Apistogramma ortegai, new species, is described from small streams tributaries of the Ampiyacu River near Pebas, in easternPeru. It belongs to the Apistogramma regani species group and is distinguished from all other species of Apistogrammaby the combination of contiguous caudal spot to bar 7, presence of abdominal stripes, short dorsal-fin lappets in both sexes,absence of vertical stripes on the caudal fin, and reduced number of predorsal and prepelvic scales.

Reliable taxonomy underpins communication in all of biology, not least nature conservation and sustainable use of ecosystem resources. The flexibility of taxonomic interpretations, however, presents a serious challenge for end-users of taxonomic concepts. Users need standardised and continuously harmonised taxonomic reference systems, as well as high-quality and complete taxonomic data sets, but these are generally lacking for non-specialists. The solution is in dynamic, expertly curated web-based taxonomic tools.

The Pan-European Species-directories Infrastructure (PESI) worked to solve this key issue by providing a taxonomic e-infrastructure for Europe. It strengthened the relevant social (expertise) and information (standards, data and technical) capacities of five major community networks on taxonomic indexing in Europe, which is essential for proper biodiversity assessment and monitoring activities. The key objectives of PESI were: 1) standardisation in taxonomic reference systems, 2) enhancement of the quality and completeness of taxonomic data sets and 3) creation of integrated access to taxonomic information.

This paper describes the results of PESI and its future prospects, including the involvement in major European biodiversity informatics initiatives and programs.

Geophagus mirabilis, new species, is endemic to the rio Aripuanã drainage upstream from Dardanelos/Andorinhas falls.The new species is distinguished from all other species of the genus by the presence of one to five large black spots arrangedlongitudinally along the middle of the flank, in addition to the black midlateral spot that is characteristic of species in thegenus and by a pattern of iridescent spots and lines on the head in living specimens. It is further distinguished from allcongeneric species, except G. camopiensis and G. crocatus, by the presence of seven (vs. eight or more) scale rows in thecircumpeduncular series below the lateral line (7 in G. crocatus; 7-9 in G. camopiensis). Including the new species, five cichlids and 11 fish species in total are known only from the upper rio Aripuanã, and 15 fish species in total are known only from the rio Aripuanã drainage

Muscicapa dauurica Pallas, 1811 is shown to be an available name and the oldest available name for the Asian Brown Flycatcher

A recent phylogenetic analysis of the Myxinidae based on the 16S rRNA gene resulted in synonymization of Paramyxine with Eptatretus. This created homonymy of Paramyxine fernholmi with Eptatretus fernholmi and Paramyxine wisneri with Eptatretus wisneri. In order to resolve this nomenclatural dilemma, we made a more extensive phylogenetic assessment of the Myxinidae and examined the nomenclature of the family. We used 75 sequences (37 of which new for this study) of a 561 bp fragment of the 16S rRNA gene, representing 33 species, and 72 sequences (37 of which new for this study) of a 687 bp fragment of the cytochrome c oxidase subunit I (COI) gene, representing 23 species, to reconstruct the phylogeny of Myxinidae. The monophyly of the subfamily Myxininae, traditionally characterized by having a single pair of external gill openings, was rejected (0.50 Bayesian posterior probability) by the 16S analysis, but supported by the COI and combined COI+16S analyses (0.99 and 0.81 Bpp, respectively). The monophyly of the subfamily Eptatretinae, characterized by having several pairs of external gill openings, was not supported by the 16S analysis and rejected by the COI and combined COI+16S analysis due to the placement of Eptatretus lopheliae as the earliest branch of Myxinidae (0.71 and 0.57 Bpp, respectively). Eptatretus lopheliae and Eptatretus rubicundus formed a monophyletic group and were allocated to a new genus, Rubicundus, characterized by the presence of an elongated tubular nostril and reddish coloration. A new monotypic subfamily, Rubicundinae, was proposed for Rubicundus. The synonymy of the genera Paramyxine and Quadratus with Eptatretus was confirmed. E. fernholmi is renamed Eptatretus luzonicus. Eptatretus wisneri was renamed Eptatretus bobwisneri. Petromyzon cirrhatus Forster, 1801, Homea banksii Fleming, 1822, and Bdellostoma forsteri Müller, 1836 are synonyms, but no type specimens are known to exist. Petromyzon cirrhatus was designated as type species of Eptatretus, conserving present usage. Gastrobranchus dombeyi Shaw, 1804 has priority over other names for Chilean myxinids. Bdellostoma stoutii was designated as type species of Polistotrema Gill. The validity of the Western Atlantic Myxine limosa as distinct from the Eastern Atlantic Myxine glutinosa was confirmed.

Gustaf Johan Billberg’s review of ichthyology, published in Swedish in 1833 in the Linnéska samfundets handlingar, mentions92 fish taxa at genus and species level, 41 of which represent new taxa, unnecessary replacement names, or unjustifiedemendations. Billberg presents his own classification of fishes, in which five new family names are introduced:Ballistidae, Diodontidae, Ooididae, Chironectidae, and Macrorhyncidae. Diodontidae has priority over Diodontidae Bonaparte, 1835. Macrorhyncidae was published earlier than Gempylidae Gill, 1862, but the latter has priority by prevailingusage.Billberg mentions 61 genera of fishes, 41 of them listed only by name. Six generic names proposed by Billberg are available as unjustified emendations: Myxinus, Petromyzus, Scylia, Mustellus, Zyganna, and Ballistes. Brachionus is anunnecessary replacement name. Aphrus, Capriscus, Exormizus, Enneophthalmus, and Oedaus are nomina nuda. Eight new genera of fishes are proposed: Anodon, Posthias, Orbis, Sphaeroides, and Ooides are junior synonyms; Cotilla is anomen oblitum in relation to Sufflamen Jordan, 1916; Tropigaster a nomen oblitum in relation to Aracana Gray, 1835;and Tetragonizus a nomen oblitum in relation to Lactoria Jordan & Fowler, 1902.Billberg lists 31 species of fishes. Three represent new combinations; two are nomina nuda. The following 14 newspecies are described based on literature: Raja forskohlii, Cephaloptera dumerillii, Myliobatis lacepedei, Scylia russelii,Anodon macropterus, Cotilla frenata, Monacanthus blochii, M. sebae, M. cuvieri, M. marcgravii, Tetraodon striatus,Orbis psittacinus, Orbis punctulatus, and Orbis guttatus. All of those are invalid, except Scylia russelii, which is a species inquirenda. The following nine species group names are unnecessary replacement names and consequentlyinvalid: Raja arabica, Myliobatis rissoi, Scylia isabellina, Anodon cirrhosus, Anodon cornutus, Zyganna voracissima,Centrina broussonetii, Acipenser vulgaris, and Acipenser ichthyocolla.Three species of pipefishes of the family Syngnathidae are described and figured by Billberg from drawings ofspecimens observed on the Swedish West Coast. Syngnathus virens and S. pustulatus are junior synonyms of S. typhle Linnaeus, 1758. Syngnathus palmstruchii is a junior synonym of Entelurus aequoreus (Linnaeus, 1758).

Fish species names based on the family name of Eduard Rüppell are reviewed, and it is concluded that Nemachilichthys ruppelli correct name for Cobitis rupellii Sykes, 1839

Danio dangila is widely distributed in the Ganga and lower Brahmaputra basins of India, Nepal and Bangladeshand distinguished by the cleithral spot in the shape of a short vertical stripe (vs. a round spot in all similar species).Four new species are described, similar to D. dangila but with round cleithral spot and each diagnosed byspecies specific colour pattern. Danio assamila, new species, is reported from the upper and middle Brahmaputradrainage in India. Danio catenatus, new species, and D. concatenatus, new species, occur in rivers of the western slope of the Rakhine Yoma, Myanmar. Danio sysphigmatus, new species, occurs in the Sittaung drainage and smal lcoastal drainages in southeastern Myanmar. Those five species, collectively referred to as chain danios, make upa distinctive group within Danio, diagnosed by elevated number of unbranched dorsal-fin rays, long rostral andmaxillary barbels, complete lateral line, presence of a prominent cleithral spot, horizontal stripes modified intoseries of rings formed by vertical bars between horizontal dark stripes, and pectoral and pelvic fins each with the unbranched first ray prolonged and reaching well beyond the rest of the fin. Danio meghalayensis is resurrected from the synonymy of D. dangila, with D. deyi as a probable junior synonym. Danio meghalayensis has a colour pattern similar to that of chain danios with vertical bars bridging parallel horizontal stripes but usually predominantly stripes instead of series of rings, a smaller cleithral spot and shorter barbels, and the unbranched ray in the pectoral and pelvic fins is not prolonged. Danio meghalayensis is known only from the Brahmaputra drainagein Meghalaya, India. The geographical distribution of the chain danios represents a unique pattern for the region, and may be explained by different climate and river drainage systems during the latest glacial period

Danio feegradei Hora is redescribed based on recently collected specimens from small coastal streams on the western slope of the Rakhine Yoma, ranging from the Thade River drainage southward to slightly north of Kyeintali. Danio absconditus,new species, is described from the Kyeintali Chaung and small coastal streams near Gwa, south of the range of D. feegradei. Both species are distinguished from other Danio by the presence of a dark, elongate or round spot at the baseof the caudal fin and a cleithral marking composed of a small black spot margined by a much smaller orange spot. Danio feegradei is characterized by the colour pattern, with series of white spots along the otherwise dark side; D. absconditusby about 7–11 dark vertical bars on the abdominal side. Within Danio, the presence of a complete lateral line, cleithralspot, and 14 circumpeduncular scales is shared with D. dangila and similar species, but these character states may be plesiomorphicas suggested by the shared presence of cleithral spot and complete lateral line in Devario and Betadevario. In other Danio the cleithral spot is absent, the lateral line is short or absent, and the circumpeduncular scale count is lower(10–12). Twenty teleost species are reported from streams on the western slope of the Rakhine Yoma, all probably endemic.The parapatric distribution of D. absconditus and D. feegradei is unique within the genus, and may be partly explainedby changes in eustatic sea levels.

Chalinochromis cyanophleps is described from nine specimens, the largest 129 mm SL, from Namansi. It differs fromother species of Chalinochromis in plain trunk colouration, absence of black stripes on the head, relatively narrow lips, presence of tricuspid jaw teeth, and presence of five rather than four dentary lateralis foramina. The blue iridescent stripe below the eye is shared with other lamprologin cichlids, but is broader and more conspicuous in C. cyanophleps.

Chalinochromis cyanophleps occurs at depths between 6 and 45 m in rocky habitats along the Tanzanian coast of Lake Tanganyika,from Mvuna Island south to Kalala Island, a stretch of about 90 km. Field observations were made of specimens up to 18 cm total length. The COI DNA barcode sequence differs by 1.8% from that of C. popelini.

Danio htamanthinus, new species, is described from small streams in the vicinity of Htamanthi on the middle Chindwin River. It is most similar to D. choprae and D. flagrans from the Ayeyarwaddy River drainage, sharing the same elaborate colour pattern with dark vertical bars and a red interstripe along the posterior side, but is distinguished by the absence of a P+1 stripe and presence of a P stripe represented only by small spots. The uncorrected p-distance in the mitochondrial COI gene separates D. htamanthinus from D. choprae by 4.3% and from D. flagrans by 7.5%. The largest specimen is only 22.9 mm in standard length (male holotype), but the holotype and one other male, 19.5 mm SL, feature sex-specific pectoral-fin tubercles, and a female as small as 16.6 mm SL has ripening ova.In a phylogenetic analysis based on COI sequences, D. htamanthinus is sister taxon of D. flagrans+D. choprae, and those three species are sister group of D. margaritatus+D.erythromicron.

Neolamprologus timidus, new species, is described from Ulwile Island and adjacent localities on the Tanzanian coast of Lake Tanganyika. The species was observed or collected along about 100 km of coastline from KolwePoint, Cape Mpimbwe, south to Kisi Island. It is distinguished from the most similar species, N. furcifer, by presenceof scales on most of the cheek, long pectoral fin and pelvic fin with the second ray longer than the first. Neolamprologus timidus is sympatric with N. furcifer at Kolwe Point and south to Kampempa Point, and at Lupitaand Ulwile Islands south to Kisi Island, but N. furcifer is otherwise absent from the range of N. timidus. Two morphologically distinct forms are recognized in N. furcifer. Samples of N. furcifer from Ulwile Island and slightly more southern localities possess a caudal fin with rounded lobes and long middle rays, appearing onlyslightly emarginate. Samples of N. furcifer from Udachi and nearby localities possess pointed caudal-fin lobeswith greatly elongated streamers, similar to N. timidus and to N. furcifer from other parts of Lake Tanganyika, including the type specimens from the southern part of the lake. The variation in caudal-fin shape may be an expression of character displacement as it occurs in the area of sympatry between N. timidus and N. furcifer. MitochondrialDNA sequences are nearly identical in samples of N. furcifer with pointed or rounded caudal fin. A molecular phylogenetic analysis of a large set of lamprologin cichlids using two mitochondrial genes corroborates earlier analyses and places N. furcifer and N. timidus in different clades with different species of Neolamprologus, Julidochromis, Chalinochromis, and Telmatochromis despite sharing a unique combination of fin and bodyshape, and colour pattern. A 4648 base-pair multiloci analysis of a smaller number of species using fragments ofthree mitochondrial and two nuclear genes resolves N. furcifer and N. timidus in sister clades, but the N. timidus clade also includes Telmatochromis brachygnathus, and N. furcifer is sister species of Chalinochromis brichardi.

Danio annulosus, new species, is described from a small pool below the Shuvolong Falls in the Kaptai Lake system in Bangladesh. It shares with chain danios (D. assamila, D. dangila, D. catenatus, D. concatenatus, and D. sysphigmatus) a colour pattern consisting of series of dark rings with light interspaces along the side, complete lateral line, 14 cir-cumpeduncular scales, a produced first ray in the pectoral fin, and a black humeral spot. It differs from other chain danios in possessing much shorter pectoral and pelvic fins, and a humeral spot that is slightly wider than deep instead of round or deeper than wide. The mitochondrial cytochrome c oxidase subunit I (COI) sequence separates D. annulosus from the most similar species, D. catenatus by a p-distance of 3.4%. Although recorded from only a single locality, Danio annulosus is expected to have a wider distribution in the Karnafuli River drainage

The native distribution of the small labyrinth fish species Pseudosphromenus cupanus includes southern India and Sri Lanka. According to literature it has a range including also Pakistan, Bangladesh, Myanmar, Malaysia, and Indonesia (Sumatra) but there are no voucher specimens or reliable observations from those areas. The distribution record of P. cupanus was inflated partly by including P. dayi as a synonym. Pseudosphronemus dayi is native to the Western Ghats in India, but the origin of the aquarium importation in 1907 was reported as both Cochin (=Kochi) and Malacca (=Malaysia), the latter locality obviously in error. The basis for the Sumatra record is an obviously mislabeled sample of P. dayi from Pulau Weh close to Sumatra. The basis for reporting the species from Pakistan, Myanmar or Bangladesh could not be located. Misidentified museum specimens from Myanmar and Pakistan identified as P. cupanus were never published on. Pseudosphromenus cupanus has been considered recently to be extinct in Bangladesh, but in fact it never occurred there.

cichlid species first collected by Alfred Russell Wallace in the upper Rio Negro in 1852, lost during the transport toEngland but documented in drawings, is described as Crenicichla monicae on the basis of three specimens collected by the Swedish Amazonas Expedition 1923–1925. Crenicichla monicae is most similar to C. johanna, C. rosemariae, and one undescribed species which are characterized by cycloid scales, distinguishing them from other species of the genus in which most scales are ctenoid. Crenicichla monicae is recorded only from the lower Rio Uaupés and lower Rio Ic¸ana,tributaries of the upper Rio Negro, and is sympatric with the similar species C. johanna and C. lenticulata. It isdistinguished from all other species of Crenicichla by the color pattern in females, with scattered dark spots on the upperhalf of the side and on the dorsal and caudal fins. Crenicichla monicae is a member of the C. lugubris species group,characterized by very small scales in a large number along the middle of the side (89–126 scales in E1 row), blunt snout,and particular ontogenetic transformation of color pattern

Garra mini, new species, is described from the Shuvolong, Shailopropat and Chingthong waterfalls in the Kar-nafuli and Sangu River drainages. The largest specimens recorded is 46.8mm SL and specimens over 40mm SL have reached reproductive size. Alongside G.ethelwynnae (28mm SL) and G.poecilura (44.5mm SL), G.miniis one of the smallest species in the genus. Garra mini is diagnosed by morphological and meristic characters in combination, particularly the numerous small predorsal scales and the presence of a contrasted dark stripe along the middle of the side, and also by the DNA barcode sequence (cytochrome oxidase subunit I, COI) with three unique substitutions

Teleocichla preta nov. sp. inhabits the rapids along the Rio Xingu and lower portion of the Rio Iriri. It is the largest species in the genus, reaching 121·3 mm standard length (L_S) while others do not reach more than 87·8 mm L_S. Teleocichla preta is distinguished from all other species of Teleocichla by the unique blackish (in live specimens) or dark brown (preserved specimens) overall colouration of the body, which masks the faint vertical bars or zig-zag pattern of blotches on the flanks. Teleocichla preta also has a deeper body and a deep laterally compressed caudal peduncle, unlike any other congener, as well as a stout lower pharyngeal tooth plate bearing molariform teeth on its median area.