8,544 research outputs found

    Study of Myxosporea (Myxozoa), infecting worldwide mullets with description of a new species

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    Existing data on Myxozoa parasites infecting mullets were reviewed. The validity of nine species names was updated. Sixteen species were registered during analysis of original material collected in the Mediterranean, Black, Azov, and Japan Seas in 2004–2005. A new bivalvulid myxozoan parasite, Myxobolus adeli n. sp., was described from the inner organs of the golden grey mullet Liza aurata (Risso, 1810) collected in the Mediterranean (Ebro Delta, Spain), Black Sea (Kerch Strait, Ukraine), and Azov Sea (Genichesk, Ukraine) coastal waters. It is characterized by the presence of elongated, spindle-like cysts 0.5–1.3 mm in size, filled with wide transverse-oval spores about 6.2Γ—7.2Γ—4.6 ΞΌm in size, with two equal polar capsules measuring about 3.0Γ—1.8 ΞΌm and short polar filament, turned into four coils. The obtained data show that this species differs from all previously described Myxobolus spp. with equal polar capsules. Comparative study of Myxobolus spp. recorded in worldwide mullets indicates a close relationship with M. adeli n. sp. and Myxobolus improvisus Isjumova, 1964 registered in mullets. Probably, the last species includes representatives of some different species, infecting freshwater and marine hosts

    Current state of the zoobenthos at the Crimean shores of the Black Sea

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    The analysis of current state of zoobenthos at the Crimean shores of the Black Sea is fulfilled. The general features of taxonomical structure, regional peculiarities of bottom fauna development and species number distribution pattern with depth are considered. The results obtained testify the absence of species number reduction at the Crimean coastal zone of the Black Sea over the 2nd half of the XX century. Total number of the macrozoobenthos species registered in the Crimea water area exceeds 560. Filter-feeding mollusks (Chamelea gallina and Modiolula phaseolina first of all) became the most pronounced β€œevolutioning” species, determining the quantitative changes of the bottom fauna over the soft-bottoms of the southwestern Crimea during the period 1930-s – 1990-s. The shift to lesser depths: from the zone of the mussel silts (26-50 m) to the silty-sand (13-25 m) of the most productive benthal belt of the southwestern Crimea is marked. Meiobenthos (eumeiobenthos) of the Crimean shelf includes more than 522 species in total. Formation of specific meiofauna composition in areas of the methane gas seeping is marked. The presence of 38 species and 6 genera of Nematoda, which are registered only in the given conditions testify to this

    Microfungi of the Ponto-Caspian basin (сheck-list, synonymy)

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    The monograph presents the results of the inventory and revision of the taxonomic composition of microfungi from the waters of the Ponto-Caspian basin, mainly the Russian, Ukrainian and Romanian sectors of the Black Sea and the Volga basin. Information about fungi from other sectors of the Black, Azov, and Caspian seas is scarce. In this monograph of the fungi we document 600 species, members of Phylums Basidiomycota (3 species), Ascomycota (371), Zygomycota (26), Blastocladiomycota (4), Chytridiomycota (19), yeasts from Phylums Basidiomycota (26) and Ascomycota (33), fungi-like organisms from Phylums Oomycota (83), Hyphochytriomycota (2), Labyrinthulomycota (14), and Microsporidia (19) (the group of organisms related to fungi, with a controversial systematic status). The list consists of modern (valid) names of species and genera indicated in the Index Fungorum database, but the information on each taxon has been compared and, if necessary, supplemented with data from the MycoBank database. In the work, next to the species names are conventional symbols indicating the salinity of the water and substrates from of which the micromycete was isolated. There are Indexes of Genera and their synonyms (1577), of Species, intraspecific taxa and their synonyms (4626 names), as well as Author of fungal names (1550) at the end of the book. The monograph is prepared as a reference book and practical guide for mycologists, ecologists, hydrobiologists, parasitologists, graduate and undergraduate students, and teachers of universities.Π’ ΠΌΠΎΠ½ΠΎΠ³Ρ€Π°Ρ„ΠΈΠΈ ΠΈΠ·Π»ΠΎΠΆΠ΅Π½Ρ‹ Ρ€Π΅Π·ΡƒΠ»ΡŒΡ‚Π°Ρ‚Ρ‹ ΠΈΠ½Π²Π΅Π½Ρ‚Π°Ρ€ΠΈΠ·Π°Ρ†ΠΈΠΈ ΠΈ Ρ€Π΅Π²ΠΈΠ·ΠΈΠΈ таксономичСского состава Π²ΠΎΠ΄Π½Ρ‹Ρ… микроскопичСских Π³Ρ€ΠΈΠ±ΠΎΠ² ΠΈΠ· Π²ΠΎΠ΄ΠΎΠ΅ΠΌΠΎΠ² ΠŸΠΎΠ½Ρ‚ΠΎ-Каспийского бассСйна, прСимущСствСнно российского, украинского ΠΈ румынского сСкторов Π§Ρ‘Ρ€Π½ΠΎΠ³ΠΎ моря ΠΈ бассСйна Ρ€. Π’ΠΎΠ»Π³ΠΈ. БвСдСния ΠΎ Π³Ρ€ΠΈΠ±Π°Ρ… ΠΈΠ· Π΄Ρ€ΡƒΠ³ΠΈΡ… сСкторов Π§Ρ‘Ρ€Π½ΠΎΠ³ΠΎ моря, Π° Ρ‚Π°ΠΊΠΆΠ΅ Каспийского ΠΈ Азовского ΠΌΠΎΡ€Π΅ΠΉ малочислСнны. Π’ ΠΌΠΎΠ½ΠΎΠ³Ρ€Π°Ρ„ΠΈΡŽ Π²ΠΊΠ»ΡŽΡ‡Π΅Π½Ρ‹ Π³Ρ€ΠΈΠ±Ρ‹ 600 Π²ΠΈΠ΄ΠΎΠ² ΠΈΠ· ΠΎΡ‚Π΄Π΅Π»ΠΎΠ² Basidiomycota (3 Π²ΠΈΠ΄Π°), Ascomycota (371), Zygomycota (26), Blastocladiomycota (4), Chytridiomycota (19), Π΄Ρ€ΠΎΠΆΠΆΠ΅Π²Ρ‹Π΅ Π³Ρ€ΠΈΠ±Ρ‹ ΠΈΠ· ΠΎΡ‚Π΄Π΅Π»ΠΎΠ² Basidiomycota (26) ΠΈ Ascomycota (33), Π³Ρ€ΠΈΠ±ΠΎΠΏΠΎΠ΄ΠΎΠ±Π½Ρ‹Π΅ ΠΎΡ€Π³Π°Π½ΠΈΠ·ΠΌΡ‹ ΠΈΠ· ΠΎΡ‚Π΄Π΅Π»ΠΎΠ² Oomycota (83), Hyphochytriomycota (2), Labyrinthulomycota (14), Π° Ρ‚Π°ΠΊΠΆΠ΅ Microsporidia (19) (Π³Ρ€ΡƒΠΏΠΏΠ° родствСнных Π³Ρ€ΠΈΠ±Π°ΠΌ ΠΎΡ€Π³Π°Π½ΠΈΠ·ΠΌΠΎΠ² с нСясным систСматичСским статусом). Бписок составлСн ΠΏΠΎ соврСмСнным (Π²Π°Π»ΠΈΠ΄Π½Ρ‹ΠΌ) названиям Π²ΠΈΠ΄ΠΎΠ² ΠΈ Ρ€ΠΎΠ΄ΠΎΠ², ΡƒΠΊΠ°Π·Π°Π½Π½Ρ‹Ρ… Π² Π±Π°Π·Π΅ Index Fungorum, Π½ΠΎ информация ΠΏΠΎ ΠΊΠ°ΠΆΠ΄ΠΎΠΌΡƒ таксону Π±Ρ‹Π»Π° сопоставлСна ΠΈ, ΠΏΡ€ΠΈ нСобходимости, Π΄ΠΎΠΏΠΎΠ»Π½Π΅Π½Π° ΠΈΠ· Π±Π°Π·Ρ‹ MycoBank. Π’ Ρ€Π°Π±ΠΎΡ‚Π΅ рядом с Π½Π°Π·Π²Π°Π½ΠΈΠ΅ΠΌ Π²ΠΈΠ΄Π° располоТСны условныС символы, ΡƒΠΊΠ°Π·Ρ‹Π²Π°ΡŽΡ‰ΠΈΠ΅ Π½Π° ΡΠΎΠ»Ρ‘Π½ΠΎΡΡ‚ΡŒ Π²ΠΎΠ΄Ρ‹ ΠΈ субстрат, с ΠΊΠΎΡ‚ΠΎΡ€ΠΎΠ³ΠΎ Π±Ρ‹Π» Π²Ρ‹Π΄Π΅Π»Π΅Π½ ΠΌΠΈΠΊΡ€ΠΎΠΌΠΈΡ†Π΅Ρ‚. Π’ ΠΊΠΎΠ½Ρ†Π΅ ΠΊΠ½ΠΈΠ³ΠΈ Ρ€Π°Π·ΠΌΠ΅Ρ‰Π΅Π½Ρ‹ Β«Π£ΠΊΠ°Π·Π°Ρ‚Π΅Π»ΠΈΒ» Ρ€ΠΎΠ΄ΠΎΠ² ΠΈ ΠΈΡ… синонимов (1577), Π²ΠΈΠ΄ΠΎΠ², Π²Π½ΡƒΡ‚Ρ€ΠΈΠ²ΠΈΠ΄ΠΎΠ²Ρ‹Ρ… таксонов ΠΈ ΠΈΡ… синонимов (4626 Π½Π°Π·Π²Π°Π½ΠΈΠΉ), Π° Ρ‚Π°ΠΊΠΆΠ΅ Π°Π²Ρ‚ΠΎΡ€ΠΎΠ² Π½Π°Π·Π²Π°Π½ΠΈΠΉ Π³Ρ€ΠΈΠ±ΠΎΠ² (1550 ΠΈΠΌΠ΅Π½). ΠœΠΎΠ½ΠΎΠ³Ρ€Π°Ρ„ΠΈΡ ΠΏΠΎΠ΄Π³ΠΎΡ‚ΠΎΠ²Π»Π΅Π½Π° Π² качСствС справочного ΠΈ практичСского пособия для ΠΌΠΈΠΊΠΎΠ»ΠΎΠ³ΠΎΠ², экологов, Π³ΠΈΠ΄Ρ€ΠΎΠ±ΠΈΠΎΠ»ΠΎΠ³ΠΎΠ², ΠΏΠ°Ρ€Π°Π·ΠΈΡ‚ΠΎΠ»ΠΎΠ³ΠΎΠ², аспирантов, студСнтов ΠΈ ΠΏΡ€Π΅ΠΏΠΎΠ΄Π°Π²Π°Ρ‚Π΅Π»Π΅ΠΉ Π’Π£Π—ΠΎΠ²

    ВаксономичСский статус Neoechinorhynchus agilis (Acanthocephala, Neoechinorhynchidae), с описаниСм Π΄Π²ΡƒΡ… Π½ΠΎΠ²Ρ‹Ρ… Π²ΠΈΠ΄ΠΎΠ² Ρ€ΠΎΠ΄Π° ΠΎΡ‚ ΠΊΠ΅Ρ„Π°Π»Π΅Π²Ρ‹Ρ… Ρ€Ρ‹Π± (Teleostei, Mugilidae) Атлантики ΠΈ ΠŸΠ°Ρ†ΠΈΡ„ΠΈΠΊΠΈ

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    Π¨ΠΈΡ€ΠΎΠΊΠΎΠ΅ гСографичСскоС распространСниС, Π±ΠΎΠ³Π°Ρ‚Ρ‹ΠΉ список хозяСв, Π° Ρ‚Π°ΠΊΠΆΠ΅ Π·Π½Π°Ρ‡ΠΈΡ‚Π΅Π»ΡŒΠ½Π°Ρ Π²Π°Ρ€ΠΈΠ°Π±Π΅Π»ΡŒΠ½ΠΎΡΡ‚ΡŒ мСтричСских ΠΏΡ€ΠΈΠ·Π½Π°ΠΊΠΎΠ² Π°ΠΊΠ°Π½Ρ‚ΠΎΡ†Π΅Ρ„Π°Π»Ρ‹ Neoechinorhynchus agilis (Rudolphi, 1819) ставит вопрос ΠΎ таксономичСском статусС этого Π²ΠΈΠ΄Π°. Для провСдСния ΡΡ€Π°Π²Π½ΠΈΡ‚Π΅Π»ΡŒΠ½ΠΎΠ³ΠΎ морфологичСского Π°Π½Π°Π»ΠΈΠ·Π° Π±Ρ‹Π» использован Ρ‚ΠΈΠΏΠΈΡ‡Π½Ρ‹ΠΉ ΠΌΠ°Ρ‚Π΅Ρ€ΠΈΠ°Π» Π ΡƒΠ΄ΠΎΠ»ΡŒΡ„ΠΈ ΠΈ Π²Π°ΡƒΡ‡Π΅Ρ€Π½Ρ‹Π΅ экзСмпляры Π―ΠΌΠ°Π³ΡƒΡ‚ΠΈ, Π° Ρ‚Π°ΠΊΠΆΠ΅ собствСнный ΠΌΠ°Ρ‚Π΅Ρ€ΠΈΠ°Π», собранный Π² Π·Π°ΠΏΠ°Π΄Π½ΠΎΠΉ части Π’ΠΈΡ…ΠΎΠ³ΠΎ ΠΎΠΊΠ΅Π°Π½Π° ΠΈ сСвСро-восточной АтлантикС. Π’ Ρ€Π΅Π·ΡƒΠ»ΡŒΡ‚Π°Ρ‚Π΅ исслСдования Π±Ρ‹Π»ΠΎ ΠΎΠ±Π½Π°Ρ€ΡƒΠΆΠ΅Π½ΠΎ Ρ‚Ρ€ΠΈ Π²ΠΈΠ΄Π° Π°ΠΊΠ°Π½Ρ‚ΠΎΡ†Π΅Ρ„Π°Π» Neoechinorhynchus, Π² Ρ‚ΠΎΠΌ числС Π΄Π²Π° Π²ΠΈΠ΄Π° ΠΈΠ· Атлантики: N. (N.) agilis ΠΈ N. (H.) personatus Tkach, Sarabeev et Shvetsova, sp. n., ΠΈ ΠΎΠ΄ΠΈΠ½ Π²ΠΈΠ΄ ΠΈΠ· Π’ΠΈΡ…ΠΎΠ³ΠΎ ΠΎΠΊΠ΅Π°Π½Π°, N. (H.) yamagutii Tkach, Sarabeev et Shvetsova, sp. n. ΠžΠΏΠΈΡΠ°Π½Π½Ρ‹Π΅ Π² Ρ€Π°Π±ΠΎΡ‚Π΅ Π²ΠΈΠ΄Ρ‹ Ρ…ΠΎΡ€ΠΎΡˆΠΎ Ρ€Π°Π·Π»ΠΈΡ‡Π°ΡŽΡ‚ΡΡ ΠΊΠ°ΠΊ морфологичСски, Ρ‚Π°ΠΊ ΠΈ мСтричСски. Π Π°Π·Π΄Π΅Π»Π΅Π½ΠΈΠ΅ N. agilis Π½Π° Ρ‚Ρ€ΠΈ Π²ΠΈΠ΄Π°, Π΄Π²Π° ΠΈΠ· ΠΊΠΎΡ‚ΠΎΡ€Ρ‹Ρ… описаны Π²ΠΏΠ΅Ρ€Π²Ρ‹Π΅, являСтся основой для дальнСйшСго пСрСсмотра Π½Π°Ρ…ΠΎΠ΄ΠΎΠΊ этой Π°ΠΊΠ°Π½Ρ‚ΠΎΡ†Π΅Ρ„Π°Π»Ρ‹ ΠΈΠ· Ρ€Π°Π·Π½Ρ‹Ρ… Ρ€Π΅Π³ΠΈΠΎΠ½ΠΎΠ² ΠΈ ΠΎΡ‚ Ρ€Π°Π·Π½Ρ‹Ρ… хозяСв.The wide variability in morphological features, geographical and host ranges of mullet acanthocephalan parasite Neoechinorhynchus agilis (Rudolphi, 1819), raises the question of taxonomic status of this species. Rudolphi’s type and Yamaguti`s voucher specimens, as well as our own material from the WW Pacific and NE Atlantic region were used herein to provide comparative morphological analysis. The study revealed three different species of Neoechinorhynchus, N. (N.) agilis and N. (H.) personatus Tkach, Sarabeev et Shvetsova, sp. n. in the Atlantic and N. (H.) yamagutii Tkach, Sarabeev et Shvetsova, sp. n. in the Pacific. Strong morphological and morphometric differences were found between three described herein species from different hosts and regions. The dividing of N. agilis into three species, two of them are new, provides a basis for the further revision of host-geographical records of mullet acanthocephalan parasites

    Redescription of Ligophorus mediterraneus Sarabeev, Balbuena & Euzet, 2005 (Monogenea: Ancyrocephalidae) with some methodological notes

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    A redescription of Ligophorus mediterraneus Sarabeev, Balbuena & Euzet, 2005, based on original material from the Black and Mediterranean Seas, is presented and new diagnostic characters for its recognition are proposed. The unlikely wide range of variation in the angle between the shaft and point of the anchors, reported for this species and for some others in the genus, is analysed, and the structure of the ventral bar in Ligophorus spp. is described and its taxonomic significance discussed

    Lamellodiscus aff. euzeti Diamanka, Boudaya, Toguebaye & Pariselle, 2011 (Monogenea: Diplectanidae) from the gills of Cheimerius nufar (Valenciennes) (Pisces: Sparidae) collected in the Arabian Sea, with comments on the distribution, specificity and historical biogeography of Lamellodiscus spp.

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    Specimens of Lamellodiscus Johnston & Tiegs, 1922 (Monogenea: Diplectanidae) were collected from the gills of Cheimerius nufar (Valenciennes) (Sparidae) in the Arabian Sea. All of these parasites belonged to one and the same species, which is morphologically very close to L. euzeti Diamanka, Boudaya, Toguebaye & Pariselle, 2011. A different host, distant locality and small morphological differences compared with the original description of L. euzeti acted as a stimulus for a detailed redescription. The specimens from the Arabian Sea differ slightly in the details of the male copulatory organ (MCO) from the type-specimens of L. euzeti, which were re-examined, and from the respective drawings in its original description. Such differences include a longer inner process of the large element of the accessory piece associated with the proximal part of the copulatory tube, a longer point on the small element of the accessory piece associated with the distal part of the copulatory tube, and the presence of a smooth or slightly folded inner margin of this element rather than structures resembling spines which occur in the typespecimens of L. euzeti. Therefore, the present specimens infecting C. nufar in the Indo-Pacific may represent a different, but morphologically very similar species to the Atlantic form L. euzeti; consequently, they are recognised here as Lamellodiscus aff. euzeti. This form belongs to the β€˜ignoratus s. str.’ subgroup of the genus. The composition of this subgroup is redefined to comprise 17 species, including L. corallinus Paperna, 1965 but excluding L. acanthopagri Roubal, 1981, and the morphology of the MCO of representatives of this group is clarified. A link between the diversity of Lamellodiscus species and the ancestral origin of present-day sparid species in the Tethys Sea is suggested. It is shown that Lamellodiscus spp. exhibit rather high levels of specificity to their hosts, since half of them parasitise only a single host species and c.90% infect closely related host species. Comparison of the levels of host-specificity of the species of this genus with other narrowly specific genera of the Dactylogyridea revealed that their estimations are comparable. The possibility of intrahost speciation within Lamellodiscus is discussed. It is shown that a co-evolutionary model is more discernible if it includes data on the occurrence of morphologically similar species from different regions and host taxa

    Redescriptions of Ligophorus cephali Rubtsova, Balbuena, Sarabeev, Blasco-Costa & Euzet, 2006 and L. chabaudi Euzet & Suriano, 1977 (Monogenea: Ancyrocephalidae), with notes on the functional morphology of the copulatory organ

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    Redescriptions of Ligophorus cephali Rubtsova, Balbuena, Sarabeev, Blasco-Costa & Euzet, 2006 and L. chabaudi Euzet & Suriano, 1977 based on original material from the Black Sea, the Mediterranean Sea and the Sea of Japan are presented. A comparison of samples of these two species from different regions was carried out with the aid of principal components analysis. The occurrence of L. chabaudi on Mugil cephalus in the Sea of Japan was confirmed. The functional morphology of the male copulatory organ was examined, and the use of the shape of this structure in the taxonomy of Ligophorus Euzet & Suriano, 1977 is discussed

    Descriptions of eight new species of Ligophorus Euzet & Suriano, 1977 (Monogenea: Ancyrocephalidae) from Red Sea mullets

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    Eight new species of Ligophorus Euzet & Suriano, 1977 (Monogenea: Ancyrocephalidae) are described from two species of mullets from the Red Sea. Ligophorus bykhowskyi n. sp. and L. zhangi n. sp. from Crenimugil crenilabris (Forsskal) differ from other species of the genus in the structure of the male copulatory organ, which has a simple accessory piece and a wide copulatory tube that arises from a large, single-chambered, expanded base. Ligophorus simpliciformis n. sp., L. bipartitus n. sp., L. campanulatus n. sp., L. mamaevi n. sp., L. lebedevi n. sp. and L. surianoae n. sp. from Liza carinata (Valenciennes) are differentiated on the basis of the morphometrics of the hard parts of the haptor and male copulatory organ. The eight species represent the first records of species directly attributed to Ligophorus from the Red Sea. Measurements of the haptoral hard-parts and the male copulatory organ of the new species are analysed with the aid of Principal Component Analysis. Three morphological types of male copulatory organ, five types of anchor, and two types of ventral and three types of dorsal bars were distinguished among these species. L. bykhowskyi and L. zhangi from C. crenilabris have the same type of male copulatory organ and anchors. Those species from Liza carinata have only one common morphological character, a thick copulatory tube, but have two types of accessory piece, four types of anchors and three types of bars. All species of Ligophorus found on mullets in the Red Sea have an accessory piece without a distal bifurcation and thus differ from most species of this genus from other regions of the world’s oceans
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