In this second part of the revision of Afrotropical Afrocrania Hincks, 1949 (= Pseudocrania Weise, 1892, not Pseudocrania MCoy, 1851), a group of Galerucinae restricted to Africa, additional material is revised. Herein, species in which the males lack deep head cavities, partly horned antennomeres, or extended elytral extrusions, but usually have small post-scutellar extrusions or depressions, are considered. Material of Afrocrania pauli (Weise, 1903), comb. n. (= Candezea pauli Weise, 1903), and A. famularis (Weise, 1904), comb. n. (= Monolepta famularis Weise, 1904; = Candezea atripennis Laboissière, 1931, syn. n.) is studied. Lectotypes are designated for A. pauli, A. famularis and C. atripennis. Six new species, A. aequatoriana sp. n., A. minima sp. n., A. nigra sp. n., A. occidentalis sp. n., A. pallida sp. n. and A. weisei sp. n. are described. Distribution patterns are mapped. Together with the already revised species there are 16 valid Afrocrania species are hitherto known. Its phylogenetic position within the Galerucinae is discussed, identification keys to males and females for all known taxa are presented.
Dioncopseudobenedenia Yamaguti, 1965 (Monogenea: Capsalidae) is redefined. Dioncopseudobenedenia kala Yamaguti, 1965 (type species) is redescribed from type material from Hawaii and from new specimens from Heron Island, Queensland, Australia and New Caledonia. We made detailed observations on D. macracantha Yamaguti, 1968 from type material from Hawaii, and from new material from Heron Island and New Caledonia. Dioncopseudobenedenia ancoralis sp. n. is described from the gill chamber of Siganus lineatus (Valenciennes) from Green Island and Heron Island, Australia and from New Caledonia. This study confirms that only one pair of large central sclerites is present on the haptor in Dioncopseudobenedenia species. The male copulatory organ in species of Dioncopseudobenedenia is a penis contained in a fluid-filled space (= penis canal) with weakly muscular walls. Dioncopseudobenedenia kala and D. ancoralis bear a sclerite at the tip of the penis. In D. macracantha, the structure of the penis, which has no terminal sclerite, indicates it may combine the functions of a penis and a cirrus. Dioncopseudobenedenia is compared with Calicobenedenia Kritsky et Fennessy, 1999, the other capsalid genus with a single pair of large sclerites on the haptor. The large haptoral sclerites in species of Dioncopseudobenedenia resemble accessory sclerites, whereas those of C. polyprioni Kritsky et Fennessy, 1999 resemble hamuli. Observations of oncomiracidia confirmed that the large haptoral sclerites in D. kala are accessory sclerites. Haptoral morphology suggests that different Dioncopseudobenedenia spp. employ different means of attachment. Mating behaviour was observed twice between two different pairs of D. kala specimens from Heron Island. Two preserved specimens from Nouméa, New Caledonia had structures near the dorsal vaginal pore that we interpret as spermatophores. This is the first report of spermatophores in a capsalid inhabiting the gill chamber. The geographic distribution of Dioncopseudobenedenia spp. is discussed.
The first part of a revision of the European species of the genus Rhabdomastix Skuse, 1890 is presented. The history of taxonomic research on Rhabdomastix is reviewed, relationships of the genus are discussed, and the subgeneric classification outlined and re-assessed. A new subgenus, Lurdia subgen. n., is established for species centred around R. lurida (Loew, 1873), and Palaeogonomyia Meunier, 1899 and Sacandaga Alexander, 1911, previously considered subgenera, are synonymized with Rhabdomastix. A revision of the European species of Lurdia subgen. n. is presented. Two species are redescribed, Rhabdomastix (Lurdia) lurida (Loew, 1873) and R. (L.) inclinata Edwards, 1938, and the lectotype of the former is designated. Descriptions are provided of seven species, viz. R. (L.) mendli sp. n. (Switzerland, Germany, Italy), R. (L.) sublurida sp. n. (Czech Republic, Slovakia), R. (L.) furva sp. n. (Slovakia), R. (L.) loewi sp. n. (Switzerland, Germany, Austria, Italy), R. (L.) robusta sp. n. (Czech Republic, Slovakia), R. (L.) falcata sp. n. (Switzerland, Germany, Bulgaria) and R. (L.) tatrica sp. n. (Slovakia). Male and female terminalia are illustrated for all the species (except female falcata), and a key to species is appended.
The second and final part of a revision of the European species of the genus Rhabdomastix Skuse, 1890 is presented. The subgenus Rhabdomastix s. str. is revised. Seven species are redescribed, Rhabdomastix (Rhabdomastix) japonica Alexander, 1924, R. (R.) laeta (Loew, 1873), R. (R.) borealis Alexander, 1924, R. (R.) edwardsi Tjeder, 1967, R. (R.) subparva Starý, 1971, R. (R.) hirticornis (Lackschewitz, 1940) and R. (R.) beckeri (Lackschewitz, 1935). Three new synonyms are proposed. Lectotypes of four pertinent nominal species are designated. Descriptions are provided of six species, viz. R. (R.) laetoidea sp. n. (Czech Republic, Slovakia, Bulgaria, Ukraine), R. (R.) crassa sp. n. (France, Czech Republic, Slovakia), R. (R.) corax sp. n. (Bulgaria, Greece), R. (R.) eugeni sp. n. (France, Switzerland, Germany, Czech Republic, Slovakia, Italy, Romania, Bulgaria, Greece, Ukraine, Armenia), R. (R.) filata sp. n. (Bulgaria, Greece, European Russia, Turkey, Georgia, Armenia) and R. (R.) georgica sp. n. (Georgia). Male and female terminalia are illustrated for all the species, and a key to species is appended.
A new subfamily Homalomitrinae is established for two enigmatic Neotropical genera, Homalomitra Borgmeier, 1931 and Sphaeromitra gen. n. which are diagnosed on the basis of newly discovered characters. All available specimens of the group are revised. Two new species of Homalomitra, H. antiqua sp, n. (Costa Rica, Brazil) and H. tenuior sp. n. (female only; Colombia, Ecuador) are described and the remaining species of the genus, H. ecitonis Borgmeier, 1931 (type species, Brazil) and H. albuquerquei Mourgués-Schurter, 1987 (Costa Rica) are redescribed. A key to Homalomitra species is given. Sphaeromitra inepta gen. et sp. n. is described from Peru. Phylogenetic relationships of Homalomitrinae, both its genera and all species included are discussed.
This study is a revision of the Iberian Merodon Meigen, 1803 species, including an illustrated key, a discussion of taxonomic characters and a morphological diagnosis for all included species. Descriptions are provided for nine new species: M. antonioi sp. n., M. arundanus sp. n., M. cabanerensis sp. n., M. crypticus sp. n., M. hurkmansi sp. n., M. legionensis sp. n., M. longispinus sp. n., M. luteihumerus sp. n. and M. quercetorum sp. n. The taxon M. escorialensis Strobl, 1909 is redescribed and lectotype is designated. Lectotypes are designated for four taxa: M. albifrons Meigen, 1822; M. spinipes obscuritarsis Strobl in Czerny & Strobl, 1909; M. spicatus Becker, 1907; and M. spinipes grossus Gil Collado, 1930. Three varieties are redefined and considered as valid species: M. obscuritarsis Strobl in Czerny & Strobl, 1909 (as var. of spinipes); M. grossus Gil Collado, 1930 (as var. of spinipes); M. unicolor Strobl in Czerny & Strobl, 1909 (as var. of aeneus). The following new synonymies are proposed: M. affinis Gil Collado, 1930 syn.n. (= junior synonym of M. longicornis Sack, 1913); M. lusitanicus Hurkmans, 1993 syn.n. (= junior synonym of M. serrulatus Wiedemann in Meigen, 1822); M. andalusiacus Paramonov, 1929 syn.n., M. bolivari Gil Collado, 1930 syn.n., M. hispanicus Sack, 1931 syn.n. (= all three are junior synonyms of M. unguicornis Strobl in Czerny & Strobl, 1909); M. spicatus Becker, 1907 syn.n. (= junior synonym of M. chalybeus Wiedemann in Meigen, 1822); M. fuerteventurensis Barkemeyer, 2002 syn. n. (= junior synonym of M. obscuritarsis Strobl, 1909); and M. spinipes grossus (Gil Collado, 1930) syn.n. (= junior synonym of M. albifrons Meigen, 1822). Status of M. serrulatus Wiedemann in Meigen, 1822 is revised. Four species: M. longicornis Sack, 1913, M. pumilus Macquart, 1849, M. ottomanus Hurkmans, 1993 and M. segetum (Fabricius, 1794) are new for the Iberian Peninsula. Male genitalia are illustrated for all the species and a key of the 34 Iberian species (+ M. hurkmansi sp. n.) for males and females (except for the unknown female of M. longispinus sp. n.) is appended. Distribution and biological data for the Iberian species are also included. A brief zoogeographic discussion is also presented. The level of endemism of genus Merodon on the Iberian Peninsula is extremely high (almost 50%).
Monozoic cestodes of the genus Khawia Hsü, 1935 (Caryophyllidea: Lytocestidae), parasites of cyprinid fish in Europe, Asia, Africa and North America, are revised on the basis of taxonomic evaluation of extensive materials, including recently collected specimens of most species. This evaluation has made it possible to critically assess the validity of all 17 nominal species of the genus and to provide redescriptions of the following seven species considered to be valid: Khawia sinensis Hsü, 1935 (type species); K. armeniaca (Cholodkovsky, 1915); K. baltica Szidat, 1941; K. japonensis (Yamaguti, 1934); K. parva (Zmeev, 1936); K. rossittensis (Szidat, 1937); and K. saurogobii Xi, Oros, Wang, Wu, Gao et Nie, 2009. Several new synonyms are proposed: Khawia barbi Rahemo et Mohammad, 2002 and K. lutei Al-Kalak et Rahemo, 2003 are synonymized with K. armeniaca; K. coregoni Kritscher, 1990 with Caryophyllaeus laticeps (Pallas, 1781) (family Caryophyllaeidae); K. cyprini Li, 1964 and K. iowensis Calentine et Ulmer, 1961 with K. japonensis; K. dubia (Szidat, 1937) (syn. Bothrioscolex dubius Szidat, 1937) with K. rossittensis; and Tsengia neimongkuensis Li, 1964 and T. xiamenensis Liu, Yang et Lin, 1995 with K. sinensis. Khawia prussica (Szidat, 1937) (syn. Bothrioscolex prussicus Szidat, 1937) is considered to be species incertae sedis, but its morphology indicates it may belong to Caryophyllaeus Gmelin, 1790 (Caryophyllaeidae). The molecular analysis of all seven valid species, based on comparison of sequences of two nuclear ribosomal and two mitochondrial genes, has shown that the species form three major groups clustered according to their fish hosts. Five species from common and crucian carp and goldfish were grouped together, whereas K. armeniaca from barbels (Barbinae) and K. baltica from tench (Tinca) formed separate clades. In contrast, geographical distribution does not seem to play a crucial role in grouping of individual taxa. A phylogenetic tree based on morphological characters was incongruent with that inferred from molecular data, which indicates that some morphological traits may be homoplastic. A key to identification of all species of Khawia based on morphological characteristics is provided.
A revisionary study revealed two species of monogeneans, Dactylogyrus crucis Rogers, 1967 and Dactylogyrus lythruri sp. n., parasitising Lythrurus Jordan (formerly a subgenus of Notropis Rafinesque, 1818). New records and updated taxonomy of seven of 12 known minnows of the genus of Lythrurus are provided for D. crucis. A record of Dactylogyrus attenuatus Mizelle et Klucka, 1953 (syn. Dactylogyrus umbratilus [Kimpel, 1939], nomen nudum) on Lythrurus umbratilis (Girard) is referrable to D. crucis. Dactylogyrus lythruri is described from eight species of Lythrurus. It most closely resembles Dactylogyrus beckeri Cloutman, 1987, but is distinguished by having a smaller base of the male copulatory organ (MCO) and lacking a ventral enlargement of the distal end of the basal process. Previous reports of Dactylogyrus banghami Mizelle et Donahue, 1944 and Dactylogyrus cf. beckeri Cloutman, 1987 from Lythrurus atrapiculus (Snelson) and Lythrurus bellus (Hay) from Alabama, and Dactylogyrus confusus Mueller, 1938 from L. umbratilis in Illinois are herein relegated to D. lythruri. Four species of Lythrurus appeared not to be infected with Dactylogyrus., Donald G. Cloutman, Andrew B. Adrian, Chris T. McAllister, Bruce W. Stallsmith, Thomas J. Fayton and Henry W. Robison., and Obsahuje bibliografii
The New World species of Loxocera Meigen are revised including two new species, L. (Imantimyia) ignyodactyla Buck sp. n. from Costa Rica (first record of the genus from the Neotropical region) and L. (Imantimyia) ojibwayensis Buck sp. n. from Ontario, Canada. Loxocera californica Capelle is synonymized with L. collaris Loew and lectotypes are designated for L. pleuritica Loew and L. cylindrica var. obsoleta Johnson (both synonyms of L. cylindrica Say). The New World species are diagnosed and a key to species is provided. The male and female terminalia of Loxocera are described in detail for the first time, and their functional morphology is discussed. Eggs of most species are described and a key to the known eggs of Loxocera is provided. A phylogenetic framework for the Holarctic subgenera and species groups of Loxocera is developed based on morphological characters of the adult flies. The Old World subgenus Platystyla Macquart is synonymized with Loxocera s. str., and Imantimyia Frey is reinstated as a valid subgenus including all Holarctic species previously placed in Loxocera s. str. except the L. aristata species group. This leads to the following new subgeneric combinations: L. (L.) malaisei Frey comb. n., L. (L.) matsumurai Iwasa comb. n., L. (L.) monstrata Iwasa, comb. n., and L. (L.) omei Shatalkin comb. n. The species groups of Imantimyia are redefined, i.e. the L. achaeta-group (7 spp.), the L. fulviventris-group (4 spp.), and the L. albiseta-group (1 sp.). The Oriental subgenus Asiopsila Shatalkin is referred to Psila Meigen s. l. as a subgenus based on characters of the egg, resulting in fourteen new generic combinations: Psila (Asiopsila) brevibuccata (Shatalkin) comb. n., P. (A.) burmanica (Frey) comb. n., P. (A.) decorata (de Meijere) comb. n., P. (A.) derivata (Shatalkin) comb. n., P. (A.) formosana (Hennig) comb. n., P. (A.) freidbergi (Shatalkin) comb. n., P. (A.) humeralis (de Meijere) comb. n., P. (A.) kambaitensis (Frey) comb. n., P. (A.) limpida (Shatalkin) comb. n., P. (A.) maculipennis (Hendel) comb. n., P. (A.) michelseni (Shatalkin) comb. n., P. (A.) pleuralis (Frey) comb. n., P. (A.) primigena (Shatalkin) comb. n., and P. (A.) vittipleura (Shatalkin) comb. n.