13 research outputs found

    Description of a new Tardigrade, Macrobiotus barbarae (Eutardigrada : Macrobiotidae) from the Dominican Republic

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    A moss sample collected in the Dominican Republic contained tardigrades and their eggs, including adults and eggs of a new species, Macrobiotus barbarae sp. nov. The new species belongs to the harmsworthi group and it is most similar to M. ovostriatus Pilato et PatanĂš, 1998 and M. pseudonuragicus Pilato et al., 2004 in the character of egg areolation. It differs from M. ovostriatus above all by larger body size and wider buccal tube, better developed oral cavity armature (the first band of teeth is present and the second band of teeth forms a ring of triangular teeth) and indentation of hind lunulae. M. barbarae sp. nov. differs also from M. pseudonuragicus in details of the egg projections (in M. pseudonuragicus the terminal portion of processes is short, not elongated and divided into several short points whereas in the new species the terminal parts are elongated and generally not divided). Differences between the new species and other similar members of the harmsworthi group are also discussed

    Small is beautiful : the first phylogenetic analysis of Bryodelphax Thulin, 1928 (Heterotardigrada, Echiniscidae)

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    The phyletic relationships both between and within many of tardigrade genera have been barely studied and they remain obscure. Amongst them is the cosmopolitan Bryodelphax, one of the smallest in terms of body size echiniscid genera. The analysis of newly-found populations and species from the Mediterranean region and from South-East Asia gave us an opportunity to present the first phylogeny of this genus, which showed that phenotypic traits used in classical Bryodelphax taxonomy do not correlate with their phyletic relationships. In contrast, geographic distribution of the analysed species suggests their limited dispersal abilities and seems to be a reliable predictor of phylogenetic affinities within the genus. Moreover, we describe three new species of the genus. Bryodelphax australasiaticus sp. nov., by having the ventral plate configuration VII:4-4-2-4-2-2-1, is a new member of the weglarskae group with a wide geographic range extending from the Malay Peninsula through the Malay Archipelago to Australia. Bryodelphax decoratus sp. nov. from Central Sulawesi (Celebes) also belongs to the weglarskae group (poorly visible ventral plates VII:4-2-2-4-2-2-1) and is closely related to the recently described Bryodelphax arenosus Gąsiorek, 2018, but is differentiated from the latter by well-developed epicuticular granules on the dorsum. Finally, a new dioecious species, Bryodelphax nigripunctatus sp. nov., is described from Mallorca and, by the reduced ventral armature (II/III:2-2-(1)), it resembles Bryodelphax maculatus Gąsiorek et al., 2017. The latter species, known so far only from northern Africa, is recorded from Europe for the first time. A taxonomic key to the genus members is also presented

    Limno-Terrestrial Tardigrada of Sub-Antarctic Islands—An Annotated Review

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    Research on the limno-terrestrial Tardigrada fauna of the Sub-Antarctic zone began almost 120 years ago. Here we present an overview of the literature data on the presence of tardigrades on sub-Antarctic islands, including the substrates on which they have been found. From 32 published sources, we found original data on the occurrence of 49 currently valid species on six sub-Antarctic islands/island groups. Of these, 9 species (18%) were originally described from this zone, another 13 species (26%) were described from Continental or Maritime Antarctica, almost half of these species (22 species—45%) were originally described from European localities, and the remaining 5 species (10%) were originally described from South America, Africa, or Australia. The validity of the records of individual species is discussed. We consider the presence of 29 species in the Sub-Antarctic to be doubtful. We ascertained a total of 90 combinations of species and islands or island groups. More than half (64%) of these will require confirmation in the future because we currently consider them doubtful. We can conclude that the tardigrade fauna of the sub-Antarctic islands is only very superficially known, and the occurrence of most species in this zone must be verified

    Three Echiniscidae species (Tardigrada: Heterotardigrada) new to the Polish fauna, with the description of a new gonochoristic Bryodelphax Thulin, 1928

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    During a faunistic survey in the Pieniny and Tatra Mountains three species of Echiniscidae new to Poland, including one new to science, were found. Bryodelphax instabilis sp. nov. is characterised by an instable number of ventral plates, deep faceting of the scapular plate, having dorsal plates covered either with pseudopores or pores, and striking sexual dimorphism. Two first records, namely Echiniscus militaris and E. spiniger, are rare taxa of upland-mountain character, which have already been reported from a few European countries since the original description at the beginning of the XX^{th} century. The interspecific appendage length variability and development of pedal plates in the spinulosus group, to which E. spiniger belongs, and their taxonomic importance is discussed. Notes relating to sexual dimorphism within the newly recorded Pseudechiniscus facettalis, are also presented. Echiniscus testudo is reported from the Polish part of the Tatra Mountains for the first time. Succeeding findings confirm the high tardigrade \alpha-diversity in the Polish mountain ranges. An amended key for Polish Heterotardigrada is provided

    A new species of Tardigrada Bryodelphax brevidentatus sp. nov. (Heterotardigrada : Echiniscidae) from China (Asia)

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    A new heterotardigrade, Bryodelphax brevidentatus sp. nov. is described from moss sample collected in China. The new species is most similar to Bryodelphax tatrensis (Węglarska) but differs from it mainly by the different appearance of the dentate collar (different in shape and length of teeth), shorter cirri A and shorter claws

    FIGURES 1–8 in New taxonomic position of several Macrobiotus species (Eutardigrada: Macrobiotidae)

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    FIGURES 1–8. Macrobiotus subintermedius (syntype) (Figs. 1–4): 1—bucco-pharyngeal apparatus in lateral view (Phase Contrast = PhC); 2—pores on the caudal cuticle (arrows) (Differential Interference Contrast); 3—pores on the anterior cuticle (arrows) (PhC); 4—egg (PhC). Macrobiotus pustulatus (holotype) (Figs. 5–8; PhC): 5—bucco-pharyngeal apparatus in ventral view; 6—claws of the first pair of legs; 7—pores on the dorsal posterior cuticle; 8—pores on the ventral posterior cuticle. Scale bars: 1, 5, 6 = 5 ”m; 2, 3, 4, 7, 8 = 10 ”m.Published as part of <i>Guidetti, Roberto, Bertolani, Roberto & Degma, Peter, 2007, New taxonomic position of several Macrobiotus species (Eutardigrada: Macrobiotidae), pp. 61-68 in Zootaxa 1471 (1)</i> on page 64, DOI: 10.11646/zootaxa.1471.1.6, <a href="http://zenodo.org/record/10088041">http://zenodo.org/record/10088041</a&gt

    FIGURES 9–18 in New taxonomic position of several Macrobiotus species (Eutardigrada: Macrobiotidae)

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    FIGURES 9–18. Macrobiotus lazzaroi (Figs. 9–12; PhC): 9—bucco-pharyngeal apparatus in ventral view (paratype); 10—claws of the second pair of legs (holotype); 11—pores on dorsal cuticle (holotype); 12—egg. Macrobiotus spertii (holotype) (Figs. 13–18; PhC): 13—bucco-pharyngeal apparatus in ventral view; 14—macroplacoids within the pharynx; 15—claws of the first pair of legs (arrow = accessory points on main branch); 16—egg; 17—egg processes of another egg; 18—egg processes of a further egg. Scale bars: 9, 10, 15, 17, 18 = 5 ”m; 11–14, 16 = 10 ”m.Published as part of <i>Guidetti, Roberto, Bertolani, Roberto & Degma, Peter, 2007, New taxonomic position of several Macrobiotus species (Eutardigrada: Macrobiotidae), pp. 61-68 in Zootaxa 1471 (1)</i> on page 65, DOI: 10.11646/zootaxa.1471.1.6, <a href="http://zenodo.org/record/10088041">http://zenodo.org/record/10088041</a&gt

    Bryodelphax brevidentatus Kaczmarek, Michalczyk & Degma, 2005, sp. nov.

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    Bryodelphax brevidentatus sp. nov. (Figs. 1, 3–4, 7– 9) Type material. Holotype and 40 paratypes: Asia, China, Sichuan Province, Kangding Nature Reserve, 2650 m asl, August 2002, moss sample from rocks, Ms K. Ratyńska. Type depositories. Holotype and 10 paratypes (1 slide) are deposited in the Natural History Collections, Faculty of Biology, A. Mickiewicz University, Umultowska 89, 61­ 614 Poznań, Poland, 14 paratypes (2 slides) are deposited in the Department of Animal Taxonomy and Ecology, A. Mickiewicz University, Poznań, 8 paratypes (1 slide) are deposited in the Department of Zoology, Faculty of Natural Sciences, Comenius University, Slovakia, 8 paratypes (1 slide) are deposited in the Department of Biology, McMurry University, Abilene, Texas, U.S.A. Description. Holotype (female): Total body length without hind legs 136.0 (Fig. 1). Body coloured light orange, eyes absent or not visible after preparation. Apart from head appendages, only lateral appendages cirri A present. Internal cirri 5.0 long, cephalic papilla 3.0 long, external cirri 12.0 long. Appendages cirrus A 28.0 long (20.6% of body length). Clava oval. Ventral plates absent. Dorsal plates covered with dense and regular granulation (about 0.5–0.7 in diameter), distinctly larger on scapular and terminal plates (about 0.7–1.0 in diameter). In addition to granulation, slightly larger irregularly distributed pores are visible on entire plates but more densely distributed on margin of plates (about 1.0 in diameter). Scapular plate divided into two parts by median, longitudinal and thin stripe. Paired plates divided into two unequal anterior and posterior parts by transverse and very thin stripe without granulation. Paired plates 2 with crenulated posterior margin. Median plates 1 and 2 divided into two unequal parts (Fig. 1). Median plate 3 undivided and triangular in shape. Granules on median plates distinctly smaller then those on other plates (about 0.3 in diameter). Terminal plate with two longitudinal and thin stripes which divide the plate into three parts. Spine on the first pair of legs and papilla on fourth pair present. Dentate collar on fourth pair of legs with 5 small, triangular teeth arranged irregularly (Figs. 3–4, 7– 9). Claws of fourth pair of legs 7.0 long. External claws of all legs smooth, internal claws with very small spur 1.0 long near their base (oriented downwards). Remarks. Measurements of 16 randomly selected specimens (females) (holotype and paratypes) are given in Table 1. The paratypes are similar to the holotype and differs from them mainly by different number of collar teeth and size of some characters (Tab. 1). Etymology. The name brevidentatus refers to the general appearance of dentate collar in the new species, brevis = short, dentatus = toothed. Differential Diagnosis. Bryodelphax brevidentatus sp. nov. is most similar to B. tatrensis (Figs. 2, 5–6, 10– 12) by the presence of similar dorsal sculpture and by the presence of a dentate collar on the fourth pair of legs. The new species differs from B. tatrensis by much smaller and differently shaped teeth on the dentate collar (wide and short in B. brevidentatus and slender, sharp and long in B. tatrensis); relatively smaller claws, similar in length on all legs (in B. tatrensis, claws on IV pair of legs are distinctly longer than others). In addition, the new species differs from: 1. Bryodelphax alzirae by different colour of the body (brick red in B. alzirae and light orange in B. brevidentatus sp. nov.), presence of pores in the cuticle (only irregular granulation in B. alzirae), absence of small supplementary plates (three pairs of such plates in B. alzirae), much smaller number of teeth in dentate collar (12 teeth in B. alzirae and 47 in B. brevidentatus sp. nov.). 2. B. mateusi by different colour of the body (colourless or yellowish in B. mateusi) and by absence of small supplementary plates (six pairs of such plates in B. mateusi). 3. B. amphoterus by different colour of the body (colourless or very slightly rose in B. amphoterus) and different sculpture (more evident granulation with slightly stellate shape in B. amphoterus), shorter cirri A (about 40.0–50.0 in B. amphoterus and less than 30.0 in B. brevidentatus sp. nov.), generally smaller number of teeth in dentate collar and lacking of spur on external claws, terminal plates divided in three parts by unsculptured stripes (not marked in the description and drawing of B. amphoterus). We are grateful to Ms Katarzyna Ratyńska who collected material for us, Professor Barbara Wçglarska for the loan of the type material of B. tatrensis and Dr. Wojciech Magowski for making a phase contrast microscope available to us.Published as part of Kaczmarek, Ɓukasz, Michalczyk, Ɓukasz & Degma, Peter, 2005, A new species of Tardigrada Bryodelphax brevidentatus sp. nov. (Heterotardigrada: Echiniscidae) from China (Asia), pp. 33-38 in Zootaxa 1080 on pages 34-38, DOI: 10.5281/zenodo.17036

    Lepidoptera of different grassland types across the Morava floodplain

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    Volume: 34Start Page: 39End Page: 4
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