Systematic studies of Festuca (Poaceae) occurring in China compared with taxa in North America

2003 ◽  
Vol 81 (10) ◽  
pp. 1008-1028 ◽  
Author(s):  
Xiang Chen ◽  
Susan G Aiken ◽  
Michael J Dallwitz ◽  
Patrice Bouchard

Members of the genus Festuca in China were studied from an illustrated database developed using the DELTA (DEscription Language for Taxonomy) software package. The database includes the place of valid publication of scientific names; the location of type specimens when known; whether we have examined the type specimens; synonymy; information on habitat, distribution, subgeneric classification, and taxonomic notes; and approximately 200 images. Five subgenera and 58 species including aggregates are recognized. Six taxa are not assigned to a subgenus at this time. Species descriptions of 400–500 words were generated in Chinese and English and are available on the Internet at http://cdelta.ibcas.ac.cn and as a CD-ROM in English and Chinese from the first author. INTKEY has been used to produce parallel and diagnostic descriptions of 120–130 words for 58 species of the genus Festuca for the Flora of China treatment in English. INTKEY and other DELTA programs were used to assess taxa throughout the database and in a detailed study of 11 flat-leaved taxa that appear to have their centre of diversity in China. The awnless taxa from China that were considered belong to the genus Festuca, not Poa. All the flat-leaved Festuca studied are sufficiently morphologically unique to be treated as species distinct from any found in North America. Clustering and phylogenetic methodologies were used to assess subgeneric and sectional classifications. A new section is proposed, Parviglumae sect. nov.Key words: Festuca, Subulatae, DELTA, China, systematics.

2021 ◽  
Author(s):  
Rudolf Meier ◽  
Bonny Blaimer ◽  
Eliana Buenaventura ◽  
Emily Hartop ◽  
Thomas von Rintelen ◽  
...  

AbstractHalting biodiversity decline is one of the most critical challenges for humanity, but biodiversity assessment and monitoring are hampered by taxonomic impediments. We here distinguish between a “dark taxon impediment” caused by a large number of undescribed species and a “superficial description impediment” caused by species descriptions so imprecise that type specimens have to be consulted in order to resolve species identities. Recently, Sharkey et al. (2021) proposed to address the dark taxon impediment for Costa Rican braconid wasps by describing 403 species based on barcode clusters (“BINs”) computed by BOLD Systems. The default assumption of the revision is that BIN=Species (e.g., BOLD:ACM9419 becomes Bracon federicomatarritai Sharkey, sp. nov.) and therefore the diagnoses of most species consist only of a consensus barcode. We here argue that this type of “minimalist revision” is unnecessary and undesirable. It is unnecessary because barcode clusters (e.g. BINs) already provide grouping statements that overcome many of the obstacles associated with dark taxon impediments. However, minimalist revisions are also undesirable and problematic because the diagnoses are only based on one character system – that in the case of Sharkey et al. was poorly analyzed. Furthermore, the revision relies on units that violate basic rules of reproducibility because the BINs were delimited by a proprietary algorithm (RESL) that is applied to a mixture of public and private data. Here, we illustrate that many of the BINs described as species are unstable when the available public data are reanalyzed, reiterate that COI mostly measures time of divergence, and that BOLD Systems violates key principles of open science. We conclude by urging authors, reviewers, editors, and grantors to only publish and fund projects that adhere to modern standards of reproducibility.


1988 ◽  
Vol 62 (2) ◽  
pp. 218-233 ◽  
Author(s):  
John Mark Malinky

Concepts of the family Hyolithidae Nicholson fide Fisher and the genera Hyolithes Eichwald and Orthotheca Novak have been expanded through time to encompass a variety of morphologically dissimilar shells. The Hyolithidae is here considered to include only those hyolithid species which have a rounded (convex) dorsum; slopes on the dorsum are inflated, and the venter may be flat or slightly inflated. Hyolithes encompasses species which possess a low dorsum and a prominent longitudinal sulcus along each edge of the dorsum; the ligula is short and the apertural rim is flared. The emended concept of Orthotheca includes only those species of orthothecid hyoliths which have a subtriangular transverse outline and longitudinal lirae covering the shell on both dorsum and venter.Eighteen species of Hyolithes and one species of Orthotheca from the Appalachian region and Western Interior were reexamined in light of more modern taxonomic concepts and standards of quality for type material. Reexamination of type specimens of H. similis Walcott from the Lower Cambrian of Newfoundland, H. whitei Resser from the Lower Cambrian of Nevada, H. billingsi Walcott from the Lower Cambrian of Nevada, H. gallatinensis Resser from the Upper Cambrian of Wyoming, and H. partitus Resser from the Middle Cambrian of Alabama indicates that none of these species represents Hyolithes. Hyolithes similis is here included under the new genus Similotheca, in the new family Similothecidae. Hyolithes whitei is designated as the type species of the new genus Nevadotheca, to which H. billingsi may also belong. Hyolithes gallatinensis is referred to Burithes Missarzhevsky with question, and H. partitus may represent Joachimilites Marek. The type or types of H. attenuatus Walcott, H. cecrops Walcott, H. comptus Howell, H. cowanensis Resser, H. curticei Resser, H. idahoensis Resser, H. prolixus Resser, H. resseri Howell, H. shaleri Walcott, H. terranovicus Walcott, and H. wanneri Resser and Howell lack shells and/or other taxonomically important features such as a complete aperture, rendering the diagnoses of these species incomplete. Their names should only be used for the type specimens until better preserved topotypes become available for study. Morphology of the types of H.? corrugatus Walcott and “Orthotheca” sola Resser does not support placement in the Hyolitha; the affinities of these species are uncertain.


Phytotaxa ◽  
2016 ◽  
Vol 272 (1) ◽  
pp. 94 ◽  
Author(s):  
ZHONG-SHUAI ZHANG ◽  
XIANG-YUN ZHU ◽  
LING-LU LI ◽  
SHAN-WEN JIANG ◽  
WEN-LI CHEN

Ptilagrostis Grisebach (1852: 447) is a small genus of the grass family, including approximately 11 species (Wu & Phillips 2006, Barkworth 2007). It occurs in both Asia and North America with about eight species distributed in Qinghai-Tibet Plateau, its diversity center. Ptilagrostis yadongensis Keng & Tang (1985: 44) is one of the species that occurs in this region, which was described based on materials from Yadong, China, the southern slope of Himalayas. The paper was published in a Chinese journal, viz. Journal of Southwest Agriculural University, and had not been noticed until 2005 (Peterson et al. 2005, Wu & Phillips 2006). The author pointed out that P. yadongensis is distinguished from its morphological close, Ptilagrostis concinna (Hooker 1897: 230) Roshevitz (1934: 75) by linear panicles with fewer spikelets, longer and unequal glumes, and shorter and glabrous anthers.


Zootaxa ◽  
2021 ◽  
Vol 4933 (4) ◽  
pp. 543-556
Author(s):  
PO-WEI CHEN ◽  
HUI-CONG XIE ◽  
XUE WU ◽  
CHU-ZE SHEN ◽  
ZHU-QING HE

There are 29 species or subspecies in genus Hexacentrus occurring in Asia, Africa and Australia. Because of its similar appearance, it is not easy to distinguish them by traditional methods. In this study, we collected samples and sequenced COI genes from wide range. By reconstructing the gene tree, we found one new species, H. formosanus Chen et He sp. nov., from Taiwan. The new species is similar to H. expansus or H. inflatissimus, but differs from the former in male Cu2 vein of left tegmina curved and slender, and spectrum of male left tegmina slender and subsquare; differs from the later by body size smaller and female tegmina narrow and short. The type specimens are deposited in National Museum of Natural Science, Taichung, Taiwan (NMNS). H. japonicus hareyamai is treated as species level, H. hareyamai stat. nov. 


Phytotaxa ◽  
2018 ◽  
Vol 373 (1) ◽  
pp. 95
Author(s):  
TIM BÖHNERT ◽  
FEDERICO LUEBERT ◽  
MAXIMILIAN WEIGEND

The genus Atriplex Linnaeus (1753: 1052) (Chenopodiaceae Vent.; placed in Amaranthaceae Juss. s. l. in APG IV 2016) comprises about 300 species distributed mainly in subtropical, temperate, and subarctic regions of the world and is mostly adapted to dry conditions on often saline soils (Sukhorukov & Danin 2009, Kadereit et al. 2010, Iamonico 2013, APG IV 2016). The genus is highly diverse in Eurasia, Australia and North America. South America is another centre of diversity with ca. 55 species, 45 of which are considered as native (Brignone et al. 2016). A recent and exhaustive taxonomical synopsis of Atriplex for South America was published by Brignone et al. (2016), but there are also regional taxonomic revisions, e.g., for Chile by Rosas (1989), or Argentina by Múlgura de Romero (1981, 1982 & 1984).


Zootaxa ◽  
2013 ◽  
Vol 3620 (3) ◽  
pp. 483-499 ◽  
Author(s):  
DAVID EVANS WALTER ◽  
SARAH LATONAS

The oribatid mite genus Protoribates Berlese (Haplozetidae) is reviewed for North America and the genus diagnosis is revised to account for the North American species, Protoribates robustior (Jacot, 1937) is redescribed and newly reported from western North America and a new species from Alberta is described. Protoribates haughlandae sp. n. is bisexual, heterotridactylous, and lives primarily in the peat soils of fens and bogs. Protoribates robustior is all-female, monodactylous, and occurs primarily in dry forests or in dry, treeless sites dominated by grasses, sedges, and shrubs. Both species feed on fungal hyphae and spores, but P. haughlandae also is an opportunistic predator and/or necrophage of small arthropods and P. robustior gut contents often include material that resembles plant cell walls. Examination of type specimens confirms that Protoribates prionotus (Woolley, 1968) is a junior synonym of the widespread Protoribates lophotrichus (Berlese, 1904). A key to differentiate Lagenobates from Protoribates and to identify the 7 species of the latter that are known or reported from North America is provided.


Phytotaxa ◽  
2015 ◽  
Vol 212 (1) ◽  
pp. 102
Author(s):  
Lang-Sheng Yang ◽  
Guo-Qing Zhuang

Lilium saccatum S. Y. Liang (1987: 540) was published in the Flora of Xizangica based on the material of Qinghai-Xizang Expedition (No. 74-3754) collected on July 30th, 1974. In the protologue, the author compared this species to L. souliei (Franchet) Sealy (1950: 296) and indicated that the former had basally saccate tepals compared to the latter, and based on this point the new species was recognized. However, the original description and type specimens of L. souliei has already displayed this feature (Fig. 3J–M in Sealy 1950; our Fig. 1A), until now, this feature has not been listed in both the Flora of Reipublicae Popularis Sinicae (Liang 1980), and Flora of China (Liang & Tamura 2000).


2002 ◽  
Vol 76 (1) ◽  
pp. 76-94 ◽  
Author(s):  
Frederick A. Sundberg ◽  
Linda B. McCollum

Kochaspids are an informal group of ptychopariid trilobites that were both abundant and widespread in the early Middle Cambrian of North America. Based on the reassociation of pygidia and cranidia of some kochaspids, Kochiella Poulsen, 1927, is redefined and Hadrocephalites n. gen. is proposed. Hadrocephalites includes taxa previously assigned by Rasetti and Palmer to Schistometopus Resser, 1938a. Schistometopus is considered nomen dubium. Representatives of Kochiella and Hadrocephalites from the Pioche Shale and Carrara Formation of Nevada are described, including the new species Kochiella rasettii, K. brevaspis, Hadrocephalites lyndonensis, and H. rhytidodes. Other kochaspids previously assigned to Kochaspis Resser, 1935; Eiffelaspis Chang, 1963; Schistometopus; and Kochiella are discussed and some are reassigned. The type specimens of Kochiella augusta (Walcott, 1886); K. crito (Walcott, 1917b); K. chares (Walcott, 1917a); K. mansfieldi Resser, 1939; K. arenosa Resser, 1939; Hadrocephalites carina (Walcott, 1917b), and H. cecinna (Walcott, 1917b) are re-illustrated.


Zootaxa ◽  
2020 ◽  
Vol 4809 (1) ◽  
pp. 111-131
Author(s):  
STEVEN FEND ◽  
PILAR RODRIGUEZ

Four new species of the lumbriculid genus Eremidrilus Fend & Rodriguez, 2003 are described from Idaho, Montana, and New Mexico. The new species all have a filiform proboscis, club-shaped atria in X, each with two functional vasa deferentia, and spermathecae paired in both XI and XII. Male pores of Eremidrilus artzaini n. sp., E. humboldti n. sp., and E. gilita n. sp. are all associated with distinctive porophores, but these structures are absent in E. montanensis n. sp. The new species are easily distinguished from California Eremidrilus species, all of which have spermathecae only in XI. New observations of type specimens of Eremidrilus allegheniensis (Cook, 1971), a species with two spermathecal segments, known only from eastern USA, confirm differences in atrial morphology, and also document unusual spermathecal porophores and ventral glands. 


Zootaxa ◽  
2020 ◽  
Vol 4748 (1) ◽  
pp. 182-194 ◽  
Author(s):  
JING ZHANG ◽  
ERNST BROCKMANN ◽  
QIAN CONG ◽  
JINHUI SHEN ◽  
NICK V. GRISHIN

We obtained whole genome shotgun sequences and phylogenetically analyzed protein-coding regions of representative skipper butterflies from the genus Carcharodus Hübner, [1819] and its close relatives. Type species of all available genus-group names were sequenced. We find that species attributed to four exclusively Old World genera (Spialia Swinhoe, 1912, Gomalia Moore, 1879, Carcharodus Hübner, [1819] and Muschampia Tutt, 1906) form a monophyletic group that we call a subtribe Carcharodina Verity, 1940. In the phylogenetic trees built from various genomic regions, these species form 7 (not 4) groups that we treat as genera. We find that Muschampia Tutt, 1906 is not monophyletic, and the 5th group is formed by currently monotypic genus Favria Tutt, 1906 new status (type species Hesperia cribrellum Eversmann, 1841), which is sister to Gomalia. The 6th and 7th groups are composed of mostly African species presently placed in Spialia. These groups do not have names and are described here as Ernsta Grishin, gen. n. (type species Pyrgus colotes Druce, 1875) and Agyllia Grishin, gen. n. (type species Pyrgus agylla Trimen, 1889). Two subgroups are recognized in Ernsta: the nominal subgenus and a new one: Delaga Grishin, subgen. n. (type species Pyrgus delagoae Trimen, 1898). Next, we observe that Carcharodus is not monophyletic, and species formerly placed in subgenera Reverdinus Ragusa, 1919 and Lavatheria Verity, 1940 are here transferred to Muschampia. Furthermore, due to differences in male genitalia or DNA sequences, we reinstate Gomalia albofasciata Moore, 1879 and Gomalia jeanneli (Picard, 1949) as species, not subspecies or synonyms of Gomalia elma (Trimen, 1862), and Spialia bifida (Higgins, 1924) as a species, not subspecies of Spialia zebra (Butler, 1888). Sequencing of the type specimens reveals 2.2-3.2% difference in COI barcodes, the evidence that combined with wing pattern differences suggests a new status of a species for Spialia lugens (Staudinger, 1886) and Spialia carnea (Reverdin, 1927), formerly subspecies of Spialia orbifer (Hübner, [1823]). 


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