Journal of Ecology and Environment

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Published online April 12, 2022
https://doi.org/10.5141/jee.22.004

Journal of Ecology and Environment (2022) 46:10

Diversity of phytoplankton from the Nakdong River, South Korea: Euglenophytes

Han Soon Kim *† and Jae Hak Lee

Department of Biology, Kyungpook National University, Daegu 41566, Republic of Korea

Correspondence to:Han Soon Kim
E-mail kimhsu@knu.ac.kr

Han Soon Kim and Jae Hak Lee contributed equally to this work.

Received: January 10, 2022; Revised: February 28, 2022; Accepted: March 8, 2022

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Background: Many investigations on phytoplankton from the Nakdong River carried out. However, since the weirs were constructed, only changes in phytoplankton biomass and dominant species have been restrictively studied in phytoplankton investigations in the Nakdong River. Added to this, any investigation on the phytoplankton flora has not been done in the Nakdong River. The aim of this study is to elucidate the characteristics of phytoplankton communities in the Nakdong River with the weirs built in it.
Results: We observed a total of 103 taxa of Euglenophytes belonging to 8 genera from middle-lower part of the Nakdong River. The genus Trachelomonas was the most abundant group making up 40 taxa, followed Lepocinclis (20), Phacus (17), Strombomonas (14), Euglena (5), Colacium (3), Monomorphina (3) and Menoideum (1). Among them, a total of 22 taxa including Colacium (1), Lepocinclis (8), Phacus (4), Strombomonas (4) and Trachelomonas (5) were reported for the first time in Korea, and 86 taxa including those new to Korea were first recorded in the Nakdong River. All the species are illustrated with photomicrographs, and new to Korean species briefly discussed with regard to their taxonomy together with photomicrographs.
Conclusions: The present study, a total of 22 taxa including one species of Colacium, 8 taxa of Lepocinclis, 4 taxa of Phacus, 4 taxa of Strombomonas and 5 taxa of Trachelomonas were reported for the first time in Korea, and 86 taxa including those new to Korea were first recorded in the Nakdong River.

Keywords: Euglenophytes, phytoplankton diversity, Nakdong River, photomicrographs

The Nakdong River is the second longest river on the Korean peninsula with a length of about 510 km and a watershed area of 23,860 km2. As many as 13 million people reside in the basin area. The Nakdong River provides a source of portable and living water to approximately 10 million citizens in not only metropolitan cities such as Daegu, Busan, and Changwon but also many smaller cities. Sixteen large-scale weirs were built in 2012 as part of the Four Major Rivers Project with eight along the Nakdong River included in it with the goal of securing water quantity, mitigating the consequences of droughts and preventing against flooding. The weir construction project interrupts natural water flow and makes a distinct change in the aquatic ecosystem such as hydrological features, water qualities and aquatic communities including freshwater algae (Cha et al. 2015).

In particular, the eight weirs constructed in the Nakdong River substantially changed the river ecosystem overall in terms of not only epilithic diatom assemblages but also hydraulic and hydrologic factors such as water flow reduction, the consequently increasing hydraulic retention time and physico-chemical properties (Lee et al. 2021; Park et al. 2021). Added to this, every summer sees blue-green algal blooms by dominated species such as Microcystis aeruginosa, Aphanizomenon flos-aquae, Anabaena planktonica in the Nakdong River.

Under these circumstances, the phytoplankton community in the Nakdong River can be affected by hydraulic and hydrological variations such as water flow reduction, an increasing retention time and physico-chemical properties following the weir construction.

Many investigations on phytoplankton flora in Korea have been conducted across various regions since Skvortzow (1929) reported 58 diatoms taxa in Lake Seoho, Suwon. And, most of the studies were carried out in lentic waterbodies such as dams, reservoirs and swamps (Chung 1976; Chung 1979; Chung et al. 1972a; Chung et al. 1972b; Kim 1997; Kim 2013a; Kim 2013b; Kim 2013c; Kim 2014a; Kim 2014b; Kim 2018; Kim et al. 1995; Kim et al. 2009; Kim et al. 2020; Kim and Chung 1993a; Kim and Chung 1993b; Kim and Kim 2017). Meanwhile, investigations have been done relatively on a smaller scale in lotic waterbodies (Cho et al. 1993; Choi et al. 2007; Chung et al. 1965; Chung et al. 1968; Chung et al. 1994; Chung et al. 2013; Jeong et al. 2010; Kim 2003; Kim 2004; Kim and Boo 1996; Kim and Lee 1991; Lee et al. 2002; Lee and Jung 2004; Park et al. 1995; Seo and Chung 1994).

Especially, phytoplankton investigations in the Nakdong River were performed primarily at downstream sections including estuary reservoirs before the weir construction (Cho et al. 1993; Choi et al. 2007; Chung et al. 1994; Kim 2004; Kim and Lee 1991; Seo and Chung 1994). Since the weirs were constructed, only changes in phytoplankton biomass and dominant species have been restrictively studied in phytoplankton investigations in the Nakdong River (Lee et al. 2018). Added to this, any investigation on the phytoplankton flora has not been done in the Nakdong River.

Meanwhile, the first report regarding the distribution of Euglenophytes across Korea was published in 1956 (Chung), and many floristic and taxonomic studies of Euglenophytes have been performed in different regions of Korea, most of which surveyed a regional flora including various habitats such as reservoirs, swamps, ditches and ponds (Conforti and Ruiz 2001; Conforti and Ruiz 2002; Chung 1975; Chung and Chang 1957; Chung and Kim 1992; Chung and Kim 1993; Kim 2013c; Kim and Boo 1996; Kim and Boo 1998; Kim et al. 1998; Kim et al. 2000a; Kim et al. 2000b; Wui and Kim 1987). Over 340 taxa of Euglenophytes are known currently in Korea (Kim 2018; Lee and Kim 2015), 30 of which have been found in the main stream section of the Nakdong River until now (Cho et al. 1993; Choi et al. 2007; Chung et al. 1994; Chung et al. 2000; Chung et al. 2013; Kim and Lee 1991; Seo and Chung 1994).

The aim of this study is to elucidate the characteristics of phytoplankton communities in the Nakdong River with the weirs built in it.

Study site

The Nakdong River is the second longest river in South Korea with a river length of about 510 km flows from north to south of Korean peninsula, and the Nakdong River estuary dam is located in the mouth of the river and eight weirs at middle-lower part were constructed in 1987 and 2012, respectively (Fig. 1). The total watershed area is 23,860 km2 and reside about 13 million person in the basin area. The Nakdong River water used as drinking and living water for approximately 10 million in meteropolitan cities Daegu, Busan and Changwon and many smaller cyties.

Figure 1. Map showing the sampling sites and eight weirs and estuary dam of the Nakdong River. SJ: SangJu; ND: Nakdan; GM: Gumi; CG: Chilgok; GG: Gangjeong-Goryeong; DS: Dalseong; HC: Hapcheon-Changnyeong; CH: Changnyeong-Haman.

Sample collection, identification and water quality parameters

Over 2,500 samples in 10 sites of four weirs–Gangjeong-Goryeong (GG), Dalseong (DS), Hapcheon-Changnyeong (HC), Changnyeong-Haman (CH) and estuary dam were collected from June 2017 to December 2020, at a week to month intervals, from the surface layer, middle and lower water depth using a plankton net (mesh size: 20 µm) and Vandorn sampler (Fig. 1). All living materials were immediately examined, and after an initial examination, materials were fixed with 5% formalin for permanent preservation and detail identification. Microscopic examinations were conducted at a magnification of 400 to 630× using a Zeiss microscope (Axio Imager. A2; Carl Zeiss Microscopy GmbH, Göttingen, Germany), and photomicrographs were taken with an AxioCam HRC camera (Carl Zeiss). Species identification was performed using relevant literatures (Ciugulea and Triemer 2010; Huber-Pestalozzi 1955; Tell and Conforti 1986; Wolowski and Hindak 2005). Water quality parameters used data of the ministry of environmental (National Institute of Environmental Research, NIER) (Table 1).

Table 1 . Physico-chemical and hydrological parameters of the sampling sites from Nakdong River during the surveyed periods.

Sampling sitespHEC (uS/cm)TN (mg/L)NH3-N (mg/L)NO3-N (mg/L)TP (mg/L)PO4-P (mg/L)HRT (day)
St. 18.4246.12.4740.0691.8240.0410.0136.7–16.3
St. 28.1369.23.3230.1082.5610.0460.013
St. 38.3319.33.0650.0862.3740.0430.0133.7–6.1
St. 48.1353.43.2160.0902.3970.0440.0143.9–5.9
St. 57.9308.32.8540.0782.1720.0400.015
St. 67.9288.32.2980.0571.6770.0360.0103.8–5.4
St. 77.8283.12.5760.0551.9400.0350.012
St. 88.0275.12.5710.0611.9060.0390.014
St. 98.0272.92.5140.0651.8770.0390.015
St. 108.0268.42.5210.0961.8360.0360.012

Each environment variable value is presented as the mean.

EC: electrical conductivity; TN: total nitrogen; TP: total phosphorus; PO4-P: phosphate phosphorus; NO3-N: nitrate nitrogen; NH3-N: ammonium nitrogen; HRT: hydraulic retention time.


Environmental characteristics

Water environmental factors in the surveyed region presented in Table 1. The mean nutrients concentration for total nitrogen (TN), nitrate nitrogen (NO3-N), ammonium nitrogen (NH3-N), total phosphorus (TP), and phosphate phosphorus (PO4-P) appeared mesotrophic to eutrophic level. Hydraulic retention time was between 3.7–16.3 days and 15 days (mean 10 days).

Euglenophytes flora in Nakdong River

We observed Euglenophytes of 103 taxa from the middle-downstream section of Nakdong River. The genus Trachelomonas was the most abundant group making up 40 taxa, and were observed 3 taxa of Colacium, Euglena (5), Lepocinclis (20), Menoideum (1), Monomorphina (3), Phacus (17) and Strombomonas (14) (Table 2). A total of 22 taxa; Colacium (1); Lepocinclis (8); Phacus (4); Strombomonas (4) and Trachelomonas (5) were new to Korea. All of the species were illustrated with light-photomicrographs and briefly described with regarded to their taxonomy of the 22 taxa new to Korea (Figs. 2-135).

Table 2 . List of Euglenophytes species found in the Nakdong River.

List of speciesPrevious studyThis studyList of speciesPrevious studyThis study
Astasia lagenula+Strombomonas acuminataa+
Colacium elongatumb+Strombomonas acuminata var. amphora+
Colacium simplexa+Strombomonas australicab+
Colacium vesiculosuma+Strombomonas borystehniensisb+
Euglena desesa+Strombomonas costata++
Euglena ehrenbergiia+Strombomonas fluviatilisa+
Euglena gaumei+Strombomonas gibberosaa+
Euglena gracilis+Strombomonas girardiana+
Euglena oblongaa+Strombomonas maximaa+
Euglena proxima++Strombomonas napiformis var. brevicolis++
Euglena viridis+Strombomonas schauinslandiia+
Euglena sp.+Strombomonas tetrapterab+
Eutreptiella gymnastica+Strombomonas triquetraa+
Lepocinclis acus++Strombomonas urceolataa+
Lepocinclis acus var. hyalinab+Strombomonas verrucosa+
Lepocinclis acus var. longissimab+Strombomonas verrucosa var. zmiewikab+
Lepocinclis constrictab+Strombomonas sp.+
Lepocinclis fusiformisa+Trachelomonas abruptaa+
Lepocinclis fusiformis var. amphyrinchusb+Trachelomonas alliaa+
Lepocinclis fusiformis var. majora+Trachelomonas armataa+
Lepocinclis globulus+Trachelomonas armata var. steiniia+
Lepocinclis gracilicaudaa+Trachelomonas australica var. rectangularisb+
Lepocinclis hungpanchiaoensisb+Trachelomonas bacilliferaa+
Lepocinclis marsoniia+Trachelomonas cerviculaa+
Lepocinclis ovum++Trachelomonas cordata var. minora+
Lepocinclis ovum var. conicaa+Trachelomonas cylindricaa+
Lepocinclis ovum var. dimidio-minora+Trachelomonas cylindrica var. decollata+
Lepocinclis ovum var. ovata+Trachelomonas dubiaa+
Lepocinclis oxyuris++Trachelomonas dybowskiia+
Lepocinclis playfairiana+Trachelomonas hexangulata var. repandaa+
Lepocinclis reeuwykiana var. kriegerib+Trachelomonas hispida++
Lepocinclis salina++Trachelomonas hispida var. coronataa+
Lepocinclis spirogyrab+Trachelomonas intermedia++
Lepocinclis spirogyroidesa+Trachelomonas klebsiia+
Lepocinclis wangiib+Trachelomonas lefevrei++
Menoidium pelluciduma+Trachelomonas lemmermanniib+
Monomophina nordstedtii++Trachelomonas mirabilis var. affinisa+
Monomorphina pyruma+Trachelomonas novab+
Monomorphina trypanona+Trachelomonas oblonga++
Phacus anomalusb+Trachelomonas oblonga var. australicaa+
Phacus caudatus+Trachelomonas pavlovskoensisa+
Phacus curvicauda++Trachelomonas pavlovskoensis f. ellipsoideaa+
Phacus cylindraeusb+Trachelomonas planctonica++
Phacus elegansa+Trachelomonas planctonica var. oblongaa+
Phacus glaberb+Trachelomonas playfairia+
Phacus helikoidesa+Trachelomonas pulcherimaa+
Phacus limnophilaa+Trachelomonas pulcherima var. minora+
Phacus lefevreia+Trachelomonas raciborskiia+
Phacus longicauda++Trachelomonas similisa+
Phacus longicauda var. insecta++Trachelomonas stokesianaa+
Phacus longicauda var. rotunda+Trachelomonas stokesiib+
Phacus orbicularisa+Trachelomonas sydneyensis var. minimaa+
Phacus raciborskiia+Trachelomonas variansa+
Phacus ranulusa+Trachelomonas varians var. globosaa+
Phacus smulkowskianuab+Trachelomonas verrucosa f. irregularisa+
Phacus suecicusa+Trachelomonas volvocina++
Phacus tortus++Trachelomonas woronichinianab+
Phacus undulatusa+

aIndicates new records for Nakdong River, bindicates new records for Korea.


Figs. 2-15. (2) Colacium elongatum, (3) C. simplex, (4) C. vesiculosum, (5) E. deses, (6) E. ehrenbergii, (7) E. oblonga, (8) E. proxima, (9) E. sp., (10) Lepocinclis constricta, (11) L. conica, (12) L. ovum, (13) L. ovum var. dimidio-minor, (14) L. globulus, (15) L. steinii. Scale bars = 10 μm.

Taxonomic descriptions

Colacium elongatum Playfair (Fig. 2)

Ciugulea and Triemer 2010, p. 5; Huber-Pestalozzi 1955, p. 127, pl. 23, Figure 111.

Cell elongate cylindrical, attached by mucilaginous stalk, group into colonies; chloroplast numerous, disc shaped, with a pyrenoid, periplast fine striated. Cell length 15−30 µm, breadth 8−12 µm.

Lepocinclis acus var. hyalina (Klebs) D.A. Kapustin (Fig. 17)

Ciugulea and Triemer 2010. p. 67.

Figs. 16-29. (16) Lepocinclis acus, (17) L. acus var. hyalina, (18–20) L. acus var. longissima, (21) L. tripteris, (22) Phacus limnophila, (23) Menoideum pellucidum, (24) Lepocinclis caudata, (25) L. gracilicauda, (26) L. fusiformis, (27) L. fusiformis var. amphirhynchus, (28) L. fusiformis var. major, (29) L. hungpanchiaoensis. Scale bars = 10 μm.

Cell narrow, long cylindrical, colorless, rod-like paramylon. Anterior with contractile vacuole. Pellicle strips very fine. Cell length 120−140 µm, breadth 12−13 µm.

Lepocinclis acus var. longissima (Deflandre) D.A. Kapustin (Figs. 18-20)

Wolowski and Hindak 2005, Figures 9, 10.

Cell narrow, long cylindrical, rod-like paramylon. Anterior with eyespot and contractile vacuole. Longitudinal pellicle strips fine. Cell length 260−280 µm, breadth 10−12 µm.

Lepocinclis constricta Matvienko (Fig. 10)

Syn.: Euglena gymnodiniodes Zakrys

Wolowski and Hindak 2005, Figures 66, 67.

Figs. 66-77. (66) Phacus orbicularis, (67) P. platalea, (68) P. triqueter, (69) P. undulatus, (70) P. hamatus, (71) P. pleuronectes, (72) Strombomonas acuminata, (73–76) S. borystheniensis, (77) S. scauinslandii. Scale bars = 10 μm.

Cells gourd-shaped, broad fusiform to longitudinal hexagonal shaped constricted in the middle part of lateral sides; anterior end narrowly projected and truncate; posterior end broadly rounded, with a thin, long straight cauda; periplasts spirally striated; paramylon bodies numerous, globose to ovoid. Cell length 28−31 µm, breadth 14−16 µm, caudal length 8−9 µm.

Lepocinclis fusiformis var. amphyrinchus Nygaard (Fig. 27)

Yamagishi and Akiyama 1998, 20: 42.

Cells broad fusiformis, anterior end conically narrowed and projected into truncately rounded, apex shallowly bilobed; posterior ends conically produced into a short caudal process; lateral sides roundly swelled; periplasts spirally striated; paramylon two, large ring-like plate; chloroplast disc shaped. Cell length 34−38 µm, breadth 21−24 µm.

Lepocinclis hungpanchiaoensis Chu (Fig. 29)

Yamagishi and Akiyama 1995, 14: 32.

Cells broad ovoid, anterior end conically narrowed, shallow prominentally bilobed at one side just below the end; posterior ends gradually narrowed, with a short pointed cauda; lateral sides roundly swelled; periplasts spirally striated; paramylon two, ring-like plate. Cell length 44−47 µm, breadth 21−23 µm. This species only has been known from the east-north Asia (Japan and China).

Lepocinclis reeuwykiana var. kriegeri Conrad (Fig. 36)

Huber-Pestalozzi 1955, p. 147. pl. 28. Figure 140; Yamagishi and Akiyama 1995, 14: 33.

Figs. 30-38. (30, 31) Lepocinclis oxyuris, (32) L. spirogyroides, (33, 34) L. salina, (35) L. marssonii, (36) L. reeuwykiana var. kriegeri, (37) L. spirogyra, (38) L. wangii. Scale bars = 10 μm.

Cells long fusiform; anterior end narrowly produced and truncate, slightly depressed; posterior end gradually narrowed and projected into a long, straight cauda; periplasts spirally striated; paramylon bodies two, ring-like plate. Cell length 54−60 µm, breadth 11−13 µm.

Lepocinclis spirogyra Korschikov (Fig. 37)

Yamagishi and Akiyama 1989, 10: 49, Wolowski and Hindak 2005, Figures 259, 260.

Figs. 39-44. (39) Phacus elegans, (40, 41) P. longicauda, (42) P. helicoides, (43) P. ranula, (44) P. tortus. Scale bars = 10 μm.

Cells fusiform; anterior end slightly narrowed, rounded; posterior end projected into a straight, long cauda; periplasts left-handed striated by rows of small verruca; chloroplasts plate-shaped; paramylon bodies two, ring-like plate. Cell length 45−54 µm, breadth 20−23 µm, cauda 6-10 µm.

Lepocinclis wangii Chu (Fig. 38)

Yamagishi and Akiyama 1989, 10: 53.

Cells broad fusiform; anterior end conically narrowed, rounded, shallow prominently bilobed at just below the end, and one side produced into a beak-like process; posterior ends gradually narrowed in to a long, straight cauda; periplasts spirally striated; paramylon two, ring-like plate. Cell length 50−53 µm, breadth 25−30 µm, cauda 12−13 µm. This species only has been known from the east-north Asia (Japan and China).

Phacus anomalus F.E. Fritsch & M.F. Rich (Figs. 47, 48)

Huber-Pestalozzi 1955, p. 204. Figure 260; Yamagishi and Akiyama 1995, 14: 39.

Figs. 45-65. (45, 46) Phacus acuminatus, (47, 48) P. anomalus, (49) P. curvicauda, (50, 51) P. smulkowskianus, (52) P. inflexus, (53) P. cylindraceus, (54, 55) P. suecicus, (56) P. horridus, (57, 58) P. raciborskii, (59) P. glaber, (60) Monomorphina nordstedtii, (61–63) M. pyrum, (64, 65) M. trypanon. Scale bars = 10 μm.

Cells asymmetric ovoid to broad ellipsoid, with two distinct dissimilar halves-the one half large, thick, the other slightly smaller, thinner and slightly twisted; one face with a broad deep furrow, the other with a shallow one extending entirely, in vertical view asymmetric; anterior ends narrowed, asymmetrically rounded; posterior end broadly, truncately rounded, with a short, oblique cauda; lateral sides slightly swelled; periplasts longitudinally striated; paramylon bodies two, circular plate. Cell length 25−30 µm, breadth 20−22 µm.

Phacus cylindraceus T.G. Popova (Fig. 53)

Popova 1955, p. 213, pl. 86, Figure 11; Yamagishi and Akiyama 1995, 14: 42.

Cells small, long cylindrical to fusiform; anterior ends slightly narrowed, obliquely truncate, shallowly bilobed and one side projected; posterior end gradually narrowed into a obtuse projection; lateral sides nearly straight and parallel or slightly swelled at midregion; periplasts obliquely striated; paramylon bodies two, lod-like, one large and the other small. Cell length 22−25 µm, breadth 6−8 µm.

Phacus glaber (Deflandre) Pochmann (Fig. 59)

Huber-Pestalozzi 1955, p. 238, pl. 55, Figure 340; Ciugulea and Triemer 2010, p. 97, Figures A–C.

Cells broad ovoid to elliptic; anterior ends truncately rounded, slightly concave at center, with a median papilla; posterior end broadly rounded, with a straight or slightly curved cauda; periplasts longitudinally striated, without any granules or spines; paramylon bodies two, large, parietal disc-like plate. Cell length 45−50 µm, breadth 22−24 µm.

Phacus smulkowskianus (Zakrys) W.-H.Kusber (Figs. 50, 51)

Ciugulea and Triemer 2010, p. 121, Figures A–D.

Cells fusiform to long-ovoid, spirally twisted throughout their entire length, 1.5–2 turns; anterior end narrowed and truncate, with a central small papilla; posterior end tapering into a twisted, straight cauda; lateral margins undulated in side view; periplasts spirally striated; paramylon bodies two, circular or ovoidal plate, one large and the other small. Cell length 30−40 µm, breadth 15−18 µm.

Strombomonas australica (Playfair) Deflandre (Fig. 86)

Huber-Pestalozzi 1955, p. 391, pl. 81, Figure 851A.

Figs. 78-89. (78) Strombomonas urceolata, (79) S. verrucosa var. zmiewika, (80) S. napiformia var. brevicolis, (81) S. ovalis, (82, 83) S. triquetra, (84, 85) S. tetraptera, (86) S. australica, (87) S. gibberosa, (88) S. costata, (89) S. maxima. Scale bars = 10 μm.

Lorica long, slender fusiform; anterior ends gradually narrowed, with a long, cylindrical collar, collar mouth irregularly serrated; posterior ends gradually narrowed into a long, straight, conical cauda; wall rough, with irregularly scattered small granules. Lorica length 58−60 µm, breadth 18−20 µm, collar length 11 µm, diameter 6 µm, cauda length 12 µm.

Strombomonas borystehniensis (Roll) Popova (Figs. 73−76)

Syn.: Strombomonas verrucosa var. borystehniensis (Roll) Deflandre

Huber-Pestalozzi 1955, p. 371, pl. 77, Figure 793; Yamagishi and Akiyama 1994, 13: 75; Ciugulea and Triemer 2010. p. 128.

Lorica longer than broad, ellipsoid to ovoid; anterior ends with short collar, posterior ends rounded or slightly narrowed, with very short tail; periplast with many irregular granules; chloroplast numerous discoid. Lorica length 23−32 µm, breadth 18−23 µm.

Strombomonas tetraptera Balech & Dastugue (Figs. 84, 85)

Huber-Pestalozzi 1955, p. 391, pl. 81, Figure 851A.

Lorica twisted, fusiform to cylindrical in lateral view; quadrangular with concaved sides and rounded angular in vertical view; anterior ends slightly narrowed, with short and broad collar, mouth slightly irregular and oblique; posterior ends conically tapered into a short cauda; lateral sides longitudinally swelled or nearly straight and undulated for twisting of the periplast; wall rough, with irregularly scattered verrucae. Lorica length 37−40 µm, breadth 23−26 µm.

Strombomonas verrucosa var. zmiewika (Svirenko) Deflandre (Fig. 79)

Huber-Pestalozzi 1955, p. 370, pl. 77, Figure 791.

Lorica broad ellipsoid to ovoid; anterior end gradually narrowed into a short, broad, cylindric collar; posterior end abruptly narrowed, with a long straight, conical cauda; wall irregularly verrucose. Lorica length 40-45 µm, breadth 20−21 µm, neck length 4−5 µm, diameter 5 µm.

Trachelomonas australica var. rectangularis Deflandre (Figs. 112, 113)

Huber-Pestalozzi 1955, p. 304, pl. 65, Figure 561.

Figs. 90-116. (90) Trachelomonas oblonga, (91) T. oblonga var. australica, (92) T. cordata var. minor, (93) T. verrucosa f. irregularis, (94) T. stokesiana, (95) T. stokesii, (96) T. volvocina, (97, 98) T. woronichiniana, (99) T. acanthostoma var. minor, (100) T. intermedia, (101) T. cylindrica, (102) T. cylindrica var. decollata, (103) T. abrupta, (104) T. klebsii, (105, 106) T. nova, (107) T. cervicula, (108) T. varians, (109) T. varians f. globosa, (110, 111) T. lefevrei, (112, 113) T. australica var. rectangularis, (114) T. hispida, (115) T. hispida var. coronata, (116) T. mirabilis var. affinis. Scale bars = 10 μm.

Lorica broad cylindrical; anterior and posterior ends angularly rounded; lateral sides straight and parallel; flagella apertures without collar, but surrounded by a circle of spines; wall covered with short and sharp minute spines. Lorica length 29−31 µm, breadth 18−20 µm.

Trachelomonas lemmermannii Wolozynska (Figs. 132, 133)

Huber-Pestalozzi 1955, p. 321, pl. 69, Figure 637.

Figs. 117-135. (117) Trachelomonas armata, (118) T. armata var. steinii, (119) T. hexangulata var. repanda, (120) T. pavlovskoensis var. ellipsoidea, (121) T. pavlovskoensis, (122) T. allia, (123) T. raciborskii, (124) T. sydneyensis var. minima, (125) T. bacillifera var. minima, (126) T. planktonica, (127) T. planktonica var. oblonga, (128) T. playfairi, (129) T. similis, (130) T. dybowskii, (131) T. dubia, (132, 133) T. lemmermannii, (134) T. pulcherima, (135) T. pulcherima var. minor. Scale bars = 10 μm.

Lorica cylindrical; anterior ends truncately rounded; flagellum apertures without a collar; posterior ends narrowed into a short, broad conical apex; lateral sides straight and parallel; wall covered with many puncta. Lorica length 26−28 µm, breadth 12−13 µm.

Trachelomonas nova Drezepolski (Figs. 105, 106)

Huber-Pestalozzi 1955, p. 314, pl. 68, Figure 604.

Lorica obovoid; anterior ends slightly narrowed, rounded; posterior ends slightly, conically narrowed; flagellum apertures without a collar, but surrounded by a circle of spines; wall covered with short spines. Lorica length 23−25 µm, breadth 19−20 µm.

Trachelomonas stokesii Drezepolski (Fig. 95)

Huber-Pestalozzi 1955, p. 282, pl. 61, Figure 476.

Lorica obovoid; anterior ends rounded; posterior ends slightly narrowed and rounded; flagellum apertures without a collar; wall finely punctate. Lorica length 14−15 µm, breadth 12−13 µm.

The present study found that phytoplankton communities of the Nakdong River showed a high species diversity (total 769 taxa, unpublished), investigating a total of 103 taxa of Euglenophytes at the middle-lower part of the Nakdong River. The genus Trachelomonas was the most abundant group making up 40 taxa, followed Lepocinclis (20), Phacus (17), Strombomonas (14), Euglena (5), Colacium (3), Monomorphina (3) and Menoideum (1). Among them, a total of 22 taxa including Colacium (1), Lepocinclis (8), Phacus (4), Strombomonas (4) and Trachelomonas (5) were reported for the first time in Korea, and 86 taxa including those new to Korea were first recorded in the Nakdong River. Meanwhile, 12 taxa including Astasia lagenula, Phacus caudatus, Strombomonas girardiana recorded in the previous studies were not observed in this research. Most of the euglenoids species observed in the Nakdong River are known to prefer to small and organically polluted eutrophic environments (Munawar 1972; Padisak et al. 2009; Reynolds et al. 2002; Tell and Conforti 1986; Wolowski and Walne 2007). The highest species diversity of Euglenophytes was observed during summer, especially in July where water temperatures remain high after heavy rain. It is assumed that the species were introduced from small swamps formed on the riverside by heavy rain during summer.

Many floristic and taxonomic studies on euglenophytes have been done across various regions in lentic waterbodies such as swamps, reservoirs and ponds in South Korea (Chung 1975; Chung and Chang 1957; Chung and Kim 1992; Chung and Kim 1993; Conforti and Ruiz 2001; Conforti and Ruiz 2002; Kim 2013c; Kim and Boo 1998; Kim et al. 1998; Kim et al. 2000a; Kim et al. 2000b; Wui and Kim 1987). Over 340 taxa of Euglenophytes have been recorded in Korea (Lee and Kim 2015; Kim 2018). Thirty taxa of Euglenophytes have been found in the main stream section of the Nakdong River (Cho et al. 1993; Choi et al. 2007; Chung et al. 1994; Chung et al. 2000; Chung et al. 2013; Kim and Lee 1991; Seo and Chung 1994).

Also, a great deal of studies have been done on phytoplankton communities in lotic environments of the four major rivers including the Han River and the Nakdong River (Cho et al. 1993; Choi et al. 2007; Chung et al. 1965; Chung et al. 1968; Chung et al. 1994; Chung et al. 2000; Chung et al. 2013; Jeong et al. 2010; Jung et al. 2003; Kim 2003; Kim 2004; Kim and Boo 1996; Kim and Lee 1991; Lee and Chang 1997; Lee and Jung 2004; Lee et al. 2002; Seo and Chung 1994; Son 2013). The total number of phytoplankton species in these lotic river ecosystems varies significantly from 72 taxa to 466 taxa depending on researchers. Also, the species richness of euglenophytes showed a significant difference from 0 to 36 taxa according to researchers (Table 3). It is estimated that the great differences in phytoplankton composition in similar habitats come mainly from different volumes of literature materials, depth of taxonomic knowledge among researchers, research periods and sampling times rather than from differences in practical phytoplankton communities.

Table 3 . Composition of the Euglenophytes of the Nakdong River and another lentic and lotic waters for different periods in South Korea.

ReferencesSiteSampling periodEug. Sp. NumberComposition ratio (%)Tot. Sp. Number
This studyNR2018–202010313.4769 (include Diatoms)
Kim and Lee (1991)NR1988–198942197 (include Diatoms)
Cho et al. (1993)NR1991–199231.3227 (include Diatoms)
Chung et al. (1994)NR19932411.9201 (exclude Diatoms)
Seo and Chung (1994)NR1992–19939186 (include Diatoms)
Kim (2004)NR1995–199636 (no list)7.9456 (include Diatoms)
Lee et al. (2002)NR2000–2001Unknown(include as others)239 (include Diatoms)
Chung et al. (2013)NR1983–2004303.7817 (include Diatoms)
Son (2013)NR2012Unknown(include as others)72 (include Diatoms)
Park et al. (1995)KHR1990–19913115.3203 (exclude Diatoms)
Lee and Chang (1997)HR1995–199632.1145 (include Diatoms)
Jung et al. (2003)HR2001–2002103.7267 (include Diatoms)
Lee and Jung (2004)HR1945–2004123.7332 (include Diatoms)
Kim and Boo (1996)KR1994–199637Only Euglenoid
Jeong et al. (2010)YR2004–2005Unknown(include as others)265 (include Diatoms)
Kim (2003)YR1995–199663 (no list)13.5466 (include Diatoms)
Kim and Chung (1993b)Tchokjibul S.1990–19918027.4292 (exclude Diatoms)
Sajipo S.1990–19919731.2311 (exclude Diatoms)
Kim (2001)Woopo S.19986418.1353 (include Diatoms)
Conforti and Ruiz (2001), Conforti and Ruiz (2002)Chunam R.199196Only Euglenoid
Kim (2018)Cheonjin L20174913.1376 (exclude Diatoms)

NR: Nakdong River; HR: Han River; KR: Kum River; YR: Youngsan River; KHR: Kumho River; S.: Swamp; R.: Reserver; L.: Lake; Eug. Sp.: Euglenophytes Spcies; Tot. Sp.: Total species.



The phytoplankton communities of the Nakdong River after the weir construction significantly changed compared to before they were built. In particular, the total number of all species including Euglenophytes as well as the total amount of biomass saw a remarkable increase. The Euglenophytes community at the middle-lower part of the Nakdong River is similar to that in lentic waterbodies such as shallow eutrophic reservoirs and swamps given the high species diversity and composition ratio (Conforti and Ruiz 2001; Conforti and Ruiz 2002; Kim 2001; Kim and Chung 1993a; Kim and Chung 1993b) (Table 3). The results suggest that water environments in the middle-lower section of the Nakdong River is changing to resemble lentic ecosystems such as swamps and reservoirs given the increasing retention time and nutrient concentration following the construction of the weirs.

The present study, a total of 103 taxa of Euglenophytes were found from middle-lower part of the Nakdong River. The genus Trachelomonas was the most abundant group making up 40 taxa, followed Lepocinclis (20), Phacus (17), Strombomonas (14), Euglena (5), Colacium (3), Monomorphina (3) and Menoideum (1). Among them, a total of 22 taxa including Colacium (1), Lepocinclis (8), Phacus (4), Strombomonas (4) and Trachelomonas (5) were reported for the first time in Korea, and 86 taxa including those new to Korea were first recorded in the Nakdong River.

Syn.: Synonym

Var.: Variety

Fiig.: Fiigure

EC: Electrical conductivity

TN: Total nitrogen

TP: Total phosphorus

PO4-P: Phosphate phosphorus

NO3-N: Nitrate nitrogen

NH3-N: Ammonium nitrogen

HRT: Hydraulic retention time

HSK designed this study and wrote the manuscript. HSK and JHL participated in field works and reviewed/edited the manuscript. All authors read and approved the final manuscript.

  1. Cha SM, Kang MJ, Park Y, Lee SW, Kim JH. Water quality changes according to the midstream weir construction in the Yeongsan River, Korea. Desalin Water Treat. 2015;53(11):3066-71. https://doi.org/10.1080/19443994.2014.922735.
    CrossRef
  2. Cho KJ, Chung IK, Lee JA. Season dynamicsof phytoplankton community in the Naktong River estuary, Korea. Korean J Phycol. 1993;8(1):15-28.
  3. Choi CM, Kim JH, Kim WI, Lee JS, Chung GB, Lee JT, et al. Phytoplankton flora and community structure in the lower Nakdong River. Korean J Environ Agric. 2007;26(2):159-70. https://doi.org/10.5338/KJEA.2007.26.2.159.
    CrossRef
  4. Chung IK, Kang YJ, Kwon OS, Seo JK. The ecology of phytoplankton in the Naktong estuary. Algae. 2000;15(2):99-110.
  5. Chung IK, Kim NL, Song EH, Lee JE, Lee SR. Literature survey on the phytoplankton flora in the Nakdong River estuary, Korea. Korean J Fish Aquat Sci. 2013;46(4):467-87. https://doi.org/10.5657/KFAS.2013.0467.
    CrossRef
  6. Chung J, Kim HS, Kim YJ. Sturcture of phytoplankton community in the Nakdong River Estuary Dam. Korean J Limnol. 1994;27(1):33-46.
  7. Chung J, Kim HS. Fresh-water algae new to Korea (II). Korean J Phycol. 1992;7(2):173-83.
  8. Chung J, Kim HS. Fresh-water algae new to Korea (III). Korean J Phycol. 1993;8(1):37-46.
  9. Chung J, Kim SD, Lee KS. Fresh-water algae from Jae Ju Do island (I). Korean J Limnol. 1972a;5(1):13-23.
  10. Chung J, Kim SD, Lee KS. Fresh-water algae from Jae Ju Do island (II). Korean J Limnol. 1972b;5(3):15-31.
  11. Chung J. A study on the Cyanophyceae from Chun Ra Book Do area. Korean J Bot. 1976;19(1):19-30.
  12. Chung J. A study on the Euglenophyceae from Chon La Book Do area. Res Rev Kyungpook Natl Univ. 1975;20:233-42.
  13. Chung J. A study on the fresh-water algae from Chungchong Book Do area. Korean J Limnol. 1979;12(1-2):41-53.
  14. Chung YH, Chang YK. A study on the Euglena in the area of Seoul (II). Univ Seoul Coll Thes Sci Nat. 1957;5:119-28.
  15. Chung YH, Kay ES, Park DW. A study on the microflora of the Han River(II): the phytoplanktons and its seasonal variaton in the area of the Chun-chon and the Chung-pyong reservoir of the Han River. Korean J Bot. 1968;11(2):1-30.
  16. Chung YH, Shim JH, Lee MJ. A study on the microflora of the Han River I. The phytoplanktons and the effect of the marine water in the lower course of the Han River. Korean J Bot. 1965;8(4):7-29.
  17. Chung YH. A study on the Euglena in the area of Seoul. Univ Seoul Coll Thes Sci Nat. 1956;3:49-55.
  18. Ciugulea I, Triemer RE. A color atlas of photosynthetic euglenoids. East Lansing: Michigan State University Press; 2010. 196 p.
  19. Conforti V, Ruiz L. Euglenophytes from Chunam reservoir (South Korea) II Trachelomonas EHR. Algol Stud. 2001;102:117-45. https://doi.org/10.1127/algol_stud/104/2002/81.
    CrossRef
  20. Conforti V, Ruiz L. Euglenophytes from Chunam reservoir (South Korea) I Euglena EHR., Lepocinclis PERTY and Phacus DUJ. Algol Stud. 2002;104:81-96.
    CrossRef
  21. Huber-Pestalozzi G. [Euglenophyceen]. Stuttgart: Schweizerbart; 1955. German.
    CrossRef
  22. Jeong EJ, Na JE, Kim GM, Shim SS, Lee HY. Water temperature and community of phytoplankton in Youngsan River, Korea. Korean J Environ Biol. 2010;28(2):56-63.
  23. Jung SW, Lee JH, Yoo JS. Environmental studies of the lower part of the Han River V. Blooming characteristics of phytoplankton communities. Algae. 2003;18(4):255-62. https://doi.org/10.4490/ALGAE.2003.18.4.255.
    CrossRef
  24. Kim HS, Chung J. Ecological study of phytoplankton on some reservoir (Changnyong county). Korean J Limnol. 1993a;26(3):203-21.
  25. Kim HS, Chung J. Freshwater algal flora of natural swamps in Changnyong county. Korean J Limnol. 1993b;26(4):305-19.
  26. Kim HS, Lee JH, Kim JH. A checklist of freshwater algae from Mt. Sinbul alpine wetlands in South Korea. Nova Hedwig. 2020;111(1-2):1-38. https://doi.org/10.1127/nova_hedwigia/2020/0584.
    CrossRef
  27. Kim HS, Takahashi E, Chung J. Morphologic and taxonomic studies on scale-bearing Chrysophyta from Naktong River estuary lake, Pusan, in Korea. Korean J Limnol. 1995;28(1):87-99.
  28. Kim HS. Anabaena koreana sp. nov. (Cyanophyceae), a new species, and new record of fresh-water blue-green algae from Korea. J Ecol Environ. 2013;36(4):293-302.
    CrossRef
  29. Kim HS. Desmids from Korea; 1. Desmidiaceae 1 (Micrasterias). J Ecol Environ. 2014a;37(4):285-98. https://doi.org/10.5141/ecoenv.2014.
    CrossRef
  30. Kim HS. Diversity of phytoplankton species in Cheonjin Lake, northeastern South Korea. J Ecol Environ. 2018;42(4):29. https://doi.org/10.1186/s41610-018-0080-5.
    CrossRef
  31. Kim HS. New record of fresh-water green algae (Chlorophytes) from Korea. J Ecol Environ. 2013;36(4):303-14. https://doi.org/10.5141/ecoenv.2013.303.
    CrossRef
  32. Kim HS. New records of Euglenophyta from Korea. J Ecol Environ. 2013c;36(4):339-46. https://doi.org/10.5141/ecoenv.2013.339.
    CrossRef
  33. Kim HS. Records of desmids (Chlorophyta) newly found in Korea. J Ecol Environ. 2014b;37(4):299-313. https://doi.org/10.5141/ecoenv.2014.
    CrossRef
  34. Kim HS. Seasonal changes of phytoplankton community in the Woopo and Mokpo swamp. Korean J Limnol. 2001;34(2):90-7.
  35. Kim HS. Silica-scaled chrysophytes (Synurophyceae) in several reservoirs, swamps and a highland pond from Changnyong county, Korea. Algae. 1997;12(1):1-10.
  36. Kim JH, Kim HS. New records of freshwater algae from Korea. J Species Res. 2017;6(3):224-31. https://doi.org/10.12651/JSR.2017.6.3.224.
    CrossRef
  37. Kim JH, Park YJ, Kim HS. Silica-scaled chrysophytes (Synurophyceae) from Jeju Island, Korea. Nova Hedwig. 2009;89(1-2):201-18. https://doi.org/10.1127/0029-5035/2009/0089-0201.
    CrossRef
  38. Kim JT, Boo SM, Coute A. Taxonomic and floristic accounts of the genus Trachelomonas Ehrenberg 1833 (Euglenophyceae) from Korea. Korean J Limnol. 2000b;33(2):80-108.
  39. Kim JT, Boo SM, Zakrys B. Contribution to the knowledge of the genus Phacus Dujardin 1841 (Euglenophyceae) in Korea. Nova Hedwig. 2000a;71(1-2):37-67. https://doi.org/10.1127/nova/71/2000/37.
    CrossRef
  40. Kim JT, Boo SM, Zakrys B. Floristic and taxonomic accounts of the genus Euglena (Euglenophyceae) from Korean fresh waters. Algae. 1998;13(2):173-97.
    CrossRef
  41. Kim JT, Boo SM. Floristic and taxonomic accounts of the genus strombomonas (Euglenophyceae) from Korean fresh waters. Algae. 1998;13(3):275-82.
  42. Kim JT, Boo SM. Seasonal changes of the euglenoid species and the biomass in the Kumgang River. Algae. 1996;11(4):375-9.
  43. Kim JW, Lee HY. A study on phytoplankton communities in the reservoir of Nakdong River estuary. Korean J Limnol. 1991;24(3):143-51.
  44. Kim YJ. Dynamics of phytoplankton community in Youngsan River. Algae. 2003;18(3):207-15. https://doi.org/10.4490/ALGAE.2003.18.3.
    CrossRef
  45. Kim YJ. Monthly variations of phytoplankton communities in the mid and lower parts of the Nakdong River. Algae. 2004;19(4):329-37. https://doi.org/10.4490/ALGAE.2004.19.4.329.
    CrossRef
  46. Lee HJ, Park HK, Cheon SU. Effects of weir construction on phytoplankton assemblages and water quality in a large river system. Int J Environ Res Public Health. 2018;15(11):2348. https://doi.org/10.3390/ijerph15112348.
    Pubmed KoreaMed CrossRef
  47. Lee JB, Kim HS. National list of species of Korea. Flagellates. Incheon: National Institute of Biological Resources; 2015. p. 194.
  48. Lee JH, Chang M. Environmental studies of the lower of Han River II. Phytoplankton dynamics. Korean J Limnol. 1997;30(3):193-202.
  49. Lee JH, Jung SW. Environmental studies in the lower part of the Han River -VII. Long term variations and prospect of the phytoplankton community. Algae. 2004;19(4):321-7. https://doi.org/10.4490/ALGAE.2004.19.4.321.
    CrossRef
  50. Lee JH, Kwon JN, Yang SY. Seasonal variation of phytoplankton community in the Naktong River. Algae. 2002;17(4):267-73. https://doi.org/10.4490/ALGAE.2002.17.4.267.
    CrossRef
  51. Lee KL, Choi JS, Lee JH, Jung KY, Kim HS. Response of epilithic diatom assemblages to weir construction on the Nakdong River, Republic of Korea. Ecol Indic. 2021;126:107711. https://doi.org/10.1016/j.ecolind.2021.107711.
    CrossRef
  52. Munawar M. Ecological studies of Euglenineae in certain polluted and unpolluted environments. Hydrobiologia. 1972;39(3):307-20. https://doi.org/10.1007/BF00046647.
    CrossRef
  53. Padisak J, Crossetti LO, Naselli-Flores L. Use and misuse in the application of the phytoplankton functional classification: a critical review with updates. Hydrobiologia. 2009;621:1-19. https://doi.org/10.1007/s10750-008-9645-0.
    CrossRef
  54. Park CW, Kim YJ, Chung J. Structure of phytoplankton community in the Kumho River. Korean J Limnol. 1995;28(1):49-60.
  55. Park HK, Lee HJ, Heo J, Yun JH, Kim YJ, Kim HM, et al. Deciphering the key factors determining spatio-temporal heterogeneity of cyanobacterial bloom dynamics in the Nakdong River with consecutive large weirs. Sci Total Environ. 2021;755(Pt 2):143079. https://doi.org/10.1016/j.scitotenv.2020.143079.
    Pubmed CrossRef
  56. Popova TG. [Manual for identification of the freshwater algae of the USSR. Euglenids]. Moscow: Sovetskaya Nauka; 1955. 119 Fiigures; p. 282. Russian.
  57. Reynolds CS, Huszar V, Kruk C, Flores LN, Melo S. Towards a functional classification of the freshwater phytoplankton. J Plankton Res. 2002;24(5):417-28. https://doi.org/10.1093/plankt/24.5.417.
    CrossRef
  58. Seo JK, Chung IK. The phytoplankton community structure in the Nakdong River mouth. Korean J Limnol. 1994;27(3):227-50.
  59. Skvortzow BW. Fresh-water diatoms from Korea, Japan. Manila: Bureau of Printing; 1929.
  60. Son HJ. The analysis of phytoplankton community structure in the middle-lower part of the Nakdong River. J Korean Soc Environ Eng. 2013;35(6):430-5. https://doi.org/10.4491/KSEE.2013.35.6.430.
    CrossRef
  61. Tell G, Conforti V. [Euglenophyta pigmentadas de la Argentina]. Berlin: J. Cramer. p. 301. Spanish.
    CrossRef
  62. Wolowski K, Walne PL. Strombomonas and Trachelomonas species (Euglenophyta) from south-eastern USA. Eur J Phycol. 2007;42(4):409-31. https://doi.org/10.1080/09670260701702508.
    CrossRef
  63. Wotowski K, Hindak F. Atlas of Euglenophytes. Cracow: VEDA; 2005. 136 pp.
  64. Wui IS, Kim BH. The flora of the fresh-water algae in Chol-La Nam-Do, Korea (I) Euglenophyceae. Korean J Phycol. 1987;2(1):119-27.
  65. Yamagishi T, Akiyama M. Photomicrographs of the fresh-water algae. Tokyo: Uchida Rokakuho; 1989.
  66. Yamagishi T, Akiyama M. Photomicrographs of the fresh-water algae. Tokyo: Uchida Rokakuho; 1994.
  67. Yamagishi T, Akiyama M. Photomicrographs of the fresh-water algae. Tokyo: Uchida Rokakuho; 1995.
  68. Yamagishi T, Akiyama M. Photomicrographs of the fresh-water algae. Tokyo: Uchida Rokakuho; 1997.
  69. Yamagishi T, Akiyama M. Photomicrographs of the fresh-water algae. Tokyo: Uchida Rokakuho; 1998.
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