Han River December 20112–1640 [85]
Bukhan River2011–20150–810
(August 2014)
[18]
Namhan River2011–20150–75
(September 2015)
[18]
SwitzerlandLake Zürich1995–19963.1–23
(December 1995)
[86]
ThailandPhayao LakeJune 2012–February 20130–12.0 (October 2012)0.1–1.1 [87]
North AmericaEastern Ontario Lake and the Upper Saint Lawrence River1996–19975–20
(September 1996)
2–25
(September 1996)
[88]
July 1998, September 19980–20
(September 1998)
0–60
(September 1998)
[89]
Ontario Lake2007 published0–200 (August–September) [90]
Saint Lawrence River2000–20018–600–26 [19]
2007 published10–6010–60 [90]
Wales, U.K.Nine reservoirsJuly 2019–August 20200.3–4200.57–58 [91]
United States of AmericaCalifornia AqueductAugust 1990–October 19903–48 (August 1990) [24]
July 1991–November 1991 0–78 [24]
Cheney ReservoirAugust 1999–October 20000–37 (July 2000)0–2 [14]
May 2001–June 20151–113 (July) [20]
Diamond Valley LakeMay 20000–750
(May 2000)
[25]
October 20042–63
(October 2004)
[25]
Eagle Creek Reservoir2008–20100–109.4
(October 2009)
0–223.7
(May 2010)
[49]
January 2013–December 20130–77.3
(May 2013)
0–111.8
(May 2013)
[28,29]
McDaniel Lake1983–20020–330–90 [92]
San Vicente Reservoir199623 [93]
Winnebago LakeAugust 20, 199618 (August 1996) 133 (August 1996) [40]
Three water supply reservoirs1999–20020–2 (September 2000)0–46 (September 2000) [41]
Four ReservoirsMay 2001–December 20120–1330–224 [94]
Drinking water ReservoirNovember 2013–December 2013, 06/2014–August 2014 10–289
(August 2014)
[27,95]
Note: DWTPs: drinking water treatment plants; RW: raw water; MRSNWDP = nine sampling sites along the main canal of the Middle Route of South-to-North Water Diversion Project; LWSP = local water supply plant, Shanghai, China.
Table 4. Influencing factors to geosmin, 2-methyl isoborneol, β-cyclocitral, and β-ionone in different freshwater bodies of the world.
Table 4. Influencing factors to geosmin, 2-methyl isoborneol, β-cyclocitral, and β-ionone in different freshwater bodies of the world.
Geosmin2-Methyl Isoborneolβ-Cyclocitralβ-Ionone
CHL+TL–CN–January 2009–December 2009 [23]
CR–US–August 1999–October 2000 [14]
REC–CN–August 2019 [21]
TL–CN–June 2009–May 2010 [64]
TL–CN–January 2009–December 2009 [23]
REC–CN–August 2019 [21]
ETL–CN–August 2020–November 2021 [50]
LR–CN–2022 [51]
TL–CN–June 2009–May 2010 [64]
TL–CN–January 2009–December 2009 [23]
DL–CN–June 2002–May 2003 [46]
LR–CN–2022 [51]
TEL–CN–05/18–09/19 [48]
TL–CN–June 2009–May 2010 [64]
TL–CN–January 2009–December 2009 [23]
DL–CN–June 2002–May 2003 [46]
#DECL–CN–September 2011–August 2012 (This study)
SL–CN–September 2017 [22]
CL–CN–September 2017 [22]
TL–CN–September 2017 [22]
TL–CN–June 2009–May 2010 [64]
DL–CN–June 2002–May 2003 [46]
WR–DE–May–October 2006–2009 [16]
ER–US–2008–2010 [49]
DECL–CN–September 2011–August 2012 (This study) SL–CN–September 2017 [22]
CL–CN–September 2017 [22]
TL–CN–September 2017 [22]
DL–CN–June 2002–May 2003 [46]
ER–US–2008–2010 [49]
DECL–CN–September 2011–August 2012 (This study)
SWDP–CN–September 2018–August 2019 [71]
DECL–CN–September 2011–August 2012 (This study)
SL–CN–September 2017 [22]
CL–CN–September 2017 [22]
TL–CN–September 2017 [22]
SWDP–CN–September 2018–August 2019 [71]
CYA+PL–TH–June 2012–February 2013 [87]
BR–KR–2011–2015 [18]
NR–KR–2011–2015 [18]
PAL–KO–June 2012–September 2012 [15]
LL–CN–May–September 2016 [45,69]
DWR–US–November 2013–December 2013 [27]
YC–CN–2018–2019 [47]
ETL–CN–August 2020–November 2021 [50]
DL–CN–June 2002–May 2003 [46]DL–CN–June 2002–May 2003 [46]
#DECL–CN–September 2011–August 2012 (This study)
DL–CN–June 2002–May 2003 [46]
ER–US–2008–2010 [49]
DECL–CN–September 2011–August 2012 (This study)
DL–CN–June 2002–May 2003 [46]
ER–US–2008–2010 [49]
DECL–CN–September 2011–August 2012 (This study)DECL–CN–September 2011–August 2012 (This study)
PHY+ REC–CN–August 2019 [21]
MIC+TL–CN–January 2009–December 2009 [23]
CA–US–August 1990 [24]
BR–KR–2011–2015 [18]
NR–KR–2011–2015 [18]
LW–US–August 20, 1996 [40]
DECL–CN–September 2011–August 2012 (This study)
TL–CN–June 2009–May 2010 [64]
TL–CN–January 2009–December 2009 [23]
YC–CN–2018–2019 [47]
LL–CN–May–September 2016 [45,69]
TL–CN–June 2009–May 2010 [64]
WCL–CN–December 2013 [42]
ECL–August 2012, December 2012 [33]
TL–CN–January 2009–December 2009 [23]
DL–CN–June 2002–May 2003 [46]
LW–US–August 20, 1996 [40]
TL–CN–June 2009–May 2010 [64]
TL–CN–January 2009–December 2009 [23]
DL–CN–June 2002–May 2003 [46]
#DECL–CN–September 2011–August 2012 (This study)
TL–CN–June 2009–May 2010 [64]
DL–CN–June 2002–May 2003 [46]
DL–CN–June 2002–May 2003 [46]DECL–CN–September 2011–August 2012 (This study)DECL–CN–September 2011–August 2012 (This study)
DOL+PAL–KO–June 2012–September 2012 [82]
WCL–CN–December 2013 [42]
RW–JP–October 2010–September 2012 [78]
DL–CN–June 2002–May 2003 [46]
BR–KR–2011–2015 [18]
NR–KR–2011–2015 [18]
Diamond Valley Lake in the US [25]
DECL–CN–September 2011–August 2012 (This study)
DECL–CN–September 2011–August 2012 (This study)DECL–CN–September 2011–August 2012 (This study)
# DL–CN–June 2002–May 2003 [46]
YC–CN–2018–2019 [47]
DECL–CN–September 2011–August 2012 (This study)
MER+NR–KR–2011–2015 [18]
# YC–CN–2018–2019 [47]
OSC+ TL–CN–June 2009–May 2010 [64]
RW–JP–October 2010–September 2012 [78]
#TL–CN–June 2009–May 2010 [64]YC–CN–2018–2019 [47]TL–CN–June 2009–May 2010 [64]TL–CN–June 2009–May 2010 [64]
PHO+LK–JP–September 1989–1990.10 [9]RW–JP–October 2010–September 2012 [78]
HR–CN–January 2009–December 2009 [58]
LK–JP–September 1989–October 1990 [9]
LK–JP–1994–1997 [17]
YC–CN–2018–2019 [47]
PLA+ECR–US–January 2013–December 2013 [28]
ER–US–2008–2010 [49]
MR–CN–2009–2012 [60]
DL–CN–June 2002–May 2003 [46]
ER–US–2008–2010 [49]
NP–CN–2017–2020 [73]
# YC–CN–2018–2019 [47]
PSE+SVR–US–1996 [93]
LSK–US–1996 [93]
LY–JP–2022 [80]
TL–CN–2021 [65]
SWDP–CN–September 2018–August 2019 [71]
SR–CN–April–July 2018 [63]
QR–CN–May 2016–September 2016 [61]
SWDP–CN–September 2018–August 2019 [71]
ETL–CN–August 2020–November 2021 [50]
NP–CN–2017–2020 [73]
YQR-CN–2018–2021 [74]
#ER–US–2008–2010 [49]ER–US–2008–2010 [49]
CYL+ER–US–2008–2010 [49]
COE+LS–JP–September–October 2009 [77]
LYN+ CA–US–August 1990 [24]
DIA+ DWR–US–November 2013–December 2013 [27]
# ER–US–2008–2010 [49]
ACT+PL–TH–June 2012–February 2013 [87]
LK–JP–1994–1997 [17]
PAL–KO–June 2012–September 2012 [82]
ECR–US–January 2013–December 2013 [28]
FP–CN–April 2006–January 2007 [70]
#PAL–KO–June 2012–September 2012 [15]
FLA+ ECR–US–January 2013–December 2013 [29]
PRO+ECR–US–January 2013–December 2013 [29]
GEN+PAL–KO–07–10/2020 [84]QR–CN–May 2016–September 2016 [61]
LSR–CN–July 2010–November 2011 [59]
QCS Reservoir–CN–2021 [62]
PAL–KO–July–October 2020 [84]
T+TL–CN–June 2009–May 2010 [64]
REC–CN–August 2019 [21]
YQR–CN–2018–2021 [74]
DECL–CN–September 2011–August 2012 (This study)
TL–CN–June 2009–May 2010 for p–MIB [64]
FR–CN–December 2000–July 2003 [57]
YC–CN–2018–2019 [47]
TL–CN–June 2009–May 2010 [64]
TEL–CN–05/18–09/19 [48]
TL–CN–June 2009–May 2010 for p–ION [64]
ER–US–2008–2010 [49]TL–CN–June 2009–May 2010 for d–MIB [64] DECL–CN–September 2011–August 2012 (This study)TL–CN–June 2009–May 2010 for d–ION [64]
#DECL–CN–September 2011–August 2012 (This study)ER–US–2008–2010 [49] August 2012DECL–CN–September 2011–August 2012 (This study)DECL–CN–September 2011–August 2012 (This study)
pH+ DECL–CN–September 2011–August 2012 (This study)
LL–CN–May 2016–09 [45,69]
#DECL–CN–September 2011–August 2012 (This study)
ER–US–2008–2010 [49]
FR–CN–December 2000–July 2003 [57]
ER–US–2008–2010 [49]
DECL–CN–September 2011–August 2012 (This study)DECL–CN–September 2011–August 2012 (This study)
DO+REC–CN–August 2019 [21]TL–CN–June 2009–May 2010 [64] TL–CN–June 2009–May 2010 for d–ION [64]
SL–CN–September 2017 [22]
TL–CN–June 2009–May 2010 [64] August 2012
DECL–CN–September 2011–August 2012 (This study)TL–CN–June 2009–May 2010 [64]SL–CN–September 2017 [22]
TL–CN–June 2009–May 2010 for p–ION [64]
#DECL–CN–September 2011–August 2012 (This study)
TL–CN–September 2017 [22]
ER–US–2008–2010 [49]
SL–CN–September 2017 [22]
CL–CN–September 2017 [22]
TL–CN–September 2017 [22]
ER–US–2008–2010 [49]
DECL–CN–September 2011–August 2012 (This study)DECL–CN–September 2011–August 2012 (This study)
CL–CN–September 2017 [22]
TL–CN–September 2017 [22]
CON+DECL–CN–September 2011–August 2012 (This study)DECL–CN–September 2011–August 2012 (This study)
#ER–US–2008–2010 [49]FR–CN–December 2000–July 2003 c
ER–US–2008–2010 [49]
DECL–CN–September 2011–August 2012 (This study)DECL–CN–September 2011–August 2012 (This study)
WD+ ETL–CN–August 2020–November 2021 [50]
TUR#PAL–KO–June 2012–September 2012 [15]
TDS+ER–US–2008–2010 [49]ER–US–2008–2010 [49]
ORP#ER–US–2008–2010 [49]ER–US–2008–2010 [49]
TN+REC–CN–August 2019 [21]TL–CN–September 2017 [44]TL–CN–September 2017 [44]TL–CN–September 2017 [44]
LR–CN–2022 [51]
#DECL–CN–September 2011–August 2012 (This study)
SL–CN–September 2017 [22]
CL–CN–September 2017 [22]
TL–CN–September 2017 [22]
ETL–CN–September 2017 [44]
ER–US–2008–2010 [49]
DECL–CN–September 2011–August 2012 (This study)
SL–CN–September 2017 [22]
CL–CN–September 2017 [22]
TL–CN–September 2017 [22]
ER–US–2008–2010 [49]
ETL–CN–August 2020–November 2021 [50]
DECL–CN–September 2011–August 2012 (This study)DECL–CN–September 2011–August 2012 (This study)
SL–CN–September 2017 [22]
CL–CN–September 2017 [22]
TL–CN–September 2017 [22]
NO3+DECL–CN–September 2011–August 2012 (This study)
SL–CN–September 2017 [22]
LR–CN–2022 [51]
SWDP–CN–September 2018–August 2019 [71]SWDP–CN–September 2018–August 2019 [71]SL–CN–September 2017 [22]
SWDP–CN–September 2018–August 2019 [71]
ETL–CN–September 2017 [44]
#TL–CN–September 2017 [22]
ETL–CN–September 2017 [44]
ER–US–2008–2010 [49]
DECL–CN–September 2011–August 2012 (This study)
SL–CN–September 2017 [22]
CL–CN–September 2017 [22]
TL–CN–September 2017 [22]
ER–US–2008–2010 [49]
DECL–CN–September 2011–August 2012 (This study)DECL–CN–September 2011–August 2012 (This study)
CL–CN–September 2017 [22]
TL–CN–September 2017 [22]
TKN+ER–US–2008–2010 [49]
# ER–US–2008–2010 [49]
NH4+SL–CN–September 2017 [22]DECL–CN–September 2011–August 2012 (This study)
ER–US–2008–2010 [49]
SL–CN–September 2017 [22]
LR–CN–2022 [51]
LL–CN–May-September 2016 [45,69]
#DECL–CN–September 2011–August 2012 (This study)
CL–CN–September 2017 [22]
TL–CN–September 2017 [22]
ETL–CN–September 2017 [44]
ER–US–2008–2010 [49]
SL–CN–September 2017 [22]
CL–CN–September 2017 [22]
TL–CN–September 2017 [22]
FR–CN–December 2000–July 2003 [57]
DECL–CN–September 2011–August 2012 (This study)DECL–CN–September 2011–August 2012 (This study)
CL–CN–September 2017 [22]
TL–CN–September 2017 [22]
TP+ TL–CN–January 2009–December 2009 [23]
ER–US–2008–2010 [49]
ETL–CN–August 2020–November 2021 [50]
WCL–CN–December 2013 [42]
TL–CN–January 2009–December 2009 [23]
TEL–CN–05/18–09/19 [48]
WCL–CN–December 2013 [42]
TL–CN–January 2009–December 2009 [23]
CL–CN–September 2017 [22]YC–CN–2018–2019 [47] DECL–CN–September 2011–August 2012 (This study)
CL–CN–September 2017 [22]
#DECL–CN–September 2011–August 2012 (This study)
SL–CN–September 2017 [22]
TL–CN–September 2017 [22]
ETL–CN–September 2017 [44]
ER–US–2008–2010 [49]
DECL–CN–September 2011–August 2012 (This study)
SL–CN–September 2017 [22]
CL–CN–September 2017 [22]
TL–CN–September 2017 [22]
DECL–CN–September 2011–August 2012 (This study)SL–CN–September 2017 [22]
TL–CN–September 2017 [22]
DIPCL–CN–September 2017 [22]
#SL–CN–September 2017 [22]SL–CN–September 2017 [22]
CL–CN–September 2017 [22]
SL–CN–September 2017 [22]
CL–CN–September 2017 [22]
DOP#SL–CN–September 2017 [22]SL–CN–September 2017 [22]
CL–CN–September 2017 [22]
SL–CN–September 2017 [22]
CL–CN–September 2017 [22]
PO4+WCL–CN–December 2013 [42] WCL–CN–December 2013 [42]
LL–CN–May–September 2016 [45,69]
#DECL–CN–September 2011–August 2012 (This study)DECL–CN–September 2011–August 2012 (This study)DECL–CN–September 2011–August 2012 (This study)DECL–CN–September 2011–August 2012 (This study)
N/P+ETL–CN–September 2017 [44]ETL–CN–September 2017 [44]ETL–CN–September 2017 [44]ETL–CN–September 2017 [44]
LR–CN–2022 [51]
# YC–CN–2018–2019 [47]
UV254+
SL–CN–September 2017 [22] SL–CN–September 2017 [22]
#CL–CN–September 2017 [22]SL–CN–September 2017 [22]
CL–CN–September 2017 [22]
CL–CN–September 2017 [22]
SUVA+ LL–CN–May–September 2016 [45,69]
SL–CN–September 2017 [22]
#SL–CN–September 2017 [22]
CL–CN–September 2017 [22]
SL–CN–September 2017 [22]
CL–CN–September 2017 [22]
TL–CN–September 2017 [22]
CL–CN–September 2017 [22]
COD+YQR–CN–2018–2021 [74]DECL–CN–September 2011–August 2012 (This study)
YQR–CN–2018–2021 [74]
#DECL–CN–September 2011–August 2012 (This study) DECL–CN–September 2011–August 2012 (This study)DECL–CN–September 2011–August 2012 (This study)
DOC+ DECL–CN–September 2011–August 2012 (This study)
CL–CN–September 2017 [22]SL–CN–September 2017 [22]
CL–CN–September 2017 [22]
CL–CN–September 2017 [22]
#DECL–CN–September 2011–August 2012 (This study)
SL–CN–September 2017 [22]
TL–CN–September 2017 [22]
DECL–CN–September 2011–August 2012 (This study)DECL–CN–September 2011–August 2012 (This study)
SL–CN–September 2017 [22]
TL–CN–September 2017 [22]
MC+August 2012August 2012
DECL–CN–September 2011–August 2012 (This study)DECL–CN–September 2011–August 2012 (This study)
ER–US–2008–2010 [49]
#ER–US–2008–2010 [49]
GSM+ ER–US–2008–2010 [49]
CL–CN–September 2017 [22]
TL–CN–January 2009–December 2009 [23]
ETL–CN–September 2017 [44]
TL–CN–2020 published [35]
TL–CN–January 2009–December 2009 [23]
ETL–CN–September 2017 [44]
TL–CN–2020 published [35]
CL–CN–September 2017 [22]
SL–CN–September 2017 [22]
TL–CN–January 2009–December 2009 [23]
ETL–CN–September 2017 [44]
DECL–CN–September 2011–August 2012 (This study)
# TL–CN–2020 published [35]
SL–CN–September 2017 [22]
TL–CN–September 2017 [22]
TL–CN–September 2017 [22]
MIB+ER–US–2008–2010 [49]
CL–CN–September 2017 [22]
TL–CN–January 2009–December 2009 [23]
ETL–CN–September 2017 [44]
TL–CN–2020 published [35]
TL–CN–January 2009–December 2009 [23]
ETL–CN–September 2017 [44]
TL–CN–2020 published [35]
CL–CN–September 2017 [22]
TL–CN–January 2009–December 2009 [23]
ETL–CN–September 2017 [44]
DECL–CN–September 2011–August 2012 (This study)
#TL–CN–2020 published [35]
SL–CN–September 2017 [22]
TL–CN–September 2017 [22]
SL–CN–September 2017 [22]
TL–CN–September 2017 [22]
CYC+TL–CN–2020 published [35]
TL–CN–January 2009–December 2009 [23]
ETL–CN–September 2017 [44]
TL–CN–2020 published [35]
TL–CN–January 2009–December 2009 [23]
ETL–CN–September 2017 [44]
TL–CN–2020 published [35]
TL–CN–January 2009–December 2009 [23]
ETL–CN–September 2017 [44]
ION+TL–CN–2020 published [35]
SL–CN–September 2017 [22]
CL–CN–September 2017 [22]
TL–CN–January 2009–December 2009 [23]
ETL–CN–September 2017 [44]
TL–CN–2020 published [35]
CL–CN–September 2017 [22]
TL–CN–January 2009–December 2009 [23]
ETL–CN–September 2017 [44]
TL–CN–2020 published [35]
TL–CN–January 2009–December 2009 [23]
ETL–CN–September 2017 [44]
#TL–CN–September 2017 [22]SL–CN–September 2017 [22]
TL–CN–September 2017 [22]
Note: +: There is a positive correlation between T/O compound and each indicator. #: There is no correlation between the T/O compound and each indicator. −: There is a negative correlation between T/O compound and each indicator. CHL = chlorophyll-a; CYA = cyanobacteria; PHY = phycocyanin; MIC = Microcystis; DOL = Dolichospermum; MER = Merismopedia; OSC = Oscillatoria; PHO = Phormidium; PLA = Planktothrix; PSE = Pseudanabaena; CYL = Cylindrospermopsis raciborskii; COE = Coelosphaerium; LYN = Lyngbya; DIA = Diatom; ACT = actinomycetes; FLA = Flavobacterium; PRO = α-proteobacteria; GEN = 2-methyl isoborneol synthesis gene; T = temperature; DO = dissolved oxygen; CON = conductivity; WD = water depth; TUR = turbidity; TDS = total dissolved solids; ORP = oxidation-reduction potential; TN = total nitrogen; NO3 = nitrate; TKN = total Kjeldahl nitrogen; NH4 = ammonia nitrogen; TP = total phosphorus; DIP: dissolved inorganic phosphate; DOP: dissolved organic phosphate; PO4 = orthophosphate; N/P = N/P ratio; UV = UV254; SUVA = specific UV absorbance; COD = potassium permanganate index; DOC = dissolved organic carbon; MC = microcystin; GSM = geosmin; MIB = 2-methyl isoborneol; CYC = β-cyclocitral; ION = β-ionone; CN = China; DE = Germany; JP = Japan; KO = Korea; KR = South Korea; TH = Thailand; US = United States; DECL = drinking water intakes in Eastern Chaohu Lake [this study]; CL = Chaohu Lake; ECL = Eastern Chaohu Lake; WCL = Western Chaohu Lake; TL = Taihu Lake; ETL = East Taihu Lake; SL = Songhua Lake; DL = Dianchi Lake; DVL = Diamond Valley Lake; PAL = Paldang Lake; PL = Phayao Lake; LL = seven landscape lakes in Beijing; LS = Lake Shinji; LSK = Lake Skinner; LK = Lake Kasumigaura; LY = Lake Y; LW= Lake Winnebago; YC = Lake Yangcheng; TEL = 13 eutrophic lakes in China; LR = Liangxi River; CR = Cheney Reservoir; ECR = Eagle Creek Reservoir; SVR = San Vicente Reservoir; SR = Shiyan Reservoir; SWDP = nine sampling sites along the main canal of the Middle Route of South-to-North Water Diversion Project; QCS = QCS Reservoir; NP = Nanping Reservoir; QR = Qingcaosha Reservoir; MR = Miyun Reservoir; WR = Wahnbach Reservoir; LSR = Lushui Reservoir; FR = Feng-Shen Reservoir; YQR = Yuqiao Reservoir; REC = seven important reservoirs in eastern China; DWR = drinking water reservoir; FH = FH Reservoir; BR = Bukhan River; HR = Huangpu River; NR = Namhan River; CA = California Aqueduct; RW = raw water from drinking water treatment plants; FP = fishponds.
Table 5. Minimum, maximum, and average values of biological, physicochemical indices, and microcystins observed in the eastern drinking water source of Chaohu Lake from September 2011 to August 2012.
Table 5. Minimum, maximum, and average values of biological, physicochemical indices, and microcystins observed in the eastern drinking water source of Chaohu Lake from September 2011 to August 2012.
IndexesMinimumMaximumMean
Chlorophyll-a (µg·L−1)5.375.625.7
Cyanobacterial density (×104 cells·mL−1)0.121.99.4
Microcystis spp. density (×104 cells·mL−1)0.018.55.6
Dolichospermum spp. density (×104 cells·mL−1)0.117.13.7
Temperature (°C)63119
pH7.38.88.1
Dissolved oxygen (mg·L−1)6.012.49.4
Conductivity (μS·cm−1)293416329
Total nitrogen (mg·L−1)0.483.291.67
Nitrate (mg·L−1)0.091.460.59
Ammonia nitrogen (mg·L−1)0.060.380.19
Total phosphorus (mg·L−1)0.020.190.08
Orthophosphate (mg·L−1)0.000.020.00
Potassium permanganate index (mg·L−1)3.88.35.5
Dissolved organic carbon (mg·L−1)3.715.824.22
MC-LR (μg·L−1)0.071.900.53
MC-RR (μg·L−1)0.123.730.79
MC-YR (μg·L−1)0.004.180.82
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Shang, L.; Ke, F.; Xu, X.; Feng, M.; Li, W. Temporal Dynamics and Influential Factors of Taste and Odor Compounds in the Eastern Drinking Water Source of Chaohu Lake, China: A Comparative Analysis of Global Freshwaters. Toxins 2024, 16, 264. https://doi.org/10.3390/toxins16060264

AMA Style

Shang L, Ke F, Xu X, Feng M, Li W. Temporal Dynamics and Influential Factors of Taste and Odor Compounds in the Eastern Drinking Water Source of Chaohu Lake, China: A Comparative Analysis of Global Freshwaters. Toxins. 2024; 16(6):264. https://doi.org/10.3390/toxins16060264

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Shang, Lixia, Fan Ke, Xiangen Xu, Muhua Feng, and Wenchao Li. 2024. "Temporal Dynamics and Influential Factors of Taste and Odor Compounds in the Eastern Drinking Water Source of Chaohu Lake, China: A Comparative Analysis of Global Freshwaters" Toxins 16, no. 6: 264. https://doi.org/10.3390/toxins16060264

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