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Features of the Maechidiini (Scarabaeidae: Melolonthinae) genera Maechidius Macleay, 1819, Epholcis Waterhouse, 1875 and Paramaechidius Frey, 1969 are critically revised and a new synonymy is proposed: Maechidius = Epholcis syn. nov. = Paramaechidius syn. nov. A key to and an annotated checklist of Maechidiini from the Indo-Australian transition zone are presented for the first time. Thirty-five new species are described, namely Maechidius aiyura sp. nov., M. alesbezdeki sp. nov., M. awu sp. nov., M. babyrousa sp. nov., M. bintang sp. nov., M. boessnecki sp. nov., M. brocki sp. nov., M. caperatus sp. nov., M. ciliatus sp. nov., M. crypticus sp. nov., M. dani sp. nov., M. deltouri sp. nov., M. dendrolagus sp. nov., M. hamatus sp. nov., M. kazantsevi sp. nov., M. konjo sp. nov., M. lapsus sp. nov., M. legalovi sp. nov., M. leucopsar sp. nov., M. longipes sp. nov., M. mailu sp. nov., M. maleo sp. nov., M. merdeka sp. nov., M. miklouhomaclayi sp. nov., M. nepenthephilus sp. nov., M. owenstanleyi sp. nov., M. riedeli sp. nov., M. similis sp. nov., M. skalei sp. nov., M. sougb sp. nov., M. suwawa sp. nov., M. trivialis sp. nov., M. ursus sp. nov., M. weigeli sp. nov. and M. yamdena sp. nov. Six new synonyms are proposed: Maechidius Macleay, 1819 = Epholcis Waterhouse, 1875 syn. nov. = Paramaechidius Frey, 1969 syn. nov., Maechidius esau Heller, 1914 = M. setosus Moser, 1920 syn. nov. = M. setosellus Frey, 1969 syn. nov., Maechidius heterosquamosus Heller, 1910 comb. rest. = Paramaechidius clypeatus Frey, 1969 syn. nov. and Maechidius paupianus Heller, 1910 = M. arrowi Frey, 1969 syn. nov. The first records of Maechidiini from the Tanimbar Islands (Yamdena), Sangihe Islands (Sangir) and Lesser Sunda Islands (Bali) are documented, of which the latter two are the northern- and westernmost known records of Maechidius and of the tribe Maechidiini. Lectotypes are designated for 23 species. Fifteen new combinations are proposed and the original combination to Maechidius is restored for four species. Ecological data are presented for the first time for selected Papuan and Wallacean species. Type material of Wallacean and Papuan Maechidiini is depicted for the first time. A key to species is given. In total, 78 species of Maechidiini are confirmed for the Indo-Australian transition zone.
The geographical range of the typically host-specific species of chewing lice (Phthiraptera) is often assumed to be similar to that of their hosts. We tested this assumption by reviewing the published records of twelve species of chewing lice parasitizing wild and domestic chicken, one of few bird species that occurs globally. We found that of the twelve species reviewed, eight appear to occur throughout the range of the host. This includes all the species considered to be native to wild chicken, except Oxylipeurus dentatus (Sugimoto, 1934). This species has only been reported from the native range of wild chicken in Southeast Asia and from parts of Central America and the Caribbean, where the host is introduced. Potentially, this discontinuous distribution is due to a low tolerance for dry environments, possibly exacerbated by competitive exclusion by Cuclotogaster heterographus (Nitzsch, 1866). Our examinations of O. dentatus also revealed that this species differs significantly from other species of Oxylipeurus in the male and female genitalia, head structure and chaetotaxy, and other morphological characters. We therefore here erect the monotypic genus Gallancyra gen. nov. for O. dentatus, and redescribe the type species.
Revision of the endemic Malagasy leafhopper tribe Platyjassini (Hemiptera: Cicadellidae: Iassinae)
(2020)
The leafhopper tribe Platyjassini, endemic to Madagascar, is revised, largely based on specimens obtained in a recent bioinventory project led by the California Academy of Sciences. Platyjassini was previously known based on the type genus, Platyjassus Evans, 1953, and four described species. Betsileonas marmorata (Blanchard, 1840), the largest leafhopper recorded from Madagascar, presently known from a few specimens collected > 100 years ago and recently considered a genus and species incertae sedis within Cicadellidae, is newly placed in Platyjassini. Fourteen new genera and 54 new species are described and illustrated, and three new combinations are proposed. Pachyjassus gen. nov. includes three new species: Pachyjassus alatus sp. nov., Pachyjassus basifurcatus sp. nov. and Pachyjassus ranomafanensis sp. nov. Pallijassus gen. nov. is erected to include two species previously placed in Platyjassus, Pallijassus reticulatus (Evans, 1959) comb. nov. and Pallijassus stenospatulatus (Evans, 1959) comb. nov. Petalojassus gen. nov. includes one new species, Petalojassus ochrescens sp. nov. Phaiojassus gen. nov. includes seven new species: Phaiojassus acutus sp. nov., Phaiojassus bispinosus sp. nov., Phaiojassus constrictus sp. nov., Phaiojassus grandis sp. nov., Phaiojassus spatulatus sp. nov., Phaiojassus undulatus sp. nov. and Phaiojassus unispinosus sp. nov. Pictojassus gen. nov. includes three new species: Pictojassus kirindiensis sp. nov., Pictojassus productus sp. nov. and Pictojassus tulearensis sp. nov. Platyjassella gen. nov. includes six new species: Platyjassella ancora sp. nov., Platyjassella andohahelensis sp. nov., Platyjassella attenuata sp. nov., Platyjassella cormorana sp. nov., Platyjassella emarginata sp. nov. and Platyjassella immaculata sp. nov. Platyjassula gen. nov. includes four new species: Platyjassula cyclura sp. nov., Platyjassula heterofurca sp. nov., Platyjassula isofurca sp. nov. and Platyjassula mahajangensis sp. nov. In addition to the type species, Platyjassus viridis Evans, 1953, Platyjassus includes 11 new species: Platyjassus acutus sp. nov., Platyjassus asymmetricus sp. nov., Platyjassus fisheri sp. nov., Platyjassus griswoldi sp. nov., Platyjassus harinhalai sp. nov., Platyjassus irwini sp. nov., Platyjassus pedistylus sp. nov., Platyjassus pennyi sp. nov., Platyjassus pictipennis sp. nov., Platyjassus symmetricus sp. nov. and Platyjassus vestigius sp. nov. Plerujassus gen. nov. includes one new species, Plerujassus brunnescens sp. nov., in addition to Plerujassus appendiculatus (Evans, 1959) comb. nov., previously placed in Platyjassus. Plexijassus gen. nov. includes one new species, Plexijassus caliginosus sp. nov. Pseudocurtara gen. nov. includes three new species: Pseudocurtara minima sp. nov., Pseudocurtara nigripicta sp. nov. and Pseudocurtara quadrata sp. nov. Pseudocyrta gen. nov. includes one new species, Pseudocyrta hyalina sp. nov. Pseudomarganana gen. nov. includes two new species: Pseudomarganana olivacea sp. nov. and Pseudomarganana rosea sp. nov. Pulchrijassus gen. nov. includes eight new species: Pulchrijassus anjozorobensis sp. nov., Pulchrijassus eunsunae sp. nov., Pulchrijassus pallescens sp. nov., Pulchrijassus roseus sp. nov., Pulchrijassus rubrilineatus sp. nov., Pulchrijassus sindhuae sp. nov., Pulchrijassus talatakelyensis sp. nov. and Pulchrijassus toamasinensis sp. nov. Punctijassus gen. nov. includes three new species: Punctijassus circularis sp. nov., Punctijassus compressus sp. nov. and Punctijassus ivohibensis sp. nov. Illustrated keys to genera and species are provided.
Three species of Lophogastrida and eight Mysida are documented for samples from 5161–5497 m bottom depth in the Angola Basin. Previously known latitudinal ranges are extended southward for five species, and bathymetric ranges extended beyond 5000 m for six species. Upon revision of the subfamily Petalophthalminae (Mysidae), four species previously attributed to the genus Petalophthalmus are integrated into Ipirophthalmus gen. nov. as I. liui gen. et comb. nov., I. caribbeanus gen. et comb. nov., I. oculatus gen. et comb. nov., and I. macrops gen. et comb. nov., mainly based on the structure of eyes and presence of setae on the telson. Petalophthalmus cristatus sp. nov. is described based on its reduced cornea and the structure of eyestalks, rostrum, mandibles, and telson. The structure of mouthparts, foregut and maxillipeds suggests an omnivorous mode of life. The diagnosis of the tribe Calyptommini (Mysidae: Erythropinae) is widened to cover the 3-segmented, uniramous fourth male pleopod and the non-incised eyeplate with horn-like rudiments of eyestalks in Abyssomysis cornuta gen. et sp. nov. The structure of mandibles, foregut, and second maxilliped suggest detritus feeding in this species. Keys to the Calyptommini and Petalophthalminae are given.
Cloeon perkinsi was described from South Africa in 1932 by Barnard. Despite being relatively common in Africa, it was mentioned in the literature quite rarely, and its known distribution to date includes most of sub-Saharan Africa. Material collected recently in Ethiopia, Israel, Saudi Arabia, and Yemen extends its distribution in East Africa, Arabian Peninsula and the Levant. We examined this material, and provide a re-description of adults (females and males) and nymphs of the species. It represents a much-needed urge mainly due to inconsistencies in literature reports regarding colouration, and sometimes incomplete morphological description of all stages. We demonstrate the intraspecific morphological variability that we have witnessed, and provide information regarding the range of habitats colonised by C. perkinsi. Based on geological and climatic history of the studied region, taken together with among countries genetic distances of the mitochondrial barcoding gene COI, we propose colonisation mechanisms for the north-easternmost limit of distribution. The fragmented distribution pattern of the species highlights the conservation importance of isolated aquatic habitats in the region, as well as current knowledge gaps.
We re-examined the type material of five of the seven described species of the marine tardigrade genus Angursa Pollock, 1979, namely, A. abyssalis Renaud-Mornant, 1981, A. bicuspis Pollock, 1979 (type species), A. capsula Bussau, 1992, A. lanceolata Renaud-Mornant, 1981, and A. lingua Bussau, 1992. In addition, we describe A. seisuimaruae sp. nov. from the Sea of Kumano, Japan. Based on new data obtained, we amend the diagnosis of this genus, provide a taxonomic key to species, and discuss their geographical distributions.
The species of the genus Enicospilus Stephens, 1835 in Saudi Arabia are reviewed. Six species have previously been recorded from Saudi Arabia: E. brevicornis (Masi, 1939), E. capensis (Thunberg, 1822), E. nervellator Aubert, 1966, E. perlatus Shestakov, 1926, E. psammus Gauld & Mitchell, 1978 and E. oculator Seyrig, 1935. Five new species are described and illustrated in this paper: Enicospilus arabicus Gadallah & Soliman sp. nov., E. mirabilis Soliman & Gadallah sp. nov., E. pseudoculator Gadallah & Soliman sp. nov., E. shadaensis Gadallah & Soliman sp. nov. and E. splendidus Rousse, Soliman & Gadallah sp. nov. Twelve species are newly recorded for the fauna of Saudi Arabia, thus raising the total number to 23 species: E. bicoloratus Cameron, 1912, E. divisus (Seyrig, 1935), E. dubius (Tosquinet, 1896), E. grandiflavus Townes & Townes, 1973, E. odax Gauld & Mitchell, 1978, E. oweni Gauld & Mitchell, 1976, E. pacificus (Holmgren, 1868), E. pallidus (Taschenberg, 1875), E. rundiensis Bischoff, 1915, E. senescens (Tosquinet, 1896), Enicospilus sp. 1 and Enicospilus sp. 2 cf. bicoloratus Cameron, 1912. The unknown male of E. odax is described for the first time. The COI barcodes of 17 specimens were sequenced, compared to the existing data and uploaded to the BOLD Systems database. An illustrated key and an annotated faunistic list of all species of Enicospilus in Saudi Arabia are also provided. Finally, we discuss the biogeographical and ecological significance of the Enicospilus fauna in Saudi Arabia.
The genus Paharia Distant, 1905 is reviewed based on the description of a new species, Paharia oorschoti sp. nov., and redescription of the allied Paharia putoni (Distant, 1892), both from Turkey. The relationships among Paharia, Subpsaltria Chen, 1943 and Tibicina Kolenati, 1857 of the tribe Tibicinini Distant, 1905 are discussed. The morphology of the exuviae of Pa. oorschoti sp. nov. and S. yangi Chen 1943 is described and compared. Tibicina insidiosa Boulard, 1977 is transferred to Paharia to become Paharia insidiosa comb. nov. A key to all species of Paharia is provided.
Ten new species belonging to three new genera (Atlantisina gen. nov., Bathycyclopora gen. nov., Calvetopora gen. nov.) of umbonulomorph bryozoans from northeastern Atlantic seamounts, islands, and the continental slope are introduced. We furthermore erect the new family Atlantisinidae fam. nov. for these genera. Eight new species belong to the new genus Atlantisina: Atlantisina atlantis gen. et sp. nov. (type species), A. acantha gen. et sp. nov., A. gorringensis gen. et sp. nov., A. inarmata gen. et sp. nov., A. lionensis gen. et sp. nov., A. meteor gen. et sp. nov., A. seinensis gen. et sp. nov., and A. tricornis gen. et sp. nov. The genus Bathycyclopora gen. nov. is introduced for ?Phylactella vibraculata Calvet from the Azores, and also includes Bathycyclopora suroiti gen. et sp. nov. The type species of Calvetopora gen. nov. is Lepralia inflata Calvet from the Gulf of Cadiz; this genus also includes Calvetopora otapostasis gen. et sp. nov. and another species left in open nomenclature. Of the 13 species described herein, 11 occur on seamounts and islands, and nine species are endemic to a single seamount, island or station. The present results show that bryozoans provide striking examples of the function of seamounts as areas of endemism, most likely intrinsically linked to the low dispersal abilities of bryozoan larvae.
Tortonian teleost otoliths from northern Italy: taxonomic synthesis and stratigraphic significance
(2017)
The Tortonian fish otoliths of northern Italy have been studied for more than a century and represent one of the best known otolith-based teleost faunas in the Miocene of the Mediterranean Basin. Yet with the growing knowledge on Recent otoliths, an updated taxonomic overview of this fauna is needed. Moreover, new material from hemipelagic Tortonian marls sampled at nine localities is described herein, revealing 109 taxa of which 88 are recognised at species level. Four of these are new: Coryphaenoides biobtusus sp. nov., “Merluccius” rattazzii sp. nov., Neobythites auriculatus sp. nov. and Lesueurigobius stironensis sp. nov. The compilation of previously studied and newly acquired material revealed a total of 118 nominal Tortonian species. At generic level, the fauna is characterised by many modern forms; more than 90% can be assigned to present day genera. At species level, however, more than half of the represented taxa are extinct. Based on the fossil otolith record, the Tortonian fauna of the Mediterranean is most similar to that of the Langhian (Badenian) of the Central Paratethys by sharing many extinct Miocene species, but it is also very close to that of the Pliocene Mediterranean, by sharing many modern Atlantic-Mediterranean forms. The Tortonian fauna is further characterised by many species that are apparently confined to the upper Miocene, resulting in a unique combination of its taxonomic composition.
The Chimarra lehibemavo species-group, new and endemic to Madagascar (Trichoptera, Philopotamidae)
(2017)
The Chimarra lehibemavo group is described to include thirteen new species: Chimarra lehibemavo sp. nov., C. cebegepi sp. nov., C. fenoevo sp. nov., C. forcellinii sp. nov., C. fotobohitra sp. nov., C. gattolliati sp. nov., C. gensonae sp. nov., C. jejyorum sp. nov., C. hamatra sp. nov., C. makiorum sp. nov., C. moramanga sp. nov., C. saha sp. nov. and C. tamara sp. nov. The adults are easily recognizable by their large size, yellow colour and the structure of the male genitalia. The membranous tergum IX and the absence of the mesal lobe of tergum X are observed in other lineages, but the strong asymmetrical deformation of the phallotheca is apomorphic. The group is monophyletic with unknown affinities, but a preliminary phylogenetic placement is suggested following genetic analysis of two specimens. With one exception, the species have restricted geographical distributions in Madagascar and inhabit rivers in eastern pristine rainforests.
In Southeast Asia, bats of the genus Tylonycteris Peters, 1872 have traditionally been classified into two wide-ranging species, T. pachypus (Temminck, 1840) and T. robustula Thomas, 1915. Our comparative phylogeographic analyses based on two mitochondrial and seven nuclear genes, combined with our multivariate morphological analyses, show that these species actually represent cryptic species complexes that share a similar biogeographic history in three major regions, i.e., Sundaland, southern Indochina, and northern Indochina. Our molecular dating estimates suggest that Pleistocene climatic oscillations and sea level changes have repeatedly isolated ancestral populations of Tylonycteris spp. in distant bamboo forest refugia. The analyses indicate, however, that populations of the T. pachypus complex were less affected by forest fragmentation in mainland Southeast Asia than those of the T. robustula complex. Accordingly, we propose several taxonomic changes within the genus Tylonycteris: the species T. fulvida and T. malayana are revalidated, and a new species, T. tonkinensis Tu, Csorba, Ruedi & Hassanin sp. nov., endemic to northern Indochina, is described.
Umborotula bogorensis (Weber, 1890) is a freshwater sponge species that is recorded occasionally, mainly on islands and peninsulas of Australasia. Less than 10 records with morphological descriptions and illustrations have been published so far, and the most recent record is dated 1978. A list of the few voucher specimens from museum collections is provided here together with the rich unpublished Sasaki collection from Japan, Korea, and Taiwan, recently deposited in a Japanese museum. The present new record from Northeast Thailand enlarges the geographic range of U. bogorensis to the Indochina mainland. A comparison of historical data vs present Thai records is performed by morpho-analysis(SEM) as well as biogeographic, ecological and climatic data. Results show low variability in shape and size of the diagnostic morphotraits in populations scattered over the wide geographic range. Here we also formally accept the new taxonomic status (rank elevation) of the previous suborder Spongillina as a new order Spongillida. The presence of this potentially threatened species in the Sakaerat Biosphere Reserve, together with its possible long-term persistence in the Bogor Botanical Garden, may support its conservation. Only a census of the known, extremely scattered populations will define the status of this species.
Four monoraphid taxa belonging to the genera Achnanthes, Psammothidium and Planothidium were found during the ongoing taxonomic revision of the freshwater and limno-terrestrial diatoms of the Maritime Antarctic region. The present paper describes these four taxa as new based on detailed light and scanning electron microscopy observations: Achnanthes kohleriana Kopalová, Zidarova & Van de Vijver sp. nov., Planothidium wetzelectorianum Kopalová, Zidarova & Van de Vijver sp. nov., Psammothidium confusoneglectum Kopalová, Zidarova & Van de Vijver sp. nov. and Psammothidium superpapilio Kopalová, Zidarova & Van de Vijver sp. nov. The morphology and ecology of all four taxa are discussed and the species are compared with morphologically similar taxa.
We revise the Panjange nigrifrons group in Borneo and document an unexpected diversity in western Sarawak forests. Five species occur within 80 km from Kuching, each species being known from its type locality only. Further species occur east until Niah, but the genus seems to be absent from Sabah. We contrast this with another pholcid genus (Aetana Huber, 2005), which is diverse in Sabah and westward until Niah, but does not seem to occur in central and western Sarawak. Five species are newly described: Panjange kapit Huber, sp. nov., Panjange kubah Huber, sp. nov., Panjange niah Huber, sp. nov., Panjange pueh Huber, sp. nov., Panjange seowi Huber, sp. nov.; Panjange tahai (Huber, 2011) comb. nov. is transferred from Pholcus.
The existing literature on the Odonata inhabiting the three large divisions of the Pacific Ocean (Micronesia, Melanesia, Polynesia) is revised taking into consideration earlier discussions on the species origin, historical faunistic records, various palaeogeographical models proposed for the area, general data on the biology and ecology of this insect order. Special emphasis is paid on the incomplete data set for the region and inconsistency of the exploration of this vast area. The taxonomy and fauna of the Pacific Odonata is far from complete which makes it very difficult to provide any plausible hypothesis on the biogeographical pattern that we observe today.
The widely accepted view of long distance dispersal from a centre of origin as the only possible means for species to occupy remote oceanic island archipelagos is critically reviewed. There are seven phenomena in the current Odonata distribution that cannot be explained only by random gene transfer mediated by wind dispersal.
Those are called “oddities”, however, they are believed to be regularities of past geological events and modern day human associated activities within the Pacific.
The rationale for each of them is explained in details and illustrated with distribution maps following the current taxonomy of the group.
A new approach is suggested to tackle the question of the origin of the Pacific Odonata by relating the higher taxa distribution to the geological events and palaeontology of the families. It is not intended to be a new hypothesis yet before more systematic studies of the taxonomy and fauna of the group. Therefore, it is believed that the new method suggested here will increase the attention of the scientific community and will boost studies on this insect order within the Pacific Ocean. Discussion on its applicability is provided with attention to details that are difficult to be explained with the Pacific Odonata palaeontology as we know it for the moment.
We provide the current holdings of Meropeidae in the Florida State Collection of Arthropods (FSCA). To date, FSCA holds a well-curated collection of extant meropeids representing 17 U.S. states and Western Australia (n = 316 Merope tuber Newman, fi ve Austromerope poultoni Killington). Merope tuber records from Vermont, Texas, and South Carolina are published here for the fi rst time. A total of 298 pinned M. tuber and four pinned
A. poultoni; six M. tuber specimens preserved in 95% ethanol; and 12 M. tuber and one A. poultoni sputter-coated with gold-palladium for SEM are available for researchers interested in studying this unique family of insects.
The island arc of the Lesser Antilles lies at the eastern margin of the Caribbean Sea in the Western Hemisphere, and stretches from the eastern end of the islands of the Greater Antilles (at the Virgin Islands), south to a position near the continental islands of Trinidad and Tobago at the north eastern corner of South America. The islands are a part of the West Indian Islands biodiversity “hotspot” and have been available for terrestrial colonization for about the past 15 million years. This is a status report on present knowledge of the beetle faunas of these islands, which is composed of 90 families, 1210 genera, and 2612 recognized species. Many additional species are not yet identified, or are unnamed, or remain to be discovered. Reported for the first time from the Lesser Antilles are four families, 49 genera, 105 species, and 1253 new island records. The largest families are Curculionidae (588 species), Staphylinidae (389 species), Chrysomelidae (181 species), Tenebrionidae (142 species), Cerambycidae (138 species), Scarabaeidae (127 species), and Carabidae (126 species). There are differing patterns of species distributions: 154 species are probably introduced by human activities; 985 are endemic species (limited to a single island); 465 are species endemic to more than one island of the Lesser Antilles; 212 are species limited to just islands of the West Indies; and 800 are native (naturally occurring) species which also have part of their distributional range in North, Central, or South America. Most of the widely distributed beetle fauna has probably come from South America by over-water dispersal. There is no compelling evidence for a vicariance origin of any part of the beetle fauna. Earlier colonists have had more time to form endemic genera (18) and endemic species. The more widely distributed species probably represent distributions achieved in and since the Pleistocene.
Ichneumonidae are incredibly diverse, yet there have been few Guatemalan ichneumonid studies. We studied the phenology of 215 specimens of Zagryphus zulaya Gauld (Hymenoptera: Ichneumonidae: Tryphoninae), most captured in a light trap and two Malaise traps in a montane (1850m) forest from 2002 to 2014. One of the Malaise traps caught over 95% of the specimens. The results suggest that Z. zulaya is most abundant in May, June, July, and August, the rainy season. Zagryphus vegai Gauld is newly recorded from Guatemala; it was previously known only from Costa Rica. It was found at an altitude of 1850m, though its previous known range was 700m to 1500m.
The study of the Portuguese marine ichthyofauna has a long historical tradition, rooted back in the 18th Century. Here we present an annotated checklist of the marine fishes from Portuguese waters, including the area encompassed by the proposed extension of the Portuguese continental shelf and the Economic Exclusive Zone (EEZ). The list is based on historical literature records and taxon occurrence data obtained from natural history collections, together with new revisions and occurrences. It comprises a total of 1191 species, distributed among 3 superclasses, 4 classes, 42 orders, 212 families and 617 genera. If considering only the EEZ and present territorial waters, this list represents an increase of 230 species (27.8%) and of 238 species (29.0%), when compared to the information available in FishBase (2012) and in the last checklist of marine and estuarine fishes of Portugal (1993), respectively. The order Perciformes shows the highest diversity, with 54 families, 162 genera and 299 species. Stomiidae (80 species), Myctophidae (71 species) and Macrouridae (37 species) are the richest families. From the listed species, 734 are present off mainland Portugal, 857 off the Azores and 766 off Madeira. Within the limits of the examined area, three species are reported for the first time in mainland Portugal and twenty-nine records are identified as doubtful. A total of 133 species have been recorded from the extended Portuguese continental shelf (2 off mainland Portugal, 117 off the Azores and 14 off Madeira), two of which are common to the Azores and Madeira extensions. Biogeographically, the Atlantic group is the most important (548 species – 46.01%), followed by the Lusitanian group (256 species – 21.49%), the African group (71 species – 5.96%), the Boreal group (34 species – 2.85%), the Mediterranean group (31 species – 2.60%), the Macaronesian group (21 species – 1.76%), the Atlantic/African group (19 species – 1.60%) and the Mediterranean/African and the Arctic groups, each with only 1 species (0.08%). Regarding the preferences for vertical habitat, the demersal fishes are the most important group (305 species – 25.61%), followed by the mesopelagic group (228 species – 19.14%), the bathypelagic group (164 species – 13.77%), the benthopelagic group (147 species – 12.34%), the bathydemersal group (115 species – 9.66%), the reef-associated group (88 species – 7.39%), the pelagic group (74 species – 6.21%), the epipelagic group (58 species – 4.87%) and 1 species (0.08%) of the benthic group. The oceanic habitat is the best represented group comprising 446 species (37.45%), followed by the shelf group (199 species – 16.71%), the slope group (164 species – 13.77%), the inner shelf group (89 species – 7.47%), the coastal group (70 species – 5.88%), the outer shelf group (29 species – 2.43%) and the oceanic/shelf group (7 species – 0.59%).
The genus Dadagulella gen. nov. is described to include 16 species of small, dentate, ovateacuminate Afrotropical snails. An identification key is provided and biogeography, anatomy and systematics are discussed. The type species is the Kenyan D. radius (Preston, 1910) comb. nov., whose name has informally been used for part of the group in the past. Substantial intraspecific variation occurs in three species: D. radius itself, D. browni (van Bruggen, 1969) comb. nov. and D. minuscula (Morelet, 1877) comb. nov. (= Ennea fi scheriana Morelet, 1881) (non Gulella minuscula Emberton & Pearce, 2000) . We recognise subspecies within each of these: D.radius radius (Preston, 1910) comb. nov., D. r. calva (Connolly, 1922) comb. et stat. nov., D. browni browni (van Bruggen, 1969) comb. nov., D. b. mafi ensis subsp. nov., D. b. semulikiensis subsp. nov., D. minuscula minuscula (Morelet, 1877) comb. nov., D. m. mahorana subsp. nov. Six new Tanzanian species are described: D. cresswelli sp. nov., D. delta sp. nov., D. ecclesiola sp. nov., D. frontierarum sp. nov., D. minareta sp. nov., and D. pembensis sp. nov. The genus includes seven other previously described species: D. cuspidata (Verdcourt, 1962) comb. nov.; D. rondoensis (Verdcourt, 1994) comb. nov.; D. conoidea (Verdcourt, 1996) comb. nov.; D. selene (van Bruggen & Van Goethem, 1999) comb. nov.; D. meredithae (van Bruggen, 2000) comb. nov.; D. nictitans (Rowson & Lange, 2007) comb. nov.; and D. delgada (Muratov, 2010) comb. nov.
Four taxa belonging to the complex of species around Achnanthidium minutissimum were found during the ongoing taxonomic revision of the Antarctic freshwater and limno-terrestrial diatom flora. Two taxa were previously described as Achnanthidium lailae and A. sieminskae. Two others were formerly identified as A. minutissimum but detailed light and scanning electron microscopical observations revealed sufficient morphological differences compared to the type of A. minutissimum, to justify their separation and description as new taxa: Achnanthidium indistinctum and A. maritimo-antarcticum. The morphology and ecology of all four taxa are discussed comparing the species with morphologically similar taxa. The biogeographical consequences of the splitting of the former A. minutissimum complex in the Antarctic Region are discussed.
The biogeographic significance of Diplopoda is substantiated by 50 maps documenting indigenous occurrences of the 16 orders, the three Spirostreptida s. l. suborders – Cambalidea, Epinannolenidea, Spirostreptidea – and all higher taxa including Diplopoda itself. The class is indigenous to all continents except Antarctica and islands/archipelagos in all temperate and tropical seas and oceans except the Arctic; it ranges from Kodiak Island and the northern Alaskan Panhandle, United States (USA), southern Hudson Bay, Canada, and near or north of the Arctic Circle in Iceland, continental Scandinavia, and Siberia to southern “mainland” Argentina, the southern tips of Africa and Tasmania, and Campbell Island, subantarctic New Zealand. The vast, global distribution is interrupted by sizeable, poorly- or unsampled areas including the Great Basin, USA; the Atacama Desert region of Chile and neighboring countries; southern South American islands; the central Kalahari and Sahara deserts; the Gobi Desert, Mongolia, and all of north-central and western China; from north of the Caspian Sea, Russia, to central Kazakhstan; and the “Outback” of central Australia. Five Arabian countries lack both samples and published records of indigenous diplopods – Bahrain, Kuwait, Oman, Qatar, and United Arab Emirates – as do Turks and Caicos, in the New World, and Mauritania and possibly Egypt, Africa. New records, including the first for Chilognatha from Botswana and the first specific localities from Northern Territory, Australia, are cited in the Appendix. Increased emphasis on mappings in taxonomic research is warranted along with investigations of insular “species swarms” that constitute a microcosm of the early evolution of the class. The largest “species swarm” in the Diplopoda is Diplopoda itself!