CAS 246395 (field code: HTP 900), 70.3 mm SL male, GenBank MN010585, east coast of Zanzibar, Tanzania, Africa (GPS coordinates: 6°10'30"S; 39°32'28"E), 75 m, collected by H.T. Pinheiro, B. Shepherd, and L.A. Rocha, 14 December 2018; Figure 1.

CAS 246396 (HTP 883), 56.8 mm SL female, GenBank MN010586, east coast of Zanzibar, Tanzania, Africa, 70 m, 07 December 2018; CAS 246397 (HTP 901), 61.3 mm SL male, GenBank MN010587, east coast of Zanzibar, Tanzania, Africa, 75 m, 14 December 2018; Figure 2 (A1, A2); CAS 246398 (HTP 902), 57.4 mm SL female, GenBank MN010588, east coast of Zanzibar, Tanzania, Africa, 75 m, 14 December 2018; Figure 2 (B1, B2); CAS 246399 (HTP 903), 54.3 mm SL female, east coast of Zanzibar, Tanzania, Africa, 75 m, 14 December 2018; Figure 2 (C1, C2). All type specimens collected by H.T. Pinheiro, B. Shepherd, and L.A. Rocha.

Cirrhilabruswakanda shares similar meristic characters to other members of this genus. However, it is readily distinguished from all other Cirrhilabrus in having the following combination of colouration and morphological characters: caudal fin strongly lanceolate in males; both sexes with a series of purple scales (in life and in preservation) arranged in a chain-link pattern across dorsal two-thirds of body.

Dorsal-fin rays XI,9; anal-fin rays III,9; dorsal and anal-fin soft rays branched except first ray unbranched in two individuals; last dorsal and anal-fin ray branched to base; pectoral-fin rays 14–15 (15/15), upper two unbranched; pelvic-fin rays I,5; principal caudal-fin rays 7+6, uppermost and lowermost unbranched; upper procurrent caudal-fin rays 6, lower procurrent caudal-fin rays 6; lateral line interrupted, with dorsoanterior series of pored scales 16–19 (17/17) and midlateral posterior peduncular series 8–9 (9/9); scales above lateral line to origin of dorsal fin 2; scales below lateral line to origin of anal fin 6; median predorsal scales 4–5 (4); median prepelvic scales 5; rows of scales on cheek 2; circumpeduncular scales 15–16 (15); gill rakers 8–9 (8) + 8–9 (8) = 16–18 (16); pseudobranchial filaments 8–10; vertebrae 9+16; epineurals 13 (Figure 3).

Body moderately elongate and compressed, depth 3.1–3.4 (3.2) in SL, width 2.1–2.6 (2.6) in depth; head length 3.2–3.6 (3.2) in SL; snout pointed, its length 3.4–3.9 (3.9) in HL; orbit diameter 3.6–4.7 (4.7) in HL; depth of caudal peduncle 1.7–2.1 (2.1) in HL. Mouth small, terminal, and oblique, with maxilla almost reaching 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 very small conical teeth medial to upper canines; lower jaw with a single stout pair of canines anteriorly which protrude obliquely outward and are slightly lateral to medial pair of upper jaw; no teeth on roof of mouth.

Posterior margin of preoperculum with 30–32 (32) very fine serrated; margins of posterior and ventral edges of preoperculum free to about level of middle pupil. Anterior nostril in short membranous tube, located nearer to orbit than snout tip; posterior nostril larger, roughly ovoid to rectangular, located just medial and anterior to upper edge of eye. Scales cycloid; head scaled except snout and interorbital space; four large scales on opercle; a broad naked zone on membranous edge of preopercle; a row of large, elongate, pointed scales along base of dorsal fin, one per element, scales progressively shorter posteriorly on soft portion of fin; anal fin with a 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; a horizontal series of greatly enlarged scales extend two-thirds distance to central posterior margin of caudal fin; pectoral fins naked except for a few small scales at extreme base; a single large scale at base of each pelvic fin, about three-fourths length of pelvic spine.

Origin of dorsal fin above third lateral-line scale, predorsal length 3.0–3.2 (3.1) in SL; first 1–4 dorsal-fin spines progressively longer, fifth to sixth subequal, eighth to tenth longest, 2.1–2.6 (2.6) 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, 1.6–1.9 (1.6) in HL, remaining rays progressively shorter; origin of anal fin below base of ninth dorsal-fin spine; third anal-fin spine longest, 2.4–3.0 (3.0) in HL; interspinous membranes of anal fin extended as on dorsal fin; anal-fin soft rays relatively uniform in length, sixth longest, 1.5–2.1 (1.8) in HL; dorsal and anal-fin rays barely reaching caudal-fin base; caudal fin of males lanceolate; pectoral fins short, reaching vertical between bases of fifth or sixth dorsal-fin spines, longest ray 1.4–1.6 (1.6) in HL; origin of pelvic fins below lower base of pectoral fins; pelvic fins short, not reaching past anal fin origin, longest ray 1.5–1.9 (1.7) in HL.

Based on colour photographs and specimens when freshly dead, and field photos of live individuals (Figures 1; 2A1; 4A; 4B; 5A): head ochreous yellow; lower part of head whitish to pale pink (yellowish when freshly dead), purple stripe present from mid-upper lip to mid-upper edge of orbit; second stripe of similar colour present from lower edge of maxilla to mid-lower edge of orbit; interorbital and upper part of snout yellowish, with a series of very fine white stripes; preoperculum prominently purple on outer edge; iris bright yellow, greenish on the upper edge, with orange ring around pupil; body pale mauve to purplish-pink, with a faint region of paler yellowish-pink below middle part of dorsal fin; body with a network of dark purple scales arranged in a chain-link pattern from just after dorsal fin origin to edge of caudal peduncle, absent from lower third of body; dorsal-fin bluish-purple, bright fuchsia on distal half; posterior dorsal fin yellowish hyaline with a faint blue medial band, sometimes broken into spots; distal edge of dorsal fin narrowly bright blue; caudal fin bluish hyaline with a pair of concentric bright blue chevrons converging at lanceolatus terminus; coloured portion of chevron marking bright fuchsia to magenta; anal-fin similar to dorsal fin, distal edge narrowly bright blue; pelvic fins hyaline to translucent magenta; pectoral fins pinkish hyaline.

Similar to males described above. Head and body more subdued in colouration, pinkish-purple to lilac (Figure 4C), deepening to yellow post mortem (Figures 2B1; 2C1).

(Figures 2A2; 2B2; 2C2; 6A): head and body pale tan; fine white stripes on interorbital and nape remain; infraorbitals, frontals, and pre-maxilla weakly purple; preoperculum, dentary, angular, and articular bones strongly purple; scales in chain-link formation deep purple; median fins translucent, except rays weakly purple; pelvic and pectoral fins translucent hyaline.

The specific epithet refers to the fictional East African nation of Wakanda, home of the superhero Black Panther, as is the case for the new species, which has remained hidden from the world for a long time. To be treated as a noun in apposition. The common name refers to the fictional metal vibranium, a rare substance found on Wakanda that is woven into Black Panther’s suit. The purple chain-link scale pattern of the new species is reminiscent of this detail.

Cirrhilabruswakanda is presently known only from the east coast of Zanzibar, Tanzania. The species inhabits deep shelves consisting of small patch reefs dominated by rhodolith and sponge beds, at depths between 50 and 80 m.

Pairwise comparison of mitochondrial sequence data suggests that Cirrhilabruswakanda is most closely related to C.rubrisquamis Randall & Emery (1983), differing by 0.6% in mitochondrial COI (uncorrected pairwise distance). Such marginal differences in sequence data between closely related sister species is not uncommon in Cirrhilabrus, even when stark morphological differences are present (Tea et al., 2016; Victor, 2016; Allen & Hammer, 2017). It also appears to be closely related to C.blatteus Springer & Randall (1974) (1.9% difference in COI) and C.sanguineus Cornic (1987) (1.5% difference in COI). These four species share the following character combination: short pelvic fins (not or barely reaching anal-fin origin); relatively unmarked dorsal and anal fins; males with a strongly lanceolate caudal fin (except in C.rubrisquamis); both sexes with a pair of prominent facial stripes above and below the orbit; and both sexes with prominent purple scales and osseus elements that persist, and stain purple, respectively, even in preservation.

In Cirrhilabruswakanda the purple scale pattern presents as a scattered, chain-link motif (Figure 1; 2; 4; 5A). In the other related species, the purple scales are manifested as: two rows dorsally and laterally in C.blatteus (Figure 5B); an oblique mid-dorsal saddle in C.sanguineus (Figure 5C); a crosshatch network anteriorly in C.rubrisquamis(Figure 5D). Aside from details in live colouration, Cirrhilabruswakanda differs from: C.blatteus in having a higher number of pored lateral line scales (24–28 vs. 21–24); C.sanguineus in having one fewer median prepelvic scale (5 vs. 6) and fewer pseudobranchial filaments (8–10 vs. 11), and further from C.rubrisquamis in having a lanceolate caudal fin.

The four species are part of a larger complex of fairy wrasses that includes five other species from the western Pacific Ocean: Cirrhilabrusjordani, C.earlei, C.roseafascia, C.lanceolatus, and C.shutmani. Together, these nine species form the Cirrhilabrusjordani complex. Previous morphological and molecular studies have also shown support for this grouping (Tea and Gill 2017; Tea et al. 2018).

Cirrhilabruswakanda possess several osseus elements and fin rays that stain naturally purple in ethanol (Figure 6A). Only a handful of other Cirrhilabrus share this character. Springer and Randall (1974) first noted this occurrence in Cirrhilabrusblatteus (Figure 6B). Subsequently, Randall (1995) made note of its reoccurrence in Cirrhilabrusrubrisquamis and Cirrhilabrussanguineus. Tea et al. (2018) expanded this list to include Cirrhilabrusearlei (Figure 6C). Incidentally, these species are all closely related members of the jordani complex, with C.wakanda, C.rubrisquamis, C.sanguineus and C.blatteus occurring in the western Indian Ocean, and C.earlei occurring in the western Pacific Ocean. However, since the purple post-preservation staining is not found in the other Pacific Ocean species (C.jordani, C.shutmani, C.roseafascia, and C.lanceolatus), the distribution of this character within the jordani complex sensu lato is paraphyletic and is therefore not synapomorphic for this group of fairy wrasses.

Cirrhilabrusblatteus – Red Sea, off Saudi Arabia: CAS 235080, 56.2 mm SL; 63.4 mm SL; 65.1 mm SL; Cirrhilabrusearlei – Palau: CAS 213114, 56.5 mm SL.