Cenozoic magmatic phases of the Costa Rican island arc (Cordillera de Talamanca)

Author(s):  
Jelle Zeilinga de Boer ◽  
Mark S. Drummond ◽  
Marc J. Bordelon ◽  
Marc J. Defant ◽  
Hervé Bellon ◽  
...  
Phytotaxa ◽  
2020 ◽  
Vol 461 (3) ◽  
pp. 185-194
Author(s):  
MARCO CEDEÑO-FONSECA ◽  
THOMAS B. CROAT ◽  
ALEJANDRO ZULUAGA ◽  
MICHAEL MITTERMEIER ◽  
MARIO A. BLANCO

Two species of Monstera, apparently endemic to Costa Rica, are newly described and illustrated. Monstera juliusii occurs in the southern Costa Rican portion of the Cordillera de Talamanca at 1600–2250 m, and has been confused with M. standleyana in herbaria. Monstera monteverdensis occurs in the Guanacaste and Tilarán cordilleras, and the northwestern part of the Cordillera Central, at 500–2300 m, and has been confused with M. epipremnoides, M. lentii and M. lechleriana in herbaria. Phenology and suggested conservation categories according to the IUCN Red List criteria are indicated for both new taxa.


Lankesteriana ◽  
2017 ◽  
Vol 17 (2) ◽  
Author(s):  
Adam P. Karremans ◽  
Melissa Díaz-Morales

Stelis dies-natalis y Stelis aenigma, pertenecientes a un grupo de especies en su mayoría Centroamericanas colocadas alternativamente en el género Dracontia, son descritas e ilustradas basadas en material vivo. Ambas se encontraron en robledales de altura en diferentes picos de la Cordillera de Talamanca en Costa Rica. La primera, S. dies-natalis, se encontró en los Cerros Buena Vista y Urán, es similar a S. hydra pero se puede distinguir por la inflorescencia relativamente corta, las flores morado oscuro con un labelo amarillo cubierto por verrugas morado oscuro, los pétalos apiculados y el labelo con un apículo brevemente acuminado. La segunda, S. aenigma, que se pensaba inicialmente que se trataría un segundo espécimen de S. dies-natalis cuando se colectó en el Cerro Utyum, pero se puede distinguir fácilmente por las inflorescencias con pocas flores que apenas supera el tamaño de la hoja, las flores rojizas, el labelo sigmoideo y la antera obtusa y cuculada. Stelis platystylis, una especie previamente conocida de México a Nicaragua, es ilustraba basada en material vivo de Costa Rica. 


1988 ◽  
Vol 62 (03) ◽  
pp. 419-423 ◽  
Author(s):  
Baba Senowbari-Daryan ◽  
George D. Stanley

Two Upper Triassic sphinctozoan sponges of the family Sebargasiidae were recovered from silicified residues collected in Hells Canyon, Oregon. These sponges areAmblysiphonellacf.A. steinmanni(Haas), known from the Tethys region, andColospongia whalenin. sp., an endemic species. The latter sponge was placed in the superfamily Porata by Seilacher (1962). The presence of well-preserved cribrate plates in this sponge, in addition to pores of the chamber walls, is a unique condition never before reported in any porate sphinctozoans. Aporate counterparts known primarily from the Triassic Alps have similar cribrate plates but lack the pores in the chamber walls. The sponges from Hells Canyon are associated with abundant bivalves and corals of marked Tethyan affinities and come from a displaced terrane known as the Wallowa Terrane. It was a tropical island arc, suspected to have paleogeographic relationships with Wrangellia; however, these sponges have not yet been found in any other Cordilleran terrane.


Island Arc ◽  
1998 ◽  
Vol 7 (3) ◽  
pp. 596-607
Author(s):  
F RYER ◽  
S UJIMOTO ◽  
S EKINE ◽  
J OHNSON ◽  
K ASAHARA ◽  
...  

Planta Medica ◽  
2015 ◽  
Vol 81 (11) ◽  
Author(s):  
JJ Araya ◽  
M Chavarría ◽  
A Pinto-Tomás ◽  
C Murillo ◽  
L Uribe ◽  
...  

2010 ◽  
Vol 30 (S 01) ◽  
pp. S150-S152
Author(s):  
G. Jiménez-Cruz ◽  
M. Mendez ◽  
P. Chaverri ◽  
P. Alvarado ◽  
W. Schröder ◽  
...  

SummaryHaemophilia A (HA) is X-chromosome linked bleeding disorders caused by deficiency of the coagulation factor VIII (FVIII). It is caused by FVIII gene intron 22 inversion (Inv22) in approximately 45% and by intron 1 inversion (Inv1) in 5% of the patients. Both inversions occur as a result of intrachromosomal recombination between homologous regions, in intron 1 or 22 and their extragenic copy located telomeric to the FVIII gene. The aim of this study was to analyze the presence of these mutations in 25 HA Costa Rican families. Patients, methods: We studied 34 HA patients and 110 unrelated obligate members and possible carriers for the presence of Inv22or Inv1. Standard analyses of the factor VIII gene were used incl. Southern blot and long-range polymerase chain reaction for inversion analysis. Results: We found altered Inv22 restriction profiles in 21 patients and 37 carriers. It was found type 1 and type 2 of the inversion of Inv22. During the screening for Inv1 among the HA patient, who were Inv22 negative, we did not found this mutation. Discussion: Our data highlight the importance of the analysis of Inv22 for their association with development of inhibitors in the HA patients and we are continuous searching of Inv1 mutation. This knowledge represents a step for genetic counseling and prevention of the inhibitor development.


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