收藏切换
Diatom distribution and its relationship to sediment property in the Minjiang Estuary, southeast China
收藏切换
PDF
Linnan SHEN1, 2, Aiguo GAO1, Chao LI1, *, Min CHEN2
Acta Oceanologica Sinica | 2017, 36(10) : 20 - 30
Less
收藏切换
Acta Oceanologica Sinica | 2017, 36(10): 20-30
Diatom distribution and its relationship to sediment property in the Minjiang Estuary, southeast China
Full
Linnan SHEN1, 2, Aiguo GAO1, Chao LI1, *, Min CHEN2
Affiliations
  • 1 College of Ocean and Earth Sciences, Xiamen University, Xiamen 361102, China
  • 2 Geology Laboratory of Marine and Coastal, Third Institute of Oceanography, State Oceanic Administration, Xiamen 361005, China
Published: 2017-10-01 doi: 10.1007/s13131-017-1070-7
Outline
收藏切换

The distribution of diatoms in surface sediments in the Minjiang Estuary, southeast China, was investigated in 2009. Total 56 species and other species belonging to 25 genera were identified, among them 11 species were dominant over 5%. Dominant species included Actinocyclus ehrenbergii, Coscinodiscus curvatulus, C. divisus, C. jonesianus, C. radiatus, C. rothii, C. subtilis, Cyclotella stylorum, Epithemia hyndmanii, Hydrosera whampoensis, and Trachyneis aspera. Diatom abundance varied spatially, with the absolute abundance of diatoms ranging from 13 valves/g to 11×104 valves/g, and averaging 2.5×104 valves/g. A canonical correspondence analysis (CCA) was used to explain the relationships between diatom distribution and sediment properties in the Minjiang Estuary. CCA revealed that the major elements (Fe2O3, Na2O, CaO, MgO, TiO2, SiO2, Al2O3, and K2O) were closely related to diatom abundance. Four diatom assemblages were distinguished, representing different sediment properties, which may assist late Quaternary palaeoceanographic reconstructions of the Minjiang Estuary.

diatom  /  surface sediment  /  Minjiang Estuary  /  canonical correspondence analysis  /  sediment properties
Linnan SHEN, Aiguo GAO, Chao LI, Min CHEN. Diatom distribution and its relationship to sediment property in the Minjiang Estuary, southeast China[J]. Acta Oceanologica Sinica, 2017 , 36 (10) : 20 -30 . DOI: 10.1007/s13131-017-1070-7
Diatoms, microscopic algae found in almost all aquatic habitats (Round et al., 1990; Dawes, 1998; Cibic et al., 2007; Krause et al., 2011), play an important role in the global biogeochemical cycle. Nelson et al. (1995) estimated that more than 40% of all primary production is attributable to diatoms. Each diatom habitat has its own characteristic diatom flora, developed under distinct environmental variables (Hendey, 1964). Diatom assemblages from surface sediments reflect physical and chemical characteristics of the river water masses in the area (Jiang et al., 2001). Using diatom assemblages as environmental variables has some advantages: (1) they have a short life span and therefore respond rapidly to environmental changes; (2) they are small, and their hard tests preserve well in sediments; (3) they are abundant and diverse; (4) they are widely distributed and almost immobile, and their ecological and taxonomy distribution is well known (Facca and Sfriso, 2007; Smol and Stoermer, 2010; Li et al., 2015). Before carrying out palaeoceanographical reconstructions using fossil diatom records, studies on diatoms from the surface sediments and their relationships with local environments are necessary (Sancetta, 1982; Jiang et al., 2005; Roubeix et al., 2008; Shen et al., 2017). In recent decades, researchers have developed methods of using diatom assemblages to monitor different envorpnmental variables in Chinese estuaries and adjacent areas (Zong et al., 2010; Lin et al., 2012; Xiao, 2013; Yu et al., 2013; Liu et al., 2015). Various studies have been carried out in the Minjiang Estuary using foraminifera (Li et al., 2015), stable isotopes (Liu et al., 2016), trace metals (Xu et al., 2014; Zhou et al., 2014), organic pollutants (Zhang et al., 2003, 2004) and phytoplankton (Zhang et al., 2011; Dai et al., 2016). So far, however, little work has been done on diatoms.
The Minjiang River is the longest river (2 959 km) in Fujian Province, southeast China. The drainage basin of the Minjiang River has an area of approximately 6.1×104 km2, accounting for half of the total area of Fujian Province (Li et al., 2015). The average annual runoff is 1.75×103 m3/s. Every year, an average of 6×109 m3 fresh water with a sediment load of 6.56×106 tons is transported into the East China Sea through the Minjiang River (Liu et al., 2001; Gao et al., 2012), and about 50% of the sediment is deposited in its estuary. Sediments include chemical composites deposited in the estuary, which become one of the most important records to demonstrate the degree of interaction between land and sea as well as industrial pollution (Zhou et al., 2004). However, in comparison with some American and European estuaries, our understanding of the chemical composition of the Minjiang Estuary is limited because of the short history of research in this area (Chen et al., 2002).
Thus, the objectives of this paper were (1) to explore the diatom distribution in surface sediments of the Minjiang Estuary and (2) to distinguish diatom assemblages in different areas and discuss the factors affecting diatom preservation in the Minjiang Estuary.
The Minjiang River belongs to a subtropical monsoon climate, and the highest and lowest rainfall takes place in summer and winter, respectively. The high-flow periods are generally from April to July (average 3.2×103 m3/s), and the low-flow periods are from October to March of the next year (average 0.62×103 m3/s) (Yang et al., 2007). The annual average water temperature is 19.9°C with a range of 9.8–32.2°C. The Minjiang Estuary is divided into two branches (the South Channel and the North Channel) upstream of the area shown in Fig. 1. The mean width of the South Channel is 1 km, and is wider than the North Channel, which is 0.5 km wide (Zhang et al., 2015). Near the river mouth the outflow is blocked by the Langqi Island and subsequently divides into two branches. A submerged delta develops at the front of the river mouth with water depths less than 15 m (Chen et al., 1998). The Minjiang Estuary is affected by tidal currents, river runoff and waves. The tidal and river currents are the dominant forces in the region (Liu et al., 2015). The estuary is affected by formal semi-diurnal tides (Zhang et al., 2011).
The sampling stations were selected and distributed along the Minjiang Estuary, southeast China, on the margin of the northwest Pacific Ocean (Fig. 1). Surficial sediment samples were collected by grab sampling in 2009 from 25 sites using the R/V Yanping 2.
All samples were processed at the diatom analysis laboratory in Xiamen University, and the samples were prepared according to Håkansson (1984). Carbonates and organic material were removed using 10% HCl and 30% H2O2, respectively; subsequent washings in distilled water were used to remove the chemicals from the solution and to produce 2 mL of concentrated diatom suspension. After complete homogenization a subsample was transferred to a cover slip and air-dried. Permanent slides were made with Canada balsam (Håkansson, 1984).
Diatom species were observed and identified using an Olympus BX51 optical microscope (Olympus Corporation, Tokyo, Japan) with magnification of 800× and 1 000× (oil immersion). In this study, for each sample at least 300 diatom valves were counted and identified in random transects from at least three slides. For incomplete valves, if more than half the frustule was present, the diatom was counted as a whole. Using illustrations in the literature (Jin et al., 1965, 1992; Lawson and Rushforth, 1975; Grimes and Rushforth, 1982; John, 1983; Round et al., 1990; Cheng et al., 1996, 2012; Lange-Bertalot, 2000; Witkowski, 2001; Guo, 2003; Qi and Li, 2004; Smol and Stoermer, 2010), each specimen was identified to species level or, if this was not possible, at least to genus level.
For grain size analysis untreated sediments were dried, weighed, mixed with sodium hexametaphosphate and water, soaked and then wet sieved through a set of standard sieves larger than 63 μm. The dry weights were then determined with an analytical balance (resolution of 0.000 1 g) at 1Φ intervals, and the grains (<63 μm) were analyzed using a Mastersizer 2000 laser diffraction particle sizer (USA), with the detected sizes ranging from 0.02 to 2 000 μm. The results of grain size analysis were plotted on the Wentworth scale, and sediments classified by the Shepard triangular diagram (Wu et al., 2013; Wang et al., 2014).
The sub-samples from 25 sites were dried at 60°C, ground in an agate mill to pass through a 150 screen mesh, pressed into cakes and put into a Rigaku 100e type dispersive spectrometer (ZSX-100e) to analyze the major components: SiO2, Al2O3, K2O, Fe2O3, Na2O, TiO2, CaO and MgO. Two replicates were used for standards, analytical blanks and samples.
To detect the influences of environmental variables on the distribution of diatoms, CANOCO (version 4.5) was used in the numerical analysis (ter Braak and Smilauer, 2002). Several statistical methods can be used for data analysis in CANOCO, based on the characteristics of the data set (e.g., linear or non-linear methods, direct or indirect analyses) (Jiang et al., 2001). Before choosing linear or non-linear ordination methods, a detrended correspondence analysis (DCA) was used on the diatom data to determine which method was appropriate, with gradient length as the criterion (Birks, 1995; ter Braak and Smilauer, 2002). In our database, DCA showed a first gradient length of 2.839, implying a unimodal diatom distribution. Therefore, canonical correspondence analysis (CCA) was used to determine which environmental variables were most likely to explain the highest amount of variation present in our diatom database (McCune, 1997). Species data were transformed before statistical analyses, and only species with more than 2% relative abundance in at least one sample were included in further statistical analyses (Lopes et al., 2006).
Diatoms were abundant in most of the surface sediments from the Minjiang Estuary, with abundance varying spatially (Fig. 2a). The results indicated that the highest diatom abundance occurred in Sta. MJ11, reaching 11×104 valves/g. In contrast, the sample from MJ1, in the estuary of the Minjiang River had the lowest diatom abundance (13 valves/g). The average diatom abundance of the study area was 2.5×104 valves/g.
In total, 56 species and varieties of diatoms from 25 genera were identified in the study area. According to Pokras and Molfino, when the relative percentage of an individual species reaches 10%, or even 5% under certain environmental conditions, the species can be considered dominant (Pokras and Molfino, 1986). Using this criterion, we have indicated the 11 most dominant taxa in our study in Fig. 2. Among these dominant diatoms, freshwater diatoms contained Epithemia hyndmanii (0%–7.14%) and Hydrosera whampoensis (0%–7.14%). These species were mainly distributed in the downstream estuary (Figs 2j, k). The marine diatoms Coscinodiscus curvatulus (0%–21.45%), C. divisus (0%–96.50%), C.radiatus (0%–21.90%), C. jonesianus (0%–59.06%), C. rothii (0%–16.08%), C. subtilis (0%–27.27%) and Trachyneis aspera (0%–9.09%) were found in most of the stations (Figs 2ch, l). Brackish-water species included Actinocyclus ehrenbergii (0%–7.47%) and Cyclotella stylorum (0%–8.90%). A. ehrenbergii mainly appeared in the estuary (Fig. 2b), while C. stylorum was abundant in the North Channel area (Fig. 2i).
The result of grain size analysis from the sediment samples is presented in Fig. 3. The sand content ranged from 1.63% to 83.56%, with an average of 35.02%; the silt content varied from 13.86% to 76.84%, with an average of 48.11%; the clay content varied from 0.41% to 83.24%, with an average of 16.88%. The grain size data set indicated that silt and sand accounted for more than 80% of all sediments. The sediment median size varied from 0.12Φ to 2.68Φ (with an average of 1.22Φ), and the sediment sorting and skewness ranged from 0.42 to 1.81 (with an average of 0.69) and –0.39 to 0.26 (with an average of –0.05) (Table 1), respectively. Silt and clay were mainly distributed in the outer part of estuary, whereas sand and sand silt constituted the inner estuary.
Major elements found in the sediment are listed in Table 2. The SiO2 concentrations were significantly high in the Minjiang River sediments (average 88.58%), and the minimum level was observed in front of the estuary, while the highest level was occasionally found in the upstream region. The concentration of Al2O3 was the second highest in the study area and varied from 3.41% to 8.06%, with an average of 5.76%. The concentrations of other six major elements varied: K2O, 1.64%–3.49%, average 2.73%; Fe2O3, 0.24%–1.98%, average 0.87%; Na2O, 0.30%–1.06%, average 0.56%; TiO2, 0.11%–0.60%, average 0.23%; CaO, 0.15%–0.36%, average 0.20% and MgO, 0.07%–0.47%, average 0.18%. The significantly varied concentrations of major elements indicated different distribution patterns in the study area. The high concentrations of SiO2, and low concentrations of K2O, Fe2O3, Na2O, TiO2, CaO and MgO, were associated with enriched silicate silt and sand in the area (Gao et al., 2012).
CCA revealed the relationships between diatom distribution and environmental variables; CCA outputs are given in Table 3. Monte Carlo permutation tests revealed that only nine variables (Fe2O3, SiO2, CaO, Na2O, MgO, depth, silt, clay, and sand) qualified for interpretation of the total variance in the diatom community composition (p<0.05).
The CCA based on 22 selected species and varieties of diatoms from 25 samples showed that a total of four axes explained 53.3% of the species variance. However, Axes 3 and 4 were considered to be less important to interpretation of species-environment correlations, because of low eigenvalues (Table 3). Therefore, the first two axes were selected to interpret the CCA results, explaining 21.2% and 13.9% of the variance, respectively. The species-environment correlations individually obtained for the axes were 0.857 and 0.774, respectively.
The correlation between environmental variables and the CCA axes can be inferred from Table 4. The first axis was positively correlated with depth (0.456), followed by Fe2O3 (0.431), silt (0.257) and other major elements (<0.198). SiO2 (–0.192), sand (–0.189), CaO (–0.046) and clay (–0.039) were negatively correlated with Axis 1. The second axis had a positive relationship with Na2O (0.392), CaO (0.381), Fe2O3 (0.377) and MgO (0.325) and a negative relationship with depth (–0.511), SiO2 (–0.160), K2O (–0.038) and silt (–0.032).
In the CCA diagram, the biplots of sites-environment and species-environment displayed a relationship between environmental variables and sites and species (Fig. 4). The CCA diagram for sites and environmental variables showed distribution patterns along the canonical axis (Fig. 4a). Sixteen sites were projected on the negative side of Axis 1, and nine sites (MJ2–MJ11) were projected on the positive side of Axis 1.
In the CCA scatter diagram, the diatom species were projected according to their relationship with the environmental variables in the ordination diagram (Fig. 4b). Species projection in the direction of the environmental arrow indicated a positive correlation, while species projection in the opposite direction indicated a negative correlation (Li et al., 2015). The result showed that most diatoms were negatively related to the major elements, except for species such as A. undulatus, Coscinodiscus argus, C. radiatus, C. jonesianus, C. rothii, C. subtilis and Cyclotella stylorum, which had a positive correlation with major elements (SiO2 and K2O), depth, sand and silt.
The CCA results showed the relationships between the chemical composition and samples, as well as the percentage and geographical distribution of the diatom samples in the Minjiang Estuary. The diatom at the sampling sites could be distinguished into four assemblages (Fig. 4a). The assemblages were mapped according to the sampling sites, displaying a clear spatial geographic variation (Fig. 5). The sites in the estuary (MJ1–MJ5) belonged to Assemblage I. The downstream sites from MJ6 to MJ8 were dominated by Assemblage II. Assemblage III comprised the upper and middle stream of the Minjiang River, including the North Channel area (MJ9–MJ17). Assemblage IV, with eight sites, mainly occurred in the South Channel area.
This study examined diatom distribution in surface sediments from the Minjiang Estuary. Changes in the abundance and types of diatoms indicated that environmental variations exist in this estuary.
In previous studies, high phytoplankton diversity and abundance usually occurred in surface seawater adjacent to the Minjiang Estuary. This was attributed to the effect of river input, which decreases salinity, increases the nutrient levels and provides diverse habitat for diatoms (Lin et al., 2012; Xiao, 2013; Dai et al., 2016). However, the spatial pattern of diatom abundance in the surface sediment differed from that of the surface seawater, with lower abundance in the Minjiang Estuary (Lapointe, 2000; Xu et al., 2014). The inconsistent spatial pattern of diatom abundance in the surface sediment and upper water column can be related to the sedimentary environment of the Minjiang Estuary.
The deposition rates in the Minjiang Estuary varied significantly, with a range of 0.79–3.34 cm/a, and average values of 1.97 cm/a (Shi et al., 2010). Ye et al. (2002) researched the tidal current speeds in the inner shelf of Zhejiang Provine and Fujian Province were 0.26 m/s. During the intense winter monsoon, sediments from the Changjiang River (Yangtze River) can reach the Minjiang Estuary, which increase deposition rate in the study area (Liu et al., 2007; Xu et al., 2014). The rate of deposition is important as it can influence the geographic distribution of diatoms, and a high deposition rate will increase the burial speed and dilute diatom abundance during the preservation process (Milliman et al., 1985; Xu et al., 2009; Liu et al., 2015). Sediment grain size is another important factor affecting the pattern of diatom distribution. In general, sandy silt and muddy sand have been found to be better than sand in preserving diatoms (Jesus et al., 2006; Méléder et al., 2007). In the estuary, hydrodynamics are controlled by runoff and waves; sediment tends to be coarse, consisting of sand, or silt and sand. At Sites MJ3–MJ6, the sand fraction accounted for more than 60% by weight, and diatom species and abundance were low. In the estuary, we identified 26 species and varieties of diatoms, with absolute abundance of diatoms ranging from 16 to 78 356 valves/g, and averaging 19 670 valves/g. However, at some sites such as MJ1 and MJ2, the coastal current dominated particle transport, and the sediment was relatively fine, consisting of clay or silty clay. Diatom species and abundance were high, especially at Sta. MJ2, which had an abundance of 49 906 valves/g. In the inner estuary the sediment was fine, and diatom numbers were relatively high. Therefore, the distribution of sediment grain size is clearly a critical factor controlling the variation in diatom content.
Diatom Assemblage I comprised 14 genera and 28 diatom species; the diatom abundance ranged from 13 valves/g to 49 906 valves/g and average abundance was 10 048 valves/g. The assemblage was characterized by C. asteromphalus (0%–11.7%), C. curvatulus (0%–18.18%), C. divisus (7.17%–57.14%), C. jonesianus (0%–58.11%) and C. subtilis (0%–27.27%). These dominant diatoms are marine and coastal species (Guo, 2003), and their distribution showed that this assemblage was strongly affected by the China Coastal Currents system. The assemblage also contained the freshwater species E. hyndmanii (0%–7.14%) and H. whampoensis (0%–7.14%), mainly distributed in MJ2 and MJ3 (Fig. 2), suggesting that the assemblage was affected by fresh water from the Minjiang River.
Samples from Assemblage II comprised 13 genera and 24 diatom species. Diatom abundance was higher than in Assemblage I, and varied from 544 valves/g to 78 356 valves/g; average abundance was 28 518 valves/g. The dominant diatoms mainly comprised marine and coastal species of C. jonesianus (28.70%–59.06%), C. divisus (15.79%–27.73%), C. subtilis (7.20%–23.19%), C. radiatus (5.33%–7.83%), C. rothii (4.09%–6.40%), A. ehrenbergii (0%–5.33%) and C. curvatulus (0%–5.33%), respectively. The dominant species being marine and coastal diatoms indicated that the oceanic and coastal water had a strong influence on this assemblage.
Assemblage III comprised 21 genera and 48 diatom species. Abundance ranged from 143 valves/g to 11 4886 valves/g, and the average value was 39 309 valves/g. The relative abundance of the dominant diatoms C. divisus and C. jonesianus accounted for 14.40%–67.14% and 0.47%–53.44% of the assemblage, respectively; the marine species C. rothii, C. radiatus and C. subtilis accounted for 0%–16.08%, 0.22%–15.54% and 3.66%–15.85%, respectively. Thalassiosira excentrica and Coscinodiscus argus, both cosmopolitan species (Guo, 2003), accounted for 0%–3.66% and 0%–2.36%, respectively. There was also a large number of coastal species (such as C. stylorum, C. striata and P. sulcata) in Assemblage III, which may have been affected by the shallow water depth. The samples from Assemblage III had positive SiO2 values (Fig. 4a), suggesting that they were located in an area with a relatively high SiO2 content.
Assemblage IV had few diatom species than Assemblage III, and only 8 genera and 16 diatom species were found. Diatom abundance ranged from 239 valves/g to 87 904 valves/g, and the average value was 15 698 valves/g. The relative abundance of the dominant diatoms C. divisus, C. curvatulus and C. jonesianus accounted for 31.72%–68.87%, 3.97%–21.45% and 6.34%–16.56% of the assemblage, respectively. The marine species C. subtilis, C. radiatus and C. rothii accounted for 0%–7.55%, 0%–21.90% and 0%–6.34%, respectively.
Samples from Assemblage IV had a positive correlation with sand, indicating that they were situated to coarse particles, and negative values with depth, suggesting they were characterized by shallow water depth (Fig. 4a).
Diatoms have long been used as powerful and reliable environmental indicators (Smol and Stoermer, 2010). In this study, the spatial distribution of four diatom assemblages indicated significant environmental difference in the Minjiang River. The CCA results revealed that Fe2O3, Na2O, CaO, MgO and TiO2 were highly negative to large diatom species; however, SiO2, Al2O3 and K2O had a positive correlation with most diatom species (Fig. 4b). The Fe2O3, Na2O, CaO, MgO, and TiO2 concentrations were low at most stations; in contrast, the concentrations of SiO2, Al2O3 and K2O were high throughout the study area (Table 2). The results showed that the diatom assemblages were insensitive to a selected environmental factor until it exceeded a critical standard.
Major element chemistry can also be related to sediment property (Meybeck and Helmer, 1989). SiO2 had positive correlation with sand, while Al2O3 and Fe2O3 presented positive correlation with silt, suggesting that SiO2 levels increased in coarse particles, and Al2O3 and Fe2O3 levels were higher in finer sediments (Roquin and Zeegers, 1987; Ottesen et al., 1989; Vital and Stattegger, 2000). Diagenetic elements such as Al and Fe, the major components of silica minerals, are the products of rock weathering (Xie and Yin, 1993; Yamanaka et al., 2010; Zhou et al., 2014), and these elements were clearly controlled by grain size in Minjiang River sediment. The fine sediments (such as silt and clay) usually had high Al2O3 and Fe2O3 contents (Table 2). The strong positively correlation of K2O, TiO2, CaO, and MgO with Al2O3 and Fe2O3 (Table 5), suggested that these components might originate from human activities, and weathering, and be transferred by colloidal and mineral particulates (Gibbs, 1994; Zhao and Yan, 1994; Peng et al., 2003; Zhou et al., 2014).
There were few diatoms from stations with lower concentrations of major elements because of fresh water input, such as Sites MJ1, MJ2 and MJ3 (Fig. 2, Table 2). Fresh water input changed physical and biochemistry factors (temperature, salinity, hydrodynamics and other nutrient parameters) (Boltovskoy and Wright, 1976; Murray, 2006; Li et al., 2015), and then strongly affected diatom community structure in the coastal marine environment.
(1) Total 56 species and varieties of diatoms from 25 genera were identified from 25 samples. The absolute abundance of diatoms ranged from 13 valves/g to 11×104 valves/g, with an average of 2.5×104 valves/g.
(2) Sediment properties influenced the distribution of diatoms. When sediments were fine, the diatom abundance was relatively high. CCA revealed that the major elements (Fe2O3, Na2O, CaO, MgO, TiO2, SiO2, Al2O3, and K2O) had a close relationship with diatoms. Fresh water input can affect diatom community structure in the coastal marine environment.
(3) Four diatom assemblages have been identified, representing different sediment properties. Assemblage I (estuary area) was strongly affected by the China Coastal Current and fresh water from the Minjiang River. Assemblage II (downstream area) was affected by oceanic and coastal water. Assemblage III (upper and North Channel area) was influenced by shallow water and a relatively high SiO2 content. Assemblage IV (South Channel area) was associated with coarse particles and shallow water depth. Diatom assemblages can therefore be important in late Quaternary palaeoceanographic reconstructions of the Minjiang Estuary.
The authors thank all of the investigators for their help in collecting samples and data on the cruises in November 2009.
  • The Special Fund for Basic Scientific Research Foundation of the Third Institute of Oceanography, State Oceanic Administration, China under contract No. 2016015; the National Natural Science Foundation of China under contract Nos 41306083 and 41376050.
Birks H J B. 1995. Quantitative palaeoenvironmental reconstructions. In: Maddy D, Brew J S, eds. Statistical Modelling of Quaternary Environmental Data. Technical Guide No. 5. Cambridge: Quaternary Research Association, 161–236
Boltovskoy E, Wright R C. 1976. Recent Foraminifera. Netherlands: Springer, 1–515
Chen Jingsheng, Wang Feiyue, Xia Xinghui, et al. 2002. Major element chemistry of the Changjiang (Yangtze River). Chemical Geology, 187(3–4): 231–255
Chen Zhaodi, Wu Sheng, Xia Da, et al. 1998. Chinese Bays (The Fourteenth Series): Important Estuaries (in Chinese). Beijing: China Ocean Press, 25–799
Cheng Zhaodi, Gao Yahui, Dickman M. 1996. Colour Plates of the Diatoms (in Chinese). Beijing: China Ocean Press, 1–120
Cheng Zhaodi, Gao Yahui, Liu Shicheng, et al. 2012. Marine Bacillariophyta Pennatae (I) Flora of China Seas (in Chinese). Beijing: Science Press, 1–137
Cibic T, Blasutto O, Falconi C, et al. 2007. Microphytobenthic biomass, species composition and nutrient availability in sublittoral sediments of the Gulf of Trieste (northern Adriatic Sea). Estuarine, Coastal and Shelf Science, 75(1–2): 50–62
Dai Hong, Qiu Maofu, Yang Bicheng, et al. 2016. Community characteristics of phytoplankton and relationships with environmental factors in southern part area of Minjiang estuary in Fujian Province in Summer. Journal of Fisheries Research (in Chinese), 38(1): 56–66
Dawes C J. 1998. Marine Botany. 2nd ed. New York: John Wiley and Sons, Inc, 1–484
Esper O, Gersonde R, Kadagies N. 2010. Diatom distribution in southeastern Pacific surface sediments and their relationship to modern environmental variables. Palaeogeography, Palaeoclimatology, Palaeoecology, 287(1–4): 1–27
Facca C, Sfriso A. 2007. Epipelic diatom spatial and temporal distribution and relationship with the main environmental parameters in coastal waters. Estuarine, Coastal and Shelf Science, 75(1–2): 35–49
Gao Aiguo, Zhao Dongmei, Li Chao, et al. 2012. Geochemical characteristics of the surface sediments in the Minjiang River estuary and its adjacent sea area. Marine Geology Frontiers (in Chinese), 28(5): 1–6, 20
Gibbs R J. 1994. Metals in the sediments along the Hudson River estuary. Environment International, 20(4): 507–516
Grimes J A, Rushforth S R. 1982. Diatoms of Recent Bottom Sediments of Utah Lake, Utah, USA (Bibliotheca Phycologica). Vaduz: J Cramer
Guo Yujie. 2003. Marine Bacillariophyta Centricae Flora of China Seas (in Chinese). Beijing: Science Press, 1–493
Håkansson H. 1984. The recent diatom succession of Lake HavgårdssjÖn, south Sweden. In: Mann D G, ed. Proceedings of the Seventh International Diatom Symposium. Otto Koeltz: Philadelphia, 411–429
Hendey N I. 1964. An Introductory Account of the Smaller Algae of British Coastal Waters. Fishery Investigations Series IV Part V: Bacillariophyceae (Diatoms). West Germany: H M S O London Ottokoelz Science Publishers
Jesus B, Mendes C R, Brotas V, et al. 2006. Effect of sediment type on microphytobenthos vertical distribution: modelling the productive biomass and improving ground truth measurements. Journal of Experimental Marine Biology and Ecology, 332(1): 60–74
Jiang Hui, Eiríksson J, Schulz M, et al. 2005. Evidence for solar forcing of sea-surface temperature on the North Icelandic shelf during the late Holocene. Geology, 33(1): 73–76
Jiang Hui, Seidenkrantz M S, Knudsen K L, et al. 2001. Diatom surface sediment assemblages around Iceland and their relationships to oceanic environmental variables. Marine Micropaleontology, 41(1–2): 73–96
Jin Dexiang, Chen Jinhuan, Huang Kaige. 1965. Planktonic Diatoms of China Seas (in Chinese). Shanghai: Shanghai Science and Technology Press, 1–229
Jin Dexiang, Cheng Zhaodi, Liu Shicheng, et al. 1992. Benthic Diatoms of China Seas (in Chinese). Beijing: China Ocean Press, 1–437
John J. 1983. The Diatom Flora of the Swan River Estuary, Western Australia (Bibliotheca Phycologica). Vaduz: J Cramer
Krause J W, Nelson D M, Brzezinski M A. 2011. Biogenic silica production and the diatom contribution to primary production and nitrate uptake in the eastern equatorial Pacific Ocean. Deep-sea Research Part II: Topical Studies in Oceanography, 58(3–4): 434–448
Lange-Bertalot H. 2000. Diatoms of Europe: Diatoms of the European Inland Waters and Comparable Habitats. Konigstein/Germany: Koeltz Scientific Books
Lapointe M. 2000. Modern diatom assemblages in surface sediments from the Maritime Estuary and the Gulf of St. Lawrence, Québec (Canada). Marine Micropaleontology, 40(1–2): 43–65
Lawson L L, Rushforth S R. 1975. The Diatom Flora of the Provo River, Utah, U.S.A. (Bibliotheca phycologica). Vaduz: J Cramer
Li Tao, Li Xuejie, Zhong Hexian, et al. 2015. Distribution of trace metals and the benthic foraminiferal assemblage as a characterization of the environment in the north Minjiang River Estuary (Fujian, China). Marine Pollution Bulletin, 90(1–2): 227–241
Lin Gengming, Yang Qingliang, Wang Yu, et al. 2012. Species composition and distribution characteristics of phytoplankton in northern sea of Fujian, China during withdraw of Zhe-Min coastal current. Chinese Journal Applied Environmental Biology (in Chinese), 18(3): 411–420
Liu Huatai, Guo Zhanrong, Gao Aiguo, et al. 2016. 18O and 226Ra in the Minjiang River estuary, China and their hydrological implications. Estuarine, Coastal and Shelf Science, 173: 93–101
Liu Cangzi, Jia Hailin, Chen Xiangfeng. 2001. Sedimentary texture and sedimentation in the Minjiang River estuary. Oceanologia et Limnologia Sinica (in Chinese), 32(2): 177–184
Liu Dongyan, Liu Lixue, Di Baoping, et al. 2015. Paleoenvironmental analyses of surface sediments from the Bohai Sea, China, using diatoms and silicoflagellates. Marine Micropaleontology, 114: 46–54
Liu Jinpeng, Xu Kehui, Li Anchun, et al. 2007. Flux and fate of Yangtze River sediment delivered to the East China Sea. Geomorphology, 85(3–4): 208–224
Lopes C, Mix A C, Abrantes F. 2006. Diatoms in northeast Pacific surface sediments as paleoceanographic proxies. Marine Micropaleontology, 60(1): 45–65
McCune B. 1997. Influence of noisy environmental data on canonical correspondence analysis. Ecology, 78(8): 2617–2623
Méléder V, Rincé Y, Barillé L, et al. 2007. Spatiotemporal changes in microphytobenthos assemblages in a macrotidal flat (Bourgneuf Bay, France). Journal of Phycology, 43(6): 1177–1190
Meybeck M, Helmer R. 1989. The quality of rivers: from pristine stage to global pollution. Palaeogeography, Palaeoclimatology, Palaeoecology, 75(4): 283–309
Milliman J D, Shen Huangting, Yang Zuosheng, et al. 1985. Transport and deposition of river sediment in the Changjiang estuary and adjacent continental shelf. Continental Shelf Research, 4(1–2): 37–45
Murray J W. 2006. Ecology and Applications of Benthic Foraminifera. Cambridge: Cambridge University Press, 1–440
Nelson D M, Tréguer P, Brzezinski M A, et al. 1995. Production and dissolution of biogenic silica in the ocean: revised global estimates, comparison with regional data and relationship to biogenic sedimentation. Global Biogeochemical Cycles, 9(3): 359–372
Ottesen R T, Bogen J, Bølviken B, et al. 1989. Overbank sediment: a representative sample medium for regional geochemical mapping. Journal of Geochemical Exploration, 32(1–3): 257–277
Peng Xiaotong, Zhou Huaiyang, Weng Huanxin, et al. 2003. Distribution characteristics, transfer mechanism and pollution assess of heavy metal vanadium, nickel and cobalt in sediment cores of the Zhujiang estuary. Journal of Zhejiang University (Science Edition) (in Chinese), 30(1): 103–108
Pokras E M, Molfino B. 1986. Oceanographic control of diatom abundances and species distributions in surface sediments of the Tropical and Southeast Atlantic. Marine Micropaleontology, 10(1–3): 165–188
Qi Yuzao, Li Jiaying. 2004. Flora Algarum Sinicarum Aquae Dulcis (Tomus X) (in Chinese). Beijing: Science Press, 1–137
Roquin C, Zeegers H. 1987. Improving anomaly selection by statistical estimation of background variations in regional geochemical prospecting. Journal of Geochemical Exploration, 29(1–3): 295–316
Roubeix V, Rousseau V, Lancelot C. 2008. Diatom succession and silicon removal from freshwater in estuarine mixing zones: from experiment to modelling. Estuarine, Coastal and Shelf Science, 78(1): 14–26
Round F E, Crawford R M, Mann D G. 1990. The Diatoms: Morphology and Biology of the Genera. Cambridge: Cambridge University Press, 1–760
Sancetta C. 1982. Distribution of diatom species in surface sediments of Bering and Okhotsk seas. Micropaleontology, 28(3): 221–257
Shen Linnan, Chen Min, Lan Binbin, et al. 2017. Diatom distribution as an environmental indicator in surface sediments of the West Philippine Basin. Chinese Journal of Oceanology and Limnology, 35(2): 431–443
Shi Xuefa, Liu Shengfa, Qiao Shuqing, et al. 2010. Depositional features and palaeoenvironmental records of the mud deposits in Min-Zhe Coastal mud area, East China Sea. Marine Geology & Quaternary Geology (in Chinese), 30(4): 19–30
Smol J P, Stoermer E F. 2010. The Diatoms: Applications for the Environmental and Earth Sciences. Cambridge: Cambridge University Press, 1–469
ter Braak C J F, Smilauer P. 2002. CANOCO 4.5. Biometris. Wageningen: Wageningen University and Research Centre, 1–500
Vital H, Stattegger K. 2000. Major and trace elements of stream sediments from the lowermost Amazon River. Chemical Geology, 168(1–2): 151–168
Wang Liang, Fan Dejiang, Li Weiran, et al. 2014. Grain-size effect of biogenic silica in the surface sediments of the East China Sea. Continental Shelf Research, 81: 29–37
Witkowski A. 2001. Diatom Monographs. Ruggell, Liechtenstein: ARG Gantner Verlag
Wu Rui, Gao Yahui, Fang Qi, et al. 2013. Diatom assemblages in surface sediments from the South China Sea as environmental indicators. Chinese Journal of Oceanology and Limnology, 31(1): 31–45
Xiao Ying. 2013. Study on the ecological characteristics of phytoplankton community in Minjiang Estuary. Journal of Fujian Fisheries (in Chinese), 35(4): 258–263
Xie Xuejing, Yin Binchuan. 1993. Geochemical patterns from local to global. Journal of Geochemical Exploration, 47(1–3): 109–129
Xu Kehui, Milliman J D, Li Anchun, et al. 2009. Yangtze- and Taiwan-derived sediments on the inner shelf of East China Sea. Continental Shelf Research, 29(18): 2240–2256
Xu Yonghang, Sun Qinqin, Yi Liang, et al. 2014. The source of natural and anthropogenic heavy metals in the sediments of the Minjiang River estuary (SE China): implications for historical pollution. Science of the Total Environment, 493: 729–736
Yamanaka T, Miyabe S, Sawai Y, et al. 2010. Geochemical and diatom evidence of transition from freshwater to marine environments in the Aira Caldera and Kagoshima Bay, Japan, during post-glacial sea-level rise. Journal of Asian Earth Sciences, 39(5): 386–395
Yang Yusheng, Chen Guangshui, Guo Jianfen, et al. 2007. Soil respiration and carbon balance in a subtropical native forest and two managed plantations. Plant Ecology, 193(1): 71–84
Ye Yincan, Zhuang Zhenye, Liu Dujuan, et al. 2002. Holocene depositional strength zoning in the East China Sea. Journal of Ocean University of Qingdao (in Chinese), 32(6): 941–948
Yu Yu, Song Jinming, Li Xuegang, et al. 2013. Environmental significance of biogenic elements in surface sediments of the Changjiang estuary and its adjacent areas. Journal of Environmental Sciences, 25(11): 2185–2195
Zhang Zulin, Hong Huasheng, Zhou Juliang, et al. 2003. Fate and assessment of persistent organic pollutants in water and sediment from Minjiang River estuary, Southeast China. Chemosphere, 52(9): 1423–1430
Zhang Zulin, Hong Huasheng, Zhou Juliang, et al. 2004. Phase association of polycyclic aromatic hydrocarbons in the Minjiang river estuary, China. Science of the Total Environment, 323(1–3): 71–86
Zhang Peng, Pang Yong, Pan Hongche, et al. 2015. Factors contributing to hypoxia in the Minjiang River estuary, Southeast China. International Journal of Environmental Research and Public Health, 12(8): 9357–9374
Zhang Wenlong, Zeng Congsheng, Tong Chuan, et al. 2011. Analysis of the expanding process of the Spartina Alterniflora salt Marsh in Shanyutan wetland, Minjiang River estuary by remote sensing. Procedia Environment Sciences, 10: 2472–2477
Zhao Yiyang, Yan Mingcai. 1994. Geochemistry of Sediments of the China Shelf Sea (in Chinese). Beijing: Science Press, 13–170
Zhou Huaiyang, Peng Xiaotong, Pan Jianming. 2004. Distribution, source and enrichment of some chemical elements in the sediments of the Pearl River estuary, China. Continental Shelf Research, 24(16): 1857–1875
Zhou Guohua, Sun Binbin, Zeng Daoming, et al. 2014. Vertical distribution of trace elements in the sediment cores from major rivers in east China and its implication on geochemical background and anthropogenic effects. Journal of Geochemical Exploration, 139: 53–67
Zong Yongqiang, Kemp A C, Yu Fengling, et al. 2010. Diatoms from the Pearl River estuary, China and their suitability as water salinity indicators for coastal environments. Marine Micropaleontology, 75(1–4): 38–49
Year 2017 volume 36 Issue 10
PDF
30
16
Cite this Article
BibTeX
Article Info
doi: 10.1007/s13131-017-1070-7
  • Receive Date:2016-06-28
  • Online Date:2026-04-16
  • Published:2017-10-01
Article Data
Affiliations
History
  • Received:2016-06-28
  • Accepted:2017-01-06
Funding
The Special Fund for Basic Scientific Research Foundation of the Third Institute of Oceanography, State Oceanic Administration, China under contract No. 2016015; the National Natural Science Foundation of China under contract Nos 41306083 and 41376050.
Affiliations
    1 College of Ocean and Earth Sciences, Xiamen University, Xiamen 361102, China
    2 Geology Laboratory of Marine and Coastal, Third Institute of Oceanography, State Oceanic Administration, Xiamen 361005, China

Corresponding:

References
Share
https://castjournals.cast.org.cn/joweb/aos/EN/10.1007/s13131-017-1070-7
Share to
QR

Scan QR to access full text

Cite this article
BibTeX
Citations
表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
关闭全屏
  • BibTeX
  • EndNote
  • RefWorks
  • TxT