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Article

Biotic and Abiotic Factors Affecting the Population Dynamics of Ceratium hirundinella, Peridinium cinctum, and Peridiniopsis elpatiewskyi

by
Behrouz Zarei Darki
1,* and
Alexandr F. Krakhmalnyi
2
1
Department of Marine Biology, Faculty of Marine Sciences, Tarbiat Modares University, Noor 46417-76489, Mazandaran Province, Iran
2
Institute for Evolutionary Ecology, NAS of Ukraine, 37, Lebedeva St., 03143 Kiev, Ukraine
*
Author to whom correspondence should be addressed.
Diversity 2019, 11(8), 137; https://doi.org/10.3390/d11080137
Submission received: 23 July 2019 / Revised: 1 August 2019 / Accepted: 2 August 2019 / Published: 15 August 2019
(This article belongs to the Special Issue Freshwater Algal Diversity and Bio-Indication of Water Resources)
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Abstract

:
The present research was conducted to assess the impact of abiotic and biotic factors on the growth of freshwater dinoflagellates such as Ceratium hirundinella, Peridinium cinctum, and Peridiniopsis elpatiewskyi, which reduce the quality of drinking water in the Zayandeh Rud Reservoir. To this end, 152 algal and zoological samples were collected from the reservoir located in the Central part of Iran in January, April, July, and October 2011. Abiotic factors such as pH, temperature, conductivity, transparency, dissolved oxygen, and nutrient concentration of the water were measured in all study stations. The results showed that the population dynamics of dinoflagellates in the Zayandeh Rud Reservoir was different depending on season, station, and depth. The findings proved that C. hirundinella was one of the dominant autumn planktons in the highest biovolume in the Zayandeh Rud Reservoir. While P. elpatiewskyi was present in the reservoir throughout a year with biovolume peak in summer. Accompanying bloom of P. elpatiewskyi and C. hirundinella, P. cinctum also grew in well-heated summer and autumn waters. It was further found that Ceratium density was positively correlated with sulfate ion concentrations, while the growth of P. cinctum and P. elpatiewskyi were associated, first and foremost, with NO2− and Mn.

1. Introduction

Freshwater dinoflagellates of genera Ceratium, F. Schrank 1793; Peridinium, Ehrenberg 1830; and Peridiniopsis, Lemmermann 1904, are quite often components of biocenosis in many bodies all over the world and may even cause harmful blooms that negatively affect the water quality [1,2,3,4]. Some abilities of dinoflagellates are (i) tolerance to high irradiance [5]; (ii) migration in a water column to optimize photosynthesis and growth [5]; and (iii) toxin excretion [3] allow them to compete, grow, and dominate in the phytoplankton community. Furthermore, their diversity and biomass, just like the algae diversity and abundance of the other divisions, are formed under the influence of hydrological conditions and important environmental factors such as temperature, light intensity, and nutrient concentration [6,7,8]. Thus, the population dynamics of other algae and invertebrates, as the main feeders of phytoplankton [9], is also an impacted biological factor. In other words, a dinoflagellate growth and bloom can be influenced by both abiotic and biotic factors.
Reviewing the literature, Ceratium hirundinella, (O.F. Müller) Bergh 1881, is the most widespread freshwater dinoflagellate, which is present in almost all water bodies of the world. It is also responsible for the smell and taste of drinking water [10,11]. Distribution of C. hirundinella has been properly examined under the influence of various physical and chemical factors in different latitudinal zones [12,13,14,15,16,17]. The presence of C. hirundinella in a water body is positively related to water ionic content, such as HCO3−, SO42−, Ca2+ and Mg2+ [6,18]. In turn, higher ionic content is observed in water bodies that are stratified than in those that do not [14]. However, this alga was also found both in stratified and mixed periods [16]. The growth peak of C. hirundinella is immediately above the thermocline [15].
Among genera of Peridinium and Peridiniopsis, Peridinium aciculiferum, Peridinium gatunense, Peridinium bipes, and Peridiniopsis minima are known as the causative agents of harmful bloom in freshwaters [1,2,4]. Ecology of Peridinium cinctum, (O.F. Müll.) Ehrenb. 1838, and influence of some physical [8] and chemical parameters such as nitrite and phosphorous on its growth and reproduction have already been studied [5,19,20,21]. Regel et al. [5] found out that the species has to migrate to an optimal depth for better photosynthesis (30% surface irradiance); out of which, negative growth was observed. Peridiniopsis elpatiewskyi, (Ostenf.) Bourr. 1968, is known as a subtropical form, presented from May to September with a maximum in August in the Northern Hemisphere and preferred depth near the surface [22]. Nevertheless, there is no enough knowledge of ecological growth condition of P. elpatiewskyi. Its only distribution and morphology in some water bodies throughout the different parts of the world (i.e., Cuba [23]; Israel [22]; Ukraine [24]; Greece [25]; Germany [26]; Chili [27]) has been reported.
Thus, the present research aims to assess the impact of abiotic and biotic factors on the population dynamics of freshwater dinoflagellates such as C. hirundinella, P. cinctum, and P. elpatiewskyi in the Zayandeh Rud Reservoir, of which its water is used for irrigation and drinking supply (Central Iran).

2. Materials and Methods

2.1. Study Sites

Materials for the present study were collected from the oligotrophic mountain reservoir of Zayandeh Rud, situated in the Central part of Iran on the Zayandeh Rud River in the Esfahan-Sirjan Basin. The reservoir is the most important source of pure water for four provinces in Iran. It is located at 50°15–50°45’ N; 32°30’–33°00’ E with a mean elevation of about 1950 m above mean sea level. It is elongated in an east-west orientation (40 km long and from 0.05 to 4.5 km wide). The drainage basin area covers about 41,503 km2. The maximum water-surface is 54 km2 and stores some 1470 million m3 at the highest level [28]. The maximum depth is 88 m. However, these parameters are constantly fluctuating [29]. During the investigation, the maximum depth was 51 m. Its retention time is 369 days. The main water source for the reservoir is the Zayandeh Rud River, with its temporary and permanent inflows, that is mainly fed up by melted snow water springing from the Zardkuh Bakhtiyari Mountains at the height of 4221 m above sea level [30]. The majority of water inflows (up to 80%) into the reservoir in May. With discharge waters, the reservoir is polluted with agrochemicals from agricultural fields and orchards. In the reservoir, stratification usually starts in an area located close to the dam in June and ends in late August. Sometimes, short-term stratification is observed in April [28]. The mid-summer thermocline near the dam had a depth between 20 and 22 m during the investigation and the transparency of water can reach 6.5 m in winter, while in the summer, it accounts for 3.0 m. The lower boundary of the photosynthesis layer of phytoplankton reaches to 16–17 m in winter, and it rises to 7–8 m in summer.
To conduct the study, four transects with three stations (left and right banks, and a middle station) were established for the water sampling. The first transect was considered at the water entrance where the river and one of the inflows flow into the reservoir. The second transect was located in the water body mouth. The third one was in the middle of the reservoir. The fourth transect was finally considered near the dam structure. The details of the sampling points and study transects are shown in Figure 1 and Table 1.

2.2. Sampling

In order to study the affecting factors on population dynamics of C. hirundinella, P. cinctum, and P. elpatiewskyi, some abiotic factors such as pH, surface temperature, as well as depth temperature profile, electrical conductivity (EC), transparency, total dissolved solids (TDS), dissolved oxygen (DO), chemical oxygen demand (COD), biochemical oxygen demand (BOD), mineral and organic nitrogen, phosphates, sulfates, Fe, and Mn were considered. Besides, some biotic factors including the qualitative and quantitative algal composition of all algal divisions, and cell numbers of microinvertebrates were measured at all investigated stations. The water transparency was estimated by a Secchi disk. The vertical profiles of temperature were carried out with conductivity-temperature-depth (CTD) sensors (Ocean Seven 316). Qualitative samples were taken with a planktonic net, with a mesh size of 55 µm, by sieving 100 L of water and a part of them were preserved with a 4% formaldehyde. Quantitative algological and zoological samples were also taken with a Ruttner bathometer [31,32].
Overall, 152 algal and zoological samples were collected from the surface, 5, and 10 m depths, from January to October 2011, in the middle of each season between 9:00 and 14:00. Moreover, samples were taken up to 30 m every 5 m in the middle station of the fourth transect in July to study the species behavior below and above the thermocline that has a place in this water area. Peculiarities of sampling, processing, and storage of the algological material are described in Wasser et al. [33].

2.3. Sample Analysis

The dinoflagellate cells study was conducted at the Institute of Evolutionary Ecology of the National Academy of Sciences of Ukraine (Kiev) using an Olympus BX51 light microscope with UPlanFLN 40 ×/0.67 and Plan 40 ×/0.65 Ph 2 lenses. Dinoflagellates were examined in transmitted light and a mode of fluorescence with preliminary staining of cells using Calcofluor White M2R [34]. The cell sizes were determined using the AmScope program. Photomicrographs were made with a Canon EOS 1000D camera in Adobe Photoshop CS5 Extended. Identification of other algae species was carried out with a Nikon Eclipse E200 microscope at the laboratory of the Department of Marine Biology of Tarbiat Modares University (Iran). The diatoms were processed for the purpose to delete the organic contents of the cell by warm methods before microscopic analysis [35,36]. Identification of microinvertebrates was carried out according to former reports [32,37,38]. Algal cells were counted with a Neubauer chamber conducting previously the sedimentation procedure according to Wasser et al. [33]. Cell biovolumes of each species were calculated according to the most suitable geometric models [39,40]. Total biovolumes of each phytoplankton species were calculated by multiplying the counted number of cells per milliliter by an average cell biovolume of that species. The cells of invertebrates were reckoned with a Sedgwick Rafter counter [32].

2.4. Data and Statistical Analyses

The canonical correspondence analysis (CCA) was used to determine relationships between the cell number of investigated dinoflagellates and the investigated abiotic and biotic factors. The statistical analysis was performed with the software SPSS 21.

3. Results

The study found that, among dinoflagellates, three species of C. hirundinella, P. cinctum, and P. elpatiewskyi were the structure-forming species in reservoir biocenosis (Figure 2). These species were found in the water column under the particular abiotic parameters, as presented in Table 2.
In the Zayandeh Rud Reservoir, the investigated dinoflagellates were present in different biovolumes at the water surface depending on the season and station (Figure 3). The average biovolumes for three species cells of C. hirundinella, P. cinctum, and P. elpatiewskyi were calculated 75,078.57 µm3, 59,511.49 µm3, and 14,299.84 µm3, respectively. Furthermore, their abundances were changing in a water column (Figure 4). Temperature depth profiles showed that thermal stratification was observed in the middle station of transect 4 (near the dam) and eventually stabilized during July to produce a precipitous thermocline of 6.7 °C between 20 and 22 m.
The maximum number of cells was recorded for P. elpatiewskyi at a 5 m depth near the dam in July while the minimum value was in January. However, it had not the maximum values in biovolume. Monitoring the vertical distribution showed that P. elpatiewskyi preferred to concentrate more at a depth between 5 and 15 m above the thermocline. Below that, the cell density was significantly declined. P. elpatiewskyi was replaced by C. hirundinella, which was one of the dominants in autumn plankton in the Zayandeh Rud Reservoir. Overall, C. hirundinella preferred the low flow reservoir areas (transects 3 and 4, which are located closer to the dam), where it was recorded in highest biovolume. In a water column, C. hirundinella was spread uniformly enough. Its population density decreased below the thermocline. In January and April, Ceratium cells appeared more as cysts. Accompanying bloom of P. elpatiewskyi and C. hirundinella, P. cinctum also grew in well-heated summer and autumn waters. In October, especially favorable conditions for this species occurred near the second transect at the bottom. In January, species were not detected in the samples. P. cinctum also gave preference to the depth depending on transects. In stations with insignificant depths, it went down to the bottom (station 2) while, at the deep-water stations, it focused on stratification close to the surface (middle stations of transects 3 and 4) and above the thermocline.
The investigated dinoflagellates were a part of the algal and invertebrate communities. A total of 117 species of algae and 255 invertebrates species were recorded in the course of this study in the Zayandeh Rud Reservoir. A maximum value of the phytoplankton biovolume was in October while a minimum one was observed in January (Figure 5).
Among algae, diatoms were dominant on the species diversity, but not on biovolume. The recorded maximum number of diatomic cells of 1230 cells mL−1 was in January. Three dominant species of Asterionella formosa Hassall, Cyclotella ocellata Pantocsek, and Fragilaria crotonensis Kitton contributed to the reservoir algal flora. The lowest biovolume of diatomic cells was noted in July. Dinobryon divergens O.E.Imhof together with Dinobryon sertularia Ehr. from Chrysophyta division bloomed up to 3.33 mm3 L−1 in the middle of the third transect in April. The population density of green algae and streptophytes varied from 2 to 270 cells mL−1. Chlorophyta and Streptophyta groups were dominated by Pediastrum boryanum (Turpin) Meneghini, Oocystis borgei J.Snow, and Zygnema insigne (Hass.) Kütz. The highest biovolume of green algae was observed in 10 m depth near the dam in autumn when Tetraedron minimum with its variety of T. minimum var. scrobiculatum and less Scenedesmus ellipticus vegetated. The species diversity of zooplankton in a sample ranged from one to 34 species and Protozoa was presented as the most diverse and numerous (to 120 thousand specimens m−3). Balanonema sp. (dominated in winter), Vorticella convallaria (in spring and autumn), Tetrahymena pyriformis (in autumn) of class Ciliata and Amoeba sp. (in spring) constituted the complex of the dominant species of protozoa in the reservoir. Among Metazoa, species of the phylum Arthropoda, such as Leydigia acanthocercoids (dominated in spring), Chydorus sphaericus (in spring), Cyclops sp. (at the third and fourth transects in summer and autumn), Herpetocypris sp. (in winter), Nauplius larva (in summer) and the phylum Rotifera as Notholca squamula (in spring), Keratella cochlearis (at the third and fourth transects in spring and throughout the water area in autumn), Polyarthra euryptera with Polyarthra sp. (at the first and second transects in summer), as well as Nematod sp. of the phylum Nematoda (throughout the researched period), were the most numerous.
To find the correlation between the cell number of the three studied species and abiotic and biotic factors, canonical correspondence analysis (CCA) was conducted (Figure 6). Based on the CCA, the eigenvalues of axis 1 (λ = 0.84) and 2 (λ = 0.39) explained 57.5% and 26.8% of the relationship. The C. hirundinella density was positively correlated with SO4−, BOD, COD, green, and streptophyte algae and negatively correlated with NO3−, and PO4−, while P. elpatiewskyi had a positive correlation with temperature and a negative one with EC, NO2−, and Mn. P. cinctum was associated moderately with Fe and NO2−.

4. Discussion

In the phytoplankton community of the Zayandeh Rud Reservoir, C. hirundinella, P. cinctum, and P. elpatiewskyi were the structure-forming species and their growth peaks were found between summer and late autumn. C. hirundinella, which is a well-researched species because of its conspicuous cells and cosmopolitism, in the Zayandeh Rud Reservoir, was present in water throughout a year. However, in winter and spring it appeared more as cysts and in autumn alga reaches the highest biovolume. Its vertical distribution in the water column is not uniformly above the thermocline and photic zone, which is not in conflict with a report of Hedger et al. [15]. Comparing the obtained findings with many other studies, the conclusion can be made that seasonal periodicity of the species C. hirundinella is variable and reaches the high abundance in different months depending on the world regions (Table 3).
Perhaps, firstly, in different parts of the world in the same month, the water temperature because of the solar radiance can significantly distinguish [41]. Secondly, species can inhabit water where the temperature ranges between 4 and 26 °C [14,16,17]. The present correlation analysis indicated that the species do not rely on temperature and can grow in diverse temperature condition and in stratified and mixed periods that explains its temperature spread. Indeed, in previous works, it was found that the growth of C. hirundinella depends more on ionic content of water such as Ca2+, Mg2+, PO4−, HCO3−, and lest of SO42− [6,13,14,18]. The statistical analysis of the current study determined that the main element correlated with the population of C. hirundinella is sulfate SO4−. The maximum number of the species cells was noted at notably high values of SO4− (from 100 to 236 mg L−1). Photosynthetic organisms especially vascular plants and algae acquire S at their highest oxidation number as sulfate [42]. The ATP sulfurylase sequence of five species from dinoflagellates is known but there is no information about the Ceratium species. Perhaps, S is also one of the main components of C. hirundinella cells and is used for the sulfation of its molecules such as lipids, polysaccharides, proteins, the amino acids cysteine, antioxidants, and others, as in the other algae [43]. In the Zayandeh Rud Reservoir, the main source of sulfate pollution is the runoff water, which comes into the reservoir from agricultural fields distributed in the basin, orchards where sulfate is used in fertilizers, and fish farms as domestic sewage.
Water discharge contributes to water pollution and increases not only sulfate concentration but also nitrite (NO2−) and nitrate (NO3−) that were correlated with the growth of P. cinctum and P. elpatiewskyi. When no external nitrogen source is available in the environment, even at optimal temperatures, cells of P. cinctum and P. elpatiewskyi stop their fission [20]. According to conducted statistical analysis, between NO3− and NO2−, P. cinctum and P. elpatiewskyi preferred to absorb nitrite-nitrogen as a nutrient unlike the green algae undergoing nitrate assimilation to nitrite and then reduction to ammonium [44]. Perhaps, the dinoflagellate has the enzyme complex nitrite reductase, making it competitive in an algological community [31]. The temperature was the second-strongest factor correlated with cells of P. cinctum and P. elpatiewskyi. Their growth temperature ranged from 11 to 25 °C during the whole investigated period. The species were present in the plankton of the reservoir throughout a year, with their biovolume peaks in summer. In general, in the Zayandeh Rud Reservoir, P. cinctum was characterized by a small number of cells compared to some of the world’s water bodies (Table 3). It could not compete with P. elpatiewskyi, which grew up with it under the same ecological conditions and in the same period of the year. Under stratification, P. cinctum migrated to the surface, which is a bit in contrary to that reported by Regel et al. in the South Australia Lake [5]. Furthermore, it was found out that Mn, and to a much lesser extent Fe, were the required trace elements for growth of P. cinctum and P. elpatiewskyi. pH was weakly variable correlating with the abundance of the dinoflagellate, nevertheless, pH is a factor that contributes to the control of dinoflagellate blooms [45].
Concerning the biotic factor, the variability of C. hirundinella was positively moderately associated with the divisions Chlorophyta and Streptophyta. This fact may point that C. hirundinella and green-streptophyte algae are coexist well and a joint population growth attests to favorable abiotic environmental factors (temperature, EC, pH, and others) for them. P. cinctum was negatively associated with Bacillariophyta. When the diatomic biovolume declined, its biovolume was increased showing that phytoplankton species dominance shifted between these divisions [46]. Moreover, Duarte et al. [47] also concluded that phytoplankton communities with lower diversity were dominated by dinoflagellates and exhibit higher cell numbers and production than communities with higher diversity. This was possible because dinoflagellates had multiple life-form strategies consistent with their diverse habitat specializations, but rely on impoverished bloom species pools, whereas diatoms had a relatively uniform bloom strategy based on species-rich pools and exhibit limited habitat specialization [48]. The population of P. elpatiewskyi was positively correlated with Xanthophyta. Concerning Metazoa and Protozoa, all three investigated dinoflagellates had a weak correlation. The cells of P. elpatiewskyi, probably due to their size, was the most consumable. Although, overall, invertebrates prefer to feed with smaller cells of green algae, which grow at this time [9,21]. On the other hand, many dinoflagellates produce chemicals which cause them to be unable to be swallowed by invertebrates, enhancing their survival and competitive ability [49]. Moreover, these algae have long generation times and their losses due to grazing were low by comparison with those of other planktonic algae [16]. The cases of consumption of P. cinctum by fish that had not been investigated in this work also were known [50].
The quality of the water stored in the Zayandeh Rud Reservoir is typically very good [51], but surface and water column growth of C. hirundinella and P. elpatiewskyi, that appear during warm, calm periods when the water level is low, may impair the quality of water used for drinking. Therefore, according to the present study, it was firstly important to monitor the parameters such as SO4−, which was correlated with C. hirundinella growth, and NO2− associated with P. cinctum and P. elpatiewskyi growth, in order to take measures to control the use of fertilizers in orchards, agricultural fields, and domestic sewage, which are the main causes of water pollution by these ions.

5. Conclusions

The current investigation allowed the changes in population dynamics of the three dominant dinoflagellates, such as C. hirundinella, P. cinctum and P. elpatiewskyi, to be identified, under the influence of the biotic and abiotic variables, in the Zayandeh Rud Reservoir (Central Iran). The statistically significant moderate correlations were ultimately established between abiotic parameters and dinoflagellates under consideration. C. hirundinella was positively correlated, first and foremost, with SO4−, while P. cinctum and P. elpatiewskyi had a negative correlation with NO2− and Mn. Furthermore, the findings proved that biotic factors influenced the growth of the three dinoflagellates less. The results of the present study would help the Zayandehroud Reservoir managers to adopt the most ecologically appropriate measures to maintain the quality of drinking water. However, endeavors to gain better insight, with high-resolution and longer duration of data collection, are needed in order to draw a comprehensive conclusion.

Author Contributions

Methodology, formal analysis, investigation, and data curation: B.Z.D. and A.F.K.; conceptualization, writing—original draft preparation, writing—review and editing, visualization, supervision, project administration, and funding acquisition: B.Z.D.

Funding

The study was funded by the Isfahan Regional Water Company, project number 90/159.

Acknowledgments

The authors would like to thanks A. Aslani, H. Karamalian, and A. Zahabsaniei for their expert comments and advice about the investigated area.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Hirabayashi, K.; Yoshizawa, K.; Yoshida, N.; Ariizumi, K.; Kazama, F. Long-Term Dynamics of Freshwater Red Tide in Shallow Lake in Central Japan. Environ. Health Prev. Med. 2007, 12, 33–39. [Google Scholar] [CrossRef] [PubMed]
  2. Yatigammana, S.K.; Ileperuma, O.A.; Perera, M.B.U. Water pollution due to a harmful algal bloom: A preliminary study from two drinking water reservoirs in Kandy, Sri Lanka. J. Natl. Sci. Found. Sri Lanka 2011, 39, 91–94. [Google Scholar] [CrossRef]
  3. Viner-Mozzini, Y.; Zohary, T.; Gasith, A. Dinoflagellate bloom development and collapse in Lake Kinneret: A sediment trap study. J. Plankton Res. 2003, 25, 591–602. [Google Scholar] [CrossRef]
  4. Rengefors, K.; Legrand, C. Toxicity in Peridinium aciculiferum an adaptive strategy to outcompete other winter phytoplankton. Limnol. Oceanogr. 2001, 46, 1990–1997. [Google Scholar] [CrossRef]
  5. Regel, R.H.; Brookes, J.D.; Ganf, G.G. Vertical migration, entrainment and photosynthesis of the freshwater dinoflagellate Peridinium cinctum in a shallow urban lake. J. Plankton Res. 2004, 26, 143–157. [Google Scholar] [CrossRef]
  6. Margalef, R.; Mir, M.; Estrada, M. Phytoplankton composition and distribution as an expression of properties of reservoirs. Can. Water Res. J. 1982, 7, 26–50. [Google Scholar] [CrossRef]
  7. Padisak, J.; Hajnal, E.; Naselli-flores, L.; Dokulil, M.T.; Noges, P.; Zohary, T. Convergence and divergence in organization of phytoplankton communities under various regimes of physical and biological control. Hydrobiologia 2010, 639, 205–220. [Google Scholar] [CrossRef]
  8. Lopez, N.L.; Rondon, C.A.R.; Zapata, A.; Jimenez, J.; Vilamil, W.; Arenas, G.; Rincon, C.; Sanchez, T. Factors controlling phytoplankton in tropical high-mountain drinking-water reservoirs. Limnetica 2012, 31, 305–322. [Google Scholar]
  9. Agrawal, A.A. Algal defense, grazers, and their interactions in aquatic trophic cascades. Acta Oecol. 1998, 19, 331–337. [Google Scholar] [CrossRef]
  10. Heaney, S.I.; Talling, J.F. Ceratium hirundinella—Ecology of a complex, mobile and successful plant. In Forty-Eighth Annual Report for the Year Ended 31 March 1980; Freshwater Biological Association: Ambleside, UK, 1980; pp. 27–40. [Google Scholar]
  11. Whittington, J.; Sherman, B.; Green, D.; Oliver, R.L. Growth of Ceratium hirundinella in a subtropical Australian reservoir: The role of vertical migration. J. Plankton Res. 2000, 22, 1025–1045. [Google Scholar] [CrossRef]
  12. Kawabata, Z.; Kagawa, H. Distribution pattern of the dinoflagellate Ceratium hirundinella (O. F. Müller) Bergh in a reservoir. Hydrobiologia 1988, 169, 319–325. [Google Scholar] [CrossRef]
  13. Sigee, D.C.; Levado, E.; Dodwell, A.J. Elemental composition of depth samples of Ceratium hirundinella (Pyrrophyta) within a stratified lake: An X-ray microanalytical study. Aquat. Microb. Ecol. 1999, 19, 177–187. [Google Scholar] [CrossRef]
  14. Perez-Martınez, C.; Sanchez-Castillo, P. Temporal occurrence of Ceratium hirundinella in Spanish reservoirs. Hydrobiologia 2001, 452, 101–107. [Google Scholar] [CrossRef]
  15. Hedger, R.D.; Olsen, N.R.B.; George, D.G.; Malthus, T.J.; Atkinson, P.M. Modelling spatial distributions of Ceratium hirundnella and Microcystis spp. in a small productive British lake. Hydrobiologia 2004, 528, 217–227. [Google Scholar] [CrossRef]
  16. MacDonagh, M.E.; Casco, M.A.; Claps, M.C. Colonization of a Neotropical Reservoir (Córdoba, Argentina) by Ceratium hirundinella (O. F. Müller) Bergh. Ann. Limnol. Int. J. Limnol. 2005, 41, 291–299. [Google Scholar] [CrossRef]
  17. Hart, R.C.; Wragg, P.D. Recent blooms of the dinoflagellate Ceratium in Albert Falls Dam (KZN): History, causes, spatial features and impacts on a reservoir ecosystem and its zooplankton. Water SA 2009, 35, 455–468. [Google Scholar] [CrossRef]
  18. Bruno, S.F.; McLaughlin, J.J.A. The nutrition of the freshwater dinoflagellate Ceratium hirundinella. J. Protozool. 1977, 24, 548–553. [Google Scholar] [CrossRef]
  19. Pfiester, L.A. Periodicity of Ceratium hirundinella (O.F.M.) Dujardin and Peridinium cinctum (O.F.M.) Ehrenberg in relation to certain ecological factors. Castanea 1971, 36, 246–257. [Google Scholar]
  20. Grigorszky, I.; Kiss, K.T.; Béres, V. The effects of temperature, nitrogen, and phosphorus on the encystment of Peridinium cinctum, Stein (Dinophyta). Hydrobiologia 2006, 563, 527–535. [Google Scholar] [CrossRef]
  21. Belkinova, D.; Padisák, J.; Gecheva, G.; Cheshmedjiev, S. Phytoplankton based assessment of ecological status of Bulgarian lakes and comparison of metrics within the water framework directive. Appl. Ecol. Environ. Res. 2014, 12, 83–103. [Google Scholar] [CrossRef]
  22. Pollinger, B.U.; Hickel, B. Dinoflagellata associations in subtropical lake. Arch. Hydrobiol. 1991, 120, 267–285. [Google Scholar]
  23. Popovsky, J. Some thecate Dinoflagellates from Cuba. Arch. Protistenkd. 1970, 112, 252–258. [Google Scholar]
  24. Krakhmalniy, A. Morphology of Peridiniopsis elpatiewskyi (Ostenf.) Bourr. (Dinophyta) theca. Int. J. Algae 2009, 11, 25–33. [Google Scholar] [CrossRef]
  25. Katsiapi, M. Assessing Water Quality of Greek Lakes and Reservoirs Using Ecological and Molecular Markers. Ph.D. Thesis, Aristotle University of Thessaloniki, Thessaloniki, Greece, 2012; p. 148. [Google Scholar]
  26. Täuscher, L. Checklisten und Gefährdungsgrade der Algen des Landes Brandenburg. Verh. Bot. Ver. Berl. Brandenbg. 2013, 146, 109–128. [Google Scholar]
  27. Ascencio, E.; Rivera, P.; Cruces, F. Morphology of Peridiniopsis elpatiewskyi (Ostenfeld) Bourrelly (Dinophyceae) found for the first time in Chilean inland waters. Gayana Bot. 2015, 72, 42–46. [Google Scholar] [CrossRef]
  28. Pourmoghaddas, H. Water Quality and Health Issues in the Zayandeh Rud Basin; International Water Management Institute: Isfahan, Iran, 2006; p. 30. [Google Scholar]
  29. Shahmansuri, M. Investigation of Trophic State and Thermal Stratification of Reservoir of Zayandeh Rood; Regional Water Company of Esfahan: Isfahan, Iran, 2005; p. 159. [Google Scholar]
  30. Hoseiniabri, H. Zayandeh Rud River from Headwaters to Wetland; Golha Publication: Isfahan, Iran, 1996; p. 91. [Google Scholar]
  31. Becker, E.W. Microalgae: Biotechnology and Microbiology; Cambridge University Press: Cambridge, UK, 2008; p. 293. [Google Scholar]
  32. Pechenik, J.A. Biology of the Invertebrates; Wm. C. Brown Publishers: Dubuque, IA, USA, 1991; p. 567. [Google Scholar]
  33. Wasser, S.P.; Kondrateva, N.V.; Masyuk, N.P.; Palamar-Mordvintseva, G.M. Algae: Reference Book; Wasser, S.P., Kondrateva, N.V., Masyuk, N.P., Palamar-Mordvintseva, G.M., Eds.; Nauk. Dumka: Kiev, Ukraine, 1989; p. 608. (In Russian) [Google Scholar]
  34. Fritz, L.; Triemer, R.E. A rapid simple technique utilizing Calcofluor White M2R for the visualization of Dinoflagellate thecal plates. J. Phycol. 1985, 21, 662–664. [Google Scholar] [CrossRef]
  35. Lange-Bertalot, H. Diatoms of Europe: Diatoms of the European inland waters and comparable habitats. In Navicula Sensu Stricto. 10 Genera Separated from Navicula Sensu Lato. Frustulia.; A.R.G. Gantner Verlag K.G.: Ruggell, Lichtenstein, 2001; Volume 2, p. 526. [Google Scholar]
  36. Proshkina-Lavrenko, A.I. Diatoms of the USSR: Fossil and Recent; Nauka Press: Leningrad, Russia, 1974; p. 40. (In Russian) [Google Scholar]
  37. Parker, T.J.; Haswell, W.A. Textbook of Zoology: Invertebrates; Macmillan: London, UK, 1972; p. 874. [Google Scholar]
  38. Barnes, R.S.K.; Calow, P.; Olive, P.J.W.; Golding, D.W.; Spicer, J.I. The Invertebrates: A Synthesis, 3rd ed.; Wiley-Blackwell Publisher: Hoboken, NJ, USA, 2001; p. 512. [Google Scholar]
  39. Sun, J.; Liu, D. Geometric models for calculating cell biovolume and surface area for phytoplankton. J. Plankton Res. 2003, 25, 1331–1346. [Google Scholar] [CrossRef] [Green Version]
  40. Vadrucci, M.; Mazziotti, C.; Fiocca, A. Cell biovolume and surface area in phytoplankton of Mediterranean transitional water ecosystems: Methodological aspects. Transit. Waters Bull. 2013, 7, 100–123. [Google Scholar]
  41. Perez-Martınez, C.; Sanchez-Castillo, P. Winter dominance of Ceratium hirundinella in a southern north-temperate reservoir. J. Plankton Res. 2002, 24, 89–96. [Google Scholar] [CrossRef]
  42. Prioretti, L.; Gontero, B.; Hell, R.; Giordano, M. Diversity and regulation of ATP sulfurylase in photosynthetic organisms. Front. Plant Sci. Front. 2014, 5, 597. [Google Scholar] [CrossRef] [PubMed]
  43. Giordano, M.; Prioretti, L. Sulphur and Algae: Metabolism, Ecology and Evolution. In The Physiology of Microalgae; Borowitzka, M.A., Beardall, J., Raven, J.A., Eds.; Springer: Dordrecht, The Netherlands, 2014; pp. 185–209. [Google Scholar]
  44. Sanz-Luque, E.; Chamizo-Ampudia, A.; Llamas, A.; Galvan, A.; Fernandez, E. Understanding nitrate assimilation and its regulation in microalgae. Front. Plant Sci. 2015, 6, 899. [Google Scholar] [CrossRef] [PubMed]
  45. Hinga, K.R. CO-occurrence of dinoflagellate blooms and high pH in marine enclosures. Mar. Ecol. Prog. Ser. 1992, 86, 181–187. [Google Scholar] [CrossRef]
  46. Coria-Monter, E.; Monreal-Gomez, M.A.; Salas-de-Leon, D.A.; Aldeco-Ramırez, J.; Merino-Ibarra, M. Differential distribution of diatoms and dinoflagellates in a cyclonic eddy confined in the Bay of La Paz, Gulf of California. J. Geophys. Res. Oceans 2014, 119, 6258–6268. [Google Scholar] [CrossRef]
  47. Duarte, P.; Macedo, M.F.; Cancela da Fonseca, L. The relationship between phytoplankton diversity and community function in a coastal lagoon. In Marine Biodiversity: Patterns and Processes, Assessment, Threats, Management and Conservation, Proceedings of the 38th European Marine Biology Symposium, Aveiro, Portugal, 8–12 September 2003; Queiroga, H., Cunha, M.R., Cunha, A., Moreira, M.H., Quintino, V., Rodrigues, A.M., Serodio, J., Warwick, R.M., Eds.; Developments in Hydrobiology; Springer: Dordrecht, The Netherlands, 2006; Volume 183, pp. 3–18. [Google Scholar]
  48. Smayda, T.J. Adaptive Ecology, Growth Strategies and the Global Bloom Expansion of Dinoflagellates. J. Oceanogr. 2002, 5, 281–294. [Google Scholar] [CrossRef]
  49. Huntley, M.; Sykes, P.; Rohan, S.; Marin, V. Chemically-mediated rejection of dinoflagellate prey by the copepods Calanus pacificus and Paracalanus parvus: Mechanism, occurrence and significance. Mar. Ecol. Prog. Ser. 1986, 28, 105–120. [Google Scholar] [CrossRef]
  50. Spataru, P. The feeding habits of Tilapia galilaea (Artedi) in Lake Kinneret (Israel). Aquaculture 1976, 9, 47–59. [Google Scholar] [CrossRef]
  51. Darki, B.Z.; Darki, L.Z.; Akkafi, H.R.; Mirzai, M. Taxonomic composition of algae and its indicator role in the ecosystem of the Zayandeh Rud River, Iran. Inland Water Biol. 2013, 6, 285–293. [Google Scholar] [CrossRef]
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Figure 1. Schematic map of Zayandeh Rud Reservoir showing the sampling stations. The transects corresponding sampling stations on the left bank are denoted by 2−, 3−, 4−, while on the right bank by 2+, 3+, 4+, and the middle stations by 1, 2, 3, 4.
Figure 1. Schematic map of Zayandeh Rud Reservoir showing the sampling stations. The transects corresponding sampling stations on the left bank are denoted by 2−, 3−, 4−, while on the right bank by 2+, 3+, 4+, and the middle stations by 1, 2, 3, 4.
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Figure 2. Dominant species of dinoflagellates inhabiting the Zayandeh Rud Reservoir: 1—Ceratium hirundinella, 2–4—Peridinium cinctum, 5–7—Peridiniopsis elpatiewskyi; 1, 2, 5—ventral view, 3, 6—dorsal view, 4—antapical view (antapex), 7—apical view (apex). C1–C6—cingulum plates; Sa, Sd, Sp–sulcal plates; 1′–4′, 1” –7”, 1”’ –5”’, 1”” –2””—thecal plates.
Figure 2. Dominant species of dinoflagellates inhabiting the Zayandeh Rud Reservoir: 1—Ceratium hirundinella, 2–4—Peridinium cinctum, 5–7—Peridiniopsis elpatiewskyi; 1, 2, 5—ventral view, 3, 6—dorsal view, 4—antapical view (antapex), 7—apical view (apex). C1–C6—cingulum plates; Sa, Sd, Sp–sulcal plates; 1′–4′, 1” –7”, 1”’ –5”’, 1”” –2””—thecal plates.
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Figure 3. The biovolumes of the investigated species at the surface in different stations (2−, 3−, 4−, 2+, 3+, 4+, 1, 2, 3, 4) and months (January, April, July, and October) in the Zayandeh Rud Reservoir in 2011. CH, C. hirundinella; PC, P. cinctum; PE, P. elpatiewskyi.
Figure 3. The biovolumes of the investigated species at the surface in different stations (2−, 3−, 4−, 2+, 3+, 4+, 1, 2, 3, 4) and months (January, April, July, and October) in the Zayandeh Rud Reservoir in 2011. CH, C. hirundinella; PC, P. cinctum; PE, P. elpatiewskyi.
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Figure 4. Vertical distribution of C. hirundinella, P. cinctum, and P. elpatiewskyi (black line) and depth temperature profile (the red one) in the Zayandeh Rud Reservoir at the middle stations of the third and fourth transects in January, April, July, and October 2011.
Figure 4. Vertical distribution of C. hirundinella, P. cinctum, and P. elpatiewskyi (black line) and depth temperature profile (the red one) in the Zayandeh Rud Reservoir at the middle stations of the third and fourth transects in January, April, July, and October 2011.
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Figure 5. The seasonal variations in biovolumes of C. hirundinella (CH), P. cinctum (PC), P. elpatiewskyi (PE) and phytoplankton groups (Cyanophyta, Bacillariophyta, Euglenophyta, Chrysophyta, Xanthophyta, Chl+Str: Chlorophyta and Streptophyta) on average throughout the Zayandeh Rud Reservoir in January, April, July, and October 2011.
Figure 5. The seasonal variations in biovolumes of C. hirundinella (CH), P. cinctum (PC), P. elpatiewskyi (PE) and phytoplankton groups (Cyanophyta, Bacillariophyta, Euglenophyta, Chrysophyta, Xanthophyta, Chl+Str: Chlorophyta and Streptophyta) on average throughout the Zayandeh Rud Reservoir in January, April, July, and October 2011.
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Figure 6. Canonical correspondence analysis (CCA) biplot showing the relationships between the cell number of C. hirundinella (CH), P. cinctum (PC), P. elpatiewskyi (PE), and abiotic and biotic variables of algal divisions (Cyan: Cyanophyta, Bac: Bacillariophyta, Eug: Euglenophyta, Chrys: Chrysophyta, Xan, Xanthophyta, Chl+Str, Chlorophyta plus Streptophyta) and invertebrates.
Figure 6. Canonical correspondence analysis (CCA) biplot showing the relationships between the cell number of C. hirundinella (CH), P. cinctum (PC), P. elpatiewskyi (PE), and abiotic and biotic variables of algal divisions (Cyan: Cyanophyta, Bac: Bacillariophyta, Eug: Euglenophyta, Chrys: Chrysophyta, Xan, Xanthophyta, Chl+Str, Chlorophyta plus Streptophyta) and invertebrates.
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Table
Table 1. Geographic coordinates and depths of the middle station of each transect on the Zayandeh Rud Reservoir.
Table 1. Geographic coordinates and depths of the middle station of each transect on the Zayandeh Rud Reservoir.
TransectsGeographic CoordinatesDepth (m)
JanuaryAprilJulyOctober
150°31’45.74” E–32°42’56.38” N1.21.41.51.0
250°36’31.58” E–32°43’09.32” N10.578.35.5
350°39’56.68” E–32°44’08.97” N322728.423.5
450°44’02.37” E–32°44’01.72” N514849.343
Table
Table 2. The value ranges of abiotic water factors restricted to the samples where C. hirundinella, P. cinctum, and P. elpatiewskyi (CH, PC, and PE) were present over the study period in the Zayandeh Rud Reservoir. Abbreviations: TDS, total dissolved solids; EC, electrical conductivity; DO, dissolved oxygen; COD, chemical oxygen demand; BOD, biochemical oxygen demand.
Table 2. The value ranges of abiotic water factors restricted to the samples where C. hirundinella, P. cinctum, and P. elpatiewskyi (CH, PC, and PE) were present over the study period in the Zayandeh Rud Reservoir. Abbreviations: TDS, total dissolved solids; EC, electrical conductivity; DO, dissolved oxygen; COD, chemical oxygen demand; BOD, biochemical oxygen demand.
Abiotic and Biotic VariablesSpecies
CHPCPE
Min–MaxMean ± S.DMin–MaxMean ± S. DMin–MaxMean ± S.D
Transparency (m)0.3–6.23.3 ± 1.762.8–4.23.6 ± 0.570.68–6.23.25 ± 1.83
TDS (ppm)150–260191.1 ± 37.21152–262195.8 ± 41.4152–262192.2 ± 35.9
pH7.4–8.78.04 ± 0.446.7–8.47.9 ± 0.466.7–8.78.02 ± 0.45
Temperature (T, °C)6.4–25.614.8 ± 5.611–25.617.5 ± 4.911–25.615.06 ± 5.69
EC (μS cm−1)230–413329.5 ± 66.09230–413295 ± 43.26230–413324.6 ± 64.2
DO (mg L−1)5.2–8.37.8 ± 1.355.2–8.37.1 ± 0.915.2–8.37.7 ± 1.24
NO3− (mg L−1)3.8–12.69.8 ± 4.973.8–12.68.02 ± 3.123.8–12.69.64 ± 4.2
NO2− (mg L−1)0.055–0.150.07 ± 0.030.052–0.110.06 ± 0.030.052–0.110.06 ± 0.03
PO4− (mg L−1)0.02–0.170.06 ± 0.030.02–0.170.06 ± 0.030.02–0.170.06 ± 0.03
SO4− (mg L−1)14.6–236.646.2 ± 49.314.6–236.655.6 ± 56.414.6–236.644.3 ± 50.05
Fe (mg L−1)0.002–0.20.06 ± 0.060.002–0.100.025 ± 0.0380.002–0.150.06 ± 0.06
Mn (mg L−1)0.003–0.0060.003 ± 0.0020.001–0.0060.002 ± 0.0010.001–0.0060.003 ± 0.002
COD (mg L−1)2–5712.24 ± 12.722–5714.3 ± 13.62–5711.7 ± 12.79
BOD (mg L−1)1–2914.25 ± 14.591–297.53 ± 6.51–296.24 ± 5.79
Table
Table 3. The population density of C. hirundinella (CH), P. cinctum (PC), and P. elpatiewskyi (PE) in some water bodies of the world.
Table 3. The population density of C. hirundinella (CH), P. cinctum (PC), and P. elpatiewskyi (PE) in some water bodies of the world.
SpeciesWater BodyMax Cell Number, Cells mL−1DepthPeriod of TimeAuthors
CHZayandeh Rud Reservoir, Iran400SurfaceIn OctoberCurrent study
Albert Falls Dam (South Africa)5000-In OctoberHart and Wragg [17]
The Ishitegawa Reservoir (Japan)1300SurfaceIn JulyKawabata, Kagawa [12]
Rio Tercero Reservoir1244Photic zonelater summerMacDonagh et al. [16]
Esthaite Water (England)1000In the 0–5 m layerIn SeptemberHeaney and Talling [10]
Bermejales Reservoir (Spain)247-In DecemberPerez-Martınez, Sanchez-Castillo [14]
Lake Kinneret (Israel)35Photic zonein MayPollinger, Hickel [22]
PCZayandeh Rud Reservoir, Iran50At the bottom (5.5 m)In OctoberCurrent study
Torrens Lake (South Australia)460Below the surface mixed layerIn January (summer month)Regel et al. [5]
Man-made lake near Tokyo420--Pollinger, Hickel [22]
PEZayandeh Rud Reservoir, Iran1500At a 5 m depthIn JulyCurrent study
Lake Kinneret (Israel)100Near the surfaceIn summerPollinger, Hickel [22]

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Zarei Darki, B.; Krakhmalnyi, A.F. Biotic and Abiotic Factors Affecting the Population Dynamics of Ceratium hirundinella, Peridinium cinctum, and Peridiniopsis elpatiewskyi. Diversity 2019, 11, 137. https://doi.org/10.3390/d11080137

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Zarei Darki B, Krakhmalnyi AF. Biotic and Abiotic Factors Affecting the Population Dynamics of Ceratium hirundinella, Peridinium cinctum, and Peridiniopsis elpatiewskyi. Diversity. 2019; 11(8):137. https://doi.org/10.3390/d11080137

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Zarei Darki, Behrouz, and Alexandr F. Krakhmalnyi. 2019. "Biotic and Abiotic Factors Affecting the Population Dynamics of Ceratium hirundinella, Peridinium cinctum, and Peridiniopsis elpatiewskyi" Diversity 11, no. 8: 137. https://doi.org/10.3390/d11080137

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