Monozoic cestodes of the recently amended genus Promonobothrium Mackiewicz, 1968 (Cestoda: Caryophyllidea), parasites of suckers (Cypriniformes: Catostomidae) in North America, are reviewed, with information on their host specificity, distribution and data on the scolex morphology of seven species studied for the first time using scanning electron microscopy (SEM). Evaluation of type and voucher specimens from museum collections and newly collected material of most species indicated the following valid nominal species: Promonobothrium minytremi Mackiewicz, 1968 (type species); P. ingens (Hunter, 1927); P. hunteri (Mackiewicz, 1963); P. ulmeri (Calentine et Mackiewicz, 1966); P. fossae (Williams, 1974) and P. mackiewiczi (Williams, 1974). Rogersus Williams, 1980 with its only species R. rogersi is transferred to Promonobothrium based on morphological and molecular data. Promonobothrium currani sp. n. and P. papiliovarium sp. n. are described from Ictiobus bubalus (Rafinesque) and Ictiobus niger (Rafinesque), and Erimyzon oblongus (Mitchill), respectively. The newly described species can be distinguished from the other congeners by the morphology of the scolex, the position of the anteriormost vitelline follicles and testes, the presence of postovarian vitelline follicles and the shape of the ovary. Molecular phylogenetic analyses of six species based on sequences of the small and large subunits of the nuclear ribosomal RNA genes (ssrDNA, lsrDNA) confirmed the monophyletic status of the genus and supported the validity of the species analysed. A key to identification of all species of Promonobothrium based on morphological characteristics is provided., Mikuláš Oros, Jan Brabec, Roman Kuchta, Anindo Choudhury, Tomáš Scholz., and Obsahuje bibliografii
Lepeophtheirus simplex Ho, Gómez et Fajer-Avila, 2001 is a parasite of Sphoeroides annulatus (Jenyns), an economically important fish species, with potential for aquaculture, in northwestern Mexico. The goal of this study was to describe the developmental stages under experimental conditions and seasonal fecundity of this parasite on wild fish. There are two naupliar, one copepodid, two chalimus and two pre-adult stages preceding the adult of L. simplex. The results support previous findings, which point out that the life cycle of the caligid copepods includes only six post-naupliar stages. The generation time from egg extrusion to adult for L. simplex was approximately 10 days at 22 °C. The body length of the ovigerous females ranged between 2.2 and 4.1 mm, and its fecundity between 12 and 36 eggs per string. Fecundity was negatively correlated with the egg size and positively correlated with the egg string length. Our data did not reveal significant differences in fecundity among sampling months, but ovigerous females were significantly larger in March (when water temperature was 22 °C) than in June and July (when water temperature was 30 °C). To some extent, our fecundity results contrast with those found in species of sea lice from higher latitudes. Undoubtedly, biological information on different species of sea lice from different environmental conditions will enhance our understanding of their infection strategies and will be valuable, given the increasing interest in marine fish farming in Mexico., Francisco Neptalí Morales-Serna, Ana Inés Rivas-Salas, Samuel Gómez, Emma Josefina Fajer-Ávila., and Obsahuje bibliografii
The taxonomy of Diplectanum Diesing, 1858, a genus of monopisthocotylean monogeneans, remains unsettled and needs to be revised based on new morphological criteria. Recent studies in monopisthocotyleans have shown that the muscle arrangement in the posterior attachment organ (haptor) differs between congeneric species and can be used as an additional criterion in genus-level taxonomy. To explore the possibility of using the haptoral musculature and nervous system in the taxonomy of Diplectanum, we conducted a detailed confocal-microscopy study of three species of Diplectanum (D. aculeatum Parona et Perugia, 1889, D. sciaenae van Beneden et Hesse, 1863 and D. similis Bychowsky, 1957) with phalloidin staining for muscle and indirect immunostaining for 5HT and FMRFamide. A further goal was to clarify the functional mechanics of the haptor and the role of its essential components (squamodiscs and anchors) in attachment to the host. The system of connecting bars and gaffing anchors was found to have a complex musculature consisting of 23 muscles in D. aculeatum and D. sciaenae, and 21 muscles in D. similis. The squamodiscs were shown to be operated by several groups of muscles attached primarily to the area termed the squamodisc fulcrum. Most of the haptoral musculature is identical in D. aculeatum and D. sciaenae and these species differ only in the presence of a muscle sheath around the tissue strand between the squamodiscs in D. sciaenae and in the different patterns of superficial squamodisc muscles. Diplectanum similis shows more significant differences from the other two species: besides lacking two of the haptoral muscles, it also differs in the shapes and arrangement of several other muscles. The nervous system of all three species conforms to the general pattern typical for the Dactylogyroidea and shows little variation between species., Anatoly A. Petrov, Evgenija V. Dmitrieva, Maryana P. Popyuk, Pavel I. Gerasev, Sergey A. Petrov., and Obsahuje bibliografii
Trematode sporocysts and rediae reproduce by parthenogenesis, forming clonal groups in the molluscan host. It has recently become popular to consider these groups as eusocial colonies, with division of labour between rediae morphs: small 'soldiers' incapable of reproduction defend the colony, while large rediae reproduce. Alternatively, clonal groups can be considered as self-sustaining infrapopulations. We tested these two hypotheses in the light of new data on rediae of Himasthla elongata (Mehlis, 1831) from snails Littorina littorea (Linnaeus) concerning ultrastructure, growth character and composition of their groups. Clonal groups under study contained rediae of different age and maturity stages: small (young) rediae, rediae with early cercarial embryos, rediae with late embryonic cercariae, rediae with fully formed motile cercariae, rediae with redial embryos and degenerating rediae. Small rediae had a reproductive organ, the germinal mass, whereas most large rediae with developing cercariae did not, which contradicts the eusocialconcept. Overall distribution of rediae by size and by gut to body length ratio was bimodal, which agrees with the eusocial concept ('soldiers' and 'reproductives' as modal size classes). On closer inspection, however, the bimodal size-frequency distributions (SFD) turned out to be the sum of unimodal SFD of rediae at various stages of maturity. The overall bimodality was determined by the character of redial growth resulting in a relatively low occurrence of intermediate morphs and by the developmental arrest in young rediae. The facts that small rediae can attack other rediae and concentrate in the anterior parts of the mollusc can be explained by age-related feeding preferences and niche segregation. They are unlikely to be associated with the 'colony' defence against invaders. To sum up, clonal groups of H. elongata rediae in our study represented self-sustaining infrapopulations., Kirill V. Galaktionov, Irina M. Podvyaznaya, Kirill E. Nikolaev, Ivan A. Levakin., and Obsahuje bibliografii
Seven new species of chewing lice in the genus Resartor Gustafsson et Bush, 2017 are described and illustrated. They are: Resartor albofulvus sp. n. ex Heterophasia desgodinsi desgodinsi (Oustalet); Resartor apimimus sp. n. ex Heterophasia picaoides wrayi (Ogilvie-Grant); Resartor aterrimus sp. n. ex Minla ignotincta mariae La Touche; Resartor extraneus sp. n. ex Lioparus chrysotis swinhoii (Verreaux); Resartor guangxiensis sp. n. ex Trochalopteron milnei sinianum Stresemann; Resartor longisuturalis sp. n. ex Actinodura cyanouroptera wingatei (Ogilvie-Grant); Resartor seminudus sp. n. ex Leiothrix argentauris tahanensis (Yen). All species differ in the shape of the head, shape of the male genitalia and abdominal chaetotaxy. A checklist and a key to the species of Resartor are provided., Daniel Roland Gustafsson, Xingzhi Chu, Sarah Elizabeth Bush, Fasheng Zou., and Obsahuje bibliografii