Plectorhinchus caeruleonothus, a new species of sweetlips (Perciformes: Haemulidae) from northern Australia and the resurrection of P. unicolor (Macleay, 1883), species previously confused with P. schotaf (Forsskål, 1775).

Two distinct haemulid fishes from Australia and the Indo-Australian Archipelago respectively have long been confused with Plectorhinchus schotaf (Forsskål, 1775). Plectorhinchus caeruleonothus sp. nov. is described from 17 specimens collected off western and far northern Australia, between the Monte Bello Islands, Western Australia and Torres Strait, Queensland. It has also been confirmed outside this range by photographs taken at Ningaloo Reef and Exmouth Gulf, Western Australia, and at Claremont Isles and Lizard Island, Queensland. The new species is unique among the genus in having a combination of dorsal-fin rays XII, 18-20, lateral-line scales 56-61, gill rakers 7-9 on the upper limb and 18-20 on the lower limb of the first arch, nostrils minute, and fresh colouration in adults including body uniformly grey, cheek, opercles and posterior margin of the opercular membrane uniformly blue-grey, and rim of orbit and upper edge of maxilla dusky yellow. In contrast to its closest congeners, the juveniles have a distinctive pattern of narrow creamish-white to pale grey stripes on a dark grey to chocolate brown background on the head and body, and oblique dark stripes progressing with growth to spots on the caudal fin. Plectorhinchus unicolor (Macleay, 1883) from Japan to northern Australia is resurrected from the synonomy of P. schotaf and redescribed on the basis of the holotype and 24 non-type specimens. Plectorhinchus unicolor is most similar to P. schotaf, but can be distinguished by fresh colouration, modal dorsal and pectoral-fin ray counts and DNA barcoding. Plectorhinchus schotaf appears to be restricted to the region from southeast Africa to the Arabian Sea, including the Red Sea and Persian Gulf. Plectorhinchus griseus (Cuvier in Cuvier & Valenciennes, 1830) from Indian and Sri Lankan Seas has previously been treated as a junior synonym of P. schotaf, but in accordance with Smith (1962), is here confirmed as a valid species, readily distinguished from the latter by a concavity in the lateral profile of the snout in adults, deep body and high soft dorsal-fin ray count. Comparison of the CO1 genetic marker utilised in DNA barcoding also resulted in significant genetic divergences between the new species, P. unicolor and their closest sampled congeners. Some behavioural observations are also presented for the species treated, including aggressive interactions between individuals of the new species, the likes of which have not previously been recorded among species of Plectorhinchus.

Redescription of Parapercis macrophthalma (Pietschmann, 1911) and description of a new species of Parapercis (Pisces: Pinguipedidae) from Taiwan.

Parapercis macrophthalina is confirmed as a valid species and redescribed on the basis of the holotype and other specimens collected from the type locality, Taiwan, and Japan. It is morphologically similar to P. muronis Tanaka, 1918, but differs in having five vertical transverse bars that extend well below the lateral line versus five oblique transverse bars, with the third to fifth bars ending on or above the lateral line. A new species is also described on the basis of a specimen collected from southwestern Taiwan. It is distinct in having numerous pores interconnected by canals on the head, forming 10 vertical or oblique rows on the cheek and opercular apparatus, predorsal scales extending to the level of the posterior margin of the eye, four dorsal-fin spines, six oblique bars laterally on the body, and a combination of other characters. A key to species of Parapercis with narrow transverse bars on the upper body is provided.

Review of Australian species of Plectranthias Bleeker and Selenanthias Tanaka (Teleostei: Serranidae: Anthiadinae), with descriptions of four new species.

Australian species of the anthiadine genera Plectranthias and Selenanthias are reviewed. Twenty-two species of Plectranthias and two species of Selenanthias are recorded from Australian waters: Plectranthias sp. 1 from a seamount north of Middleton Reef and Norfolk Ridge, Tasman Sea; P. alleni Randall from off southwest Western Australia; P. azumanus (Jordan Richardson) from off southwest Western Australia; P. bennetti Allen Walsh from Holmes Reef, Coral Sea; P. cruentus Gill Roberts from Lord Howe Island, and possibly off Stradbroke Island, Queensland; P. ferrugineus n. sp. from the North West Shelf and Arafura Sea; P. fourmanoiri Randall from Christmas Island and Holmes Reef, Coral Sea; P. grahami n. sp. from off central New South Wales, Tasman Sea; P. inermis Randall from Christmas Island; P. japonicus (Steindachner) from the Arafura Sea and North West Shelf; P. kamii Randall from the Coral Sea, Lord Howe Island and Christmas Island; P. lasti Randall Hoese from the North West Shelf and off Marion Reef, Queensland; P. longimanus (Weber) from the Timor Sea, Great Barrier Reef, Coral Sea and southern Queensland; P. maculicauda (Regan) from southeastern Australia; P. mcgroutheri n. sp. from the North West Shelf; P. megalophthalmus Fourmanoir Randall from northeast of the Whitsunday Islands, Queensland; P. melanesius Randall from southeastern Queensland and a seamount north of Middleton Reef; P. moretonensis n. sp. from off Stradbroke Island, Queensland; P. nanus Randall from the Cocos (Keeling) Islands, Christmas Island, Great Barrier Reef and Coral Sea; P. retrofasciatus Fourmanoir Randall from the Great Barrier Reef; P. robertsi Randall Hoese from off Queensland, Coral Sea; P. winniensis (Tyler) from the Great Barrier Reef and Coral Sea; Selenanthias analis Tanaka from the North West Shelf and Arafura Sea; and S. barroi (Fourmanoir) from west of Lihou Reef, Coral Sea. Five of the species represent new records for Australia: P. azumanus, P. kamii, P. megalophthalmus, P. melanesius and S. barroi. Previous records of P. megalophthalmus from the North West Shelf are based on misidentified specimens of P. lasti. Records of P. wheeleri from the North West Shelf are based on specimens here identified as P. mcgroutheri n. sp. A record of P. yamakawai Yoshino from Christmas Island is based on a misidentified specimen of P. kamii. Plectranthias retrofasciatus was previously recorded from the Great Barrier Reef as P. pallidus Randall Hoese, here shown to be a junior synonym of P. retrofasciatus. Video-based records of P. kelloggi from the Great Barrier Reef appear to be based on P. retrofasciatus. Identification keys, diagnoses, character summaries, photographs and Australian distribution information are presented for all species. Full descriptions are provided for the new species and for those newly recorded from Australia.

Three new species of Australian anthiadine fishes, with comments on the monophyly of Pseudanthias Bleeker (Teleostei: Serranidae).

Three new species of anthiadine species are described from specimens trawled from Australian waters. Pseudanthias paralourgus n. sp. is described from five specimens collected off southeastern Queensland. It resembles P. elongatus (Franz, 1910) from Japan to the South China Sea, but differs in male live coloration. The remaining two species are assigned to the genus Tosana Smith Pope, 1906, which is newly diagnosed to include the two new species and the type species from southern Japan to the South China Sea, T. niwae Smith Pope, 1906. The two new species, T. dampieriensis n. sp. described from three specimens from off Western Australia and T. longipinnis n. sp. described from 42 specimens from off eastern Australia, differ from each other and from T. niwae in various meristic and morphometric details. Pseudanthias paralourgus co-occurs with T. longipinnis. Molecular phylogenetic analysis of mitochondrial COI yielded a tree with the three Tosana species forming the sister group of a clade consisting of P. paralourgus n. sp., P. elongatus and the type species of Pseudanthias Bleeker, 1871, P. pleurotaenia (Bleeker, 1857). Our preliminary phylogenetic analyses suggest that Pseudanthias comprises a polyphyletic assemblage of species that also includes Nemanthias Smith, 1954, Luzonichthys Herre, 1936, Tosanoides Kamohara, 1953, Odontanthias Bleeker, 1873, and Serranocirrhitus Watanabe, 1949, thus highlighting the need for a revised generic classification of species currently assigned to Pseudanthias.

Scorpaena regina, a new scorpionfish (Teleostei: Scorpaenidae) from the east coast of Queensland, Australia.

The new, small-sized scorpionfish, Scorpaena regina, is described on the basis of 59 specimens from the east coast of Queensland, Australia, from depths of 2-57 m. The new species is most similar to the southwestern Pacific species, S. bulacephala and the Hawaiian endemic S. colorata, all three species being distinguished from all other Indo-Pacific species of Scorpaena by the following combination of characters: exposed cycloid scales covering the anteroventral surface of the body and pectoral-fin base, the lateral surface and dorsal margin of the lacrimal without spines, and the lateral surface of the maxilla without longitudinal ridges. The new species differs from S. bulacephala and S. colorata in having lower numbers of pectoral-fin rays, scale rows below the lateral line, and total gill rakers [13-17 (mode 16), 11-14 (12), and 13-17 (14 or 15), respectively], a simple anterior lacrimal spine, posterior tip of the pectoral fin (seventh or eighth ray longest) not reaching to vertical through first anal-fin spine, smaller body size (maximum size 64.5 mm SL), and shallower habitat (2-57 m). Morphological ontogenetic changes in the relative lengths of some body proportions in the new species are also discussed.

Epinephelus fuscomarginatus (Perciformes: Epinephelidae), a new species of grouper from off the Great Barrier Reef, Australia.

A new species of epinephelid fish from northeastern Australia is described based on five specimens 408-564 mm SL collected by deep water demersal dropline fishing. Epinephelus fuscomarginatus sp. nov. is known from the Capricorn Channel, off the southern end of the Swain Reefs, Qld, Australia, in depths of 220-230 m. It is distinguished by a combination of dorsal-fin rays XI, 14, pectoral-fin rays 17, anal-fin rays III, 8, caudal-fin rounded, lateral-line scales 60-67, gill rakers 9-10 + 16-19 = 25-28, body depth 3.0-3.4 in SL, angle of preopercle broadly rounded, bearing 4-9 small non-prominent serrae, midlateral part of lower jaw with 2 rows of teeth, tooth patches on vomer and palatines narrow, in 2-3 and 2-4 rows, respectively, and coloration including broad dark brown margins to the soft dorsal, anal and caudal fins. There are no dark spots on the head, body, or fins at any known size and in subadults there are two faint pale brown bars radiating from the eye to the posterior margin of the opercle, and diffuse irregular brown wavy bars and blotches on the sides of the body. Comparison of the mitochondrial cytochrome c oxidase subunit 1 (CO 1) genetic marker utilised in DNA barcoding produced modest but consistent genetic divergences of 1.10% and 2.70 % between E. fuscomarginatus sp. nov. and its closest sampled congeners, E. magniscuttis and E. epistictus, respectively. Further evidence is presented to indicate that populations of E. epistictus currently recognised from the Indian Ocean east to the Indo-Australian Archipelago may be distinct from those from the Sea of Japan to the East China Sea.

Three new species of Parapercis (Perciformes: Pinguipedidae) and first records of P. muronis (Tanaka, 1918) and P. rubromaculata Ho, Chang Shao, 2012 from Australia.

Three new species of pinguipedid fishes from northern Australia are described based on specimens collected by deep water demersal trawling. Parapercis algrahami sp. nov. is recorded from off Dunk Island, Qld, south to Newcastle, NSW, in 67-333 m. It is distinct in having five narrow transverse dark bars across the upper body and a dark spot dorsally on the caudal-fin base, 6 canine teeth in outer row at front of lower jaw, palatines with 1-2 rows of teeth, and predorsal scales extending far forward on the nape to the posterior portion of the interorbital region. Parapercis imamurai sp. nov. is recorded from off Saumarez Reef, Qld, south to off Coffs Harbour, NSW, in 256-405 m. It is unique in having colouration that includes a broad dusky bar from lower margin of eye across the suborbital region and three broad dusky bands crossing the body between the middle of the soft dorsal-fin and the caudal-fin base, 10 canine teeth in outer row at front of lower jaw, and the fifth dorsal-fin spine longest. Parapercis pogonoskii sp. nov. is unique in having a combination of three reddish-brown vertical bars on the upper body between the anterior and posterior portions of the soft dorsal fin, the soft dorsal fin with two large dusky blotches and caudal-fin base with a dusky blotch in the upper corner, 8-10 canine teeth in outer row at front of lower jaw, fifth dorsal-fin spine longest, angle of subopercle with a single broad spine, and angle of preopercle with 4-5 large widely-separated spines. Comparison of the mitochondrial cytochrome c oxidase subunit 1 (CO 1) genetic marker utilised in DNA barcoding produced significant genetic divergences of at least 8.1% and 14.1% between P. algrahami sp. nov. and P. pogonoskii sp. nov. respectively and their closest sampled congeners.        The geographic range of Parapercis rubromaculata Ho, Chang Shao, 2012 is extended from Taiwan to the southern hemisphere waters off Western Australia, based on specimens collected from Shark Bay, north to Ashmore Terrace, in depths of 56-107 m. A revised diagnosis for the species is presented, meristic, morphometric and DNA barcoding data for the two populations are compared, and a detailed description of the colouration of fresh and preserved specimens from Australia is provided. Previous records of Parapercis macrophthalma (Pietschmann, 1911) from Western Australia are established as misidentifications of Parapercis muronis (Tanaka, 1918) and the latter is thereby confirmed from the southern hemisphere and Australian waters for the first time. Comparative meristic, morphometric and DNA barcoding data is provided for populations of P. muronis from Japan, Philippines and Western Australia.

Description of a new species of Tomiyamichthys from Australia with a discussion of the generic name.

Tomiyamichthys levisquama is described as a new species from the Northern Territory and Queensland, Australia from estuaries and soft bottom marine environments. It is distinctive in body and head shape, head coloration and by the absence of ctenoid scales on the body. It is compared with the related species Tomiyamichthys russus (Cantor 1849), which has ctenoid scales on the posterior part of the body. The validity of the name Tomiyamichthys over Flabelligobius is discussed, with both genera being described in the same paper, here accepting Tomiyamichthys as the appropriate name.

Parapercis nigrodorsalis (Perciformes: Pinguipedidae), a new species of sandperch from northern New Zealand and the Norfolk Ridge, Tasman Sea and remarks on P. binivirgata (Waite, 1904).

A new species of pinguipedid fish, Parapercis nigrodorsalis, is described from 17 specimens collected off the North Island of New Zealand and Wanganella Bank, Norfolk Ridge, Tasman Sea, in depths of 56-280 m. The species has also been photographed underwater off the Poor Knights Islands Reserve and Burgess Island, Mokohinau Group, in New Zealand. It is most similar to Parapercis binivirgata (Waite, 1904) in morphology, coloration and meristic values, but is unique among the genus in having a combination of dorsal-fin rays V, 23, anal-fin rays I, 19, lateral-line scales 57-63, vomer with 1-2 irregular rows of robust conical teeth, palatines with 1-2 rows of small teeth, angle of subopercle smooth, 10 abdominal and 22 caudal vertebrae, and coloration, including seven broad reddish-brown bands on the upper body between the spinous dorsal-fin and the caudal peduncle, most bands bifurcated into close-set double bars with black smudge-like blotches below, and membrane of the spinous dorsal fin black. Comparison of the mitochondrial cytochrome c oxidase subunit 1 (CO 1) genetic marker utilised in DNA barcoding produced a genetic divergence of 5.38% and 7.63% between the new species and its two closest sampled congeners. The holotype of P. binivirgata is identified from two specimens previously regarded as syntypes, some revisions are made to meristic data in the original description of the latter, and a detailed description of the revised geographic range of P. binivirgata is provided.  

Is aseptic loosening truly aseptic?

Surgeons who treat osteomyelitis or infected implants think that microorganisms can live on and around implanted biomaterials and necrotic bone without clinical manifestations of infection. Gristina and Costerton, in their seminal work, suggested that such bacteria persist within biofilms and that they are often overlooked when diagnosis is based on standard microbiologic culture techniques. Subsequent studies using specialized techniques including sonication to remove adherent bacteria and direct detection using various forms of microscopy have confirmed that bacteria are present in many culture-negative cases. This led to the suggestion that at least some cases of failed orthopaedic implants that were considered aseptic loosening based on the absence of clinical signs of infection and the failure to isolate bacteria may actually have an infectious etiology. In addition to biofilms, potentially important concepts that also may contribute to false-negative culture results include the failure to recognize small colony variants induced during growth in vivo and the presence of bacteria inside host cells including osteoblasts. Importantly, bacteria persisting as small colony variants within biofilms and/or inside osteoblasts also may be an explanation for the recurrent nature of musculoskeletal infection.