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1.
J Environ Radioact ; 100(10): 866-74, 2009 Oct.
Article in English | MEDLINE | ID: mdl-19631426

ABSTRACT

The Proserpina dam was built in Roman times to provide drinking water to Emerita Augusta (today's Mérida in SW Spain). During maintenance work, a sediment core was extracted, offering an excellent opportunity to analyze the historical environmental impacts of the dam and its reservoir over the 2000 years since Roman times. In order to establish an accurate chronology, (14)C ages were determined by accelerator mass spectrometry (AMS). Core samples were assayed for their content in uranium and thorium series isotopes, (40)K, and the anthropogenic radionuclides (137)Cs, (90)Sr, and (239+240)Pu. Potassium-40 presented the highest activity level and was not constant with depth. The uranium and thorium series were generally in equilibrium, suggesting there had been no additional input of natural radionuclides. The presence of (137)Cs was only found in relation with the global fallout in the early 1960s. Multi-element assays were performed using the PIXE and PIGE techniques. Some variations in the multi-element concentrations were observed with depth, but the sediment core could be considered as clean, and no presumptive anthropogenic pollutants were found. Nevertheless, an unusually high Zn content was detected at depths corresponding to pre-Roman times, due to geological anomalies in the area.


Subject(s)
Fresh Water/chemistry , Geologic Sediments/chemistry , Radioisotopes/analysis , Water Supply/analysis , Carbon Radioisotopes/analysis , Cesium Radioisotopes/analysis , Elements , Environmental Pollution/history , History, Ancient , Plutonium/analysis , Potassium Radioisotopes/analysis , Radiation Monitoring , Radiometric Dating , Roman World , Spain , Strontium Radioisotopes/analysis , Thorium/analysis , Uranium/analysis
2.
J Microsc ; 224(Pt 3): 298-305, 2006 Dec.
Article in English | MEDLINE | ID: mdl-17210062

ABSTRACT

One of the abnormalities of bone architecture is osteoporosis as occurring in post-menopausal women. Especially long bones, such as femur, become more fragile and more prone to fracture. The efficiency of several osteoporosis preventative treatments based on oestrogen and progestin in bone structure and mineral recovery was studied using ovariectomized Wistar rats as an osteoporosis experimental model. Diagonal cross-sections of the proximal epiphysis of femoral bones were analysed using nuclear microscopy techniques in order to map and determine the concentration profiles of P, Ca, S, Fe and Zn from the epiphysis to diaphysis and across the cortical and trabecular bone structures. In control animals (not ovariectomized), the S and Zn contents significantly characterized differences between cortical and trabecular bone structures, whereas P and Ca showed increased gradients from the epiphyseal region to the diaphysis. After ovariectomy the differences observed were differential according to the type of hormonal supplementation. A significant decrease in P and Ca contents and depletion of minor and trace minerals, such as S, Fe and Zn, were found for both cortical and trabecular bone structures after ovariectomy relative to controls. Bone mineral contents were reversed to control levels by synthetic oestrogen supplementation, and combined oestrogen and progesterone treatment. Recovery was more evident in the femoral epiphysis and neck than in the diaphysis. The use of oestrogen alone did not lead to bone recovery after ovariectomy. Alterations in bone mineral composition observed for animals receiving synthetic oestrogen and combined oestrogen and progesterone supplement might reflect beneficial structural changes in critical regions of long bones, mostly affected in post-menopausal osteoporosis.


Subject(s)
Bone Density/drug effects , Osteoporosis/prevention & control , Rats/anatomy & histology , Animals , Bone Density/physiology , Calcium/metabolism , Elements , Femur Neck/diagnostic imaging , Femur Neck/physiopathology , Hormone Replacement Therapy , Osteoporosis/physiopathology , Phosphates/metabolism , Radiography , Rats, Wistar , Sulfur/metabolism , Zinc/metabolism
3.
Biol Trace Elem Res ; 101(1): 37-46, 2004 Oct.
Article in English | MEDLINE | ID: mdl-15516701

ABSTRACT

For the past years, different therapies based on steroid hormone supplementation or modulators of estrogen receptors have been used after menopause to prevent or manage osteoporosis. Although these treatments seem to be beneficial, they have some negative effects in the uterus and breast. The objective of this study was to assess variations for the concentrations of K, Ca, Mn, Fe, Cu, Zn, and Se in uterine tissue of Wistar rats. Ovariectomized rats were subjected to estrogen, progesterone, raloxifene, and tibolone supplementation and compared with nonovariectomized control animals. Elemental contents determined by the particle-induced X-ray emission (PIXE) technique revealed major alterations in Fe, Ca, Mn, and Se in the uterus of ovariectomized rats relative to control animals. After ovariectomy, a significant increase in Ca and Fe and a significant decrease in Mn and Se contents were determined in the uterus. For the ovariectomized groups in which animals received raloxifene, tibolone, estrogen, and estrogen combined with progesterone supplementation, an overall recovery in Mn, Fe, and Se contents was verified. Elemental concentration in the progesterone-supplemented group did not significantly differ from ovariectomized animals receiving placebo. The alterations found for ovariectomized animals receiving placebo and progesterone suggest tissue impairment and trace element imbalance, contrasting with the remaining supplemented groups where an enhancement of tissue activity might justify similar concentration levels relative to controls, because most of the elemental contents altered after ovariectomy.


Subject(s)
Hormone Replacement Therapy , Trace Elements/analysis , Uterus/chemistry , Animals , Estrogens/pharmacology , Female , Norpregnenes/pharmacology , Progesterone/pharmacology , Raloxifene Hydrochloride/pharmacology , Rats , Selective Estrogen Receptor Modulators/pharmacology
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