Amphipoda of the Atlantic and Arctic Coasts of North America: Anonyx (Lysianassidae)

1968 ◽  
Vol 25 (5) ◽  
pp. 943-1060 ◽  
Author(s):  
Donald H. Steele ◽  
Pierre Brunel

In place of the widely ranging, abundant, and variable species Anonyx nugax, previously recorded from Canadian Atlantic and Arctic waters, eight less variable species of this genus are here recognized, one of which (sarsi) is new to science. Detailed descriptions, figures, distribution maps and a key applying to all sizes are given. The study of the species is based on examination of available type-specimens and the use of new characters. The systematics of the genus is discussed in a chronological review of all the relevant literature, and the status of several species is revised.Since the young of large and small species are similar among themselves, and have sometimes been wrongly described as distinct species, they are also described and illustrated at two sizes. Mature males are distinguished by elongated second antennae equipped with calceoli, in most species by the armature of the second and third uropods, and sometimes by their enlarged eyes.Three species are characterized by a row of spines accompanying single setae on the hind margin of segment 6 of peraeopods 3–4, and by a rather unprominent upper lip. One may distinguish them as follows. The large (> 33 mm) A. laticoxae has short spines on peraeopods 3–4, an anteriorly well-expanded first coxa, and an unconstricted short-spined inner ramus of uropod 2. Anonyx compactus is smaller (12–17 mm), has one elongated ventral spine on each of the first two flagellar segments of antenna 1, a posterior projection marked off by an angle from the lateral plate of metasome segment 3, a strongly parachelate peraeopod 1 with a perpendicular palm, and a fairly strongly subchelate peraeopod 2. Anonyx sarsi is of medium size (20–31 mm), has a very low and unprominent upper lip and, on the outer ramus of uropod 2, small similar-sized spines on the proximal two-thirds of the inner margin (no such spines in laticoxae and compactus); the female has tufts instead of a row of setae on the dorsal margin of the fourth peduncular segment of antenna 2, but otherwise the species is morphologically similar to A. nugax.The other five species are characterized by a row of pairs of long setae on the hind margin of segment 6 of peraeopods 3–4 and, except nugax, have a rather prominent upper lip. Except in ochoticus and lilljeborgi, uropod 2 bears spines on the inner margin of its outer ramus. Anonyx ochoticus is the smallest (9–11 mm) species, and has on urosome segment 1 a prominent dorsal keel well overlapping the next urosome segments. Anonyx debruyni, rather small (15–21 mm), has a parachelate peraeopod 1 with an oblique palm, a very strongly subchelate peraeopod 2, most prominent and pointed upper lip and interantennal angle, and, on the outer ramus of uropod 2, only two small spines on the distal half of the inner margin. Anonyx lilljeborgi is small (9–18 mm), has a very prominent but high and usually evenly rounded upper lip, a concave cephalic ventral margin (like debruyni), and a lateral plate of metasome segment 2 with a nearly toothless postero-ventral corner. Anonyx nugax is the largest (31–44 mm) species, with a little-projecting upper lip, a prominent tooth at the postero-ventral corner of metasome lateral plate 2, a short posterior projection, with a nearly straight ventral margin, on the lateral plate of metasome segment 3 and, on the inner margin of the outer ramus of uropod 2, a row of similar-size small spines not extending into the distal third of the ramus. Anonyx pacificus is also large (27–34 mm) and similar to nugax, but differs in the more prominent and pointed upper lip, the longer and ventrally concave posterior projection on metasome lateral plate 3, and, on the outer ramus of uropod 2, spines which increase in size distally and reach into the distal third of the inner margin.Three species, nugax, lilljeborgi, and sarsi, have a circumpolar arctic-boreal distribution, the latter chiefly in shallow water (< 50 m). Four (pacificus, laticoxae, ochoticus, and compactus) are colder-water forms apparently of Pacific origin and all new for the North Atlantic. The distribution of debruyni is uncertain.

1993 ◽  
Vol 50 (3) ◽  
pp. 249-364 ◽  
Author(s):  
K. A. Kron

Rhododendron sect. Pentanthera G. Don (Ericaceae) comprises a group of closely related, highly ornamental plants which are commonly called ‘azaleas'. Thirteen of the fifteen species recognized in this section are indigenous to North America. One species (R. molle) is native to Japan and China, and one species (R. luteum) is indigenous to the Caucasus region. Phylogenetic analysis of the species within the section indicates that R. molle is the sister to the rest of the section. It is the sole member of R. subsect. Sinensia. The remaining species form a monophyletic group recognized as R. subsect. Pentanthera. Within this subsection the presence of a blotch on the upper corolla lobe defines two primarily orange to red-flowered groups. The first group has a Tertiary Period disjunct distribution and comprises R. luteum, R. austrinum and R. occidentale. The second group is indigenous to eastern North America and comprises R. calendulaceum, R. cumberlandense, R. flammeum, R. prunifolium and R. alabamense. In both groups the cladistically basal species has white flowers with a yellow blotch on the upper corolla lobe (R. occidentale, R. alabamense, respectively). The pink to white early flowering species R. canescens, R. periclymenoides and R. prinophyllum do not form a monophyletic group.Phenetic analyses indicate that the eastern Asian taxon, R. molle, is best recognized as one species with two geographical subspecies; Rhododendron prinophyllum is quite distinct from R. canescens and R. periclymenoides. The latter two species are very similar morphologically, but their similarities are due to the retention of primitive characters and they should be recognized as distinct species. Rhododendron calendulaceum can be distinguished from R. cumberlandense using a combination of morphological and phenological characters. The various taxa previously segregated out of R. viscosum are merely extreme forms of a widespread and variable species and are not given any formal rank. No subspecific taxa are recognized for R. occidentale. Distribution maps, keys to the species, species descriptions and specimen citations are included.


Phytotaxa ◽  
2014 ◽  
Vol 181 (5) ◽  
pp. 261 ◽  
Author(s):  
Leonardo Maurici Borges ◽  
José Rubens Pirani

Megadiverse genera usually have a complex taxonomy. One factor influencing this complexity is concerned to synonyms, which are often numerous in widespread and morphologically variable species. In this article we examined the case of Mimosa longepedunculata and M. tocantina, two sympatric narrowly distributed species from central Brazil, considered to be synonyms in Barneby’s monograph. We show that this was an inaccurate taxonomic decision related to a misinterpretation of the type specimens and, possibly, also to sampling biases in field works. The definition of each species is here clarified and M. tocantina is reestablished and considered a distinct species from M. longepedunculata, having M. pseudosetosa as a new synonym. A regional identification key for the species is provided together with data on distribution and habitat, flowering and fruiting, conservation status, etymology, and notes on morphology. Illustrations, pictures and a full description of M. longepedunculata are also presented.


Plants ◽  
2021 ◽  
Vol 10 (5) ◽  
pp. 868
Author(s):  
Grzegorz J. Wolski ◽  
Samar Nour-El-Deen ◽  
Alicja Cienkowska ◽  
Daniel Bożyk ◽  
Wagieh El-Saadawi

An annotated checklist of the pleurocarpous moss genus Plagiothecium in Eurasia is presented for the first time based on a thorough review of the literature. Data have been compiled from previous relevant works conducted on the genus over more than 70 years and published up to the end of June 2020 for 107 Eurasian countries (and islands). Sectional classification is based on molecular phylogeny of the genus published recently. A total of 41 taxa are reported, including 29 species and 12 infraspecific taxa (nine varieties and three forms) belonging to eight sections. The highest numbers of taxa were found in China (20 taxa), the Russian Federation (20 taxa) and Japan (18 taxa), while the smallest numbers of taxa were recorded in the Middle East, Central Asia and the islands area. Not a single species of Plagiothecium was recorded in 26 regions, whereas P. denticulatum, P. nemorale and P. cavifolium turned out to be the most widespread species in the entire study area. They were recorded in most of the surveyed countries and islands. For each accepted taxon, information on relevant literature, synonyms, distribution within Eurasia and globally are provided. Comments on each taxon, ecological preferences, and notes on doubtful records are also included. Additionally, distribution maps for each recognised taxon are supplied. This checklist can enlighten and foster a better understanding of the distribution, diversity, and ecology of Plagiothecium in Eurasia and provides an incentive for future research on the genus.


Phytotaxa ◽  
2022 ◽  
Vol 531 (1) ◽  
pp. 54-62
Author(s):  
SHUI-HU JIN ◽  
YI-FEI LU ◽  
WEI-JIE CHEN ◽  
XIAO-FENG JIN

Based on literature survey, examination of type specimens and fieldwork, seven names of Carex are synonymized in the present paper: viz. Carex hypoblephara reduced to a synonym of C. glossostigma; C. dayunshanensis and C. wuyishanensis to synonyms of C. graciliflora; C. dolichogyne to a synonym of C. truncatigluma; C. kwangtoushanica to a synonym of C. tatsiensis; and C. martini to a synonym of C. rhynchophora. The holotype of Carex fokienensis is identified and confirmed at P. The putative endemic species Carex macrosandra (basionym: C. lanceolata var. macrosandra) is synonymized to C. lanceolata, whereas C. cavaleriensis, considered a synonym of the former, is here recognized as a distinct species. A lectotype is designated for C. lanceolata var. macrosandra.


2011 ◽  
Vol 9 (4) ◽  
pp. 709-730 ◽  
Author(s):  
Alejandro Londoño-Burbano ◽  
César Román-Valencia ◽  
Donald C. Taphorn

We review species of Parodon Valenciennes, 1850 from the Magdalena, Cauca, Orinoco, Amazonas, Atrato and Caribbean-Guajira River basins of Colombia using meristic and morphological characters. We recognize eight valid species, five previously described: P. apolinari Myers, from the Orinoco River basin; P. buckleyi Boulenger and P. pongoensis (Allen) from the upper Amazon; P. caliensis Boulenger, from the upper Cauca River drainage; and P. suborbitalis Valenciennes, from Lake Maracaibo basin. Three new species are described: P. alfonsoi, from the lower Magdalena River drainage; P. magdalenensis, from the middle Magdalena and upper Cauca River drainages; and P. atratoensis, from the Atrato River basin. We redescribe Parodon suborbitalis using type specimens and topotypes, and designate lectotypes. A taxonomic key is included for identification of the species, as well as geographic distribution maps.


Zootaxa ◽  
2017 ◽  
Vol 4358 (2) ◽  
pp. 271 ◽  
Author(s):  
VIRIDIANA LIZARDO ◽  
FEDERICO ESCOBAR ◽  
OCTAVIO ROJAS-SOTO

In this study, we systematized available distribution data, obtained from biological databases and relevant literature, for Mexican species belonging to the tribe Phanaeini. The main objectives were to provide an overall description of the distribution records in biological collections, to detect potential sampling biases, to describe the seasonality of collections and to obtain species distribution models using the Desktop GARP algorithm. A total of 5,562 records, corresponding to 32 species in Mexico, were compiled, including the recently described Phanaeus zoque Moctezuma & Halffter, 2017. This compilation includes 784 unique collection records at 325 localities. These records were mainly distributed along the Trans-Mexican Volcanic Belt, the Sierra Madre Oriental and Sierra Madre Occidental mountain ranges and throughout the states of Chiapas and Veracruz. The Mexican High Plateau, the state of Tlaxcala and the Yucatan Peninsula are lacking in records. Distribution maps were created for species of three genera (Phanaeus MacLeay, 1819, Coprophanaeus Olsoufieff, 1924, and Sulcophanaeus Olsoufieff, 1924) and for 29 species present in Mexico. These species distributions are largely delimited by geomorphological features and vegetation types and coincide with expert descriptions of this tribe; some species show expanded distribution ranges. These maps provide a starting point for further analyses, the planning of future field studies, and the verification of possible new species in the Mexican territory. 


2002 ◽  
Vol 13 (3) ◽  
Author(s):  
Jens-Peter Kopelke

Euura auritae and Euura cinereae are distinct species making spindle-shaped stem galls on Salix aurita and on Salix cinerea, respectively. Different morphological criteria and no-choice as well as multiple choice oviposition experiments have proved E. auritae and E. cinereae to be distinct species. Euura cinereae on S. cinerea is distributed at least over Southern Norway, Germany and Austria, but within its distribution area it may occur patchily. A recent paper doubted that the type specimens of E. cinereae had been reared from S. cinerea, but rather that they had been reared from S. aurita. However, as discussed in the present paper, they give no convincing evidence that E. cinereae occurs on S. aurita rather than on S. cinerea in Finland.


Bothalia ◽  
1992 ◽  
Vol 22 (1) ◽  
pp. 59-57 ◽  
Author(s):  
N. E. Helme ◽  
H. P. Linder

Wachendorfia Burm. is a small genus endemic to the Cape Floral Region. Pour species are recognised in this study. Two species were originally described by Burman in 1757 and these were followed by numerous other descriptions of what is essentially one very variable species  (W. paniculaia Burm.). This variation is discussed and reasons are given as to why the recognition of formal infraspecific taxa is inappropriate. Formal taxonomic descriptions, distribution maps and a key to the species are provided. Rhizome morphology, leaf anatomy and pollen and seed coat structures were investigated and illustrations are provided. A cladogram was inferred and this is consistent with an ecological speciation model for the genus. The two species with the most restricted distribution (W. brachyandra W.F. Barker and W. pamfiora W.F. Barker) are considered to be the most recently evolved. Features of systematic and ecological interest (e.g. floral enantiomorphy) are discussed.


Bothalia ◽  
1971 ◽  
Vol 10 (3) ◽  
pp. 419-426
Author(s):  
J. H. Ross

Recently Brenan. in Kew Bull. 21 : 477-480 (1968). upheld  Acacia brevispica Harms and A. schweinfurthii Brenan Exell as distinct species and recognized two subspecies within A. brevispica. These conclusions differ from earlier results published by Ross Gordon- Gray in Brittonia 18: 44-63 (1966). Consequently it was considered necessary to re-examine these species in preparation for the account of  Acacia for the Flora of Southern Africa. Distribution maps of the two species are provided and the differences between the species tabulated and discussed. Despite certain difficulties in Natal. Brenan's taxonomic conclusions are adopted. A map showing the distribution of  A. schweinfurthii and  A. brevispica subsp. dregeana in Natal is provided and a selection of Natal specimens cited.


Zootaxa ◽  
2010 ◽  
Vol 2510 (1) ◽  
pp. 55 ◽  
Author(s):  
EDUARDO SUAREZ-MORALES

Specimens of monstrilloid copepods collected and described in the early 20 th century by G.O. Sars from the coasts of Norway and deposited in the Sars Collection (University of Oslo) were re-examined. Monstrilla leucopis Sars, 1921 was described based on female and male specimens, but the species was later synonymized with M. conjunctiva Giesbrecht, 1902 by several authors. Females of this species were analyzed and compared with closely related congeners, particularly with M. conjunctiva. This analysis includes the description of previously unknown morphological details following upgraded descriptive standards in this group. Evidence was found to support the notion that the female type specimens from Kvalø, Norway represent a distinct species; thus, M. leucopis is redescribed and reinstated as a valid taxon. Previous tropical records of female M. conjunctiva are questionable, but differences with M. leucopis can be found in body and antennule proportions, the structure of the genital spines and fifth legs, and most probably, their geographical ranges. Furthermore, M. leucopis has a modified thick-walled seta on the endopods of legs 2–4, so far a unique character among monstrilloids. The single male specimen labeled as M. leucopis in the Sars Collection was also examined and it is not the male of this species as depicted by G.O. Sars (1921). It is in fact a male of M. longiremis Giesbrecht, 1893, a species for which a short supplementary description and taxonomic comments are also provided herein. The male of M. leucopis also shares some important characters with that of M. conjunctiva, but also with another male specimen that was questionably assigned to the latter species; this male probably represents an undescribed species.


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