Branchiomma iliffei, Tovar-Hernández & Knight-Jones, 2006
publication ID |
https://doi.org/ 10.11646/zootaxa.1189.1.1 |
publication LSID |
lsid:zoobank.org:pub:B57B9D66-6191-4BFE-A17D-9CA97CEF4C7D |
persistent identifier |
https://treatment.plazi.org/id/03818780-A402-FFC3-FEEC-F9B1FD62FE7D |
treatment provided by |
Felipe |
scientific name |
Branchiomma iliffei |
status |
sp. nov. |
Branchiomma iliffei View in CoL sp. nov.
Figures 7A–K View FIGURE 7 , 8B–C View FIGURE 8 , 9K–M View FIGURE 9 , 10G View FIGURE 10 , 11F View FIGURE 11
Material examined
Type material: Holotype [ LACMAHF POLY 2129 ] Bahamas, Exuma Cays, Basil Minn’s Cave , 23° 28’ N, 75° 45’ W, Sta. 45, LH03233, in marine entrance pool, algae and sediment scooped up from bottom (strong sulphuric acid odour from black silt), Coll. L. Harris, Jan. 11, 2003 GoogleMaps . Paratypes [ LACMAHF POLY 2130 ] (3), sample location and date as for holotype .
Nontype material: Curaçao [ZMA] V. Pol. 0068.01, Spaansche Water, in mangrove roots, 0–1 m, Coll. C. J. van der Horst, Apr. 3, 1920 (1); V. Pol. 1404, Saint Croix Krausse, lagoon sea side, July 15, 1955, on muddy sand flat with clumps of Rhizophora sp. sea grasses, Cassiopeia sp. , 0–2 m, Coll. P. Wagenaar Hummelinck (4).
Description
The following description is based mainly on the holotype, with data in parenthesis for the paratypes.
Body elongate, 19.5 (23–32) mm long without crown, thorax 3 mm long (3.5), 2 mm wide. Body colour dark brown with interramal dark brown spots, small, difficult to distinguish against the background colour of the body. Radiolar crown short (onequarter of the body length), 6 (8) mm long. Radioles united at the base by short dark green web or membrane, consist of 13 pairs (13–14) with green and maroon bands, each band occupying space of two or three pinnules), and stylodes with inner region maroon. Radioles with apinnulate tips, as long as equivalent space of 10 pinnules. Basal stylode unpaired, medium length, subdigitiform; stylode width one half of the rachis width. Stylodes: 16 pairs [m, m, m, m, m, l, l, l, l, l, l, l, l, l, l, l], all subdigitiform ( Fig. 9L View FIGURE 9 ), with long pairs only 1–1.5 times as long the medium ones ( Fig. 9M View FIGURE 9 ); width of those from basal region of radiole one half of the rachis width, as in those of the medial region. Eyes big, near to the radiolar tip, covering whole of side of radiolar rachis ( Fig. 7C View FIGURE 7 ), with those from median and distal region surrounded by an accumulation of pigment cells, and lenses coneshaped. Dorsal lips short, onequarter length of radioles, triangular and with a distinct orange longitudinal ridge (midrib) with some small dark olive green spots. Midline faecal groove deep on first segment forming mounds each side, collar well separated dorsally ( Figs 7A View FIGURE 7 , 8B View FIGURE 8 ); ventral lappets triangular, not overlapping ( Figs 7B View FIGURE 7 , 8C View FIGURE 8 ). Thorax with eight segments. Thoracic tori extending to sides of green ventral shields ( Fig. 7B View FIGURE 7 ). Collar chaetae slender, weakly geniculate, arranged in compact fascicles. Thoracic notochaetae arranged within each fascicle in irregular oblique rows of superior and inferior chaetae; each superior chaeta slender, weakly geniculate, knee region slightly wider than shaft ( Fig. 7F View FIGURE 7 ); inferior chaetae with knee up to twice as wide as shaft ( Fig. 7G View FIGURE 7 ). Avicular uncini with the crest surmounted by three rows of teeth (side view) occupying one half of the crest with four or five teeth per row ( Figs 7D View FIGURE 7 , 11F View FIGURE 11 ), and with short, curved manubrium ( Fig. 7E View FIGURE 7 ). Abdomen with 65 (66–69) segments. Tori smaller than those in thorax (less than a half its length). Most fascicles of abdominal chaetae forming single compact tufts ( Fig. 10G View FIGURE 10 ), outer chaetae geniculate ( Figs 7K View FIGURE 7 ), arranged in a Cshaped arc around a cluster of more slender shafted capillary chaetae ( Fig. 7K View FIGURE 7 ); number of chaetae per fascicle decreasing gradually towards newer posterior segments. Abdominal uncini with short straight manubrium ( Fig. 7E View FIGURE 7 ). Faecal groove passes around right side of body from the last thoracic segment to second segment of ventral abdomen and on to bilobed pygidium. Tubes made of brown, fine sand.
Remarks
Branchiomma illifei differs from B. nigromaculatum , B. bairdi and B.conspersum in having stylodes of similar shape and size throughout the radiole (lacking macrostylodes). The species differs from Branchiomma curtum (and others in the B. cingulatum group, PKJ pers. obs) in being more elongate, with a longer thorax, and bearing more numerous stylodes, but its most distinguishing character is the remarkable size of its eyes, which take up most of the width of the rachis in side view ( Fig. 7C View FIGURE 7 ).
Type locality Bahamas, Exuma Cays, Basil Minn’s Cave , 23° 28’ N, 75° 45’ W GoogleMaps .
Distribution Bahamas and Curaçao.
Etymology
This species is named in honour of Dr. Tom Iliffe (Texas A & M University at Galveston) in recognition of his research on Bahamas.
m, B 25 m, C, E–F, L 67 m, D, G 125 m, H 33 m, J 17 m, M 100 m.
Discussion
Wide geographical distributions of polychaete species, whether or not they are referred to as cosmopolitan, are often suspect. Detailed study usually finds that more than one species is involved. It is less timeconsuming to synonymise species, than to spend time studying each in fine detail. The distribution of Branchiomma nigromaculatum given above is now more limited than that in general polychaete literature. The Cape Verde Island records, apparently the only proven ones outside of the West Atlantic tropical waters, could have been distributed by flotsam using the Gulf Stream / North Atlantic current / North equatorial current gyre. However, some species really do have a wide, if not a cosmopolitan, distribution. The wider, somewhat linear distribution of Branchiomma curtum Ehlers from Chile, New Zealand, Cape Verde Islands and Mexico may have been assisted by ballast water from ships.
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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