Cirrhilabrus shutmani, a new species of fairy wrasse from the Babuyan Islands, northern Philippines (Teleostei: Labridae)

Abstract

Cirrhilabrus shutmani, new species, is described on the basis of four specimens from Didicas Volcano, Babuyan Islands, Cagayan province, northern Philippines. The holotype and three paratypes were collected at a depth of 50-70 m, along denuded rubble slopes. The new species belong to a complex consisting of C. blatteus, C. claire, C. earlei, C. jordani, C. lanceolatus, C. roseafascia, C. rubrisquamis and C. sanguineus. Aside from similar nuptial male colouration, the nine species share the following character combination: relatively short pelvic fins (not or barely reaching anal-fin origin, except for C. claire with relatively long pelvic fins); a pair of stripes on head (in both sexes); and, dorsal and anal fins without obvious stripes or spots. It differs from the other members of its group in lacking any stripes on the upper and lower body, and in having the following live colouration details: upper part of nape dusky red; dorsal and anal fin bright red with dusky markings; pelvic fins bright red, dusky anteriorly; caudal fin bright yellow basally with distal half bright red. We also present new distribution records for C. claire, C. earlei and C. lanceolatus, as well as a brief mention of a possibly new, related species from the Ogasawara Islands.

Full text

Accepted by W. Holleman: 22 Sept. 2017; published: 30 Oct. 2017
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ZOOTAXA
ISSN 1175-5326 (print edition)
ISSN
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Copyright © 2017 Magnolia Press
Zootaxa 4341 (1): 077
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088
http://www.mapress.com/j/zt/
Article
77
https://doi.org/10.11646/zootaxa.4341.1.6
http://zoobank.org/urn:lsid:zoobank.org:pub:245B75EA-7339-4CF6-B2A5-17D859835C62
Cirrhilabrus shutmani, a new species of fairy wrasse from the Babuyan Islands,
northern Philippines (Teleostei: Labridae)
YI-KAI TEA
1
& ANTHONY C. GILL
2,3,4
1
90 Carillon Avenue, Newtown, NSW 2042, Australia. E-mail: teayk1@gmail.com
2
Macleay Museum and School of Life and Environmental Sciences, A12 – Macleay Building, The University of Sydney, New South
Wales 2006, Australia. E-mail: anthony.c.gill@sydney.edu.au
3
Ichthyology, Australian Museum, 1 William Street, Sydney, New South Wales 2010, Australia
4
Corresponding author
Abstract
Cirrhilabrus shutmani, new species, is described on the basis of four specimens from Didicas Volcano, Babuyan Islands,
Cagayan province, northern Philippines. The holotype and three paratypes were collected at a depth of 50–70 m, along
denuded rubble slopes. The new species belong to a complex consisting of C. blatteus, C. claire, C. earlei, C. jordani, C.
lanceolatus, C. roseafascia, C. rubrisquamis and C. sanguineus. Aside from similar nuptial male colouration, the nine spe-
cies share the following character combination: relatively short pelvic fins (not or barely reaching anal-fin origin, except
for C. claire with relatively long pelvic fins); a pair of stripes on head (in both sexes); and, dorsal and anal fins without
obvious stripes or spots. It differs from the other members of its group in lacking any stripes on the upper and lower body,
and in having the following live colouration details: upper part of nape dusky red; dorsal and anal fin bright red with dusky
markings; pelvic fins bright red, dusky anteriorly; caudal fin bright yellow basally with distal half bright red. We also pres-
ent new distribution records for C. claire, C. earlei and C. lanceolatus, as well as a brief mention of a possibly new, related
species from the Ogasawara Islands.
Key words: ichthyology; taxonomy; Didicas Volcano; colouration
Introduction
The labrid genus Cirrhilabrus Temminck & Schlegel (1845) consists of small, planktivorous fishes found mostly
on rubble slopes spanning the tropical Indo-Pacific region. Allen et al. (2015) listed 51 nominal species in the
genus. Five other species have been described since: Cirrhilabrus isosceles Tea et al. (2016), C. hygroxerus Allen
& Hammer (2016), C. rubeus Victor (2016), C. africanus Victor (2016), and C. efatensis Walsh et al. (2017),
bringing the current nominal species count to 56. Increased deepwater exploration and aquarium fish collection has
allowed for the discovery of several new species, as well as the expansion of previously documented geographical
distributions of various species. We herein describe an additional species in the genus from four specimens
collected for the aquarium trade from Didicas Volcano, Babuyan Islands, northern Philippines. We also present
new distribution records for C. claire, C. earlei, and C. lanceolatus. Additionally, we discuss a possible new
species of Cirrhilabrus with similar combination of colour patterns and fin characters from Ogasawara, which
currently remains known only from photos taken in the field.
Materials and methods
Methods of counting and measuring follow Randall & Masuda (1991), except gill raker counts were counted as
upper (epibranchial) + lower (ceratobranchial), with the angle raker included in the second count. In the description
that follows, data are presented for all type specimens, followed where variation was noted by data for the holotype

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in parentheses. Where counts were recorded bilaterally, both counts are presented and separated by a slash; the first
count is the left. Types are deposited in the Australian Museum, Sydney (AMS), National Museum of the
Philippines, Manila, Philippines (PNM), Western Australian Museum, Perth (WAM) and the Zoological Reference
Collection of the Lee Kong Chian Natural History Museum at the National University of Singapore (ZRC).
Distribution records for various Cirrhilabrus species are based on published photos (in particular, those in Kuiter
2010), underwater photographs, and verifiable literature accounts.
Cirrhilabrus shutmani n. sp.
Magma Fairy-wrasse
Figures 1–6, 8A, Tables 1–2
Holotype. PNM 15354, 55.7 mm SL male, northern Philippines, Cagayan province, Babuyan Islands, Didicas
Volcano (19.08 N, 122.21 E), 50–70 m, rubble slopes, collected by M. Baghukan & D.G. Acutin, 25 August 2016.
Paratypes. AMS I. 47290-001, 44.2 mm SL male, WAM P.34787-001, 45.2 mm SL male, ZRC 55885, 39.5
mm SL male, all collected with holotype.
Diagnosis. Cirrhilabrus shutmani shares similar meristic counts to the other species in its complex, but differs
from congeners in the following live colouration details: upper part of nape dusky red; dorsal and anal fin bright
red with dusky markings; pelvic fins bright red, dusky, and unmarked; caudal fin bright yellow basally with distal
half bright red.
Description. Dorsal-fin rays XI,9; anal-fin rays III,9; dorsal and anal-fin soft rays branched except first ray
unbranched; last dorsal and anal-fin ray branched to base; pectoral-fin rays 15/15, upper two unbranched; pelvic-
fin rays I,5; principal caudal-fin rays 7 + 6, upper and lowermost unbranched; upper procurrent caudal rays 4–5 (5),
lower procurrent caudal rays 4–5 (5); lateral line interrupted, with dorsoanterior series of pored scales 15/15–16
(15/16) and midlateral posterior peduncular series 6–8/6–8 (6/6); scales above lateral line to origin of dorsal fin 2–
3/2–3 (3/3); scales below lateral line to origin of anal fin 7/7; median predorsal scales 4; median prepelvic scales 6;
rows of scales on cheek 2; circumpeduncular scales 16; gill rakers 3–5 + 8–9 = 11–14 (5 + 9); pseudobranchial
filaments 7–9 (9).
Body moderately elongate and compressed, depth 3.5–3.8 (28.9) in SL, width 7.0–10.8 (7.0) in SL; head
length 3.2–3.4 (3.2) in SL; snout pointed, its length 3.3–3.9 (3.3) in HL; orbit diameter 3.5–3.7 (3.5) in HL; depth
of caudal peduncle 2.2–2.4 (2.2) in HL. Mouth small, terminal, and oblique, with maxilla almost reaching a vertical
at front edge of orbit; dentition typical of genus with three pairs of canine teeth present anteriorly at side of upper
jaw, first forward-projecting, next two strongly recurved and outcurved, third longest; an irregular row of small
conical teeth medial to upper canines; lower jaw with single stout pair of canines anteriorly which protrude
obliquely outward and are slightly lateral to medial pair of upper jaw; canine teeth in lower jaw followed by two
smaller, conical teeth; sides of lower jaw with a series of small conical teeth, which continue across front of jaw
behind canine; no teeth on roof of mouth.
Posterior margin of preopercle with 23–32 (32/32) very fine serrae; margins of posterior and ventral edges of
preoperculum free to about level of middle pupil. Nostrils small, located anterior to upper edge of eye in a short
membranous tube. Scales cycloid; head scaled except snout and interorbital space; 7 large scales on opercle; broad
naked zone on membranous edge of preopercle; row of large, elongate, pointed scales along base of dorsal fin, one
per element, longest about two-fifths length of spines, scales progressively shorter posteriorly on soft portion of
fin; anal fin with similar basal row of scales; last pored scale of lateral line (posterior to hypural plate) enlarged and
pointed; one scale above and below last pored scale also enlarged; horizontal series of greatly enlarged scales
extend two-thirds distance to central posterior margin of caudal fin; pectoral fins naked except for few small scales
at extreme base; single large scale at base of each pelvic fin, about three-fourths length of pelvic spine.
Origin of dorsal fin above second lateral-line scale, predorsal length 3.0–3.3 (3.3) in SL; first 1–3 dorsal-fin
spines progressively longer, third and fourth subequal, fifth longest, 2.4–2.8 (2.4) in HL; interspinous membranes
of dorsal fin in males extend beyond dorsal-fin spines, with each membrane extending in a pointed filament beyond
spine; fifth dorsal-fin soft ray longest, 2.0–2.2 (2.0) in HL, remaining rays progressively shorter; origin of anal fin
below base of ninth dorsal-fin spine; third anal-fin spine longest, 2.8–3.0 (3.0) in HL; interspinous membranes of
anal fin extended as on dorsal fin; anal-fin soft rays relatively uniform in length, fifth longest, 1.6–1.9 (1.6) in HL;

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dorsal and anal-fin rays barely reaching caudal-fin base; caudal fin of TP males rounded, length 1.1–1.2 (1.2) in
HL; pectoral fins short, reaching a vertical between bases of 5th or 6th dorsal-fin spines, longest ray 1.5–2 (1.5) in
HL; origin of pelvic fins below lower base of pectoral fins; pelvic fins moderately long, but not reaching anal fin
spine, longest ray 1.9–2.1 (1.9) in HL.
FIGURE 1. Cirrhilabrus shutmani n. sp., freshly euthanized male holotype, PNM 15354, 55.7 mm SL, Didicas Volcano,
Babuyan Islands, northern Philippines. Photo by S.K. Tea.
FIGURE 2. Cirrhilabrus shutmani n. sp., preserved male holotype, PNM 15354, 55.7 mm SL, Didicas Volcano, Babuyan
Islands, northern Philippines. Photo by Y.K. Tea.

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FIGURE 3. Cirrhilabrus shutmani n. sp., male holotype, PNM 15354, 55.7 mm SL, from Didicas Volcano, Babuyan Islands,
northern Philippines. Image reversed. Photo by B.P. Shutman.
FIGURE 4. Cirrhilabrus shutmani n. sp., male, approximately 50 mm TL, from Didicas Volcano, Babuyan Islands, northern
Philippines. Specimen not retained. Photo by B.P. Shutman.

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FIGURE 5. Cirrhilabrus shutmani n. sp., males, A) approximately 57 mm TL, B) approximately 60 mm TL, C) approximately
65 mm TL, all from Didicas Volcano, Babuyan Islands, northern Philippines. Specimens not retained. Photos by B.P. Shutman.

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Colouration of male in life (based on colour photographs of the holotype and paratype when freshly dead, and
aquarium photos of live individuals; Figures 1, 3, 4, 5 & 8A): head and body bright red to orange; lower part of
head sometimes washed with magenta; lilac to magenta stripe weakly present from behind upper orbit to upper
edge of operculum; second stripe of same colour weakly present from behind lower orbit to lower part of cheek;
lilac to magenta stripes continue past eye anteriorly on to snout, the upper stripe reaching mid-upper lip; lower part
of operculum sometimes washed with magenta; upper part of nape and sometimes narrow area below dorsal-fin
dusky red; interorbital and upper part of snout sometimes with 3–5 fine white stripes; iris bright yellow to orange,
dusky dorsally, with bluish grey submarginal ring around pupil; lower part of abdomen bright red to orange-red,
sometimes washed with magenta; anterior two-thirds of body bright red, fading gradually to bright orange
posteriorly; dorsal fin bright red with single row of large orange scales basally, often dusky anteriorly between first
and second dorsal fin spines; more extensive dusky grey-red area sometimes present on anterior three quarters of
fin; distal margin of fin narrowly bright blue to purple; anal fin similar to dorsal fin, but usually without dusky
markings; caudal fin bright yellow, orange basally, with distal half of fin bright red; pelvic fins bright red, dusky
anteriorly, narrowly bright purple-blue on leading edge; pectoral fins reddish hyaline.
TABLE 1. Proportional measurements of type specimens of Cirrhilabrus shutmani expressed as a percentage of the
standard length.
Holotype Paratypes
PNM 15354 AMS I.47290-001 WAM P.34787-
001
ZRC 55885
Sex male male male male
Standard length (mm) 55.7 44.2 45.2 39.5
Body depth 28.9 27.4 26.5 26.8
Body width 14.2 9.3 12.4 11.6
Head length 29.3 29.6 30.5 30.9
Snout length 8.8 8.6 8.8 7.8
Orbit diameter 8.3 8.4 8.4 8.4
Interorbital width 7.7 7.5 7.1 7.3
Upper jaw length 8.2 8.5 7.3 5.4
Caudal-peduncle depth 13.3 13.1 12.8 12.9
Caudal-peduncle length 12.6 12.2 13.5 13.2
Predorsal length 30.5 31.9 32.1 32.9
Preanal length 58.7 57.7 58.0 58.5
Prepelvic length 34.8 32.6 36.1 34.4
Dorsal-fin base 61.2 58.6 58.8 58.2
First dorsal spine 4.8 5.4 6.0 5.3
Longest dorsal spine 12.2 12.2 12.8 10.9
Longest dorsal ray 14.9 14.5 15.3 13.9
Anal-fin base 29.4 28.3 28.3 28.4
First anal spine 6.1 5.7 6.2 4.6
Second anal spine 9.7 8.8 10.0 8.6
Third anal spine 9.9 9.7 10.8 10.6
Longest anal ray 17.4 17.6 17.7 16.2
Caudal-fin length 23.7 25.6 27.2 26.1
Pectoral-fin length 19.4 18.3 18.8 15.4
Pelvic spine length 8.3 8.2 7.7 8.0
Pelvic fin length 15.8 14.7 14.4 15.7

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Colouration of initial phase in life (based on colour photographs and aquarium photos of live individuals):
Similar to males; dorsal and anal fins hyaline red without dusky markings; pelvic fins hyaline red; caudal fin pale
yellow hyaline at base, translucent to reddish hyaline distally.
Colouration in preservative; Figure 2: similar to colour in life; dusky markings remain; red markings become
pale tan; dorsal, anal and pelvic fins greyish hyaline; caudal fin greyish hyaline, base pale yellow; pectoral fins
hyaline.
Etymology. Named in honour of Barnett Paul Shutman, who first provided photos as well as the type
specimens of the new species (via Aquarium Iwarna, Singapore). The common name, magma fairy wrasse, alludes
to its live colouration, as well as the type location of Didicas Volcano, an active volcano part of the “Pacific Ring of
Fire” at the southern end of the Luzon Volcanic Arc.
Distribution and habitat. Cirrhilabrus shutmani is known only from the type locality, Didicas Volcano in the
Babuyan Islands at the northern tip of the Philippines (Figure 6). It appears to inhabit steep slopes comprised
mostly of volcanic rubble at depths ranging from 50–70 m.
Comparisons. Cirrhilabrus shutmani appears to be closely related to C. blatteus Springer & Randall (1974),
C. claire Randall & Pyle (2001), C. earlei Randall & Pyle (2001), C. jordani Snyder (1904), C. lanceolatus Randall
& Masuda (1991), C. roseafascia Randall & Lubbock (1982), C. rubrisquamis Randall & Emery (1983) and C.
sanguineus Cornic (1987). The nine species are distinguished from congeners in having the following character
combination: relatively short pelvic fins (not or barely reaching anal-fin origin, except for C. claire with relatively
long pelvic fins); a pair of stripes on head (in both sexes); and, dorsal and anal fins without obvious stripes or spots.
Cirrhilabrus shutmani is readily distinguished from the other eight species in live colouration (Figure 7–8; Table
2), and further from C. blatteus, C. earlei, C. lanceolatus, C. roseafascia and C. sanguineus in lacking a lanceolate
caudal fin (however, see Remarks). Aside from live colouration, C. shutmani differs from C. jordani in having one
fewer median predorsal scales (4 vs 5) and fewer lower gill rakers (8–9 vs 11). Based on Randall & Pyle’s (2001)
morphometric data for similar-sized specimens of C. earlei, C. shutmani differs in having a shorter head length
(29.3–30.9 vs 34.0–35.4 % SL), a smaller orbit (8.3–8.4 vs 8.9–10.2 % SL), a greater caudal peduncle depth (12.8–
13.3 vs 15.5–16.0 % SL), a shorter 1
st
dorsal fin spine (4.8–6.0 vs 9.4–10.5 % SL), a longer anal fin base (28.3–29.4
vs 24.2–25.6 % SL), shorter first, second and third anal fin spines (4.6–6.2 vs 8.1–8.9; 8.6–10.0 vs 11.1–13.3; 9.7–
10.8 vs 12.8–13.5 % SL, respectively), shorter pelvic fin spine (7.7–8.3 vs 12.4–13.4 % SL) and shorter pelvic fin
(14.4–15.8 vs 20.4–24.7 % SL).
Remarks. The live colouration and absence of a lanceolate caudal fin in C. shutmani should be treated as
provisional. Members of the genus Cirrhilabrus are sexually dimorphic and protogynous, and often diagnosed by
their terminal phase (male) colouration. Males of C. blatteus, C. earlei, C. jordani, C. lanceolatus and C.
roseafascia often attain standard lengths greater than 70 mm, with total lengths frequently exceeding 100 mm
(especially for C. lanceolatus and C. roseafascia). The largest known specimen of C. shutmani is the male
holotype, at 55.7 mm SL, leading us to believe that the specimens in the type series are not fully mature. Its close
relationship with the other members of the species complex suggests that it may be capable of attaining greater
lengths, and may develop a lanceolate caudal fin. In describing C. earlei, Randall & Pyle (2001) alluded to its small
size (largest specimen 69.1 mm SL). B.D. Greene and R. Whitton later collected a specimen measuring
approximately 100 mm SL (140 mm TL), showing that the species does attain lengths greater than previously
thought (Figure 9). The new specimen also possessed a strongly lanceolate caudal fin, a feature noted as absent in
the original description of C. earlei. Whereas Tea et al. (2016) commented on the unreliability of using caudal fin
morphology as a character for classification (indeed, C. claire, C. jordani and C. rubrisquamis lack a lanceolate
caudal fin), the character might be expected in larger individuals of C. shutmani. In support of this, B. Shutman
sent us a photograph of an aquarium specimen of approximately 65 mm TL that shows a weakly lanceolate caudal
fin (Figure 5C).
We here provide new, previously unrecorded distribution records for C. claire, C. earlei, and C. lanceolatus
(Figure 6). Cirrhilabrus claire was previously known only from the type locality of Rarotonga, Cook Islands. It has
since been collected and observed from Mo’orea, French Polynesia (Figure 8I). Cirrhilabrus earlei was previously
known only from Palau. It has since been collected in Kwajalein Atoll, Marshall Islands, for the aquarium trade
(Figure 8B) and by B.D. Greene (BPBM 39701). B.D. Greene, R.L. Pyle and J.L. Earle have also photographed
and collected the species from across the Federated States of Micronesia, in Pohnpei (Figure 9), Majuro, Puluwat
(BPBM 40802), Gray Feather Bank, Ulithi and Yap. Cirrhilabrus lanceolatus was previously known only from

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Okinawa and the Izu Peninsula, Japan, but has since been collected from Scarborough Shoals, South China Sea,
western Philippines, by aquarium fish collectors (Figure 8F).
FIGURE 6. Distribution records for selected species of Cirrhilabrus: closed star, C. shutmani; open circles, C. jordani; closed
circles, C. earlei; closed triangles, C. lanceolatus; open triangles, C. roseafascia; open star, C. earlei + C. roseafascia; closed
square, C. blatteus; open square, C. sanguineus; closed crosses, C. rubrisquamis; open crosses, C. claire.
FIGURE 7. Cirrhilabrus jordani, male, approximately 95 mm TL, aquarium specimen from Hawaii. Image reversed, specimen
not retained. Photo by Y.K. Tea.

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FIGURE 8. Males of selected Cirrhilabrus species. All are in nuptial display except D, F and I. A) C. shutmani n. sp.,
aquarium specimen from Didicas Volcano, Babuyan Islands, northern Philippines (photo by D. Laux); B) C. earlei, aquarium
specimen from Kwajalein Atoll, Marshall Islands (photo by T. lauderdale); C) C. jordani, aquarium specimen from the
Hawaiian Islands (photo by Y.K. Tea); D) C. blatteus, Israel, Gulf of Aqaba (photo by J.E. Randall); E) C. roseafascia,
aquarium specimen from Coral Sea, Australia (photo by Y.K. Tea); F) C. lanceolatus, aquarium specimen from Scarborough
Shoal, South China Sea, western Philippines (photo by B.P. Shutman); G) C. sanguineus, aquarium specimen from Mauritius
(photo by H. Tanaka); H) C. rubrisquamis, aquarium specimen from the Maldives (photo by T. Lauderdale); I) C. claire,
aquarium specimen from Mo’orea, French Polynesia (photo by Y.K. Tea).
FIGURE 9. Cirrhilabrus earlei, male, approximately 100 mm SL (140 mm TL), collected from Pohnpei, Micronesia. Photo by
B.D. Greene & R. Whitton.

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FIGURE 10. Unknown Cirrhilabrus, male, approximately 70 mm TL, A) not displaying, B) in nuptial display, photographed
in the Ogasawara Islands. Photo by S. Kobayashi.
In addition, we are aware of a Cirrhilabrus with a similar combination of colouration and fin-shape characters,
photographed in the Ogasawara Islands (Figure 10). Its live colouration details and differences from the other nine
species are summarized in Table 2. Its nuptial colouration is very similar to that of C. shutmani (cf. Figures 8A and
10). Specimens are needed to evaluate the identity of this species.
Acknowledgements
We thank S.K. Tea, K. Lim, J. Comendador and M. McGrouther for curatorial assistance. B.P. Shutman provided
the holotype and paratypes via Iwarna Aquafarm, Singapore. We also thank S.K. Tea, B.P. Shutman, I. Pollock, T.
Lauderdale, D. Laux, J.E. Randall, S. Spruce, S. Kobayashi, B.D. Greene and R. Whitton for providing excellent
photographs of various Cirrhilabrus species. B.D. Greene, R.L. Pyle, J.L. Earle, R. Kimura and B.P. Shutman
provided valuable distribution records for C. earlei, C. claire, and C. lanceolatus.

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PDUJLQEULJKW
SXUSOHEOXH
3DOHSLQNWR
\HOORZRUDQJH
%ULJKW\HOORZ 3DOH\HOORZ
ZLWKGDUNEOXH
ZHGJHVKDSHG
VSRWVSRWQRW
UHDFKLQJEOXH
DQWHULRUHGJHRI
ILQ
3DOH\HOORZ
JUHHQZLWKGDUN
EOXHVSRWVSRW
VXIIXVHGDQG
UHDFKLQJEOXH
DQWHULRUHGJHRI
ILQ
3DOHSLQN 3DOHSLQN 3DOHSLQNWR
SXUSOH
3DOH\HOORZWR
RUDQJH
VRPHWLPHV
GXVN\
3LQNWRSLQNLVK
UHG
&DXGDOILQ %ULJKW\HOORZ
ZLWKUHGGLVWDO
KDOI
3LQNWRSXUSOH
GRUVDOO\DQG
YHQWUDOO\ZLWK
EURDGREOLTXH
EOXHPDUJLQV
%ULJKWUHG
VRPHWLPHV
ZLWK\HOORZ
VWUHDNV
3DOH\HOORZLVK
K\DOLQHFHQWUDO
UD\VZLWKEULJKW
EOXHOLQHV
FRQYHUJLQJWR
WLSRIFDXGDOILQ
3DOH\HOORZ
JUHHQGRUVDOO\
DQGYHQWUDOO\
ZLWKEURDG
REOLTXH
JUHHQLVKEOXH
PDUJLQV
%ULJKW\HOORZ
EDVDOO\\HOORZ
JUH\GLVWDOO\
ZLWKDSDLURI
EULJKWEOXH
FKHYURQV
FRQYHUJLQJWRWLS
RIFDXGDOILQ
3DOHSLQNZLWK
DSDLURIEULJKW
EOXHFKHYURQV
FRQYHUJLQJWR
WLSRIFDXGDO
ILQ
3LQNWRPDJHQWD
ZLWKEULJKWEOXH
VXEPDUJLQDOEDQG
<HOORZWR
RUDQJHSLQN
ZLWKGXVN\
JUHHQWREODFN
PDUJLQHGJHG
RQWKHLQVLGH
ZLWKEOXH
3LQNWRSLQNLVK
UHGGRUVDOO\
DQGYHQWUDOO\
ZLWKJUHHQLVK
EOXHPDUJLQV
FRQYHUJLQJWR
WLSRIFDXGDOILQ
)DFLDO
PDUNLQJV
/LODFWR
PDJHQWD
VWULSHVDERYH
DQGEHORZ
H\HZHDNO\
SUHVHQW
3XUSOHWR
SXUSOHUHG
VWULSHDERYH
H\HVWURQJO\
SUHVHQWVWULSH
EHORZH\H
ZHDNO\
SUHVHQW
%ULJKWUHG
VWULSHVDERYH
DQGEHORZH\H
VWURQJO\
SUHVHQW
3LQNWRUHGGLVK
SLQNVWULSHV
VWURQJO\
SUHVHQWORZHU
VWULSHH[WHQGLQJ
WRSHFWRUDOILQ
EDVH
2UDQJHUHGWR
SXUSOHVWULSHV
VWURQJO\
SUHVHQWORZHU
VWULSHH[WHQGLQJ
WRSHFWRUDOILQ
EDVH
/DUJHUHGVSRWRQ
RSHUFXOXP
EHKLQGH\H
IDFLDOVWULSHV
SUHVHQWRQO\
GXULQJQXSWLDO
GLVSOD\
/LODFWR
ODYHQGHU
VWULSHVDERYH
DQGEHORZH\H
ZHDNO\SUHVHQW
/LODFWRODYHQGHU
VWULSHVDERYHDQG
EHORZH\HSUHVHQW
RQO\GXULQJ
QXSWLDOGLVSOD\
3XUSOHVWULSHV
DERYHDQG
EHORZH\H
VWURQJO\
SUHVHQW
3LQNLVKUHG
VWULSHVVWURQJO\
SUHVHQWORZHU
VWULSHH[WHQGLQJ
WRSHFWRUDOILQ
EDVH
6WULSHRQ
XSSHUERG\
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GXULQJQXSWLDO
GLVSOD\DQG
FRQQHFWHGWR
XSSHUH\H
VWULSH
3UHVHQWDQG
FRQQHFWHGWR
XSSHUH\H
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3UHVHQWDQG
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XSSHUH\H
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3UHVHQWDQG
FRQQHFWHGWR
XSSHUH\HVWULSH
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FRQQHFWHGWR
XSSHUH\HVWULSH
3UHVHQWHQGLQJ
DWGRUVDOILQ
RULJLQ
$EVHQW $EVHQWSUHVHQW
RQO\GXULQJ
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DQGFRQQHFWHGWR
XSSHUH\HVWULSH
3UHVHQWDQG
FRQQHFWHGWR
ORZHUH\H
VWULSH
3UHVHQWHQGLQJ
DWGRUVDOILQ
RULJLQ
FRQQHFWHGWR
XSSHUH\HVWULSH
RQO\LQQXSWLDO
GLVSOD\
6WULSHVRQ
ORZHUERG\
$EVHQW GDUN
SXUSOHVWULSHV
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SUHVHQWRQO\
GXULQJQXSWLDO
GLVSOD\DVD
OLODFVWULSH
DERYHDQDOILQ
6RPHWLPHVZLWK
IDLQWRUDQJH
SLQNVWULSH
DERYHDQDOILQ
$EVHQWSUHVHQW
RQO\GXULQJ
QXSWLDOGLVSOD\
DVDIDLQWOLODF
VWULSHDERYH
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3XUSOHVWULSH
SUHVHQW
PLGODWHUDOO\
$EVHQWEXW
ZLWKEURDG
REOLTXH
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VWULSHZHDNO\
SUHVHQWZLWK
QDUURZREOLTXH
SDOH\HOORZLVK
EDQGEHKLQG
SHFWRUDOILQ

TEA & GIL L
88
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Zootaxa 4341 (1) © 2017 Magnolia Press
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