skip to main content
US FlagAn official website of the United States government
dot gov icon
Official websites use .gov
A .gov website belongs to an official government organization in the United States.
https lock icon
Secure .gov websites use HTTPS
A lock ( lock ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

Explore Research Products in the PAR
It may take a few hours for recently added research products to appear in PAR search results.


  • NSF Public Access
  • Search Results
  • The millipede family Striariidae Bollman, 1893. IX. The identity of Striaria californica Cook, 1899, and the new genus Bayaria for Striaria nana Loomis, 1936, with a key to genera and an annotated checklist of the Striariidae (Diplopoda, Chordeumatida, Striarioidea)
Title: The millipede family Striariidae Bollman, 1893. IX. The identity of Striaria californica Cook, 1899, and the new genus Bayaria for Striaria nana Loomis, 1936, with a key to genera and an annotated checklist of the Striariidae (Diplopoda, Chordeumatida, Striarioidea)
The identity of Striaria californica Cook, described in 1899 from a single female, is established on the basis of additional specimens collected by Cook in 1929 and determined to be that species by Loomis (1936) as well as specimens from the San Francisco Bay region, likely to be from near the original collection locality. We propose Amplaria californica (Cook, 1899) new combination. A new genus, Bayaria Shear & Marek n. gen., is established for Striaria nana Loomis, 1936 Bayaria nana (Loomis, 1936) new combination. Striaria carmela Chamberlin, 1947, is a junior synonym of Bayaria nana. A key to the 16 genera of Striariidae and an annotated checklist of the 52 species are provided.  more » « less
Award ID(s):
1916368
PAR ID:
10557807
Author(s) / Creator(s):
;
Publisher / Repository:
Mapress
Date Published:
Journal Name:
Zootaxa
Volume:
5463
Issue:
4
ISSN:
1175-5326
Page Range / eLocation ID:
524 to 544
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. ; ; ; (, Zootaxa)
    A new genus and species of short-tailed whipscorpion (Schizomida: Hubbardiidae Cook, 1899) is described based on specimens collected in the Venezuelan state of Amazonas. The new genus differs from other Neotropical genera in the presence of six setae on opisthosomal tergite II, the absence of seta Dm4 on the flagellum in both sexes, the female flagellum comprising four segments, and the median lobes of the spermatheca being four times longer than the lateral lobes. Jipai longevus gen. et sp. nov. increases the count of South American schizomid genera to fourteen and the count of species to 57. The type locality of the new taxon is situated in the Guiana region of Amazonia s. l., where three other hubbardiid genera have also been recorded. This discovery contributes to the understanding of Amazonian schizomid diversity and highlights the need for further sampling in this diverse, vulnerable and poorly explored area. 
    more » « less
  2. ; ; (, Ornithology)
    Abstract We applied an integrative taxonomic framework to evaluate the systematics of the Neotropical Black-and-white Becard (Pachyramphus albogriseusSclater 1857). Combining phylogenomic (ultraconserved elements), morphological, and vocalization data, we confirmed that this species is polyphyletic; some individuals form a clade sister to P. polychopterus and should be afforded species rank as P. salviniRichmond 1899 (Slender-billed Becard), whereas the remaining subspecies of P. albogriseus (Broad-banded Becard) are sister to P. major. We found that P. salvini differs from P. albogriseus in song, color of the lores, wing-bar width, body size, and bill width. Whereas P. albogriseus occurs in montane forest in Costa Rica and Panama (ssp. ornatus) and along the eastern slope of the Andes from northern Venezuela to southern Peru (ssp. albogriseus), P. salvini is found in the lowlands from Pacific Colombia south to northwest Peru and in the Río Marañón drainage. The latter also occurs, possibly only seasonally, along the eastern slope of the Andes, where the two species’ ranges approach closely. We treat P. a. guayaquilensisZimmer 1936 as a junior synonym of P. salviniRichmond 1899, and P. a. coronatusPhelps and Phelps 1953 as a junior synonym of P. a. albogriseusSclater 1857. This study provides a striking example of a major problem for comparative biology: underestimated and mischaracterized diversity. We argue that there are likely many more cases like this awaiting discovery. 
    more » « less
  3. ; ; (, ZooKeys)
    null (Ed.)
    The taxonomic concept of the genus Machleida Fåhraeus, 1870 is tested and revised based on newly identified material. The following new species are described: Machleida banachi , M. flagstaffensis , M. tarskii , and M. zofiae Kamiński. Machleida capillosa Wilke, 1925 is considered as a junior subjective synonym of Asida devia Péringuey, 1899. Asida lecta Péringuey, 1899 (= Pseudomachla recurva Wilke, 1925) (transferred to Afrasida ), Machleida nossibiana Fairmaire, 1897 (transferred to Scotinesthes ), and Machleida tuberosa Wilke, 1925 (interpreted as incertae sedis in Asidini) are excluded from Machleida . An identification key for the species of the newly revised Machleida is provided. The present paper brings the total number of species within the genus to six ( M. banachi sp. nov. ; M. devia (Péringuey, 1899); M. flagstaffensis sp. nov. ; M. nodulosa Fåhraeus, 1870; M. tarskii sp. nov. ; M. zofiae Kamiński sp. nov. ). The morphology of female terminalia (ovipositor and genital tubes) is described for the genus for the first time. 
    more » « less
  4. ; ; ; ; ; ; ; ; (, ZooKeys)
    This catalogue includes all valid family-group (six subtribes), genus-group (55 genera, 33 subgenera), and species-group names (1009 species and subspecies) of Sepidiini darkling beetles (Coleoptera: Tenebrionidae: Pimeliinae), and their available synonyms. For each name, the author, year, and page number of the description are provided, with additional information (e.g., type species for genus-group names, author of synonymies for invalid taxa, notes) depending on the taxon rank. Verified distributional records (loci typici and data acquired from revisionary publications) for all the species are gathered. Distribution of the subtribes is illustrated and discussed. Several new nomenclatural acts are included. The generic names Phanerotomea Koch, 1958 [= Ocnodes Fåhraeus, 1870] and Parmularia Koch, 1955 [= Psammodes Kirby, 1819] are new synonyms (valid names in square brackets). The following new combinations are proposed: Ocnodesacuductusacuductus (Ancey, 1883), O. acuductusufipanus (Koch, 1952), O. adamantinus (Koch, 1952), O. argenteofasciatus (Koch, 1953), O. arnoldiarnoldi (Koch, 1952), O. arnoldisabianus (Koch, 1952), O.barbosai (Koch, 1952), O.basilewskyi (Koch, 1952), O.bellmarleyi (Koch, 1952), O. benguelensis (Koch, 1952), O. bertolonii (Guérin-Méneville, 1844), O. blandus (Koch, 1952), O. brevicornis (Haag-Rutenberg, 1875), O. brunnescensbrunnescens (Haag-Rutenberg, 1871), O. brunnescensmolestus (Haag-Rutenberg, 1875), O. buccinator (Koch, 1952), O. bushmanicus (Koch, 1952), O. carbonarius (Gerstaecker, 1854), O. cardiopterus (Fairmaire, 1888), O. cataractus (Koch, 1952), O. cinerarius (Koch, 1952), O. complanatus (Koch, 1952), O. confertus (Koch, 1952), O. congruens (Péringuey, 1899), O. cordiventris (Haag-Rutenberg, 1871), O. crocodilinus (Koch, 1952), O. dimorphus (Koch, 1952), O. distinctus (Haag-Rutenberg, 1871), O. dolosus (Péringuey, 1899), O. dorsocostatus (Gebien, 1910), O. dubiosus (Péringuey, 1899), O. ejectus (Koch, 1952), O. epronoticus (Koch, 1952), O. erichsoni (Haag-Rutenberg, 1871), O. ferreiraeferreirae (Koch, 1952), O. ferreiraezulu (Koch, 1952), O. fettingi (Haag-Rutenberg, 1875), O. fistucans (Koch, 1952), O. fraternus (Haag-Rutenberg, 1875), O. freyi (Koch, 1952), O. freudei (Koch, 1952), O. fulgidus (Koch, 1952), O. funestus (Haag-Rutenberg, 1871), O. gemmeulus (Koch, 1952), O. gibberosulus (Péringuey, 1908), O. gibbus (Haag-Rutenberg, 1879), O. globosus (Haag-Rutenberg, 1871), O. granisterna (Koch, 1952), O. granulosicollis (Haag-Rutenberg, 1871), O.gridellii (Koch, 1960), O. gueriniguerini (Haag-Rutenberg, 1871), O. guerinilawrencii (Koch, 1954), O. guerinimancus (Koch 1954), O. haemorrhoidalishaemorrhoidalis (Koch, 1952), O. haemorrhoidalissalubris (Koch, 1952), O. heydeni (Haag-Rutenberg, 1871), O. humeralis (Haag-Rutenberg, 1871), O. humerangula (Koch, 1952), O. imbricatus (Koch, 1952), O.imitatorimitator (Péringuey, 1899), O. imitatorinvadens (Koch, 1952), O. inflatus (Koch, 1952), O. janssensi (Koch, 1952), O. javeti (Haag-Rutenberg, 1871), O. junodi (Péringuey, 1899), O. kulzeri (Koch, 1952), O. lacustris (Koch, 1952), O. laevigatus (Olivier, 1795), O. lanceolatus (Koch, 1953), O. licitus (Peringey, 1899), O. luctuosus (Haag-Rutenberg, 1871), O. luxurosus (Koch, 1952), O. maputoensis (Koch, 1952), O. marginicollis (Koch, 1952), O. martinsi (Koch, 1952), O. melleus (Koch, 1952), O. mendicusestermanni (Koch, 1952), O. mendicusmendicus (Péringuey, 1899), O. miles (Péringuey, 1908), O. mimeticus (Koch, 1952), O. misolampoides (Fairmaire, 1888), O. mixtus (Haag-Rutenberg, 1871), O. monacha (Koch, 1952), O. montanus (Koch, 1952), O. mozambicus (Koch, 1952), O. muliebriscurtus (Koch, 1952), O. muliebrismuliebris (Koch, 1952), O. muliebrissilvestris (Koch, 1952), O. nervosus (Haag-Rutenberg, 1871), O.notatum (Thunberg, 1787), O. notaticollis (Koch, 1952), O. odorans (Koch, 1952), O. opacus (Solier, 1843), O. osbecki (Billberg, 1815), O. overlaeti (Koch, 1952), O. ovulus (Haag-Rutenberg, 1871), O. pachysomaornata (Koch, 1952), O. pachysomapachysoma (Péringuey, 1892), O. papillosus (Koch, 1952), O. pedator (Fairmaire, 1888), O. perlucidus (Koch, 1952), O. planus (Koch, 1952), O. pretorianus (Koch, 1952), O. procursus (Péringuey, 1899), O. protectus (Koch, 1952), O. punctatissimus (Koch, 1952), O. puncticollis (Koch, 1952), O. punctipennisplanisculptus (Koch, 1952), O. punctipennispunctipennis (Harold, 1878), O. punctipleura (Koch, 1952), O. rhodesianus (Koch, 1952), O. roriferus (Koch, 1952), O. rufipes (Harold, 1878), O. saltuarius (Koch, 1952), O.scabricollis (Gerstaecker, 1854), O. scopulipes (Koch, 1952), O. scrobicollisgriqua (Koch, 1952), O. scrobicollissimulans (Koch, 1952), O. semirasus (Koch, 1952), O. semiscabrum (Haag-Rutenberg, 1871), O. sericicollis (Koch, 1952), O.similis (Péringuey, 1899), O. sjoestedti (Gebien, 1910), O. spatulipes (Koch, 1952), O. specularis (Péringuey, 1899), O. spinigerus (Koch, 1952), O. stevensoni (Koch, 1952), O. tarsocnoides (Koch, 1952), O. temulentus (Koch, 1952), O. tenebrosusmelanarius (Haag-Rutenberg, 1871), O. tenebrosustenebrosus (Erichson, 1843), O. tibialis (Haag-Rutenberg, 1871), O. torosus (Koch, 1952), O. transversicollis (Haag-Rutenberg, 1879), O. tumidus (Haag-Rutenberg, 1871), O. umvumanus (Koch, 1952), O. vagus (Péringuey, 1899), O. vaticinus (Péringuey, 1899), O. verecundus (Péringuey, 1899), O. vetustus (Koch, 1952), O. vexator (Péringuey, 1899), O. virago (Koch, 1952), O. warmeloi (Koch, 1953), O. zanzibaricus (Haag-Rutenberg, 1875), Psammophanesantinorii (Gridelli, 1939), and P.mirei (Pierre, 1979). The type species [placed in square brackets] of the following genus-group taxa are designated for the first time, Ocnodes Fåhraeus, 1870 [ Ocnodesscrobicollis Fåhraeus, 1870], Psammodophysis Péringuey, 1899 [ Psammodophysisprobes Péringuey, 1899], and Trachynotidus Péringuey, 1899 [ Psammodesthoreyi Haag-Rutenberg, 1871]. A lectotype is designated for Histrionotusomercooperi Koch, 1955 in order to fix its taxonomic status. Ulamus Kamiński is introduced here as a replacement name for Echinotus Marwick, 1935 [ Type species. Aviculaechinata Smith, 1817] (Mollusca: Pteriidae) to avoid homonymy with Echinotus Solier, 1843 (Coleoptera: Tenebrionidae). 
    more » « less
  5. ; ; ; (, Plant Ecology)
    Abstract The disruptive effects of tertiary species on otherwise positive pairwise species interactions (e.g. context-dependent parasitism in pollinator syndromes) is well-known. However, few—if any—studies have investigated how invasive plants affect interactions between facilitative plants and their native plant communities. Further, if tertiary invasive species can change interactions among native species from positive to negative, then a tertiary native should be capable of the same phenom for pairwise interactions between natives and invasives. Our previous research indicates invasive black mustard ( Brassica nigra ) changes interaction signs for otherwise positive species interactions between the dominant, native facilitator California buckwheat ( Eriogonum fasciculatum ) and its co-dominant beneficiary California sagebrush ( Artemisia californica ) in semi-arid California coastal sage scrub habitat. Here, E. fasciculatum and A. californica seedlings increased B. nigra shoot growth in pairwise species interactions in the greenhouse. However, in three-way species interactions, E. fasciculatum and A. californica together reduced B. nigra SLA, height, and reproductive potential while not increasing shoot DW. In three-way species interactions, B. nigra did not significantly reduce E. fasciculatum facilitation of A. californica . Also surprisingly, light competition with B. nigra resulted in an increase in A. californica height , which reduced the negative effects of A. californica light competition on shade-intolerant E. fasciculatum. In an additive field experiment, A. californica protected E. fasciculatum from facilitating germination and growth of B. nigra when water competition was minimized. Taken together, this study demonstrates the importance of studying species interactions between competitive, native perennials in the current ecological context of invaded ecosystems. 
    more » « less
  • Citation Formats
  • MLA
  • APA
  • Chicago
  • BibTeX
  • Save / Share this Record
  • Send to Email