The Spanish Occupation of the Central Lowlands of South America: Santa Cruz de la Sierra la Vieja

Author(s):  
Horacio Chiavazza
Keyword(s):  
Author(s):  

Abstract A new distribution map is provided for Elsinoe australis Bitancourt & Jenkins. Hosts: Citrus. Information is given on the geographical distribution in EUROPE, Italy (Sicily), SOUTH AMERICA, Argentina (Santa Fe, Tucuman), Bolivia (Santa Cruz), Brazil (Minas Gerais, Rio Grande do Sul, Rio de Janeiro, Sao Paulo), Paraquay, Uruguay.


1998 ◽  
Vol 47 ◽  
pp. 309
Author(s):  
S Miura ◽  
J.A. Adauno ◽  
C Hugo ◽  
T Kamiya ◽  
N Liboshi ◽  
...  

Author(s):  
I. J. Gamundí

Abstract A description is provided for Cyttaria darwinii. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. DISEASE: A highly evolved and highly specific obligate parasite causing often spectacular cankers only on branches of Nothofagus species. Fruitbodies only appear on the cankers; this fungus does not cause wood decay. HOSTS: Nothofagus antarctica, N. betuloides, N. dombeyi, N. pumilio, Nothofagus sp. (Fagaceae); more than 70% of all records are from N. antarctica and N. pumilio. GEOGRAPHICAL DISTRIBUTION: SOUTH AMERICA: Argentina (Chubut, Neuquén, Río Negro, Santa Cruz, Tierra del Fuego); Chile (Aisén, Los Lagos, Magallanes y Antártica Chilena, Bío-Bío, Maule). Highest recorded altitude: 1700 m. TRANSMISSION: Not known, but presumably infection is by wind-dispersed ascospores. The reasons postulated by INGOLD (1988) for evolution of the golf ball shape of fruitbodies of Cyttaria espinosae [IMI Descriptions No. 1593] are doubtless also valid for this species.


2015 ◽  
Vol 89 (5) ◽  
pp. 748-761 ◽  
Author(s):  
Sergio E. Miquel ◽  
Pablo E. Rodriguez

AbstractA remarkable fossil assemblage composed of five gastropod taxa is described from the Early Miocene of Santa Cruz (Patagonia, Argentina) in southernmost South America. The assemblage includes extinct and living genera South America, and on geographic distributions and represent background new information on spatial and across time distributions as well as identification of new taxa. A new taxon,Patagocharopa enigmatican. gen. n. sp., is tentatively assigned to Charopidae.Gastrocopta patagonican. sp. (Vertiginidae) represents the oldest record ofGastrocoptain Argentina and the southernmost record for the Americas.Punctum patagonicumn. sp. (Punctidae) represents the first record ofPunctumfor continental South America, and characterized by a protoconch with traces of axial costulae and a teleoconch with strong radial ribs.Zilchogyra miocenican. sp. is the first Miocene record of the charopid genusZilchogyra. Fragments of a possibleScolodonta(Scolodontidae) are recorded. Overall, the assemblage represents an important and useful paleoenvironmental tool. This fauna suggests that a more temperate and humid environment than today—with a more dense vegetation cover—was prevalent at this site during the Early Miocene.


Bionomina ◽  
2019 ◽  
Vol 16 (1) ◽  
pp. 83-87
Author(s):  
OMAR M. ENTIAUSPE-NETO ◽  
DANIEL LOEBMANN

The neotropical colubrid snake genus Chironius Fitzinger, 1826 comprises 22 species, distributed from Central America, at Honduras, to South America, in Uruguay and Argentina (Dixon et al. 1993; Hamdan & Fernandes 2015); this genus is diagnosed by the presence of 10–12 dorsal scale rows and hemipenis with single lobe and sulcus, centrally spinous, distally calyculate, acapitate and with a proximal naked pocket (Dixon et al. 1993). Chironius laurenti Dixon, Wiest & Cei, 1993 is a large sized colubrid, distributed in Bolivia, at departments of Beni, Cochabamba and Santa Cruz, and in Brazil, in Acre, Mato Grosso and Mato Grosso do Sul (Dixon et al. 1993; Miranda et al. 2014; Ferreira et al. 2017).


2003 ◽  
Vol 109-110 ◽  
pp. 77-86 ◽  
Author(s):  
Maria Teresa Civalero ◽  
Nora Viviana Franco
Keyword(s):  

2017 ◽  
Vol 38 (1) ◽  
pp. 15-30 ◽  
Author(s):  
Adriana Albino ◽  
Santiago Brizuela ◽  
Sergio Vizcaíno

Squamates form a substantial part of the present-day South American herpetofauna, and their fossils constitute an indispensable evidence for understanding the origin and evolution of the main taxa. Squamates are relatively common in Miocene localities of Patagonia, especially in levels of the late early Miocene Santa Cruz Formation. In this contribution, remains of the three species of the extinct iguanidErichosaurusAmeghino 1899 (E. diminutus,E. bombimaxillaandE. debilis) are redescribed, and new squamate specimens are reported for first time. The genusErichosaurusis considered invalid.Erichosaurus debilis,E. diminutusand a new specimen are recognized as indeterminate species of the extant polichrotinePristidactylus, whereasE. bombimaxillaremains as an indeterminate iguanid. Snakes are represented by an indeterminate colubrid. All these specimens, together with a tupinambine teiid previously described for the same formation, represent the southernmost fossil record of squamates in South America and indicate the occurrence of the iguanidPristidactylus, the teiidTupinambisand the colubrid snakes south to their present distribution as back as during the early Miocene.


1993 ◽  
Vol 67 (S29) ◽  
pp. 1-76 ◽  
Author(s):  
Thomas M. Bown ◽  
John G. Fleagle

The family Palaeothentidae contains some of the dentally more specialized of the small-bodied marsupials of South America and was a clade almost equivalent with the Abderitidae in having been the most abundant caenolestoids. They were unquestionably the most diverse, containing two subfamilies, nine genera, and 19 species, with a distribution ranging from Colombia to Tierra del Fuego. The best and most continuous record of the Palaeothentidae is from Patagonian Argentina where eight genera and 17 species are recognized. There, the Palaeothentidae ranged in age from the Deseadan (later Oligocene) through the late Santacrucian (middle Miocene—the Santacrucian record lasting from about 19.4 m.y. to considerably less than 16.05 m.y. before the present). The family appears to have survived longer in Colombia. The palaeothentine Palaeothentes boliviensis (Bolivia) and the incertae sedis genus and species Hondathentes cazador (Colombia) are the only taxa restricted to an extra-Argentine distribution.Two palaeothentid subfamilies are recognized. The subfamily Acdestinae is new and is erected to accommodate four genera and five species of herbivorous to frugivorous palaeothentids known from the Deseadan through the middle–late Santacrucian. Three of those genera are new (Acdestoides, Acdestodon, and Trelewthentes), as are three acdestine species placed in the genera Acdestodon, Trelewthentes, and Acdestis. The largely faunivorous Palaeothentinae includes four genera and 13 species; the genera Propalaeothentes and Carlothentes are new and new species are described for the genera Propalaeothentes (2) and Palaeothentes (3). Carlothentes is named for Ameghino's Deseadan species Epanorthus chubutensis, and Ameghino's genus Pilchenia is resurrected to accommodate Deseadan P. lucina. New species include: Acdestodon bonapartei, Trelewthentes rothi, Acdestis lemairei, Palaeothentes marshalli, P. migueli, P. pascuali, and Propalaeothentes hatcheri.The Palaeothentinae contains more generalized palaeothentid species than does the Acdestinae, but also includes some very specialized forms. The most generalized known palaeothentid is the Colombian Hondathentes cazador. Both the Acdestinae and Palaeothentinae have large- and small-bodied species; Palaeothentes aratae was the largest palaeothentid (about 550 g), and P. pascuali n. sp. the smallest (about 50 g). The oldest known members of both subfamilies consist of five of the six largest palaeothentids.The evolutionary history of the Palaeothentidae is complicated by thick sequences containing no fossils, several lacunae in sequences that yield fossils, and a continent-wide distribution of localities. By far the densest and most continuous record of the family exists in the coastal Santa Cruz Formation of Patagonian Argentina. Three major clades exist within the Palaeothentidae: 1) the incertae sedis species Hondathentes cazador; 2) the Acdestinae; and 3) the Palaeothentinae (including the new genus Propalaeothentes). The evolution of dental characters in these clades is documented with the aid of 719 new specimens (about 80% of the hypodigm of the family), most of which (about 90% of the new specimens) have precise stratigraphic data.Biostratigraphic study of the new samples was assisted by a new technique of temporal analysis of paleosols and by radiometric age determinations, the latter indicating that the upper part of the Pinturas Formation (16.6 Ma) is older than the lower part of the Santa Cruz Formation (16.4 Ma) and that the top of the marine Monte León Formation (Grupo Patagonica) is older than either (19.4 Ma).Fifty-two gnathic and dental characters were used to identify the taxonomy and to reconstruct the phylogeny of the Palaeothentidae. Analysis of sequencing of appearances of derived characters documents rampant convergences at all taxonomic levels and considerable phenotypic plasticity (variable percent representation of different mutable character morphs) in the organization of the palaeothentid dentition. Certain highly generalized character states survive for the duration of the family in some lineages, whereas others are phenotypically lost for a time and then reappear as a minor percentage of character variability. In general, replacement faunas of palaeothentids were morphologically more generalized than their antecedent forms. The high rate of character mutability and the survival and reappearance of generalized dental characters in the Palaeothentidae were probably related to massive events of pyroclastic deposition that periodically caused at least local extinctions of small mammal populations throughout the duration of the Patagonian middle Tertiary. Dental character regression indicates that palaeothentids arose prior to the Deseadan from a relatively large-bodied marsupial having generalized tribosphenic molars with more or less bunodont cusps; probably an unknown member of the Didelphidae.


Author(s):  
I. J. Gamundí

Abstract A description is provided for Cyttaria hookeri. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. DISEASE: A highly evolved and highly specific obligate parasite causing cankers only on branches of Nothofagus species. Fruitbodies only appear on the cankers; this fungus does not cause wood decay. HOSTS: Nothofagus antarctica, N. obliqua(?), N. pumilio, Nothofagus sp. (Fagaceae) [about 75% of all records are from N. antarctica]. GEOGRAPHICAL DISTRIBUTION: SOUTH AMERICA: Argentina (Chubut, Neuquén, Río Negro, Santa Cruz, Tierra del Fuego); Chile (Aisén, La Araucanía, Magallanes y Antártica Chilena, Bío-Bío). Highest recorded altitude: 1800m. TRANSMISSION: Not known, but presumably infection is by wind-dispersed ascospores. The reasons postulated by INGOLD (1988) for evolution of the golf ball shape of fruitbodies of Cyttaria espinosae Lloyd [IMI Descriptions No. 1593] are doubtless also valid for this species.


Zootaxa ◽  
2008 ◽  
Vol 1858 (1) ◽  
pp. 37
Author(s):  
MARCELA L. MONNÉ ◽  
MIGUEL A. MONNÉ

A key to the genera of South American Lepturini and keys to the South American species of Cyphonotida, Euryptera, Lycochoriolaus, Megachoriolaus and Strangalia are provided. Megachoriolaus clarkei Monné & Monné new species is described from Brazil (Rondônia) and Bolivia (Santa Cruz). The following new synonymies are proposed: Euryptera latipennis var. virgata Gounelle, 1911 and Euryptera brasiliensis Fuchs, 1956 = Euryptera latipennis Lepeletier & Audinet-Serville, 1828; Euryptera rotundipennis Fuchs, 1956 = Lycochoriolaus angustatus (Melzer, 1935). The following species are transferred from Euryptera: Lycochoriolaus ater (Gounelle, 1911) new combination, Megachoriolaus atripennis (Bates, 1870) new combination, M. bicolor (Gounelle, 1911) new combination and M. venustus (Breme, 1844) new combination. Lectotype designations are proposed for the following species: Euryptera leonina Gounelle, 1911, Euryptera latipennis var. virgata Gounelle, 1911 and Euryptera bicolor Gounelle, 1911.


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