Origin of chromite nodules in podiform chromitite from the Kızıldağ ophiolite, southern Turkey

2021 ◽  
Vol 139 ◽  
pp. 104443
Author(s):  
Chen Chen ◽  
Christina Yan Wang ◽  
Wei Tan ◽  
Zhuo-Sen Yao
Keyword(s):  
Southern Turkey ◽  
Podiform Chromitite

The Age of Autonomy

2018 ◽  
Author(s):  
Stefan Winter
Keyword(s):  
Eighteenth Century ◽  
Paradigm Shift ◽  
Large Scale ◽  
Social Disparities ◽  
Local Autonomy ◽  
Economic Context ◽  
Southern Turkey ◽  
Leadership Structure ◽  
Landed Gentry ◽  
Tribal Leadership

This chapter follows the rise to power of the Shamsins, the Bayt al-Shillif, and associated ʻAlawi families as Ottoman tax concessionaries. It shows that their position of local autonomy, rather than having evolved out of some domestic or “tribal” leadership structure, resulted from a paradigm shift in Ottoman provincial administration as well as from a very favorable economic context, in particular the development of commercial tobacco farming in the northern highlands around Latakia. If the eighteenth century witnessed the emergence of a veritable Ottoman–ʻAlawi landed gentry, it also saw increasing social disparities lead to large-scale emigration away from the highlands toward the coastal and inland plains as well as toward the Hatay district of what is today southern Turkey.

scholarly journals Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome Resembling Juvenile Idiopathic Arthritis: A Single-Center Experience from Southern Turkey

2021 ◽  
pp. 1-6
Author(s):  
Rabia Miray Kisla Ekinci ◽  
Sibel Balci ◽  
Haldun Dogan ◽  
Serdar Ceylaner ◽  
Celal Varan ◽  
...  
Keyword(s):  
Juvenile Idiopathic Arthritis ◽  
Pericardial Effusion ◽  
Early Onset ◽  
Joint Space ◽  
Coxa Vara ◽  
Single Center ◽  
The Third ◽  
Single Center Experience ◽  
Southern Turkey

Camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome, caused by biallelic pathogenic mutations in the <i>PRG4</i> gene, is characterized by early-onset camptodactyly, noninflammatory arthropathy, coxa vara deformity, and rarely, pericardial effusion. Herein, we report 3 patients with CACP syndrome from 2 unrelated families. All patients are female, born to consanguineous parents, and had camptodactyly since the first years of their lives. Two patients had a prior diagnosis of juvenile idiopathic arthritis. Hip changes were present in 2 patients, and 2 of 3 patients had undergone surgery for camptodactyly. Routine echocardiographic evaluations were normal during the 2-year follow-up. This paper represents the third study including CACP patients from Turkey. Clinically, all 3 patients resembled juvenile idiopathic arthritis cases and received unnecessary medication. There is also an ongoing need for improving awareness of CACP and an effective treatment focusing on the lubrication of the joint space in CACP patients.

scholarly journals Inconsistent magnetic polarities in magnetite- and greigite-bearing sediments: Understanding complex magnetizations in the late Messinian in the Adana Basin (southern Turkey)

2012 ◽  
Vol 13 (10) ◽  
pp. n/a-n/a ◽  
Author(s):  
Stella Lucifora ◽  
Francesca Cifelli ◽  
Massimo Mattei ◽  
Leonardo Sagnotti ◽  
Domenico Cosentino ◽  
...  
Keyword(s):  
Southern Turkey

scholarly journals Pervasive Palaeogene remagnetization of the central Taurides fold-and-thrust belt (southern Turkey) and implications for rotations in the Isparta Angle

2011 ◽  
Vol 184 (3) ◽  
pp. 1090-1112 ◽  
Author(s):  
Maud J. M. Meijers ◽  
Douwe J. J. van Hinsbergen ◽  
Mark J. Dekkers ◽  
Demir Altıner ◽  
Nuretdin Kaymakcı ◽  
...  
Keyword(s):  
Thrust Belt ◽  
Fold And Thrust Belt ◽  
Isparta Angle ◽  
Southern Turkey
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