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New collection records for Calusamyia hribari Coher (Diptera: Keroplatidae) are presented. Sufficient material has been amassed to make some statements about the species’ distribution, seasonality, and morphology. Calusamyia hribari occurs throughout the inhabited Florida Keys, from Key Largo to Key West. New island records include Boca Chica Key, Crawl Key, Summerland Key, Geiger Key, Dredger’s Key, Upper Matecumbe Key, Key Largo, Long Key, Tavernier, Windley Key, and Fat Deer Key. As yet it has not been collected from any uninhabited islands within wildlife refuges. About five times more males than females have been collected. Most specimens have been collected in the summer months, with May being the peak of abundance in traps. Females have two spermathecae, similar to other keroplatids.
This is the second part of a study of a large collection of Siphonophoridae Cook, 1895 from Brazil. Here, those without an abrupt division between the head and rostrum are considered. Two species have been distinguished and are described as Siphonophora setaepromissa sp. nov. and S. tuberculata sp. nov. Siphonophora hebetunguis (Attems, 1951) from the same region has many similarities with the two new species and is redescribed from type material. Comparisons have also been made with S. fuhrmanni Carl, 1914, and comments are made on the genera Cordillerium Verhoeff, 1941, Pterozonium Attems, 1951, Rhinosiphora Verhoeff, 1924, and Siphonophora Brandt, 1837. Finally, some suggestions for characters to look at in future collections of siphonophorids are made based on experience of this collection.
Small-scale phenotypic differentiation along complex stream gradients in a non-native amphipod
(2019)
Background: Selective landscapes in rivers are made up by an array of selective forces that vary from source to downstream regions or between seasons, and local/temporal variation in fitness maxima can result in gradual spatio-temporal variation of phenotypic traits. This study aimed at establishing freshwater amphipods as future model organisms to study adaptive phenotypic diversification (evolutionary divergence and/or adaptive plasticity) along stream gradients.
Methods: We collected Gammarus roeselii from 16 sampling sites in the Rhine catchment during two consecutive seasons (summer and winter). Altogether, we dissected n = 1648 individuals and quantified key parameters related to morphological and life-history diversification, including naturally selected (e.g., gill surface areas) as well as primarily sexually selected traits (e.g., male antennae). Acknowledging the complexity of selective regimes in streams and the interrelated nature of selection factors, we assessed several abiotic (e.g., temperature, flow velocity) and biotic ecological parameters (e.g., conspecific densities, sex ratios) and condensed them into four principal components (PCs).
Results: Generalized least squares models revealed pronounced phenotypic differentiation in most of the traits investigated herein, and components of the stream gradient (PCs) explained parts of the observed differences. Depending on the trait under investigation, phenotypic differentiation could be ascribed to variation in abiotic conditions, anthropogenic disturbance (influx of thermally polluted water), or population parameters. For example, female fecundity showed altitudinal variation and decreased with increasing conspecific densities, while sexual dimorphism in the length of male antennae—used for mate finding and assessment—increased with increasing population densities and towards female-biased sex ratios.
Conclusions: We provide a comprehensive protocol for comparative analyses of intraspecific variation in life history traits in amphipods. Whether the observed phenotypic differentiation over small geographical distances reflects evolutionary divergence or plasticity (or both) remains to be investigated in future studies. Independent of the mechanisms involved, variation in several traits is likely to have consequences for ecosystem functions. For example, leaf-shredding in G. roeselii strongly depends on body size, which varied in dependence of several ecological parameters.
Thirty-six species of various thecate hydroids occur in two recent, deep-water collections from off New Caledonia. Of these, nine are new, namely Solenoscyphus subtilis Galea, sp. nov., Hincksella immersa Galea, sp. nov., Synthecium rectangulatum Galea, sp. nov., Diphasia alternata Galea, sp. nov., Dynamena opposita Galea, sp. nov., Hydrallmania clavaformis Galea, sp. nov., Symplectoscyphus acutustriatus Galea, sp. nov., Symplectoscyphus elongatulus Galea, sp. nov. and Zygophylax niger Galea, sp. nov. The male and female gonothecae of Caledoniana decussata Galea, 2015, the female gonothecae of Caledoniana microgona Galea, 2015, as well as the gonothecae of both sexes of Solenoscyphus striatus Galea, 2015 are described for the first time. The systematic position of the genera Solenoscyphus Galea, 2015 and Caledoniana Galea, 2015 is discussed on both morphological and molecular grounds, and both are confidently placed within the family Staurothecidae Maronna et al., 2016. In light of the molecular data, the genera Billardia Totton, 1930 and Dictyocladium Allman, 1888 are assigned to the families Syntheciidae Marktanner-Turneretscher, 1890 and Symplectoscyphidae Maronna et al., 2016, respectively. The previously undescribed gonothecae of Hincksella neocaledonica Galea, 2015, and the male gonothecae of Sertularella tronconica Galea, 2016, were found. Thyroscyphus scorpioides Vervoort, 1993, a peculiar hydroid with putative stem nematothecae, is redescribed and assigned to the new genus Tuberocaulus Galea, gen. nov. Noteworthy new records from the study area are: Tasmanaria edentula (Bale, 1924), Hincksella sibogae Billard, 1918, Dictyocladium reticulatum (Kirchenpauer, 1884), Salacia sinuosa (Bale, 1888) and Billardia hyalina Vervoort & Watson, 2003. Most species are illustrated to facilitate their identification, and the morphology of the new ones is compared to that of their related congeners.
Genera of Cryptognathini (Coleoptera: Coccinellidae) are discussed and a key to all recognized genera is provided. Cryptognatha is revised, and species of this genus are keyed. New species, authored by González and Hanley, are Cryptognatha pam, C. kellie, C. hannah, C. whitney, C. karla, C. celia, C. shelia, C. gayle, C. della and C. vicki. The following new synonymies are proposed: Cryptognatha simillima Sicard = Cryptognatha gemellata Mulsant, Cryptognatha fryii Crotch = Cryptognatha pudibunda Mulsant, Cryptognatha bryanti Brèthes = Cryptognatha pudibunda Mulsant. Lectotypes are here designated for Cryptognatha amicta Gorham, C. weisei Brèthes, C. pudibunda Mulsant and C. fryii Crotch.
Twenty new species are described in Pentilia Mulsant (Coleoptera: Coccinellidae: Scymninae: Cryptognathini) by Gordon and González: Pentilia bernadette, P. chelsea, P. dianna, P. elena, P. ernestine, P. estelle, P. kari, P. jasmine, P. jody, P. kendra. P. krystal, P. lora, P. mable, P. muriel, P. nichole, P. nadine. P. paulette, P. rachael, P. sadie and P. traci. A lectotype is here designated for Pentilia egena Mulsant.
Seventy-four species, forms and varieties of Cubitermes Wasmann, 1906 have been studied, including taxa placed in synonymy with other species. Within this group of taxa, the enteric valve, mainly of the workers and soldiers, provided the best and the only clear-cut criteria for distinguishing some major subsets that are proposed here as species groups.The genus Cubitermes is re-described; the morphologies of the enteric valves are described in detail including the number of spatulae at the downstream end of the primary cushions; the possible presence of crests or bulges near the downstream end of the primary cushions; the overall shape of the primary cushions; the number of lateral supporting bristles; the kind of symmetry of the valve; and the structure of the secondary cushions. These characteristics are used to define nine species groups. For now, these groups have no taxonomic ranking but are helpful as regards species recognition. Identification keys for species groups are provided for soldiers and workers together with a partial key for imagines. Geographical ranges of the groups are also provided. On the basis of enteric valve morphology, some synonymies can no longer be validated: (a) C. planifrons Sjöstedt, 1924 is not a synonym of C. fungifaber (Sjöstedt, 1896); (b) C. kemneri Emerson, 1928 is not a synonym of C. zenkeri (Desneux, 1904); and (c) C. fungifaber var. elongata Sjöstedt, 1924 does not belong to the species C. fungifaber. Cubitermes planifrons and C. kemneri become valid again and C. fungifaber var. elongata is an invalid name.
A recent survey of the mangroves around Hong Kong revealed the presence of seven species of the genus Elaphropeza Macquart, 1827. All belong to a group of yellow species that occur exclusively in mangroves. Three species were previously known: Elaphropeza calcarifera Bezzi, 1912 and E. xanthocephala Bezzi, 1912, both from Taiwan, and E. riatanae Shamshev & Grootaert, 2007 from Singapore. Four species are new to science: Elaphropeza furcatella sp. nov., E. guenardi sp. nov., E. hongkongensis sp. nov. and E. hongshulin sp. nov. All seven species are described or an extended diagnosis is provided. All species are figured and NGS barcodes are made available. A key is given for the Hong Kong species and their siblings from Singapore and Taiwan. Remarkable is that five of the seven species are more or less closely related to species occurring in Singapore. Genetic distances and morphologic differences are congruent. The species turnover between the northern part and the southern part of the South China Sea is high, with only one of the seven species present in both regions.
Background: Developmental biology relies to a large extent on the observation and comparison of phenotypic traits through time using high resolution microscopes. In this context, transparent model organisms such as the zebrafish Danio rerio in which developing tissues and organs can be easily observed and imaged using fluorescent proteins have become very popular. One limiting factor however is the acquisition of a sufficient amount of data, in standardized and reproducible conditions, to allow robust quantitative analysis. One way to improve this is by developing mounting methods to increase the number of embryos that can be imaged simultaneously in near-to-identical orientation.
Results: Here we present an improved mounting method allowing semi-automated and high-content imaging of zebrafish embryos. It is based on a 3D-printed stamp which is used to create a 2D coordinate system of multiple μ-wells in an agarose cast. Each μ-well models a negative of the average zebrafish embryo morphology between 22 and 96 h-post-fertilization. Due to this standardized and reproducible arrangement, it is possible to define a custom well plate in the respective imaging software that allows for a semi-automated imaging process. Furthermore, the improvement in Z-orientation significantly reduces post-processing and improves comparability of volumetric data while reducing light exposure and thus photo-bleaching and photo-toxicity, and improving signal-to-noise ratio (SNR).
Conclusions: We present here a new method that allows to standardize and improve mounting and imaging of embryos. The 3D-printed stamp creates a 2D coordinate system of μ-wells in an agarose cast thus standardizing specimen mounting and allowing high-content imaging of up to 44 live or mounted zebrafish embryos simultaneously in a semi-automated, well-plate like manner on inverted confocal microscopes. In summary, image data quality and acquisition efficiency (amount of data per time) are significantly improved. The latter might also be crucial when using the services of a microscopy facility.
Four new species in the genus Amphicnaeia (Coleoptera: Cerambycidae: Lamiinae) are described: A. panamensis Wappes, Santos-Silva and Galileo and A. fuscofasciata Wappes, Santos-Silva and Galileo from Panama; A. bezarki Wappes, Santos-Silva and Galileo from Venezuela; and A. rileyi Wappes, Santos-Silva and Galileo from Costa Rica and Panama. Amphicnaeia affinis Breuning, 1940 is placed in synonymy with A. lineata Bates, 1866, and the species newly recorded from the Brazilian state of Minas Gerais. Amphicnaeia cordigera Aurivillius, 1920 is transferred to Rosalba Thomson, 1864, resulting in a new combination, and Rosalba rufescens Breuning, 1940, is found to be a junior synonym of the former. The holotypes of A. vitticollis Breuning, 1940, and A. villosula (Thomson, 1868) are illustrated for the first time.
Walter Biese described Littoridina santiagensis Biese, 1944 (Cochliopidae) from Estero Dehesa in 1944 based exclusively on external shell features and a second allopatric population in Yeso Spring three years later. Since 2011 different samplings have been carried out at the type locality and have only provided specimens of the morphologically similar invasive mudsnail Potamopyrgus antipodarum Gray, 1843 (Tateidae), raising doubts about the identity of the species. The recent finding of two snail morphotypes in Yeso Spring, a thick shelled form congruent with type specimens of L. santiagensis and a slender one morphologically associable to P. antipodarum, allowed comparative studies, including the taxonomic analysis of additional populations with similar shell morphology occurring in central Chile. A DNA barcoding (COI) approach identified the slender form from Yeso Spring in Maipo Basin and a second population from the contiguous Rapel Basin indeed as the invasive P. antipodarum; however, L. santiagensis was recovered among species of Potamolithus Pilsbry, 1896 (Tateidae), justifying the Potamolithus santiagensis (Biese, 1944) comb. nov. Besides recognition of three other populations as belonging to Potamolithus, the molecular analysis also suggests trans-Andean dispersal of this group of snails in the Southern Cone of South America.
The gigas species group of the subgenus Canthidium (Neocanthidium) is defi ned and described. This species group is composed of three described species [C. gigas Balthasar, 1939, Brazilian Atlantic Forest, including intrusions into Cerrado, C. bokermanni (Martínez et al., 1964), Chaco and western Cerrado in Brazil, Bolivia, Paraguay, and Argentina, and C. kelleri (Martínez et al., 1964), Brazilian Cerrado and neighbouring open areas] and three new species: Canthidium stofeli sp. nov. from the western and southern regions of the Brazilian Amazon, Canthidium feeri sp. nov. from French Guiana, and Canthidium ayri sp. nov. from the Brazilian Atlantic Forest. We present descriptions and redescriptions, illustrations, an identifi cation key and comments on the distributions of the species of the gigas group.
Virpazaria Gittenberger, 1969 is distributed in the Balkan Peninsula (Albania, Montenegro and Croatia) and inhabits the shallow subterranean habitat (MSS) on limestone base rock. Reviewing historical and recently collected material, two species, Virpazaria (Virpazaria) gittenbergeri Fehér & Erőss sp. nov. and Virpazaria (Virpazaria) pesici Fehér & Deli sp. nov., are introduced as new to science. The conservation status of the new species are assessed using IUCN criteria. Two taxa, Virpazaria (Virpazaria) pageti alexanderi Reischütz & Subai, 2012 and Virpazaria (Aemiliella) ripkeni pastorpueri Reischütz et al., 2011, are synonymized with their nominate subspecies. Some new distribution records, as well as geological and geomorphological data about the known locations for Virpazaria, are presented.
The Tallahatta Formation, Lisbon Formation, and Gosport Sand are the three lithostratigraphic units that make up the lower-to-middle Eocene Claiborne Group. In Alabama, these marine units are among the most fossiliferous in the state and a long history of scattered reports have attempted to document their fossil diversity. In this study, we examined 20 931 elasmobranch and bony fish elements, including otoliths, derived from Claiborne Group units in Alabama and identified 115 unequivocal taxa. Among the taxa identified, one new species is described, Carcharhinus mancinae sp. nov., and Pseudabdounia gen. nov. is a new genus erected to include two species formerly placed within Abdounia Capatta, 1980. New taxonomic combinations proposed include Pseudabdounia claibornensis (White, 1956) gen. et comb. nov., Pseudabdounia recticona (Winkler, 1874) gen. et comb. nov., Physogaleus alabamensis (Leriche, 1942) comb. nov., and Eutrichiurides plicidens (Arambourg, 1952) comb. nov. We also report the first North American paleobiogeographic occurrences of Aturobatis aff. A. aquensis Adnet, 2006, Brachycarcharias atlasi (Arambourg, 1952), Eutrichiurides plicidens comb. nov., Galeorhinus louisi Adnet & Cappetta, 2008, Ginglymostoma maroccanum Noubhani & Cappetta, 1997, Gymnosarda sp., Mennerotodus sp., Rhizoprionodon ganntourensis (Arambourg, 1952), Stenoscyllium aff. S. priemi Noubhani & Cappetta, 1997, Trichiurus oshosunensis White, 1926, and the first North American occurrence for a fossil member of the Balistidae Risso, 1810. Our sample also included 26 taxa that represented first paleobiogeographic occurrences for Alabama, including Abdounia beaugei (Arambourg, 1935), Albula eppsi White, 1931, Ariosoma nonsector Nolf & Stringer, 2003, Anisotremus? sp., Anomotodon sp., Brachycarcharias twiggsensis (Case, 1981), Burnhamia daviesi (Woodward, 1889), Eoplinthicus yazooensis Capetta & Stringer, 2002, Galeorhinus ypresiensis (Casier, 1946), Gnathophis meridies (Frizzell & Lamber, 1962), Haemulon? obliquus (Müller, 1999), Hypolophodon sylvestris (White, 1931), Malacanthus? sulcatus (Koken, 1888), Meridiania cf. M. convexa Case, 1994, Palaeocybium proosti (Storms, 1897), Paraconger sector (Koken, 1888), Paralbula aff. P. marylandica Blake, 1940, Phyllodus toliapicus Agassiz, 1844, Propristis schweinfurthi Dames, 1883, Pycnodus sp., Pythonichthys colei (Müller, 1999), Scomberomorus stormsi (Leriche, 1905), Signata stenzeli Frizzell & Dante, 1965, and Signata nicoli Frizzell & Dante, 1965, and the first Paleogene occurrences in Alabama of a member of the Gobiidae Cuvier, 1816. A biostratigraphic analysis of our sample showed stratigraphic range extensions for several taxa, including the first Bartonian occurrences of Eoplinthicus yazooensis, Jacquhermania duponti (Winkler, 1876), Meridiania cf. M. convexa, Phyllodus toliapicus, and “Rhinobatos” bruxelliensis (Jaekel, 1894), range extensions into the late Ypresian and Bartonian for Tethylamna dunni Cappetta & Case, 2016 and Scoliodon conecuhensis Cappetta & Case, 2016, the first late Ypresian records of Galeorhinus louisi, the first Lutetian occurrence of Gymnosarda Gill, 1862, and a range extension for Fisherichthys aff. F. folmeri Weems, 1999 into the middle Bartonian. Larger biostratigraphic and evolutionary trends are also documented, such as the acquisition of serrations in Otodus spp., possible population increases for the Rhinopterinae Jordan & Evermann, 1896 and Carcharhiniformes Compagno, 1973 in the Bartonian, and the apparent diversification of the Tetraodontiformes Berg, 1940 during the same stage. This study helps better our understanding of earlyto-middle Eocene elasmobranch and bony fish diversity, paleobiogeography, and biostratigraphy in the Gulf Coastal Plain of North America.
Neopanorpa van der Weele, 1909 is the second largest genus in Panorpidae, and over 170 Oriental species have been reported hitherto. In this paper, we describe two new species: Neopanorpa luojishana sp. nov. and Neopanorpa xingmini sp. nov. from Southwest China. We also report the first discovery of the male of Neopanorpa ocellaris (Navás, 1908) from Guangxi and Guizhou, China, a species recorded from Sikkim previously. Neopanorpa brevivalvae Chou & Wang, 1988 is synonymized with Neopanorpa lungtaushana Cheng, 1957. In addition, Neopanorpa furcula nom. nov. is proposed for Neopanorpa furcata Zhou, 2005, a junior homonym preoccupied by Neopanorpa furcata (Hardwicke, 1825). The biogeographical implications of some Neopanorpa species are discussed in brief.
There are 214 species of the suborder Tipulomorpha (Diptera) known from Panama. Of these, 162 species were described by the noted American entomologist, Charles Paul Alexander, from Panama during the period from 1912 through 1979. Panama hosts two of the four families found within the Tipulomorpha: Limoniidae (197 species) and Tipulidae (17 species). We have records of only three species from multiple provinces (n = 2) within Panama and 211 species from just one province. The vast majority of the latter are known from a single location within their respective provinces. There are 142 endemic species (66.4%) included in Panama’s Tipulomorpha fauna, with the remainder being found elsewhere in South America (48 species), Central America (44), Mexico (23 species), the Caribbean (14 species), and the United States (4 species). Whereas, this taxonomic group has benefited from collecting in the Canal Zone and the popular western highlands in Chiriqui Province, we know little or nothing of the distribution of species within the country, their natural history, or their relationship to water quality.
First records of Elachistinae are given from Thailand. Ten species of Elachistinae are reported, eight of which are described as new: Urodeta longa Sruoga & Kaila sp. nov., Elachista buszkoi Sruoga & Kaila sp. nov., E. oryx Sruoga & Kaila sp. nov., E. pellineni Sruoga & Kaila sp. nov., E. capricornis Sruoga & Kaila sp. nov., E. phichaiensis Sruoga & Kaila sp. nov., E. loeiensis Sruoga & Kaila sp. nov. and E. siamensis Sruoga & Kaila sp. nov. The new species are diagnosed and illustrated with photographs of the adults and genitalia. One species remains unidentified to species level.
In two separate occurrences, graduates of the Oregon Forest Pest Detector program discovered the exotic Agrilus cyanescens (Ratzeburg) (Coleoptera: Buprestidae) in Portland, Oregon, damaging a backyard shrub, Lonicera involucrata (Rich.) Banks ex Spreng. (Caprifoliaceae). Although first detected in the USA 99 years ago, the known occurrence nearest to Oregon is in Utah.
Jeekelosoma Mauriès, 1985, is upgraded from subgenus status under Eviulisoma Silvestri, 1910 to full genus status. The type species, Jeekelosoma abadi (Mauriès, 1985) is redescribed based on topotypical material from a cave in Morocco. Jeekelosoma heptarachne sp. nov. and J. viginti sp. nov. are described from two further Moroccan caves.