A new R package to parse plant species occurrence records into unique collection events efficiently reduces data redundancy.

Biodiversity data aggregators, such as Global Biodiversity Information Facility (GBIF) suffer from inflation of the number of occurrence records when data from different databases are merged but not fully reconciled. The ParseGBIF workflow is designed to parse duplicate GBIF species occurrence records into unique collection events (gatherings) and to optimise the quality of the spatial data associated with them. ParseGBIF provides tools to verify and standardize species scientific names according to the World Checklist of Vascular Plants taxonomic backbone, and to parse duplicate records into unique 'collection events', in the process compiling the most informative spatial data, where more than one duplicate is available, and providing crude estimates of taxonomic and spatial data quality. When GBIF occurrence records for a medium-sized vascular plant family, the Myrtaceae, were processed by ParseGBIF, the average number of records useful for spatial analysis increased by 180%. ParseGBIF could therefore be valuable in the evaluation of species' occurrences at the national scale in support for national biodiversity plans, identification of plant areas important for biodiversity, sample bias estimation to inform future sampling efforts, and to forecast species range shifts in response to global climate change.

Revision of the emRhagovelia/em emangustipes/em complex (Insecta: Hemiptera: Veliidae) from Colombia.

Water striders of the genus Rhagovelia Mayr, 1865 (Insecta: Hemiptera: Veliidae) have colonized the water surface mainly in lotic freshwater systems, but also in coastal marine environments. They are characterized by the swimming fan in the distal tarsomere of the middle leg that allows them to quickly maneuver. In the Americas, it was subdivided into four monophyletic complexes (angustipes, collaris, obesa and robusta), one paraphyletic grade (abrupta), each with several groups of species, and one additional group (varipes). However, the taxonomy of this genus still has inconsistencies due to its morphological complexity and to the misinterpretation of characters. For this reason, we present a revision of the species of the angustipes complex occurring in Colombia. Material deposited in nine biological collections was examined, including several types. A total of 3,674 specimens  were studied, belonging to 26 valid species, of which R. boyacensis sp. nov., R. graziae sp. nov. and R. molanoi sp. nov., are described as new; and R. angustipes Uhler, 1894 is recorded from the country for the first time. Furthermore, eleven species are redescribed and twelve are considered synonyms. Finally, a key to the species of the angustipes complex occurring in Colombia is presented, as well as updated distribution maps.

Anatomic glossary of mesopleural structures in Bethylidae (Hymenoptera: Chrysidoidea)

The mesopleuron of Bethylidae has many structures that are used in taxonomic and phylogenetic studies. The lack of understanding of these structures has generated independent terminologies and a series of confusing terms, hampering effective scientific communication. A morphological study and literature review were made in order to solve these problems. Our study resulted in an anatomic glossary with 49 terms that presented a large number of synonyms and polysemies. The glossary standardizes the terms used in the Bethylidae mesopleuron and in other Hymenoptera groups, which will facilitate hypotheses of primary homology in comparative biology.(AU)

Anatomic glossary of mesopleural structures in Bethylidae (Hymenoptera: Chrysidoidea)

Abstract The mesopleuron of Bethylidae has many structures that are used in taxonomic and phylogenetic studies. The lack of understanding of these structures has generated independent terminologies and a series of confusing terms, hampering effective scientific communication. A morphological study and literature review were made in order to solve these problems. Our study resulted in an anatomic glossary with 49 terms that presented a large number of synonyms and polysemies. The glossary standardizes the terms used in the Bethylidae mesopleuron and in other Hymenoptera groups, which will facilitate hypotheses of primary homology in comparative biology.

Anatomic glossary of mesopleural structures in Bethylidae (Hymenoptera: Chrysidoidea)

Abstract The mesopleuron of Bethylidae has many structures that are used in taxonomic and phylogenetic studies. The lack of understanding of these structures has generated independent terminologies and a series of confusing terms, hampering effective scientific communication. A morphological study and literature review were made in order to solve these problems. Our study resulted in an anatomic glossary with 49 terms that presented a large number of synonyms and polysemies. The glossary standardizes the terms used in the Bethylidae mesopleuron and in other Hymenoptera groups, which will facilitate hypotheses of primary homology in comparative biology.

Revision of the American genus Platyvelia Polhemus & Polhemus, 1993 (Heteroptera: Gerromorpha: Veliidae)

ABSTRACT The subfamily Veliinae (Heteroptera: Gerromorpha: Veliidae) includes ten genera worldwide, seven of which are endemic to the American continent. Here, we provide a revision of Platyvelia Polhemus and Polhemus, 1993, which is distributed from the United States to northern Argentina, and included nine valid species prior to this study. Six species are redescribed, the synonymies of P. egregia (Drake and Harris, 1935) and P. verdica (Drake, 1951) with P. brachialis (Stål, 1860) are proposed, a lectotype is designated for P. annulipes, and two species groups are erected based on male characters: the P. annulipes group and the P. brachialis group. Keys to the species groups and species within each group, photos, and distribution maps are also included.

Studies on neotropical Phasmatodea XX: A new genus and 16 new species from French Guiana.

The present paper describes 16 new species and one new genus from French Guiana and numerous taxonomic changes are proposed prior to the publication of a comprehensive guide to the Phasmatodea of French Guiana. The following 16 new species are described and illustrated: Phanocles procerus n. sp., Phanocloidea lobulatipes n. sp., Cladomorphus guianensis n. sp., Hirtuleius gracilis n. sp., Parastratocles rosanti n. sp., Parastratocles fuscomarginatus n. sp., Paraprisopus apterus n. sp., Paraprisopus multicolorus n. sp., Agrostia longicerca n. sp., Isagoras similis n. sp., Paragrostia brulei n. sp., Prexaspes globosicaput n. sp., Prexaspes guianensis n. sp., Dinelytron cahureli n. sp., Prisopus clarus n. sp. and Prisopus conocephalus n. sp.. The new genus Paragrostia n. gen. is established for the newly described Paragrostia brulei n. sp. and Paragrostia flavimaculata (Heleodoro, Mendes Rafael, 2017) n. comb. the latter of which is here transferred from Agrostia Redtenbacher, 1906.                Fifty-six new combinations are proposed with species transferred to other genera: Bacteria pallidenotata Redtenbacher, 1908, is transferred to Phanocloidea Zompro, 2001 (n. comb.); Bacteria maroniensis Chopard, 1911 is transferred to Phanocles Stål, 1875 (n. comb.); Cladomorphus gibbosus (Chopard, 1911) is transferred to Hirtuleius Stål, 1875 (n. comb.); Stratocles soror Redtenbacher, 1906, Parastratocles lugubris (Redtenbacher, 1906) and Parastratocles cryptochloris (Rehn, 1904) are transferred to Brizoides Redtenbacher, 1906 (n. comb.); Stratocles xanthomela (Olivier, 1792), Stratocles forcipatus Bolívar, 1896 and Stratocles tessulatus (Olivier, 1792) are transferred to Parastratocles (n. comb.); Olcyphides cinereus (Olivier, 1792), Perliodes affinis Redtenbacher, 1906, Perliodes nigrogranulosus Redtenbacher, 1906, Perliodes sexmaculatus Redtenbacher, 1906, Isagoras rugicollis (Gray, 1835), Isagoras sauropterus Rehn, 1947, Brizoides viridipes (Rehn, 1905) and Brizoides graminea Redtenbacher, 1906 are transferred to Agrostia Redtenbacher, 1906 (n. comb.); Agrostia flavimaculata Heleodoro, Mendes Rafael, 2017 is transferred to Paragrostia n. gen. (n. comb.); Isagoras affinis Chopard, 1911, Isagoras chocoensis Hebard, 1921, Isagoras metricus Rehn, 1947 and Isagoras schraderi Rehn, 1947 are transferred to Tenerella Redtenbacher, 1906 (n. comb.); Xerosoma glyptomerion Rehn, 1904 is transferred to Isagoras Stål, 1875 (n. comb.); Isagoras venosus (Burmeister, 1838), Paraphasma paulense Rehn, 1918 and Paraphasma quadratum (Bates, 1865) are transferred to Prexaspes Stål, 1875 (n. comb.); Prexaspes (Prexaspes) cneius (Westwood, 1859) is transferred to Tenerella Redtenbacher, 1906 (n. comb.); Prexaspes lateralis (Fabricius, 1775) is transferred to Paraphasma Redtenbacher, 1906 (n. comb.); Isagoras santara (Westwood, 1859) and Prexaspes olivaceus Chopard, 1911 are transferred to Periphloea Redtenbacher, 1906 (n. comb.); Dinelytron agrion Westwood, 1859 is transferred to Paraprisopus Redtenbacher, 1906 (n. comb.); Anarchodes atrophicus (Pallas, 1772) is transferred to Ignacia Rehn, 1904 (n. comb.); Planudes asperus Bellanger Conle, 2013, Planudes brunni Redtenbacher, 1906, Planudes cortex Hebard, 1919, Planudes crenulipes Rehn, 1904, Planudes funestus Redtenbacher, 1906, Planudes melzeri Piza, 1937, Planudes molorchus (Westwood, 1859), Planudes paxillus (Westwood, 1859), Planudes perillus Stål, 1875, Planudes pygmaeus (Redtenbacher, 1906) and Planudes taeniatus Piza, 1944 are transferred to Isagoras Stål, 1875 (n. comb.); Prisopoides atrobrunneus Heleodoro Rafael, 2020, Prisopoides brunnescens Heleodoro Rafael, 2020, Prisopoides caatingaensis Heleodoro Rafael, 2020 and Prisopoides villosipes (Redtenbacher, 1906) are transferred to Prisopus Peletier de Saint Fargeau Serville, 1828 (n. comb.); Melophasma antillarum (Caudell, 1914), Melophasma brachypterum Conle, Hennemann Gutiérrez, 2011, Melophasma colombianum Conle, Hennemann Gutiérrez, 2011 and Melophasma vermiculare Redtenbacher, 1906 are transferred to Paraprisopus Redtenbacher, 1906 (n. comb.); Prexaspes (Elasia) ambiguus (Stoll, 1813), Prexaspes (Elasia) brevipennis (Burmeister, 1838), Prexaspes (Elasia) pholcus (Westwood, 1859), Prexaspes (Elasia) viridipes Redtenbacher, 1906 and Prexaspes (Elasia) vittata (Piza, 1985) are transferred to Prexaspes Stål, 1875 (n. comb.).                Twenty-six new synonymies are established: Perliodes Redtenbacher, 1906 and Chlorophasma Redtenbacher, 1906 are synonymised with Agrostia Redtenbacher, 1906 (n. syn.); Chlorophasma Redtenbacher, 1906 is synonymised with Agrostia Redtenbacher, 1906 (n. syn.); Elasia Redtenbacher, 1906 is synonymised with Prexaspes Stål, 1875 (n. syn.); Prisopoides Heleodoro Rafael, 2020 is synonymised with Prisopus Peletier de Saint Fargeau Serville, 1828 (n. syn.); Melophasma Redtenbacher, 1906 is synonymised with Paraprisopus Redtenbacher, 1906 (n. syn.); Bacteria crassipes Chopard, 1911 is synonymised with Bacteria pallidenotata Redtenbacher, 1908 (n. syn.); Perliodes grisescens Redtenbacher, 1906 and Metriophasma (Metriophasma) pallidum (Chopard, 1911) are synonymised with Agrostia cinerea (Olivier, 1792) (n. syn.); Perliodes nigrogranulosus Redtenbacher, 1906 and Metriophasma (Metriophasma) ocellatum (Piza, 1937) are synonymised with Isagoras rugicollis (Gray, 1835) (n. syn.); Isagoras chopardi Hebard, 1933 is synonymised with Tenerella cneius (Westwood, 1859) (n. syn.); Isagoras proximus Redtenbacher, 1906 is synonymised with Isagoras glyptomerion (Rehn, 1904) (n. syn.); Chlorophasma hyalina Redtenbacher, 1906 is synonymised with Agrostia graminea (Redtenbacher, 1906) (n. syn.); Isagoras nitidus Redtenbacher, 1906 is synonymised with Anisa flavomaculatus (Gray, 1835) (n. syn.); Prexaspes acuticornis (Gray, 1835) is synonymised with Prexaspes servillei (Gray, 1835) (n. syn.); Prexaspes nigromaculatus Chopard, 1911 is synonymised with Periphloea santara (Westwood, 1859) (n. syn.); Prexaspes (Elasia) janus Kirby, 1904 is synonymised with Paraphasma maculatum (Gray, 1835) (n. syn.); Prexaspes dictys (Westwood, 1859) is synonymised with Prexaspes brevipennis (Burmeister, 1838) (n. syn.); Parastratocles aeruginosus Redtenbacher, 1906: 107 is synonymised with Parastratocles forcipatus Bolívar, 1896 (n. syn.); Parastratocles carbonarius (Redtenbacher, 1906: 106) is synonymised with Parastratocles lugubris (Redtenbacher, 1906) (n. syn.); Prisopus spinicollis Burmeister, 1838, Prisopus spiniceps Burmeister, 1838 and Prisopus cornutus Gray, 1835 are synonymised with Prisopus ohrtmanni (Lichtenstein, 1802) (n. syn.); the genus Planudes Stål, 1875 is synonymised with Isagoras Stål, 1875 (n. syn.); Pseudophasma annulipes (Redtenbacher, 1906) is synonymised with Pseudophasma blanchardi (Westwood, 1859) (n. syn.); Ignacia appendiculatum (Kirby, 1904) is synonymised with Anarchodes atrophicus (Pallas, 1772) (n. syn.).                Isagoras obscurum Guérin-Méneville, 1838 is shown to have been erroneously synonymised with Isagoras rugicollis (Gray, 1835) and is here re-established as a valid species (rev. stat.). Pseudophasma castaneum (Bates, 1865) is re-established as a valid species here (rev. stat.).                Paraprisopus Redtenbacher, 1906 and the entire tribe Paraprisopodini are transferred to Pseudophasmatidae: Pseudophasmatinae (n. comb.).                Lectotypes are designated for Perliodes grisescens Redtenbacher, 1906, Isagoras plagiatus Redtenbacher, 1906.Neotypes are designated for Agrostia cinerea (Olivier, 1792), Prexaspes ambiguus (Stoll, 1813), Prisopus horridus (Gray, 1835) and Prisopus sacratus (Olivier, 1792).

Taxonomical revision of the genus Hypseocharis in Peru and Bolivia / Revisión taxonómica del género Hypseocharis en Perú y Bolivia

Abstract In the present study we revised the genus Hypseocharis in Bolivia and Peru. A total number of 105 herbarium specimens were revised to evaluate the morphological diversity across the range of the genus. In a subset of 24 complete individuals a multivariate morphometric analysis was performed to evaluate the morphological characters historically used to differentiate the "species" of the genus Hypseocharis. A revision of the herbarium material indicated that there are no sharp lines dividing the different "species" with the only exception of H. tridentata. The multivariate analysis indicated that H. bilobata, H. malpasensis and H. pedicularifolia all occupy the same morphospace as H. pimpinellifolia and there are no individual morphological characters or suites of characters permitting the differentiation of distinct taxa. This confirms earlier findings from Argentina: There are only two species in the genus, widespread Hypseocharis pimpinellifolia and H. tridentata. Hypseocharis pilgeri, originally described from Peru, can also not be differentiated from H. pimpinellifolia. We propose the recognition of only two species: H. pimpinellifolia with variously pinnate to bipinnate leaves with a terminal leaflet at most marginally larger than the lateral ones, flowers with 15 anthers and capsular fruits as differing from H. tridentata with pinnate leaves with the terminal leaflet much larger than the lateral ones, flowers with 5 anthers and schizocarpic fruits. Hypseocharis pimpinellifolia is a widespread and polymorphic species, ranging from Ancash (Peru) to La Rioja (Argentina) and comprises forms with white, yellow, orange, and red corollas and with simply pinnate to very finely bipinnate leaves.

Resumen En el presente estudio se realizó una revisión taxonómica del género Hypseocharis en Bolivia y Perú. Se analizó la diversidad morfológica abarcando toda la distribución geográfica del género Hypseocharis utilizando 105 especímenes de herbario. Un análisis multivariado morfométrico fue aplicado a 24 individuos completos para evaluar los caracteres históricos utilizados para diferenciar las especies dentro del género. La revisión del material de herbario mostró una distinción de la especie H. tridentata, pero no se confirmó una clara separación entre las "especies" H. bilobata, H. malpasensis, H. pedicularifolia y H. pimpinellifolia. Todas ocupan el mismo morfo espacio con similares caracteres morfológicos, apoyando previos estudios en Argentina, donde solamente se describieron dos especies: H. pimpinellifolia y H. tridentata, esta última proveniente de Argentina y con solo un espécimen de Bolivia. Nuestros resultados también mostraron que H. pilgeri, originalmente descrita en Perú, tampoco se diferencia de H. pimpinellifolia. Por lo tanto, proponemos la distinción de solamente dos especies en el género: H. pimipinellifolia con hojas variables pinnadas o bipinnadas, con foliolos terminales un poco más grandes que los foliolos laterales; flores con 15 anteras y tipo de fruto capsular. Mientras que H. tridentata posee hojas pinnadas con foliolos terminales mucho más grandes que los laterales; flores con 5 anteras y tipo de fruto esquizocarpo. Hypseocharis pimpinellifolia es una especie ampliamente distribuida desde Ancash (Perú) hasta La Rioja (Argentina) morfológicamente variable incluyendo varios tipos de hojas, desde simples pinnadas hasta bipinnadas y flores blancas, amarillas, naranjas o rojas.

Taxonomic revision of Dichotomius (Selenocopris) nisus (Olivier, 1719) and Dichotomius (Selenocopris) superbus (Felsche, 1901)

Abstract Within the subgenus Dichotomius (Selenocopris) Burmeister 1846, D. nisus (Olivier, 1789) and D. superbus (Felsche, 1901) had been historically arranged in the "Nisus" section by Luederwaldt, however, according to the revised classification of the subgenus, the two species now belong to different species groups. In this paper, the taxonomic history concerning the species once included by Luederwaldt in the "Nisus" section is revised and discussed. The following new synonyms are proposed: Pinotus taunayi (Luederwaldt, 1931) as a subjective synonym of D. geminatus (Arrow, 1913), and Pinotus taunayi pilosus (Luederwaldt, 1931) as a subjective synonym of D. nisus. Lectotypes are designated for D. nisus and Pinotus garbei. Redescriptions, diagnoses and updated distribution data are provided for D. nisus and D. superbus. The diagnostic characters of the male genitalia of these species are described and illustrated for the first time.

A revision of the genera and species of the Neotropical family Mesembrinellidae (Diptera: Oestroidea).

The Neotropical family Mesembrinellidae is revised. A total of 53 valid, extant species are included in the family, including 15 described as new and 38 redescribed based on study of type and non-type material and of the literature. A total of 18 primary types were examined. An additional ca. 2300 specimens, belonging to 47 species, were studied in detail, including dissection and photographic documentation of terminalia, with many females illustrated for the first time. Keys to subfamilies, genera, species-groups and species are provided. Type specimens of six species housed in South American institutions could not be obtained for study, i.e., M. bequaerti Séguy, 1925 and the five recently described species M. andina (Wolff et al., 2014), M. carvalhoi (Wolff et al., 2013b), M. cordillera (Wolff Ramos-Pastrana in Wolff et al., 2017), M. obscura (Wolff in Wolff et al., 2017) and Laneella patriciae (Wolff, 2013). We accept the synonymy, proposed by previous authors, of Eumesembrinella Townsend, 1931 with Mesembrinella Giglio-Tos, 1893. In addition, we synonymize the genera Albuquerquea Mello, 1967, Giovanella Bonatto in Bonatto Marinoni, 2005, Henriquella Bonatto in Bonatto Marinoni, 2005, Huascaromusca Townsend, 1918 and Thompsoniella Guimarães, 1977 with Mesembrinella Giglio-Tos, 1893, synn. nov., retaining three valid genera in the family: Laneella Mello, 1967, Mesembrinella and Souzalopesiella Guimarães, 1977. Laneella nigripes Guimarães, 1977 and Mesembrinella bellardiana Aldrich, 1922 are fixed as the type species of the genera Laneella Mello, 1967 and Mesembrinella Giglio-Tos, 1893, respectively, under Article 70.3 of the ICZN Code. We separate Mesembrinella into the following species-groups: M. latifrons (Mello, 1967), M. spicata Aldrich, 1925, M. bolivar (Bonatto in Bonatto Marinoni, 2005), M. aeneiventris (Wiedemann, 1830), M. bicolor (Fabricius, 1805), and M. anomala (Guimarães, 1977). The following 15 new species are described: Laneella fusconitida Whitworth, sp. nov. from Costa Rica, Ecuador and Venezuela, Laneella fuscosquamata Whitworth, sp. nov. from Guatemala and Mexico, Laneella purpurea Whitworth, sp. nov. from Costa Rica, Mesembrinella bullata Whitworth, sp. nov. from Bolivia, Mesembrinella chantryi Whitworth, sp. nov. from French Guiana and Brazil, Mesembrinella epandrioaurantia Whitworth, sp. nov. from Venezuela, Mesembrinella guaramacalensis Whitworth, sp. nov. from Venezuela, Mesembrinella longicercus Whitworth, sp. nov. from Bolivia, Mesembrinella mexicana Whitworth, sp. nov. from Mexico, Mesembrinella nigrocoerulea Whitworth, sp. nov. from Costa Rica, Ecuador and Venezuela, Mesembrinella serrata Whitworth, sp. nov. from Peru, Mesembrinella velasquezae Whitworth, sp. nov. from Venezuela, Mesembrinella violacea Whitworth, sp. nov. from Costa Rica, Mesembrinella woodorum Whitworth, sp. nov. from Ecuador, and Mesembrinella zurquiensis Whitworth, sp. nov. from Costa Rica. Mesembrinella abaca Hall, 1948 is proposed as a junior synonym of Mesembrinella socors (Walker, 1861), syn. nov. Lectotypes are designated for Dexia randa Walker, 1849 (now Mesembrinella) and Mesembrinella pictipennis Aldrich, 1922. We analyze the most extensive DNA-barcode dataset for Mesembrinellidae to date, encompassing the three genera considered valid and including 188 sequences (178 new) from 35 species, with data for 23 species provided for the first time. The topology of the resulting Neighbor-Joining tree is mostly congruent with morphology; however, some species show considerable genetic variation that is not reflected by morphology. Finally, we include a corrigendum to the recent Zootaxa paper on Nearctic Calliphora Robineau-Desvoidy (Diptera: Calliphoridae) by Tantawi et al.

A proposal towards classification of the Raspy Crickets (Orthoptera: Stenopelmatoidea: Gryllacrididae) with zoogeographical comments: An initial contribution to the higher classification of the Gryllacridines.

In this contribution to the study of gryllacridines or raspy crickets (Orthoptera: Gryllacrididae), a new proposal for classification of this family is provided, dividing it into two subfamilies and ten tribes that includes most of the 114 known genera to date (including the new genera described here). It describes and redefines two subfamilies: Hyperbaeninae n. subf. and Gryllacridinae n. sensu, ten tribes: Phryganogryllacridini n. trib., Capnogryllacridini n. trib., Asarcogryllacridini n. trib., Hyperbaenini n. trib., Paragryllacridini n. trib., Ametrini n. trib., Ametroidini n. trib., Gryllacridini n. sensu., Eremini n. trib. and Progryllacridini n. trib.; ten genera: Claudiagryllacris n. gen., Griffinigryllacris n. gen., Gorochovgryllacris n. gen., Ingrishgryllacris n. gen., Rentzgryllacris n. gen., Willemsegryllacris n. gen., Karnygryllacris n. gen., Brunnergryllacris n. gen., Bianigryllacris n. gen. and Hugelgryllacris n. gen.; seven genera groups: Gryllacrae n. group. (placed under Gryllacridini n. trib. comprising ten genera: Caustogryllacris, Eugryllacris, Gryllacris, Lyperogryllacris, Nesogryllacris, Ocellarnaca, Phlebogryllacris, Prosopogryllacris, Willemsegryllacris n. gen. and Xanthogryllacris), Metriogryllacrae n. group. (under Gryllacridini grouped Metriogryllacris, Homogryllacris, Pseudasarca n. stat. and Furcilarnaca), Anancistrogerae (Anancistrogera, Ancistrogera, Angustogryllacris, Aphanogryllacris, Celebogryllacris), Triaenogryllacrae n. group. (under Gryllacridinae only comprising Triaenogryllacris) the next groups under Ametrini n. trib.: Ametrae n. group. (comprising two genera: Ametrus and Pareremus), Apotrechae n. group. (including three genera: Apotrechus, Apterolarnaca and Bianigryllacris n. gen.) and Apteronomae n. group. (comprising two genera: Ametrosomus and Apteronomus). The status of Dictogryllacris reinst. stat., was restored, previously transferred by Gorochov 2003 as subgenus of Capnogryllacris and to Pseudasarca n. stat. as full genus status is proposed. One genera, one subgenus and one fossil species are synonymized: Xiphogryllacris n. syn. (under Hyalogryllacris) and †Gryllacris brevippennis n. syn. (under †Macrelcana ungeri). The subgenus Glolarnaca n. stat. (included under Zalarnaca), is considered as full genus in Gryllacridinae (Gryllacridini). 57 new combinations are proposed, with particular emphasis on Niphetogryllacris, placing 36 of the 43 existing species of the genus: Pissodogryllacris tesellata n. comb., Willemsegryllacris barnesi n. comb. (previously placed under Gryllacris), Afrogryllacris nigripceps n. comb. (previously placed under in Barombogryllacris), Anancistrogera nigroscutata n. comb., A. cornualis n. comb. and A. genualis n. comb. (included by Karny in Caustogryllacris and by Gorochov in the subgenus Pseudolarnaca, here transfered to Anancistrogera), Hugelgryllacris tchancha n. comb. (before in Psilogryllacris), Diaphanogryllacris annandalei n. comb., D. barkudensis n. comb., D. dravida n. comb., D. gravelyi n. comb., Claudiagryllacris finoti n. comb. C. stigmata n. comb., C. lemur n. comb., C. fryeri n. comb., Stictogrtllacris pungens n. comb., S. madagassa n. comb., S. genufuscata n. comb., S. vosseleri n. comb., S. difficilis n. comb., S. paulani n. comb., Stictogryllacris signoreti n. comb., S. indecisa n. comb., S. conspersa n. comb., S. pittarellii n. comb., S. ametroides n. comb., S. jacobi n. comb., S. kilimandjarica n. comb., S. meruensis n. comb.; S. neglecta n. comb.; S. submutica n. comb., Griffinigryllacris reunionis n. comb., G. adelungi n. comb., G. mauritiana n. comb., Karnygryllacris occipitalis n. comb., K. atriceps n. comb., K. brevipennis n. comb., K. humilis n. comb., K. scurra n. comb., K. triocellata n. comb., K. pittarellii n. comb., K. grylloides n. comb., Brunnergryllacris testaceus n. comb. and B. eximia n. comb (previously placed under Niphetogryllacris), Rentzgryllacris sechellensis n. comb. (before in Prosopogryllacris and the three subspecies are treated as full species), Gorochovgryllacris navicula n. comb. (transferred from Brachybaenus), Bianigryllacris trilobus n. comb., B. bilobus n. comb., B. digitatus n. comb., B. fallax n. comb., B. nigrigeniculatus n. comb., B. parvospinus n. comb., B. quadratus n. comb. and B. transversus n. comb. (previously placed under Apotrechus), Hyalogryllacris orthoxipha n. comb. (previously placed under Xiphogryllacris), Afroneanias glauningi n. comb., A. sphinix n. comb. and Ingrishgryllacris brevifalcatus n. comb. (previously placed under Ametroides and Glomeremus respectively). A key to the identification of the subfamilies and tribes is provided, plus historical background of the major taxonomic works on the group and the few contributions on ecology, morphology, and behavior is also done. It also discusses the status of fossil taxa thought to belong to the family. A preliminary analysis of the zoogeography of the family from the parameters of richness, diversity and distribution patterns of different groups studied, and also, some final comments on what has been achieved in this contribution are give, what is missing to the study of gryllacridines to the future and some problems that still affect the taxonomy to genera and species level. Finally, a check list in which all family taxa are included with the new classification is provided, with some comments on their distribution and taxonomic status if necessary.

Revision of black fungus gnat species (Diptera, Sciaridae) described from the Hawaiian Islands by D.E. Hardy and W.A. Steffan, and a contribution to the knowledge of the sciarid fauna of the Galápagos Islands.

On the Hawaiian Islands 22 sciarid species were detected, belonging to the following ten genera: Austrosciara Schmitz Mjöberg, Bradysia Winnertz, Corynoptera Winnertz, Cratyna Winnertz, Epidapus Haliday, Hyperlasion Schmitz, Lycoriella Frey, Phytosciara Frey, Pseudolycoriella Menzel Mohrig and Scatopsciara Edwards. The revision resulted in new combinations for the following five species: Austrosciara hawaiiensis (Hardy) comb. n., Corynoptera prominens (Hardy) comb. n., Cratyna adrostylata (Hardy) comb. n., Cr. longicosta (Hardy) comb. n., and Scatopsciara hoyti (Hardy) comb. n. Eight species were declared as new synonyms: Bradysia bishopi Steffan, 1973 = B. centidens Vilkamaa, Hippa Mohrig, 2012 syn. n.; B. crassicornis (Skuse, 1890) = B. molokaiensis (Grimshaw, 1901) syn. n. and = B. aspercera Mohrig, 2016 syn. n.; B. radicum (Brunetti, 1912) = B. spatitergum (Hardy, 1956) syn. n.; Corynoptera prominens (Hardy, 1956) = C. gladiota Mohrig, 2004 syn. n.; Cosmosciara hartii (Johannsen, 1912) = Plastosciara (Plastosciara) latipons Hardy, 1956 syn. n.; Hyperlasion wasmanni (Schmitz, 1918) = Scythropochroa magnisensoria Hardy, 1956 syn. n.; and Scatopsciara hoyti (Hardy, 1956) = Sc. spiculata Vilkamaa, Hippa Mohrig, 2012 syn. n. These four species are new reports for Hawai'i, three of them are new to science: Epidapus pallidus (Séguy), Pseudolycoriella nigrofemoralis Mohrig, Kauschke Broadley sp. n., Scatopsciara hardyi Mohrig, Kauschke Broadley sp. n. and Sc. steffani Mohrig, Kauschke Broadley sp. n. A lectotype was designated for Bradysia radicum (Brunetti) in order to fix the name. All new and revised species are figured.        The species Bradysia bishopi Steffan, 1973, B. ocellaris (Comstock, 1882), B. radicum (Brunetti, 1912), Cosmosciara hartii (Johannsen, 1912), Pseudolycoriella planiforceps (Steffan, 1971) and Scatopsciara steffani Mohrig, Kauschke Broadley sp. n. are reported from the Galápagos Islands.

Revision of Brazilian species of Aleochara Gravenhorst of the subgenus Aleochara (Coleoptera: Staphylinidae: Aleocharinae).

Adults and larvae of Aleochara are found in fly-infested habitats, where the larvae are ectoparasitoids of fly pupae. There are three subgenera recorded in Brazil. This study provides a taxonomic revision of Brazilian species of the subgenus Aleochara. As a result, we recognize seven species in Brazil, A. bonariensis Lynch, A. bugnioni Fauvel, A. lustrica Say, A. chrysorrhoa Erichson and three species described by Sharp: A. auricoma, A. mundana and A. prisca. Redescriptions and illustrations of the male and female genitalia are provided for all species. Nomenclatural changes: A. bugnioni is considered a new junior synonym of A. lateralis Erichson, and A. pseudochrysorrhoa Caron, Mise Klimaszewski is a new junior synonymy of A. bonariensis. In addition, the type of A. verecunda Sharp, was not studied and the name is considered as species inquirenda, while A. curtula (Goeze) is not confirmed in Brazil and its Neotropical records is discussed. Finally, a key to species is provided and an updated checklist of the Brazilian species of Aleochara (Aleochara), including synonyms, is compiled.

Clinical relevance of official anatomical terminology: the significance of using synonyms / Relevancia clínica de la terminología anatómica oficial: la importancia de usar sinónimos

Terminologia Anatomica is a unique collection of technical terms that enable communication in anatomy and medicine across the world. However, current anatomical terminology also contains some internal inconsistencies and discrepancies in regard to clinical terminology. Thus, a number of terms are not logically related to the names of similar anatomical entities, or the names of corresponding physiological and pathological conditions. Moreover, during clinical practice many anatomical terms have commonly been replaced by new, clinical idioms. These terminological discrepancies represent an impediment to learning and teaching in medical and health professions programs. In this paper it is proposed that the relevant synonyms should be introduced into Terminologia Anatomica in the same way as currently the case for the kidney (ren/nephros) and uterine tube (tuba uterina/salpinx). This change would significantly reduce inconsistencies in nomenclature and make anatomical terminology more logical, easier to understand and memorize. Furthermore, it would better align anatomy with other branches of medicine and medical education.

Terminologia Anatomica es una colección única de términos técnicos que permiten la comunicación en anatomía y medicina en todo el mundo. Sin embargo, la terminología anatómica actual también contiene algunas inconsistencias internas y discrepancias con respecto a la terminología clínica. Por lo tanto, varios términos no están lógicamente relacionados con los nombres de entidades anatómicas similares, o los nombres de las correspondientes condiciones fisiológicas y patológicas. Además, durante la práctica clínica muchos términos anatómicos han sido comúnmente reemplazados por nuevos modismos clínicos. Estas discrepancias terminológicas representan un impedimento para el aprendizaje y la enseñanza en los programas médicos y profesionales de la salud. En este trabajo se propone que los sinónimos relevantes se introduzcan en la terminología anatómica de la misma manera que en la actualidad, como en el caso del riñón (ren / nephros) y la tuba uterina (tuba uterina / salpinx). Este cambio reduciría significativamente las inconsistencias en la nomenclatura y haría la terminología anatómica más lógica, más fácil de entender y memorizar. Además, alinearía mejor la anatomía con otras áreas de la medicina y la educación médica.

Taxonomic notes on the genera Scatella and Scatophila (Diptera: Ephydridae) with a remark on Trixoscelis chilensis (Trixoscelididae).

Two new combinations are proposed in Scatella for Ephydra australis Walker, 1853 and Opomyza guttata Macquart, 1843. Two species are resurrected from synonymy: Scatella lacustris (Meigen, 1830), revised status and Trixoscelis chilensis (Schiner, 1868), revised status (Trixoscelididae). Nine new synonyms are suggested: Scatella insularis Mathis Wirth, 1981 = S. australis (Walker, 1853); S. lutosa nigripes Oldenberg, 1923 = S. obsoleta Loew, 1861; S. septempunctata Malloch, 1933 = S. gratiellae Canzoneri Raffone, 1987 = S. septemfenestrata Lamb, 1912; S. tenuicosta Collin, 1930 = S. lacustris (Meigen, 1830); S. vulgata Cresson, 1931 = S. guttata (Macquart, 1843); Scatophila zlobini Krivosheina, 2009 = S. hirtirostris Sturtevant and Wheeler, 1954; S. grisescens Frey, 1915 = S. mesogramma (Loew, 1869); S. planiceps (Boheman, 1853) = S. quadriguttata (Meigen, 1830).

The Ciidae (Coleoptera) of New Brunswick, Canada: New records and new synonyms.

The Ciidae of New Brunswick, Canada are reviewed. Seventeen species are recorded for New Brunswick, including the following 10 species that are newly recorded for the province: Ceracis singularis (Dury), Ceracis thoracicornis (Ziegler), Cis angustus Hatch, Cis fuscipes Mellié, Cis horridulus Casey, Cis striatulus Mellié, Dolichocis laricinus (Mellié), Malacocis brevicollis (Casey), Orthocis punctatus (Mellié), and Plesiocis cribrum Casey. Additional locality data are provided for the following species previously known from the province: Cis americanus Mannerheim, Cis creberrimus Mellié, Cis levettei (Casey), Cis submicans Abeille de Perrin, Dolichocis manitoba Dury, Hadreule elongatula (Gyllenhal), and Octotemnus glabriculus (Gyllenhal). Seven synonyms are proposed here; Cis pistoria Casey with Cis submicans Abeille de Perrin; Cis fraternus Casey, Cis macilentus Casey and Cis striolatus Casey with Cis striatulus Mellié; Dolichocis indistinctus Hatch with Dolichocis laricinus (Mellié); and Octotemnus denudatus Casey and Octotemnus laevis Casey with Octotemnus glabriculus (Gyllenhal). Lindgren funnel traps provided the majority of specimens for 15 of the 17 species reported from New Brunswick and were the sole source of specimens for seven of the 10 species newly reported here, suggesting they are a very useful tool for sampling Ciidae in the forests of New Brunswick.

A commented list of Scaphopoda (Mollusca) found along the Brazilian coast, with two new synonymies in the genus Gadila Gray, 1847

This review aims to present an updated checklist of scaphopods, based mainly on literature database. There is a total of 40 species (six families) for Brazil, including information about the distribution and bathymetric range of each taxon. We propose two synonyms with the aid of morphometry of the shell, for the genus Gadila: G. longa as junior synonym of G. elongata and G. robusta as junior synonym of G. pandionis.

Uma lista atualizada dos escafópodes da costa brasileira pertencentes a seis famílias é apresentada baseada principalmente em dados da literatura. Há um total de 40 espécies para o Brasil, incluindo informações sobre a distribuição e a faixa batimétrica de cada táxon. Nós propomos dois sinônimos com o auxílio da morfometria da concha, para o gênero Gadila: G. longa como sinônimo júnior de G. elongata e G. robusta como sinônimo júnior de G. pandionis.

Assessment of inter- and intra-cultivar variations in olive using SSR markers

Olive (Olea europaea L.) production in the world has been made by using many cultivars, and the genetic uniformity of commercial cultivars is important for standard olive oil and table olive production. The genetic variation among and within commonly cultivated olive cultivars in Turkey was analyzed using SSR markers. A total of 135 leaf samples were collected from 11 commonly cultivated olive cultivars from 11 provinces in four geographical regions of Turkey. Seven SSR primer pairs generated 46 SSR markers, and the number of SSR markers per primer pair ranged from 4 (UDO-14) to 9 (GAPU-89) with an average of 6.57. This high level of SSR polymorphism suggests that olive production in Turkey has been made using genetically diverse olive cultivars and this high level of genetic variation is probably due to the location of Turkey in the center of the origin of olive. The UPGMA dendrogram, developed to visualize the estimated genetic relationships among the 135 samples, demonstrated that the clustering of olive cultivars was not based on geographical regions of cultivation. Presence of genetic variation was detected within a nationwide grown Turkish olive cultivar, called 'Gemlik'. Olive growers successfully discriminated olive cultivars with distinct morphological and pomological characters. However, there was some confusion about the identification of cultivars with similar phenotypic traits. To prevent misidentification of olive cultivars and to minimize intra-cultivar variation, certified propagation materials which were characterized using DNA based molecular markers should be used during the establishment of new olive orchards.

Assessment of inter- and intra-cultivar variations in olive using SSR markers

Olive (Olea europaea L.) production in the world has been made by using many cultivars, and the genetic uniformity of commercial cultivars is important for standard olive oil and table olive production. The genetic variation among and within commonly cultivated olive cultivars in Turkey was analyzed using SSR markers. A total of 135 leaf samples were collected from 11 commonly cultivated olive cultivars from 11 provinces in four geographical regions of Turkey. Seven SSR primer pairs generated 46 SSR markers, and the number of SSR markers per primer pair ranged from 4 (UDO-14) to 9 (GAPU-89) with an average of 6.57. This high level of SSR polymorphism suggests that olive production in Turkey has been made using genetically diverse olive cultivars and this high level of genetic variation is probably due to the location of Turkey in the center of the origin of olive. The UPGMA dendrogram, developed to visualize the estimated genetic relationships among the 135 samples, demonstrated that the clustering of olive cultivars was not based on geographical regions of cultivation. Presence of genetic variation was detected within a nationwide grown Turkish olive cultivar, called 'Gemlik'. Olive growers successfully discriminated olive cultivars with distinct morphological and pomological characters. However, there was some confusion about the identification of cultivars with similar phenotypic traits. To prevent misidentification of olive cultivars and to minimize intra-cultivar variation, certified propagation materials which were characterized using DNA based molecular markers should be used during the establishment of new olive orchards.

Sinopse das espécies neotropicais do grupo nitida do gênero Apenesia (Hymenoptera, Bethylidae)

Two species are described and illustrated: Apenesia quelata sp. nov. and A. trivisa sp. nov. New geographic records and data on morphostructural variation of A. membranaceus Lanes & Azevedo, 2004, A. paraensis Kieffer, 1910, A. quadrata Evans, 1963, A. serrulata Azevedo & Batista, 2002, e A. williamsi Evans, 1966 are provided. Two species are synonymyzed: A. laticeps Evans, 1963 as junior synonym of A. quadrata Evans, 1963; A. truncaticeps (Kieffer, 1910) as junior synonym of A. paraensis Kieffer, 1910. The female of A. quadrata is described and illustrated for the first time. Key to the species of the nitida species-group based on males is provided.

São descritas e ilustradas duas espécies: Apenesia quelata sp. nov. e A. trivisa sp. nov. São fornecidos registros geográficos novos e dados sobre variações morfoestruturais de A. membranaceus Lanes & Azevedo, 2004, A. paraensis Kieffer, 1910, A. quadrata Evans, 1963, A. serrulata Azevedo & Batista, 2002 e A. williamsi Evans, 1966. Duas espécies são sinonimizadas: A. laticeps Evans, 1963 como sinônimo júnior de A. quadrata Evans, 1963; A. truncaticeps (Kieffer, 1910) como sinônimo júnior de A. paraensis Kieffer, 1910. A fêmea de A. quadrata é descrita e ilustrada pela primeira vez. É fornecida chave de identificação para as espécies do grupo nitida, baseada em machos.