Revision of the milliped genus Auturus (Polydesmida: Platyrhacidae)

1982 ◽  
Vol 60 (12) ◽  
pp. 3249-3267 ◽  
Author(s):  
Rowland M. Shelley

The milliped genus Auturus consists of the valid species evides (Bollman), mcclurkini Causey, louisianus (Chamberlin), and erythropygos (Brandt), the last two of which are divided into two subspecies each. The other four nominal species are relegated to appropriate synonymies. Auturus evides, louisianus, and mcclurkini occur in the central United States, along the Mississippi River from central Minnesota to the Gulf of Mexico. Auturus erythropygos is widely allopatric and occurs in the southeastern United States from northern North Carolina to northern Florida. The four species are anatomically similar, and all occur exclusively in association with moist, decaying hardwood logs or stumps. They can be distinguished only by details of the male gonopods, particularly the orientation of the terminal calyx and the position of the solenomerite within the calyx. Auturus evides, louisianus, and erythropygos are phenotypically similar and appear to be closely related; mcclurkini, however, possesses a number of unique characters and represents a separate line of descent. The genus Illiniums, recently synonymized with Auturus, is revived on the basis of published illustrations of its type species, I. beattyi Shear.

Zootaxa ◽  
2009 ◽  
Vol 2243 (1) ◽  
pp. 53-56 ◽  
Author(s):  
IVAN MARIN

The palaemonoid family Anchistioididae Borradaile, 1915 includes a single genus Anchistioides Paulson, 1875 with four known valid species: Anchistioides compressus Paulson, 1875 (type species), A. willeyi (Borradaile, 1899), A. australiensis (Balss, 1921) and A. antiguensis (Schmitt, 1924). Borradaile (1915) suggested two more species within the genus Amphipalaemon Nobili, 1901 (a junior synonym of Anchisitioides Paulson), Amphipalaemon gardineri Borradaile, 1915 (= Anchistioides gardineri) and Amphipalaemon cooperi Borradaile, 1915 (= Anchistioides cooperi) which were later synonomyzed with Anchisitioides willeyi by Gordon (1935), who also suggested their conspecificity with Anchistioides australiensis. At the present time, Anchistioides australiensis is a valid species (Bruce, 1971; Chace & Bruce, 1993) based on specific morphological features such as the presence of sharp postorbital tooth, oblique distal lamela of scaphocerite and sharply produced spines on posterodorsal angles of sixth abdominal somite (see Bruce, 1971: fig. 9). The other Indo-Pacific species, Anchistioides compressus and A. willeyi, can be clearly identified by specific form of scaphocerite, the presence of a well marked blunt postorbital tubercle in A. willeyi which is absent in A. compressus (e.g., Bruce, 1971) and the number of ventral rostral teeth (3-4 large ventral rostral teeth present in A. willeyi while up to 8 small ventral rostral teeth in A. compressus (Paulson, 1875; Gordon, 1935)). Anchistioides antiguensis is clearly separated geographically being known only from the tropical Western Atlantic and Caribbean region (Schmitt, 1924; Holthuis, 1951; Wheeler & Brown, 1968; Martinez-Iglesias, 1986; Markham et al, 1990; Ramos-Porto et al, 1998; Cardoso, 2006).


2013 ◽  
Vol 145 (6) ◽  
pp. 603-625 ◽  
Author(s):  
Mar Ferrer-Suay ◽  
Jesús Selfa ◽  
Juli Pujade-Villar

AbstractAlloxysta Förster, 1869 (Hymenoptera: Figitidae) type material of 19 nominal species deposited in the Canadian National Collection of Insects (Ottawa, Ontario, Canada) and the United States National Museum of Natural History (Washington, District of Columbia, United States of America) were studied. Nine species are treated as valid: A. australiae (Ashmead, 1900), A. commensuratus Andrews, 1978, A. japonicus (Ashmead, 1904), A. lachni (Ashmead, 1885), A. longiventris Baker, 1896, A. minuscula Andrews, 1978, A. nothofagi Andrews, 1976, A. vandenboschi Andrews, 1978, and A. xanthopsis (Ashmead, 1896). The following synonymies are established: A. affinis (Baker, 1896) and A. quebeci Andrews, 1978 junior synonyms of A. castanea (Hartig, 1841); A. alaskensis Ashmead, 1902 and A. coniferensis Andrews, 1978 junior synonyms of A. macrophadna (Hartig, 1841); A. bicolor (Baker, 1896) and A. anthracina Andrews, 1978 junior synonyms of A. obscurata (Hartig, 1840); A. dicksoni Andrews, 1978 junior synonym of A. pilipennis (Hartig, 1840); and A. leguminosa (Weld, 1920), A. megourae (Ashmead, 1887), and A. rauchi Andrews, 1978 junior synonyms of A. brevis (Thomson, 1862). The type material of A. schlingeri Andrews, 1978 and A. halli Andrews, 1978 could not be found and we consider them as nomina dubia. Alloxysta vandenboschi Andrews is removed from synonymy with A. obscurata and considered a valid species. Comments on the type material are given. Complete redescriptions and images are presented for the valid species.


Weed Science ◽  
1996 ◽  
Vol 44 (3) ◽  
pp. 575-578 ◽  
Author(s):  
Barry J. Brecke ◽  
Piotr Tobola

Wild poinsettia is a serious weed in several crops, including peanut, grown in the southeastern United States. A study was conducted over 3 yr at Jay, FL, to characterize the growth and development of wild poinsettia grown from seed collected at Plains, GA; Marianna, FL; and Baton Rouge, LA. Seedlings from each selection were transplanted to the field and were grown either alone or in competition with peanut. Observations made throughout the growing season indicated that the Louisiana selection flowered later, grew to a larger size, produced more leaf area and biomass, and caused greater light attenuation and peanut yield reduction than the other two selections. The Georgia selection produced the smallest plants, least leaf area and biomass, and was least competitive with peanut. The Florida selection was intermediate for these parameters. Wild poinsettia dry biomass production was reduced by 78 to 83% when grown with peanut compared with monoculture wild poinsettia.


2019 ◽  
Vol 34 (2) ◽  
pp. 467-479 ◽  
Author(s):  
Ryan C. Bunker ◽  
Ariel E. Cohen ◽  
John A. Hart ◽  
Alan E. Gerard ◽  
Kim E. Klockow-McClain ◽  
...  

Abstract Tornadoes that occur at night pose particularly dangerous societal risks, and these risks are amplified across the southeastern United States. The purpose of this study is to highlight some of the characteristics distinguishing the convective environment accompanying these events. This is accomplished by building upon previous research that assesses the predictive power of meteorological parameters. In particular, this study uses the Statistical Severe Convective Risk Assessment Model (SSCRAM) to determine how well convective parameters explain tornado potential across the Southeast during the months of November–May and during the 0300–1200 UTC (nocturnal) time frame. This study compares conditional tornado probabilities across the Southeast during November–May nocturnal hours to those probabilities for all other November–May environments across the contiguous United States. This study shows that effective bulk shear, effective storm-relative helicity, and effective-layer significant tornado parameter yield the strongest predictability for the November–May nocturnal Southeast regime among investigated parameters. This study demonstrates that November–May southeastern U.S. nocturnal predictability is generally similar to that within other regimes across the contiguous United States. However, selected ranges of multiple parameters are associated with slightly better predictability for the nocturnal Southeast regime. Additionally, this study assesses conditional November–May nocturnal tornado probabilities across a coastal domain embedded within the Southeast. Nocturnal coastal tornado predictability is shown to generally be lower than the other regimes. All of the differences highlight several forecast challenges, which this study analyzes in detail.


Author(s):  
Malinda Maynor Lowery

The Lumbee tribe of North Carolina, including approximately 55,000 enrolled members, is the largest Indian community east of the Mississippi River. Lumbee history serves as a window into the roles that Native people have played in the struggle to implement the founding principles of the United States, not just as “the First Americans,” but as members of their own nations, operating in their own communities’ interests. When we see US history through the perspectives of Native nations, we see that the United States is not only on a quest to expand rights for individuals. Surviving Native nations like the Lumbees, who have their own unique claims on this land and its ruling government, are forcing Americans to confront the ways in which their stories, their defining moments, and their founding principles are flawed and inadequate. We know the forced removals, the massacres, the protests that Native people have lodged against injustice, yet such knowledge is not sufficient to understand American history. Lumbee history provides a way to honor, and complicate, American history by focusing not just on the dispossession and injustice visited upon Native peoples, but on how and why Native survival matters. Native nations are doing the same work as the American nation—reconstituting communities, thriving, and finding a shared identity with which to achieve justice and self-determination. Since the late 19th century, Lumbee Indians have used segregation, war, and civil rights to maintain a distinct identity in the biracial South. The Lumbees’ survival as a people, a race, and a tribal nation shows that their struggle has revolved around autonomy, or the ability to govern their own affairs. They have sought local, state, and federal recognition to support that autonomy, but doing so has entangled the processes of survival with outsiders’ ideas about what constitutes a legitimate Lumbee identity. Lumbees continue to adapt to the constraints imposed on them by outsiders, strengthening their community ties through the process of adaptation itself. Lumbee people find their cohesion in the relentless fight for self-determination. Always, that struggle has mattered more than winning or losing a single battle.


Zootaxa ◽  
2007 ◽  
Vol 1418 (1) ◽  
pp. 1-628 ◽  
Author(s):  
CARL J. FERRARIS

A checklist of Recent and fossil catfishes (Order Siluriformes) is presented, summarizing taxonomic literature published through 2005. From 4624 nominal species group names and 810 genus group names, 3093 species are recognized as valid, and are distributed among 478 genera and 36 families. Distributional summaries are provided for each species, and nomenclatural synonymies, including relevant information on all name-bearing types, are included for all taxa. One new name is proposed herein: Clariallabes teugelsi, as a replacement for Clarias (Allabenchelys) dumerili longibarbis David & Poll, 1937, which is preoccupied by Clarias longibarbis Worthington, 1933, but has been treated as a valid species of Clariallabes by Teugels. Acrochordonichthys melanogaster Bleeker, 1854, is designated as type species of Acrochordonichthys Bleeker, 1857, inasmuch as no earlier valid designation has been found. A new genus Pseudobagarius, is proposed for the “pseudobagarius group” of species formerly placed in Akysis. The status of 228 species group names remains unresolved and 31 names based on otoliths ascribed to catfishes are listed but not placed into the checklist. The current emphasis given to catfish taxonomy at present is likely to result in a dramatic increase in the total number of valid taxa as well as major changes in the membership of some of the higher level taxa recognized here.


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