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Article

An Annotated Checklist of Algae from the Order Synurales (Chrysophyceae) of Viet Nam

1
A.N. Severtsov Institute of Ecology and Evolution, Russian Academy of Sciences, 33 Leninsky Prospect, 119071 Moscow, Russia
2
K.A. Timiryazev Institute of Plant Physiology, Russian Academy of Sciences, 35 Botanical Street, 127276 Moscow, Russia
3
Coastal Branch of Joint Vietnam-Russia Tropical Science and Technology Research Center, 30 Nguyen Thien Thuat, Nha Trang 650000, Vietnam
*
Author to whom correspondence should be addressed.
Diversity 2023, 15(2), 183; https://doi.org/10.3390/d15020183
Submission received: 12 December 2022 / Revised: 17 January 2023 / Accepted: 19 January 2023 / Published: 28 January 2023
(This article belongs to the Special Issue Algae Biodiversity: Natural and Anthropogenic Impacts)

Abstract

:
This paper presents an annotated list of the Mallomonas and Synura taxa (order Synurales, class Chrysophyceae) found in Viet Nam. This list is based on materials from long-term studies (from 2008 to 2020) of 371 freshwater localities in 18 provinces in the country. A total of 67 taxa (morphotypes) of the genus Mallomonas and 7 of the genus Synura were reported. For each species, the range of abiotic environmental parameters under which they were found is given, as well as comments on the distribution of these taxa within Viet Nam and the tropical region.

1. Introduction

The algae of the order Synurales (Chrysophyceae) are unicellular or colonial organisms. They are distinguished from the other members of Chrysophyceae by their flagellar apparatus, cholorophyll-c composition, and the presence of bilaterally symmetrical silica scales that form an armor around the cell [1]. According to the latest review, the order includes three genera: Mallomonas Perty, Synura Ehrenberg, and Neotessella Jo, Kim, Shin, Škaloud & Siver [2]. The genera Mallomonas and Synura are among the most diverse in the number of species from this order and the whole Chrysophyceae class. The genus Mallomonas includes more than 200 species [1,3], and Synura includes more than 50 [4]. The species concept for this group is based on the morphology of scales and bristles, studied by transmission or scanning electron microscopy (TEM or SEM), and is considered one of the best among the protists [5]. Molecular data, in general, justify the scale and bristle morphology to provide reliable characteristics for species delimitation [4,6,7,8,9,10].
Studies of silica-scaled chrysophytes in the tropical region using electron microscopy began in the late 1970s [11]. To date, there is information about the flora of the synuralean algae of Bangladesh [11], Malaysia [12,13], Singapore [13], Sri Lanka [14], tropical China [15,16] and Australia [12], India [17,18], Nigeria [19,20], Papua New Guinea [21], Indonesia [22,23,24], Madagascar [25], Kenya [26], Republic of Chad [27], Zimbabwe [28], Cameroon [29,30], South Africa [31,32,33], Costa Rica [34], Jamaica [28], Ecuador [35], Guatemala [28], Panama [36], Belize [37], Colombia [28,38], and Brazil [28,39,40,41,42]. However, this region is still poorly studied and requires further research [1].
We have carried out long-term studies of the flora of Viet Nam, which made it possible to find and describe a large number of species of algae from the order Synurales. The studies covered various geographical parts of the country, such as Northern Viet Nam [43], mountainous and coastal regions of Central Viet Nam [44,45,46,47,48], Southern Viet Nam [49,50,51], and the flora of some islands [52]. Taking into account the number of studied habitats and the number of published works, it became necessary to generalize data on the distribution of synuralean algae in Viet Nam. This is the aim of this work.

2. Materials and Methods

Plankton studies on different types of water bodies were carried out from 2008 to 2020 in various regions of Viet Nam [43,44,45,46,47,48,49,50,51,52]. In total, samples from 371 localities in Viet Nam were included in our studies of synuralean algae (Figure 1).
The samples were collected from 18 provinces located in the northern, central, and southern parts of the country. Below is a list of the provinces studied, the abbreviations used in the text (in bold), and the years of sampling:
Bắc Kạn Province—BB, 2019 [43];
Hà Nội administrative area—BV, 2019 [43];
Ninh Bình Province—NB, 2019 [43];
Thanh Hoá Province—TH, 2019 [43];
Quảng Bình Province—QB, 2016 [48];
Quảng Trị Province—QT, 2019 [48];
Thừa Thiên Huế Province—TTH, 2019 [48];
Bình Định Province—BD, 2018 [48];
Phú Yên Province—PY, 2018 [48];
Khánh Hòa Province—KH, 2008–2018 [44,45,46,48];
Đắk Lắk Province—DL, 2010, 2014 [48];
Lâm Đồng Province—LD, 2010, 2012, 2014, 2018 [47,48];
Đồng Nai Province—DN, 2010, 2012, 2014, 2015, 2018 [49,51];
Bình Thuận Province—BT, 2012–2014 [51];
Bến Tre and Trà Vinh provinces (Mekong Delta)—M, 2018 [50];
Kiên Giang Province, Phú Quốc Island—PQ, 2015 [52];
Bà Rịa—Vũng Tàu Province, Con Dao Archipelago, Côn Sơn Island—CD, 2015 [52].
Sampling occurred during expeditions of the Joint Vietnam–Russia Tropical Science and Technology Research Center (“Ecolan 3.2” project). Basic characteristics of the localities, climate parameters, and distribution of described species are represented in [43,44,45,46,47,48,49,50,51,52].
Samples were collected using a plankton net with 20 μm mesh. For electron microscopy studies, an aliquot of each sample was washed three times by repeated centrifugation with deionized water. Drops of each washed sample were dried directly onto stubs for Scanning Electron Microscopy (SEM) or grids for Transmission Electron Microscopy (TEM) or digested (4–5 min) in sulfuric acid with potassium dichromate before mounting. For SEM studies, samples were dried on aluminum stubs, coated with gold for 10 min with a JEE-4X (JEOL, Tokyo, Japan) sputter coater, and observed with a JEOL 6510 LV scanning electron microscope. For TEM studies, samples were dried onto formvar-coated grids (EMS FF200-Cu-50, Electron Microscopy Sciences, Hatfield, PA, USA) and observed with a JEM-1011 TE microscope. Specific conductance, pH, and temperature measurements were made with a Hanna HI 9828 device (Hanna Instruments, Inc., Smithfield, RI, USA).

3. Results

A total of 74 taxa from the order Synurales were identified at the 371 localities in Viet Nam.
Mallomonas acaroides Perty emend. Iwanoff (Figure 2A).
This species was found in five localities in three provinces of Viet Nam: LD, BB, NB.
Parameters: pH 6.5–8.2 (7.4 ± 0.4), specific conductance 16–368 (174 ± 63) µS cm−1, temperature 20–31 (24 ± 2) °C.
This is a widespread species and common component of phytoplankton in water bodies and rivers in temperate latitudes [1]. It is rare in the tropics where it was recorded previously in China [15,16] and the mountainous regions of Zimbabwe [28].
M. adamas Harris & Bradley (Figure 2B).
This species was found in 14 localities in seven provinces: PQ, DN, LD, KH, BD, PY, TTH.
Parameters: pH 5.7–7.5 (6.5 ± 0.2), specific conductance 6–100 (50 ± 8) µS cm−1, temperature 25–37 (32 ± 1) °C.
A rare species that occurs sporadically in different regions—in Australia and in a number of countries in Europe and Asia [1]. In the tropical region, it has been recorded in Malaysia [12].
M. akrokomos Ruttner (Figure 2C).
This species was found in four localities in three provinces: LD, PY, TTH.
Parameters: pH 5.9–6.8 (6.5 ± 0.2), specific conductance 22–138 (85 ± 30) µS cm−1, temperature 24–35 (31 ± 3) °C.
It is considered a cosmopolitan species [1]; however, unpublished molecular data indicate that this species represents a complex of cryptic taxa. The tropical strain we isolated forms a separate branch on the phylogenetic tree (unpublished). In the tropics, this morphotype was rarely noted in Brazil [28], Zimbabwe [28], China [15,16], India [17,18], and Ecuador [35].
M. bangladeshica (Takahashi & Hayakawa) Siver & Wolfe (Figure 2D).
This species was found in seven localities in five provinces: KH, DL, PY, BV, TTH.
Parameters: pH 5.8–7.5 (6.6 ± 0.3), specific conductance 74–250 (137 ± 25) µS cm−1, temperature 28–36 (31 ± 1) °C.
It is a rare, mostly tropical species [1]. This species is known from Bangladesh [11], Sri Lanka [14], tropical China [15,16], India [18], Indonesia [22], and Papua New Guinea [21]. Two localities are known in Europe, Romania [53] and Portugal [54].
M. binocularis Siver (Figure 2E).
This species was found in four localities in three provinces: DN, KH, TTH.
Parameters: pH 4.8–6.9 (5.5 ± 0.6), specific conductance 10–96 (42 ± 22) µS cm−1, temperature 24–34 (29 ± 3) °C.
This is a very rare species, previously considered endemic to North America. This taxon was described from a pond in Florida, USA [55]. Subsequently, it was also found in North Carolina and southern New Jersey, USA [56]. Identification of this species in Viet Nam indicates its wider distribution.
M. bronchartiana Compère (Figure 2F).
This species was found in 38 localities in eight provinces: CD, DN, KH, BT, DL, BD, PY, QT.
Parameters: pH 4.8–8 (6.7 ± 0.1), specific conductance 26–382 (109 ± 14) µS cm−1, temperature 25–36 (32 ± 0.1) °C.
A revision of published records related to M. bronchartiana [57] made it possible to confirm that the taxon was previously recorded in a number of African countries [27,28,58], the Amazon tropics [40], Jamaica [28], Malaysia [12], India [17], and Indonesia [22].
M. cattiensis Gusev, Doan-Nhu & Nguyen-Ngoc (Figure 2G).
This species was described from Viet Nam [59] and was found in 13 localities in seven provinces: DN, KH, BT, DL, BD, PY, TTH.
Parameters: pH 4.8–7.6 (6.5 ± 0.2), specific conductance 22–592 (109 ± 45) µS cm−1, temperature 25–36 (31 ± 1) °C.
This species was also recorded on the Java Island, Indonesia [22], and in Papua New Guinea, where it was identified as M. morrisonensis ([21], 1993, Figures 10 and 11, p. 115).
M. caudata Iwanoff (Figure 2H).
This species was found in 48 localities in 13 provinces: DN, LD, KH, BT, BB, QB, DL, BD, PY, BV, TH, QT, TTH.
Parameters: pH 5.9–8.6 (7.1 ± 0.1), specific conductance 16–235 (74 ± 7) µS cm−1, temperature 17–35 (28 ± 1) °C.
This species belongs to widespread taxa, especially in the temperate zone [1]. In the tropics, it has been recorded in Brazil [28,39], Panama [36], the tropics and subtropics of China [15,16], and India [17,18].
M. ceylanica Dürrschmidt & Cronberg (Figure 2I).
This species was found in 15 localities in nine provinces: CD, KH, BT, QB, DL, BD, NB, QT, TTH.
Parameters: pH 5.5–7.8 (6.8 ± 0.2), specific conductance 33–666 (226 ± 58) µS cm−1, temperature 17–37 (30 ± 2) °C.
This species was originally described from Sri Lanka [14]. Later, it was found only in a few tropical water bodies in China [16], India [17,18], and South Korea [9].
M. collucata Gusev & Kulikovskiy (Figure 2J).
This species was described from Viet Nam [60] and was found in one locality in one province: PQ.
Parameters: pH 5.3, specific conductance 17 µS cm−1, temperature 29 °C. This species is endemic to Viet Nam.
M. crassisquama (Asmund) Fott (Figure 2K).
This species was found in 62 localities in 12 provinces: DN, LD, KH, QN, QB, DL, BD, PY, BV, TH, QT, TTH.
Parameters: pH 6.0–8.6 (7.1 ± 0.1), specific conductance 16–373 (76 ± 7) µS cm−1, temperature 17–37 (29 ± 1) °C.
It is a widespread species, especially in temperate latitudes [1]. This species is less common in the tropics; it is known from Sri Lanka [14], Jamaica [28], Zimbabwe [28], Colombia [28,38], Guatemala [28], China [15,16], India [18], Nigeria [19,20], Brazil [40], and Ecuador [35].
M. crassisquama var. papillosa Siver & Skogstad (Figure 2L).
This species was found in four localities in two provinces: LD and QB.
Parameters: pH 6.5–7.1 (6.8 ± 0.2), specific conductance 16–110 (55 ± 24) µS cm−1, temperature 18–24 (22 ± 2) °C.
This is a rare taxon. It was believed that the distribution of this taxon was limited to the northern regions of temperate latitudes [1,61]. Our findings refute this assumption. However, it should be noted that this variety has a dubious status. It differs from the type variety M. crassisquama only in the presence of large and conspicuous papillae on the scale surface [1,62]. However, some studies have shown that the presence, size, and number of papillae on the surface of the scales of the M. crassisquama morphotype are rather variable features, to the extent that scales covered with papillae or without papillae can be present on the same cell [63]. However, since revisions and more detailed comparative studies of M. crassisquama var. crassisquama and M. crassisquama var. papillosa have not been made, we consider M. crassisquama var. papillosa in this work as an independent taxon.
M. cf. cristata Dürrschmidt (Figure 2M).
This taxon was found in 11 localities in seven provinces: PQ, DN, BT, QB, DL, PY, TTH.
Parameters: pH 5–7.3 (6.1 ± 0.3), specific conductance 13–63 (36 ± 5) µS cm−1, temperature 18–34 (30 ± 2) °C.
Mallomonas cristata was described from Chile [64]. It was later found in many habitats throughout the world [1]. In the tropical region, the species is known from Madagascar [25], Brazil [41,42], and Ecuador [35]. Specimens from Viet Nam differ mainly by serrated bristles, while only 1–2 small teeth on the distal portion of bristles were originally described for M. cristata. The structure of the bristles is one of the characteristics for distinguishing species of the genus Mallomonas, in particular, in the sections Mallomonas and Striatae [65,66,67]. With a high degree of probability, this is a new species for science, but additional studies of the scales and bristle morphology and molecular data are needed to describe it.
M. distinguenda Gusev, Doan-Nhu, Nguyen-Ngoc & Kapustin (Figure 2N).
This species was described from Viet Nam [68] and was found in nine localities in four provinces: PQ, DN, BT, TTH.
Parameters: pH 4.6–6.9 (5.7 ± 0.4), specific conductance 10–311 (58 ± 34) µS cm−1, temperature 24–34 (30 ± 1) °C.
This species is endemic to Viet Nam.
M. elevata Han Soon Kim (Figure 2O).
This species was found in nine localities in five provinces: LD, KH, BD, PY, TTH.
Parameters: pH 4.7–7.4 (5.8 ± 0.3), specific conductance 6–248 (61 ± 26) µS cm−1, temperature 23–35 (31 ± 1) °C.
The species was recently described from the subtropics of South Korea [69]. We found this species for the first time outside the type habitat.
M. elongata Reverdin (Figure 2P).
This species was found in three localities in two provinces: QB, PY.
Parameters: pH 7.0–7.4 (7.2 ± 0.1), specific conductance 117–118 (118 ± 1) µS cm−1, temperature 18–36 (26 ± 11) °C.
Mallomonas elongata is considered as a widespread species in temperate latitudes [1]. In the tropical region, the species was found in Brazil [28,40], the highlands of Colombia [28], the mountainous regions of Guatemala, the tropical and subtropical regions of China [15], and India [18]. Mallomonas elongata is characterized by the acute or rounded V-rib, which is hooded and continuous with the short anterior submarginal rib; scales and V-rib outlines are often asymmetrical [65,70]. Previous records of M. elongata from Asia [12,15,16] and all the above-mentioned records in the tropics correspond to a different morphotype, which is probably a new species not yet described (see Mallomonas sp. 1 in [43,49]).
M. favosa f. favosa K.H. Nicholls (Figure 2Q).
This species was found in 34 localities in 10 provinces: PQ, CD, DN, LD, KH, BT, DL, BD, PY, TTH.
Parameters: pH 4.6–7.8 (6.1 ± 0.2), specific conductance 3–380 (69 ± 14) µS cm−1, temperature 24–38 (32 ± 1) °C.
Mallomonas favosa f. favosa is considered a cosmopolitan species [71]. It was described in Canada [72] and was later reported from other parts of the world [1]. In the tropical region, Mallomonas favosa f. favosa was found in Malaysia [12], China [16], Papua New Guinea [21], and Brazil [41,42].
M. favosa f. gemina Dürrschmidt & Croome (Figure 2R).
This species was found in 53 localities in 11 provinces: PQ, CD, DN, KH, BT, DL, BD, PY, NB, QT, TTH.
Parameters: pH 4.6–8.0 (6.4 ± 0.1), specific conductance 10–923 (154 ± 29) µS cm−1, temperature 24–39 (32 ± 0.1) °C.
Mallomonas favosa f. gemina was described in Malaysia [12] and was later found in Indonesia [21], South Korea [73], and Madagascar [25].
M. fimbriata Gusev (Figure 2S).
This species was described from Viet Nam [74] and was found in four localities in three provinces: PQ, KH, BT.
Parameters: pH 4.6–7.1 (5.2 ± 0.5), specific conductance 25–112 (66 ± 18) µS cm−1, temperature 24–31 (28 ± 1) °C.
Scales of Mallomonas fimbriata were also reported from one locality in Malaysia as Mallomonas sp. 3 ([12], Figure 49, p. 294).
M. fragariformis Gusev, Kapustin, Shkurina, Martynenko (Figure 2T).
This species was described from Viet Nam [75] and was found in eight localities in six provinces: PQ, CD, BT, TTH, PY, QT.
Parameters: pH 6.0–8.7 (6.6 ± 0.5), specific conductance 37–329 (163 ± 61) µS cm−1, temperature 30–36 (32 ± 2) °C.
Scales of Mallomonas fragariformis were also reported from Indonesia [22].
M. furtiva Gusev, Čertnerová, Škaloudová, Škaloud (Figure 3A).
This species was described from Viet Nam [76] and was found in 24 localities in nine provinces: PQ, CD, DN, LD, KH, BT, BD, PY, TTH.
Parameters: pH 5.2–7.9 (6.3 ± 0.1), specific conductance 10–3000 (275 ± 138) µS cm−1, temperature 20–38 (30 ± 1) °C.
Outside Viet Nam, it was found in the Indonesian part of New Guinea [23] and Malaysia ([12] as M. cf. rasilis, Figure 41, p. 292).
M. grata E.Takahashi (Figure 3B).
This species was found in 11 localities in nine provinces: DN, LD, KH, DL, BD, BV, NB, TH, QT.
Parameters: pH 5.8–7.6 (7.1 ± 0.2), specific conductance 21–468 (151 ± 56) µS cm−1, temperature 23–36 (30 ± 1) °C.
Mallomonas grata was described from a pond in Japan [77]. It has rare finds in India [17,18], South Korea ([78] as Mallomonas sp. 2, Figure 49, p. 429), China [15,16], Singapore, and Malaysia [13]. It is noted that it is a rare species and is endemic to Southeast and East Asia [13].
M. gusakovii Gusev, Kapustin, Martynenko, Guseva & Kulikovskiy (Figure 3C).
This species was described from Viet Nam [79] and was found in two localities in one province: PQ.
Parameters: pH 4.7–5.1, specific conductance 25–1200 µS cm–1, temperature 29–31 °C.
This species is endemic to Viet Nam.
M. guttata var. guttata Wujek (Figure 3D).
This species was found in 68 localities in 12 provinces: PQ, CD, DN, LD, KH, BT, QB, DL, BD, PY, QT, TTH.
Parameters: pH 4.1–8.6 (6.5 ± 0.1), specific conductance 10–3000 (216 ± 69) µS cm–1, temperature 18–39 (32 ± 0.4) °C.
It is considered a widespread taxon [1]. In the tropical region, it was recorded in most of the studied countries: Bangladesh [11], Indonesia ([24], as M. perforata Cronberg & Hickel, Figures 5–11, p. 108), Malaysia [12], Sri Lanka [14], Costa Rica [34], Jamaica [28], Zimbabwe [28], China [15,16], Papua New Guinea [21], India [17,18], Madagascar [25], Nigeria [19,20], Brazil [41,42], Colombia [38], and Ecuador [35].
M. guttata var. simplex Nicholls (Figure 3E).
This species was found in 43 localities in 10 provinces: PQ, DN, LD, KH, BT, DL, BD, PY, QT, TTH.
Parameters: pH 4.9–8.5 (6.6 ± 0.1), specific conductance 9–3000 (120 ± 73) µS cm−1, temperature 24–38 (30 ± 0.5) °C.
It is considered a rare species, described from Canada [80] and known from China [16,81]. M. guttata var. simplex is a dubious taxon, different from the M. guttata var. guttata in that the depressions on the central field are few and arranged in one row. In our samples, both varieties were often found together. Moreover, cells were found with scales containing both several rows and single rows of depressions [49]. A more detailed study and revision of these two taxa are needed.
M. harrisiae E.Takahashi (Figure 3F).
This species was found in five localities in two provinces: PQ and TTH.
Parameters: pH 4.7–6.9 (5.8 ± 0.5), specific conductance 6–37 (28 ± 6) µS cm−1, temperature 30–35 (32 ± 1) °C.
Mallomonas harrisiae is a very rare taxon that was first described from Japan [82] and was recently found in China [83]. Viet Nam is the third country where this species has been found.
M. hexareticulata Jo, Shin, Kim, Siver & Andersen (Figure 3G).
This species was found in 20 localities in nine provinces: PQ, KH, BT, QB, DL, BD, BV, TH, TTH.
Parameters: pH 5.3–8.2 (6.9 ± 0.2), specific conductance 13–329 (116 ± 19) µS cm−1, temperature 18–34 (30 ± 1) °C.
This species was recently described from the water bodies of South Korea [7]. We confirmed the findings of this species in Viet Nam both on the basis of both morphological and molecular approaches (unpublished).
M. kenyana (Wujek & Asmund) Kapustin & Gusev (Figure 3H).
This species was found in 95 localities in 14 provinces: DN, LD, KH, BT, BB, QB, DL, BD, PY, BV, NB, TH, QT, TTH.
Parameters: pH 5.9–9.2 (7.4 ± 0.1), specific conductance 18–955 (181 ± 18) µS cm–1, temperature 17–64 (30 ± 1) °C.
This taxon was first described as Mallomonas cyathelata Wujek & Asmund var. kenyana Wujek & Asmund [26]. It is a predominantly tropical species known from Kenya [26], Zimbabwe [28], Guatemala [28], China [15], Papua New Guinea [21], Indonesia [22], India [17,18], Madagascar [25], Nigeria [19,20], Colombia [38], Brazil [84], and the subtropics of the USA [85].
M. korshikovii Gusev (Figure 3I).
This species was described from Viet Nam [45] and was found in 10 localities in seven provinces: PQ, CD, KH, BT, BD, PY, TH.
Parameters: pH 5.0–7.2 (6.5 ± 0.2), specific conductance 55–3000 (736 ± 377) µS cm−1, temperature 30–36 (33 ± 1) °C.
This species is endemic to Viet Nam.
M. lamii Gusev, Kulizin, Guseva, Shkurina & Kulikovskiy (Figure 3J).
This species was described from Viet Nam [86] and was found in 35 localities in 11 provinces: CD, DN, KH, BT, DL, BD, PY, M, TH, QT, TTH.
Parameters: pH 5.8–8.1 (6.8 ± 0.1), specific conductance 15–2370 (247 ± 83) µS cm−1, temperature 28–39 (31 ± 0.4) °C.
Despite the fact that this species has large and conspicuous scales that are easy to detect when processing samples, it has not yet been found outside of Viet Nam. Thus, this taxon can be considered as an endemic species for this territory. However, given the fact that the species occurs quite often, it can be assumed that it should be found in neighboring regions as well.
M. loricata Gusev, Shkurina & Kulikovskiy (Figure 3K).
This species was described from Viet Nam [87] and was found in 25 localities in eight provinces: KH, BT, DL, BD, PY, BV, QT, TTH.
Parameters: pH 6.0–8.3 (6.9 ± 0.1), specific conductance 32–247 (99 ± 11) µS cm−1, temperature 27–37 (33 ± 1) °C.
Mallomonas loricata was also recorded in Singapore and Malaysia under the epithet M. matvienkoae ([13], 2007, Figure 7, p. 225). It can be assumed that this taxon has a wide distribution in the tropical region. By now, it can be considered endemic to Southeast Asia.
M. lusca Gusev & Kezlya (Figure 3L).
This species was described from Viet Nam [88] and was found in six localities in three provinces: DN, KH, BT.
Parameters: pH 5.9–7.1 (6.6 ± 0.2), specific conductance 23–311 (95 ± 50) µS cm−1, temperature 29–34 (31 ± 1) °C.
Scales of Mallomonas lusca were also reported from one locality in Malaysia [12]. This species is endemic to Southeast Asia.
M. mangofera Harris & Bradley var. mangofera apud Dürrschmidt [89] (Figure 3M).
This species was found in 25 localities in 10 provinces: CD, DN, LD, KH, QN, DL, BD, BV, NB, TH.
Parameters: pH 4.8–9.0 (7.0 ± 0.2), specific conductance 10–955 (275 ± 49) µS cm−1, temperature 20–36 (31 ± 1) °C.
Scales, observed in Viet Nam, are quite similar to ones described from Chile under the name M. mangofera var. mangofera ([89], Figures 6–10, p. 181 and Figures 11–16, p. 183). Scale specimens of M. mangofera var. mangofera from the type locality in Great Britain [90], as well as the other scales from Europe (for example, [91], Figure J, p. 730; [92]), differ in the presence of the base plate pores on the posterior flange, a large window without secondary layer at the base of the V-rib, and in the peculiarities of papillae ornamentation of the shield. Further investigations are necessary for an understanding of the relationship between these two morphotypes of Mallomonas mangofera. Our unpublished data indicate that these are different species. However, until a revision of this group is made, we present this taxon as M. mangofera var. mangofera apud Dürrschmidt [89].
In the tropical region, this morphotype has been found in Bangladesh [11], Malaysia [12], Jamaica [28], China [15,16], Papua New Guinea [21], India [18], Madagascar [25], Brazil [41,42,85], Colombia [38], Ecuador [35], and Indonesia [23].
M. mangofera var. foveata (Dürrschmidt) Kristiansen (Figure 3N).
This species was found in 35 localities in 13 provinces: PQ, CD, DN, LD, KH, BT, BB, DL, BD, PY, TH, QT, TTH.
Parameters: pH 4.7–8.0 (6.6 ± 0.2), specific conductance 10–740 (218 ± 44) µS cm−1, temperature 22–39 (32 ± 1) °C.
The taxon is considered cosmopolitan [71]. Not all morphotypes in our studies had an internal reticulation formed by a secondary silica layer on the surface of the scales, while the type specimens from Chile had such a reticulation [89]. However, our studies of cultures have shown that, within the same monoclonal culture, secondary reticulation may or may not be present on scales. The taxon was found in the tropical region in Malaysia [12], Sri Lanka [14], Jamaica [28], Zimbabwe [28], Colombia [28,38], China [15,16], India [18], Madagascar [25], Brazil [41,42], Ecuador [35], and Indonesia [23].
M. cf. mangofera var. reticulata (Cronberg) Kristiansen (Figure 3O).
This species was found in 26 localities in 10 provinces: PQ, CD, DN, KH, BB, DL, BD, PY, QT, TTH.
Parameters: pH 4.6–7.9 (6.2 ± 0.2), specific conductance 10–666 (147 ± 38) µS cm−1, temperature 22–39 (31 ± 1) °C.
Mallomonas cf. mangofera var. reticulata is an incompletely described taxon that requires additional revision, but it can be argued with certainty that it should have species status. This taxon belongs to the group of taxa Mallomonas mangofera from the section Torquatae series Mangoferae, which includes many morphospecies. Several characteristics that were used for distinguishing taxa in this group have unclear taxonomic significance. In particular, this applies to the presence or absence of reticulation and its form (triangular, polygonal, and circular). Scales of Mallomonas mangofera f. reticulata, according to the original description and holotype given by Cronberg based on material from Zimbabwe [28], have a network of triangular meshes. Scales from Viet Nam have rounded or polygonal meshes. The morphotype found in Viet Nam and the African morphotype also differ in the shape of the scales, and most likely they should be considered different species based on morphological differences. However, we present our taxon as M. cf. mangofera var. reticulata because the significance of such a feature as the shape of the internal reticulation is not yet clear, and further revision of this group is required. Scales identified as Mallomonas mangofera var. reticulata with polygonal or rounded meshes were recorded in China ([16], Figures 56 and 57, p. 892 and [93], Figure 47, p. 35). Mallomonas mangofera f. reticulata with a similar structure was recorded in Malaysia ([13], Figure 5, p. 253). Moreover, this morphotype was identified as Mallomonas mangofera var. mangofera in Cronberg ([28], Figure 44, p. 214), Kristiansen ([94], Figure 46), Wei & Kristiansen ([95], Figure 52), and Hansen ([25], Figure 35, p. 161). Nemcova et al. ([96], Figures 29 and 30, p. 17) presented both morphotypes from French water bodies, with triangular ([96], Figure 30, p. 17) and polygonal ([96], Figure 29, p. 17) reticulation, under the name Mallomonas mangofera var. reticulata. To date, this morphotype, in addition to the regions mentioned above, is also known from Jamaica [28], India [18], and Indonesia [23].
M. mangofera var. sulcata Dürrschmidt (Figure 3P).
This species was found in six localities in five provinces: QN, BD, PY, QT, TTH.
Parameters: pH 5.0–7.3 (6.4 ± 0.3), specific conductance 28–119 (60 ± 16) µS cm−1, temperature 30–37 (33 ± 1) °C.
Mallomonas mangofera var. sulcata is a very rare and not fully described variety from the M. mangofera complex. It was described in a Chilean water body [89]. Subsequently, it was also found in one locality in Singapore [13]. Mallomonas mangofera var. sulcata differs from other taxa of the M. mangofera complex by the presence of grooves (narrow long depressions) along the submarginal ribs. Although only two long depressions are indicated in the diagnosis of the species, in the accompanying illustrations, there are more of them on some scales, and they can have different shapes ([89], p. 189, Figure 37). In Singapore and Viet Nam, similar morphotypes have been found with numerous depressions, narrower than those illustrated for organisms from the type habitat. Perhaps these are scales of a different taxon than the one described from Chile. Further investigations are needed to clarify the taxonomic status of this organism and taxonomic significance of such characters as the number and shape of the depressions on the shield.
M. cf. mangofera var. gracilis (Dürrschmidt) Kristiansen (Figure 3Q).
This species was found in five localities in three provinces: BB, NB, TTH.
Parameters: pH 5–7.9 (6.4 ± 0.6), specific conductance 28–480 (149 ± 97) µS cm−1, temperature 22–34 (30 ± 2) °C.
M. mangofera var. gracilis is a very rare and not fully described variety from the M. mangofera complex. It was described from Chile [89]; subsequently, single finds were noted in Denmark [97], Finland [98], Malaysia [12], and China [16]. The diagnostic characters of this variety are rather dubious. This variety differs from the type variety of M. mangofera by the shield with a weakly developed pattern of papillae, which are fused together to some extent, and with a pit-like depression with a pore at the base of the posterior submarginal rib. These characteristics can also be represented by weakly silicified scales of other species of this complex. It is also unclear whether scales identified as Mallomonas mangofera var. gracilis from such distant areas represent one species. Since the ultrastructure of the scales found in Viet Nam corresponds to the description of Mallomonas mangofera var. gracilis, we present this taxon in this list. However, further studies of this morphotype are required.
M. matvienkoae B. Asmund & Kristiansen var. siveri Wujek & L.C. Saha (Figure 3R).
This species was found in 3 localities in 2 provinces: DN, NB.
Parameters: pH 5.2–7.8 (6.8 ± 1), specific conductance 10–480 (290 ± 175) µS cm−1, temperature 24–34 (29 ± 4) °C.
Mallomonas matvienkoae var. siveri is a very rare taxon, described in India [18]. Findings in Viet Nam are the first outside the type habitat. Our unpublished molecular data indicate that the rank of this taxon should be raised to the species level.
M. minuscula Gusev, Guseva, Kezlya & Kulikovskiy (Figure 3S).
This species was described from Viet Nam [99] and was found in 14 localities in eight provinces: PQ, CD, LD, KH, BB, BD, PY, TTH.
Parameters: pH 4.7–7.9 (6 ± 0.2), specific conductance 16–242 (94 ± 21) µS cm−1, temperature 22–37 (32 ± 1) °C.
Based on these data, we expect a wider distribution of this species in Southeast Asia, but so far it is endemic to Viet Nam.
M. morrisonensis Croome & P.A.Tyler (Figure 3T).
This species was found in 56 localities in 13 provinces: PQ, DN, LD, KH, BT, DL, BD, PY, BV, NB, TH, QT, TTH.
Parameters: pH 4.1–8.0 (6.3 ± 0.1), specific conductance 10–539 (104 ± 14) µS cm−1, temperature 22–38 (31 ± 0.1) °C.
This species is distributed in tropical and subtropical regions [1]. The taxon was described from water bodies of Australia [100]. In the tropical region, it was recorded in Malaysia [12], China [15], India [17,18], Madagascar [25], and Brazil [42].
M. multisetigera Dürrschmidt (Figure 4A).
It was found in 12 localities in seven provinces: PQ, CD, KH, BT, BD, M, TTH.
Parameters: pH 4.7–7.2 (6.4 ± 0.2), specific conductance 25–2370 (409 ± 218) µS cm−1, temperature 29–39 (33 ± 1) °C.
This species is considered a cosmopolitan taxon [1]. In the tropical region, it is known from Jamaica [28], China [16], Madagascar [25], Nigeria [19,20], Brazil [42,101], Indonesia [23], and Ecuador [35].
M. neoampla Gusev & Siver (Figure 4B).
This species was described from Viet Nam [102] and was found in 11 localities in three provinces: KH, TH, TTH.
Parameters: pH 5.3–7.4 (6.2 ± 0.2), specific conductance 28–263 (93 ± 21) µS cm−1, temperature 30–35 (32 ± 1) °C.
It is a rare species also found in Malaysia [13]. This species is endemic to Southeast Asia.
M. ocellata Dürrschmidt & Croome (Figure 4C).
This species was found in 14 localities in eight provinces: LD, KH, BT, QB, DL, BD, PY, TTH.
Parameters: pH 5.5–7.3 (6.5 ± 0.2), specific conductance 23–148 (62 ± 12) µS cm−1, temperature 17–36 (29 ± 2) °C.
This is a rare species [1,13]. It is known from Malaysia, from where it was described in 1985 [12], Singapore [13], China [16], and Japan [103,104].
M. cf. ouradion Harris & Bradley (Figure 4D).
This species was found in five localities in four provinces: PQ, DN, PY, TTH.
Parameters: pH 4.7–6.6 (5.5 ± 0.4), specific conductance 10–55 (36 ± 10) µS cm−1, temperature 24–30 (28 ± 1) °C.
It is a fairly rare species with a scattered distribution [1]. It was originally described in Great Britain [105]. However, our findings in Viet Nam differ from the scales recorded in the temperate zone. In contrast to the original description of M. ouradion, the Vietnamese scales are smaller and have a different outline, a wide posterior border, a V-rib shifted to the center of the scales, and a poorly developed anterior submarginal rib and well-developed anterior flanges. Apparently, this morphotype is distributed in the tropical region and is a species new to science; however, there are insufficient data to describe it, so we mention it here as M. cf. ouradion.
M. papillosa Harris & Bradley (Figure 4E).
This species was found in four localities in three provinces: CD, DN, TTH.
Parameters: pH 5.3–7.0 (6.4 ± 0.7), specific conductance 28–65 (43 ± 14) µS cm−1, temperature 33–36 (34 ± 1) °C.
This species is considered cosmopolitan and is often found in the temperate zone [1]. However, in the tropical region, it is quite rare. Single finds are known from Malaysia [12], the highlands of Colombia [28], China [15,16], Papua New Guinea [21], India [18], Madagascar [25], Brazil [42], Indonesia [23], and Ecuador [35].
M. paragrandis Gusev (Figure 4F).
This species was described from Viet Nam [106] and was found in 95 localities in 13 provinces: PQ, CD, DN, KH, BT, DL, BD, PY, M, NB, TH, QT, TTH.
Parameters: pH 4.8–8.5 (6.8 ± 0.1), specific conductance 10–3000 (199 ± 54) µS cm−1, temperature 25–39 (32 ± 0.1) °C.
It is one of the most common species of the genus in Viet Nam. It has also been found in Indonesia [22] and Madagascar ([25] as M. matvienkoae f. matvienkoae, Figure 15, p. 154).
M. parvula Dürrschmidt (Figure 4G).
This species was found in one locality in one province: NB.
Parameters: pH 7.4, specific conductance 480 µS cm−1, temperature 34 °C.
It belongs to common species of temperate latitudes [1]. It is rare in the tropical region, recorded in China [15], Nigeria [19,20], and Ecuador [35].
M. peronoides (K.Harris) Momeu & L.S.Péterfi (Figure 4H).
This species was found in 50 localities in 14 provinces: CD, DN, KH, BT, BB, DL, BD, PY, M, BV, NB, TH, QT, TTH.
Parameters: pH 5.7–8.6 (7.2 ± 0.1), specific conductance 10–2370 (318 ± 56) µS cm−1, temperature 22–39 (32 ± 0.1) °C.
It is considered a widespread species, but it is more common in tropical areas [1], where it is known from Sri Lanka [14], Zimbabwe [28], China [15,16], India [17,18], Madagascar [25], Nigeria [19,20], Brazil [40,41,42], and Indonesia [22].
M. plumosa Croome & P.A. Tyler (Figure 4I).
This species was found in 31 localities in nine provinces: CD, DN, LD, KH, BT, DL, PY, QT, TTH.
Parameters: pH 4.8–8.6 (6.4 ± 0.2), specific conductance 10–293 (88 ± 14) µS cm−1, temperature 24–36 (30 ± 1) °C.
Mallomonas plumosa is a rare species described from Australia, in Tasmania [99]. The species was also found in New Zealand and South and Southeast Asia [1]. It is known from the tropical region in China [16], India [17,18], and Indonesia [22].
M. portae-ferreae Péterfi & Asmund (Figure 4J).
This species was found in 11 localities in eight provinces: KH, BT, DL, BD, M, BV, NB, TH.
Parameters: pH 6.8–9.2 (7.5 ± 0.2), specific conductance 65–2370 (433 ± 206) µS cm−1, temperature 28–34 (31 ± 1) °C.
The species is considered a cosmopolitan taxon, but it is distributed mainly in regions with a warm climate [1]. It was found in the tropics in Bangladesh [11], Sri Lanka [14], Republic of Chad [107], Zimbabwe [28], tropical China [15,16], India [17,18], Indonesia [22,23], South Africa [33], and Brazil [28].
M. pseudobronchartiana Gusev, Siver & Shin (Figure 4K).
This species was described from Viet Nam [57] and was found in two localities in two provinces: DN, DL.
Parameters: pH 5.9–6.1, specific conductance 22–119 µS cm−1, temperature 28–29 (29 ± 1) °C.
Outside Viet Nam, this species has been observed in South Korea ([73] as M. bronchartiana, Figures 4 and 5, p. 211; [9] as M. sp. 1, Figure 11, p. 939) and multiple regions in the United States ([108,109,110] as M. bronchartiana).
M. pseudomatvienkoae Jo, Shin, Kim, Siver & Andersen (Figure 4L).
This species was found in 79 localities in 15 provinces: PQ, CD, DN, LD, KH, BT, DL, BD, PY, M, BV, NB, TH, QT, TTH.
Parameters: pH 4.1–8.2 (6.4 ± 0.1), specific conductance 6–2370 (155 ± 36) µS cm−1, temperature 23–39 (31 ± 0.1) °C.
This species from the M. matvienkoae complex was recently described based on combined morphological and molecular studies of strains isolated from South Korea [7]. This morphotype was also found in India ([17] as M. matvienkoae var. matvienkoae, Figure 15, p. 350), Colombia ([38] as M. matvienkoae var. matvienkoae, Figure 21, p. 159), and Indonesia [22]. This taxon is widespread in Viet Nam, and, therefore, it should also be a common species in other regions of tropical and subtropical Asia. It is possible that this morphotype was not previously illustrated separately, as it was considered to belong to M. matvienkoae.
M. pseudocratis Dürrschmidt (Figure 4M).
This species was found in four localities in two provinces: QB and NB.
Parameters: pH 7.1–7.8 (7.5 ± 0.2), specific conductance 104–480 (315 ± 92) µS cm−1, temperature 17–34 (24 ± 5) °C.
M. pseudocratis is a widespread species, but it has a scattered distribution [1]. In the tropics, it is known from China [15] and India [18].
M. punctifera Korshikov (Figure 4N).
This species was found in two localities in one province: LD.
Parameters: pH 6.5–6.6, specific conductance 16–164 µS cm−1, temperature 20–23 °C.
Mallomonas punctifera is a common species in northern temperate latitudes [1]. In the tropics, it has been reported only from Malaysia [12] and China [15,16].
M. punctostriata Gusev & Kulikovskiy (Figure 4O).
This species was described from Viet Nam [60] and was found in two localities in two provinces: PQ, KH.
Parameters: pH 5.0–7.0, specific conductance 1200–3000 µS cm−1, temperature 31–34 °C.
M. punctostriata was found only in Viet Nam. Both habitats are located near the sea coast and have high mineralization.
M. rasilis Dürrschmidt (Figure 4P).
This species was found in 32 localities in 14 provinces: PQ, CD, DN, LD, KH, BT, BB, DL, BD, PY, BV, NB, TH, TTH.
Parameters: pH 4.7–9 (6.9 ± 0.2), specific conductance 22–711 (169 ± 34) µS cm−1, temperature 19–64 (32 ± 1) °C.
M. rasilis is considered a widespread species [1], but the finds of this species require verification, and the taxon needs revision [77]. M. rasilis was described from Chile [89]. In the tropics and subtropics, the species was found in Korea ([73] as M. sp. 4, Figures 52 and 53), Sri Lanka [14], China [16,84], Madagascar [25], and Indonesia [24].
M. siderea Gusev & Kulikovskiy (Figure 4Q).
This species was described from Viet Nam [111] and was found in six localities in six provinces: QB, PY, NB, TH, QT, TTH.
Parameters: pH 4.7–9.0 (6.9 ± 0.2), specific conductance 22–711 (169 ± 34) µS cm−1, temperature 19–64 (32 ± 1) °C.
It is a rare species in Viet Nam. One collar scale of this species has also been recorded in Malaysia under the name M. grata ([13], Figure 4, p. 253). Thus, this species can be considered endemic to Southeast Asia.
M. skvortsovii Gusev, Doan-Nhu, Nguyen-Ngoc & Kapustin (Figure 4R).
This species was described from Viet Nam [68] and was found in two localities in two provinces: PQ, DN.
Parameters: pH 5.2–6.4, specific conductance 10–119 µS cm−1, temperature 24–30 °C.
It is a very rare species endemic to Viet Nam.
M. sorohexareticulata Jo, Shin, Kim, Siver & Andersen (Figure 4S).
This species was found in 35 localities in 10 provinces: PQ, DN, LD, KH, BT, QB, DL, BD, QT, TTH.
Parameters: pH 4.6–8.0 (6.4 ± 0.1), specific conductance 9–104 (44 ± 4) µS cm−1, temperature 17–36 (31 ± 1) °C.
This species from the M. matvienkoae complex was recently described based on combined morphological and molecular studies of strains isolated from South Korea [7]. Scales with a similar ultrastructure under the name Mallomonas matvienkoae were reported from tropical China ([15], Figure 14, p. 175; [16], Figure 21, p. 887), Madagascar ([25], Figure 13, p. 154), and Nigeria ([19], Figure 5, p. 101). It can be assumed that this species should also be common in other regions of tropical and subtropical Asia.
M. spinosa Gusev emend. Wei & Kristiansen (Figure 4T).
This species was described from Viet Nam [112] and was found in 28 localities in 12 provinces: PQ, CD, DN, KH, BT, DL, BD, PY, M, TH, QT, TTH.
Parameters: pH 4.7–8.0 (6.7 ± 0.1), specific conductance 25–1591 (198 ± 68) µS cm−1, temperature 28–36 (32 ± 0.1) °C.
The scale of this species was first found in Malaysia, but due to insufficient material, the authors did not describe this species and referred it as Mallomonas sp. 1 [12]. This taxon was also recorded in China, in the province of Hainan [16], and in Indonesia [22].
M. splendens (G.S. West) Playfair emend. Croome, Dürrschmidt & P.A. Tyler (Figure 5A).
This species was found in 40 localities in nine provinces: PQ, CD, DN, LD, KH, BT, PY, QT, TTH.
Parameters: pH 4.6–7.2 (6.0 ± 0.1), specific conductance 10–1240 (123 ± 45) µS cm−1, temperature 20–36 (30 ± 1) °C.
This species has a limited distribution, primarily in Asia and Australia [1]. The modern diagnosis is based on the study of material using electron microscopy from Australia [113]. It has the form of M. splendens f. arnhemensis, which is distinguished by a depression in the central field at the angle of a V-shaped rib [113], which was also found in Viet Nam and Indonesia. Since it is difficult to distinguish this feature in the TEM images, we do not consider this form separately in this work. Based on electron microscopy data, M. splendens has been recorded from Australia [12], Malaysia [12], China [16], Indonesia [22], and Papua New Guinea [21].
M. striata Asmund sensu lato (Figure 5B).
It was found in one locality in one province: TTH.
Parameters: pH 6.5, specific conductance 51 µS cm−1, temperature 30 °C.
Mallomonas striata is considered a cosmopolitan taxon [1,114]. However, recently it has been shown that M. striata is a complex of species that can be morphologically distinguished by the structure of bristles, the shape of scales, and the number and arrangement of structural elements on the surface of scales [66,67,115,116]. Only one scale was found, in general, corresponding to the type of Mallomonas striata in ultrastructure, so we reported it as M. striata sensu lato. This species is rare in the tropics and has been recorded in Costa Rica [34], Colombia [38], and Jamaica [28].
M. striata var. serrata Harris & Bradley (Figure 5C).
It was found in one locality in one province: LD.
Parameters: pH 7.1, specific conductance 38 µS cm−1, temperature 20 °C.
This taxon is considered cosmopolitan [1]. It differs from the type variety in the structure of the bristles and the shape of the scales [115]. In the tropical region, it was recorded in Malaysia [12], Brazil [28,41,42], Jamaica [28], Zimbabwe [28], Papua New Guinea [21], Madagascar [25], Ecuador [35], and Indonesia [23].
M. tonsurata Teiling (Figure 5D).
This species was found in 102 localities in 16 provinces: PQ, CD, DN, LD, KH, QN, BT, QB, DL, BD, PY, M, BV, TH, QT, TTH.
Parameters: pH 4.8–8.6 (7.0 ± 0.1), specific conductance 9–2370 (126 ± 26) µS cm−1, temperature 17–39 (31 ± 0.1) °C.
It is a cosmopolitan species [1,71]. It was found in the tropics in most of the studied countries: Malaysia [12,13], Singapore [13], Sri Lanka [14], Republic of Chad [27], Zimbabwe [28], highlands of Colombia [28], Guatemala [28], tropical China [15,16], India [18], Nigeria [19,20], Indonesia [22], and Brazil [28,40].
M. tropica Dürrschmidt & Croome (Figure 5E).
This species was found in eight localities in four provinces: CD, KH, BD, TTH.
Parameters: pH 4.1–7.0 (5.9 ± 0.4), specific conductance 28–286 (125 ± 37) µS cm−1, temperature 31–36 (33 ± 1) °C.
It is a very rare species and was found in Viet Nam for the first time after the description from a water body in Malaysia [12].
M. velari Gusev, Siver & Shin (Figure 5F).
This species was described from Viet Nam [57] and was found in two localities in two provinces: PQ, DN.
Parameters: pH 4.7–5.2, specific conductance 10–25 µS cm−1, temperature 24–29 °C.
It is a very rare species endemic to Viet Nam.
M. vietnamica Gusev, Kezlya & Tran (Figure 5G).
This species was described from Viet Nam [117] and was found in one locality in one province: BV.
Parameters: pH 7.8, specific conductance 153 µS cm−1, temperature 25 °C.
It is a very rare species endemic to Viet Nam.
Synura australiensis Playfair (Figure 5H).
This species was found in 19 localities in six provinces: DN, LD, KH, BT, DL, TTH.
Parameters: pH 4.8–7.5 (6.1 ± 0.2), specific conductance 10–133 (56 ± 10) µS cm−1, temperature 22–35 (28 ± 1) °C.
It is a widespread species in the tropical region [1]. In particular, it is known from Australia [12], Brazil [28,39], Zimbabwe [28], Papua New Guinea [21], India [17,18], and Madagascar [25].
S. echinulata Korshikov (Figure 5I).
This species was found in 36 localities in nine provinces: PQ, CD, DN, LD, KH, BT, DL, PY, TTH.
Parameters: pH 4.6–8.0 (6.1 ± 0.1), specific conductance 10–96 (42 ± 4) µS cm−1, temperature 22–38 (30 ± 1) °C.
It is a widespread taxon in various climatic zones [1]. In the tropics, this morphotype was found in most of the studied countries.
S. cf. longitubularis Jo, Shin, Kim & Siver (Figure 5J).
This species was found in 174 localities in 17 provinces: PQ, CD, DN, LD, KH, BT, BB, QB, DL, BD, PY, M, BV, NB, TH, QT, TTH.
Parameters: pH 4.9–10.0 (6.9 ± 0.1), specific conductance 9–2370 (160 ± 18) µS cm−1, temperature 17–34 (31 ± 0.1) °C.
Synura cf. longitubularis is one of the most widespread taxa of synuralean algae in Viet Nam. However, the identification of this taxon based on morphological data is problematic [8]. Synura longitubularis was recently described in South Korea based on molecular data [8] and is almost indistinguishable from S. curtispina Petersen & Hansen in terms of the scale ultrastructure. Our unpublished data on 15 strains from 12 water bodies of four provinces of Viet Nam, using the ITS rDNA marker, indicate that only S. longitubularis was found in water bodies of Viet Nam; however, more research is needed on the distribution of this taxon. Since S. longitubularis is morphologically indistinguishable from S. curtispina, a correct analysis of the previous finds in the tropics is not possible. It can only be noted that this morphotype was found in almost all studied tropical countries.
S. mammillosa E.Takahashi (Figure 5K).
This species was found in 10 localities in six provinces: PQ, LD, QB, BD, PY, TTH. Parameters: pH 4.6–7.4 (6.4 ± 0.3), specific conductance 16–1200 (167 ± 121) µS cm−1, temperature 17–34 (25 ± 2) °C.
It is considered a widespread species [1]. It was found in the tropics in Brazil [28,40,42], China [15], Madagascar [25], Nigeria [19,20], Ecuador [35], Colombia [38], and Indonesia [23].
S. papillosa Kapustin, Gusev & Siver (Figure 5L).
This species was described from Viet Nam [118] and was found in 45 localities in 10 provinces: PQ, CD, DN, KH, BT, DL, BD, PY, QT, TTH.
Parameters: pH 4.6–8.0 (6.2 ± 0.1), specific conductance 10–3000 (187 ± 76) µS cm−1, temperature 24–39 (31 ± 1) °C.
Synura papillosa is quite widespread and is found both in warm climates and in temperate regions of North America [118].
S. petersenii Korshikov sensu lato (Figure 5M,N).
It was found in nine localities in four provinces: DN, LD, KH, BT.
Parameters: pH 5.7–7.6 (6.6 ± 0.2), specific conductance 14–740 (205 ± 96) µS cm−1, temperature 20–32 (27 ± 1) °C.
Synura petersenii is a complex of closely related cryptic and pseudocryptic taxa that requires molecular methods for correct identification [4,5,8,119,120]. Therefore, the correct identification of the scales found in Viet Nam is impossible. In the tropical region, they were noted in most of the countries studied, but since it is not possible to correctly identify them, a detailed distribution analysis is not given here.
S. sphagnicola (Korshikov) Korshikov (Figure 5O).
This species was found in 12 localities in four provinces: PQ, LD, QT, TTH.
Parameters: pH 4.7–7.3 (6.3 ± 0.3), specific conductance 9–66 (38 ± 5) µS cm−1, temperature 24–37 (33 ± 1) °C.
Synura sphagnicola is a widespread taxon that prefers acidic conditions [1]. In the tropics, this species was found in Malaysia [12], China [15], Nigeria [19,20], Brazil [41,42,85], and Ecuador [35].

4. Discussion

Our investigations of algae from the order Synurales have revealed an exceptionally high diversity in Viet Nam. There are now 67 Mallomonas taxa and 7 Synura taxa that have been reported from Viet Nam. Among them, 21 species of the genus Mallomonas [45,57,59,60,68,74,75,76,79,86,87,88,99,102,106,111,112,117] and one species of the genus Synura were described from Vietnam [118]. Moreover, 18 unidentified morphotypes of Mallomonas scales and one of Synura have also been reported in freshwaters of the country [43,46,48,50,51,52]. All of these taxa are presumably new species for science, which require more detailed morphological and molecular studies for description. The number of described new species of the genus Mallomonas from Viet Nam is approximately 10% of the known species of the genus. About one-third of the known species of this genus have now been found in Viet Nam. Many Mallomonas species found in the country are known only from Viet Nam or have a limited distribution in Southeast Asia.
Among the synuralean algae found in Vietnam, cosmopolitan and widespread species accounted for one third of the total number of taxa while species restricted to tropical and subtropical latitudes accounted for more than half (Figure 6).
This taxonomic diversity of synuralean algae (74 taxa) exceeds values for other studied tropical countries. For example, 55 taxa of synuralean algae in the Asian tropics were recorded in subtropical and tropical areas of China [15,16], 38 were found in Indonesia [22,23,24,121], 37 in Malaysia [12,13], 35 in India [17,18], 14 in Sri Lanka [14], and 11 in Bangladesh [11]. In other tropical areas, quite high diversity has been recorded in Madagascar—29 taxa of synuralean algae [25]. In other tropical countries, the number of recorded taxa was lower than 20.
The highest taxonomic diversity of synuralean algae in our studies was observed in natural water bodies, most of which were located in protected areas with reduced anthropogenic impact [43,48,49,51]. Most endemic and rare species were found in such habitats. Most eutrophic and hypereutrophic artificial water bodies (reservoirs and ponds) have a reduced number of synuralean species [43,48]. Most of the territory of Viet Nam is under serious anthropogenic pressure, especially lowland areas [122,123,124]. Additional efforts are needed for the development of protected natural areas. They should include entire landscape complexes of unique terrestrial and aquatic habitats. Algae of the order Synurales can be good marker taxa for identifying such unique aquatic ecosystems.

Author Contributions

E.G., supervision, sampling, writing and drafting of the manuscript, identification; N.M., sample preparation, editing of the manuscript; N.S., sample preparation, editing of the manuscript, measurements; P.T.H., sampling, measurements, editing of the manuscript; T.D.D., sampling, writing and drafting of the manuscript; N.T.H.T., sampling, writing and drafting of the manuscript. All authors contributed to the drafts and gave final approval for publication. All authors have read and agreed to the published version of the manuscript.

Funding

Financial support was provided by the Russian Science Foundation (20-14-00211) for the sample processing, microscopy, and identification. Analysis of environmental parameters was performed within the state assignment of Ministry of Science and Higher Education of the Russian Federation (themes No. 122042700045-3 and AAAA-A18-118042490059-5).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

The authors are grateful to the staff members of the Joint Vietnam–Russia Tropical Science and Technology Research Center for their assistance in management and sampling. We also thank the anonymous reviewers for their helpful comments.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Kristiansen, J.; Preisig, H.R. Chrysophyta and Haptophyta Algae, 2nd part: Synurophyceae. In Süsswasserflora Von Mitteleuropa (Freshwater Flora of Central Europe); Büdel, B., Gärtner, G., Krienitz, L., Preisig, H.R., Schagerl, M., Eds.; Spektrum Akademisher Verlag, Springer: Berlin, Germany, 2007; pp. 1–252. ISBN 978-3-8274-1701-5. [Google Scholar]
  2. Kristiansen, J.; Škaloud, P. Chrysophyta. In Handbook of the Protists, 2nd ed.; Archibald, J.M., Simpson, A.G.B., Slamovits, C.H., Eds.; Springer International Publishing: Cham, Switzerland, 2017; pp. 331–366. [Google Scholar] [CrossRef]
  3. Guiry, M.D.; Guiry, G.M. AlgaeBase. World-Wide Electronic Publication, National University of Ireland, Galway. Available online: https://www.algaebase.org (accessed on 6 December 2022).
  4. Škaloud, P.; Škaloudová, M.; Jadrná, I.; Bestová, H.; Pusztai, M.; Kapustin, D.; Siver, P.A. Comparing morphological and molecular estimates of species diversity in the freshwater genus Synura (Stramenopiles): A model for understanding diversity of eukaryotic microorganisms. J. Phycol. 2020, 56, 574–591. [Google Scholar] [CrossRef]
  5. Škaloud, P.; Kristiansen, J.; Škaloudová, M. Developments in The Taxonomy of Silica-Scaled Chrysophytes—From Morphological and Ultrastructural to Molecular Approaches. Nord. J. Bot. 2013, 31, 385–402. [Google Scholar] [CrossRef]
  6. Jo, B.Y.; Shin, W.; Boo, S.M.; Kim, H.S.; Siver, P.A. Studies on Ultrastructure and Three-Gene Phylogeny of the Genus Mallomonas (Synurophyceae). J. Phycol. 2011, 47, 415–425. [Google Scholar] [CrossRef] [PubMed]
  7. Jo, B.Y.; Shin, W.; Kim, H.S.; Siver, P.A.; Andersen, R.A. Phylogeny of the Genus Mallomonas (Synurophyceae) and Descriptions of Five New Species on the Basis of Morphological Evidence. Phycologia 2013, 52, 266–278. [Google Scholar] [CrossRef] [Green Version]
  8. Jo, B.Y.; Kim, J.I.; Škaloud, P.; Siver, P.A.; Shin, W. Multigene Phylogeny of Synura (Synurophyceae) and Descriptions of Four New Species Based on Morphological and DNA Evidence. Eur. J. Phycol. 2016, 51, 413–430. [Google Scholar] [CrossRef] [Green Version]
  9. Siver, P.A.; Jo, B.Y.; Kim, J.I.; Shin, W.; Lott, A.M.; Wolfe, A.P. Assessing the Evolutionary History of The Class Synurophyceae (Heterokonta) Using Molecular, Morphometric, and Paleobiological Approaches. Am. J. Bot. 2015, 102, 921–941. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  10. Čertnerová, D.; Čertner, M.; Škaloud, P. Molecular Phylogeny and Evolution of Phenotype in Silica-Scaled Chrysophyte Genus Mallomonas. J. Phycol. 2019, 55, 912–923. [Google Scholar] [CrossRef] [PubMed]
  11. Takahashi, E.; Hayakawa, T. The Synuraceae (Chrysophyceae) in Bangladesh. Phykos 1979, 18, 129–147. [Google Scholar]
  12. Dürrschmidt, M.; Croome, R. Mallomonadaceae (Chrysophyceae) from Malaysia and Australia. Nord. J. Bot. 1985, 5, 285–298. [Google Scholar] [CrossRef]
  13. Neustupa, J.; Řezáčová, M. The genus Mallomonas (Mallomonadales, Synurophyceae) in Several Southeast Asian Urban Water Bodies—The Biogeographical Implications. Nova Hedwig. 2007, 84, 249–259. [Google Scholar] [CrossRef]
  14. Dürrschmidt, M.; Cronberg, G. Contribution to The Knowledge of Tropical Chrysophytes: Mallomonadaceae and Paraphysomonadaceae from Sri Lanka. Algol. Stud. 1989, 54, 15–37. [Google Scholar]
  15. Wei, Y.X.; Yuan, X.P. Studies on Silica-Scaled Chrysophytes from the Tropics and Subtropics of China. Nova Hedwig. 2001, 122, 169–187. [Google Scholar]
  16. Wei, Y.X.; Yuan, X.P.; Kristiansen, J. Silica-Scaled Chrysophytes from Hainan, Guangdong Provinces and Hong Kong Special Administrative Region, China. Nord. J. Bot. 2014, 32, 881–896. [Google Scholar] [CrossRef]
  17. Saha, L.C.; Wujek, D.E. Scale-bearing Chrysophytes from Tropical Northeast India. Nord. J. Bot. 1990, 10, 343–355. [Google Scholar] [CrossRef]
  18. Wujek, D.E.; Saha, L.C. Scale-Bearing Chrysophytes (Chrysophyceae and Synurophyceae) from India. II. Nova Hedwig. 1996, 112, 367–377. [Google Scholar]
  19. Wujek, D.E.; Adesalut, A.; Nwankwo, D.I. Silica scaled Chrysophyceae and Synurophyceae (Chrysophyta) from Nigeria. II. Lake Lekki. Trop. Freshwat. Biol. 2003, 12, 99–103. [Google Scholar] [CrossRef]
  20. Wujek, D.E.; Kadiri, M.O.; Dziedzic, R.M. Silica-scaled Chrysophyceae and Synurophyceae from Nigeria. III. Chrysophytes from rivers of Edo State. Fottea 2010, 10, 93–98. [Google Scholar] [CrossRef]
  21. Vyverman, W.; Cronberg, G. Scale Bearing Chrysophytes from Papua New Guinea. Nord. J. Bot. 1993, 13, 111–120. [Google Scholar] [CrossRef]
  22. Kapustin, D.A.; Gusev, E.S. Silica-Scaled Chrysophytes from West Java (Indonesia) Including Description of a New Chrysosphaerella Species. Nova Hedwig. 2019, 148, 11–20. [Google Scholar] [CrossRef]
  23. Gusev, E.; Kapustin, D.; Martynenko, N.; Kulikovskiy, M. Diversity of Silica-Scaled Chrysophytes (Stramenopiles: Chrysophyceae) from Indonesian Papua. Diversity 2022, 14, 726. [Google Scholar] [CrossRef]
  24. Cronberg, G.; Hickel, B. Mallomonas fenestrata sp. nov. and M. perforata sp. nov. (Chrysophyceae, Mallomonadaceae) from Tropical Lakes. Nord. J. Bot. 1985, 5, 105–110. [Google Scholar] [CrossRef]
  25. Hansen, P. Silica-scaled Chrysophyceae and Synurophyceae from Madagascar. Arch. Protistenkd. 1996, 147, 145–172. [Google Scholar] [CrossRef]
  26. Wujek, D.E.; Asmund, B. Mallomonas cyathellata sp. nov. and Mallomonas cyathellata var. kenyana var. nov. (Chrysophyceae) studied by means of scanning and transmission electron microscopy. Phycologia 1979, 18, 115–119. [Google Scholar] [CrossRef]
  27. Compère, P. Mallomonas bronchartiana, Chrysophycée nouvelle du lac Tchad. Bull. Jard. Bot. Nat. Belg. Bull. Nat. Plantentuin Belg. 1974, 44, 61–63. [Google Scholar] [CrossRef]
  28. Cronberg, G. Scaled Chrysophytes from the Tropics. Nova Hedwig. 1989, 95, 191–232. [Google Scholar]
  29. Piątek, J. Mallomonas camerunensis sp. nov. (Chrysophyceae, Stramenopiles) from a shallow puddle in the Guineo Congolian rainforest (Cameroon). Pol. Bot. J. 2015, 60, 119–126. [Google Scholar] [CrossRef] [Green Version]
  30. Piątek, J.; Łukaszek, M. Mallomonas cronbergiae (Chrysophyceae, Stramenopiles), a new species from the Guineo-Congolian rainforest in Cameroon. Pol. Bot. J. 2016, 61, 199–204. [Google Scholar] [CrossRef] [Green Version]
  31. Němcová, Y.; Bulant, P.; Kristiansen, J. Mallomonas solea-ferrea and Mallomonas siveri (Stramenopiles): Two new taxa from the Western Cape (South Africa). Nova Hedwig. 2011, 93, 375–384. [Google Scholar] [CrossRef]
  32. Němcová, Y.; Kreidlová, J. Two new species of Mallomonas (Chrysophyceae: Synurales): Mallomonas temonis and Mallomonas divida. Phytotaxa 2013, 87, 11–18. [Google Scholar] [CrossRef] [Green Version]
  33. Vuuren, S.J.; Levanets, A.; Kapustin, D.; Swanepoel, A. Morphology, ecology and geographic distribution of three Mallomonas (Phylum Ochrophyta) species from the Vaal River, South Africa. S. Afr. J. Bot. 2022, 149, 160–169. [Google Scholar] [CrossRef]
  34. Wujek, D.E. Scale bearing Chrysophyceae (Mallomonadaceae) from North-Central Costa Rica. Brenesia 1984, 22, 309–313. [Google Scholar]
  35. Wujek, D.E.; Dziedic, R.M. Silica-scaled Chrysophytes from Ecuador. Gayana Bot. 2005, 62, 1–8. [Google Scholar] [CrossRef] [Green Version]
  36. Wujek, D.E. Scale bearing Chrysophyceae from the Panama Canal. Jpn. J. Phycol. 1986, 34, 83–86. [Google Scholar]
  37. Carty, S.; Wujek, D.E. A new species of Peridinium and new records of dinoflagellates and silica-scaled chrysophytes from Belize. Caribbean J. Sci. 2003, 39, 136–139. [Google Scholar]
  38. Vigna, M.S.; Duque, S.R.; Nunez-Avellaneda, M. Tropical silica-scaled chrysophyte flora (Chrysophyceae and Synurophyceae) from Colombia. Nova Hedwig. 2005, 128, 151–166. [Google Scholar]
  39. Franceschini, I.M.; Couté, A. Quelques Chrysophycées (Algae, Chromophyta) à écailles siliceuses de l’extrême sud-est du Brésil. Algol. Stud. Arch. Hydrobiol. 1991, 62, 31–45. [Google Scholar]
  40. Kristiansen, J.; Menezes, M. Silica-scaled Chrysophytes from an Amazonian flood-plain lake, Mussurá Lake, northern Brazil. Algol. Stud. Arch. Hydrobiol. 1998, 90, 97–118. [Google Scholar] [CrossRef]
  41. Couté, A.; Franceschini, I.M. Scale-Bearing Chrysophytes from Acid Water of Florianopolis, Santa Catarina Island, South Brazil. Algol. Stud. 1998, 88, 37–61. [Google Scholar] [CrossRef]
  42. Franceschini, I.M.; Kristiansen, J.M. New records of scale-bearing chrysophytes for Florianópolis, Santa Catarina Island, Southern Brazil. Algol. Stud. Arch. Hydrobiol. 2004, 111, 63–77. [Google Scholar] [CrossRef]
  43. Gusev, E.; Martynenko, N.; Tran, H. Studies on Algae from the Order Synurales (Chrysophyceae) in Northern Vietnam. Diversity 2021, 13, 602. [Google Scholar] [CrossRef]
  44. Gusev, E.S.; Nguyen, T.H.T. Silica-Scaled Chrysophytes (Chrysophyceae and Synurophyceae) from Vietnam (Khanh Hoa and Quang Nam provinces). Nova Hedwig. 2011, 93, 191–199. [Google Scholar] [CrossRef]
  45. Gusev, E.S. Studies on Synurophycean Algae from Mangrove Wetlands (Vietnam). Nova Hedwig. 2013, 142, 87–95. [Google Scholar]
  46. Gusev, E.S.; Doan-Nhu, H.; Nguyen-Ngoc, L.; Guseva, E.E.; Phan Tan, L. Silica-Scaled Chrysophytes from Cam Ranh Peninsula (Khanh Hoa Province, Vietnam). Nova Hedwig. 2019, 148, 63–76. [Google Scholar] [CrossRef]
  47. Doan-Nhu, H.; Thi-Tinh, T.; Gusev, E.; Kulikovskiy, M.; Phan-Tan, L.; Nguyen-Ngoc, L. Taxonomic Composition of Silica-Scaled Chrysophytes in a Tropical Mountain Reservoir. Inland Wat. Biol. 2021, 14, 490–499. [Google Scholar] [CrossRef]
  48. Gusev, E.; Martynenko, N. Diversity of Silica-Scaled Chrysophytes in Central Vietnam. Water 2022, 14, 65. [Google Scholar] [CrossRef]
  49. Gusev, E.S.; Doan-Nhu, H.; Nguyen-Ngoc, L. Silica-Scaled Chrysophytes from Cat Tien National Park (Dong Nai Province, Vietnam). Nova Hedwig. 2017, 105, 347–364. [Google Scholar] [CrossRef]
  50. Gusev, E.S.; Gusakov, V.A.; Guseva, E.E.; Kulikovskiy, M.S.; Tsvetkov, A.I.; Dịnh, C.N. Flora of Silica-Scaled Chrysophytes (Chrysophyceae: Synurales, Paraphysomonadales) of the Mekong Delta. Inland Wat. Biol. 2020, 13, 349–357. [Google Scholar] [CrossRef]
  51. Gusev, E.S.; Guseva, E.E.; Dien, T.D.; Kulikovskiy, M.S. Flora of Silica-Scaled Chrysophytes (Chrysophyceae) of Two Provinces in Southern Viet Nam. Inland Wat. Biol. 2022, 15, 205–216. [Google Scholar] [CrossRef]
  52. Gusev, E.; Martynenko, N.; Kapustin, D.; Doan-Nhu, H.; Nguyen-Ngoc, L. Diversity of Silica-Scaled Chrysophytes of Two Tropical Islands: Phu Quoc and Con Son (Viet Nam). Life 2022, 12, 1611. [Google Scholar] [CrossRef]
  53. Řezáčová, M.; Škaloud, P. A contribution to the knowledge of the silica-scaled chrysophytes in eastern Hungary. Czech Phycol. 2004, 4, 67–73. [Google Scholar]
  54. Calado, A.J.; Craveiro, S.C. Notes on the ecology of Synurophycean algae found in Portugal. Nord. J. Bot. 1995, 15, 641–654. [Google Scholar] [CrossRef]
  55. Siver, P.A. Two new taxa in the Section Papillosae of the genus Mallomonas (Synurophyceae) from the Ocala National Forest, Florida, USA. Nord. J. Bot. 2002, 22, 123–128. [Google Scholar] [CrossRef]
  56. Siver, P.A.; Lott, A.M. The Scaled Chrysophyte Flora from the Pinelands National Preserve of Southern New Jersey, U.S.A. Nova Hedwig. 2010, 136, 167–180. [Google Scholar] [CrossRef]
  57. Gusev, E.S.; Siver, P.A.; Shin, W. Mallomonas bronchartiana Compère Revisited: Two New Species Described from Asia. Cryptogam. Algol. 2017, 38, 3–16. [Google Scholar] [CrossRef]
  58. Cronberg, G. Scaled chrysophytes from the Okavango Delta, Botswana, Africa. Nova Hedwig. 1996, 114, 91–108. [Google Scholar]
  59. Gusev, E.S.; Doan-Nhu, H.; Nguyen-Ngoc, L. Mallomonas cattiensis sp. nov. (Synurales, Chrysophyceae), a New Species from Viet Nam. Phytotaxa 2015, 221, 188–192. [Google Scholar] [CrossRef]
  60. Gusev, E.S.; Kulikovskiy, M.S. Two new species of genus Mallomonas from swamp localities in Vietnam. Phytotaxa 2020, 468, 121–129. [Google Scholar] [CrossRef]
  61. Siver, P.A.; Voloshko, L.N.; Gavrilova, O.V.; Getsen, M.V. The scaled chrysophyte flora of the Bolshezemelskaya tundra (Russia). Nova Hedwig. 2005, 128, 125–150. [Google Scholar]
  62. Siver, P.A.; Skogstad, A. Morphological variation and ecology of Mallomonas crassisquama (Chrysophyceae). Nord. J. Bot. 1988, 8, 99–107. [Google Scholar] [CrossRef]
  63. Bessudova, A.Y.; Tomberg, I.V.; Firsova, A.D.; Kopyrina, L.I.; Likhoshway, Y.V. Silica-scaled chrysophytes in lakes Labynkyr and Vorota of the Sakha (Yakutia) Republic, Russia. Nova Hedwig. 2019, 148, 35–48. [Google Scholar] [CrossRef]
  64. Dürrschmidt, M. Mallomonas cristata sp. nov. (Chrysophyceae, Synuraceae) from South Chilean Inland Waters. Phycologia 1981, 20, 298–302. [Google Scholar] [CrossRef]
  65. Asmund, B.; Kristiansen, J. The Genus Mallomonas (Chrysophyceae). A Taxonomic Survey Based on The Ultrastructure of Silica Scales and Bristles. Opera Bot. 1986, 85, 1–128. [Google Scholar]
  66. Němcová, Y.; Rott, E. Diversity of Silica-Scaled Chrysophytes in High-Altitude Alpine Sites (North Tyrol, Austria) Including a Description of Mallomonas pechlaneri sp. nov. Cryptogam. Algol. 2018, 39, 63–83. [Google Scholar] [CrossRef]
  67. Gusev, E.; Němcová, Y.; Kulikovskiy, M. Mallomonas voloshkoae sp. nov. (Synurales, Chrysophyceae) and distribution of M. pechlaneri in mountain lakes of Siberia. Phytotaxa 2022, 530, 221–229. [Google Scholar] [CrossRef]
  68. Gusev, E.S.; Doan-Nhu, H.; Nguyen-Ngoc, L.; Kapustin, D.A. Two New Species of the Genus Mallomonas from the Cat Tien National Park (Viet Nam): Mallomonas distinguenda and Mallomonas skvortsovii. Phytotaxa 2016, 273, 59–64. [Google Scholar] [CrossRef]
  69. Kim, H.S.; Kim, J.H.; Shin, W.; Jo, B.Y. Mallomonas elevata sp. nov. (Synurophyceae), a new scaled Chrysophyte from Jeju Island, South Korea. Nova Hedwig. 2014, 98, 89–102. [Google Scholar] [CrossRef]
  70. Asmund, B. Electron microscope observations on Mallomonas species and remarks on their occurrence in some Danish ponds and lakes. III. Dan. Bot. Ark. 1959, 18, 1–50. [Google Scholar]
  71. Kristiansen, J. Cosmopolitan chrysophytes. Syst. Geog. Plants 2000, 70, 291–300. [Google Scholar] [CrossRef]
  72. Nicholls, K.H. Four new Mallomonas species of the Torquatae series (Chrysophyceae). Canadian J. Bot. 1984, 62, 1583–1591. [Google Scholar] [CrossRef]
  73. Kim, J.; Hee Park, Y.; Jung Kim, H. Silica-Scaled Chrysophytes (Synurophyceae) from Jeju Island, Korea. Nova Hedwig. 2009, 89, 201–218. [Google Scholar] [CrossRef]
  74. Gusev, E.S. A new species of the genus Mallomonas (Synurales, Chrysophyceae), Mallomonas fimbriata, sp. nov. Phytotaxa 2015, 195, 291–296. [Google Scholar] [CrossRef]
  75. Gusev, E.; Kapustin, D.; Skurina, N.; Martynenko, N.; Phan Trong, H. Mallomonas fragariformis sp. nov. (Synurales, Chrysophyceae), a new tropical chrysophyte species. Phytotaxa 2022, 576, 123–130. [Google Scholar] [CrossRef]
  76. Gusev, E.S.; Čertnerová, D.; Škaloudová, M.; Škaloud, P. Exploring Cryptic Diversity and Distribution Patterns in the Mallomonas kalinae/rasilis Species Complex with a Description of a New Taxon—Mallomonas furtiva sp. nov. J. Eukaryot. Microbiol. 2018, 65, 38–47. [Google Scholar] [CrossRef] [PubMed]
  77. Takahashi, E. Studies on genera Mallomonas, Synura and other plankton in fresh-water with electron microscope. IV. On two new species of Mallomonas found in ditches at Tsuruoka in North-East of Japan. Bull. Yamagata Univ. Agric. Sci. 1963, 4, 169. [Google Scholar]
  78. Kim, J.H.; Kim, H.S. Seasonal occurrence of silica-scaled chrysophytes in a small eutrophic swamp, South Korea. Nova Hedwig. 2011, 93, 411–436. [Google Scholar] [CrossRef]
  79. Gusev, E.S.; Kapustin, D.A.; Martynenko, N.A.; Guseva, E.E.; Kulikovskiy, M.S. Mallomonas gusakovii sp. nov. (Chrysophyceae, Synurales), a New Species from Phu Quoc Island, Vietnam. Phytotaxa 2019, 406, 199–205. [Google Scholar] [CrossRef]
  80. Nicholls, K.H. Descriptions of four new Mallomonas taxa (Mallomonadaceae, Chrysophyceae). J. Phycol. 1989, 25, 292–300. [Google Scholar] [CrossRef]
  81. Wei, Y.X.; Kristiansen, J. Studies on silica-scaled chrysophytes from Fujian Province, China. Chin. J. Ocean. Limnol. 1998, 16, 256–266. [Google Scholar] [CrossRef]
  82. Takahashi, E. Studies on Genera Mallomonas and Synura, and Other Plankton in Fresh Water with the Electron Microscope. IX. Mallomonas harrisae sp. nov. (Chrysophyceae). Phycologia 1975, 14, 41–44. [Google Scholar] [CrossRef]
  83. Wei, Y.-X.; Yuan, X.-P. Studies on Silica-Scaled Chrysophytes from Zhejiang, Jiangsu and Jiangxi Provinces, China. Nova Hedwig. 2013, 142, 163–179. [Google Scholar]
  84. Franceschini, I.M.; Couté, A.; Silva, A.J. Synurophyceae et Chrysophyceae à écailles siliceuses du rio dos Sinos, RS, Brésil. Algol. Stud. 1996, 80, 59–85. [Google Scholar]
  85. Wujek, D.E. Chrysophyceae (Mallomonadaceae) from Florida. Fla. Sci. 1984, 3, 160–170. [Google Scholar]
  86. Gusev, E.; Kulizin, P.; Guseva, E.; Shkurina, N.; Kulikovskiy, M. Mallomonas lamii sp. nov. (Synurales, Chrysophyceae), a New Species Bearing Large Scales Described from the Tropics. Phytotaxa 2019, 423, 266–272. [Google Scholar] [CrossRef]
  87. Gusev, E.; Shkurina, N.; Kulikovskiy, M. Mallomonas loricata sp. nov. (Synurales, Chrysophyceae), a New Tropical Species from Section Plantae. Phytotaxa 2021, 500, 225–233. [Google Scholar] [CrossRef]
  88. Gusev, E.; Kezlya, E. Mallomonas lusca sp. nov.—A rare species from Southeast Asia. Phytotaxa 2021, 529, 105–112. [Google Scholar] [CrossRef]
  89. Dürrschmidt, M. A Taxonomic Study of the Mallomonas mangofera Group (Mallomonadaceae, Chrysophyceae), Including the Description of four New Taxa. Plant Syst. Evol. 1983, 143, 175–196. [Google Scholar] [CrossRef]
  90. Harris, K.; Bradley, D.E. A taxonomic study of Mallomonas. J. Gen. Micr. 1960, 22, 750–777. [Google Scholar] [CrossRef] [Green Version]
  91. Péterfi, L.S.; Momeu, L.; Padisák, J.; Varga, V. Silica-scaled chrysophytes from permanent and temporary waters of Hortobágy, eastern Hungary. Hydrobiologia 1998, 369, 339–351. [Google Scholar] [CrossRef]
  92. Škaloud, P.; Škaloudová, M.; Pichrtová, M.; Němcová, Y.; Kreidlová, J.; Pusztai, M. www.chrysophytes.eu—A Database on Distribution and Ecology of Silica-Scaled Chrysophytes in Europe. Nova Hedwig. 2013, 142, 141–146. [Google Scholar]
  93. Wei, Y.X.; Yuan, X.P. Studies on silica-scaled chrysophytes from the Daxinganling Mountains and Wudalianchi Lake Regions, China. Nova Hedwig. 2015, 101, 299–315. [Google Scholar] [CrossRef]
  94. Kristiansen, J. Silica-scaled chrysophytes from China. Nord. J. Bot. 1989, 8, 539–552. [Google Scholar] [CrossRef]
  95. Wei, Y.X.; Kristiansen, J. Occurrence and Distribution of Silica-scaled Chrysophytes in Zhejiang, Jiangsu, Hubei, Yunnan and Shandong Provinces, China. Arch. Protistenk. 1994, 144, 433–449. [Google Scholar] [CrossRef]
  96. Němcová, Y.; Kreidlová, J.; Kosová, A.; Neustupa, J. Lakes and pools of Aquitaine region (France)—A biodiversity hotspot of Synurales in Europe. Nova Hedwig. 2012, 95, 1–24. [Google Scholar] [CrossRef]
  97. Hansen, A.F.; Johansen, J.E.; Skovgard, A. Floristik undersøgelse af skælbærende gulalger i Dyrehaven. Urt 1993, 17, 13–18. [Google Scholar]
  98. Hällfors, G.; Hällfors, S. Records of Chrysophytes with Siliceous Scales (Mallomonadaceae and Paraphysomonadaceae) from Finnish Inland Waters. In Flagellates in Freshwater Ecosystems; Jones, R., Ilmavirta, V., Eds.; Kluwer Academic Publishers: Dordrecht, The Netherlands; Boston, MA, USA; London, UK, 1988; pp. 1–29. [Google Scholar]
  99. Gusev, E.; Guseva, E.; Kezlya, E.; Kulikovskiy, M. Mallomonas minuscula sp. nov. (Synurales, Chrysophyceae), a new member in the section Torquatae from Vietnam. Fottea 2019, 19, 132–137. [Google Scholar] [CrossRef] [Green Version]
  100. Croome, R.L.; Tyler, P.A. Mallomonas morrisonensis (Chrysophyceae) a New Species from Australia. Br. Phycol. J. 1983, 18, 383–389. [Google Scholar] [CrossRef] [Green Version]
  101. Wujek, D.E.; Bicudo, C.E.M. Scale-bearing chrysophytes from the state of São Paulo, Brazil, 2: Additions to the flora. Braz. J. Bot. 2004, 64, 915–918. [Google Scholar] [CrossRef]
  102. Gusev, E.; Siver, P.A. Mallomonas neoampla sp. nov. from Vietnam, a New Species That Bridges the Gap Between Fossil and Modern Taxa. Nova Hedwig. 2017, 104, 521–528. [Google Scholar] [CrossRef]
  103. Ito, H. Chrysophytes in the southern part of Hyogo prefecture, Japan (I). Chrysophyte flora in three ponds and reservoir. Jpn. J. Phycol. 1990, 38, 327–332. [Google Scholar]
  104. Ito, H. Chrysophytes in the southern part of Hyogo prefecture, Japan (II). Mallomonas. Jpn. J. Phycol. 1991, 39, 253–262. [Google Scholar]
  105. Harris, K.; Bradley, D.E. Some Unusual Chrysophyceae Studied in the Electron Microscope. Microbiology 1958, 18, 71–83. [Google Scholar] [CrossRef] [Green Version]
  106. Gusev, E.S. A new species in genus Mallomonas Perty (Synurales, Chrysophyceae) from Vietnam. Int. J. Algae 2015, 17, 351–362. [Google Scholar] [CrossRef]
  107. Compère, P. Mallomonas portae-ferreae: Peterfi & Asmund (Chrysophycée) au lac Tchad. Bull. Jard. Bot. Nat. Belg. Bull. Nat. Plantentuin Belg. 1973, 43, 236–237. [Google Scholar] [CrossRef]
  108. Siver, P.A. The Biology of Mallomonas: Morphology, Taxonomy and Ecology; Kluwer Academic: Dordrecht, Netherlands, 1991; pp. 1–230. [Google Scholar] [CrossRef]
  109. Siver, P.A.; Lott, A.M. Further observations on the scaled Chrysophycean and Synurophycean flora of the Ocala National Forest, Florida, USA. Nord. J. Bot. 2006, 24, 211–233. [Google Scholar] [CrossRef]
  110. Siver, P.A.; Lott, A.M. Do Scaled Chrysophytes Have a Biogeography? Evidence from the East Coast of North America. Freshw. Biol. 2012, 57, 451–467. [Google Scholar] [CrossRef]
  111. Gusev, E.; Kulikovskiy, M. Mallomonas siderea sp. nov. (Synurales, Chrysophyceae), a New Tropical Species from the Section Torquatae. Nova Hedwig. 2021, 113, 291–301. [Google Scholar] [CrossRef]
  112. Gusev, E.S. A New Species of the Genus Mallomonas (Synurophyceae), Mallomonas spinosa sp. nov., from Vietnam. Phytotaxa 2012, 66, 1–5. [Google Scholar] [CrossRef]
  113. Croome, R.; Diirrschmidt, M.; Tyler, P.A. Light and Electron Microscopical Investigation of Mallomonas splendens (G.S. West) Playfair (Mallomonadaceae, Chrysophyceae). Nova Hedwig. 1985, 41, 463–470. [Google Scholar]
  114. Kristiansen, J. The genus Mallomonas (Synurophyceae): A taxonomic survey based on the ultrastructure of silica scales and bristles. Opera Bot. 2002, 139, 1–218. [Google Scholar]
  115. Neustupa, J.; Němcová, Y. A geometric morphometric study of the variation in scales of Mallomonas striata (Synurophyceae, Heterokontophyta). Phycologia 2007, 46, 123–130. [Google Scholar] [CrossRef] [Green Version]
  116. Gusev, E.; Martynenko, N. Silica-Scaled Chrysophytes of Teletskoye Lake and Adjacent Area with a Description of a New Species from the Genus Mallomonas. Diversity 2022, 14, 1040. [Google Scholar] [CrossRef]
  117. Gusev, E.; Kezlya, E.; Tran, H.; Kulikovskiy, M. Mallomonas vietnamica sp. nov. (Synurales, Chrysophyceae), a New Species, That Shares Some Features with Fossil Taxa. Cryptogam. Algol. 2021, 42, 39–46. [Google Scholar] [CrossRef]
  118. Siver, P.A.; Kapustin, D.; Gusev, E. Investigations of two-celled colonies of Synura formerly described as Chrysodidymus with descriptions of two new species. Eur. J. Phycol. 2018, 53, 245–255. [Google Scholar] [CrossRef]
  119. Škaloud, P.; Kynčlová, A.; Benada, O.; Kofroňová, O.; Škaloudová, M. Toward a Revision of the Genus Synura, Section Petersenianae (Synurophyceae, Heterokontophyta): Morphological Characterization of Six Pseudo-Cryptic Species. Phycologia 2012, 51, 303–329. [Google Scholar] [CrossRef]
  120. Škaloud, P.; Škaloudová, M.; Procházková, A.; Němcová, Y. Morphological Delineation and Distribution Patterns of Four Newly Described Species within the Synura petersenii Species Complex (Chrysophyceae, Stramenopiles). Eur. J. Phycol. 2014, 49, 213–229. [Google Scholar] [CrossRef]
  121. Vyverman, W. A systematic account of the algal flora of the seasonal swamps in the southern part of Irian Jaya (Indonesia). In Recent Trends in Algal Taxonomy; Vidyavati Mahato, A.K., Ed.; Associated Publishing Co.: New Delhi, India, 2006; Volume 2, pp. 3–19. [Google Scholar]
  122. Le, T.P.Q.; Ho, T.C.; Duong, T.T.; Nguyen, T.B.N.; Vu, D.A.; Pham, Q.L.; Seidler, C. Water quality of the Red River system in the period 2012–2013. J. Vietnam. Environ. 2014, 6, 191–195. [Google Scholar] [CrossRef]
  123. Hoang, T.T.H.; Nguyen, T.K.; Le, P.Q.; Dang, D.K.; Duong, T.T. Assessment of the water quality downstream of Red River in 2015 (Vietnam). J. Vietnam. Environ. 2015, 8, 167–172. [Google Scholar] [CrossRef]
  124. Petrisor, A.; Hamma, W.; Nguyen, H.D.; Randazzo, G.; Muzirafuti, A.; Stan, M.; Tran, V.T.; Astefănoaiei, R.; Bui, Q.; Drago, V.D.; et al. Degradation of Coastlines under the Pressure of Urbanization and Tourism: Evidence on the Change of Land Systems from Europe, Asia and Africa. Land 2020, 9, 275. [Google Scholar] [CrossRef]
Figure 1. Geographical position of the studied area.
Figure 1. Geographical position of the studied area.
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Figure 2. Scales of Mallomonas (A) M. acaroides. (B) M. adamas. (C) M. akrokomos. (D) M. bangladeshica. (E) M. binocularis. (F) M. bronchartiana. (G) M. cattiensis. (H) M. caudata. (I) M. ceylanica. (J) M.collucata. (K) M. crassisquama. (L) M. crassisquama var. papillosa. (M) M. cf. cristata. (N) M. distinguenda. (O) M. elevata [48]. (P) M. elongata. (Q) M. favosa f. favosa. (R) M. favosa f. gemina. (S) M. fimbriata. (T) M. fragariformis. Scale bars: (F,P): 5 μm; (A,C,DE,HI,K,MN,QT): 2 μm; (B,G,J,L,O,S): 1 μm. TEM: (A,C,DE,HK,MT); SEM: (B,F,G,L).
Figure 2. Scales of Mallomonas (A) M. acaroides. (B) M. adamas. (C) M. akrokomos. (D) M. bangladeshica. (E) M. binocularis. (F) M. bronchartiana. (G) M. cattiensis. (H) M. caudata. (I) M. ceylanica. (J) M.collucata. (K) M. crassisquama. (L) M. crassisquama var. papillosa. (M) M. cf. cristata. (N) M. distinguenda. (O) M. elevata [48]. (P) M. elongata. (Q) M. favosa f. favosa. (R) M. favosa f. gemina. (S) M. fimbriata. (T) M. fragariformis. Scale bars: (F,P): 5 μm; (A,C,DE,HI,K,MN,QT): 2 μm; (B,G,J,L,O,S): 1 μm. TEM: (A,C,DE,HK,MT); SEM: (B,F,G,L).
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Figure 3. Scales of Mallomonas. (A) M. furtiva. (B) M. grata. (C) M. gusakovii. (D) M. guttata var. guttata. (E) M. guttata var. simplex. (F) M. harrisiae. (G) M. hexareticulata. (H) M. kenyana. (I) M. korshikovii. (J) M. lamii. (K) M. loricata. (L) M. lusca. (M) M. mangofera var. mangofera. (N) M. mangofera var. foveata. (O) M. cf. mangofera var. reticulata. (P) M. mangofera var. sulcata. (Q) M. cf. mangofera var. gracilis. (R) M. matvienkoae var. siveri. (S) M. minuscula. (T) M. morrisonensis. Scale bars: (CF,HO,R,T): 2 μm; (A,B,G,P,Q,S): 1 μm. TEM: (A,CF,HT); SEM: (B,G).
Figure 3. Scales of Mallomonas. (A) M. furtiva. (B) M. grata. (C) M. gusakovii. (D) M. guttata var. guttata. (E) M. guttata var. simplex. (F) M. harrisiae. (G) M. hexareticulata. (H) M. kenyana. (I) M. korshikovii. (J) M. lamii. (K) M. loricata. (L) M. lusca. (M) M. mangofera var. mangofera. (N) M. mangofera var. foveata. (O) M. cf. mangofera var. reticulata. (P) M. mangofera var. sulcata. (Q) M. cf. mangofera var. gracilis. (R) M. matvienkoae var. siveri. (S) M. minuscula. (T) M. morrisonensis. Scale bars: (CF,HO,R,T): 2 μm; (A,B,G,P,Q,S): 1 μm. TEM: (A,CF,HT); SEM: (B,G).
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Figure 4. Scales of Mallomonas. (A) M. multisetigera. (B) M. neoampla. (C) M. ocellata. (D) M. cf. ouradion. (E) M. papillosa. (F) M. paragrandis. (G) M. parvula [43]. (H) M. peronoides. (I) M. plumosa. (J) M. portae-ferreae. (K) M. pseudobronchartiana. (L) M. pseudomatvienkoae. (M) M. pseudocratis. (N) M. punctifera. (O) M. punctostriata. (P) M. rasilis. (Q) M. siderea. (R) M. skvortsovii. (S) M. sorohexareticulata. (T) M. spinosa. Scale bars: (B): 5 μm; (K): 3 μm; (A,CJ,LN,P,RT): 2 μm; (O,Q,S): 1 μm. TEM: (AJ,LO,Q,R,T); SEM: (K,P,S).
Figure 4. Scales of Mallomonas. (A) M. multisetigera. (B) M. neoampla. (C) M. ocellata. (D) M. cf. ouradion. (E) M. papillosa. (F) M. paragrandis. (G) M. parvula [43]. (H) M. peronoides. (I) M. plumosa. (J) M. portae-ferreae. (K) M. pseudobronchartiana. (L) M. pseudomatvienkoae. (M) M. pseudocratis. (N) M. punctifera. (O) M. punctostriata. (P) M. rasilis. (Q) M. siderea. (R) M. skvortsovii. (S) M. sorohexareticulata. (T) M. spinosa. Scale bars: (B): 5 μm; (K): 3 μm; (A,CJ,LN,P,RT): 2 μm; (O,Q,S): 1 μm. TEM: (AJ,LO,Q,R,T); SEM: (K,P,S).
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Figure 5. Scales of Mallomonas and Synura. (A) M. splendens. (B) M. striata sensu lato [48]. (C) M. striata var. serrata. (D) M. tonsurata. (E) M. tropica. (F) M. velari. (G) M. vietnamica. (H) Synura australiensis. (I) S. echinulata. (J) S. cf. longitubularis. (K) S. mammillosa. (L) S. papillosa. (M,N) S. petersenii sensu lato (S. spp. from S. petersenii complex). (O) S. sphagnicola. Scale bars: (AJ,LO): 2 μm; (K): 1 μm. TEM: (BO); SEM: (A).
Figure 5. Scales of Mallomonas and Synura. (A) M. splendens. (B) M. striata sensu lato [48]. (C) M. striata var. serrata. (D) M. tonsurata. (E) M. tropica. (F) M. velari. (G) M. vietnamica. (H) Synura australiensis. (I) S. echinulata. (J) S. cf. longitubularis. (K) S. mammillosa. (L) S. papillosa. (M,N) S. petersenii sensu lato (S. spp. from S. petersenii complex). (O) S. sphagnicola. Scale bars: (AJ,LO): 2 μm; (K): 1 μm. TEM: (BO); SEM: (A).
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Figure 6. Diagram showing the proportions of taxa with cosmopolitan, widespread, scattered, and tropical and subtropical distributions. Cosmopolitan, widespread taxa were identified based on [1,71], other categories—on the basis of literature analysis.
Figure 6. Diagram showing the proportions of taxa with cosmopolitan, widespread, scattered, and tropical and subtropical distributions. Cosmopolitan, widespread taxa were identified based on [1,71], other categories—on the basis of literature analysis.
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Gusev, E.; Martynenko, N.; Shkurina, N.; Huan, P.T.; Dien, T.D.; Thanh, N.T.H. An Annotated Checklist of Algae from the Order Synurales (Chrysophyceae) of Viet Nam. Diversity 2023, 15, 183. https://doi.org/10.3390/d15020183

AMA Style

Gusev E, Martynenko N, Shkurina N, Huan PT, Dien TD, Thanh NTH. An Annotated Checklist of Algae from the Order Synurales (Chrysophyceae) of Viet Nam. Diversity. 2023; 15(2):183. https://doi.org/10.3390/d15020183

Chicago/Turabian Style

Gusev, Evgeniy, Nikita Martynenko, Nataliya Shkurina, Phan Trong Huan, Tran Duc Dien, and Nguyen Thi Hai Thanh. 2023. "An Annotated Checklist of Algae from the Order Synurales (Chrysophyceae) of Viet Nam" Diversity 15, no. 2: 183. https://doi.org/10.3390/d15020183

APA Style

Gusev, E., Martynenko, N., Shkurina, N., Huan, P. T., Dien, T. D., & Thanh, N. T. H. (2023). An Annotated Checklist of Algae from the Order Synurales (Chrysophyceae) of Viet Nam. Diversity, 15(2), 183. https://doi.org/10.3390/d15020183

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