Sporolithon indopacificum Maneveldt & P.W.Gabrielson, 2017

Maneveldt, G. W., Gabrielson, P. W. & Kangwe, J., 2017, Sporolithon indopacificum sp. nov. (Sporolithales, Rhodophyta) from tropical western Indian and western Pacific oceans: First report, confirmed by DNA sequence data, of a widely distributed species of Sporolithon, Phytotaxa 326 (2), pp. 115-128 : 118-123

publication ID

https://doi.org/ 10.11646/phytotaxa.326.2.3

DOI

https://doi.org/10.5281/zenodo.13701113

persistent identifier

https://treatment.plazi.org/id/03FE87EA-8E01-FF8B-9D8C-F9477D3E18A0

treatment provided by

Felipe

scientific name

Sporolithon indopacificum Maneveldt & P.W.Gabrielson
status

sp. nov.

Sporolithon indopacificum Maneveldt & P.W.Gabrielson sp. nov. ( Figs 3–15 View FIGURES 3–8 View FIGURES 9–15 )

Holotype:— L 3964509 !, 06.vi.2016, leg. J. S. Kangwe, J. Nene & K. Mohammed, collection number T16 /01 ( Fig. 3 View FIGURES 3–8 ), free-living rhodolith occurring intertidally (and exposed at low water of spring tide) in a mixed rocky/muddy substrate, variably also dominated by seagrasses and algal turfs. Fragments of the holotype are in UWC and NCU.

Isotypes:— L 3964510!, L 3964511! and UWC T 16/01. Fragments of the isotypes housed in L are also in NCU.

Type Locality:— Tanzania. Zanzibar Island, Chwaka Bay , Mapopwe Creek (06°10 ’ 38.24 ” S; 39°25 ’ 41.27 ” E) GoogleMaps .

Etymology:— ‘ indopacificum ’ in reference to the species’ distribution in both the tropical western Indian and Pacific oceans.

Description

DNA Sequences:—Three rbc L sequences were obtained, one from the holotype, L 3964509, 1384 bp long (GenBank MG051266) and one from each isotype L 3964510 (GenBank MG051267) and L 3964511 (GenBank MG051268), both 691 bp long, and from the holotype a psb A sequence (GenBank MG051270), 850 bp long ( Table 1). Over comparable lengths the rbc L sequences were identical to each other. Both the rbc L sequences and the psb A sequence are diagnostic for S. indopacificum .

Habit and morphology:—Plants non-geniculate, free-living as spherical rhodoliths measuring roughly 35–50 mm in diameter ( Fig. 3 View FIGURES 3–8 ). Thalli lumpy with crowded, mostly contiguous, swollen protuberances ( Figs 3, 4 View FIGURES 3–8 ). Surface texture matt with freshly collected, living plants brownish pink to maroon in colour. Individual rhodoliths comprise solely this species overgrowing itself in a superimposed manner of variably thin (60 μm) to thick (> 1200 μm) crusts ( Fig. 5 View FIGURES 3–8 ).

Anatomy:—Thallus dorsiventrally organised, monomerous and haustoria absent ( Figs 6, 7 View FIGURES 3–8 ). Medulla extremely thin and plumose (non-coaxial) ( Figs 6, 7 View FIGURES 3–8 ), composed of 3–10 filaments aligned more or less parallel to substratum, measuring no more than 50 μm thick. Medullary filaments comprise square to elongate cells, measuring 10–37 μm in length and 5–8 μm in diameter. Cortex comprises the bulk of the thallus ( Fig. 6 View FIGURES 3–8 ). Cortical filaments comprise square to elongate cells, measuring 5–30 μm in length and 4–12 μm in diameter. Contiguous medullary and cortical filaments joined primarily by secondary pit connections; cell fusions absent to rare. Subepithallial initials square to rectangular, measure 5–15 μm in length and 5–12 μm in diameter, and are similar in size to subtending cells. Epithallial cells single layered (2 layers when shedding), flattened with flared upper corners ( Fig. 8 View FIGURES 3–8 ), and measure 3–5 μm in length and 4–12 μm in diameter. Trichocytes absent (thus far not observed in any species of Sporolithales).

Reproduction:—No gametangial material observed. Tetra/bisporangial chambers clustered in sori in a superficially raised layer( Figs4 View FIGURES 3–8 , 9,11–13 View FIGURES 9–15 ),3–5cells(incl.epithallial cell)above surrounding thallus surface.Individual tetra/bisporangial chambers uniporate ( Figs 10, 14 View FIGURES 9–15 ), clustered in large groups ( Figs 9, 11 View FIGURES 9–15 ), and have floors flush with ( Fig. 12 View FIGURES 9–15 ) to sunken ( Fig. 13 View FIGURES 9–15 ) 4 cell layers below surrounding vegetative surface. Chambers longitudinally elliptical, measuring 30–45 μm in diameter and 85–110 μm high, separated by 0–4 sterile paraphyses (mostly 0–1) comprised of 3–5 elongate cells each ( Figs 14, 15 View FIGURES 9–15 ) that are no different to immediately surrounding vegetative filaments. Chambers possess a basal layer of elongate cells ( Fig. 15 View FIGURES 9–15 ). Chamber pores measure 8–17 μm in diameter and surrounded by 8–13 rosette cells ( Fig. 10 View FIGURES 9–15 ) that are no different from the surrounding sorus surface cells. Entire tetra/bisporangial sori appear to be sloughed off from the outer thallus ( Fig. 4 View FIGURES 3–8 ); no buried chambers observed. Chambers bear only one tetra/bisporangium ( Figs 14, 15 View FIGURES 9–15 ) measuring 65–90 μm in length and 25–40 μm in diameter. Most sporangia not cleaved ( Fig. 14 View FIGURES 9–15 ). Other sporangia either zonately arranged bisporangia ( Fig. 15 View FIGURES 9–15 ) or incompletely divided tetrasporangia with ‘T’-shaped pattern of division ( Fig. 14 View FIGURES 9–15 ). Tetra/bisporangia bear apical pore plugs ( Figs 10, 14, 15 View FIGURES 9–15 ) and borne on a single stalk cell ( Fig. 14 View FIGURES 9–15 ).

Distribution:— Fiji and Tanzania based on DNA sequences.

J

University of the Witwatersrand

S

Department of Botany, Swedish Museum of Natural History

K

Royal Botanic Gardens

UWC

University of the Western Cape

NCU

University of North Carolina Herbarium

L

Nationaal Herbarium Nederland, Leiden University branch

T

Tavera, Department of Geology and Geophysics

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