Revision of Pittosporum (Pittosporaceae) in Australia

2000 ◽  
Vol 13 (6) ◽  
pp. 845 ◽  
Author(s):  
Lindy W. Cayzer ◽  
Michael D. Crisp ◽  
Ian R. H. Telford

Following a phylogenetic analysis using morphology, Pittosporum is here monographed and recircumscribed as a monophyletic genus, by including the small genus Citriobatus and by excluding a new genus, described in the accompanying paper as Auranticarpa. Within Australia and its associated territories, 20 species are now recognised in Pittosporum, including the four from Citriobatus, three of which are given new combinations (P. spinescens, P. lancifolium and P. multiflorum). Citriobatus linearis requires a new name (P. viscidum). Four species are reinstated or confirmed at species level (P. angustifolium, P. ligustrifolium, P. nativitatis and P. wingii), and P. trilobum is described for the first time.

Zootaxa ◽  
2018 ◽  
Vol 4415 (2) ◽  
pp. 357 ◽  
Author(s):  
DENIS J. BROTHERS

The genus Aglaotilla Brothers, gen. nov., is described for 14 striking species of Australian Mutillidae related to Ephutomorpha André, 1902, characterized by bright metallic coloration and strong punctation. The description of both sexes is possible through sex associations revealed by rearings from mud nests and trap nests. Both sexes of the type species, Ephutomorpha submetallescens Turner, 1916, are described and illustrated, the male for the first time. New combinations and a new name are proposed, as follows: Aglaotilla aeruginosa (Smith, 1879), comb. nov. (from Mutilla); A. australis (André, 1898), comb. nov. (from Mutilla); A. cuprea (André, 1901), comb. nov., stat. nov. (from Mutilla); A. dilecta (Turner, 1916), comb. nov. (from Ephutomorpha); A. ignita (Smith, 1855), comb. nov. (from Mutilla); A. metallica (Smith, 1855), comb. nov. (from Mutilla); A. mira (André, 1895), comb. nov. (from Mutilla (Sphaerophthalma [sic.])); A. nigroaenea (Smith, 1855), comb. nov. (from Mutilla); A. picturata (Turner, 1914), comb. nov. (from Ephutomorpha); A. semicuprea (André, 1898), comb. nov. (from Mutilla); A. submetallescens (Turner, 1916), comb. nov. (from Ephutomorpha); A. viridatis (Smith, 1855), comb. nov. (from Mutilla); A. viridiaurea (André, 1895), comb. nov. (from Mutilla (Sphaerophthalma [sic.])); A. discolor Brothers, nom. nov. (= Ephutomorpha aeneidorsis Turner, 1916, not Ephutomorpha lauta var. aeneidorsis André, 1903). 


Zootaxa ◽  
2019 ◽  
Vol 4681 (1) ◽  
pp. 1-136 ◽  
Author(s):  
MATHIAS HARZHAUSER ◽  
BERNARD LANDAU

We present a critical evaluation of the taxonomy, stratigraphy and biogeography of the turritellid gastropods of the Miocene Paratethys Sea. 159 species-level names and 6 infrasubspecific names have been used for Paratethyan Turritellidae since 1848. Of these, only 35 species are accepted herein as valid species, with some uncertainties due to poor preservation or limited access to type material. Maximum diversities occurred during the early middle Miocene (Langhian, Badenian) coinciding with the Miocene Climatic Optimum. Whilst early Miocene turritellid assemblages are characterized by large to very large species of Peyrotia, Turritella and Allmonia, middle Miocene assemblages are predominated by medium-sized species of Archimediella, Helminthia, Oligodia and Ptychidia. The taxonomic composition of these faunas, with representatives of Archimediella, Helminthia, Mesalia and Vermicularia suggests a biogeographic affiliation with Atlantic and especially West African faunas.                Turritellinella new gen. is established as new genus for the eastern Atlantic-Mediterranean Turritella tricarinata/communis complex. Viennella is described as new genus with Turritella incisaeformis Csepreghy-Meznerics 1956 as type species. Allmonia new gen. is introduced as new genus for European Cenozoic Protominae previously placed in Protoma. For the first time, inner lirae are documented as conchological features of Turritellidae.                Six species are described as new, three within the Turritellinae: Archimediella carpathica new sp., Ptychidia erynella new sp. and Viennella ignorata new sp., and three within the Pareorinae: Mesalia sovisi new sp., Mesalia stryriaca new sp. and Mesalia bohnhavasae new sp.. Ptychidia austrorotundata new nom. is proposed as new name Turritella turris rotundata Schaffer 1912, non Turritella rotundata Grzybowski 1899. We designate lectotypes for Turritella gradata Menke in Hörnes, 1855, Haustator striatellatus Sacco, 1895, Allmonia carniolica (Stache, 1858) and Allmonia alterniplicata (Sacco, 1895). Neotypes are designated for Archimediella abundans (Handmann, 1882), Archimediella hoernesi (Rolle, 1856), Ptychidia partschi (Rolle, 1856), Ptychidia? ernesti (Handmann, 1882). Rhabdosis Townes, 1970 (Hymenoptera, Ichneumonidae) is a junior homonym of Rhabdosis Handmann 1882 (Gastropoda, Turritellidae) and will need a new name. 


2020 ◽  
Vol 62 (1-2) ◽  
pp. 69-108
Author(s):  
S. Y. Kondratyuk ◽  
D. K. Upreti ◽  
G. K. Mishra ◽  
S. Nayaka ◽  
K. K. Ingle ◽  
...  

Eight species, new for science, i.e.: Lobothallia gangwondoana S. Y. Kondr., J.-J. Woo et J.-S. Hur and Phyllopsora dodongensis S. Y. Kondr. et J.-S. Hur from South Korea, Eastern Asia, Ioplaca rinodinoides S. Y. Kondr., K. K. Ingle, D. K. Upreti et S. Nayaka, Letrouitia assamana S. Y. Kondr., G. K. Mishra et D. K. Upreti, and Rusavskia indochinensis S. Y. Kondr., D. K. Upreti et S. Nayaka from India and China, South Asia, Caloplaca orloviana S. Y. Kondr. and Rusavskia drevlyanica S. Y. Kondr. et O. O. Orlov from Ukraine, Eastern Europe, as well as Xanthoria ibizaensis S. Y. Kondr. et A. S. Kondr. from Ibiza Island, Spain, Mediterranean Europe, are described, illustrated and compared with closely related taxa. Fominiella tenerifensis S. Y. Kondr., Kärnefelt, A. Thell et Feuerer is for the first time recorded from Mediterranean Europe, Huriella loekoesiana S. Y. Kondr. et Upreti is provided from Russia for the first time, and H. pohangensis S. Y. Kondr., L. Lőkös et J.-S. Hur for the first time from China, Phoma candelariellae Z. Kocakaya et Halıcı is new to Ukraine, and Staurothele frustulenta Vain. is recorded from the Forest Zone of Ukraine for the first time. Twelve new combinations, i.e.: Bryostigma apotheciorum (for Sphaeria apotheciorum A. Massal.), Bryostigma biatoricola (for Arthonia biatoricola Ihlen et Owe-Larss.), Bryostigma dokdoense (for Arthonia dokdoensis S. Y. Kondr., L. Lőkös, B. G. Lee, J.-J. Woo et J.-S. Hur), Bryostigma epiphyscium (for Arthonia epiphyscia Nyl.), Bryostigma lobariellae (for Arthonia lobariellae Etayo), Bryostigma lapidicola (for Lecidea lapidicola Taylor), Bryostigma molendoi (for Tichothecium molendoi Heufl. ex Arnold), Bryostigma neglectulum (for Arthonia neglectula Nyl.), Bryostigma parietinarium (for Arthonia parietinaria Hafellner et Fleischhacker), Bryostigma peltigerinum (for Arthonia vagans var. peltigerina Almq.), Bryostigma phaeophysciae (for Arthonia phaeophysciae Grube et Matzer), Bryostigma stereocaulinum (for Arthonia nephromiaria var. stereocaulina Ohlert), are proposed based on results of combined phylogenetic analysis based on mtSSU and RPB2 gene sequences. Thirty-one new combinations for members of the genus Polyozosia (i.e.: Polyozosia actophila (for Lecanora actophila Wedd.), Polyozosia agardhiana (for Lecanora agardhiana Ach.), Polyozosia altunica (for Myriolecis altunica R. Mamut et A. Abbas), Polyozosia antiqua (for Lecanora antiqua J. R. Laundon), Polyozosia bandolensis (for Lecanora bandolensis B. de Lesd.), Polyozosia behringii (for Lecanora behringii Nyl.), Polyozosia caesioalutacea (for Lecanora caesioalutacea H. Magn.), Polyozosia carlottiana (for Lecanora carlottiana C. J. Lewis et Śliwa), Polyozosia congesta (for Lecanora congesta Clauzade et Vězda), Polyozosia eurycarpa (for Lecanora eurycarpa Poelt, Leuckert et Cl. Roux), Polyozosia expectans (Lecanora expectans Darb.), Polyozosia flowersiana (Lecanora flowersiana H. Magn.), Polyozosia fugiens (for Lecanora fugiens Nyl.), Polyozosia invadens (for Lecanora invadens H. Magn.), Polyozosia juniperina (for Lecanora juniperina Śliwa), Polyozosia latzelii (for Lecanora latzelii Zahlbr.), Polyozosia liguriensis (for Lecanora liguriensis B. de Lesd.), Polyozosia massei (for Myriolecis massei M. Bertrand et J.-Y. Monnat), Polyozosia mons-nivis (for Lecanora mons-nivis Darb.), Polyozosia oyensis (for Lecanora oyensis M.-P. Bertrand et Cl. Roux), Polyozosia percrenata (for Lecanora percrenata H. Magn.), Polyozosia persimilis (for Lecanora hagenii subsp. persimilis Th. Fr.), Polyozosia poeltiana (for Lecanora poeltiana Clauzade et Cl. Roux), Polyozosia prominens (for Lecanora prominens Clauzade et Vězda), Polyozosia prophetae-eliae (for Lecanora prophetae-eliae Sipman), Polyozosia salina (for Lecanora salina H. Magn.), Polyozosia schofieldii (for Lecanora schofieldii Brodo), Polyozosia sverdrupiana (for Lecanora sverdrupiana Øvstedal), Polyozosia torrida (for Lecanora torrida Vain.), Polyozosia wetmorei (for Lecanora wetmorei Śliwa), Polyozosia zosterae (for Lecanora subfusca? zosterae Ach.)) are proposed.


Phytotaxa ◽  
2013 ◽  
Vol 146 (1) ◽  
pp. 1 ◽  
Author(s):  
PETER B. HEENAN ◽  
ROB D. SMISSEN

The generic taxonomy of the Nothofagaceae is revised. We present a new phylogenetic analysis of morphological characters and map these characters onto a recently published phylogenetic tree obtained from DNA sequence data. Results of these and previous analyses strongly support the monophyly of four clades of Nothofagaceae that are currently treated as subgenera of Nothofagus. The four clades of Nothofagaceae are robust and well-supported, with deep stem divergences, have evolutionary equivalence with other genera of Fagales, and can be circumscribed with morphological characters. We argue that these morphological and molecular differences are sufficient for the four clades of Nothofagaceae to be recognised at the primary rank of genus, and that this classification will be more informative and efficient than the currently circumscribed Nothofagus with four subgenera.        Nothofagus is recircumscribed to include five species from southern South America, Lophozonia and Trisyngyne are reinstated, and the new genus Fuscospora is described. Fuscospora and Lophozonia, with six and seven species respectively, occur in New Zealand, southern South America and Australia. Trisyngyne comprises 25 species from New Caledonia, Papua New Guinea and Indonesia. New combinations are provided where necessary in each of these genera.


Zootaxa ◽  
2010 ◽  
Vol 2481 (1) ◽  
Author(s):  
CARLOS MOLINERI

The 12 species previously placed in Tortopus together with 3 species newly described here, are revised and included in a phylogenetic analysis. Based on synapomorphic characters on the nymphs and adults of both sexes, Tortopus is restricted to T. igaranus Needham & Murphy, T. circumfluus Ulmer, T. harrisi Traver, T. zottai (Navás), T. bellus Lugo-Ortiz & McCafferty, and T. arenales sp. nov., and the genus is defined by: female parastyli receptors with long furrows anterior to sockets; penes entirely flattened; male ninth abdominal sternum almost separated in two portions by a median notch; mesosternum with furcasternal protuberances contiguous only on basal corner; and nymphs with two subapical tubercles on mandibular tusks. Tortopsis is newly described for T. bruchianus (Navás), T. limoncocha sp. nov., T. obscuripennis (Domínguez), T. parishi (Banks), T. primus (McDunnough), T. puella (Pictet), T. sarae (Domínguez), T. spatula sp. nov., and T. unguiculatus (Ulmer). Tortopsis is characterized by: R sector of female fore wing without additional veins between R 2 and IR; female parastyli receptors C or V-shaped, with sockets opening towards median line; male gonopore associated with a claw-like structure; penes separated from the base; parastyli more than 5 times length of pedestals; parastyli curved in lateral view; nymphs with a single subapical tubercle on mandibular tusks. The study of available type material permitted inclusion of comparative diagnoses, with figures and redescriptions as needed. The male imago of the type species of Tortopus (T. igaranus Needham & Murphy) is described for the first time, as are the female adults of Tortopus bellus Lugo-Ortiz & McCafferty and T. harrisi Traver. Three new Neotropical species based on male and female adults are described: Tortopus arenales and Tortopsis limoncocha from Ecuador, and Tortopsis spatula from Colombia. Keys to separate the adults and nymphs of the genera of Polymitarcyidae, and for male and female adults of all the species of Tortopus and Tortopsis are presented, as well as line drawings, pictures and SEM photographs of important structures.


2011 ◽  
Vol 80 (1) ◽  
pp. 79-85 ◽  
Author(s):  
Joanna Mytnik-Ejsmont ◽  
Dariusz L. Szlachetko

A new genus of Orchidaceae (Polystachyinae), <em>Isochilostachya</em>, is described. It is morphologically similar to <em>Polystachya </em>Hook. but is distinct by the narrower, grass-like leaves arranged in the upper part of the stem, long and acuminate floral bracts and sepals, and long clavate or capitate hairs densely arranged on the lip. A comprehensive description of the new genus is provided. A list of examined specimens and information about distribution, habitat, and altitude for each species are presented. A position of the members of the new genus in the cladogram recently obtained from molecular analyses of Polystachyinae is briefly discussed. A taxonomic key to Polystachyinae is included. Eleven new combinations on species level are validated. Eight lectotypes are designated. Most of the species of <em>Isochilostachya</em> are endemic to particular mountains of the Eastern Arc (Eastern Afromontane hotspot) in north-east Tanzania therefore a brief discussion about their restricted distribution is provided.


2021 ◽  
Vol 85 ◽  
pp. 29-56
Author(s):  
Jonah M. Ulmer ◽  
István Mikó ◽  
Andrew R. Deans ◽  
Lars Krogmann

The Waterston’s evaporatorium (=Waterston’s organ), a cuticular modification surrounding the opening of an exocrine gland located on metasomal tergite 6, is characterized and examined for taxonomic significance within the parasitoid wasp family Ceraphronidae. Modification of the abdominal musculature and the dorsal vessel are also broadly discussed for the superfamily Ceraphronoidea, with a novel abdominal pulsatory organ for Apocrita being discovered and described for the first time. Cuticular modification of T6, due to the presence of the Waterston’s evaporatorium, provides a character complex that allows for genus- and species-level delimitation in Ceraphronidae. The matching of males and females of a species using morphology, a long standing challenge for the group, is also resolved with this new character set. Phylogenetic analysis including 19 Waterston’s evaporatorium related characters provides support for current generic groupings within the Ceraphronidae and elaborates on previously suggested synapomorphies. Potential function of the Waterston’s organ and its effects on the dorsal vessel are discussed.


2002 ◽  
Vol 33 (2) ◽  
pp. 185-237 ◽  
Author(s):  
Jason P.W. Hall

AbstractA phylogenetic revision of the Neotropical riodinid genus Calydna Doubleday and relatives is presented. A phylogenetic analysis for all twenty species of Calydna using thirty-eight characters of adult morphology generated four most parsimonious cladograms. Calydna is characterised to contain eighteen species, divided here into three monophyletic species groups with the relationship caieta group + (thersander group + hiria group). A new genus Echydna Hall gen. n. is described for the most basal clade, containing chaseba Hewitson and punctata C. & R. Felder, which are transferred from Calydna (combs. n.). The taxonomy, morphology, biogeography and biology of both genera are discussed, locality data is listed and mapped, and the adults and male and female genitalia are illustrated for all species. Concealed male abdominal androconial scales, which phylogenetically unite the thersander and hiria groups, are reported for the first time outside of the tribes Symmachiini and Nymphidiini. Two new species are described, Calydna jeannea sp. n. and Calydna nicolayi sp. n., and the replacement name fissilisima is provided for the unavailable name fissilis Stichel; maculosa Bates is transferred from Calydna to Callistium Stichel (comb. n.).


Zootaxa ◽  
2019 ◽  
Vol 4683 (3) ◽  
pp. 301-335 ◽  
Author(s):  
FRANK E. ETZLER

The genus Limonius Eschscholtz, 1829 was last treated as a whole by Candèze (1860). Since then, members have been placed in eight other genera: Cidnopus Thomson, 1859; Gambrinus LeConte, 1853; Elathous Reitter, 1890; Kibunea Kishii, 1966; Limoniscus Reitter, 1905; Nothodes LeConte, 1861; Pheletes Kiesenwetter, 1858; and Solskyana Dolin, 1978. Based on the examination of adult and larval characters, five genera are recognized: Elathous Reitter, 1890; Gambrinus LeConte, 1853; Limonius Eschscholtz, 1829; Pheletes Kiesenwetter, 1858; and Tetralimonius new genus. Limoniscus Reitter, 1905 and Sichuanelater Platia and Gudenzi, 2006 are new synonymies of Gambrinus LeConte, 1853; Micrathous Lane, 1971, Neoathousius Schimmel and Platia, 1991 and Solskyana Dolin, 1978 are all new synonymies of Limonius. A total of 84 new combinations are proposed: Nearctic: Elathous huguenini (Van Dyke, 1932) new combination; Gambrinus angulatus (Motschulsky, 1859) new combination; Gambrinus bicolor (Van Dyke, 1932) new combination; Gambrinus clypeatus (Motschulsky, 1859) new combination; Gambrinus confusus (LeConte, 1853) new combination; Gambrinus cribriceps (Van Dyke, 1943) new combination; Gambrinus crotchii (Horn, 1872) new combination; Gambrinus flavomarginatus (Knull, 1938) new combination; Gambrinus fulvipilis (Candèze, 1860) new combination; Gambrinus griseus (Beauvois, 1805) new combination; Gambrinus humidus (Lane, 1941) new combination; Gambrinus interstitialis (Melsheimer, 1846) new combination; Gambrinus lanchesteri (Lane, 1941) new combination; Gambrinus meridianus (Knull, 1947) new combination; Gambrinus mirus (LeConte, 1853) new combination; Gambrinus norahae (Al Dhafer, 2009) new combination; Gambrinus olentangyi (Knull, 1947) new combination; Gambrinus plebejus (Say, 1825) new combination; Gambrinus propexus (Candèze, 1860) new combination; Gambrinus rudis (Brown, 1933) new combination; Gambrinus rufihumeralis (Lane, 1941) new combination; Gambrinus seminudus (Van Dyke, 1932) new combination; Gambrinus shircki (Lane, 1965) new combination; Gambrinus sinuifrons (Fall, 1907) new combination; Gambrinus snakensis (Lane, 1965) new combination; Gambrinus stigma (Herbst, 1806) new combination; Gambrinus pictus (Van Dyke, 1932) new combination; Gambrinus ulkei (Horn, 1871) new combination; Gambrinus ursinus (Van Dyke, 1932) new combination; Gambrinus venablesi (Wickham, 1913) new combination; Limonius brevis (Van Dyke, 1932) new combination; Limonius sordidus (Van Dyke, 1932) new combination; Pheletes lecontei (Lane, 1971) new combination; Tetralimonius definitus (Ziegler, 1845) new combination; Tetralimonius humeralis (Candèze, 1860) new combination; Tetralimonius maculicollis (Motschulsky, 1860) new combination; Tetralimonius nimbatus (Say, 1825) new combination; Tetralimonius ornatulus (LeConte, 1857) new combination. Palearctic: Gambrinus elegans (Buysson, 1891) new combination; Gambrinus gibbosus (Platia and Gudenzi, 2006) new combination. Gambrinus henanensis (Schimmel, 2006) new combination; Gambrinus hinakurai (Kishii, 1998) new combination; Gambrinus katoi (Kishii, 2002) new combination; Gambrinus kawaharai (Kishii, 2002) new combination; Gambrinus kucerai (Schimmel, 2006) new combination; Gambrinus nanshanensis (Arimoto and Hiramatsu, 2013) new combination; Gambrinus naomii (Kishii, 1997) new combination; Gambrinus shaanxiensis (Schimmel, 2006) new combination; Gambrinus suturalis (Gebler, 1844) new combination; Gambrinus takabai (Kishii, 1997) new combination; Gambrinus violaceus (Müller, 1821) new combination; Gambrinus wittmeri (Chassain, 1998) new combination; Gambrinus yamato (Kishii, 1998) new combination; Gambrinus yujii (Arimoto, 2013) new combination; Gambrinus zhejiangensis (Schimmel, 2015) new combination; Limonius brancuccii (Schimmel and Platia, 1991) new combination; Limonius decorus (Gurjeva, 1975) new combination; Limonius exiguus (Schimmel and Platia, 1991) new combination; Limonius hartmanni (Schimmel, 1998) new combination; Limonius hiermeieri (Schimmel and Platia, 1991) new combination; Limonius hirtus (Dolin, 1978) new combination; Limonius hubeiensis (Kishii and Jiang, 1996) new combination; Limonius kubani (Schimmel, 1996) new combination; Limonius loebli (Schimmel and Platia, 1991) new combination; Limonius longicornis (Schimmel and Platia, 1991) new combination; Limonius macedonicus (Cate and Platia, 1989) new combination; Limonius marginellus brusteli (Leseigneur, 2004) new combination; Limonius manaliensis (Schimmel and Platia, 1991) new combination; Limonius miandamensis (Schimmel and Platia, 1991) new combination; Limonius minusculus (Schimmel and Platia, 1991) new combination; Limonius nigronitidus (Han and Lee, 2012) new combination; Limonius platiai (Mertlik, 1996) new combination; Limonius pseudopilosus (Platia and Gudenzi 1985) new combination; Limonius recticornis (Schimmel and Platia, 1991) new combination; Limonius riesei (Platia, 1988) new combination; Limonius rusticus (Schimmel and Platia, 1991) new combination; Limonius schurmanni (Platia and Gudenzi, 1998) new combination; Limonius sinensis (Schimmel and Platia, 1994) new combination; Limonius singularis (Schimmeland Platia, 1991) new combination; Limonius stapfi (Schimmel, 2007) new combination; Limonius turcicus (Platia, 2004) new combination; Limonius wittmeri (Schimmel and Platia, 1991) new combination; Tetralimonius quercus (Olivier, 1790) new combination; Tetralimonius reitteri (Gurjeva, 1976) new combination. The following 12 North American species are removed from synonymy and recognized as valid species: Gambrinus interstitialis (Melsheimer, 1846) status resurrected; Gambrinus propexus (Candèze, 1860) status resurrected; Gambrinus shircki (Lane, 1965) status resurrected; Gambrinus snakensis (Lane, 1965) status resurrected; Gambrinus ulkei (Horn, 1871) status resurrected; Limonius anceps LeConte, 1853 status resurrected; Limonius dubitans LeConte, 1853 status resurrected; Limonius infuscatus Motschulsky, 1859 status resurrected; Limonius pilosulus Candèze, 1891 status resurrected; Limonis semianeus LeConte, 1853 status resurrected. Tetralimonius humeralis (Candèze, 1860) status resurrected; Tetralimonius maculicollis (Motschulsky, 1860) status resurrected. New replacement names are proposed for three homynyms: Limonius schimmeli Etzler new name for Neoathousius ferrugineus Schimmel and Platia, 1991; Elathous malatyanus Etzler new name for Elathous bicolor Platia, 2010, not Elathous bicolor (LeConte, 1853); and Microdesmes carteri Etzler new name for Limonius angulatus Carter, 1939 (= Microdesmes angulatus). Limonius kondratieffi Al Dhafer, 2009 is a new synonymy of Elathous bicolor (LeConte, 1853). A key to genera, generic descriptions, notes on species, and definitions of important characters are provided. 


2015 ◽  
Vol 89 (1) ◽  
pp. 72-81 ◽  
Author(s):  
William I. Ausich ◽  
Mark A. Wilson ◽  
Olev Vinn

AbstractStudy of new collections of the Wenlock and Pridoli, Silurian, crinoids from Saaremaa, western Estonia, result in taxonomic revision, expanded ranges, and new taxa. Eucalyptocrinites regularis and Periechocrinus laevis are recognized outside of Sweden for the first time. Desmidocrinus laevigatus Ausich et al., 2012 is reassigned to Methabocrinus. Because the type species of Methabocrinus was previously known only from glacial sediments, the age and provenance of this genus are constrained for the first time. A new crotalocrinitid, Velocrinus coniculus new genus and species, is described. Although the Pridoli faunas of western Estonia contain only twelve species-level taxa assigned to nine genera, this fauna is one of the four richest Pridoli faunas known.


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