An archaeomagnetic study of the Ishtar Gate, Babylon.

Data from the marriage of paleomagnetism and archaeology (archaeomagnetism) are the backbone of attempts to create geomagnetic field models for ancient times. Paleointensity experimental design has been the focus of intensive efforts and the requirements and shortcomings are increasingly well understood. Some archaeological materials have excellent age control from inscriptions, which can be tied to a given decade or even a specific year in some cases. In this study, we analyzed fired mud bricks used for the construction of the Ishtar Gate, the entrance complex to the ancient city of Babylon in Southern Mesopotamia. We were able to extract reliable intensity data from all three phases of the gate, the earliest of which includes bricks inscribed with the name of King Nebuchadnezzar II (605 to 562 BCE). These results (1) add high quality intensity data to a region relatively unexplored so far (Southern Mesopotamia), (2) contribute to a better understanding of paleosecular variation in this region, and the development of an archaeomagnetic dating reference for one of the key regions in the history of human civilizations; (3) demonstrate the potential of inscribed bricks (glazed and unglazed), a common material in ancient Mesopotamia, to archaeomagnetic studies; and (4) suggest that the gate complex was constructed some time after the Babylonian conquest of Jerusalem, and that there were no substantial chronological gaps in the construction of each consecutive phase. The best fit of our data (averaging 136±2.1 ZAm2) with those of the reference curve (the Levantine Archaeomagnetic Curve) is 569 BCE.

Distinct genetic variation and heterogeneity of the Iranian population.

Iran, despite its size, geographic location and past cultural influence, has largely been a blind spot for human population genetic studies. With only sparse genetic information on the Iranian population available, we pursued its genome-wide and geographic characterization based on 1021 samples from eleven ethnic groups. We show that Iranians, while close to neighboring populations, present distinct genetic variation consistent with long-standing genetic continuity, harbor high heterogeneity and different levels of consanguinity, fall apart into a cluster of similar groups and several admixed ones and have experienced numerous language adoption events in the past. Our findings render Iran an important source for human genetic variation in Western and Central Asia, will guide adequate study sampling and assist the interpretation of putative disease-implicated genetic variation. Given Iran's internal genetic heterogeneity, future studies will have to consider ethnic affiliations and possible admixture.