Direction of dispersion of cochineal (Dactylopius coccus Costa) within the Americas

Antiquity ◽  
2001 ◽  
Vol 75 (287) ◽  
pp. 73-77 ◽  
Author(s):  
Luis C. Rodríguez ◽  
Marco A. Méndez ◽  
Hermann M. Niemeyer
Keyword(s):  
Phylogenetic Analysis ◽  
North America ◽  
South America ◽  
Natural Dyes

Dactylopius coccus has been used in Mexico and Peru as a source of natural dyes since pre-Columbian times. A phylogenetic analysis of the genus Dactylopius, and the disjoint distribution of D. coccus, suggest that the origin of D. coccus is South America and was introduced into North America by sea routes.

scholarly journals The first phylogenetic analysis of Palpigradi (Arachnida) – the most enigmatic arthropod order

2014 ◽  
Vol 28 (4) ◽  
pp. 350 ◽  
Author(s):  
Gonzalo Giribet ◽  
Erin McIntyre ◽  
Erhard Christian ◽  
Luis Espinasa ◽  
Rodrigo L. Ferreira ◽  
...  
Keyword(s):  
Phylogenetic Analysis ◽  
North America ◽  
South America ◽  
Molecular Phylogeny ◽  
Long Range ◽  
Analytical Method ◽  
Ribosomal Genes ◽  
Point Of View ◽  
Two Alternatives

Palpigradi are a poorly understood group of delicate arachnids, often found in caves or other subterranean habitats. Concomitantly, they have been neglected from a phylogenetic point of view. Here we present the first molecular phylogeny of palpigrades based on specimens collected in different subterranean habitats, both endogean (soil) and hypogean (caves), from Australia, Africa, Europe, South America and North America. Analyses of two nuclear ribosomal genes and COI under an array of methods and homology schemes found monophyly of Palpigradi, Eukoeneniidae and a division of Eukoeneniidae into four main clades, three of which include samples from multiple continents. This supports either ancient vicariance or long-range dispersal, two alternatives we cannot distinguish with the data at hand. In addition, we show that our results are robust to homology scheme and analytical method, encouraging further use of the markers employed in this study to continue drawing a broader picture of palpigrade relationships.

scholarly journals Phylogeny and biogeography of some Cretaceous spatangoid echinoids with special emphasis on taxa from the Western Interior Seaway

2020 ◽  
pp. 1-11
Author(s):  
Steven Byrum ◽  
Bruce S. Lieberman
Keyword(s):  
Phylogenetic Analysis ◽  
North America ◽  
South America ◽  
Sea Level ◽  
North Africa ◽  
Marine Invertebrate ◽  
Western Interior Seaway ◽  
Biogeographic Patterns ◽  
Family Level ◽  
Character Matrix

Abstract Members of the echinoid order Spatangoida, a highly diverse and abundant marine invertebrate clade, were important denizens of the Cretaceous Western Interior Seaway (WIS), an epicontinental seaway that divided North America in two during an interval of greenhouse conditions between roughly 100 and 65 million years ago. A phylogenetic analysis of spatangoids was conducted using a character matrix of 32 characters from 21 species. Species that occur in the WIS were considered comprehensively, and species from other regions such as South America, Europe, and North Africa were also incorporated into the analysis. Phylogenetic patterns retrieved are largely congruent with preexisting family-level classifications; however, species within several genera, especially Hemiaster and Heteraster, need to be reassigned so that classification better reflects phylogeny. The genera Washitaster and Heteraster are closely related, as are Mecaster, Palhemiaster, and Proraster; Pliotoxaster, Macraster, and Hemiaster; and Micraster and Diplodetus. Biogeographic patterns were also considered using the phylogeny, and several episodes of vicariance and range expansion were identified. These were possibly related to some of the various major episodes of sea-level rise and fall during the Cretaceous. In particular, Valangian–mid-Aptian regressions may have caused vicariance within Heteraster and Washitaster while other early spatangoid vicariance may be related to regressions during the late Aptian–early Cenomanian. Further, vicariance caused by regressions during the mid-Cenomanian–Maastrichtian may have driven diversification within Micraster and Diplodetus. Last, transgressions during the late Aptian–early Cenomanian seem to have spurred prominent range expansions in Mecaster and Hemiaster.

Effects of insecticides on adults and eggs of Drosophila suzukii (Diptera, Drosophilidae)

2017 ◽  
Vol 43 (2) ◽  
pp. 208 ◽  
Author(s):  
Daniele Cristine Hoffmann Schlesener ◽  
Jutiane Wollmann ◽  
Juliano De Bastos Pazini ◽  
Anderson Dionei Grützmacher ◽  
Flávio Roberto Mello Garcia
Keyword(s):  
North America ◽  
South America ◽  
Chemical Control ◽  
Stone Fruits ◽  
Drosophila Suzukii ◽  
Ovicidal Effect ◽  
Mere Presence ◽  
South Of Brazil ◽  
Different Cultures ◽  
First Time

Drosophila suzukii (Diptera, Drosophilidae) is an exotic species, endemic to Asia and currently a pest to small and stone fruits in several countries of North America and Europe. It was detected in 2013 for the first time in South America, in the south of Brazil. Unlike most drosophilids, this species deserves special attention, because the females are capable of oviposit inside healthy fruits, rendering their sale and export prohibited. Despite the confirmed existence of this species in different states of Brazil, this insect is yet been to be given the pest status. Nevertheless, the mere presence of this species is enough to cause concern to producers of small fruits and to justify further investigation for it’s control, especially chemical control for a possible change in status. Therefore, the goal of this work was to evaluate, in laboratory, mortality of D. suzukii adults and ovicidal effect when exposed to different insecticides registered for species of the Tephritidae and Agromyzidae families in different cultures. The insecticides deltamethrin, dimethoate, spinosad, fenitrothion, phosmet, malathion, methidathion, and zeta-cypermethrin resulted in mortality to 100 % of the subjects three days after the treatment (DAT). Regarding the effects over eggs, it was  established that the insecticides fenitrothion, malathion, and methidathion deemed 100 % of the eggs not viable, followed by phosmet and diflubenzuron, which also caused elevated reduction in the eclosion of larvae two DAT.

Phylogenetic analysis of Foot-and-Mouth Disease Virus type O circulating in the Andean region of South America during 2002–2008

2011 ◽  
Vol 152 (1-2) ◽  
pp. 74-87 ◽  
Author(s):  
Viviana Malirat ◽  
Ingrid Evelyn Bergmann ◽  
Renata de Mendonça Campos ◽  
Gustavo Salgado ◽  
Camilo Sánchez ◽  
...  
Keyword(s):  
Phylogenetic Analysis ◽  
South America ◽  
Disease Virus ◽  
Virus Type ◽  
Foot And Mouth Disease ◽  
Mouth Disease ◽  
Andean Region ◽  
Mouth Disease Virus ◽  
Foot And Mouth ◽  
Disease Virus Type

BIOSYSTEMATIC STUDIES ON XANTHIUM: TAXONOMIC APPRAISAL AND ECOLOGICAL STATUS

1959 ◽  
Vol 37 (2) ◽  
pp. 173-208 ◽  
Author(s):  
Doris Löve ◽  
Pierre Dansereau
Keyword(s):  
North America ◽  
South America ◽  
Ecological Status ◽  
Distinct Species ◽  
Eastern North America ◽  
Flowering Response ◽  
Short Day ◽  
Stable Species ◽  
Enormous Variation

The following paper is an evaluation of the taxonomic and ecological status of the genus Xanthium L. A review of its systematics demonstrates that many so-called "species" described on material from Europe actually have their origin in America, except one, X. strumarium s. str., which seems to have a Mediterranean–European center of dispersal. Another conclusion drawn is that Xanthium consists of only two distinct species: X. spinosum L. and X. strumarium L. The former is a relatively stable species, the latter an enormously variable one readily subdivided into a number of minor taxonomic entities.Ecologically, in eastern North America at least, Xanthium is primarily a beach plant, which prefers open habitats and succumbs to crowding. The seeds are most often dispersed by water and wind. It enters easily into ruderal habitats, but only as long as these are open and unshaded.The generalized short-day flowering response in this genus supports our hypothesis that Xanthium has a tropical–subtropical origin, and we feel that it has its center in Central and/or South America, whence it has spread over the continents north and southward.There is no evidence for any sterility barriers separating the entities of X. strumarium, but we feel that an intense inbreeding with an occasional outbreeding is responsible for the enormous variation, often resulting in small, local, but unstable taxa.

Revised circumscription of Nothofagus and recognition of the segregate genera Fuscospora, Lophozonia, and Trisyngyne (Nothofagaceae)

Phytotaxa ◽  
2013 ◽  
Vol 146 (1) ◽  
pp. 1 ◽  
Author(s):  
PETER B. HEENAN ◽  
ROB D. SMISSEN
Keyword(s):  
Phylogenetic Analysis ◽  
South America ◽  
Papua New Guinea ◽  
New Genus ◽  
New Caledonia ◽  
Sequence Data ◽  
Morphological Characters ◽  
New Combinations ◽  
Southern South America ◽  
Dna Sequence Data

The generic taxonomy of the Nothofagaceae is revised. We present a new phylogenetic analysis of morphological characters and map these characters onto a recently published phylogenetic tree obtained from DNA sequence data. Results of these and previous analyses strongly support the monophyly of four clades of Nothofagaceae that are currently treated as subgenera of Nothofagus. The four clades of Nothofagaceae are robust and well-supported, with deep stem divergences, have evolutionary equivalence with other genera of Fagales, and can be circumscribed with morphological characters. We argue that these morphological and molecular differences are sufficient for the four clades of Nothofagaceae to be recognised at the primary rank of genus, and that this classification will be more informative and efficient than the currently circumscribed Nothofagus with four subgenera.        Nothofagus is recircumscribed to include five species from southern South America, Lophozonia and Trisyngyne are reinstated, and the new genus Fuscospora is described. Fuscospora and Lophozonia, with six and seven species respectively, occur in New Zealand, southern South America and Australia. Trisyngyne comprises 25 species from New Caledonia, Papua New Guinea and Indonesia. New combinations are provided where necessary in each of these genera.

Phylogenetic analysis of foot-and-mouth disease virus type O re-emerging in free areas of South America

2007 ◽  
Vol 124 (1-2) ◽  
pp. 22-28 ◽  
Author(s):  
Viviana Malirat ◽  
José Júnior França de Barros ◽  
Ingrid Evelyn Bergmann ◽  
Renata de Mendonça Campos ◽  
Erika Neitzert ◽  
...  
Keyword(s):  
Phylogenetic Analysis ◽  
South America ◽  
Disease Virus ◽  
Virus Type ◽  
Foot And Mouth Disease ◽  
Mouth Disease ◽  
Mouth Disease Virus ◽  
Foot And Mouth ◽  
Disease Virus Type

scholarly journals Memoirs of a frequent flier: Phylogenomics reveals 18 long-distance dispersals between North America and South America in the popcorn flowers (Amsinckiinae)

2017 ◽  
Vol 104 (11) ◽  
pp. 1717-1728 ◽  
Author(s):  
C. Matt Guilliams ◽  
Kristen E. Hasenstab-Lehman ◽  
Makenzie E. Mabry ◽  
Michael G. Simpson
Keyword(s):  
North America ◽  
South America ◽  
Long Distance

Peronospora farinosa. [Distribution map].

1981 ◽  
Author(s):  
Keyword(s):  
South Africa ◽  
New Zealand ◽  
North America ◽  
South America ◽  
Central America ◽  
West Indies ◽  
Spinacia Oleracea ◽  
Uttar Pradesh ◽  
Distribution Map ◽  
New Distribution

Abstract A new distribution map is provided for Peronospora farinosa Kiessl. Hosts: Beet (Beta vulgaris) and other B. spp., Spinach (Spinacia oleracea), Chenopodium spp. Information is given on the geographical distribution in AFRICA, Ethiopia, Kenya, Libya, Morocco, South Africa, Tanzania, Zimbabwe, ASIA, Afghanistan, Burma, China, Hong Kong, India (Northern States) (Uttar Pradesh) (Madhya Pradesh), Iran, Iraq, Israel, Japan, Korea, Lebanon, Mongolia, Nepal, Pakistan, Taiwan, Thailand, Turkey, USSR, AUSTRALASIA & OCEANIA, Australia, New Zealand, EUROPE, Austria, Belgium, Britain, Bulgaria, Cyprus, Czechoslovakia, Denmark, France, Germany, Greece, Hungary, Iceland, Irish Republic, Italy (Sardina), Malta, Netherlands, Norway, Poland, Portugal, Romania, Spain, Sweden, Switzerland, USSR, Yugoslavia, NORTH AMERICA, Canada, Mexico, USA, CENTRAL AMERICA & WEST INDIES, Guatemala, SOUTH AMERICA, Argentina, Bolivia, Brazil (Sao Paulo), Chile, Ecuador, Peru, Uruguay.

Sign in / Sign up

Export Citation Format

Share Document