Encyonopsis palmeti Gassiole & Le Cohu, 2014
publication ID |
https://doi.org/10.11646/phytotaxa.156.3.3 |
DOI |
https://doi.org/10.5281/zenodo.15305961 |
persistent identifier |
https://treatment.plazi.org/id/03ED87D7-FF97-BC5B-FF45-6523FA84F996 |
treatment provided by |
Felipe |
scientific name |
Encyonopsis palmeti Gassiole & Le Cohu |
status |
sp. nov. |
Encyonopsis palmeti Gassiole & Le Cohu sp. nov.
Figures 54–72 View FIGURES 54–63 View FIGURES 64–67 View FIGURES 68–72 , Figs 54–63 View FIGURES 54–63 are of the holotype.
Valves lanceolate, weakly dorsiventral; apices shortly rostrate and broadly rounded. Length: 15.4–24.2 µm; breadth: 4–5.2 µm; maximum length/breadth ratio: 5.1. Axial area narrow and linear. Raphe filiform curved to the ventral side with proximal endings deflected to the dorsal side. Striae parallel at the center becoming weakly radiate towards the poles, 22–26 in 10 µm. SEM. Externally, proximal raphe endings slightly enlarged and bent towards the dorsal side; terminal raphe fissures curved to the ventral side and terminating close to the poles in drop-like endings. Internally, extremely short intermissio, 40–45 areolae in 10 µm.
Holotype: PC0143224 . Laboratoire de Cryptogamie. Muséum d'Histoire Naturelle. Paris. GoogleMaps
Isotype: BR–4279 . Jardin Botanique National de Belgique. Département Bryophyta et Thallophyta. Domaine de Bouchout. Meise. Belgique. GoogleMaps
Type locality: Ravine de l'Etang à Grand Etang . (Longitude: 55°37'52.0"E –Latitude: 21°06'11.8"S) GoogleMaps
Etymology: The specific epithet palmeti refers to « Plaine des Palmistes » (in latin palmetum) where is located the type locality.
LM Morphology ( Figs 54–63 View FIGURES 54–63 )
The valves (number of valves observed: 99) are lanceolate, and weakly dorsiventral with the dorsal margin slightly more convex than the ventral margin ( Figs 54–63 View FIGURES 54–63 ). The apices are short-rostrate and broadly rounded. The axial area is narrow and linear. The raphe is filiform, slightly curved to the ventral side but with dorsally deflected proximal endings terminating in inconspicuous central pores. The striae are parallel in the middle part of the valve and then become weakly radiate.
SEM Morphology ( Figs 64–72 View FIGURES 64–67 View FIGURES 68–72 )
Externally, the raphe slit is slightly curved to the ventral side and then becomes deflected to the dorsal side with enlarged proximal endings bent to the dorsal side ( Figs 64–66 View FIGURES 64–67 ). The terminal fissures are curved towards the ventral side and terminate close to the poles in drop-like endings ( Fig. 66 View FIGURES 64–67 ). The central area is only distinguished dorsally by three weakly shortened striae ( Fig. 66 View FIGURES 64–67 ). The striae are composed of apically-elongated areolae sometimes irregular in shape ( Figs 65, 66 View FIGURES 64–67 ), numbering around 40 in 10 µm. Internally, the raphe fissure is interrupted by an extremely short intermissio ( Fig. 67 View FIGURES 64–67 ) and the distal endings terminate in well-developed helictoglossae ( Fig. 68 View FIGURES 68–72 ). The striae form shallow depressions in which the areolae are rounded and occluded ( Fig. 69 View FIGURES 68–72 ) by “ papillae ”-like structures (Krammer 2002), although they may appear apically elongated when they are partially occluded ( Figs 68–69 View FIGURES 68–72 ). The raphe ( Fig. 70 View FIGURES 68–72 , arrow) seems to be of the key and slot type ( Krammer, 1982). As in E. cilaosensis , each level of the cingulum is composed of two opposite bands tapering near the middle of the valve where they fit together with the other bands of a different level ( Figs 71–72 View FIGURES 68–72 ). The entire cingulum could not be observed.
Ecology and distribution
E. palmeti had a high relative abundance (22%) in the type locality “Ravine de l’Etang à Grand Etang” in slighty alkaline waters (pH 7.5) with low conductivity ( Table 4 View TABLE 4 ). This species was associated with Achnanthidium catenatum (Bílý & Marvan) Lange-Bertalot (1999: 277) (16%), other Achnanthidium species (34%) and Fragilaria sp. (14%). This species was recorded from four other sites with a very low relative abundance (0.2%).
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.
Kingdom |
|
Phylum |
|
Class |
|
Order |
|
Family |
|
Genus |