A new species of Raricirrus (Annelida: Cirratuliformia) from deep-water sunken wood off California
Author
Magalhães, Wagner F.
Author
Linse, Katrin
Author
Wiklund, Helena
text
Zootaxa
2017
2017-11-22
4353
1
51
68
journal article
31361
10.11646/zootaxa.4353.1.3
a3f68dc2-99c8-474b-8fd4-75234632da0a
1175-5326
1064504
0E24007C-9CCA-403E-84B7-6D94FF6AAFC8
Raricirrus jennae
sp. nov.
Zoobank registration number: Genbank registration number:
Figures 1
–3
Material examined.
Holotype
:
Monterey Bay,
California
, “Deadwood 2” site, 36°15.41 ʹ N, 122°40.41ʹ W, associated with deployed fragments of yew (
Torreya californica
), deployed on
October 18, 2011
and retrieved on
October 26–28, 2013
by a benthic elevator and
ROV
Doc Ricketts
on an
MBARI
cruise aboard the
R/V Western Flyer,
3100 m
(
USNM
1437642).
Paratypes
same locality, date, collector and wood
type
as
holotype
(5,
USNM
1437643; 5,
USNM
1437644; 5,
FMNH
15516; 7,
FMNH
15517). Molecular voucher specimens were collected at same localities and dates as
type
material.
Additional non-type material examined:
Same locality, date and collector as
type
series, associated with Spice bush (
Calycanthus occidentalis
), Sta. WB21 (4); Lyon, Sta. WB31 (2) and Sta. WB32 (118; 1
DNA
voucher
NHMUK
2017.105); yew (
Torreya californica
), Sta. WB34 (1), Sta. WB35 (87) and Sta. WB36 (57); fern genus
Cyathea
, Sta.
WB37 (2). East Scotia Ridge E2, "Cindy's Castle", 56°5.33ʹ S, 30°19.11ʹ W, associated with tubes of
Maldanidae
polychaetes, collected
December 12, 2012
by
ROV
ISIS
on research cruise JC80 aboard RRS James Cook,
2646 m
(2,
NHMUK
2017.101-102; 1
DNA
voucher,
NHMUK
2017.103).
Description.
Holotype
6 mm
long,
1 mm
wide on mid-body segments, with 29 chaetigers (
Figs 1A
; 2A). Twenty-two
paratypes
measured
4–9.8 mm
long,
0.5–1.2 mm
wide for 19–31 chaetigers. Body short, stout to elongate, segments distinct, rounded dorsally, ventrally flat (
Fig. 1A, G
); ventral groove along body (Fig. 2A); posterior chaetigers with a ventral ridge along 8–10 segments, slightly widened (
Fig. 1G
). Live specimens not observed. Preserved specimens with uniform color, light, golden brown (Fig. 2B) to dark brown (Fig. 2A); branchiae same color of body (Fig. 2A). Dark body pigmentation precludes observation of internal features heart body only observed in one specimen from chaetigers 10–16 (
Fig.
1I
); one dissected specimen with heart body from chaetigers 10–15 (Fig. 2C).
Prostomium conical, rounded anteriorly with a pair of elongate, postero-lateral nuchal organs (
Figs 1A, B
; 2A); eyes absent. Prostomium clearly separated from peristomium by deep lateral groove and shallow dorsal groove (Fig. 2A, B). Peristomium slightly longer than prostomium, with a shallow lateral groove forming two equivalent annuli (
Figs 1A
; 2A, B). Dorsal region of peristomium slightly elevated, forming a crest extending posteriorly over chaetiger 1–2 (Fig. 2A). Dorsal tentacles absent. Branchiae usually short, present in limited number of anterior body segments, arising posterior to notopodial lobe (
Figs 1A, I
; 2A); segmental origin of first branchia not related to size (Fig. 3B); branchiae smooth or crenulated in some specimens (
Fig.
1I
).
Holotype
with branchiae on right side of chaetigers 8 and 9 and left side of chaetiger 6 (
Figs 1A
; 2A). Presence and number of branchiae variable, present on anterior half of body usually between chaetigers 3–15 (see
Table 1
).
Parapodia lateral throughout with chaetae emerging from low parapodial ridges (
Fig. 1C, D
). Chaetae of three
types
: normal capillaries, long capillaries (natatorial) and acicular spines; capillaries showing serrations along one side of blades under oil immersion. Notopodia of chaetiger 1 with two rows of normal capillaries numbering 5–6 (
paratypes
ranging from 2–8 capillaries; see
Table 1
); notopodia of chaetiger 15 with 8–10 long capillaries (
paratypes
with 4–12 either long or normal capillaries). Notopodial capillaries always longer than neurochaetae. Notopodial acicular spines from chaetiger
16 in
holotype
(
paratypes
from chaetigers 15–20); with three spines and three companion capillaries (
paratypes
with 1–3 spines and 2–6 companion capillaries); segmental origin of notopodial spines clearly size-dependent (Fig. 3A); a juvenile individual (
1.2 mm
long,
0.2 mm
wide) with notopodial spines from chaetiger 5. Notopodial acicular spines colorless, straight with blunt tip (
Figs 1F
; 2F). Neuropodia with acicular spines and companion capillaries throughout; neuropodial acicular spines colorless, straight and with blunt tips (
Figs. 1E
; 2D, E). Some specimens with long natatorial capillaries on notopodia only, slightly longer than body’s width. Anterior neuropodia of
holotype
with one acicular spine and one companion capillary (
paratypes
with 1–2 spines and 2–4 companion capillaries); mid-body neuropodia with two acicular spines and four companion capillaries (
paratypes
with 2–3 spines and 2–6 companion capillaries); last segments with two spines and two companion capillaries (
paratypes
1–2 spines and 2–4 capillaries). Acicular spines from mid-body and posterior end segments slightly longer than neuropodial spines from anterior end but of similar shape and width (
Fig. 1E, F
).
FIGURE 1.
Raricirrus jennae
sp. nov.
A, Holotype (USNM 1437642) in dorsal view; B, paratype (USNM 1437643) anterior end, lateral view; C, parapodium 8, left side; D, parapodium 21, left side; E, neuropodial spine and notopodial spine from chaetiger 8; F, neuropodial spine and notopodial spine from chaetiger 21; G, posterior end of holotype, ventral view; H, posterior segments with pygidium, dorsal view; I, anterior end in dorsal view showing heart body; J, individual with anterior end regenerating. (abbreviations: an, anus; hb, heart body; mo, mouth; mvr, mid-ventral ridge; nuO, nuchal organ; pr, prostomium; per, peristomium; py, pygidium).
TABLE 1.
GenBank accession numbers for taxa included in phylogenetic analyses
Taxon |
COI |
16S |
Acrocirridae
gen. 1 sp. 1 KJO-2009
|
FJ944530.1 |
FJ944509.1 |
Acrocirridae
gen. 1 sp. 3 KJO-2009
|
FJ944533.1 |
FJ944511.1 |
Acrocirridae
gen. 2 sp. KJO-2009
|
FJ944536.1 |
FJ944514.1 |
Acrocirridae
sp. 'horned bomber'
|
FJ944534.1 |
FJ944512.1 |
Acrocirridae
sp. 'squidworm'
|
FJ944537.1 |
FJ944515.1 |
Acrocirridae
sp. 'tiburon bomber'
|
FJ944535.1 |
FJ944513.1 |
Brada
sp. KJO-2011
|
HQ326970.1 |
HQ326963.1 |
Brada villosa
CMC01
|
HQ024270.1 |
HQ326962.1 |
Cirratulus
cf.
cirratus
MW-2014
|
KM083601.1 |
KT033724.1 |
Cirratulus cirratus
|
HM417794.1 |
DQ779609.1 |
Cirriformia chicoi
|
KM192165.1 |
KM192189.1 |
Cirriformia tentaculata
|
KR916808.1 |
KT033725.1 |
Coppingeria
sp. KJO-2011
|
HQ326971.1 |
HQ326960.1 |
Ctenodrilus
cf.
serratus
MW-2015
|
KP794931.1 |
KT033726.1 |
Ctenodrilus serratus
|
KP794932.1 |
KT033727.1 |
Ctenodrilus pacificus
|
KT934277.1 |
KT934267.1 |
Dodecaceria ater
|
KP794933.1 |
KT033728.1 |
Dodecaceria concharum
|
DQ209262.1 |
KT033729.1 |
Dodecaceria sextentaculata
|
KP794935.1 |
KT033730.1 |
Flabelligena
sp. KJO-2008
|
EU694126.1 |
EU694113.1 |
Flabelligera infundibularis
|
EU694131.1 |
EU694112.1 |
Flabelligera mundata
|
HQ326969.1 |
HQ326958.1 |
Flota
sp. KJO-2008
|
EU694129.1 |
EU694110.1 |
Macrochaeta clavicornis
|
EU791463.1 |
HQ326957.1 |
Macrochaeta
sp. KJO-2008
|
EU694125.1 |
EU694114.1 |
Raricirrus beryli
|
HE863972
|
MF414726
|
Raricirrus jennae
California wood
|
MF414724
|
MF414727
|
Raricirrus jennae
ESR vent
|
MF414725
|
MF414728
|
Timarete caribous
|
KM192173.1 |
KM192193.1 |
Timarete ceciliae
|
KM192179.1 |
KM192196.1 |
Timarete
cf.
punctata
MW-2015
|
KP794936.1 |
KT033731.1 |
Timarete punctata
|
KM192184.1 |
KM192205.1 |
Pygidium simple segment with a ventral round lobe and dorso-terminal anal aperture (
Fig. 1H
).
Remarks.
See Table 2 and Discussion for comparison among species of
Raricirrus
.
Comparative material examined:
Raricirrus beryli
Petersen & George, 1991
, holotype, ZB 1990.52, Beryl oilfield, North Sea,
100-115 m
,
12 May 1982
.
Raricirrus variabilis
Dean, 1995
, 8 Paratypes, USNM
170552
, Virgin Islands.
Raricirrus jennae
sp. nov.
is readily distinguished from all other
Raricirrus
species by the lack of serrated chaetae, presence of acicular spines, presence of capillaries on neuropodia in addition to notopodia and absence of enlarged modified (genital) spines.
Etymology.
This species is named after Dr. Jenna Judge who kindly donated the samples collected as part of her dissertation for identification and description.
Distribution.
Type
locality is Monterey Bay, off
California
,
U.S.
in
3,100 m
. This species has also been collected from
2,100–2,600 m
at deep-sea hydrothermal vent sites E2 and E
9 in
East Scotia Ridge, Southern Ocean (Fig. 4).
FIGURE 2.
Raricirrus jennae
sp. nov.
A, anterior end of holotype (USNM 1437642) in dorsal and ventral views, respectively; B, complete specimen in lateral view showing slightly inflated posterior end segments; C, dorsal region of dissected individual showing heart body from chaetigers 10 to 15; D, neuropodial spine of chaetiger 3; E, neuropodial spine from a posterior end segment; F, notopodial spine from chaetiger 20. (abbreviations: br, branchiae; hb, heart body; mo, mouth; mvg, mid-ventral groove; pr, prostomium; per, peristomium; py, pygidium).
Phylogenetic results.
The two
Raricirrus jennae
sp. nov.
specimens from
California
wood and East Scotia Ridge vent are sister taxa to
Raricirrus beryli
from shallow water (
115 m
depth) in the North Atlantic, with strong support for the clade (Fig. 5). The K2P distance between the two
R. jennae
sp. nov
specimens from different ocean basins is
0.01 in
16S and
0.02 in
COI, while the K2P distance between them and
R. beryli
is
0.11 in
16S and
0.24 in
COI. The genus
Raricirrus
,
represented by the species
R. jennae
sp. nov.
and
R. beryli
,
appears as sister group to a clade composed of
Dodecaceria
and
Ctenodrilus
(Fig. 5).