www.aucklandmuseum.com Recent collections of fishes at the Kermadec Islands and new records for the region

Thomas Trnski Auckland War Memorial Museum Clinton A.J. Duffy Department of Conservation, Auckland War Memorial Museum Malcolm P. Francis National Institute of Water and Atmospheric Research Ltd Mark A. McGrouther Australian Museum, Sydney Andrew L. Stewart Museum of New Zealand Te Papa Tongarewa Carl D. Struthers Museum of New Zealand Te Papa Tongarewa Vincent Zintzen Museum of New Zealand Te Papa Tongarewa; Department of Conservation

Abstract

Five visits to the Kermadec Islands between 2004 and 2013 have increased the number of confirmed fish species from the region. The most intensive survey of shore fishes from all island groups of the Kermadec Islands was undertaken in May 2011. Additional fishes were recorded during surveys undertaken in 2004, 2012 and 2013. The main method used was rotenone, targeting cryptic fishes, supplemented by fishes collected by night lighting, hook and line fishing, gill netting, trapping, spearing and hand-collecting. A total of 114 species of coastal fishes and an additional 12 species from deeper water were collected. Four species of coastal fishes, based on voucher material, reported here are new records for the Kermadec Islands, with an additional nine species records to be reported in a forthcoming publication. Of these 13 new records for the Kermadec Islands, all but one species were also new records for the New Zealand Exclusive Economic Zone. In addition, 12 species of deeper shelf and upper slope fishes were collected in depths to 300 m, confirming their presence at the islands.

Keywords Fish diversity; distributions; southwestern Pacific; new records

INTRODUCTION Island is a small, emergent fragment of the rim of the Macauley Caldera (13 km x 11 km x 1000 m deep) that The Kermadec Islands have been emergent above sea was formed in the last few thousand years by a magnitude level for about 0.5 million years (Latter et al., 1992). The 11 eruption (Latter et al. 1992; Lloyd et al. 1996). The existence of uplifted limestone reefs on some the islands rate of recent uplift has been rapid; for example, Curtis provides evidence that mid-late Pleistocene (0.5 million and Cheeseman islands have been uplifted by about to 12,000 years before present) subtropical communities 18 m in the last 200 years (Doyle et al., 1979). existed near the ocean surface (Brook, 1998, 1999). Considering the recent emergence of these islands, Subtidal habitat has been available for considerably and their relative isolation – a distance of 650 km or more longer with the development of the Kermadec Ridge, from the nearest reef or landmass (Trnski & de Lange, with early Miocene (about 23 million years before 2015) – all coastal species that occur at the Kermadec present (mybp)) fossils dredged from the top of the ridge Islands must have derived from adjacent populations (Brook, 1999). The presence of Patella Scutellastra through dispersal (Trnski et al., 2010). kermadecensis at the Kermadec Islands argues for The Kermadec Islands have been exposed to a very shallow water habitats along the ridge by at least the late low level of fishing effort, as there rarely has been a Pliocene (about 2.6 mybp) when this species died out human population resident at the islands, and commercial across the rest of its range (Fleming, 1973). fishing effort is relatively low and is focused on pelagic The present morphology of Raoul Island was largely fishes (Zylichet al., 2012). This is due to the remoteness produced by erosion and explosive volcanism beginning and inhospitability of the islands for human habitation from about 4,000 ybp (Lloyd & Nathan 1981). Macauley due to the lack of permanent potable water and coastal

Bulletin of the Auckland Museum 20: 463–480 http://www.aucklandmuseum.com/research/pub/bulletin/20/21 464 Thomas Trnski et al. shelter on any of the islands, and the frequent tropical The 2011 Kermadec Biodiscovery Expedition aboard storms and volcanic activity. These same conditions RV Braveheart collected at all island groups except have limited opportunities to undertake surveys of Havre Rock. Rotenone was the main method used. Each marine life of these islands (Trnski & de Lange, 2015). rotenone station was marked by a buoy and diver pairs In addition to these factors, the marine environment entered the water at 10–20 minute intervals after rotenone within 12 nautical miles of the islands has been fully was laid, so that all fishes affected were collected over protected from exploitation within the Kermadec Islands a period of 45 to 90 minutes, depending on the depth. Marine Reserve since 1990. Fishes were also collected by line fishing, dropline, The first collections of fishes from the Kermadec spear fishing, night lighting, hand net, gill net, trap, and Islands were made during the Challenger Expedition in an overnight landing on the deck of the RV Braveheart 1873-1876 and reported by Günther (1887, 1889) and (for details on collection methods, see Trnski & de Murray (1895). Only two of the 12 species collected Lange, 2015). These collections are held at the Auckland were shore fish species: Carcharhinus galapagensis Museum (AIM), Australian Museum (AMS) and NMNZ. (as Carcharias lamia) and Naucrates ductor; the other In August 2012, the Sir Peter Blake Trust species were all mesopelagic or deepwater species. organized a visit to Raoul Island as a youth leadership Since that time, each expedition to collect fishes at programme on board the HMNZS Canterbury (http:// the Kermadec Islands has generated an increase in the www.sirpeterblaketrust.org/young-blake-expeditions/ known number of coastal fish species (excluding deep kermadecs-expedition-2013/). A few fishes were water and epipelagic species) (Francis & Cole, 2010; collected, under Clinton Duffy’s supervision. All fishes Trnski & de Lange, 2015). In summary, 12 species were were collected by line fishing and are housed at AIM. reported from the Challenger Expedition, 32 species About 100 km SSW of L’Esperance Rock is the Star were recorded by Waite (1910, 1912), a summary of Bengal Bank (32°30’S, 180°00’E), rising to within of holdings at the Museum of New Zealand Te Papa 150 m of the sea surface. During a brief visit to the bank Tongarewa recorded 72 species (excluding cartilaginous on board the RV Braveheart from 26-27 April 2013 line fishes; Paulin & Stewart, 1985), and from a number of fishing was undertaken at depths of 150 to 250 m. Most voyages between 1984 and 1992, the total species of fishes were released or retained for consumption; a small coastal fishes rose to 145 species (Francis, 1993); see subset of the fishes collected are housed at AIM. Francis and Cole (2010) and Trnski & de Lange (2015) An opportunistic five-day visit to Raoul Island, for further details on these surveys. The deepwater fish L’Esperance Rock and Havre Rock in November to fauna was described by Beaumont et al. (2012), and December 2013 on board the RV Braveheart provided McMillan et al. (2011 a,b,c) recorded 56 pelagic and an opportunity to complement earlier collections. Only coastal fishes from the north Kermadec and Colville a single scientist was on board (T. Trnski), and the focus ridges. The increasing rate of newly recorded coastal of collecting was algae and invertebrates, though a few species at the Kermadec Islands is a consequence of fish collections were made and visual observations the intensification of sampling effort and technological recorded. Fishes were collected from Raoul Island, in changes through time. Boat Cove and on the west side of North Meyer Island. The main objective of the Kermadec Biodiscovery Methods included spear fishing, hook and line fishing, Expedition 2011 was to complement earlier collections hand collecting, night lighting and dipnet, and clove oil. of fishes by intensively collecting at all island groups These collections are held at AIM. Havre Rock was also and at as many locations as weather and sea conditions visited, but no fishes were collected. would allow. Here we report the results of these A brief stopover at Raoul Island in January 2015 collections and also on four other recent visits to the on board the RV Braveheart provided the opportunity region for which the information on fishes collected has for two dives on the west side of the Meyer Islands. No either not been published or is not available publicly (for fishes were collected, though photographs by Richard example, Duffy (2005)). Robinson documented five new species records, which are reported by Francis and Duffy (2015). METHODS A number of fish species reported here were recorded from the Kermadec region for the first time. Most of The collections reported here derived from five recent these new species records are documented by Roberts visits to the Kermadec Islands. The Kermadec Islands et al. (2015), and a reference to the individual chapters Expedition in November 2004 utilised the RV Southern in that book is provided in Table 1. New species records Salvor and made collections at Raoul Island and adjacent not reported by Roberts et al. (2015) are presented here islands. The party also stopped at Macauley Island, with a photograph and specimen data to confirm the and Curtis and Cheeseman Islands, but made no fish identification. Additional new species records on all five collections at these islands due to adverse sea conditions voyages were based on visual records only and, in most (Duffy, 2005). A total of nine rotenone stations, one cases, these were supported by photos or video footage station of line fishing, one station with a dropline, one (Francis & Duffy, 2015). Where no photographic spear fishing station, and an overnight landing of a flying evidence was available for visual records, these species fish on the vessel were achieved. Specimens resulting are recorded in this paper. from this survey are held at the Museum of New Zealand Shore fishes are defined as species that occur in depths Te Papa Tongarewa (NMNZ). between 0 and 50 m, and are also referred to as “coastal Kermadec fishes from recent collections 465 fishes”. Several species that were collected and that occur (12.1%), Enneapterygius kermadecensis (8.6%), at greater depths are also reported here. Institutional Limnichthys fasciatus (7.4%), Chrysiptera rapanui acronyms are consistent with Leviton et al. (1985). (6.9%), Bathystethus cultratus (6.2%), and Lotella Methodology and diagnostic characters for new phycis (5.3%). Optivus elongatus, Scorpaena cardinalis, species records follow Böhlke (1989) and Smith (2012) Scorpaenodes evides, Trachypoma macracanthus, for Muraenidae; Smith and McCosker (1999) and Suezichthys arquatus, Cirripectes alboapicalis, Randall (2005) for Ophichthidae; Bellwood and Randall Pempheris analis, Notolabrus inscriptus, Priolepis (2000) and Randall and Randall (1981) for Labridae; psygmophilia, Girella fimbriata, Anampses elegans and and Matsuura (1980) for Balistidae. Entomacrodus niuafoouensis were secondarily abundant, each contributing between 1% and 5% of total numbers. RESULTS In 2011 rotenone stations, the most abundant species in collections were C. rapanui (12.2%), P. luculentus (9.8%), A total of 5,288 fishes, representing 114 shorefish Enneapterygius kermadecensis (7.7%), Engyprosopon species in 58 families plus 12 deeper water species raoulensis (7.5%) and Scorpaenodes evides (5.5%). in nine additional families, were collected from the Secondary species in 2011 were L. phycis, S. cardinalis, Kermadec Islands and Star of Bengal Bank (Table 1, 2) T. macracanthus, Upeneus francisi, Chromis dispila, L. in the five surveys between 2004 and 2013. Of these, fasciatus, C. alboapicalis, Entomacrodus cymatobiotus, 912 (17%) were collected in 2004 and 4,302 (81%) were Entomacrodus niuafoouensis, Parablennius laticlavius, collected during the Kermadec Biodiscovery Expedition Plagiotremus tapeinosoma, Eviota kermadecensis, P. in 2011. Ninety-six percent of specimens were collected psygmophilia, and Torquigener altipinnis. from 50 rotenone stations; nine rotenone stations were Engyprosopon raoulensis was collected only at conducted in November 2004, and 41 during May 2011. two stations, both over soft sediments at Raoul Island, Bad weather during the 2004 expedition meant that and 77% of the specimens of this species came from seven of the nine stations were made in shallow rocky a single station (K2011-48) on coarse, rippled sand at reef habitats located between the beach at Denham Bay 20–23 m depth off Fishing Rock. Also collected at this Flat and Smith Bluff; two stations were conducted in station were large numbers of T. altipinnis, Maxillicosta Boat Harbour, Meyer Islands (Duffy, 2005). In 2011, 26 raoulensis and Upeneus francisi, as well as several eels stations were conducted in a variety of habitats around (Gnathophis sp.). No fish were observed prior to laying Raoul Island, including intertidal rock pools, shallow the rotenone at this station and all of the fish collected subtidal rocky reef and subtidal sand flats; five stations emerged from within the sand or strayed into the were conducted on subtidal rocky reef around Macauley rotenone cloud (for example Upeneus francisi). Island; eight around Curtis and Cheeseman Islands; Three blennies, Cirripectes alboapicalis, and two at L’Esperance Rock (Trnski and de Lange, Entomacrodus cymatobiotus and Parablennius 2015). The size range of fishes collected using rotenone laticlavius, and the endemic triplefin Enneapterygius was 7–806 mm SL, although most individuals were kermadecensis dominated rotenone collections at Curtis 15–400 mm SL (Table 1). and Cheeseman Islands in 2011, constituting 10.6%, 6.1%, The total numbers of fish species collected using 7.2% and 23.8% of specimens collected, respectively. rotenone were 47 in 2004 and was 85 in 2011. The Enneapterygius kermadecensis also represented 15.7% number of species recorded per station ranged from 10 to of specimens collected from Macauley Island. Almost 26 (average 18.9, S.E. 3.7) in 2004, and 1 to 33 (average all of the specimens of these species collected from 15.4, S.E. 1.1) in 2011. Species discovery curves for the Curtis and Cheeseman Islands came from a single station rotenone stations are shown in Fig 1. In 2011, species (K2011-76) located on the west side of Cheeseman Island. discovery was almost monotonic until the 33rd station The habitat at the site consisted of a very steep, almost (82 species, 96.6% of total species), at which point it featureless rock wall with sparse algal and invertebrate plateaued until the capture of three additional species cover (Trnski & de Lange, 2015). at the last station (Fig. 1). These additional species Rotenone collections in 2011 included a large were Priacanthus sp., Acanthurus sp. and Anampses number of infrequently collected species, with 36 (42%) caeruleopunctatus. Priacanthus sp. and Acanthurus sp. recorded from only one or two stations (Fig. 2). The are new records for New Zealand waters (Trnski, 2015d; most frequently occurring species was Pseudolabrus Struthers, 2015), whereas A. caeruleopunctatus is luculentus (83% of stations), followed by Scorpaena widely distributed and relatively common throughout cardinalis (78%), Chrysiptera rapanui (75.6%), the Kermadec archipelago (Table 1; Francis et al., 1987; Scorpaenodes evides (73.2%), Eviota kermadecensis Eddy 2011). Two families were recorded for the first (68.3%), Trachypoma macracanthus (63.4%), Chromis time in New Zealand: Isonidae, surf silversides (Trnski, dispila (58.5%) and Anarchias seychellensis and 2015b), and Priacanthidae, bigeyes (Trnski, 2015d). Plagiotremus tapeinosoma (both 51.2%). Three of these Tropical species contribute most to the diversity species were proportionally less abundant in collections recorded but, numerically, subtropical species from the southern islands (Curtis and Cheeseman dominate the Kermadec Islands environment (Francis Islands, L’Esperance Rock). They were Chrysiptera & Duffy, 2015). The most abundant species (≥ 5% of rapanui (14 and 16% at Raoul and Macauley Islands total numbers) in the 2004 rotenone collections were respectively cf. 5 and 6% at the southern islands), Eviota Pseudolabrus luculentus (20.3%), Eviota kermadecensis kermadecensis (7 and 4% cf. 1%) and Plagiotremus 466 Thomas Trnski et al.

gill net, GN gill net,

and all E. galapagensis C. most for or, collections on specimens held in museum based Records trap. spear, Tr Sp spear, rotenone,

night light, Ro light, NL night H&L hook and line, specimens, collected and released following positive identification and fin clip sample retained. Total number of specimens: size range in mm SL except for elasmobranchs, elasmobranchs, for except SL mm in range size specimens: of number Total retained. sample clip fin and identification positive following released and collected specimens, daemelii without an image as visual records from V species recorded not known; collected in mm TL; + specimen number and size of Bengal Bank specimens measured eels and Star 1985). al ., et with Leviton consistent acronyms (institutional column in Notes listed are citations and/or numbers catalogue records, all new For evidence. Table 1. duringShorefish speciesrecorded visits to five the KermadecTable Islands and Star of Bengal Bank in2012 2011, 2004, and2013. Collection method abbreviations: hand collecting, H hand collecting, Kermadec fishes from recent collections 467

468 Thomas Trnski et al.

Kermadec fishes from recent collections 469

470 Thomas Trnski et al.

Kermadec fishes from recent collections 471

Cubiceps

Table 2. of collections Recent deeper shelf (>50 Table m depth) and upper slope (>200 m depth) fishesKermadec the from Islands andStar of Bengal Bank nomeid the except line and hook using collected specimens All teleosts). for SL elasmobranchs, for TL mm range size specimens: of (number sp. collected by night light. light. night by collected sp. 472 Thomas Trnski et al.

Figure 1. Species discovery curves for rotenone stations conducted at the Kermadec Islands in November 2004 (squares) and 2011 (circles). All stations were located at Raoul Island in 2004. In 2011 collections 1–26 were made around Raoul Island, 27–31 at Macauley Island, 32–39 at Curtis and Cheeseman Islands, and 40–41 at L’Esperance Rock.

Figure 2. Frequency of species diversity in rotenone stations at the Kermadec Islands in May 2011. Total number of rotenone stations was 41. Kermadec fishes from recent collections 473 tapeinosoma (2.4 and 4.5% cf. 1%). Chromis dispila NEW SPECIES RECORDS NOT TREATED IN was most abundant in collections from L’Esperance ROBERTS ET AL. (2015) Rock (7% cf. 2.5–3% at other islands). Pseudolabrus luculentus was most abundant in collections at Raoul Family MURAENIDAE Island (10%) and L’Esperance Rock (31%) compared to Macauley (7%) and Curtis and Cheeseman islands Gymnothorax thyrsoideus (Richardson, 1845) (5%). The remaining species showed no obvious pattern New species record for the Kermadec Islands and New in abundance among islands. Of those species collected Zealand EEZ. only from Raoul Island in 2011, only Enchelycore Voucher – NMNZ P.050106 (1: 505 mm total length ramosa and Engyprosopon raoulensis occurred at four (TL)) (Figure 3) or more stations. Enchelycore ramosa is a widespread Collected at NW corner of North Meyer Island, subtropical species that also occurs in northern New Kermadec Islands (29°14.48'S, 177°52.72'W); rotenone Zealand. Its absence from rotenone collections made and hand nets, 16–18 m depth; rocky bottom interspersed around the southern Kermadec Islands could be due to with sand and gravel, corals and seaweeds. Collectors: chance or differences in habitat types sampled. Francis et C. Bedford, M. McGrouther, C. Struthers, T. Trnski, S. al. (1987) recorded it from Curtis Island and L’Esperance Ullrich, G. Wiren, V. Zintzen; 19 May 2011 (Station Rock. Engyprosopon raoulensis is known only from K2011-57). sandy substrata between 15–36 m depth off Raoul Island and 59 m depth off Norfolk Island (Amaoka & Mihara Diagnosis. Dorsal-fin origin about half-way between 1995). It is probably widespread on soft sediments at rictus of mouth and the gill opening. Teeth: conical, suitable depths around the Kermadec Islands. two rows in upper and lower jaws, two conical teeth Other methods used to complement the rotenone in median row of intermaxillary, vomerine teeth in two collections yielded a limited number of specimens (Tables rows, diverging anteriorly in large adults. Body depth 1 and 2). This was in part due to the majority of effort 17–22 in TL; pre-anal length ca. 2.5 in TL. Vertebrae: directed towards collecting and processing the rotenone predorsal fin 3–6, preanal fin 48–55, total 125–137. stations. However, in May 2011 few pelagic organisms of any sort were observed around the expedition vessel Colour. Head and body brown, head darker (sometimes at night meaning few collections were able to be made with paler snout), densely mottled with darker brown using landing nets and jigs. This contrasted with the speckling and random blotches. The gill opening often November 2004 expedition when numerous flying fishes sits in a dark brown to dusky spot. Iris brilliant white. and small squids were attracted to the vessel’s lights Some specimens purplish grey to greyish white with a at night in Denham Bay, Raoul Island. In 2011, fishing yellowish tinge. with rod and line from the drifting expedition vessel proved more effective than droplining for sampling Specimen meristics and morphometrics. upper slope fishes. Invertebrate traps set in shallow water Vertebrae: predorsal fin 4, preanal fin 50, total 133. predominantly caught moray eels and scorpaenids. The Proportions in total length (TL): head length 8.8; single Epinephelus daemelii, all but one of the Seriola body depth 18.4; predorsal-fin length 14.1; preanal fin lalandi and all but two of the Carcharhinus galapagensis length 2.5. and Mustelus sp. were released alive after a small tissue Proportions in head length (HL): snout length 7.7; eye sample (fin clip) was taken for DNA analysis. diameter 12.8, mouth gape 3.7. Four species are reported here as new records for the Kermadec Islands, three of which are new records Morphology. Premaxillary teeth 6, maxillary teeth in for the New Zealand Exclusive Economic Zone (Table 1, a single row, and about half size of premaxillary teeth; Figures 3-6); one species (Pseudojuloides elongatus) has teeth broad based, curved, pointed. Intermaxillary teeth been recorded previously from mainland New Zealand 9, as a single row, and longer than maxillary teeth. (Ayling & Russell, 1977; Francis, 2012). Nine additional Dentary teeth in two groups and two rows, the inner new records are reported from voucher specimens larger than the outer. Vomer with two large conical teeth collected at the Kermadec Islands (Roberts et al., 2015), anteriorly and two rows of molariform teeth (becoming and additional species are recorded from photographs or a single row posteriorly). visual records (Francis & Duffy, 2015). Four species were undescribed at the time of the Kermadec Biodiscovery Colour. Brown, head darker, snout pale, body with Expedition 2011: Hime pyrhistion Gomon et al., 2013 darker brown speckling and random darker blotches; gill (occurs in Australia and New Zealand); Aspasmogaster opening in a dark brown spot; iris brilliant silvery-white. sp. (endemic to the Kermadec Islands); Hypoplectrodes sp. B (the “half-banded perch” in Francis (2012) is Notes. This species can be distinguished from similar also known from Lord Howe and Norfolk islands, and species by gill opening sitting in a dark brown blotch; northern New Zealand); and Eviota kermadecensis Hoese iris brilliant white, head darker than body, and densely & Stewart, 2012 (endemic to the Kermadec Islands). The mottled with dark brown speckles and randomly-arranged addition of Chelon sp. to the list was based on a specimen blotches. The teeth have been widely reported as conical, collected in 1908 that is held in the NMNZ collection but examination of this specimen has found the dentary and (Trnski, 2015a). maxillary teeth are short, broad-based, slightly curved and 474 Thomas Trnski et al.

Figure 3. A new record for the Kermadec Islands and New Zealand: Muraenidae Gymnothorax thyrsoideus NMNZ P.050106, 505 mm TL. Photo: C. Struthers, NMNZ

Figure 4. A new record for the Kermadec Islands and New Zealand: Ophichthidae Leiuranus semicinctus AIM MA655341, 330 mm TL. Photo: C. Struthers, NMNZ

Figure 5. A new record for the Kermadec Islands: Labridae Pseudojuloides elongatus AIM MA655350, 30.0 mm SL. Note that small artefacts of tissue appear on the tip of the snout and from the anus. Photo: P. Quin, AIM Kermadec fishes from recent collections 475 pointed. Has been recorded in the genus Siderea (Randall (29°15.156'S, 177°51.316'W); sand with occasional et al., 1990; Kuiter, 1994) and G. prosopeion (Bleeker) is a rock outcrops, fringed with emergent rocks; 24–26 m; synonym (Randall, 2005). Contrary to the keys in Böhlke rotenone and handnets. Collectors: C. Bedford, M. et al. (1999) and Böhlke and McCosker (2001), the gill sits McGrouther, S. Ullrich, C. Struthers, T. Trnski, G. in a dark blotch or spot, as seen in the specimen collected Wiren, V. Zintzen; 16 May 2011 (Station K2011-41). (Fig. 3) and that published by Randall (2005: 48). This species was first recorded from the Kermadec Islands by Diagnosis. 6 branchiostegal rays; scales cycloid and Duffy (2005) based on a sight record. large on body, smaller on thorax and on nape; no scales below cheek; lateral line continuous, steeply descending Family OPHICHTHIDAE beneath posterior of soft dorsal fin.

Leiuranus semicinctus (Lay & Bennett 1839) Specimen meristics and morphometrics. New genus and species record for the Kermadec Islands Dorsal fin IX,12; anal fin III,12; pectoral fin 12 (including and New Zealand EEZ. upper rudiment); pelvic fin I,5; lateral line scales 27; gill Voucher – AIM MA655341 (1: 330 mm TL) (Figure 4) rakers 13. Collected at Herald Islands, west side of North Chanter Proportions in standard length (SL): head length 2.8; Island, Kermadec Islands (29°15.156'S, 177°51.316'W); body depth 5.6. sand with occasional rock outcrops, fringed with Proportions in head length (HL): snout length 2.9; pelvic emergent rocks; rotenone and handnets, 24–26 m. fin length 1.9; caudal fin length 1.5. Collectors: C. Bedford, M. McGrouther, C. Struthers, T. Trnski, S. Ullrich, G. Wiren, V. Zintzen; 16 May 2011 Specimen description. anterior teeth in upper and lower (Station K2011-41). jaw caniniform and larger than teeth posteriorly, no canine tooth at corner of mouth; orbit 1.4 in snout length; Diagnosis. Mouth inferior; anterior nostrils without suborbital pores 6; dorsal-fin spine 9 longest; pelvic fin conspicuous, leaf-like appendages; upper lip not fringed reaches almost to anus; no median predorsal scales; with cirri; vomerine teeth absent or up to three teeth; scale rows between origin of dorsal fin and lateral line3; pectoral fins reduced, about the size of the gill opening; lateral line continuous, dips sharply between dorsal soft dorsal-fin origin is above or slightly posterior to gill rays 7–9; scale rows between lateral line and origin of opening; tip of tail finless. Colour: white to pale yellow anal fin7; caudal peduncle depth 1.3 times length; caudal with 22–30 broad, black, saddle-like bars, only those on fin rounded. Colour in alcohol: uniformly pale. posterior of tail extending to ventral midline; saddles wider than or about equal in width to pale interspaces. Notes. Four species of Pseudojuloides have been recorded in the region. P. atavai has been recorded from Specimen meristics and morphometrics. Niue (Randall, 2005) but does not match the specimen Vertebrae: preanal 69, postanal 102, total 171. as the species has 11 soft rays in the dorsal fin, 13 rays in Proportions in total length (TL): head length 13.2; body the pectoral fin, and there are 4–5 scale rows between the depth 59.6; snout to anus length 2.3; snout to dorsal fin origin of the dorsal fin and the lateral line. P. cerasina length 13.9. has been recorded from Lord Howe Island, New Caledonia, Fiji, Samoa, and the Cook Islands (Randall Specimen description. This specimen varies from the & Randall, 1981); this species has about 8–11 median diagnosis in having expanded membranes medially on predorsal scales, 11 (to 12 according to Kuiter, 1993) the anterior nostrils and 21 dark saddles on the head soft rays in the dorsal fin, 4 scale rows between the and body, with the last four saddles reaching the ventral origin of the dorsal fin and the lateral line, and caudal fin midline of the tail. It has three. small teeth on the vomer is 1.6–1.9 in HL. The other two species have 3 (3–4 in and the median groove of the snout contains four small, P. severnsi) scale rows between the origin of the dorsal recumbent canine teeth fin and the lateral line, consistent with the specimen. P. severnsi has been recorded in New Caledonia; this Notes. This species can be distinguished from similar species has 11 dorsal-fin rays,13 pectoral-fin rays, 15–17 species by the combination of evenly-spaced dark gill rakers, 7–8 suborbital pores, about 7–9 small median saddles along the body, inferior mouth, pectoral fin about predorsal scales, scale rows from lateral line to origin of the size of the gill opening, dorsal-fin origin above the anal fin 8–8.5, a caudal peduncle usually slightly longer gill opening, and no to 3 vomerine teeth in a medial row. than depth. The specimen is confirmed as P. elongatus, usually found in shallow water (3–15 m) and confirmed Family LABRIDAE in the region from Norfolk Island and northern New Zealand (Francis, 2012). The specimen is consistent Pseudojuloides elongatus Ayling & Russell, 1977 with this species except it has only 13 gill rakers (17–19 New species record for the Kermadec Islands. for the species), has no spots of pigment, and many Voucher – AIM MA655350 (1: 30.0 mm SL) (Figure 5) morphometric proportions are outside of the published Collected on the west side of North Chanter Island, range; these mismatched characters change with growth Herald Islands off Raoul Island, Kermadec Islands and can be explained by its juvenile stage. 476 Thomas Trnski et al.

Family BALISTIDAE differences may be due to allometric growth. This Canthidermis maculata (Bloch, 1786) species can be distinguished from the only other member of the family known from NZ waters, Rhinecanthus New genus and species record for the Kermadec Islands rectangulus by the absence of the black, wedge-shaped and the New Zealand EEZ. markings on the caudal peduncle. Voucher – NMNZ P.050469 (1: 54 mm SL) (Figure 6) Collected at Stella Passage between Curtis and DISCUSSION Cheeseman islands, Kermadec Islands (30°32.286'S, 178°33.723'W), hand net at surface associated with a A total of 126 species of fishes were recorded from the floating plastic bottle (with attached gooseneck barnacles collections made in 2004, 2011, 2012 and 2013. Of these and polychaetes); Collectors: C. Struthers, W. Chinn, A. species, 114 were shorefishes. Recent expeditions to the Mangnall; 25 May 2011 (Station K2011-93). Kermadec Islands have added another 13 species of shorefishes to those previously known from the Kermadec Diagnosis. No enlarged osseous scales behind the gill Islands. Of these, four new distribution records for the opening; mouth terminal; teeth white, uneven, each one Kermadec Islands, of which three are new records for notched; a deep groove behind the eye, below nostrils; the New Zealand Exclusive Economic Zone (EEZ), are no grooves on cheek; third dorsal spine developed, reported in this paper, and nine additional distribution extending above dorsal edge of body, second dorsal records will be reported in Roberts et al. (2015). Francis rays 23–25, anal rays 20–22, and pectoral rays 14–15 and Duffy (2015) report additional species visually (usually 14); depth of body 2.27–2.91 in SL. documented during these expeditions, and in subsequent visits. From these three publications, the coastal fish Specimen meristics and morphometrics.: fauna of the Kermadec Islands has increased to 175 Dorsal-fin rays III,25; anal-fin rays 22; pectoral-fin rays species (present study, Francis & Duffy (2015), Roberts 15; vertebrae 7+11=18. et al., (2015)). A complete list of the coastal fish fauna, Proportions in standard length (SL): body depth 2.08. including new records, recorded since 2004 can be found in Appendix 1 of Francis and Duffy (2005). It is Colour. Body and head dark, lighter below, with many clear that we are still in the discovery phase of recording elongated white spots; these spots less prominent or fish diversity at the Kermadec Islands (Francis & Duffy, missing from large adult specimens; all fins dark. 2015), as additional species are likely to be recorded in future surveys, especially if alternative capture methods Notes. NMNZ P.050469 generally agrees to the are deployed. description given by Matsuura (1980), with one Eight species of fishes in Tables 1 and 2 are exception, body depth. The SL of the collected specimen endemic to the islands: Squalus raoulensis, Mustelus (54 mm SL) is outside the range of those examined sp., Aspasmogaster sp., Microbrotula punicea, Girella by Matsuura (95.4–289.5 mm SL) and therefore these fimbriata, Parma kermadecensis, Enneapterygius

Figure 6. A new record for the Kermadec Islands and New Zealand: Balistidae Canthidermis maculatus NMNZ P.050469, 54 mm SL. Photo: C. Struthers, NMNZ Kermadec fishes from recent collections 477 kermadecensis and Eviota kermadecensis. However, two Kermadec Islands is the eastward-flowing Tasman of these species (G. fimbriata and P. kermadecensis) have Front, branching off the East Australia Current (Trnski been recorded as occasional vagrants in the northern & de Lange, 2015), potentially acting as a mechanism North Island of New Zealand (Francis, 2012; Francis & for eastward dispersal of shorefishes. However, there Duffy 2015). In addition to these confirmed endemics, is strong attenuation of coastal fish taxa as the Tasman the Kermadec Islands population of Chrysiptera rapanui Front extends into the Tasman Sea (Mullaney et al., is probably an undescribed species, given its colour 2011; Francis & Duffy, 2015) and the dispersal of differences to the population at Rapanui (Easter Island) marine species to the Kermadec Islands may be also (Allen, 1991), and individuals of this species have also from islands to the north (Liggins et al., 2013). been reported from the northern North Island (Francis The maintenance of fish species at the Kermadec & Duffy, 2015). The proportion of endemic shorefishes Islands is likely dependent on a combination of (4.6%) is relatively low, which is not surprising self-recruitment and arrival of new recruits from nearby considering the short period since emergence of these islands (Trnski et al., 2010). The relative contribution of islands and the opportunity for dispersal from adjacent each of these mechanisms is unknown and is likely to be islands, and thus the opportunity for genetic transfer a fruitful area of further study. Pelagic larval duration is among these neighbouring populations. Seven of the one measure of potential dispersal from nearby islands. eight endemic species are either live bearers or have Modeling of regional currents indicates that exchange demersal eggs (the exception is G. fimbriata), which between the Kermadec Islands and mainland New likely limits the opportunity for dispersal (Francis & Zealand would take 30-50 days (Sutton et al., 2012), Cole, 2010; Francis & Duffy, 2015), and suggests the which is longer than the larval duration of most fishes. isolation of the islands selects species that are more However, that model assumed passive drift of larvae; likely to self-recruit. Even so, one of these species with incorporating larval behaviour could reduce these transit demersal eggs (P. kermadecensis) occasionally reaches times. The model is also based on average current mainland New Zealand (Francis, 2012), a dispersal conditions; occasional extreme events such as cyclones distance of over 700 km (Trnski & de Lange, 2015). could also alter the speed and direction of dispersal. Among the apex predators, the Galapagos sharks (Carcharhinus galapagensis) observed and caught near ACKNOWLEDGEMENTS the islands appear to be juveniles as they measured up to 1.5 m, whereas the size at which they reach sexual We wouldn’t have been able to collect the diversity maturity and the maximum size for the species are 2.1–2.4 of fishes recorded here without the assistance of m and 3.0 m, respectively (Last & Stevens, 2009). The Alison Ballance, Charles Bedford, Todd Chandler, protected spotted black grouper, Epinephelus daemelii Warren Chinn, Steve Hathaway, Dan Jolly, Matthew was observed at many of the dive locations. Both of Jolly, Stephen Keable, Ash Mangnall, Mandy Reid, these observations are consistent with the oceanic islands Richard Robinson, Karl Rogers, Adam Smith, Stephen of Elizabeth and Middleton Reefs (Oxley et al., 2004), Ullrich and Ged Wiren. The owners and crew of the also considered to be a remote area with low levels of RV Southern Salvor and RV Braveheart provided fish exploitation by humans. The biology, ecology, outstanding support for the expeditions in 2004, 2011 distribution and abundance of E. daemelii throughout its and 2013. Sir Peter Blake Trust, student voyagers geographic range is provided by Francis et al. (2015). and the officers and crew of the HMNZS Canterbury The presence of several species warrants mention. provided the opportunity and assistance to collect Iso sp. is known from the western Pacific from Japan to fishes during the The Young Blake Expedition to the Australia, including Lord Howe Island, and is likely to be Kermadecs Islands in August 2012. The opportunity distributed as far east as Tonga (Randall et al., 2003) and to visit Raoul Island in 2013 was provided by GNS to Samoa (Wass 1984), but is yet to be confirmed from New repair the tsunami warning system on Raoul Island. Caledonia (Fricke et al., 2011) or Norfolk Island (Francis, Identifications of several species were confirmed from 1993). Given its occurrence at the Kermadec Islands, this photos by Howard Choat, Keiichi Matsuura. This work species is likely to occur at these intermediate locations was supported (in part) by the NZ National Institute (Trnski, 2015b). This is the first record of Canthidermis of Water and Atmospheric Research Ltd (NIWA) Core maculata from New Zealand waters. This species has Funded Coasts and Oceans Programme 2: Biological a prolonged pelagic phase and the single specimen was Resources subcontract for fundamental knowledge collected under a plastic bottle floating at the surface, a of marine fish biodiversity with the Museum of New reminder that floating objects provide potential vectors for Zealand Te Papa Tongarewa. Permission to collect long-distance dispersal for some species of fishes. fishes was provided by the Department of Conservation The fish fauna is a mix of species that occur to under Coastal Permit number AM/PAS 02-03-01 the north and south of the islands, and in the regional dated 29 April 2011, and Authorisation by Director- southwest Pacific (Francis & Duffy, 2015). This is General to Undertake Specified Scientific Study in a consistent with oceanographic currents that provide Marine Reserve dated 4 May 2011. Animal welfare was opportunities for dispersal from the west, north and consistent with the conditions of the Australian Museum south (Sutton et al., 2012; Trnski & de Lange, 2015). Animal Care and Ethics Approval number 08-02 issued The most consistent surface current influencing the to M. McGrouther. 478 Thomas Trnski et al.

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Checklist of the shore and epipelagic fishes of littoralis, and a valid species of Scorpaenodes Tonga. Atoll Research Bulletin (502): 34 pp. (Actinopterygii: Scorpaenidae). Species Diversity 15: Roberts C.D., A.L. Stewart and C.D. Struthers (eds) 2015. 71–81. The Fishes of New Zealand. Te Papa Press, Wellington. Motomura, H. and C.D. Struthers 2015. Family Scorpaenidae 4 volumes, S250 + 1748 pp. [Vol. 1: S1–S250; vol. 2: – Scorpionfishes and lionfishes. Pp. 1088–1100, in: 1–574; vol. 3: 581–1152; vol. 4: 1157–1748]. Roberts C.D., A.L. Stewart, and C.D. Struthers (eds) Russell, B.C. 2015. Family Synodontidae - Lizardfishes. The Fishes of New Zealand. Volume 3. Te Papa Press, Pp. 541-546, in: Roberts, C.D, A.L. Stewart and C.D. Wellington. Struthers (eds) The Fishes of New Zealand. Volume 2. Motomura, H., C.D. Struthers, M.A. McGrouther and A.L. Te Papa Press, Wellington. Stewart 2011. Validity of Scorpaena jacksoniensis and Shao, K.-T. and J.-P. Chen 1986. Ten new records of a redescription of S. cardinalis, a senior synonym of S. cardinalfishes from Taiwan, with a synopsis of the cookii (Scorpaeniformes: Scorpaenidae). Ichthyological Family Apogonidae. Journal of the Taiwan Museum 39: Research 58: 315–332. 61–104. Mullaney, T.J., A.G. Miskiewicz, M.E. Baird, P.T.P. Burns Smith, D.G. 2012. A checklist of the moray eels of the world and I.M. Suthers 2011. Entrainment of larval fish (Teleostei: Anguilliformes: Muraenidae). Zootaxa 3474: assemblages from the inner shelf into the East Australia 1–64. Current and into the western Tasman Front. Fisheries Smith, D.G. and J.E. McCosker 1999. Ophichthidae – Snake Oceanography 20: 434–447. eels, worm eels. Pp. 1662–1669, in: Carpenter, K.E. 480 Thomas Trnski et al.

and V.H. Niem (eds) The Living Marine Resources Trnski, T. 2015c. Family Apogonidae – Cardinalfishes. Pp of the Western Central Pacific. Volume 3 Batoid 1216–1218, in: Roberts C.D., A.L. Stewart and C.D. fishes, chimaeras and bony fishes part 1 (Elopidae to Struthers (eds) The Fishes of New Zealand. Volume 4. Linophrynidae). FAO, Rome. Te Papa Press, Wellington. Smith, D.G. and A.L. Stewart 2015. Family Congridae Trnski, T. 2015d. Family Priacanthidae – Bigeyes. Pp – Conger eels. Pp. 269–283, in: Roberts C.D., A.L. 1232–1233, in: Roberts C.D., A.L. Stewart and C.D. Stewart and C.D. Struthers (eds) The Fishes of New Struthers (eds) The Fishes of New Zealand. Volume 4. Zealand. Volume 2. Te Papa Press, Wellington. Te Papa Press, Wellington. Smith-Vaniz, W.F. and H.L. Jelks 2006. Australian trevallies Trnski, T. 2015e. Family Sphyraenidae – Barracudas. Pp. of the genus Pseudocaranx (Teleostei: Carangidae), with 1599–1601, in: Roberts C.D., A.L. Stewart and C.D. description of a new species from Western Australia. Struthers (eds) The Fishes of New Zealand. Volume 4. Memoirs of Museum Victoria 63: 97–106. Te Papa Press, Wellington. Springer, V.G. 1967. Revision of the circumtropical Trnski, T. and P.J. de Lange 2015. Introduction to the shorefish genus Entomacrodus (Blenniidae: Salariinae). Kermadec Biodiscovery Expedition 2011. Bulletin Proceedings of the United States National Museum 122 of the Auckland Museum 20: 1–18. http://www. (no. 3582): 1–150, Pls. 1–30. aucklandmuseum.com/research/pub/bulletin/20/1. Stewart, A.L. 2015. Family Syngnathidae – Pipefishes Trnski, T., M.P. Francis, C.A. Duffy, S. Chiswell and W. Nelson and seahorses. Pp. 1050–1062, in: Roberts C.D., A.L. 2010. Motion in the Ocean: Biological oceanography Stewart and C.D. Struthers (eds) The Fishes of New of the Kermadec region – migration and connectivity of Zealand. Volume 3. Te Papa Press, Wellington. marine flora and fauna. Pp 27–30, in: Proceedings of Stewart, A.L., C.D. Roberts, and C.D. Struthers 2015. DEEP: Talks and thoughts celebrating diversity in New Family Pomacentridae – Damselfishes. Pp. 1406–1423 Zealand’s untouched Kermadecs, 30–31 August 2010. in: Roberts C.D., A.L. Stewart and C.D. Struthers (eds) Pew Environment Group, Wellington, New Zealand. The Fishes of New Zealand. Volume 4. Te Papa Press, Waite, E.R. 1910. A list of the known fishes of Kermadec and Wellington. Norfolk Islands, and a comparison with those of Lord Stewart, A.L. and C.D. Struthers 2015. Family Exocoetidae Howe Island. Transactions of the New Zealand Institute – Flyingfishes. Pp. 954-964, in: Roberts, C.D, A.L. 42: 370–383. Stewart and C.D. Struthers (eds) The Fishes of New Waite, E.R. 1912. Additions to the fish fauna of the Kermadec Zealand. Volume 3. Te Papa Press, Wellington. Islands. Proceedings of the New Zealand Institute 44: Struthers, C.D. 2015. Family Acanthuridae – Surgeonfishes. 28–29. Pp. 1591–1596, in: Roberts C.D., A.L. Stewart and C.D. Wass, R.C. 1984. An annotated checklist of the fishes of Struthers (eds) The Fishes of New Zealand. Volume 4. Samoa. NOAA Technical Report NMFS SSRF-781. Te Papa Press, Wellington. Winterbottom, R. and R.C. Anderson 1997. A revised Sutton, P., S. Chiswell, R. Gorman, S. Kenna, and G. checklist of the epipelagic and shore fishes of the Chagos Rickard 2012. Physical marine environment of the Archipelago, Central Indian Ocean. Ichthyological Kermadec Islands region. Science for Conservation Bulletin of the J.L.B Smith Institute of Ichthyology 66: 318. Department of Conservation, Wellington. 16 pp. 1–28. Trnski, T. 2015a. Family Mugilidae – Mullets. Pp. 941–944, Zylich, K., S. Harper and D. Zeller 2012. Reconstruction of the in: Roberts C.D., A.L. Stewart and C.D. Struthers (eds) marine catches for the Kermadec Islands (1950–2010). The Fishes of New Zealand. Volume 3. Te Papa Press, Pp 3–8, in: Palomares, M.L.D., K. Zylich, S. Harper, Wellington. D. Zeller and D. Pauly (eds.) The Marine Biodiversity Trnski, T. 2015b. Family Isonidae – Surf silversides. Pp.946– and Fisheries Catches of the Kermadec Island Group. 947, in: Roberts C.D., A.L. Stewart and C.D. Struthers A report prepared for the Global Ocean Legacy project (eds) The Fishes of New Zealand. Volume 3. Te Papa of the Pew Environment Group. The Sea Around Us Press, Wellington. Project, Fisheries Centre, UBC, Vancouver, Canada.

Thomas Trnski, Auckland War Memorial Museum, Private Bag 92018, Auckland 1142, New Zealand. Email: [email protected] Clinton A.J. Duffy, Department of Conservation, Private Bag 68908 Newton, Auckland 1145, New Zealand; Auckland Museum, Auckland, New Zealand. Malcolm P. Francis, National Institute of Water and Atmospheric Research Ltd, Private Bag 14901, Wellington, New Zealand. Mark A. McGrouther, Australian Museum, 6 College St, Sydney NSW 2010, Australia. Andrew L. Stewart, Museum of New Zealand Te Papa Tongarewa, PO Box 467, Wellington, New Zealand. Carl D. Struthers, Museum of New Zealand Te Papa Tongarewa, Wellington, New Zealand. Vincent Zintzen, Museum of New Zealand Te Papa Tongarewa, Wellington, New Zealand; Department of Conservation, PO Box 10420 The Terrace, Wellington 6143, New Zealand.