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Article

Achnanthes Bory Sensu Stricto (Bacillariophyta) from Terrestrial Habitats of Rio de Janeiro (Brazil), with Description of Achnanthes pseudoinflata sp. nov.

1
Department of Agroecology, Institute of Agricultural Sciences, Land Management and Environmental Protection, University of Rzeszów, Zelwerowicza 8B, 35-601 Rzeszów, Poland
2
Wielicka 42C/93, 30-552 Kraków, Poland
3
Department of Soil Studies, Environmental Chemistry and Hydrology, Institute of Agricultural Sciences, Land Management and Environmental Protection, University of Rzeszów, Zelwerowicza 8B, 35-601 Rzeszów, Poland
4
Environmental Research and Innovation Department (ERIN), Luxembourg Institute of Science and Technology (LIST), 41 rue du Brill, L-4422 Luxembourg, Luxembourg
*
Author to whom correspondence should be addressed.
Diversity 2020, 12(10), 375; https://doi.org/10.3390/d12100375
Submission received: 12 August 2020 / Revised: 25 September 2020 / Accepted: 27 September 2020 / Published: 29 September 2020
(This article belongs to the Special Issue Taxonomy, Ecology and Biogeography of Diatoms)

Abstract

:
The aim of the present work was to present the ecological and morphological characteristics of species from the genus Achnanthes Bory sensu stricto, which develops in terrestrial mosses near the Rio de Janeiro Botanic Garden, Brazil. A literature comparison was made with other similar species, including the LM and SEM analysis of original material bearing Achnanthes inflata (Kützing) Grunow housed at the Grunow Collection in Vienna, and data from the available literature. Samples were collected from clumps of moss growing on tree trunks, and from a concrete wall within the botanic garden. Four taxa from the genus Achnanthes were recorded: A. coarctata, A. inflata var. gibba, A. mauiensis and Achnanthes pseudoinflata sp. nov. The main morphological differences between these taxa were cell dimensions (length and width), striae and areolae density. The most common diatom species found in these samples were Humidophila sp. (90%), Humidophila contenta (74.8%), Luticola moreirae (17.9%), and Achnanthes pseudoinflata sp. nov. (7.4%).

Graphical Abstract

1. Introduction

The genus Achnanthes Bory [1] sensu stricto includes monoraphid diatoms, with mainly linear-to-lanceolate valves. Under light microscopy observation, they are often viewed in a girdle position and are clearly bent. Raphe valves with fascia reach the valve margins, while longitudinal raphe sternum run along the apical axis to the center of the valve. A rapheless valve without fascia have a sternum which are often shifted to the valve margin. Areolae are covered by perforate cribra. Cells may grow alone or create colonies. Living cells are usually attached to the substratum via mucilage stalks but are also motile. Cells of this genus can contain either two large or many small chloroplasts [2,3,4,5,6].
The type of species for this genus is Achnanthes adnata Bory [1]. This genus currently contains around 150 species, which mostly develop in marine and brackish conditions. Only a few species of Achnanthes are known from freshwater and terrestrial environments [7,8,9,10].
C.G. Ehrenberg described three Achnanthes species from Brazil, all of which are currently considered invalid: Achnanthes brasiliensis Ehrenberg nom. inval., Achnanthes incrassata Ehrenberg nom. inval. and Achnanthes ventricosa Ehrenberg nom. inval. [11]. Here, we reproduced the figure from the Clara Ehrenberg Index.
Additional records are from the J.D. Möller collection. According to the image database of algae at Charles University in Prague (https://botany.natur.cuni.cz/algo/database/, accessed 10 March 2020), Achnanthes ventricosa Ehrenberg was presented on slide A118 which originated from Brazil and was collected in 1869.
Zimmermann [12] mentioned for the first time Achnanthes mesogongyla Grunow and Achnanthes brasiliensis Ehrenberg from the state of Santa Catarina growing on Hypnos. Subsequently, Zimmermann [13] also mentioned Achnanthes inflata in the Jaburú river at the Itaparica Island (Bahia) while Zimmermann [14] observed Achnanhtes coarctata from samples collected at the Rio de Janeiro Botanical Garden. Zimmermann [15] mentioned Achnanthes longipes and Achnanthes brevipes from the Santos and Rio de Janeiro states, respectively. Zimmermann [16] described Achnanthes ambigua C. Zimmermann as a new species from Itaparica [17]. Zimmermann [18] has described Achnanthes solea C. Zimmermann from marine samples from Santos (São Paulo).
In recent years, intensive diatomological research has been carried out in Brazil, focusing both on whole assemblages and on single genera [19,20,21,22,23,24,25,26,27,28,29]. However, research on terrestrial diatoms from this area is extremely scarce (limited to the diatom Coenogonium linkii Ehrenberg [30] living inside the thalli of lichens).
The aim of this work was to describe the ecological and morphological characteristics of a new Achnanthes species and compare it with other co-occurring species. Additionally, the comparison with the original material from the Grunow collection was made with one original material from the Grunow collection (Naturhistorisches Museum Wien, Austria).

2. Materials and Methods

Study Area

Research was conducted in the Rio de Janeiro region of south-eastern Brazil, at three sampling sites (Table 1). Two sites were located in the city of Rio de Janeiro itself (in the botanical garden and its immediate vicinity), in an area with a tropical urban climate [31]. The third site was located in the vicinity of Tijuca Park, the world’s largest urban forest. This area is part of the Atlantic Rainforest, and has a humid, subtropical climate [32].
Samples were collected in March and April 2015, both from clumps of moss growing on tree trunks at a height of 150 cm, and from a concrete wall, about 15 cm above the surface of the ground in Rio de Janeiro city, Brazil (Table 1). Three samples were taken in total. Additionally, the original material of Achnanthes inflata (Kützing) Grunow [33] was observed under light microscopy (LM) and scanning electron microscopy (SEM). The sample originated from the Grunow collection slide/material n° 788, from freshwater diatomaceous earth, collected by Hochstetter at Cabbage Tree Swamp, Auckland, New Zealand.
The samples were digested in sulfochromic mixture (a mixture of concentrated sulfuric acid (VI) and potassium dichromate) in a laboratory, in order to obtain clean diatom frustules. To remove the sulfochromic mixture, the material was then centrifuged at 2500 rpm with distilled water. The cleaned diatom valves were then enclosed in synthetic Pleurax resin, ZBE Kraków, Poland (refractive index 1.75).
Diatoms were identified and counted under an LM Carl Zeiss Axio Imager A2, equipped with a 100× Plan Apochromatic objective with differential interference contrast (DIC) for oil immersion. Diatom images were captured with a Zeiss AxioCam ICc5 camera (Jena, Germany). In total, 18 slides (6 per sample) were examined. Diatoms were identified according to the following resources: Krammer and Lange-Bertalot [34], Metzeltin and Lange-Bertalot [35,36], Rumrich et al. [37], Metzeltin et al. [38].
For the SEM observations, the samples were applied to a polycarbonate membrane filter with a 3 μm mesh, attached to aluminum stubs, and sputtered with 20 nm of gold using a turbo-pumped Quorum Q 150T ES coater. Diatoms were observed using a Hitachi SU 8010 SEM. The Grunow original material was analyzed using a Leica® DMRX bright field microscope (Wetzlar, Germany) with 100× oil immersion objective. An ultrahigh-resolution analytical field emission (FE) scanning electron microscope Hitachi SU-70 (Hitachi High-Technologies Corporation, Tokyo, Japan) operated at 5 kV and 10 mm distance was used for the SEM analysis. Diatom terminology follows Round et al. [2] and Cox [4]. Species composition and the relative abundance of taxa were determined by counting 500 specimens.

3. Results

Achnanthes pseudoinflata M. Rybak, Peszek, Skoczylas, Ector & C.E. Wetzel, sp. nov.
Figure 1 (LM), Figure 2 and Figure 3 (SEM) here.
Description: Valves with rounded capitate ends. Central part bulged—wider than apices. Frustules are often connected to each other—visible in girdle view (Figure 1AC–AI and Figure 2J,K). Observed range of valve dimensions (n = 300): 15.1–38.5 µm in length and 6.9–9.6 µm in width (Table 2). Both valves with 15–17 striae per 10 µm. Fascia on the raphe valve variable, from rectangular to bow shaped (Figure 1A–P and Figure 3A,D). Axial area narrow and linear, shifted towards the cell margin on rapheless valve (Figure 1Q–AP and Figure 2E,F). Striae parallel mid-valve, becoming curvate with respect to the axial area in apices (Figure 1). Areolae clearly distinct, 18–22 per 10 µm on both valves. Areolae are also present on the valve mantle. Distal raphe endings are strongly deflected in the same direction. Proximal raphe endings are slightly deflected and teardrop shaped (Figure 2A–C and Figure 3A). Internally, the striae are separated by thickened virgae. Externally, areolae are occluded by cribra. The cribrum is attached to the valve mostly via 3 (and rarely, 2 or 4) struts (Figure 3H). Internally, areolae have round openings with recessed cribra (Figure 3I). Orbiculi are absent on the apices of rapheless valves, and few areolae (1–3) with different structures are present (Figure 3C). In the internal view, distal raphe endings end in small helictoglossae (Figure 2E). In the internal view, proximal raphe endings are strongly hooked (Figure 3D).
Holotype: slide 26943 at the Szczecin Diatom Collection hosted by the University of Szczecin (SZCZ). The holotype specimen is illustrated in Figure 1I.
Isotypes: slide 2015/1/1 and cleaned material, University of Rzeszów.
Etymology: The species epithet is used to show a similarity to Achnanthes inflata.
Locality: Brazil, Rio de Janeiro region: Rio de Janeiro, moss samples from the concrete wall, geographic coordinates: 22°57′09″ S, 43°13′40″ W.
Similar species: Achnanthes inflata (Kützing) Grunow [33] (Figure 4A–L and Figure 5F–J), A. mauiensis R.L. Lowe and A.R. Sherwood [8], A. inflata var. gibba Gandhi [39], A. inflata var. javanica Gandhi [40], A. inflatagrandis Metzeltin, Lange-Bertalot and García-Rodríguez [38], A. elata (Leuduger-Fortmorel) Gandhi [39], A. elata var. curvula Gandhi [40], A. subelata Metzeltin, Lange-Bertalot and García-Rodríguez [38] and A. longboardia A.R. Sherwood and R.L. Lowe [8].
Habitat and associated diatom flora: The described species occurred in each of the studied samples. It was most frequent (up to 7.4%) in the moss material collected from the concrete wall (sample 2015/1), but it occurred rarely in samples 2015/2 and 2015/3—only a few cells per slide. Together with Achnanthes pseudoinflata sp. nov., other species from the genus Achnanthes were found in the analyzed material (Table 2). The most frequent (not including A. pseudoinflata sp. nov.) was Achnanthes inflata var. gibba (Figure 5A–C and Figure 6A–N), which reached a 2.4% share in the assemblage in the moss sample 2015/1, collected from the concrete wall. The other two taxa occurred in much smaller numbers. Achnanthes mauiensis R.L. Lowe and A.R. Sherwood, presented in Figure 5D,E and Figure 6O–Z occurred in sample 2015/3 (up to a few cells per slide) while the only two specimens of Achnanthes coarctata (Brébisson) Grunow [33] were found in sample 2015/1. The most frequent co-existing diatoms in the studied material were Humidophila sp. (90%) and Achnanthes pseudoinflata sp. nov. (7.4%) in the sample 2015/1, and Humidophila contenta (Grunow) R.L. Lowe, Kociolek, J.R. Johansen, Van de Vijver, Lange-Bertalot and Kopalová [41] (74.8%) and Luticola moreirae Straube, Tremarin and Ludwig [28] (17.9%) in the sample 2015/3. Achnanthes pseudoinflata sp. nov. was found in sample 2015/2, but the total number of diatoms was very low. Therefore, the diatom assemblage structure was impossible to assess.

4. Discussion

The new species is clearly distinct form the material considered here as Achnanthes inflata. The analyzed material (Figure 4A–L) and our new species differ in terms of length (36–62.4 µm instead of 15.1–38.5) and width (11.5–17.7 µm instead of 6.9–9.6). Moreover, differences were also observed regarding the number of striae (9–13 in 10 µm) and the number of areolae per striae (10–12 in 10 µm), see Table 2 and Tables S1–S5. Currently, eight taxa of Achnanthes Bory sensu stricto have been identified in modern floras from South America (i.e., besides the invalid species mentioned in the introduction by C.G. Ehrenberg). They are A. brevipes var. brevipes, A. coarctata, A. elata, A. inflata var. inflata, A. inflata var. gibba, A. inflatagrandis, A. kuwaitensis, and A. subelata [19,35,36,38,44,45].
Achnanthes pseudoinflata sp. nov. occurred in all the analyzed samples. Morphologically similar individuals were reported from New Caledonia by Moser et al. (plate 84, figs 2, 3 as Achnanthes elata [46]). However, they did not give the dimensions of their specimens nor did they include a scale bar allowing us to determine the size. A practically identical specimen was also reported from Costa Rica as Achnanthes cf. inflata by Metzeltin and Lange-Bertalot (plate 108, Figure 12 [36]). The dimensions and the shape of the cell suggest that it may be the same taxon as that described in this paper as new to science. In addition, the specimens corresponding to the species described were also presented on the website of The Florida Coastal Everglades LTER Program (http://fcelter.fiu.edu, accessed date: 30 January 2019), but in this case they were identified as Achnanthes inflata.
The most similar species is A. inflata, along with its variations. Achnanthes inflata was reported from Trinidad Island (South America) as Stauroneis inflata by Kützing [47] and was later transferred to Achnanthes inflata by Grunow [33]. This transfer was based on specimens recorded from New Zealand. The dimensions and ultrastructure observed in the original material population fully corresponded to those reported in the literature (Table 2, Figure 5A–L and Figure 6F–J). The main difference between these taxa are the cell dimensions (15.1–38.5 µm length and 6.9–9.6 µm width versus 30–65(96) µm length and 10–20.1 µm width). In addition, the striae and areolae densities are different (15–17 striae and 18–22 areolae versus 8–13 striae and 9–14 areolae per 10 µm) [8,34,38,42,43]. Despite the similar cell length and areole density, Achnanthes inflata var. gibba can be distinguished based on wider valves with a lower striae density [39]. Achnanthes inflata var. javanica can be easily separated from A. pseudoinflata sp. nov. based on a much larger cell with lower striae and areole densities [40].
Taxa with similar valve outlines to A. pseudoinflata sp. nov. are A. inflatagrandis, A. elata, and A. elata var. curvula. All taxa can be distinguished based on different valve dimensions and striae densities [38,39,40]. A similar taxon, Achnanthes subelata, can be distinguished based on wider valves with lower striae and areolae density. Additionally, A. subelata can be differentiated based on rapheless valves with axial areas in the central parts of valves, not shifted to the valve margin as in A. pseudoinflata sp. nov. [38]. Achnanthes tumescens has similar cell dimensions to A. pseudoinflata sp. nov. The taxa described can be distinguished from A. tumescens by more rounded and capitated apices, more pronounced narrowing between the central parts and the apices, and a lower areolae density per 10 µm (18–22 versus 16). Additionally, A. tumescens has fewer radiate striae than those described in A. pseudoinflata sp. nov. [8]. Achnanthes longboardia is another taxon with similar dimensions to A. pseudoinflata sp. nov. Both species overlap in dimension, but can be easily distinguished based on valve outline, which is lanceolate with rounded ends in A. longboardia and undulate with capitate apices and bold central parts in A. pseudoinflata sp. nov. [8]. Achnanthes mauiensis can be easily differentiated from A. pseudoinflata sp. nov., despite similar dimensions, via more lanceolate valves with fewer capitate apices and the difference in width (5–7.5 versus 6.9–9.6 µm). See Table 2 for the valve dimensions concerning A. pseudoinflata sp. nov. and other similar taxa from the genus Achnanthes.
Achnanthes coarctata is a cosmopolitan species reported from various parts of the world with different climates, mostly from terrestrial and aerophytic habitats [6,9,38,42,48,49]. The specimens observed in this research had valve outlines and dimensions typical for this taxon. Achnanthes inflata var. gibba is a rare taxon, reported from wet rocks and mosses in India [39] and Uruguay [35]. This taxon occurred only in sample 2015/1 of the analyzed material, where it was found to be common. The specimens studied (n = 50) had a wider range in length, but a narrower range in width. Valve outlines and areole density were typical (Table 2). Until now, Achnanthes mauiensis was known only from type locality on the island of Maui in the Hawaii archipelago. With respect to the type locality, this species occurred in aerophytic habitats [8]. In the analyzed material, this species occurred rarely in samples from the rainforest. Morphologically similar taxa were reported from Sri Lanka (Ceylon) by Foged as Achnanthes coarctata (plate 5, figs 18, 19 [50]). Reports from this study and most probably from Sri Lanka suggest that this species could be widely distributed in the terrestrial and aerophytic habitats in tropical regions.
In relation to the numerous other species in the material studied, as well as the preferences of many taxa from the genus Achnanthes, it seems that Achnanthes pseudoinflata sp. nov. also prefers aerial and terrestrial habitats. These new taxa are probably widespread, but so far it has not been possible to distinguish them from similar species. Species of the genus Achnanthes are diatoms rarely identified in algological research. This is the result of their preference for terrestrial and aerophytic environments, which are still poorly investigated.

Supplementary Materials

The following are available online at https://www.mdpi.com/1424-2818/12/10/375/s1, Table S1: Dimensions, number of striae and areolae for Achnanthes pseudoinflata sp. nov., Table S2. Dimensions, number of striae and areolae for Achnanthes coarctata, Table S3. Dimensions, number of striae and areolae for Achnanthes mauiensis, Table S4. Dimensions, number of striae and areolae for Achnanthes inflata var. gibba, Table S5. Dimensions, number of striae and areolae for Achnanthes inflata originated from Grunow’s original material.

Author Contributions

M.R., L.E., C.E.W. conceived the research; Ł.S. performed fieldwork; M.R., Ł.P., T.N. analyzed the data; M.R., Ł.P., C.E.W., L.E. wrote and edited the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

The project was funded by the Ministry of Science and Higher Education under the name of “Regional Excellence Initiative” in the years 2019–2022 Project No. 026/RID/2018/19.

Acknowledgments

The authors would like to thank the tardigradologist team from the Jagiellonian University, Krakow, especially Witold Morek for sharing the material used in present research. Zlatko Levkov is thanked for taking LM images of the original material at Grunow’s Collection. We thank Anton Igersheim (Naturhistorisches Museum Wien) regarding Grunow’s original material.

Conflicts of Interest

The authors report no potential conflict of interest.

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Figure 1. Achnanthes pseudoinflata sp. nov. Light micrographs. Scale bar = 10 µm. (AP) Raphe valve. (QAB) Rapheless valve. (ACAI) Girdle view.
Figure 1. Achnanthes pseudoinflata sp. nov. Light micrographs. Scale bar = 10 µm. (AP) Raphe valve. (QAB) Rapheless valve. (ACAI) Girdle view.
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Figure 2. Achnanthes pseudoinflata sp. nov. Scanning electron microscope micrographs. Scale bar =10 µm. (AD) External view of the raphe valve. (E,F) External view of the rapheless valve. (G,H) Internal view of the raphe valve. (I) Internal view of the rapheless valve. (J) Internal girdle view of the band and rapheless valve. (K) Girdle view.
Figure 2. Achnanthes pseudoinflata sp. nov. Scanning electron microscope micrographs. Scale bar =10 µm. (AD) External view of the raphe valve. (E,F) External view of the rapheless valve. (G,H) Internal view of the raphe valve. (I) Internal view of the rapheless valve. (J) Internal girdle view of the band and rapheless valve. (K) Girdle view.
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Figure 3. Achnanthes pseudoinflata sp. nov. Scanning electron microscope micrographs. Scale bar: A–G = 5 µm; H, I = 1 µm. (A) External view of the central part of the raphe valve. (B) External view of the raphe valve apex. (C) External view of the rapheless valve apex with two non-occluded areolae (see arrows). (D) Internal view of the central part of the raphe valve. (E) Internal view of the raphe valve apex. (F) Internal view of the central part of the rapheless valve. (G) Details of the external girdle view. (H) External view of the areolae. (I) Internal view of the areolae.
Figure 3. Achnanthes pseudoinflata sp. nov. Scanning electron microscope micrographs. Scale bar: A–G = 5 µm; H, I = 1 µm. (A) External view of the central part of the raphe valve. (B) External view of the raphe valve apex. (C) External view of the rapheless valve apex with two non-occluded areolae (see arrows). (D) Internal view of the central part of the raphe valve. (E) Internal view of the raphe valve apex. (F) Internal view of the central part of the rapheless valve. (G) Details of the external girdle view. (H) External view of the areolae. (I) Internal view of the areolae.
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Figure 4. Achnanthes inflata Grunow. Photographs from the original material of Stauroneis inflata Kützing. Scale bar = 10 µm. (A) Original drawing of Stauroneis inflata Kützing 1844. (BL) Light micrographs of Achnanthes inflata Kützing (Grunow) from the original sample. (BE) Rapheless valve. (FK) Raphe valves. (L) Girdle view.
Figure 4. Achnanthes inflata Grunow. Photographs from the original material of Stauroneis inflata Kützing. Scale bar = 10 µm. (A) Original drawing of Stauroneis inflata Kützing 1844. (BL) Light micrographs of Achnanthes inflata Kützing (Grunow) from the original sample. (BE) Rapheless valve. (FK) Raphe valves. (L) Girdle view.
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Figure 5. Scanning electron microscope micrographs. Scale bar: A–G = 10 µm; I, J = 5 µm. (AC) Achnanthes inflata var. gibba Gandhi. (A) External view of the raphe valve. (B) External view of the rapheless valve. (C) Girdle view. (D,E) Achnanthes mauiensis R.L. Lowe and A.R. Sherwood. (D) External view of the rapheless valve. (E) External view of the raphe valve. (FJ) Achnanthes inflata (Kützing) Grunow from the original Grunow’s sample. (F) External view of the rapheless valve. (G) External view of the raphe valve. (H) Girdle view. (I) External view of the valve apex with distal raphe endings. (J) Internal view of the central area with proximal raphe endings.
Figure 5. Scanning electron microscope micrographs. Scale bar: A–G = 10 µm; I, J = 5 µm. (AC) Achnanthes inflata var. gibba Gandhi. (A) External view of the raphe valve. (B) External view of the rapheless valve. (C) Girdle view. (D,E) Achnanthes mauiensis R.L. Lowe and A.R. Sherwood. (D) External view of the rapheless valve. (E) External view of the raphe valve. (FJ) Achnanthes inflata (Kützing) Grunow from the original Grunow’s sample. (F) External view of the rapheless valve. (G) External view of the raphe valve. (H) Girdle view. (I) External view of the valve apex with distal raphe endings. (J) Internal view of the central area with proximal raphe endings.
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Figure 6. Light micrographs. Scale bar = 10 µm. (AN) Achnanthes inflata var. gibba Gandhi. (AE) Rapheless valve. (FK) Raphe valve. (LN) Girdle view. (OZ) Achnanthes mauiensis R.L. Lowe and A.R. Sherwood. (O) Raphe valve. (PV) Rapheless valve. (WZ) Girdle view.
Figure 6. Light micrographs. Scale bar = 10 µm. (AN) Achnanthes inflata var. gibba Gandhi. (AE) Rapheless valve. (FK) Raphe valve. (LN) Girdle view. (OZ) Achnanthes mauiensis R.L. Lowe and A.R. Sherwood. (O) Raphe valve. (PV) Rapheless valve. (WZ) Girdle view.
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Table 1. Sampling site characteristics.
Table 1. Sampling site characteristics.
Sample Signature2015/12015/22015/3
Sampling date29 March 201529 March 20153 April 2015
Geographical coordinates22°57′09″ S
43°13′40″ W
22°57′09″ S
43°13′40″ W
22°57′39″ S
43°16′21″ W
Altitude
(m a.s.l.)
6060340
HabitatMosses collected from concrete wall in Rio de Janeiro cityLichens and mosses collected from Roystonea regia L. trunk, 1.5 m above ground levelMosses collected from palm trunk growing in rainforest
Table 2. Dimensions, number of striae and areolae for the taxa from genus Achnanthes identified in these studies and the most similar to A. pseudoinflata sp. nov. R-valve—raphe valve, p-valve—rapheless valve.
Table 2. Dimensions, number of striae and areolae for the taxa from genus Achnanthes identified in these studies and the most similar to A. pseudoinflata sp. nov. R-valve—raphe valve, p-valve—rapheless valve.
TaxaLength (µm)Width (µm)Striae Density (in 10 µm)Areolae Density (in 10 µm)References
Taxa from Genus Achnanthes Identified in Studied Samples
Achnanthes pseudoinflata sp. nov.18.1–38.56.9–9.615–1718–22This study
[Supplementary Materials Table S1]
Achnanthes coarctata31.1–36.48.5–91114–15This study
[Table S2]
17–486–1510–1414–18[34]
Achnanthes mauiensis23.2–32.46.3–6.415–16~21This study
[Table S3]
20–285–7.515–1920[8]
Achnanthes inflata var. gibba24.3–49.510–12.712–1318–19 R-valve
16–18 p-valve
This study
[Table S4]
34–4014.3–1510–1218–19[39]
Achnanthes inflata31–62.411.5–17.79–12 R-valve
9–13 p-valve
12 R-valve
10–11 p-valve
Grunow’s original material
[Table S5]
(New Zealand)
30–9610–188–139–12[34]
30–6510–2010–1311–12[38]
61.5–6913.5–16.39–11No data[8]
39–6014–159–1010–14[42]
30–9610–21.19–129–12[43]
Other Taxa Similar to Achnanthes pseudoinflata sp. nov.
Achnanthes elata22–8611–198–9 R-valve
9–10 p-valve
10–11[39]
No data14–17~10 R-valve
8–9 p-valve
8–9[38]
Achnanthes elata var. curvula60–6819–218–9 R-valve
9–10 p-valve
No data[39]
88.917.88.5 R-valve
8 p-Valve
8–9[40]
Achnanthes inflata var. javanica70–8122–22.58–9 R-valve
9–9.5 p-valve
9–10 R-valve
10 p-valve
[40]
Achnanthes inflatagrandis82–10027–307–88[38]
Achnanthes longboardia19–50.58–10.513–15 R-valve
12–14 p-valve
18–19[8]
Achnanthes subelata30–439.5–1211.5–13 R-valve
10–11 p-valve
~12[38]
Achnanthes tumescens22–36.56.5–8.515–1716[8]
Achnanthes cf. inflata30–4012–13No dataNo data[36]
Achnanthes sp. cf. inflatagrandis56–6416–20No dataNo data[36]

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Rybak, M.; Peszek, Ł.; Skoczylas, Ł.; Noga, T.; Ector, L.; Wetzel, C.E. Achnanthes Bory Sensu Stricto (Bacillariophyta) from Terrestrial Habitats of Rio de Janeiro (Brazil), with Description of Achnanthes pseudoinflata sp. nov. Diversity 2020, 12, 375. https://doi.org/10.3390/d12100375

AMA Style

Rybak M, Peszek Ł, Skoczylas Ł, Noga T, Ector L, Wetzel CE. Achnanthes Bory Sensu Stricto (Bacillariophyta) from Terrestrial Habitats of Rio de Janeiro (Brazil), with Description of Achnanthes pseudoinflata sp. nov. Diversity. 2020; 12(10):375. https://doi.org/10.3390/d12100375

Chicago/Turabian Style

Rybak, Mateusz, Łukasz Peszek, Łukasz Skoczylas, Teresa Noga, Luc Ector, and Carlos E. Wetzel. 2020. "Achnanthes Bory Sensu Stricto (Bacillariophyta) from Terrestrial Habitats of Rio de Janeiro (Brazil), with Description of Achnanthes pseudoinflata sp. nov." Diversity 12, no. 10: 375. https://doi.org/10.3390/d12100375

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