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Article

Planoplatessa gen. nov.—A New, Neglected Monoraphid Diatom Genus with a Cavum

by
Maxim S. Kulikovskiy
1,*,
Anton M. Glushchenko
1,
Irina V. Kuznetsova
1 and
John Patrick Kociolek
2
1
K.A. Timiryazev Institute of Plant Physiology RAS, IPP RAS, 35 Botanicheskaya St., 127276 Moscow, Russia
2
Museum of Natural History, Henderson Building, 15th and Broadway, Boulder, CO 80309, USA
*
Author to whom correspondence should be addressed.
Plants 2022, 11(17), 2314; https://doi.org/10.3390/plants11172314
Submission received: 7 August 2022 / Revised: 23 August 2022 / Accepted: 31 August 2022 / Published: 3 September 2022
(This article belongs to the Special Issue Integrative Taxonomy of Plants)
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Abstract

:
A new monoraphid diatom genus, Planoplatessa gen. nov., is described on the basis of a detailed morphological investigation using light and scanning electron microscopy. We transferred Achnanthes joursacensis Héribaud, a species described from fossil deposits in France, to our new genus. We investigated material from Mongolia from Recent populations. This taxon is known from fossils to Recent across the Holarctic. Achnanthes joursacensis was previously transferred to the genera Planothidium and Platessa, but the morphology of A. joursacensis does not share all morphological features with these two genera. We discuss important morphological features for the delimitation of monoraphid genera based on careful morphological and molecular investigations we presented previously. Planoplatessa gen. nov. as a genus is characterized by having uniseriate striae on both the raphe and the rapheless valves, a cavum in rapheless valves only, and straight distal raphe ends on the valve face.

1. Introduction

About 16 freshwater monoraphid diatom genera previously associated with the genus Achnanthes J.B.M. Bory de Saint-Vincent 1822 [1] are currently recognized: Achnanthidium Kützing 1844 [2], Eucocconeis P.T. Cleve 1895 [3], Psammothidium Bukhtiyarova & Round 1996 [4], Karayevia Round & Bukhtiyarova 1996 [5], Rossithidium Round & Bukhtiyarova 1996 [5], Lemnicola Round & Basson 1997 [6], Crenotia Wojtal 2013 [7], Trifonovia Kulikovskiy & Lange-Bertalot 2012 [8], Gololobovia Gliwiczia Kulikovskiy, Lange-Bertalot & Witkowski 2013 [9], Skabitschewskia Kulikovskiy & Lange-Bertalot 2015 [10], Platessa Lange-Bertalot 2004 [11], Planothidium Round & Bukhtiyarova 1996, Kulikovskiy, Glushchenko, Genkal & Kociolek 2020 [12], Gogorevia Kulikovskiy, Glushchenko, Maltsev & Kociolek 2020 [13], Platebaikalia Kulikovskiy, Glushchenko, Genkal & Kociolek 2020 [14], and Gomphothidium Kociolek et al. 2022 [15].
Of the above genera, only Gliwiczia, Planothidium, and Skabitschewskia have a very interesting morphological feature that is visible under a light microscope known as a horseshoe-shaped area [10]. The morphology of this horseshoe-like structure as seen with scanning electron microscopy includes a rimmed depression or sinus and hood or cavum (see description in [16]). Interestingly, species that possess a sinus and cavum, and those species where these features are weakly expressed have been shown to be closely related to one another and included in the genus Planothidium [16]. According to molecular data, these species can be recognized as three distinct clades: (a) species with a sinus, (b) species with a cavum, or (c) species without these features [16]. The genus Skabitschewskia is characterized by having only a cavum on rapheless valves in all known species, but this genus differs from Planothidium by striae morphology [10]. Striae in Planothidium are multiseriate on both valves, whereas, in Skabitschewskia, striae are uniseriate on raphe valves and biseriate on rapheless valves [10]. In the genus Gliwiczia, a cavum is present on both valves, and the striae are also uniseriate on both valves [9].
It is evident from the data discussed above that presence and number of horseshoe-like structures and morphology of striae are important features for the delimitation of genera between freshwater monoraphid taxa. The morphology of striae between monoraphid genera was comprehensively discussed by us during the description of the new genus Platebaikalia [14]. Freshwater monoraphid genera have different combinations of striae on raphe and rapheless valves that can include the presence of uniseriate, biseriate, or multiseriate striae. On the basis of this morphological feature, we prepared a revision of the genus Platessa, a genus that was described on the basis of species with biseriate striae in both valves and the absence of horseshoe-shaped structure [17]. After this description, many species were transferred to this genus, and Platessa soon became a catch-all taxon [14]. We described eight groups within the genus Platessa, and some of these groups have subsequently been described as new genera [14]. One of the eight groups of Platessa species includes the very interesting species Platessa joursacense (Héribaud) Chudaev which has uniseriate striae on both valves, but this species possesses a cavum on the rapheless valves [18].
P. joursacense was firstly described as Achnanthes joursacensis Héribaud 1903 [19] and for a long time was a neglected taxon. The generic position of this species has been interpreted differently by several authors. This species was included in the genus Planothidum as Planothidium joursacense (Héribaud) Lange-Bertalot 1999 [20] and later in Platessa as Platessa joursacensis (Héribaud) Chudaev [18]. The reason for this taxonomical instability is, on the one hand, the presence of cavum being a feature considered typical for Planothidum and, on the other hand, uniseriate striae in both valves not being typical for Planothidum. The presence of distal raphe ends that terminate on the valve face and straight is typical for Platessa. For a long time, this species was neglected due to its rarity and limited (only Holarctic) distribution [11]. Morphology of the raphe and rapheless valves was first investigated by Chudaev et al. [18].
The aim of this publication is to provide additional morphological evidence for the monoraphid diatom, Achnanthes joursacensis Héribaud 1903 and, on the basis of the results of this study, to describe the genus Planoplatessa gen. nov.

2. Results

Planoplatessa Kulikovskiy, Glushchenko & Kociolek gen. nov.

Type species (designated here): Planoplatessa joursacensis (Héribaud) Kulikovskiy, Glushchenko & Kociolek comb. nov.

Description

Light microscopy (LM), raphe valves (Figure 1A–I). Valves broadly elliptic with broadly rounded ends. Length 9.3–19.3 µm, width 5.5–8.4 µm. Raphe straight and filiform. Central area small and roundish. Axial area moderately narrow, almost linear. Striae 17–19 in 10 µm. Striae radiate at the center of the valve; very strongly radiate and curved toward the ends.
LM, rapheless valves (Figure 1J–R). Axial area narrowly lanceolate. Striae spaced slightly wider than in raphe valves. Visible horseshoe-shaped structure is present.
Scanning electron microscopy (SEM), raphe valves (Figure 2A–F). Striae uniseriate (Figure 2A,D, white arrows). Raphe filiform and straight (Figure 2A, black arrows). Distal raphe ends straight and present on valve face outside (Figure 2C, white arrow). Central raphe ends straight and tear-shaped outside (Figure 2B, black arrows). Mantle is short, with two small areolae present in prolongation of every striae (Figure 2A, black arrowhead). Interstriae are wider than striae inside and outside (Figure 2A,D, white arrowhead). Inside, distal raphe ends in smaller helictoglossae and curved in opposite direction (Figure 2F, black arrow). Central raphe ends are slim and curved to different sides (Figure 2E, black arrows). Distal and central raphe ends are curved opposite to another. Areolae ≈ 60 in 10 µm.
SEM, rapheless valves (Figure 3A–F). Striae uniseriate (Figure 3D, black arrow). Interstriae are wider than striae. Areolae covered by silica membrane internally [18].
Externally, central area large and flat on one side of valve (Figure 3A,B, white arrows); in another part, all striae are normally present or one central stria is slightly shorter (Figure 3A,B, black arrows). Internally, a large cavum is present (Figure 3E, black arrow). Striae are situated in deep alveoli (Figure 3D,F, black arrows).

Etymology

Combining epithet refers to the similarity with two monoraphid diatom genera, Platessa and Planothidium.

New Combination

Planoplatessa joursacensis (Héribaud) Kulikovskiy, Glushchenko & Kociolek comb. nov.
Basionym: Achnanthes joursacensis Héribaud 1903, in Les Diatomées Fossiles d’Auvergne Paris: 5; pl. 11, Figures 26 and 27.
≡ Planothidium joursacense (Héribaud) Lange-Bertalot 1999, Iconographia Diatomologica 6: 283. ≡ Platessa joursacensis (Héribaud) Chudaev 2015, Novosti Sist. Nizsh. Rast. 49: 112–113.

3. Discussion

Achnanthes joursacensis was described by Héribaud from fossil material (Upper Miocene or Pontus) near Joursac Village (currently Commune), from the southern part of Central France [19]. Subsequently, this taxon was found in sediments of different Epochs of the Neogene Period, including Miocene [21] and Pliocene [22,23], as well as from the Quaternary Period, both Pleistocene [24] and Recent in Europe [25], Russia, Moscow Region [18], Russian Far East [26], Mongolia (this investigation), Japan [27], and USA [28]. The lectotype of the species was investigated and illustrated by Krammer and Lange-Bertalot, taf. 47, Figures 7–9 [29]. This taxon prefers alkaline, meso- to eutrophic lakes and lake outlets [25]. We found this taxon in weakly alkaline (pH = 8.7) Lake Khövsgöl (Mongolia) with an electrical conductivity of 236 μS·cm−1.
All findings of this species, with both LM and SEM, correspond to observations of the lectotype investigated previously. This taxon is characterized by uniseriate striae on both valves and the presence of a cavum on rapheless valves; external distal raphe ends are straight and placed on the valve face and do not extend onto the mantle [18,29]. This combination of morphological features makes this species easily recognizable. Populations of this species were found in the Holarctic, both fossil to Recent [18].
The presence of a cavum was a good reason to transfer this species to the genus Planothidium [20]. However, Planothidium as a genus is also characterized by having multiseriate striae on both valves. Planoplatessa joursacensis comb. nov., however, only has uniseriate striae [10]. External distal raphe ends extend onto the valve mantle in Planothidium; however, in Planoplatessa joursacensis comb. nov., they are straight and only occur on the valve face. As discussed above, Planothidium as a genus can be divided into three groups, one with cavum, a second with sinus, and a third without a cavum and sinus. However, all the taxa in these groups of Planothidium have multiseriate striae. Skabitschewskia is another genus with the presence of a cavum in rapheless valves. However, Skabitschewskia is characterized by uniseriate striae on the raphe valves and biseriate striae on the rapheless valves [10]. The genus Gliwiczia is characterized by the presence of a cavum and uniseriate striae on both valves similar to the situation in Planoplatessa gen. nov. However, Gliwiczia has a cavum on both raphe and rapheless valves, a situation that is unique among monoraphid genera.
Genera such as Achnanthidium, Eucocconeis, Psammothidium, Trifonovia, Gololobovia, and Gogorevia are characterized by having uniseriate striae on both valves [8,10,12,13]. However, these genera do not have a cavum, a feature that is typical for Planoplatessa gen. nov. All these genera are very easy to distinguish from Planoplatessa gen. nov. by a combination of morphological features such as valve shape, presence or absence of sternum and stauros internally and externally, and morphology of distal and central raphe ends (see Table 1). Combinations of stria morphology with the presence or absence of a cavum and stauros are important taxonomical features that were shown with molecular data to help diagnose freshwater monoraphid genera such as Achnanthidium, Psammothidium, Gogorevia, Karayevia, Planothidium, and Lemnicola [13,16,30,31,32,33,34].
Planoplatessa gen. nov. as a genus is distinguished from other known monoraphid genera. Previous transfer of A. joursacensis to the genus Platessa was based on some morphological features shared between them, especially external distal raphe ends being straight and extending onto the valve face only [18]. Transfer of taxa that were divided on some morphological features between similar genera to different genera is normal practice. We discussed the same situation with the previous transfer of Achnanthes exigua Grunow 1880 to the genera Achnanthidium and Lemnicola [13]. However, our molecular investigation of species from this complex showed that a new genus was required, which we described as Gogorevia. Future research combining morphological and molecular datasets will be necessary to further resolve relationship of the other freshwater monoraphid genera and help to identify features that allow us to not only recognize and distinguish the genera, but also diagnose monophyletic taxa and create a natural classification for them [35].

4. Materials and Methods

Samples from Mongolia were collected by M.S. Kulikovskiy on 21 July 2015 from the Khövsgöl Lake (50°59′22.8″ N, 100°42′30.4″ E; pH = 8.7; T = 11.5 °C; conductivity = 236 μS·cm−1), directly sampling benthos and designated Mn 282.
The samples were boiled in concentrated hydrogen peroxide (≈37%) to dissolve organic matter. The samples were then washed with deionized water four times at 12 h intervals. After decanting and rinsing with up to 100 mL of deionized water, the suspension was spread onto coverslips and left to dry at room temperature. Permanent diatom slides were mounted in Naphrax®. The slide was designated no. 02605. Light microscopic (LM) observations were performed using a Zeiss Scope A1 microscope equipped with an oil immersion objective (100×, n.a. 1.4, differential interference contrast (DIC)) and Zeiss AxioCam ERc 5 s camera. For scanning electron microscopy (SEM), parts of the suspensions were fixed on aluminum stubs after air-drying. The stubs were sputter-coated with 50 nm of gold. The valve ultrastructure was examined by means of a JSM-6510LV scanning electron microscope (Institute for Biology of Inland Waters RAS, Borok, Russia).

5. Conclusions

New insights into character combinations found in freshwater monoraphid diatoms are demonstrating key features used to diagnose genera. An easily recognizable feature in both light and scanning electron microscopy is a cavum, a hollow covering found in the valve interior of certain monoraphid genera. We can now recognize four monoraphid genera that possess a cavum: Planothidium, Skabitschewskia, Gliwiczia, and Planoplatessa gen. nov. These genera are recognizable from one another on the basis of whether there is a single cavum per frustule or two (found in Gliwiczia only), multiseriate versus uniseriate striae, and whether the external distal raphe ends extend onto the valve mantle or are restricted to the valve face. While we expect these groups to constitute a monophyletic lineage, formal analyses based on morphology and molecules will be needed to verify taxon relationships and monophyly.

Author Contributions

Conceptualization, M.S.K.; methodology, A.M.G. and M.S.K.; validation, A.M.G., M.S.K. and J.P.K.; investigation, A.M.G., M.S.K. and J.P.K.; resources, M.S.K.; writing—original draft preparation, A.M.G. and M.S.K.; writing—review and editing, A.M.G., M.S.K. and J.P.K.; visualization, M.S.K., I.V.K. and A.M.G.; supervision, M.S.K.; funding acquisition, M.S.K. All authors have read and agreed to the published version of the manuscript.

Funding

This publication is based on research carried out with financial support from the Russian Science Foundation (19-14-00320∏) for light and scanning electronic microscopies and the framework of state assignment of the Ministry of Science and Higher Education of the Russian Federation (theme 122042700045-3) for finishing manuscript.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the result.

Abbreviations

LM—light microscopy; SEM—scanning electron microscopy; RV—raphe valves; RLV—rapheless valves.

References

  1. Bory de Saint-Vincent, J.B.M. Dictionnaire Classique d’Histoire Naturelle; Rey et Gravier: Paris, France; Baudouin Frères: Paris, France, 1822; Volume 1, pp. 79–80. [Google Scholar]
  2. Kützing, F.T. Die Kieselschaligen Bacillarien Oder Diatomeen. Zu finden bei W. Köhne: Nordhausen, Germany, 1844; p. 152. [Google Scholar]
  3. Cleve, P.T. Synopsis of the Naviculoid Diatoms, Part II. Kongliga Sven. Vetensk. Akad. Handl. 1895, 27, 1–219. [Google Scholar] [CrossRef]
  4. Bukhtiyarova, L.V.; Round, F.E. Revision of the genus Achnanthes sensu lato. Psammothidium, a new genus based on Achnanthidium marginulatum. Diatom Res. 1996, 11, 1–30. [Google Scholar] [CrossRef]
  5. Round, F.E.; Bukhtiyarova, L.V. Four new genera based on Achnanthes (Achnanthidium) together with a re-definition of Achnanthidium. Diatom Res. 1996, 11, 345–361. [Google Scholar] [CrossRef]
  6. Round, F.E.; Basson, P.W. A new monoraphid diatom genus (Pogoneis) from Bahrain and the transfer of previously described species A. hungarica and A. taeniata to new genera. Diatom Res. 1997, 12, 71–81. [Google Scholar] [CrossRef]
  7. Wojtal, A.Z. Species composition and distribution of diatom assemblages in spring waters from various geological formation in southern Poland. Bibl. Diatomol. 2013, 59, 1–436. [Google Scholar]
  8. Kulikovskiy, M.S.; Lange-Bertalot, H.; Metzeltin, D.; Witkowski, A. Lake Baikal: Hotspot of endemic diatoms I. Iconogr. Diatomol. 2012, 23, 7–608. [Google Scholar]
  9. Kulikovskiy, M.; Lange-Bertalot, H.; Witkowski, A. Gliwiczia gen. nov., a new achananthoid diatom genus with description of four species new for science. Phytotaxa 2013, 109, 1–16. [Google Scholar] [CrossRef]
  10. Kulikovskiy, M.S.; Lange-Bertalot, H.; Kuznetsova, I.V. Lake Baikal: Hotspot of endemic diatoms II. Iconogr. Diatomol. 2015, 26, 1–657. [Google Scholar]
  11. Kulikovskiy, M.S.; Glushchenko, A.M.; Genkal, S.I.; Kuznetsova, I.V. Identification Book of Diatoms from Russia; Filigran: Yaroslavl, Russia, 2016; p. 804. [Google Scholar]
  12. Kulikovskiy, M.S.; Glushchenko, A.M.; Kuznetsova, I.V.; Genkal, S.I.; Kociolek, J.P. Gololobovia gen. nov.—A new genus from Lake Baikal with comments on pore occlusion in monoraphid diatoms. Phycologia 2020, 59, 616–633. [Google Scholar] [CrossRef]
  13. Kulikovskiy, M.S.; Maltsev, Y.I.; Glushchenko, A.M.; Kuznetsova, I.V.; Kapustin, D.A.; Gusev, E.S.; Lange-Bertalot, H.; Genkal, S.I.; Kociolek, J.P. Gogorevia, a new monoraphid diatom genus for Achnanthes exigua and allied taxa described on the basis of an integrated molecular and morphological approach. J. Phycol. 2020, 56, 1601–1613. [Google Scholar] [CrossRef]
  14. Kulikovskiy, M.S.; Glushchenko, A.M.; Genkal, S.I.; Kuznetsova, I.V.; Kociolek, J.P. Platebaikalia—A new monoraphid diatom genus from ancient Lake Baikal with comments on the genus Platessa. Fottea 2020, 20, 58–67. [Google Scholar] [CrossRef]
  15. Kociolek, J.P.; You, Q.-M.; Yu, P.; Li, Y.-L.; Wang, Y.-L.; Lowe, R.L.; Wang, Q.-X. Description of Gomphothidium gen. nov., with light and scanning electron microscopy: A new freshwater monoraphid diatom genus from Asia. Fottea 2021, 21, 1–7. [Google Scholar] [CrossRef]
  16. Jahn, R.; Abarca, N.; Gemeinholzer, B.; Mora, D.; Skibbe, O.; Kulikovskiy, M.S.; Gusev, E.S.; Kusber, W.-H.; Zimmermann, J. Planothidium lanceolatum and Planothidium frequentissimum reinvestigated with molecular methods and morphology: Four new species and the taxonomic importance of the sinus and cavum. Diatom Res. 2017, 32, 75–107. [Google Scholar] [CrossRef]
  17. Krammer, K.; Lange-Bertalot, H. Bacillariophyceae 4. Teil: Achnanthaceae, Kritische Erganzungen zu Navicula (Lineolatae), Gomphonema Gesamtliteraturverzeichnis Teil 1–4 [second revised edition] [With “Ergänzungen und Revisionen” by H. Lange Bertalot]. In Suβsswasserflora von Mitteleuropa 2(4); Ettl, H., Ed.; Spektrum Akademischer Verlad: Heidelberg, Germany, 2004; p. 468. [Google Scholar]
  18. Chudaev, D.A.; Gololobova, M.A.; Kulikovskiy, M.S. On taxonomic position of two species of achnanthoid diatoms (Achnanthidiaceae, Bacillariophyceae). Nov. Sist. Nizsch. Rast. 2015, 49, 110–116. [Google Scholar] [CrossRef]
  19. Héribaud, J. Les Diatomées Fossiles d’Auvergne; 2e mém; Librairie des Sciences Naturelles: Paris, France, 1903; p. 166. [Google Scholar]
  20. Lange-Bertalot, H. Neue Kombinationen von taxa aus Achnanthes Bory (sensu lato). Iconogr. Diatomol. 1999, 6, 276–289. [Google Scholar]
  21. Tanaka, H.; Nagumo, T. Late Miocene freshwater diatoms from Mitoku area in Misasa Town, Tottori Prefecture, Japan. Diatom 2006, 22, 17–25. [Google Scholar] [CrossRef]
  22. Tanaka, H.; Nagumo, T.; Kashima, K.; Mitsuhashi, F. Pliocene diatoms from freshwater diatomite in Yamaga Town, Kyushu, Japan. Diatom 2004, 20, 113–122. [Google Scholar] [CrossRef]
  23. Titova, L.; Hassan, A.; Mikhailov, I.; Rodionova, E.; Rasskazov, S.; Usoltseva, M. Diversity and Ecology of Diatoms in Pliocene Deposits of the Tunka Valley (Baikal Rift Zone). Diversity 2021, 13, 479. [Google Scholar] [CrossRef]
  24. Tanaka, H.; Nagumo, T.; Kashima, K. Fossil freshwater diatoms from Tsumori Formation (Middle Pleistocene) in Mashiki Town, Kumamoto Prefecture, Kyushu, Japan. Diatom 2005, 21, 119–330. [Google Scholar] [CrossRef]
  25. Cantonati, M.; Kelly, M.G.; Lange-Bertalot, H. Freshwater Benthic Diatoms of Central Europe: Over 800 Common Species Used in Ecological Assessment; Koeltz Botanical Books: Municipality, Germany, 2017; p. 942. [Google Scholar]
  26. Potapova, M. Diatoms of Bering Island, Kamchatka, Russia. Nova Hedwig. Beih. 2014, 143, 63–102. [Google Scholar] [CrossRef]
  27. Hirota, M.; Kihara, Y.; Arita, S.; Ohtsuka, T. Periphytic diatom flora of Koyama-ike pond, Tottori Prefecture, Japan. Diatom 2013, 29, 24–41. [Google Scholar]
  28. Reavie, E.D.; Axler, R.P.; Sgro, G.V.; Danz, N.P.; Kingston, J.C.; Kireta, A.R.; Brown, T.N.; Hollenhorst, T.P.; Ferguson, M.J. Diatom-based weighted-averaging transfer functions for Great Lakes coastal water quality: Relationships to watershed characteristics. J. Great Lakes Res. 2006, 32, 321–347. [Google Scholar] [CrossRef]
  29. Krammer, K.; Lange-Bertalot, H. Bacillariophyceae. 3. Teil: Centrales, Fragilariaceae, Eunotiaceae. In Süβwasserflora von Mitteleuropa. 2(3); Ettl, H., Gerloff, J., Heynig, H., Mollenhauer, D., Eds.; Gustav Fisher Verlag: Stuttgart, Germany, 1991; p. 576. [Google Scholar]
  30. Van de Vijver, B.; Wetzel, C.E.; Kopalova, K.; Zidarova, R.; Ector, L. Analysis of the type material of Achnanthidium lanceolatum Brébisson ex Kützing (Bacillariophyta) with the description of two new Planothidium species from the Antarctic Region. Fottea 2013, 13, 105–117. [Google Scholar] [CrossRef]
  31. Kulikovskiy, M.S.; Andreeva, S.A.; Gusev, E.S.; Kuznetsova, I.V.; Annenkova, N.V. Molecular phylogeny of monoraphid diatoms and raphe significance in evolution and taxonomy. Biol. Bull. 2016, 43, 398–407. [Google Scholar] [CrossRef]
  32. Tseplik, N.D.; Maltsev, Y.I.; Glushchenko, A.M.; Kuznetsova, I.V.; Genkal, S.I.; Gusev, E.S.; Kulikovskiy, M.S. Achnanthidium gladius sp. nov. (Bacillariophyceae)—A new monoraphid diatom species from Indonesia. PhytoKeys 2021, 187, 129–140. [Google Scholar] [CrossRef]
  33. Tseplik, N.D.; Maltsev, Y.I.; Glushchenko, A.M.; Kuznetsova, I.V.; Genkal, S.I.; Kociolek, J.P.; Kulikovskiy, M.S. Achnanthidium tinea sp. nov.—A new monoraphid diatom (Bacillariophyceae) species, described on the basis of molecular and morphological approaches. PhytoKeys 2021, 174, 147–163. [Google Scholar] [CrossRef] [PubMed]
  34. Tseplik, N.D.; Glushchenko, A.M.; Maltsev, Y.I.; Kuznetsova, I.V.; Genkal, S.I.; Kociolek, J.P.; Kulikovskiy, M.S. A new monoraphid diatom species from the genus Karayevia sensu lato (Bacillariophyceae: Stauroneidaceae) with remarks on taxonomy and phylogeny of the genus. Diatom Res. 2022, 37, 39–50. [Google Scholar] [CrossRef]
  35. Kociolek, J.P.; Williams, D.M. How to define a diatom genus? Notes on the creation and recognition of taxa, and a call for revisionary studies of diatoms. In Proceedings of the 8th Central European Diatom Meeting, Zagreb, Croatia, 30 September 2015. Acta Bot. Croat. 2015, 74, 1–16. [Google Scholar] [CrossRef] [Green Version]
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Figure 1. Planoplatessa joursacensis (Héribaud) Kulikovskiy, Glushchenko & Kociolek comb. nov. Slide no. 02605. Light microscopy, differential interference contrast, size diminution series. (A–I). Raphe valves. (J–R). Rapheless valves. Scale bar = 10 μm.
Figure 1. Planoplatessa joursacensis (Héribaud) Kulikovskiy, Glushchenko & Kociolek comb. nov. Slide no. 02605. Light microscopy, differential interference contrast, size diminution series. (A–I). Raphe valves. (J–R). Rapheless valves. Scale bar = 10 μm.
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Figure 2. Planoplatessa joursacensis (Héribaud) Kulikovskiy, Glushchenko & Kociolek comb. nov. Scanning electron microscopy. Raphe valves. (A). The entire valve, external view. Black arrows show the filiform and straight raphe. White arrow shows the uniseriate stria. Black arrowhead shows the valve mantle. White arrowhead shows the interstria. (B). Central area, external view. Black arrows show the central raphe ends. (C). Valve end, external view. White arrow shows the distal raphe end. (D). The whole valve, internal views. Black arrows show the filiform and straight raphe. White arrow shows the uniseriate stria. White arrowhead shows the interstria. (E). Central area, internal view. Black arrows show the deflected in opposite directions central raphe ends. (F). Valve end, internal view. Black arrow shows the helictoglossa. Scale bar (A,D) = 2 μm; (B,E) = 1 μm; (C,F) = 0.5 μm.
Figure 2. Planoplatessa joursacensis (Héribaud) Kulikovskiy, Glushchenko & Kociolek comb. nov. Scanning electron microscopy. Raphe valves. (A). The entire valve, external view. Black arrows show the filiform and straight raphe. White arrow shows the uniseriate stria. Black arrowhead shows the valve mantle. White arrowhead shows the interstria. (B). Central area, external view. Black arrows show the central raphe ends. (C). Valve end, external view. White arrow shows the distal raphe end. (D). The whole valve, internal views. Black arrows show the filiform and straight raphe. White arrow shows the uniseriate stria. White arrowhead shows the interstria. (E). Central area, internal view. Black arrows show the deflected in opposite directions central raphe ends. (F). Valve end, internal view. Black arrow shows the helictoglossa. Scale bar (A,D) = 2 μm; (B,E) = 1 μm; (C,F) = 0.5 μm.
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Figure 3. Planoplatessa joursacensis (Héribaud) Kulikovskiy, Glushchenko & Kociolek comb. nov. Scanning electron microscopy. Rapheless valves. (A). The entire valve, external view. Black arrow shows the shortened central stria. White arrow shows the central area. White arrowhead shows the interstria. (B). Central area, external view. Black arrow shows the shortened central stria. White arrow shows the central area. (C). Valve end, external view. Black arrow shows the uniseriate stria. Black (D). The whole valve, internal view. Black arrow shows the uniseriate stria, situated in deep alveola. White arrowhead shows the interstria. (E). Internal view. Black arrow shows the cavum. (F). Valve end, internal views. Black arrow shows the uniseriate stria, situated in deep alveola. Scale bar (A,D) = 2 μm; (B,E) = 1 μm; (C,F) = 0.5 μm.
Figure 3. Planoplatessa joursacensis (Héribaud) Kulikovskiy, Glushchenko & Kociolek comb. nov. Scanning electron microscopy. Rapheless valves. (A). The entire valve, external view. Black arrow shows the shortened central stria. White arrow shows the central area. White arrowhead shows the interstria. (B). Central area, external view. Black arrow shows the shortened central stria. White arrow shows the central area. (C). Valve end, external view. Black arrow shows the uniseriate stria. Black (D). The whole valve, internal view. Black arrow shows the uniseriate stria, situated in deep alveola. White arrowhead shows the interstria. (E). Internal view. Black arrow shows the cavum. (F). Valve end, internal views. Black arrow shows the uniseriate stria, situated in deep alveola. Scale bar (A,D) = 2 μm; (B,E) = 1 μm; (C,F) = 0.5 μm.
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Table
Table 1. Comparison of different freshwater monoraphid diatom genera with cavum.
Table 1. Comparison of different freshwater monoraphid diatom genera with cavum.
Planoplatessa gen. nov.SkabitschewskiaPlanothidiumGliwiczia
Type speciesP. joursacensis (Héribaud) Kulikovskiy, Glushchenko & Kociolek comb. nov.S. dispersipunctata Kulikovskiy & Lange-Bertalot 2015P. lanceolatum (Brébisson ex Kützing) Lange-Bertalot 1999G. tenuis Kulikovskiy, Lange-Bertalot & Witkowski 2013
Striae in raphe valves (RV)UniseriateUniseriateMultiseriateUniseriate
Striae in rapheless valves (RLV)UniseriateBiseriateMultiseriateUniseriate
Interstriae in RV externallyFlat, wider than striaeFlat, equal to striaeFlat, less than striaeFlat, slightly broader than striae
Interstriae in RV internallyVery prominent on striae, broader than striaeProminent, equal to or broader than striaeProminent, narrower than striaeSlightly prominent, slightly broader than striae
Interstriae in RLV externallyFlat, broader than striaeProminent, equal to or broader than striaeFlat, narrower than striaeFlat, equal to or broader than striae
Interstriae in RLV internallyVery prominent on striae, broader than striaeVery prominent (rib-like), connected with sternum, close areolae by silica layer (alveoli), narrower than striae; in some species with reduced striae the interstriae are longer and broaderEvidently raised and narrower than striaeSlightly raised, narrower than striae
Pore occlusionsSilica membraneSilica membraneHymenesSilica membrane, below the occlusion a pair of foramina lips
Distal raphe ends externallyStraight, on valve face near mantleStraight or slightly curved on valve face or extending slightly onto valve mantle; turned in opposite directionsSmoothly curved to the same direction and extending onto valve mantleStraight and extending slightly onto mantle, slightly deflected in opposite directions
Distal raphe ends internallyIn small helictoglossae; curved in the opposite directionsIn small helictoglossae; turned in different directionsIn small helictoglossae; turned in different directionsHelictoglossae almost undeveloped; slightly turned in opposite directions
Central raphe ends externallyTear-shaped, straightTear-shaped, straightTear-shaped, turned to the same direction and opposite to distal endsTear-shaped, straight
Central raphe ends internallyLinear, straight, curved in opposite directionsStraight; turned to the different directionStraight; turned in different directionsStraight; evidently turned in different directions
Axial area in RV, externallyFlat, narrow and linearNarrow and linear, sternumNarrow and linearNarrow and linear, sternum
Axial area in RV, internallyNarrow and straight, sternum evident and elevatedSternum well-developed, narrow and linearSternum well-developed, narrow and linearSternum well-developed, narrow and linear
Axial area in RLV, externallyFlat, lanceolateNarrow and linear or slightly wider to central area, in many species deep on valve faceNarrow and linear or slightly wider to central area, deep on valve faceNarrow and wider to central area, almost rhombic
Axial area in RLV, internallyFlat, lanceolateNarrow lanceolate, raised on valve face in middleNarrow and linear or wider to central area, sternum well-developedBroad rhombic sternum
Central area in RV externallySmall, circleCircle or bowtie-shaped, flat or slightly raised in centerStriae either not shortened or 1–2 slightly shortened striae forming a small circular areaStauros elevated, central nodule evidently raised
Central area in RV internallySmall, circleCircle or bowtie-shaped, raised in centerStriae shortened or 1–2 slightly shortened striae forming a small circular areaStauros strongly elevated with cavum on one side
Central area in RLV externallyFlat and large trapezium in one sideFlat, fascia in one cavum side of valveFlat hyaline area on one side, striae either not shortened or 1–2 slightly shortened striae forming a small circular areaStauros elevated
Central area in RLV internallyLarge cavum in one sideCavumSinus on one side, striae either not shortened or 1–2 slightly shortened striae forming a small circular areaStauros strongly elevated with cavum on one side
ReferencesThis investigation, [18][10][5,30][10], own data
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Kulikovskiy, M.S.; Glushchenko, A.M.; Kuznetsova, I.V.; Kociolek, J.P. Planoplatessa gen. nov.—A New, Neglected Monoraphid Diatom Genus with a Cavum. Plants 2022, 11, 2314. https://doi.org/10.3390/plants11172314

AMA Style

Kulikovskiy MS, Glushchenko AM, Kuznetsova IV, Kociolek JP. Planoplatessa gen. nov.—A New, Neglected Monoraphid Diatom Genus with a Cavum. Plants. 2022; 11(17):2314. https://doi.org/10.3390/plants11172314

Chicago/Turabian Style

Kulikovskiy, Maxim S., Anton M. Glushchenko, Irina V. Kuznetsova, and John Patrick Kociolek. 2022. "Planoplatessa gen. nov.—A New, Neglected Monoraphid Diatom Genus with a Cavum" Plants 11, no. 17: 2314. https://doi.org/10.3390/plants11172314

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