a1_Coeuritrema Mehra, 1933, previously regarded as a junior subjective synonym of Hapalorhynchus Stunkard, 1922, herein is revised to include Coeuritrema lyssimus Mehra, 1933 (type species), Coeuritrema rugatus (Brooks et Sullivan, 1981) comb. n., and Coeuritrema platti Roberts et Bullard sp. n. These genera are morphologically similar by having a ventral sucker, non-fused caeca, two testes, a pre-testicular cirrus sac, an intertesticular ovary, and a common genital pore that opens dorsally and in the sinistral half of the body. Phylogenetic analysis of the D1-D3 domains of the nuclear large subunit ribosomal DNA (28S) suggested that Coeuritrema and Hapalorhynchus share a recent common ancestor. Coeuritrema is morphologically most easily differentiated from Hapalorhynchus by having ventrolateral tegumental papillae and a definitive metraterm that is approximately 3-7× longer than the uterus. Coeuritrema comprises species that reportedly infect Asiatic softshell turtles (Testudines: Trionychidae) only, whereas Hapalorhynchus (as currently defined) comprises blood flukes that reportedly infect those hosts plus North American musk turtles (Sternotherus Bell in Gray) and mud turtles (Kinosternon Spix), both Kinosternidae, North American snapping turtles (Chelydridae), Asiatic hard-shelled turtles (Geoemydidae) and African pleurodirans (Pelomedusidae). Coeuritrema platti sp. n. infects the blood of Chinese softshell turtles, Pelodiscus sinensis (Wiegmann), cultured in the Da Rang River Basin (Phu Yen Province, Vietnam). It differs from C. lyssimus by having a narrow hindbody (< 1.6× forebody width), ventrolateral tegumental papillae restricted to the hindbody, a short cirrus sac (< 10% of corresponding body length), a transverse ovary buttressing the caeca, a short, wholly pre-ovarian metraterm (~ 10% of corresponding body length), and a submarginal genital pore., a2_It differs from C. rugatus by having small ventrolateral tegumental papillae, testes without deep lobes, and a Laurer's canal pore that opens posterior to the vitelline reservoir and dorsal to the oviducal seminal receptacle. The new species is only the second turtle blood fluke reported from Vietnam., Jackson R. Roberts, Raphael Orélis-Ribeiro, Binh T. Dang, Kenneth M. Halanych, Stephen A. Bullard., and Obsahuje bibliografii
Bothriocephalidean tapeworms parasitic in the blackfish, Centrolophus niger (Gmelin) (Perciformes: Centrolophidae), are redescribed on the basis of the evaluation of freshly collected specimens and museum material. This evaluation enabled us to supplement species diagnoses by new morphological characters of potential use for phylogenetic analyses, including the data from scanning electron microscopical observations, and to provide a key to identification of the following four species occurring in this fish: Amphicotyle heteropleura (Diesing, 1850); Milanella familiaris Kuchta et Scholz, 2008 (both Triaenophoridae); Bothriocotyle solinosomum Ariola, 1900; and Echinophallus wageneri (Monticelli, 1890) (both Echinophallidae). Large spiniform microtriches were observed on the surface of the posterodorsal margin of segments of B. solinosomum, E. wageneri and M. familiaris. The invalidity of Atelemerus Guiart, 1935, first proposed by Bray et al. (1994), is supported by the present data and its type species, A. acanthodes Guiart, 1935, is newly synonymised with E. wageneri.
Breizacanthus aznari sp. n. is described from the banded cusk-eel Raneya brasiliensis (Kaup) (Ophidiiformes: Ophidiidae) from the Patagonian coast in Argentina. Breizacanthus Golvan, 1969 is currently composed of five species (including the new species) and is characterised by the absence of trunk spines, a short cylindrical proboscis with two types of hooks and lemnisci longer than the proboscis receptacle. Breizacanthus aznari is clearly distinguished from B. chabaudi Golvan, 1969 by having 12 longitudinal rows of hooks on the proboscis, instead of 16-18. The new species resembles B. golvani Gaevskaya et Shukhgalter, 1984, B. irenae Golvan, 1969, and B. ligur Paggi, Orecchia et Della Seta, 1975, all possessing 12 longitudinal rows of hooks. However, B. aznari differs from B. golvani in having 4-5 large hooks per row (vs. 8-9) and larger eggs. The new species can be distinguished from B. irenae by the shorter body size of females, the different range of numbers of large hooks of males (4-5 and 5-6, respectively), the smaller maximum number of small hooks of females (3 and 4, respectively), and the shorter lemnisci. Breizacanthus aznari differs from B. ligur by the smaller body length of females, the smaller maximum body length of males, the different range of numbers of large hooks of males (4-5 and 5-6, respectively), and smaller lemnisci. This is the first record of a species of Breizacanthus from fishes of the order Ophidiiformes and from the Southern Hemisphere. Comparative data on species of Euzetacanthus Golvan et Houlin, 1964 and Breizacanthus are also provided.
A new harpactorine reduviid, Camptibia obscura, gen. et sp. n., from China is described. A key to related genera is provided. The functional morphology of the fore legs of this species is discussed.
Cardicola langeli n. sp. (Digenea: Aporocotylidae) infects the heart of sheepshead, Archosargus probatocephalus (Walbaum, 1792) (Perciformes: Sparidae) in the northern Gulf of Mexico off Horn Island (type locality), Mississippi, USA. The new species is described herein using light and scanning electron microscopy of adult specimens and can be most easily distinguished from the other 24 accepted species of Cardicola Short, 1953 by the combination of having (i) an ovovitelline duct that extends anteriad and that (ii) is posterior to the ootype, (iii) a male genital pore that is lateral to the oviducal seminal receptacle and (iv) a female genital pore lateral to the ootype. The new species is the only member of Cardicola so-far reported to have tegumental spines that are distally flattened and broad, rather than pointed. The new species generally resembles the two other species of Cardicola that infect sparids, i.e. Cardicola cardiocolum (Manter, 1947) (type species) from jolthead porgy, Calamus bajonado (Block et Schneider), in the Gulf of Mexico and Cardicola aurata Holzer, Montero, Repullés, Sitja-Bobadilla, Alvarez-Pellitero, Zarza et Raga, 2008, from gilthead seabream, Sparus aurata Linnaeus, in the Mediterranean Sea, by having a spheroid anterior sucker with concentric rows of minute spines anterior to the mouth and by having a similar general arrangement of the vitellarium, gonads and genitalia. However, it differs from them by having the combination of the aforementioned five features plus asymmetrical posterior caeca and a dextral posterior caecum that extends beyond the posterior margin of the ovary. Probable eggs of C. langeli n. sp. that contain a ciliated miracidium infect gill epithelium and are spheroid. An updated list of hosts, infection sites and geographic localities for the 25 accepted species of Cardicola is provided.
A new species of the Carex flava complex (Cyperaceae) is described from the Czech Republic. It is known only from the type locality and is assumed to be endemic to the Krkonoše Mts. Its systematic position along with karyological and ecological notes are presented here. The new entity proposed, Carex derelicta, is included in the subsection Serotinae of the section Ceratocystis. The distinctive features of this species are its combination of globose to shortly cylindrical female spikes, glumes of female spikes equalling or exceeding the perigynia; perigynia 2.0–2.5 mm long, not inflated, vivid green, beaks 0.4–0.7 mm long and achenes completely filling perigynia. The chromosome number n = 35 is the first reported for this taxon.
The following caryophyllidean tapeworms were found in freshwater fishes from Japan (species reported from Japan for the first time marked with an asterisk): family Caryophyllaeidae: Paracaryophyllaeus gotoi (Motomura, 1927) from Misgurnus anguillicaudatus (Cantor); Archigetes sieboldi Leuckart, 1878 from Pseudorasbora parva (Temminck et Schlegel) and Sarcocheilichthys variegatus microoculus Mori (new hosts); family Lytocestidae: *Caryophyllaeides ergensi Scholz, 1990 from Tribolodon hakuensis (Günther), T. ezoe Okada et Ikeda, Hemibarbus barbus (Temminck et Schlegel) and Chaenogobius sp. (new hosts); Khawia japonensis (Yamaguti, 1934) from Cyprinus carpio Linnaeus; K. sinensis Hsü, 1935 from H. barbus (new host) and C. carpio; *K. parva (Zmeev, 1936) from Carassius auratus langsdorfii Valenciennes in Cuvier et Valenciennes and Carassius sp. (new hosts); and *Atractolytocestus sagittatus (Kulakovskaya et Akhmerov, 1962) from C. carpio; family Capingentidae: *Breviscolex orientalis Kulakovskaya, 1962 from H. barbus (new host); and Caryophyllidea gen. sp. (probably Breviscolex orientalis) from C. carpio. The validity of C. ergensi, originally described from Leuciscus leuciscus baicalensis from Mongolia, is confirmed on the basis of an evaluation of extensive material from Japan. Atractolytocestus sagittatus (syn. Markevitschia sagittata) is tentatively considered a valid species, differing from the only congener, A. huronensis Anthony, 1958, in its considerably greater number of testes.
Alien flora of the Czech Republic is presented. In Appendix 1, 1378 alien taxa (33.4% of the total flora) are listed with information on the taxonomic position, origin, invasive status (casual, naturalized, invasive; a new category post-invasive is introduced), time of immigration (archaeophytes vs. neophytes), habitat type invaded (natural, seminatural, human-made), vegetation invaded (expressed as occurence in phytosociological alliances), mode of introduction into the country (accidental, deliberate), and date of the first record. Number of phytogeographical as well as biological and ecological attributes were compiled for each species in the database; its structure is presented in Appendix 2 as a suggestion for similar work elsewhere. Czech alien flora consists of 24.1% of taxa which arrived before 1500 (archaeophytes) and 75.9% neophytes. There are 891 casuals, 397 naturalized and 90 invasive species. Of introduced neophytes, 21.9% became naturalized, and 6.6% invasive. Hybrids contribute with 13.3% to the total number of aliens, and the hybridization is more frequent in archaeophytes (18.7%) than in neophytes (11.7%). If the 184 hybrids are excluded from the total number of aliens, there are 270 archaeophytes and 924 neophytes in the Czech flora, i.e. total of 1195 taxa. Accidental arrivals account for 53.4% of all taxa and deliberate introduction for 46.6%; the ratio is reversed for neophytes considered separately (45.5 vs. 54.5%). Majority of aliens (62.8%) are confined to human- made habitats, 11.0% were recorded exclusively in natural or seminatural habitats, and 26.2% occur in both types of habitat. Archaeophytes and neophytes occur in 66 and 83 alliances, respectively, of the phytosociological system. Flora is further analysed with respect to origin, life histories, life forms and strategies. Only 310 species (22.4% of the total number of all alien taxa) are common or locally abundant; others are rare, based on a single locality or no longer present. The following 19 taxa are reported as new for the Czech alien flora: Agrostis scabra, Alhagi pseudalhagi, Allium atropurpureum, Bromus hordeaceus subsp. pseudothominii, Carduus tenuiflorus, Centaurea ×gerstlaueri, Centaurea nigra ×phrygia, Cerastium ×maureri, Gilia capitata, Helianthus strumosus, Hieracium pannosum, Hordeum leporinum, Oenothera coronifera, Papaver atlanticum subsp. mesatlanticum, Parietaria pennsylvanica, Polypogon fugax, Rodgersia aesculifolia, Sedum pallidum var. bithynicum, Sedum stoloniferum; these represent results of our own field research as well as of herbaria search, and unpublished data from colleagues. Other 44 taxa are reported as escaping from cultivation for the first time. Twenty two archaeophytes are listed in the Red List of the Czech flora.
A complete list of all alien taxa ever recorded in the flora of the Czech Republic is presented as an update of the original checklist published in 2002. New data accumulated in the last decade are incorporated and the listing and status of some taxa are reassessed based on improved knowledge. Alien flora of the Czech Republic consists of 1454 taxa listed with information on their taxonomic position, life history, geographic origin (or mode of origin, distinguishing anecophyte and hybrid), invasive status (casual; naturalized but not invasive; invasive), residence time status (archaeophyte vs neophyte), mode of introduction into the country (accidental, deliberate), and date of the first record. Additional information on species performance that was not part of the previous catalogue, i.e. on the width of species’ habitat niches, their dominance in invaded communities, and impact, is provided. The Czech alien flora consists of 350 (24.1%) archaeophytes and 1104 (75.9%) neophytes. The increase in the total number of taxa compared to the previous catalogue (1378) is due to addition of 151 taxa and removal of 75 (39 archaeophytes and 36 neophytes), important part of the latter being the reclassification of 41 taxa as native, mostly based on archaeobotanical evidence. The additions represent taxa newly recorded since 2002 and reported in the national literature; taxa resulting from investigation of sources omitted while preparing the previous catalogue; redetermination of previously reported taxa; reassessment of some taxa traditionally considered native for which the evidence suggests the opposite; and inclusion of intraspecific taxa previously not recognized in the flora. There are 44 taxa on the list that are reported in the present study for the first time as aliens introduced to the Czech Republic or escaped from cultivation: Abies concolor, A. grandis, A. nordmanniana, Avena sterilis subsp. ludoviciana, A. ×vilis, Berberis julianae, B. thunbergii, Bidens ferulifolius, Buddleja alternifolia, Buglossoides incrassata subsp. splitgerberi, Buxus sempervirens, Corispermum declinatum, Cotoneaster dielsianus, C. divaricatus, Euphorbia myrsinites, Gleditsia triacanthos, Helleborus orientalis, Hieracium heldreichii, Koelreuteria paniculata, Lonicera periclymenum, Lotus ornithopodioides, Malus baccata, M. pumila, Miscanthus sacchariflorus, Morus alba, Muscari armeniacum, Paeonia lactiflora, Pennisetum alopecuroides, Pinguicula crystallina subsp. hirtiflora, P. grandiflora subsp. rosea, Podophyllum hexandrum, Pyracantha coccinea, Rhodotypos scandens, Rumex patientia × R. tianschanicus ‘Uteuša’, Salix cordata, Sarracenia purpurea, Sasa palmata ‘Nebulosa’, Scolymus maculatus, Spiraea japonica, Tagetes tenuifolia, Thuja occidentalis, Trifolium badium, Vaccinium corymbosum and Viburnum rhytidophyllum. All added and deleted taxa are commented on. Of the total number of taxa, 985 are classified as casuals, 408 as naturalized but not invasive, and 61 as invasive. The reduction in the number of invasive taxa compared to the previous catalogue is due to a more conservative approach adopted here; only taxa that currently spread are considered invasive. Casual taxa are strongly overrepresented among neophytes compared to archaeophytes (76.7% vs 39.4%), while naturalized but non-invasive taxa follow the reversed pattern (18.8% vs 57.4). However, these two groups do not significantly differ in the proportion of invasive taxa. Of introduced neophytes, 250 taxa (22.6%) are considered vanished, i.e. no longer present in the flora, while 23.3% became naturalized, and 4.5% invasive. In addition to the traditional classification based on introduction–naturalization–invasion continuum, taxa were classified into 18 population groups based on their long-term trends in metapopulation dynamics in the country, current state of their populations, and link to the propagule pressure from cultivation. Mapping these population groups onto the unified framework for biological invasions introduced by Blackburn et al. in 2011 made it possible to quantify invasion failures, and boom-and-busts, in the Czech alien flora. Depending on inclusion criteria (whether or not extinct/vanished taxa and hybrids are considered), alien taxa ever recorded in the Czech Republic contribute 29.7–33.1% to the total country’s plant diversity; taking into account only naturalized taxa, a permanent element of the country’s flora, the figure is 14.4–17.5%. Analysis of the dates of the first record, known for 771 neophytes, indicates that alien taxa in the flora have been increasing at a steady pace without any distinct deceleration trend; by extrapolating this data to all 1104 neophytes recorded it is predicted that the projected number would reach 1264 in 2050. Deliberate introduction was involved in 747 cases (51.4%), the remaining 48.6% of taxa are assumed to have arrived by unintentional pathways. Archaeophytes are more abundant in landscapes, occupy on average a wider range of habitat types than neophytes, but reach a lower cover in plant communities. The alien flora is further analysed with respect to representation of genera and families, origin and life history. and Nevejdou se dvě poslední jména autorů
Gyrodactylus salaris Malmberg, 1957 is a major pathogen of wild Salmo salar L. parr populations in Norway, and its delimitation from non-pathogenic species is important. The present study was undertaken to test the power of chaetotaxy to differentiate between three populations belonging to both the same and different clades (as stated by mtDNA) of G. salaris, in addition to three different species of gyrodactylids (G. salaris, G. thymalli and G. caledoniensis). The gyrodactylids were processed for chaetotaxy in situ and a maximum of 50 specimens per collection site were used to construct a generalised map over the sensilla. The sensilla were found in all populations to be symmetrically distributed around the median longitudinal axis, according to a formula of 7 dorsal (34 sensilla) and 8 ventral (44 sensilla) clusters on each side of the median line. The three Norwegian populations of G. salaris were found identical, as were the population of G. thymalli. The specimens of G. caledoniensis from Scotland, however, were found to differ from the Norwegian species G. salaris and G. thymalli by the position of one sensillum in two of the clusters. A comparison of the sensillum pattern of laboratory maintained G. salaris (River Lierelva) with results obtained ten years earlier, questions the temporal stability of the chaetotaxy pattern. The present results indicate that chaetotaxy can be used to discriminate between certain Gyrodactylus spp. but not generally.