Chaetozone adunca, Blake, 2022

Blake, James A., 2022, New species and records of Caulleriella, Chaetocirratulus and Chaetozone (Annelida, Cirratulidae) from continental shelf and slope depths of the Western North Atlantic Ocean, Zootaxa 5113 (1), pp. 1-89 : 31-37

publication ID

https://doi.org/ 10.11646/zootaxa.5113.1.1

publication LSID

lsid:zoobank.org:pub:EB01C862-025E-493F-8CA9-934B4F1626AF

DOI

https://doi.org/10.5281/zenodo.6958012

persistent identifier

https://treatment.plazi.org/id/0936557E-257C-466D-8857-A24CF9309413

taxon LSID

lsid:zoobank.org:act:0936557E-257C-466D-8857-A24CF9309413

treatment provided by

Plazi

scientific name

Chaetozone adunca
status

sp. nov.

Chaetozone adunca new species

Figures 15–16 View FIGURE 15 View FIGURE 16

urn:lsid:zoobank.org:act:0936557E-257C-466D-8857-A24CF9309413

Chaetozone sp. 11 : Blake et al. 1987: 61, 68, C-2; Maciolek et al. 1987b: D-2; Blake & Grassle 1994: 850, 855; Blake & Hilbig 1994: 883–884, 896; Hilbig 1994: 940.

Chaetozone sp. B: Maciolek et al. 1987b: D-2 (in part).

Chaetozone sp. 1 : Maciolek et al. 1987b: D-2 (in part).

Material examined. (407 specimens) Off Cape Hatteras , North Carolina , US South Atlantic ACSAR Program, coll. J.A. Blake, Chief Scientist. Sta. 9: Cruise SA-3, Rep. 1, 22 Jul 1984, 35°28.30′N, 74°47.70′W, 579 m GoogleMaps , holotype ( USNM 1660944 About USNM ) , 7 paratypes ( USNM 1660945 About USNM ); Rep. 2, 22 Jul 1984, 3°28.40′N, 74°47.50′W, 614 m GoogleMaps , 18 paratypes ( USNM 1660946 About USNM ); Rep. 3, 22 Jul 1984, 35°28.30′N, 74°47.60′W, 598 m GoogleMaps , 32 paratypes ( USNM 1660947 About USNM ); Cruise SA-4, Rep. 1, 24 May 1985, 35°28.41′N, 74°47.44′W, 640 m GoogleMaps , 23 paratypes ( USNM 1660948 About USNM ); Rep. 2, 24 May 1985, 35°28.41′N, 74°47.56′W, 603 m GoogleMaps , 9 paratypes ( USNM 1660949 About USNM ); Rep. 3, 24 May 1985, 35°28.28′N, 74°47.52′W, 623 m GoogleMaps , 25 paratypes ( USNM 1660950 About USNM ); Cruise SA-5, Rep. 1, 25 Sep 1985, 35°28.41′N, 74°47.46′W, 629 m GoogleMaps , 18 paratypes ( USNM 1660951 About USNM ); Rep. 2, 25 Sep 1985, 35°28.41′N, 74°47.47′W, 629 m GoogleMaps , 23 paratypes ( USNM 1660952 About USNM ).— MMS Cape Hatteras Survey , August 1992, coll. J.A. Blake, Chief Scientist. Sta. SA-9: 35°28.36′N, 74°47.42′W, 620 m (57, USNM 1660953 About USNM ) GoogleMaps ; Sta. CH-1: 35°42.47′N, 74°46.58′W, 804 m (15, USNM 1660954 About USNM ) GoogleMaps ; Sta. CH-3, 35°37.08′N, 74°46.12′W, 812 m (7, USNM 1660955 About USNM ) GoogleMaps ; Sta. CH-18: 35°30.01′N, 74°47.61′W, 530 m (1, USNM 1660956 About USNM ) GoogleMaps ; Sta. CH-19: 35°29.79′N, 74°46.59′W, 812 m (13, USNM 1660957 About USNM ) GoogleMaps ; Sta. CH-34: 35°25.10′N, 74°48.35′W, 775 m (8, USNM 1660958 About USNM ) GoogleMaps ; Sta. CH-41: 35°22.19′N, 74°52.31′W, 590 m (6, USNM 1660959 About USNM ) GoogleMaps ; Sta. CH-42: 35°21.28′N, 74°50.64′W, 785 m (1, USNM 1660960 About USNM ) GoogleMaps . — Off Cape Lookout , North Carolina, ACSAR, Sta. 2: Cruise SA-3, Rep. 1, 15 Jul 1984, 34°14.50′N, 75°43.90′W, 984 m (1, USNM 1660961 About USNM ) GoogleMaps ; Rep 3, 15 Jul 1984, 34°15.00′N, 75°43.70′W, 1002 m (2, USNM 1660962 About USNM ) GoogleMaps .— Off Charleston , South Carolina, ACSAR Sta. 14: Cruise SA-4, Rep. 3, 20 May 1985, 32°23.67′N, 77°01.12′W, 803 m (1, USNM 1660963 About USNM ) GoogleMaps .— Off New England, U.S. North Atlantic ACSAR Program, coll. G.W. Hampson, Chief Scientist. Sta. 4: Cruise NA-2, Rep. 1, 28 Apr 1985, 40°21.23′N, 67°32.32′W, 563 m (3, USNM 1660964 About USNM ) GoogleMaps ; Rep. 2, 28 Apr 1985, 40°21.23′N, 67°32.33′W, 572 m (6, USNM 1660965 About USNM ) GoogleMaps . Sta. 7: Cruise NA-1, Rep. 1, 10 Nov 1984, 40°27.54′N, 67°40.34′W, 560 m (19, USNM 1660966 About USNM ) GoogleMaps ; Rep. 2, 10 Nov 1984, 40°27.49′N, 67°40.29′W, 560 m (21, USNM 1660967 About USNM ) GoogleMaps ; Rep. 3, 10 Nov 1984, 40°27.52′N, 67°40.36′W, 560 m (1, USNM 1660968 About USNM ) GoogleMaps ; Cruise NA-2, Rep. 1, 28 Apr 1985, 40°27.50′N, 67°40.27′W, 560 m (10, USNM 1660969 About USNM ) GoogleMaps ; Rep. 2, 28 Apr 1985, 40°27.46′N, 67°40.22′W, 560 m (22, USNM 1660970 About USNM ) GoogleMaps ; Rep. 3, 28 Apr 1985, 40°27.44′N, 67°40.19′W, 558 m (4, USNM 1660971 About USNM ) GoogleMaps ; Cruise NA-3, Rep. 1, 06 Jul 1985, 40°27.47′N, 67°40.26′W, 556 m (22, USNM 1660972 About USNM ) GoogleMaps ; Rep. 2, 06 Jul 1985, 40°27.50′N, 67°40.22′W, 555 m (12, USNM 1660973 About USNM ) GoogleMaps ; Rep. 3, 06 Jul 1985, 40°27.48′N, 67°40.21′W, 560 m (18, USNM 1660974 About USNM ) GoogleMaps ; Sta. 12: Cruise NA-2, Rep. 2, 04 May 1985, 39°54.26′N, 70°55.07′W, 555 m (1, USNM 1660975 About USNM ) GoogleMaps ; Cruise NA-5, Rep. 2, 06 May 1986, 39°54.27′N, 70°55.17′W, 548 m (1, USNM 1660976 About USNM ) GoogleMaps ; Cruise NA-6, Rep. 2, 30 Jul 1986, 39°54.26′N, 70°55.07′W, 559 m (1, USNM 1660977 About USNM ) GoogleMaps ; Cruise NA-6, Rep. 3, 30 Jul 1986 ,, 39°54.24′N, 70°55.09′W, 563 m (1, USNM 1660978 About USNM ) GoogleMaps .

Description. A moderately sized species, holotype with 75 setigers, 10.25 mm long, 0.5 mm wide across setiger 1, increasing over swollen anterior segments to 1.1 mm wide, and then decreasing posteriorly to 0.5 mm wide. Body variable in shape, larger specimens with a swollen thoracic region ( Fig. 15A View FIGURE 15 ); most specimens with thorax only slightly enlarged ( Fig. 16A–B View FIGURE 16 ). Individual segments short, narrow, about five times wider than long at first, with some middle thoracic segments 6–8 times wider than long in some specimens; posterior cinctured segments about twice as wide as long ( Figs. 15B View FIGURE 15 , 16F View FIGURE 16 ). Venter with shallow groove along most of body, absent in posterior cinctured segments. Dorsum with narrow groove in mid-body segments ( Fig. 15A View FIGURE 15 ), reduced posteriorly. Posterior cinctured segments with deep intersegmental grooves ( Figs. 15B View FIGURE 15 , 16F View FIGURE 16 ) and a low elevated membrane from which capillaries and acicular spines emerge ( Fig. 16B View FIGURE 16 ). Color in alcohol light tan; no apparent pigmentation.

Pre-setiger region long, narrow, smooth, about as long as first ten setigers ( Fig. 15A View FIGURE 15 ). Prostomium long, narrow, triangular, pointed anteriorly, merging seamlessly with peristomium ( Fig. 15A View FIGURE 15 ); eyespots absent; nuchal organs narrow slits. Peristomium triangular, not divided into rings, with weakly developed shallow lateral grooves visible on some specimens; dorsum narrow, producing weakly developed dorsal crest ( Fig. 15A View FIGURE 15 ). Peristomium merging seamlessly with setiger 1; dorsal tentacles arising from posterior margin with first pair of branchiae lateral to tentacles ( Fig. 15A View FIGURE 15 ); second pair of branchiae dorsal to notosetae on setiger 1 and posterior to position of first branchiae; subsequent branchiae from setiger 2 in same location dorsal to notosetae; present along most of body, but most missing and reduced to stubs or scars.

Parapodia of anterior and middle segments reduced to low ridges or mounds from which setae arise; posterior parapodia swollen, with low raised membrane from which setae arise forming prominent segmental cinctures on last 20–25 setigers. Setiger 1 and thoracic segments with 9–12 capillaries in notopodia and neuropodia; capillaries mostly of moderate size; a few long, natatory-like capillaries present or absent, but not associated with sexual maturity. Acicular spines first present in holotype from setiger 58 in notopodia and setiger 55 in neuropodia; spines 1–2 at first, increasing posteriorly, transitioning into full cinctures with 14 spines in notopodia and 13 neuropodia, up to 27 spines on a side ( Fig. 16C View FIGURE 16 ); spines alternating with capillaries as long as or slightly longer than spines; cinctures with only narrow dorsal, lateral, and ventral gaps between noto- and neuropodial fascicles providing a prominent armature ( Fig. 16C–D View FIGURE 16 ). Notopodial spines clearly longer than neuropodial spines ( Fig. 16C View FIGURE 16 ). Individual spines with basal manubrium at emergence from podial lobes; spines curving and tapering gradually to narrow blunted tip at first ( Figs. 15C, E–G View FIGURE 15 , 16D–E View FIGURE 16 ); more posterior spines with narrow hooked tip ( Fig. 15H–J View FIGURE 15 ); last 3–5 cinctures bearing spines where tip of hook curves back and merges with shaft ( Figs. 15D, K View FIGURE 15 ).

Body narrowing sharply in last few cinctured segments, terminating in simple pygidium with a small, semicircular disk ventral to anal opening ( Figs. 15B View FIGURE 15 , 16F View FIGURE 16 ).

Methyl green staining. A distinct MG pattern present ( Fig. 16G View FIGURE 16 ), with the entire pre-setiger region staining intensely, with only the tip of prostomium and a diagonal transverse band between the prostomium and peristomium not staining; about 9–10 anterior segments also retaining stain laterally and ventrally; rest of body only staining weakly, with no pattern; de-stains rapidly; pre-setiger and anterior segmental stain retained well after return to alcohol.

Remarks. Chaetozone adunca n. sp. belongs to the C. curvata group and represents the eighth species to be reported with acicular spines having a narrow tip that curves back and merges with the shaft. Chaetozone adunca n. sp. differs from others in this group by having a smooth pre-setiger region that is not divided into separate rings and with most segments having the acicular spines narrowing to a blunt or curved tip, with the spines having recurved tips limited to the posteriormost cinctured segments. This transition from blunt-tipped spines to the recurved type has not been previously reported in the genus. Two other species in group are also reported in the present paper: C. anasima and C. brychiata n. sp. (see below). All known species in the C. curvata group are compared in Table 3 View TABLE 3 .

Biology. Chaetozone adunca n. sp., as Chaetozone sp. 11, was reported as among the dominant species off Cape Hatteras, North Carolina, during the ACSAR surveys ( Blake et al. 1987, Blake & Grassle 1994) and the separate Cape Hatteras Survey ( Blake & Hilbig 1994). Station 9 is an ACSAR upper continental slope station located at a depth of about 600 m in an area that exhibits high sedimentation rates and is influenced by the Western Boundary undercurrent (WBUC) and Gulf Stream ( Blake & Grassle 1994). Perhaps because of the high sedimentation rates, infaunal densities at Station 9 at an average of 46,255 individuals per m 2 were the highest found at any location along the entire U.S. Atlantic continental slope ( Blake et al. 1987; Blake & Grassle 1994). Similarly high densities were reported by Blake & Hilbig (1994) at stations (SA-9 and CH-1, CH-3, CH-18, CH-19, CH-34, CH-41 and CH-42) in the 500–800 m range as part of the separate Cape Hatteras survey.

At total of 145 species of benthic invertebrates were identified as Station SA-9 from nine samples collected on three surveys as part of the ACSAR program ( Blake & Grassle 1994). Chaetozone adunca n. sp. (as C. sp. 11) ranked 11 th out of 20 dominant species at Station 9. The five most abundant annelids identified at this site in order of abundance were Cossura longocirrata Webster & Benedict, 1887, Scalibregma inflatum, Rathke, 1843, Limnodriloides medioporus Cook, 1969, Tubificoides intermedius ( Cook, 1969) and Aricidea quadrilobata Webster & Benedict, 1887.

Chaetozone adunca n. sp. also occurred at several upper slope stations in the North Atlantic ACSAR program, but was never among the dominant species ( Maciolek et al. 1987b).

Etymology. The epithet is from the Latin, aduncus, for bent inward, in reference to the inwardly curved tip of some of the acicular spines of this species.

Distribution. U.S. Atlantic continental slope, 530–1003 m.

Kingdom

Animalia

Phylum

Annelida

Class

Polychaeta

Order

Terebellida

Family

Cirratulidae

Genus

Chaetozone

Loc

Chaetozone adunca

Blake, James A. 2022
2022
Loc

Chaetozone sp. 11

Blake, J. A. & Grassle, J. F. 1994: 850
Blake, J. A. & Hilbig, B. 1994: 883
Hilbig, B. 1994: 940
Blake, J. A. & Hecker, B. & Grassle, J. F. & Brown, B. & Wade, M. & Boehm, P. & Baptiste, E. & Hilbig, B. & Maciolek, N. & Petrecca, R. & Ruff, R. E. & Starczak, V. & Watling, L. E. 1987: 61
1987
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