Chondrophycus anabeliae Sentíes, M.T. Fujii, Cassano & Dreckmann, 2016

Sentíes, Abel, Cassano, Valéria, Dreckmann, Kurt M., Gil-Rodríguez, Candelaria, Stein, Erika M. & Fujii, Mutue T., 2016, Chondrophycus anabeliae (Rhodomelaceae, Ceramiales), a new species in the Laurencia complex from the Mexican Caribbean, Phytotaxa 283 (3), pp. 259-270 : 261-262

publication ID

https://doi.org/ 10.11646/phytotaxa.283.3.2

DOI

https://doi.org/10.5281/zenodo.13647512

persistent identifier

https://treatment.plazi.org/id/7D2987BD-FFAF-DA5F-149D-4A5B53A2F177

treatment provided by

Felipe

scientific name

Chondrophycus anabeliae Sentíes, M.T. Fujii, Cassano & Dreckmann
status

sp. nov.

Chondrophycus anabeliae Sentíes, M.T. Fujii, Cassano & Dreckmann sp. nov. ( Figs 1–18 View FIGURES 1–4 View FIGURES 5–8 View FIGURES 9–12 View FIGURES 13–18 ).

Type locality:— MEXICO, Quintana Roo, Isla Mujeres, Garrafón de Castilla ; 21° 12’ 32.28” N and 86° 43’ 17.83” W, coll. A. Sentíes, & M. C. Gil-Rodríguez s.n., tetrasporangial plant, 12 February 2007 (holotype UAMIZ 1240 About UAMIZ ). Genbank accesion number for rbc L KX815262 . Paratype: ( UAMIZ 1241 About UAMIZ ) vegetative and male plants, coll. A. Sentíes & M. T. Fujii s.n., 16 November 2008 GoogleMaps .

Etymology:—The specific epithet makes reference to “Anabel”, the ancient goddess of love in the western Caribbean Sea region.

Diagnosis:—Plants forming tufts up to 7 cm high; thalli terete to partially compressed up to 1.5 mm in diameter, arising from a discoid holdfast; cartilaginous in texture; branching irregularly alternate and spirally arranged, usually with 2–3 (4) orders of branches; ultimate branchlets are cylindrical-clavate; two pericentral cells per vegetative axial segment, production of the first pericentral cell on the side of the trichoblast basal cell, trichoblast type spermatangial branches, procarp-bearing segment with five pericentral cells, tetrasporangia produced from a particular cell with the formation of one additional fertile pericentral cell, and arranged at a right-angle in relation to fertile branchlets.

Morphology: Plants forming tufts up to 7 cm high, terete to partially compressed axes ( Figs 1–4 View FIGURES 1–4 ), cartilaginous in texture, not adhering to herbarium paper when dried. Thalli attached to the substratum by a discoid holdfast. Erect branches irregularly alternate and spirally arranged, usually with 2–3 (4) orders of branches. The main axes are partially compressed in the lower portions of the thalli, broader in the middle portions, 900–1,500 μm in diameter, and slightly narrowing towards the terete apices, 750–1,080 μm in diameter in the upper portions. Ultimate branchlets cylindrical to clavate and truncate at the apices, 800–2,950 μm long and 544–850 μm in diameter.

Vegetative structures: In surface view the outermost cortical cells are translucent, isodiametric-polygonal in the middle portions, 20–33 μm long and 10–20 μm wide, without secondary pit connections ( Fig. 5 View FIGURES 5–8 ). Subcortical cells are pigmented, larger and connected to each other by secondary pit connections ( Fig. 6 View FIGURES 5–8 ). In transverse section thalli formed by two cortical cell layers, and four or five layers of medullary cells ( Fig. 7 View FIGURES 5–8 ). The translucent outer layer of cortical cells become evident, and they are smaller than the inner layer cells, measuring 20–25 μm long and 15–17.5 μm wide in the middle portions of main axes ( Fig. 8 View FIGURES 5–8 ). These outer cortical cells are markedly projecting beyond the surface near the apices. The inner layer of cortical cells is composed of pigmented and elongated cells, measuring 50–52 μm long and 28–30 μm wide ( Fig. 8 View FIGURES 5–8 ). Medullary cells are rounded or slightly radially elongated, measuring 75–115 μm long and 45–70 μm wide in the middle portions of the main axes. Medullary cell walls uniformly thickened, but lenticular wall thickenings are absent. Each vegetative axial segment cuts off two pericentral cells ( Figs. 9, 10 View FIGURES 9–12 ) that are slightly smaller than the medullary cells of the surrounding layer.

Reproductive structures: Male branches are characteristically swollen, up to 800 μm in diameter ( Fig. 2 View FIGURES 1–4 ). In longitudinal section through a fertile branchlet, the spermatangial pits are cup-shaped, and an axial cell row is discernible at the base ( Fig. 11 View FIGURES 9–12 ). Spermatangial branches developed from two laterals on a suprabasal cell of trichoblast, terminating in a vesicular sterile cell, 37.5–40 μm long and 20–22.5 μm in diameter; partial sterility of the spermatangial branches was not seen. Spermatangia ovoid, 15–17.5 μm long and 5.0–7.5 μm in diameter with each spermatium possessing a noticeable apical nucleus ( Fig. 12 View FIGURES 9–12 ).

In female thalli, each procarp-bearing segment producing five pericentral cells ( Fig. 13 View FIGURES 13–18 ), the fifth of which becomes the supporting cell of a four-celled carpogonial branch with two groups of sterile cells ( Fig. 14 View FIGURES 13–18 ). Fully developed cystocarps are conical, with a prominent ostiole, 500–750 μm in diameter, subapically arranged with the lower half immersed within the parent branch ( Figs. 3 View FIGURES 1–4 , 15 View FIGURES 13–18 ). Carposporangia are clavate, 80–200 μm long and 20–55 μm in diameter.

Tetrasporangial branchlets are cylindrical or slightly compressed, simple or compound, 800–1,200 μm long and 850–1,175 μm in diameter ( Fig. 4 View FIGURES 1–4 ). Tetrasporangia are arranged in a right-angled pattern in relation to fertile branchlets ( Figs 4 View FIGURES 1–4 , 16 View FIGURES 13–18 ). At the apex of fertile branches, each axial segment produces one additional pericentral cell situated opposite to the existing two normal pericentral cells. The third additional cell becomes fertile, and the two pre-existing pericentral cells remain vegetative ( Fig. 17 View FIGURES 13–18 ). The additional cell cuts off two pre-sporangial cover cells distally and abaxially positioned in relation to the tetrasporangial initial ( Fig. 18 View FIGURES 13–18 ). Subsequently, one post-sporangial cover cell is produced and continues to divide, contributing to cortication around the tetrasporangia. The pre-sporangial cover cells do not divide and display a transverse-type alignment in relation to the fertile axis in surface view. Mature tetrasporangia are tetrahedrally divided, 30–130 μm in diameter ( Fig. 18 View FIGURES 13–18 ).

A

Harvard University - Arnold Arboretum

M

Botanische Staatssammlung München

C

University of Copenhagen

L

Nationaal Herbarium Nederland, Leiden University branch

T

Tavera, Department of Geology and Geophysics

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