Application of Isotopic Methods to Tracking Animal Movements

2019 ◽  
pp. 85-115 ◽  
Author(s):  
Keith A. Hobson
Keyword(s):  
Animal Movements ◽  
Isotopic Methods

scholarly journals Identifying outbreaks of Porcine Epidemic Diarrhea virus through animal movements and spatial neighborhoods

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Gustavo Machado ◽  
Carles Vilalta ◽  
Mariana Recamonde-Mendoza ◽  
Cesar Corzo ◽  
Montserrat Torremorell ◽  
...  
Keyword(s):  
Porcine Epidemic Diarrhea Virus ◽  
Animal Movements ◽  
Diarrhea Virus ◽  
Porcine Epidemic Diarrhea

scholarly journals Anatomy and Neural Pathways Modulating Distinct Locomotor Behaviors in Drosophila Larva

Biology ◽  
2021 ◽  
Vol 10 (2) ◽  
pp. 90
Author(s):  
Swetha B. M. Gowda ◽  
Safa Salim ◽  
Farhan Mohammad
Keyword(s):  
Motor Neurons ◽  
Model Systems ◽  
Neural Pathways ◽  
Animal Movements ◽  
Drosophila Larvae ◽  
The Central Nervous System ◽  
Drosophila Larva ◽  
Locomotor Behaviors ◽  
Basic Level

The control of movements is a fundamental feature shared by all animals. At the most basic level, simple movements are generated by coordinated neural activity and muscle contraction patterns that are controlled by the central nervous system. How behavioral responses to various sensory inputs are processed and integrated by the downstream neural network to produce flexible and adaptive behaviors remains an intense area of investigation in many laboratories. Due to recent advances in experimental techniques, many fundamental neural pathways underlying animal movements have now been elucidated. For example, while the role of motor neurons in locomotion has been studied in great detail, the roles of interneurons in animal movements in both basic and noxious environments have only recently been realized. However, the genetic and transmitter identities of many of these interneurons remains unclear. In this review, we provide an overview of the underlying circuitry and neural pathways required by Drosophila larvae to produce successful movements. By improving our understanding of locomotor circuitry in model systems such as Drosophila, we will have a better understanding of how neural circuits in organisms with different bodies and brains lead to distinct locomotion types at the organism level. The understanding of genetic and physiological components of these movements types also provides directions to understand movements in higher organisms.

scholarly journals Ore-Bearing Magmatic Systems with Complex Sn–Au–Ag Mineralization in the North-Eastern Verkhoyansk–Kolyma Orogenic Belt, Russia

Minerals ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 266
Author(s):  
Vera A. Trunilina ◽  
Andrei V. Prokopiev
Keyword(s):  
Active Continental Margin ◽  
Orogenic Belt ◽  
Crustal Extension ◽  
Margin Setting ◽  
The North ◽  
Magmatic Rocks ◽  
Isotopic Methods ◽  
North Eastern ◽  
Magmatic Stage ◽  
Mineral Compositions

This paper reports the results of a study of magmatic rocks with Sn–W–Au–Ag mineralization from the Kuranakh, Elikchan, and Istekh ore fields in the Northern batholith belt of the north-eastern Verkhoyansk–Kolyma orogenic belt in Eastern Russia. Using petrographic, mineralogical, geochemical, and isotopic methods, we determined the mineral compositions, petrochemistry, and geochemistry of magmatic rocks, the P–T conditions of their generation and crystallization, and their geodynamic affinity. The studied magmatic rocks have common geochemical characteristics that likely reflect the influence of fluids supplied from a long-lived, deep-seated mantle source. The ore fields are characterized by Sn–W–Au–Ag–Pb polygenetic mineralization. The magmatic and metallogenic evolution comprised five stages for the formation of magmatic rocks and ores. During the first stage (Berriasian–Barremian), arc-related magmatic rocks formed in an active continental margin setting and were associated with Au–Ag mineralization. The second, third, and fourth stages (Aptian–Campanian) took place in a crustal extension and rift setting, and were accompanied by Au–Ag and Sn–W mineralization. During the fifth (post-magmatic) stage, Sn–Ag–Sb and Pb–Ag mineralization occurred.

A comparison of three different isotopic methods for measuring body components of sheep

1978 ◽  
Vol 29 (12) ◽  
pp. 1007-1016 ◽  
Author(s):  
Timothy E. Trigg ◽  
Ernesto A. Domingo ◽  
John H. Topps
Keyword(s):  
Isotopic Methods ◽  
Body Components

scholarly journals STUDIES ON CYCLOPHOSPHAMIDE-INDUCED TOLERANCE TO SHEEP ERYTHROCYTES

1967 ◽  
Vol 125 (5) ◽  
pp. 833-845 ◽  
Author(s):  
Alan C. Aisenberg
Keyword(s):  
Tolerance Induction ◽  
Acid Synthesis ◽  
Progressive Increase ◽  
Immunological Tolerance ◽  
Receptor Sites ◽  
Deoxyribonucleic Acid Synthesis ◽  
Isotopic Methods ◽  
Radiation Induced ◽  
Immunological Suppression ◽  
Induced Tolerance

Complete immunological tolerance to sheep cells can be induced in mice when cyclophosphamide is injected together with sheep cells or up to 72 hr before or 48 hr after the antigen. As is true for radiation-induced immune suppression, the drug is most effective when given in the 24 hr prior to antigen. Complete cyclophosphamide-induced immunological suppression requires large doses of sheep cells (6.2 x 109 cells), presumably to enable antigen to reach sequestered receptor sites. The cyclophosphamide tolerance system has been analyzed with the Jerne technique to determine plaque-forming cells and with isotopic methods to measure rates of nucleic acid synthesis. This drug suppression has been found to consist of two components. The first is nonspecific injury to the lymphoid system caused by the cytotoxic drug and is related to the proportion of spleen cells killed. The second is antigen-specific immunological tolerance and appears to correlate with profound depression of deoxyribonucleic acid synthesis in the surviving cells. This tolerance is thought to be most consistent with a mechanism in which antigenic stimulation in the presence of cyclophosphamide-inhibited DNA synthesis and mitosis leads to the elimination or death of the specific immunological clone. Tolerance induction with cyclophosphamide is associated with loss of the 19S hemolysin plaques which are seen in nonstimulated mouse spleen, implicating these cells in immune responsiveness. The ability to induce tolerance is lost on the 3rd postantigen day at the end of a 24-hr period in which 19S cells have increased 8-fold and 7S cells 200-fold. The data suggest that loss of sensitivity is due to the emergence on day 3 of drug-resistant plaque-forming cells, particularly those of the 19S variety. In the succeeding days after antigen injection there is a progressive increase in the resistance of plaque-forming cells to cyclophosphamide administration.

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