Next Article in Journal
Visibility Graph Power Geometric Aggregation Operator and Its Application in Water, Energy and Food Efficiency Evaluation
Previous Article in Journal
First-Line Managers’ Experiences of Working with a Structured Support Model for Systematic Work Environment Management
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Biogenic Silica and Organic Carbon Records in Zhoushan Coastal Sea over the Past One Hundred Years and Their Environmental Indications

1
Department of Geography and Spatial Information Techniques, Ningbo University, Ningbo 315211, China
2
Institute of East China Sea, Ningbo University, Ningbo 315211, China
3
School of Geosciences, University of South Florida, Tampa, FL 33620, USA
*
Author to whom correspondence should be addressed.
Int. J. Environ. Res. Public Health 2020, 17(11), 3890; https://0-doi-org.brum.beds.ac.uk/10.3390/ijerph17113890
Submission received: 1 May 2020 / Revised: 21 May 2020 / Accepted: 26 May 2020 / Published: 30 May 2020
(This article belongs to the Section Environmental Analysis and Methods)

Abstract

:
The influence of terrestrial and marine input has dramatically changed eutrophication in coastal seas over the past 100 years. In this study, Zhoushan coastal sea (ZCS) is taken as a study area. We studied ZCS as it is a sink of the temporal and spatial variation of primary productivity, dominant species of algae, and the variation of provenance in this area over the past 100 years. We performed analysis using three sediment cores and the carbon and silicon deposition records. The analysis results demonstrate that: (1) The primary productivity in the northern area of the ZCS close to the Yangtze Estuary was the highest comparatively, but it declined slightly before 2010. The primary productivity in the southern area had an increasing trend over the past 100 years. The value of total organic carbon (TOC) in the northern area was relatively high, with an average value of 0.532% over the past 100 years, with a decreasing trend in recent years. On the contrary, TOC in the southern area was relatively low, but it was increased dramatically after 1995. (2) Diatom might play an important role in the variations. The biogenic silica (BSi) and TOC in the northern area showed a synchronous declining trend, while the BSi/TOC ratio did not change significantly. This indicates the algae population structure in this area was relatively stable over the past 100 years. The BSi/TOC ratio decreased continuously in the southern area, indicating that the dominance of diatoms was decreasing continuously. (3) The variation of diatom dominance in this area might have a great relationship with the change of nutrients’ provenance. A mean value of stable carbon isotope (δ13C) in the north of Zhoushan was −23.46‰, indicating that the terrestrial-source input was the highest. (4) The change of provenance in the study area was quite different. This illustrates that the terrestrial input impacted the largest area of ZCS while marine input became dominant in the offshore area.

1. Introduction

The Zhoushan Coastal Sea (ZCS) is located in the south of the Yangtze Estuary, west of Hangzhou Bay and near the Zhoushan Islands and Ningbo City. The marine ecological environment in the ZCS is significantly influenced by the Yangtze River. It has been proven that there was a serious eutrophication in the ZCS during the past four decades due to human activities in the drainage basin and artificial aquaculture activities in offshore areas [1,2,3,4]. The frequency of occurrence of red tide in this area has also significantly increased since 1980s, accompanied with an increasing trend of harmful algal blooming [5,6,7,8,9]. Although many studies have proven that illumination, water temperature, and nutrients are important factors that influence algae growth [10,11], it is necessary to study whether overloading nutrients and changes of nutrient ratio are a key cause of changes in the dominant algal species of red tides in the ZCS during the past four decades associated with changes of illumination and water temperature [12,13].
Currently, it is widely accepted that changes of nutrient ratio in the ZCS have been influenced by nutrients fluxes from the Yangtze River to the sea. However, the role of marine sourced nutrients in harmful algal blooming of the ZCS is still worthy of a further study, as this area is also influenced by the upwelling which may bring numerous marine sourced nutrients. The variation of nutrients and their sources in the overlying water can be kept and recorded well by core sediments in offshore areas [14,15,16]. By testing and checking parameters, such as total organic carbon (TOC), biogenic silica (BSi), and stable carbon isotope(δ13C), in core sediments and considering age frame, the sedimentary records of organic matters and their sources in the overlying water could be reconstructed. This method has been widely applied in worldwide mega estuaries, such as the Yangtze Estuary, Mississippi Estuary, Nile Estuary, Pearl River Estuary, and so on [17,18,19,20]. Researchers reconstructed records of the algae community’s variation during red tides in the East China Sea over the past century by using core sediments in offshore areas [21,22,23]. Those studies mainly focused on the sea area in the Yangtze Estuary and inner continental shelf of the East China Sea. According to the series of core test results in offshore areas in the Yangtze Estuary, the degree of dominance of dinoflagellate community presented an increasing trend in recent years, which was influenced by terrestrial source inputs from the Yangtze River [24,25]. Xing (2016) pointed out an increasing trend of degree of dominance of diatom in the South Zhejiang Offshore areas by using changes of ratio of brassicasterol to dinoflagellates sterol [26]. This trend might be related with marine source inputs, such as strengthened upwelling. This reflected that material sources played an important role in changes of local eutrophication.
The ZCS is located between the Yangtze Estuary and the South Zhejiang Offshore and is a sensitive and interactive sea area between marine sources and terrestrial sources. Influences of marine source and terrestrial source inputs on ecological environmental changes in the area during the past century could be reproduced by reconstructing the algae community structure and discussing its influencing factors. Research results can further provide directions for effective management of coastal environment. Therefore, in this study, sediments in three cores were first collected, and the main objectives include (1) analyzing sedimentary records of biogenic elements, (2) testing the sedimentary record of primary productivity and dominant species variation of algae in the ZCS over the past 100 years, and (3) revealing and assessing the spatiotemporal variations of provenance of biogenic elements in this area over time.

2. Materials and Methods

2.1. Collection of Samples

Cores at three stations A7-1, A10-4, and A11-3 (Figure 1) in the area were collected by a gravity sampler in March 2016, and then they were kept in refrigerator under −20 °C before being tested. Core A7-1 locates at 30.56 N, 122.50 E with a water depth about 20 m and a length of 170 cm. This core is nearby the north of Zhoushan Islands and in the northern coastal area of the ZCS. Core A10-4 is located at 29.42 N, 122.75 E with a water depth about 50 m and a length of 145 cm. This core presents in the southeast offshore area of the ZCS. Core A11-3 locates at 29.06 N, 122.50 E with a water depth about 40 m and a length of 140 cm, and is in the southern offshore area of the ZCS. All samples were collected by the State Key Laboratory of Estuarine and Coastal Research (East China Normal University) in May 2016. Each core was sampled at an interval of 2 cm and then stored in poly vinyl chloride sealed bags independently. For each core, the excess 210Pb(210Pbex), biogenic silica (BSi), total organic carbon (TOC) and stable carbon isotope (δ13C) were tested. A total of 45 samples were tested for 210Pbex, and a total of 225 samples for BSi, TOC, and δ13C (Table 1), respectively.

2.2. Methods

2.2.1. Pbex Test

The measurement of 210Pbex was conducted by using DeMaster (1981) [27]. About 10 g wet sample was weighed and dried under 105 °C. The dry sample was weighed again to calculate the water content. Then, the sample was grinded and screened by a 100-mesh sieve to eliminate plant roots. About 3 g of the grinded and screened sample was weighed by a balance and put into a plastic tube that was then sealed up. After waiting for a radioactive energy balance for 20 days, a deposition rate was tested by a Gamma Spectrometer (HPGe GWL-120-15 EG&G/ORTEC, Oak Ridge, TN, USA). The measurement time was set about 4 × 104 s. Total 210Pb activity (210Pbt) was determined by measuring the 46.5 keV g-ray peak, and activities of supported 210Pb (210Pbs) were determined using the g-ray peaks of 214Pb (351.9 keV) and 214Bi (609.3 and 1120.3 keV). Finally, the excess 210Pb was calculated by using the formula: 210Pbex = 210Pbt210Pbs s. The sedimentation rate of the present study was based on a constant rate supply model of 210Pbex [27,28].
The deposition rate was calculated by using the formula: r = λ × Z/(lnAz − lnA0) [29], where, r is the deposition rate; λ is the constant 0.03108 (i.e., ln2/22.3); Z is the depth of sample in the core; Az is the 210Pbex value of the sample at depth Z; A0 is the 210Pbex value of the surface sample (i.e., depth at 0). The CIC model of 210Pbex [29] was used to calculate 210Pbex values at different depths in the core.

2.2.2. Biogenic Silicon (BSi) Test

A core sample was dried under 60 °C and grinded. Then, a 110–130 mg sample was put in a 50 mL polypropylene centrifuge tube, in which 5 mL 10% H2O2 and 5 mL 1.0 mol/L HCl were added. The mixture was then processed by an ultrasonic oscillation for 30 min and then centrifuging at the rate of 4000 r/min for 5 min. After supernatant liquid was eliminated, the remainder was supplemented with 20 mL deionized water to eliminate residual HCl and H2O2. This process repeated until the pH of supernatant liquid close to 7. Next, the sample was dried overnight in an oven under 60 °C. Then, a 40 mL Na2CO3 solution was added into the centrifuging tube and heated in a water bath at 90 °C. Five hours later, the mixture was centrifuged at the rate of 4000 r/min for 5 min and 0.25 mL supernatant liquid was mixed with 17.5 mL acid ammonium molybdate completely. Another 7.5 mL reducing agent was added and the mixture was oscillated completely. After 2 h of color development, absorbance of the sample was tested at 812 nm wavelength with a Visible Spectrophotometer (7200 Unico, Shanghai, China). The test result was converted into a BSi ratio.

2.2.3. TOC and δ13C Tests

A vacuum freezing and drying sample (about 0.5 g) which was screened by an 80-mesh sieve was put into a centrifuging tube, in which 5.0 mL 10% HCl was added. The mixture was stirred continuously. Then, deionized water was added into the centrifuging tube for cleaning and centrifuging process. This process was repeated until the pH of supernatant liquid was close to 7, before the supernatant liquid was eliminated. The rest sample was dried overnight in an oven under 60 °C. About 50–60 mg of the sample was weighed by a balance and wrapped in a small stannum box. Then, the sample was crushed into sheets. TOC was measured by an element analyzer vario MACRO cube [30]. The detection limit of carbon was 8 × 106 g, the precision of the instrument was <0.01%, and the recovery efficiency was >99.5% [30]. Numerical value of δ13C was measured by a DELTA plusXP stable isotope mass spectrometer (ThermoFinnigan, San Jose, CA, USA) [31]. Stable isotopic ratios of δ13C were determined as follows: δ13C = (Rsample/Rstandard − 1) × 1000, where Rsample is the test result of ratio 13C/12C, and Rstandard is expressed relative to the Vienna Pee Dee Belemnite (V-PDB) standard. The analytical precision was ±0.2‰ for δ13C, based on the analysis of the standards [31].

3. Results and Analysis

3.1. Determination of Chronological Framework

Test results of 210Pbex are shown in Figure 2. In Figure 2, y is depth and x is ln (210Pbex). The gradient (i.e., (lnA0 − lnAz)/Z) could be changed here: r = λ/gradient [29]. The gradient at A7-1 was −41.462, so the annual average deposition rate was estimated to be at 1.560 cm. The gradient at A10-4 was −33.766, so the annual average deposition rate was estimated at 1.851 cm. The gradient at A11-3 was −43.939, so the annual average deposition rate was estimated at 1.487 cm.
According to the deposition rate, core A7-1 recorded the variation from 1905 to 2015; core A10-4 recorded from 1940 to 2015; and core A11-3 recorded from 1920 to 2015. The variation of primary productivity and provenance over the past 100 years could be revealed. Furthermore, different depths of each core could be transferred into different ages of each core, shown in Figure 3, Figure 4, Figure 5 and Figure 6, according to their corresponding deposition rates.

3.2. Primary Productivity Records

Figure 3 presents test results of TOC of three cores, the error of the results less than 0.01%. For core A7-1, TOC value declined gradually with an average value of 0.532%. The maximum and minimum of the TOC were 0.703% in 1930 and 0.303% in 2000, respectively. For core A10-4, TOC value presented an increasing trend. From 1940 to 1995, the TOC value increased slowly. In this period, the maximum and minimum were 0.445% in 1990 and 0.187% in 1955, showing an average value of 0.326%. From 1996 to 2015, TOC increased dramatically. In this period, the maximum and minimum were 0.689% in 2014 and 0.321% in 2000, with an average value of 0.486%. Per core A11-3, TOC value increased quickly during 1920–1950. The minimum and maximum of the TOC were 0.343% in 1925 and 0.649% in 1950, with an average value of 0.519%. However, the TOC value became relatively stable after 1950. The maximum and minimum of TOC were 0.704% in 1970 and 0.5434% in 2008, showing an average value of 0.630%.
During the past 100 years, the TOC values for most samples in cores A7-1 and A11-3 were around 0.6%, while TOC values for most samples in core A10-4 were only 0.4%, indicating that core A10-4 had a relatively low sediment of total organic matters. This might be due to the deepest location of core A10-4 among the three cores. However, the dramatic increase of TOC value in core A10-4 after 1995 might reveal that the deposited model of TOC has changed recently.
Test results of BSi of the three cores are shown in Figure 4. For core A7-1, BSi value was decreasing continuously. It declined slightly from 1905 to 1985. The maximum was 0.782% in 1945 and the minimum was 0.447% in 1925, with an average of 0.582%. However, BSi of samples from core A7-1 declined quickly from 1985 to 2015. The maximum was 0.637% in 1990 and the minimum was 0.369% in 2008, with an average of 0.446%. For core A10-4, the BSi value was increasing continuously, manifested by a small fluctuation during 1940–1980 and a great fluctuation during 1981–2015. The maximum and minimum of the BSi were 0.754% in 2000 and 0.371% in 1945, showing an average value of 0.507%. For core A11-3, the BSi generally increased slightly during 1920–1995. The maximum and minimum of the BSi were 0.616% in 1960 and 0.421% in 1930, with an average value of 0.513%. Then, it dropped dramatically after 1996. Its maximum and minimum were 0.568% in 2010 and 0.426% in 2005, showing an average value of 0.484%.
Generally speaking, the TOC and BSi in A7-1 both declined slightly over the past 100 years, while the TOC and BSi in A10-4 both increased. This might indicate that the primary productivity in the northern Zhoushan costal sea (ZCS) has not increased but it in the southern ZCS has increased. The TOC in A11-3 has increased while the BSi has declined since 2000, which might indicate that the advantage of diatom has declined in this core since 2000.

3.3. Provenance Analysis

Test results of δ13C of the three cores are shown in Figure 5. All the three cores were with marine-terrestrial mixed source. For core A7-1, value of δ13C was relatively high and stable during 1905–1970. The maximum and minimum numerical values of δ13C were −23.00‰ in 1940 and −23.82‰ in 1922, showing an average value of −23.34‰. During 1971–1985, the value of δ13C dropped significantly compared to that during 1905–1970. At this stage, the value of δ13C presented an increasing trend. The maximum and minimum values of δ13C were −23.33‰ in 1971 and −24.17‰ in 1985, with an average of −23.77‰. During 1986–2015, the value of δ13C presented a decreasing trend, indicating the increasing terrestrial organic input. The maximum and minimum values of δ13C were −23.29‰ in 1986 and −23.91‰ in 2014, with an average of –23.57‰. For core A10-4, the value of δ13C increased gradually from 1940 to 1995, indicating the increasing marine input. The maximum and minimum values of δ13C were −21.99‰ in 1948 and −23.71‰ in 1970, showing an average of −22.63‰. However, the value of δ13C decreased gradually from 1996 to 2015, indicating the increasing terrestrial input too. The maximum and minimum values of δ13C were −21.71‰ in 1996 and −22.57‰ in 2009, with an average of −22.24‰. For core A11-3, the value of δ13C decreased generally. The maximum and minimum values of δ13C were −22.36‰ in 1936 and –24.05‰ in 1986, with an average of −23.01‰.

4. Discussion

4.1. Variation of Dominace of Diatom in Phytoplankton

BSi represents the productivity of diatom while TOC indicates the total productivity of phytoplankton. The ratio of BSi/TOC can illustrate the dominance of diatom [30]. The results of BSi/TOC extracted from the three cores are shown in Figure 6. For core A7-1, the gradient of BSi/TOC was 0.0003, which indicates that the temporal variation of BSi/TOC was quite stable. The maximum and minimum values were 1.572 in 1935 and 0.723 in 2000, showing an average value of 1.066. This suggests that the dominance of diatom in this area was not changed dramatically over the past 100 years. For core A10-4, the BSi/TOC fluctuated greatly, and it was generally increasing continuously during 1940–1995. The gradient in this period was about 0.0024, which indicates an increasing trend. The maximum and minimum values were 2.312 in 1955 and 0.963 in 1950, showing an average value of 1.484. However, during 1996–2015, it dropped greatly compared to that during 1940–1995. The gradient during 1996–2015 was about −0.0453, indicating a dramatically decrease. During the period, the maximum and minimum values were 1.816 in 2000 and 0.868 in 2015, showing an average value of 1.307. This reflects that the dominance of diatom in this area decreased significantly. For core A11-3, the gradient was −0.0023, which indicates BSi/TOC decreasing slightly. The maximum and minimum values of BSi/TOC were 1.462 in 1930 and 0.673 in 2010, showing an average value of 0.866.
Among the three cores, BSi/TOC at A10-4 was the highest, showing the diatom taking a greater advantage than that in A7-1 and A11-3. However, this advantage at A10-4 has declined since 1986. And BSi/TOC in A11-3 has also decreased slightly. Generally, the dominance of diatom at the three cores has declined.
In this study area, the dominance of diatom showed evident temporal and spatial variations. In the northern area (A7-1), near to Yangtze Estuary, both TOC and BSi have declined continuously, and the BSi/TOC fluctuated slightly. This reflected that the primary productivity in the area continued to decline and the dominance of diatom has not changed dramatically. In the southeastern area (A10-4), both TOC and BSi increased continuously and the value of BSi/TOC increased before 1995, which proved the continuous growth both in primary productivity and the dominance of diatom. However, the growth rate of TOC was significantly higher than that of BSi after 1995, resulting in a quick reduction of BSi/TOC. This means that the primary productivity increased continuously, and the dominance of diatom declined dramatically. In the southern area (A11-3), TOC continued to increase, and it increased greatly before 1950, but the growth rate decreased significantly after 1950. The BSi presented an increasing trend before 1995, but it turned to a reduction trend after 1995. The value of BSi/TOC in this area continued to decrease, which reflected an increasing total productivity, but a decreasing productivity of diatom and decreasing dominance of the diatom. To sum up, the degree of dominance of diatom in the northern area increased. More specifically, it increased firstly and then decreased in the southeastern area, while it decreased continuously in the southern area.
As we summarized above, the dominance of diatom varied in this coastal sea. This was influenced by illumination, water temperature and nutrients ratio significantly. In this study area, water temperature changed slightly and the influence of illumination on algae was small. Yang (2013) carried out a multiple linear regression analysis and found that temperature contributed only 6.8% of interannual variation of plankton in the study area based on observed algal data during the past 20 years [32]. Han (2009) observed that temperature contributed about 9% of plankton growth in the Yangtze Estuary and its adjacent sea areas [33]. Song (2014) analyzed a direct correlation between the variation of Chlorophyll content and total suspended solid (TSS) based on a generalized additive model (GAM) and believed that illumination condition was a decisive factor of temporal and spatial distribution of plankton in sea areas [13]. Zhou et al (2017) simulated succession of algal communities and proved that temperature and illumination affected algal succession slightly [34]. In summary, the previous studies indicate that nutrient is an important factor that influences the dominance of diatom in the ZCS area.
The northern area in the ZCS is close to the Yangtze Estuary. There are overload nutrients from the Yangtze River to seas due to intensive human activities in the river basin. Tang (2009) pointed that annual average concentration of dissolved inorganic nitrogen (DIN) at Yangtze Estuary generally increased continuously in the past 50 years and it increased from 4 μmol/L in 1960s to 27 μmol/L in 2009 [35]. The annual average concentration of P also presented an increasing trend and it was increased by four times from 1966 to 1981 [36]. The total inorganic P content entered into sea areas from Yangtze Estuary in 2002 was about 1.3 times that in the middle of 1980s [37]. Adequate nutrients input is in favor of algal growth, and thus the dominance of diatom is stable in the sea area [38].
The southern area in the ZCS is far away from the Yangtze Estuary and nutrients from the Yangtze Estuary to seas have been consumed significantly in the transport process, resulting in a sharp increase of N/P [39] and forming nutrients structural features of rich nitrogen and poor phosphorus [40,41,42]. Huang (2011) pointed that N/P continued to increase in the East China Sea and it climbed up from 8.5 in 1960s to 37 in 2010s [43]. The growth rate was increasing continuously. Phosphorus limit in the southern area in the ZCS was beneficial for the growth of dinoflagellate [44,45], which led to a decreased dominance of diatom.
In the eastern area, the dominance of diatom increased gradually before 1995, but it dropped significantly after 1995, showing obvious transition characteristics. This area might be a sensitive region to illustrate the variation of provenance.

4.2. Provenance Variation of BSi and TOC

According to analysis results on value of δ13C, there were temporal and spatial variations of provenance in the study area. The highest terrestrial input was in the northern area (A7-1). The mean δ13C was −23.46‰ at A7-1, but it declined sharply in 1970s, indicating the sudden increasing of terrestrial input in 1970s. Then, from 1970 to 1985, δ13C increased, indicating increasing of marine input during the period. However, the value of δ13C began to decrease continuously after 1985, indicating that terrestrial source input still had an increasing trend. In the southeastern (A10-4) and southern (A11-3) areas, marine source input occupied a dominant role. The mean δ13C was −22.53‰ in the southeastern area and −23.01‰ in the southern area. Specifically, the value of δ13C increased before 1995 and then declined in southeastern area, indicating that terrestrial-source input weakened firstly and then increased. In the southern area (A11-3), the numerical value of δ13C declined continuously, which reflected that terrestrial source input was increasing continuously. In recent years, terrestrial input in all the three areas had an increasing trend.
The intensified influences by terrestrial-source input in northern (A7-1) and southern (A11-3) coastal areas are widely believed in correlation with diluted water input from the Yangtze River [46]. The northern area is close to the Yangtze Estuary and diluted water from the Yangtze River carries excessive nutrients which are conducive to growth of algae [47]. The southern area is further away from the Yangtze Estuary and the structure of nutrients is high N/P which restricts the growth of diatom [48].
In the southeastern area (A10-4), the farthest offshore area, the dominance of diatom increased continuously before 1995, which reflected the increased marine input. It is speculated to be influenced by the upwelling which brings abundance phosphate. This caused a relatively low value of N/P, which is conducive to diatom growth [15,49]. Lou (2011) reported that upwelling could deliver bottom nutrients to the surface of sea as a supplementation to phosphate in southeastern area of Zhoushan Islands [50]. This provides a favorable condition for diatom growth. Hence, the variation in dominance of diatom in southeastern area may be related with changes of provenance which may be caused by upwelling.

5. Conclusions

In this study, the analysis results derived from the core data demonstrate that the primary productivity was higher in the northern area of Zhoushan Islands compared to that in the southern area, which suggests that the primary productivity is positively correlated to the distance from the Yangtze Estuary. This is because the Yangtze estuary inputs overload nutrient to the study area. However, according to the results TOC and BSi data analysis, there was an increasing trend in the northern and southern areas. There were also evident temporal and spatial changes in algae community structures in the study area. The algae community structure was stable in the northern area close to the Yangtze Estuary, and the dominance of diatom in the both southern and southeastern areas generally decreased. This might be closely related with source of nutrients. According to the results of δ13C, the source of nutrients in the northern area was controlled by terrestrial source input from Yangtze diluted water. In the southern area, δ13C also presented a decreasing trend, indicating the increasing terrestrial source input. However, in the southeastern area, marine source input took a dominant role during 1940–1995. It was speculated that the phosphates were supplemented in this area by upwelling, thus facilitating diatom growth. During 1996–2015, the value of δ13C was decreasing, indicating that the increasing terrestrial source input or the upwelling become weaker. This has restricted the growth of diatom and caused a low BSi/TOC since 1995.
To sum up, the eutrophication in the largest area of Zhoushan Coastal sea over the past 100 years was infected by terrestrial source input from the Yangtze diluted water. However, in the southeastern area, the role of marine source input from upwelling should be positive to enhance eutrophication in the study area. This should remind the managers of the coastal environment that we should not only control the overloading riverine input, but also pay more attention to marine nutrients input such as upwelling in this area.

Author Contributions

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

Funding

This research project was funded by NSFC-Zhejiang Joint Fund for the Integration of Industrialization and Informatization (U1609203), National Natural Science Funded projects (71874091, 41776193, 41876215), Natural Science Foundation of Zhejiang Province (No. LQ15D020001), Scientific Research Project of Ningbo University (XYL15010).

Acknowledgments

The authors also want to express their gratitude to the editors and the anonymous reviewers for providing valuable comments and suggestions to improve the paper.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Liu, L.; Zhou, J.; Zheng, B.; Cai, W.; Lin, K.; Tang, J. Temporal and Spatial Distribution of Red Tide Outbreaks in the Yangtze River Estuary and Adjacent Waters, China. Mar. Pollut. Bull. 2013, 72, 213–221. [Google Scholar] [CrossRef] [PubMed]
  2. Gao, Y.; Deng, C.; Chen, C.; Liang, J.; Sun, L. Changes of sedimentary diatoms and resting spores over a 60 years period in the East China Sea and their environmental indication. Phycologia 2017, 56, 57–58. [Google Scholar]
  3. Cai, W. Evaluation of the ecological quality of the Yangtze estuary and adjacent waters under eutrophication pressure. Symposia of annual conference of Chinese environmental sciences and technology (vol 3). Chin. Soc. Environ. Sci. 2017, 10, 3722–3731. [Google Scholar]
  4. Wang, R.; Wang, J.; Li, F.; Yang, S.; Tan, L. Vertical distribution and indications of lipids biomarkers in the sediment core from East China Sea. Cont. Shelf Res. 2016, 122, 43–50. [Google Scholar] [CrossRef]
  5. Zhou, Y. The Influence of Nutrients on the Competition and Succession between Two Predominant Red Tide Algae of East China Sea. Master’s Thesis, Ocean University of China, Qingdao, China, 2015. [Google Scholar]
  6. Jiang, Z.; Liu, J.; Chen, J.; Chen, Q.; Yan, X.; Xuan, J.; Zeng, J. Responses of Summer Phytoplankton Community to Drastic Environmental Changes in the Changjiang (Yangtze River) Estuary during the past 50 Years. Water Res. 2014, 54, 1–11. [Google Scholar] [CrossRef]
  7. Dai, X.; Lu, D.; Guan, W.; Wang, H.; He, P.; Xia, P.; Yang, H. Newly Recorded Karlodinium Veneficum Dinoflagellate Blooms in Stratified Water of the East China Sea. Deep Sea Res. Part II: Top. Stud. Oceanogr. 2014, 101, 237–243. [Google Scholar] [CrossRef]
  8. Lou, X.; Hu, C. Diurnal Changes of a Harmful Algal Bloom in the East China Sea: Observations from GOCI. Remote Sens. Environ. 2014, 140, 562–572. [Google Scholar] [CrossRef]
  9. Zhou, C.; Place, A.R.; Yan, X.; Xu, J.; Luo, Q.; William, E.; Jiang, Y. Interactions between Karlodinium Veneficum and Prorocentrum Donghaiense from the East China Sea. Harmful Algae 2015, 49, 50–57. [Google Scholar] [CrossRef]
  10. Sun, X. The Effect of Solar Radiation on HAB Algae Growth in High Frequency HAB Occurrence Areas in ECS. Ph.D. Thesis, Ocean University of China, Qingdao, China, 2005. [Google Scholar]
  11. Zhang, S. Formation of Eucampia zoodiacus red tide in Xiamen Bay and its genetic analysis. In Symposia of Investigation on Red Tide in Xiamen Bay; Ocean Press: Beijing, China, 1993; pp. 19–28. [Google Scholar]
  12. Zhang, X. Historical Comparison on Evolution of Nutrient and Its Function on the Harmful Algae Blooms in Yangtze Estuary and Its Adjacent Sea. Ph.D. Thesis, Ocean University of China, Qingdao, China, 2012. [Google Scholar]
  13. Song, H.; Zhang, X.; Wang, B.; Sun, X.; Wang, X.; Xin, M. Bottom up and top down controls of the phytoplankton standing stock off the Changjiang Estuary. Acta Oceanol. Sin. 2014, 36, 90–100. [Google Scholar]
  14. Jin, H.; Chen, J.; Weng, H. Variations of paleoproductivity in the past decades and the environmental implications in the Changjiang Estuary in China. Acta Oceanol. Sin. 2009, 31, 113–119. [Google Scholar]
  15. Xu, G.; Liu, J.; Hu, G.; Jonell, T.N.; Chen, L. Distribution and source of organic matter in surface sediment from the muddy deposit along the Zhejiang coast, East China Sea. Mar. Pollut. Bull. 2017, 123, 1–2. [Google Scholar] [CrossRef] [PubMed]
  16. Kang, X.; Song, J.; Yuan, H.; Li, X.; Duan, L. The Sources and Composition of Organic Matter in Sediments of the Jiaozhou Bay: Implications for Environmental Changes on a Centennial Time Scale. Acta Oceanol. Sin. 2017, 36, 68–78. [Google Scholar] [CrossRef]
  17. Jia, G.; Peng, P.; Fu, J. Sedimentary records of accelerated eutrophication for the last 100 yeasr at the Pearl River Estuary. Quat. Sci. 2002, 2, 158–165. [Google Scholar]
  18. Sun, X.; Fan, D.; Liu, M.; Liao, H.; Tian, Y. Persistent Impact of Human Activities on Trace Metals in the Yangtze River Estuary and the East China Sea: Evidence from Sedimentary Records of the Last 60 Years. Sci. Total. Environ. 2019, 654, 878–889. [Google Scholar] [CrossRef]
  19. Waterson, E.J.; Canuel, E.A. Sources of Sedimentary Organic Matter in the Mississippi River and Adjacent Gulf of Mexico as Revealed by Lipid Biomarker and δ13CTOC Analyses. Org. Geochem. 2008, 39, 422–439. [Google Scholar] [CrossRef]
  20. Astrahan, P.; Silverman, J.; Gertner, Y. Spatial distribution and sources of organic matter and pollutants in the SE Mediterranean (Levantine basin) deep water sediments. Mar. Pollut. 2017, 116, 521–527. [Google Scholar] [CrossRef]
  21. Jin, H. Sedimentary Records of Changing Structures of Phytoplankton Communities for the Last Hundred Years in the Changjiang Estuary. Ph.D. Thesis, Zhejiang University, Zhejiang, China, 2009. [Google Scholar]
  22. Zhao, Z. Biogenic Silica Record in the Yangtze Estuarine Sediments: A Response to the Recent Human Activity and Eco-Modification in Catchment. Ph.D. Thesis, East China Normal University, Shanghai, China, 2010. [Google Scholar]
  23. Fan, X. Sediment Diatom Records and Eutrophication Reconstruction in the Changjiang River and Its Adjacent Area. Ph.D. Thesis, Institute of Oceanology, Chinese Academy of Sciences, Beijing, China, 2018. [Google Scholar]
  24. Ni, T.; Guan, W.; Cao, Z.; Chen, Q. Numerical study on the upwelling of Zhejiang coast in spring. J. Mar. Sci. 2014, 32, 1–13. [Google Scholar]
  25. Zhang, H. Basic Status of Marine Environmental Resources in Zhejiang Province; Ocean Press: Beijing, China, 2013. [Google Scholar]
  26. Xing, L.; Zhao, M.; Zhang, T.; Yu, M.; Duan, S.; Zhang, R.; Huh, C.-A.; Liao, W.-H.; Feng, X. Ecosystem Responses to Anthropogenic and Natural Forcing over the Last 100 Years in the Coastal Areas of the East China Sea. Holocene 2016, 26, 669–677. [Google Scholar] [CrossRef]
  27. DeMaster, D.J. The Supply and Accumulation of Silica in the Marine Environment. Geochim. Cosmochim. Acta 1981, 45, 1715–1732. [Google Scholar] [CrossRef]
  28. Zaborska, A.; Carroll, J.; Papucci, C.; Pempkowiak, J. Intercomparison of Alpha and Gamma Spectrometry Techniques Used in 210Pb Geochronology. J. Environ. Radioact. 2007, 93, 38–50. [Google Scholar] [CrossRef]
  29. McCall, P.; Robbins, J.; Matisoff, G. 137Cs and 210Pb Transport and Geochronologies in Urbanized Reservoirs with Rapidly Increasing Sedimentation Rates. Chem. Geol. 1984, 44, 33–65. [Google Scholar] [CrossRef]
  30. Li, M.; Wang, H.; Li, Y.; Ai, W.; Hou, L.; Chen, Z.; Lijun, H. Sedimentary BSi and TOC Quantifies the Degradation of the Changjiang Estuary, China, from River Basin Alteration and Warming SST. Estuar. Coast. Shelf Sci. 2016, 183, 392–401. [Google Scholar] [CrossRef]
  31. Fry, B. Food Web Structure on Georges Bank from Stable C, N, and S Isotopic Compositions. Limnol. Oceanogr. 1988, 33, 1182–1190. [Google Scholar] [CrossRef]
  32. Yang, S. Effects of Temperature on Growth of Phytoplankton in the Changjiang Estuary and Adjacent Coastal Waters. Ph.D. Thesis, Ocean University of China, Qingdao, China, 2013. [Google Scholar]
  33. Han, X. Analytical Study on Multi-Environment Factors that Influencing the Phytoplankton Growth in the Changjiang Estuary and Its Adjacent Area. Ph.D. Thesis, Ocean University of China, Qingdao, China, 2009. [Google Scholar]
  34. Zhou, Z.; Yu, R.-C.; Zhou, M.-J. Seasonal Succession of Microalgal Blooms from Diatoms to Dinoflagellates in the East China Sea: A Numerical Simulation Study. Ecol. Model. 2017, 360, 150–162. [Google Scholar] [CrossRef]
  35. Tang, H. Studies of Eutrophication Features and Eutrophication-HABs Relationship in the Changjiang Estuary and Its Adjacent Area during the Past 30 Years and Strategies on Controlling Eutrophication. Ph.D. Thesis, Ocean University of China, Qingdao, China, 2009. [Google Scholar]
  36. Li, M.; Cheng, H. Changes of dissolved silicate flux from the Changjiang River into sea and its influence since late 50 years. China Environ. Sci. 2001, 21, 193–197. [Google Scholar]
  37. Ye, S.; Ji, H.; Cao, L.; Huang, X. Red tides in the Yangtze River Estuary and adjacent sea areas: Causes and mitigation. Mar Sci. 2004, 28, 26–32. [Google Scholar]
  38. Zhou, M.; Shen, Z.; Yu, R. Responses of a coastal phytoplankton community to increased nutrient input from the Changjiang (Yangtze) River. Cont. Shelf Res. 2007, 28, 1483–1489. [Google Scholar] [CrossRef]
  39. Yang, D.; Zhao, W.; Li, J.; Wang, J. Effect of Different Phosphrous Concentration on the Growth of Skeletonema costatum. Stud. Mar. Sin. 2004, 46, 165–172. [Google Scholar]
  40. Chai, C.; Yu, Z.; Shen, Z.; Song, X.; Cao, X.; Yao, Y. Nutrient Characteristics in the Yangtze River Estuary and the Adjacent East China Sea before and after Impoundment of the Three Gorges Dam. Sci. Total. Environ. 2009, 407, 4687–4695. [Google Scholar] [CrossRef]
  41. Chen, H.; Sun, C.; Wu, Y. Analysis of trend of nutrient structure and influencing factors in Changjiang Estuary and its adjacent sea during 23 years. Mar. Environ. Sci. 2011, 30, 551–553. [Google Scholar]
  42. Wang, K.; Chen, J.; Jin, H.; Li, H.; Gao, S.; Lu, Y.; Xu, X.; Weng, H. Nutrient structure and limitation in Changjiang River Estuary and adjacent East China Sea. Acta Oceanol. Sin. 2013, 35, 128–136. [Google Scholar]
  43. Huang, J. Distributions and Changes of Nutrient Concentration in the East China Sea in Late 50 Years. Ph.D. Thesis, Ocean University of China, Qingdao, China, 2011. [Google Scholar]
  44. Jiang, Z.; Chen, J. Controlling factors of summer phytoplankton community in the Changjiang (Yangtze River) Estuary and adjacent East China Sea shelf. Cont. Shelf Res. 2015, 101, 71–84. [Google Scholar] [CrossRef]
  45. Zhang, C.; Chen, G.; Wang, Y.; Guo, C.; Zhou, J. Physiological and Molecular Responses of Prorocentrum Donghaiense to Dissolved Inorganic Phosphorus Limitation. Mar. Pollut. Bull. 2018, 129, 562–572. [Google Scholar] [CrossRef] [PubMed]
  46. Zhang, C.; Wang, X.; Shi, X.; Tang, H.; Han, X.; Xin, Y. Seasonal Variation and Spatial Distribution of Nutrients and Their Relationships with Harmful Algal Blooms in Coastal Area of the East China Sea. Environ. Sci. 2007, 11, 2416–2424. [Google Scholar]
  47. Wang, J.; Cao, J. Variation and effect of nutrient on phytoplankton community in Changjiang Estuary during last 50 years. Mar. Environ. Sci. 2012, 31, 310–315. [Google Scholar]
  48. Wang, B. Nutrient distributions and their limitation on phytoplankton in the Yellow Sea and the East China Sea. Chin. J. Appl. Ecol. 2003, 14, 1122–1126. [Google Scholar]
  49. Wang, W.; Cao, X.; Yuan, Y.; Song, X.; Yu, Z. Variation and controlling factor of nutrient distribution in Changjiang River Estuary and adjacent areas in 2012. Oceanol. Limnol. Sin. 2016, 47, 804–812. [Google Scholar]
  50. Lou, X. Remote Sensing of the Zhejiang Coastal Upwelling and Its Relationship with Red Tides. Ph.D. Thesis, Ocean University of China, Zhejiang, China, 2011. [Google Scholar]
Figure 1. Study area and location of sampling (core samples) sites (YZR–Yangtze River, ZSI–Zhoushan Islands, YZDW–Yangtze Diluted Water, ZMCC–Zhe Min Coastal Current).
Figure 1. Study area and location of sampling (core samples) sites (YZR–Yangtze River, ZSI–Zhoushan Islands, YZDW–Yangtze Diluted Water, ZMCC–Zhe Min Coastal Current).
Ijerph 17 03890 g001
Figure 2. Results of 210Pbex.
Figure 2. Results of 210Pbex.
Ijerph 17 03890 g002
Figure 3. Results of TOC.
Figure 3. Results of TOC.
Ijerph 17 03890 g003
Figure 4. Results of BSi.
Figure 4. Results of BSi.
Ijerph 17 03890 g004
Figure 5. Results of the δ13C.
Figure 5. Results of the δ13C.
Ijerph 17 03890 g005
Figure 6. The variation of ratio of BSi/TOC.
Figure 6. The variation of ratio of BSi/TOC.
Ijerph 17 03890 g006
Table 1. Testing information.
Table 1. Testing information.
TestingA7-1A10-4A11-3
210Pbex19 samples (at the depth of 1 cm, 7 cm, 13 cm, 19 cm, 27 cm, 33 cm, 41 cm, 47 cm, 55 cm, 61 cm, 69 cm, 77 cm, 81 cm, 89 cm, 97 cm, 111 cm, 125 cm, 139 cm, 153 cm, and 169 cm)19 samples (at the depth of 1 cm, 7 cm, 13 cm, 19 cm, 25 cm, 31 cm, 37 cm, 41 cm, 49 cm, 55 cm, 61 cm, 67 cm, 73 cm, 79 cm, 85 cm, 97 cm, 109 cm, 121 cm, 133 cm, and 141 cm)7 samples (at the depth of 1 cm, 13 cm, 25 cm, 35 cm, 49 cm, 62 cm, 73 cm, and 85 cm)
BSi85 samples (within the depth range 0~170 cm, at an interval of 2 cm)70 samples (within the depth range 0~140 cm, at an interval of 2 cm)70 samples (within the depth range 0~140 cm, at an interval of 2 cm)
TOC85 samples (within the depth range 0~170 cm, at an interval of 2 cm)70 samples (within the depth range 0~140 cm, at an interval of 2 cm)70 samples (within the depth range 0~140 cm, at an interval of 2 cm)
δ13C85 samples (within the depth range 0~170 cm, at an interval of 2 cm)70 samples (within the depth range 0~140 cm, at an interval of 2 cm)70 samples (within the depth range 0~140 cm, at an interval of 2 cm)
Note: 210Pbex—the excess 210Pb; BSi—biogenic silica; TOC—total organic carbon; δ13C—stable carbon isotope.

Share and Cite

MDPI and ACS Style

Xu, H.; Jiang, S.; Li, J.; Pu, R.; Wang, J.; Jin, W.; Sha, L.; Li, D. Biogenic Silica and Organic Carbon Records in Zhoushan Coastal Sea over the Past One Hundred Years and Their Environmental Indications. Int. J. Environ. Res. Public Health 2020, 17, 3890. https://0-doi-org.brum.beds.ac.uk/10.3390/ijerph17113890

AMA Style

Xu H, Jiang S, Li J, Pu R, Wang J, Jin W, Sha L, Li D. Biogenic Silica and Organic Carbon Records in Zhoushan Coastal Sea over the Past One Hundred Years and Their Environmental Indications. International Journal of Environmental Research and Public Health. 2020; 17(11):3890. https://0-doi-org.brum.beds.ac.uk/10.3390/ijerph17113890

Chicago/Turabian Style

Xu, Hao, Shangwei Jiang, Jialin Li, Ruiliang Pu, Jia Wang, Wanghai Jin, Longbin Sha, and Dongling Li. 2020. "Biogenic Silica and Organic Carbon Records in Zhoushan Coastal Sea over the Past One Hundred Years and Their Environmental Indications" International Journal of Environmental Research and Public Health 17, no. 11: 3890. https://0-doi-org.brum.beds.ac.uk/10.3390/ijerph17113890

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop