Deviata Eigner, 1995
publication ID |
https://doi.org/ 10.1093/zoolinnean/zlad044 |
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https://doi.org/10.5281/zenodo.8334787 |
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https://treatment.plazi.org/id/03D68792-FFF0-FF81-037A-3271FC1D8CF8 |
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Deviata Eigner, 1995 |
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Deviata Eigner, 1995 View in CoL View at ENA
Deviata multilineae Zhang et al., 2022 ( Fig.7A–N View Figure 7 ) Deposition of voucher specimens: Three voucher slides (No. SWY2020051501/1–3) with protargol-stained specimens were deposited in the Laboratory of Protozoology, Ocean University of China, ºingdao, China.
Cell size 150–175 × 40–60 μm (160 × 50 μm on average) in vivo (N = 6), with ratio of length to width in vivo ranging from 2.8 to 3.9; about 165 × 83 μm (140–185 × 55–116 μm), length:width ratio about 2.0:1 (1.6–2.9:1) asser protargol impregnation. Cell flexible but not contractile, outline elongate elliptical, usually with anterior part wider than the posterior one ( Fig. 7A–D, F–H View Figure 7 ). Algae in food vacuole rendered cell yellow/ greenish at low magnification ( Fig. 7A, F–H View Figure 7 ). Cytoplasm colourless, with numerous colourless globules (0.75–1.5 μm) and many transparent colourless inclusions (2–11 μm), most being spherical and located in the middle of the cell ( Fig. 7E, I View Figure 7 ). Cortical granules absent. Four macronuclear nodules, ellipsoidal-shaped, 15–18 × 13–16 μm in vivo, usually two micronuclei, each one usually located between a pair of macronuclear nodules ( Fig. 7I, K, N View Figure 7 ). Contractile vacuole about 15 μm when full, located at the equatorial level, near less cell margin ( Fig. 7A, B–D, H View Figure 7 ). Collecting canals absent. Locomotion by slowly floating in water, sometimes crawling around the substratum. No cell division, cysts, or conjugation were observed.
The adoral zone of membranelles occupies 28% of cell length in protargol preparations, composed of 23–35 membranelles ( Table 1). Paroral and endoral consisted of single-rowed dikinetids, nearly parallel to each other in most cells (intersected in two out of 15 cells examined), with the former shorter than the laưer ( Fig. 7J, M View Figure 7 ). The cytopharyngeal fibres extend posteriorly from the cytostome ( Fig. 7J View Figure 7 ). Length of cirri in vivo about 11–13 μm. Three frontal cirri, usually one buccal cirrus located right to the anterior end of the paroral and anterior of the endoral (two buccal cirri observed in three out of 20 cells), three to seven parabuccal cirri behind the right frontal cirrus ( Fig. 7J, M, N View Figure 7 ). Three frontoventral cirral rows, frontoventral cirral row 1 (FVR1) commences at right of right frontal cirrus and terminates at posterior 15% of cell length. In six out of 15 cells, FVR1 consisting of two parts: the anterior part terminates behind the proximal end of AZM, the posterior part commences at the right of several last cirri of anterior part ( Fig. 7J, N View Figure 7 ). Another two frontoventral cirral rows terminate at the rear end of the cell ( Fig. 7J, N View Figure 7 ). Eight to eleven less marginal rows, most of them located on the dorsal side; two or three right marginal rows, most of them distributed on the ventral side ( Fig. 7J, K, L, N View Figure 7 ).
Three long dorsal kineties (DK), dorsal bristles inconspicuous in vivo. DK1 with 9–17 dikinetids, DK2 with 17–27 dikinetids, DK3 with 11–17 dikinetids. Caudal cirri absent ( Fig. 7K View Figure 7 ).
18S rRNA gene sequence and phylogenetic analyses ( Figs 8 View Figure 8 , 9 View Figure 9 )
The two new 18S rRNA gene sequences obtained in this study were deposited in GenBank. Their lengths, GC-content, and accession numbers are as follows: Heterodeviata sinica 1571 bp, 45.59%, OP537913; Deviata multilineae 1630 bp, 45.77%, OP537914.
Phylogenetic trees based on 18S rRNA gene sequence data using BIandMLanalysesaremostlycongruent, therefore,onlytheMLtree isshownwithsupportsfrombothalgorithms ( Fig.2A View Figure 2 ). Accordingto the 18S rRNA gene tree, all deviatids group together in a large clade with high to full support (97%ML/1.00 BI), in which Heterodeviata sinica is placed in a subclade including D. parabacilliformis , D. rositae , and Pseudosincirra longicirrata with low support (69%ML/0.54BI). However, the position of H. sinica is not robust due to the low support for the cluster of H. sinica , D. parabacilliformis , and D. rositae in the ML tree (50%) and the incongruent topology in the BI tree ( Fig. 2C View Figure 2 ). Furthermore, the systematic relationship of Heterodeviata with related genera is shown in Figure 2B View Figure 2 .
Comparing the two new 18S rRNA sequences with seven available deviatid sequences ( Fig. 8 View Figure 8 ), Heterodeviata sinica differs from the other deviatid sequences by 31–38 nucleotide positions (corresponding to 97.5–97.9% similarity). It is noteworthy that for the sequence of Perisincirra sp. (KY855575, submiưed by Nitla from Pisa University), the morphological characterization was unavailable, but there were no nucleotides differences from Deviata brasiliensis , which suggests that Perisincirra sp. (KY855575) was misidentified, and probably is conspecific with Deviata brasiliensis . More detailed information about the nine deviatid sequences are presented within Figure 8 View Figure 8 .
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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Deviata Eigner, 1995
Song, Wenya, Dong, Jingyi, Lu, Xiaoteng, Al-Farraj, Saleh A., Song, Weibo, Hines, Hunter N. & Luo, Xiaotian 2023 |
Deviata multilineae
Zhang 2022 |