Long-Term Monitoring of Tree Population Dynamics in Desert Ecosystems: Integrating Field and Satellite Data

Arid environments are characterized by rare rain events that are highly variable, as a result of which plant populations often exhibit episodic recruitment and mortality dynamics. However, direct records and observations of such events are rare because of the slow development of woody species. In this study, we described how a decrease in annual precipitation affected acacia tree population dynamics in two hydrological regime types: small wadis and salt flats. This study combines 15 years of continuous, yearly field monitoring of individual acacia trees and data from a historical Corona satellite image, which has extended the time scope of the research. Results indicate that the annual mortality of acacia trees in small wadis reflects the cumulative effective rain events in the preceding five years, whereas the population on the salt flats was not affected by annual rainfall fluctuations. Moreover, in small wadis, rain events of less than 8 mm did not increase acacia tree survival rates. The mortality pattern and dynamics of each plot was unique, suggesting unsynchronized mortality and recruitment episodes on a regional scale. Mortality in all plots was documented both in “old” trees (i.e., recognized in 1968) and “new” trees (not recognized in 1968), but varied highly between plots. More than 50% of the dead trees recorded at the sites had died during the previous dry period (2000–2010). Combining field monitoring and historical satellite image data provided a unique database of acacia population dynamics. This record revealed the response of the acacia population to climate fluctuations and a period of episodic mortality

Clinical features and studies of erythropoiesis in Israeli Bedouins with congenital dyserythropoietic anemia type I

Abstract Congenital dyserythropoietic anemia (CDA) type I is a rare macrocytic anemia of unknown etiology. In the present study, we redefined the clinical and laboratory picture of CDA type I, some of its pathogenic aspects, and the association with thalassemia-like features in 20 patients, all of whom belong to one Bedouin tribal group and are probably descended from a common ancestor. In each case ultrastructural studies of bone marrow (BM) erythroblasts showed the classic morphological findings of CDA type I. Serological tests for CDA type II were negative. The clinical picture was variable, but mostly benign. Some patients displayed elevated hemoglobin A2 levels or high ratio of alpha- to non-alpha- globin. However, neither family studies nor complete sequence analysis of the beta-globin was compatible with beta- thalassemia. Increased erythropoiesis was manifested by a high number of BM erythroid burst-forming units. Serum erythropoietin was also elevated. BM flow cytometry studies demonstrated arrest of erythroid precursors in the S phase of the cell cycle. The ultrastructural morphological features of the erythroid precursors, showing peripheral chromatin condensation, suggest apoptosis. Additional studies are indicated to define the molecular basis of this disease.</jats:p

Clinical features and studies of erythropoiesis in Israeli Bedouins with congenital dyserythropoietic anemia type I

Congenital dyserythropoietic anemia (CDA) type I is a rare macrocytic anemia of unknown etiology. In the present study, we redefined the clinical and laboratory picture of CDA type I, some of its pathogenic aspects, and the association with thalassemia-like features in 20 patients, all of whom belong to one Bedouin tribal group and are probably descended from a common ancestor. In each case ultrastructural studies of bone marrow (BM) erythroblasts showed the classic morphological findings of CDA type I. Serological tests for CDA type II were negative. The clinical picture was variable, but mostly benign. Some patients displayed elevated hemoglobin A2 levels or high ratio of alpha- to non-alpha- globin. However, neither family studies nor complete sequence analysis of the beta-globin was compatible with beta- thalassemia. Increased erythropoiesis was manifested by a high number of BM erythroid burst-forming units. Serum erythropoietin was also elevated. BM flow cytometry studies demonstrated arrest of erythroid precursors in the S phase of the cell cycle. The ultrastructural morphological features of the erythroid precursors, showing peripheral chromatin condensation, suggest apoptosis. Additional studies are indicated to define the molecular basis of this disease.</jats:p