Mary Rose, Rollenbild, Kniestück

Signatur des Originals: S 36/F09699

Mary Rose, Rollenbild

Signatur des Originals: S 36/F09700

Rose Chéri, Rollenbild

Signatur des Originals: S 36/G00017

Geistliche Rose : ein katholisches Gebet- und Andachtsbuch

hrsg. von Andreas Büschl

Ms. lat. qu. 103 - Rituel de la Rose Croissante

Vorbesitzer: Bibliothèque et Archives du RIT. EC. ANG. ACC.-Suprème Conseil de France

Efecto de la temperatura, escarificación y concentraciones de calcio en la germinación de Gymnocalycium schickendantzii (F.A.C. Weber) Britton & Rose (Cactaceae)

Gymnocalycium schickendantzii (F.A.C. Weber) Britton & Rose (Cactaceae) es una especie endémica de Argentina. En la provincia de Mendoza las poblaciones de este cactus todavía no están siendo afectadas por las urbanizaciones y cultivos que ponen en peligro su supervivencia. Conocer aspectos sobre su germinación podría ayudar a explicar el porqué de la presencia de esta especie en su hábitat natural. El objetivo del presente trabajo fue determinar en un ensayo de germinación de G. schickendantzii el efecto de tratamientos de temperaturas de 20 y 30°C durante 25 días en laboratorio usando 3 concentraciones de calcio (1, 10 y 20 meq/l Ca), y agua como testigo con y sin escarificación, y bajo condiciones de luz blanca. Se observó que a 30°C los porcentajes de germinación, con o sin escarificación, fueron significativamente mayores que a 20°C. El efecto de la escarificación sólo ayudó a incrementar los valores de germinación cuando fueron tratadas a 20°C. Las concentraciones de calcio tienen un débil efecto en la germinación de las semillas en las mismas condiciones. El tiempo de inicio de germinación (IG) y para obtener el 50% de ella (T50) fueron mayores a 30°C tanto en las semillas escarificadas como sin escarificar.

Conidial germination of Botryosphaeria dothidea Mough.: Fr (Ces. & De Not.) and histological alterations on stems of pitahaya (Hylocereus undatus H.) (Haworth) Britton & Rose

Conidial germination of Botryosphaeria dothidea (anamorph: Fusicoccum) in sterile distilled water and 1% sterile dextrose solution was evaluated at 4, 6, 12, 24 and 36 h after incubation. Also, it was described the anatomical changes on pitahaya stems induced by this fungus, collected in the field and artificially inoculated in the laboratory. Conidial germination was less than 30% in water and it was improved when 1% dextrose was added to the water. In 1% dextrose solution the germination was 90% after 4h of incubation and 100% at 6 h. Pathogen germ tubes had entered through wounds and sometimes through stomata and hyphae colonized intra and intercellularly in the parenchyma-chlorenchyma tissues. On naturally and artificially diseased stems the main alterations were: destruction of cuticle, hyperplasia of epidermal and collenchymatous hypodermal cells and conform the advance of the pathogen a layer of lignified periderm was formed surrounding the damaged tissues; however, it couldn't stop the advance of the pathogen and the cells that surrounded the lesion suffered necrosis.

(Figures S2a-c) Phase diagrams of the upper crust, the lower crust and the upper mantle based on averaged compositions of the oceanic crust and mantle

The age of the subducting Nazca Plate off Chile increases northwards from 0 Ma at the Chile Triple Junction (46°S) to 37 Ma at the latitude of Valparaíso (32°S). Age-related variations in the thermal state of the subducting plate impact on (a) the water influx to the subduction zone, as well as on (b) the volumes of water that are released under the continental forearc or, alternatively, carried beyond the arc. Southern Central Chile is an ideal setting to study this effect, because other factors for the subduction zone water budget appear constant. We determine the water influx by calculating the crustal water uptake and by modeling the upper mantle serpentinization at the outer rise of the Chile Trench. The water release under forearc and arc is determined by coupling FEM thermal models of the subducting plate with stability fields of water-releasing mineral reactions for upper and lower crust and hydrated mantle. Results show that both the influx of water stored in, and the outflux of water released from upper crust, lower crust and mantle vary drastically over segment boundaries. In particular, the oldest and coldest segments carry roughly twice as much water into the subduction zone as the youngest and hottest segments, but their release flux to the forearc is only about one fourth of the latter. This high variability over a subduction zone of < 1500 km length shows that it is insufficient to consider subduction zones as uniform entities in global estimates of subduction zone fluxes. This article is protected by copyright. All rights reserved.