Representatives of Ligophorus Euzet et Suriano, 1977 were found on the gills of Mugil liza Valenciennes caught in southern Brazil. They were identified as Ligophorus uruguayense Failla Siquier et Ostrowski de Núñez, 2009 and Ligophorus saladensis Marcotegui et Martorelli, 2009, even though specific identification proved to be difficult due to inconsistencies in some diagnostic features reported for these two species. Therefore, a combined morphological and molecular approach was used to critically review the validity of these species, by means of phase contrast and confocal fluorescence microscopical examination of sclerotised hard parts, and assessing the genetic divergence between L. saladensis, L. uruguayense and their congeners using rDNA sequences. The main morphological differences between the two species relate to the shape of the accessory piece of the penis and the median process of the ventral bar. The accessory piece in L. uruguayense is shorter than in L. saladensis, has a cylindrical, convex upper lobe and straight lower lobe (vs with the distal tip of the lower lobe turning away from the upper lobe in the latter species). The ventral bar has a V-shaped anterior median part in L. uruguayense (vs U-shaped in L. saladensis). The two species are suggested to be part of a species complex together with L. mediterraneus Sarabeev, Balbuena et Euzet, 2005. We recommend to generalise such comparative assessment of species of Ligophorus for a reliable picture of the diversity and diversification mechanisms within the genus, and to make full use of its potential as an additional marker for mullet taxonomy and systematics., Natalia C. Marchiori, Antoine Pariselle, Joaber Pereira Jr., Jean-François Agnèse, Jean-Dominique Durand, Maarten P.M. Vanhove., and Obsahuje bibliografii
Ten new species of Myrsidea Waterston, 1915 parasitic on members of the avian families Formicariidae, Thraupidae, Tyrannidae, Troglodytidae and Icteridae are described herein. They and their type hosts are M. isacantha sp. n. ex Chamaeza nobilis Gould, M. circumsternata sp. n. ex Formicarius colma Boddaert (Formicariidae); M. cacioppoi sp. n. ex Lanio fulvus (Boddaert), M. brasiliensis sp. n. ex Tangara chilensis (Vigors), M. saviti sp. n. ex Tangara schrankii (Spix) (Thraupidae), M. rodriguesae sp. n. ex Cnipodectes subbrunneus (Sclater), M. cnemotriccola sp. n. ex Cnemotriccus fuscatus (Wied-Neuwied), M. lathrotriccola sp. n. ex Lathrotriccus euleri (Cabanis) (Tyrannidae), M. faccioae sp. n. ex Cyphorhinus arada transfluvialis (Todd) (Troglodytidae), and M. lampropsaricola sp. n. ex Lampropsar tanagrinus (Spix) (Icteridae). Among these are two new Myrsidea species described from the avian family Formicariidae, which previously had only a single described Myrsidea species, and a new host record for M. cinnamomei Dalgleish et Price, 2005 ex Attila citriniventris Sclater. Analysis of mitochondrial cytochrome oxidase I sequences for these and other neotropical Myrsidea species provides an assessment of their phylogenetic relationships and indicates that all of these newly described species are genetically distinct. We also put these descriptions into context by estimating the potential number of unnamed Myrsidea species in Brazil, given the known diversity of potential hosts and typical levels of host specificity for Myrsidea species. Our estimate indicates that Brazilian Myrsidea species diversity is likely more than an order of magnitude greater than the number of described Myrsidea species known from Brazil, highlighting the need for future work on this megadiverse ectoparasite genus.
† Pyrenicocephalus jarzembowskii, gen. et sp. n. (Hemiptera: Heteroptera: Enicocephalomorpha: Enicocephalidae: Enicocephalinae) from Early Eocene, London Clay, England, Isle of Sheppey, is described and illustrated according to the unique pyritized adult head reported as a larval enicocephalid head by Jarzembowski (1986). The head anatomy of similar and related genera of Enicocephalinae is compared and the close relationship of the new genus to a clade including the extant genera Oncylocotis, Embolorrhinus and Hoplitocoris is suggested, most probably as the sister genus to Hoplitocoris (presently with Afrotropical, East Palaearctic and Oriental range).
A key to genera of South American Deltocephalini Dallas, 1870 based on adult males is presented. Two new genera, each based on a single new species from Argentina are described and illustrated: Corrientesia gen. n. based on type species C. ochrescens sp. n. and Salnogia gen. n. based on type species S. fletcheri sp. n. A new species of Graminella DeLong, 1936, G. schrocki sp. n. from Argentina is also described and illustrated. Graminella stelliger (Berg, 1884) equals Fusanus acristylus Cheng, 1980, syn. n. A new combination, Limpica pallida (Linnavuori & DeLong, 1979) comb. n., transferred from Reventazonia Linnavuori, 1959, is also proposed. Quaziptus Kramer, 1965, is returned from Paralimnini Distant, 1908 to Deltocephalini Dallas, 1870., Yani Duan, Christopher H. Dietrich., and Obsahuje bibliografii
A combined study of morphology, stem anatomy and isozyme patterns was used to reveal the identity of sterile plants from two rivers on the Germany/France border. A detailed morphological examination proved that the putative hybrid is clearly intermediate between Potamogeton natans and P. nodosus. The stem anatomy had characteristics of both species. The most compelling evidence came from the isozyme analysis. The additive “hybrid” banding patterns of the six enzyme systems studied indicate inheritance from P. natans and P. nodosus. In contrast, other morphologically similar hybrids were excluded: P. ×gessnacensis (= P. natans × P. polygonifolius) by all the enzyme systems, P. ×fluitans (= P. lucens × P. natans) by AAT, EST and 6PGDH, and P. ×sparganiifolius (= P. gramineus × P. natans) by AAT and EST. All samples of P. ×schreberi are of a single multi-enzyme phenotype, suggesting that they resulted from a single hybridization event and that the present-day distribution of P. ×schreberi along the Saarland/Moselle border was achieved by means of vegetative propagation and long-distance dispersal. Neither of its parental species occur with P. ×schreberi or are present upstream, which suggests that this hybrid has persisted vegetatively for a long time in the absence of its parents. The total distribution of this hybrid is reviewed and a detailed account of the records from Germany is given. P. ×schreberi appears to be a rare hybrid. The risk of incorrect determination resulting from the identification of insufficiently developed or inadequately preserved plant material is discussed.
Four of 28 wild boodies or burrowing bettongs, Bettongia lesueur (Quoy et Gaimard) passed oocysts of species of Eimeria Schneider, 1875. The boodies are surviving on off-shore islands and in large predator-proof sanctuaries on the mainland where they were reintroduced. The boodie is a potoroid marsupial extinct from the mainland of Australia due to predation from red foxes and feral cats. Comparison with other species of the genus Eimeria indicates that the coccidium found represents a new species. Sporulated oocyst of Eimeria burdi sp. n. are pyriform, 21.0-24.0 µm (mean 22.6 µm) by 14.0-16.0 µm (14.9 µm), with a length/width ratio 1.31-1.71 (1.52) and 1-µm-thick yellowish bilayered wall. Micropyle is present at the thinner apex end filled with hyaline body. Polar granules are absent. Sporocysts are ellipsoidal, 10.0-13.5 µm (11.8 µm) by 7.0-8.5 µm (7.4 µm), shape index is 1.42-1.89 (1.63) and a very thin, poorly defined unilayered sporocyst wall is 0.2 µm thick with a domelike almost indistinct Stieda body. Substieda body is indistinct., Frances Hulst, Leah F. Kemp, Jan Šlapeta., and Obsahuje bibliografii
Achorovermis testisinuosus gen. et sp. n. (Digenea: Aporocotylidae) infects the heart of the smalltooth sawfish, Pristis pectinata Latham (Rhinopristiformes: Pristidae), in the eastern Gulf of Mexico. Specimens of the new genus, along with the other blood flukes that infect batoids are similar by having an inverse U-shaped intestine and a curving testis as well as by lacking tegumental spines. The new genus differs from all of the other blood flukes infecting batoids by having an elongate body (>50 × longer than wide), a testis having >100 curves, and an ovary wholly anterior to the uterus. It differs from Ogawaia glaucostegi Cutmore, Cribb et Yong, 2018, the only other blood fluke infecting a rhinopristiform, by having a body that is >50 × (vs <30 ×) longer than wide, a testis that is >75 × (vs <40 ×) longer than wide and has >100 (vs <70) curves, an ovary wholly anterior to (vs lateral and dorsal to) the seminal vesicle, a uterus wholly posterior to (vs overlapping and lateral to both) the testis and ovary, and a sinuous (vs convoluted) uterus. The new species joins a small group of chondrichthyan blood flukes that lack tegumental spines: O. glaucostegi, Orchispirium heterovitellatum Madhavi et Rao, 1970, Myliobaticola richardheardi Bullard et Jensen, 2008, Electrovermis zappum Warren et Bullard, 2019. Blood flukes infecting batoids are further unique by having a curving testis. That is, the blood flukes infecting species within Selachii are morphologically distinct from those infecting species within the Batoidea (excluding Gymnurahemecus bulbosus Warren et Bullard, 2019). Based on the morphological similarity, we suspect that the new species shares a recent common ancestor with O. glaucostegi. The discovery of the new species brings the total number of chondrichthyan blood flukes to 11 species assigned to nine genera., Micah B. Warren, Micah D. Bakenhaster, Rachel M. Scharer, Gregg R. Poulakis and Stephen A. Bullard., and Obsahuje bibliografii
Alippistrongylus bicaudatus gen. et sp. n. (Nematoda: Heligmonellidae) is described from the striped Atlantic forest rat, Delomys dorsalis (Hensel) (Rodentia: Sigmodontinae), from the province of Misiones in Argentina. The new genus and species is characterised by a synlophe of 21 unequal ridges in both sexes without a gradient in size, with two ridges weakly sclerotised and oriented perpendicularly in the dorsal left quadrant; males with a highly dissymmetrical bursa with a hypertrophied right lobe, and females with a dorsal conical appendage just posterior to the vulva, conferring a two-tailed appearance to the female worms.
New palaeodictyopterid Paraostrava stanislavi gen. n., sp. n. is described from the Upper Carboniferous (Duckmantian) deposits of the Jan Šverma Mine in northern Bohemia (Czech Republic). The new taxon based on hindwing venation is attributed to Homoiopteridae and compared with the other homoiopterid and heolid genera within Homoiopteroidea. Due to the poor state preservation of Boltopruvostia robusta, we consider this taxon as Palaeodictyoptera: Homoiopteridae of uncertain position and restore the well defined genus Ostrava Kukalová, 1960 (type species Ostrava nigra Kukalová, 1960). Some uncertainties in the current state of knowledge on the taxonomy and phylogeny of the Homoiopteridae are pointed out. The characters matrix used to separate the genera of Homoiopteroidea is included.
Frezella gen. n. is proposed to accommodate Frezella vaucheri sp. n. from poorly known auchenipterid fish, Tocantinsia piresi (Miranda Ribeiro), from the Xingú River, one of the principal tributaries of the lower Amazon River in Brazil. The new genus belongs to the Proteocephalinae because of the medullary position of the testes, ovary (yet some follicles penetrate to the cortex on the dorsal side), vitelline follicles and uterus. It differs from other proteocephaline genera in the morphology of the scolex, which includes a metascolex composed of two distinct zones: anterior, strongly wrinkled part posterior to the suckers, and posterior, sparsely folded zone. Frezella can also be differentiated by having the internal longitudinal musculature hypertrophied laterally on both sides, the presence of some ovarian follicles in the cortex on the dorsal side and the presence of additional pair of tiny, thin-walled osmoregulatory canals situated slightly dorsomedian to ventral canals. Frezella vaucheri is the first helminth parasite reported from T. piresi, which occurs in the lower reaches of the Amazon and Tocantins River basins in Brazil., Philippe Vieira Alves, Alain de Chambrier, Tomáš Scholz, José Luis Luque., and Obsahuje bibliografii