The correct order is116124310139Rest of the statem.pdf

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anubhavnigam2608

The correct order is 11 6 12 4 3 10 13 9 Rest of the statements are not correct as per the proof Solution The correct order is 11 6 12 4 3 10 13 9 Rest of the statements are not correct as per the proof.

The correct order is
11
6
12
4
3
10
13
9
Rest of the statements are not correct as per the proof
Solution
The correct order is
11
6
12
4
3
10
13
9
Rest of the statements are not correct as per the proof

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The mineralogical and structural adjustment of solid rocks to physical and chemical conditions that have been imposed at depths below the near surface zones of weathering and diagenesis and which differ from conditions under which the rocks in question originated. The word \"Metamorphism\" comes from the Greek: meta = change, morph = form, so metamorphism means to change form. In geology this refers to the changes in mineral assemblage and texture that result from subjecting a rock to conditions such pressures, temperatures, and chemical environments different from those under which the rock originally formed. There are two major kinds of metamorphism: regional and contact. Regional metamorphism. Most metamorphic rocks are the result of regional metamorphism (also called dynamothermal metamorphism). These rocks were typically exposed to tectonic forces and associated high pressures and temperatures. They are usually foliated and deformed and thought to be remnants of ancient mountain ranges. Contact metamorphism. Contact metamorphism (also called thermal metamorphism) is the process by which the country rock that surrounds a hot magma intrusion is metamorphosed by the high heat flow coming from the intrusion. The zone of metamorphism that surrounds the intrusion is called the halo (or aureole) and rarely extends more than 100 meters into the country rock. Geostatic pressure is usually a minor factor, since contact metamorphism generally takes place less than 10 kilometers from the surface.Metamorphism is defined as follows: The mineralogical and structural adjustment of solid rocks to physical and chemical conditions that have been imposed at depths below the near surface zones of weathering and diagenesis and which differ from conditions under which the rocks in question originated. The word \"Metamorphism\" comes from the Greek: meta = change, morph = form, so metamorphism means to change form. In geology this refers to the changes in mineral assemblage and texture that result from subjecting a rock to conditions such pressures, temperatures, and chemical environments different from those under which the rock originally formed. There are two major kinds of metamorphism: regional and contact. Regional metamorphism. Most metamorphic rocks are the result of regional metamorphism (also called dynamothermal metamorphism). These rocks were typically exposed to tectonic forces and associated high pressures and temperatures. They are usually foliated and deformed and thought to be remnants of ancient mountain ranges. Contact metamorphism. Contact metamorphism (also called thermal metamorphism) is the process by which the country rock that surrounds a hot magma intrusion is metamorphosed by the high heat flow coming from the intrusion. The zone of metamorphism that surrounds the intrusion is called the halo (or aureole) and rarely extends more than 100 meters into the country rock. Geostatic pressure is usually a minor factor, since contact metamorp.

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The general idea is to find a root of the polynomial and then apply Horner\'s method to remove the corresponding factor according to the Ruffini rule. This iterative scheme is numerically unstable; the approximation errors accumulate during the successive factorizations, so that the last roots are determined with a polynomial that deviates widely from a factor of the original polynomial. To reduce this error, it is advisable to find the roots in increasing order of magnitude. Wilkinson\'s polynomial illustrates that high precision may be necessary when computing the roots of a polynomial given its coefficients: the problem of finding the roots from the coefficients is in general ill-conditioned. The most simple method to find a single root fast is Newton\'s method. One can use Horner\'s method twice to efficiently evaluate the value of the polynomial function and its first derivative; this combination is called Birge–Vieta\'s method. This method provides quadratic convergence for simple roots at the cost of two polynomial evaluations per step. Closely related to Newton\'s method are Halley\'s method and Laguerre\'s method. Using one additional Horner evaluation, the value of the second derivative is used to obtain methods of cubic convergence order for simple roots. If one starts from a point x close to a root and uses the same complexity of 6 function evaluations, these methods perform two steps with a residual of O(|f(x)|9), compared to three steps of Newton\'s method with a reduction O(|f(x)|8), giving a slight advantage to these methods. When applying these methods to polynomials with real coefficients and real starting points, Newton\'s and Halley\'s method stay inside the real number line. One has to choose complex starting points to find complex roots. In contrast, the Laguerre method with a square root in its evaluation will leave the real axis of its own accord. Another class of methods is based on translating the problem of finding polynomial roots to the problem of finding eigenvalues of the companion matrix of the polynomial. In principle, one can use any eigenvalue algorithm to find the roots of the polynomial. However, for efficiency reasons one prefers methods that employ the structure of the matrix, that is, can be implemented in matrix-free form. Among these methods are the power method, whose application to the transpose of the companion matrix is the classical Bernoulli\'s method to find the root of greatest modulus. The inverse power method with shifts, which finds some smallest root first, is what drives the complex (cpoly) variant of the Jenkins–Traub method and gives it its numerical stability. Additionally, it is insensitive to multiple roots and has fast convergence with order 1 + 2.6 {\\displaystyle 1+\\Phi \\approx 2.6} even in the presence of clustered roots. This fast convergence comes with a cost of three Horner evaluations per step, resulting in a residual of O(|f(x)|2+3), which is slower than three steps of New.

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Mutants of the Drosophila dunce and rutabaga genes, which encode a cAMP-specific phosphodiesterase and a calcium/calmodulin-responsive adenylyl cyclase, respectively, are deficient in short-term memory. Altered synaptic plasticity has been demonstrated at neuromuscular junctions in these mutants, but little is known about how their central neurons are affected. This problem was examined by using the \"giant\" neuron culture, which offers a unique opportunity to analyze mutational effects on neuronal activity and the underlying ionic currents in Drosophila. On the basis of instantaneous frequency and first latency of spikes evoked by current steps, four categories of firing patterns (tonic, adaptive, delayed, and interrupted) were identified in wild-type neurons, revealing interesting parallels to those commonly observed in vertebrate CNS neurons. The distinct firing patterns are correlated with expression of different ratios of 4-aminopyridine- and tetra ethylammonium-sensitive K+ currents. Subsets of dnc and rut neurons display abnormal spontaneous spikes and altered firing patterns. Altered frequency coding in mutant neurons was demonstrated further by using stimulation protocols involving conditioning with previous activity. Abnormal spike activity and reduced K+ current remain in double-mutant neurons, suggesting that the opposite effects on cAMP metabolism by dnc and rut do not counterbalance the mutual functional defects. The aberrant spontaneous activity and altered frequency coding in different stimulus paradigms may present problems in the stability and reliability of neural circuits for information processing during certain behavioral tasks, raising the possibility of modulation in neuronal excitability as a cellular mechanism underlying learning and memory (Zhao, 1997). Not all memory genes first identified in other contexts, however, play a significant role in place memory. The DopEcR gene has been implicated in several behaviors, including a 30 min memory after courtship conditioning. This G-protein linked receptor is responsive to both dopamine and the steroid hormone ecdysone. Remarkably, DopEcR has been shown to interact with the cAMP cascade through double mutant and pharmacological tests. Using conditions that induce a robust and lasting place memory, the DopEcR mutant flies do not show a defect in memory directly after training or at 1 h post-training. This is despite the fact that the rut and cAMP-phosphodiesterase genes (dunce) are critical for place memory. It may be that DopEcR is not required for this type of learning and would be consistent with the independence of place memory from dopamine signaling. Alternatively, other redundant pathways may compensate for the reduction in DopEcR function caused by the DopEcRPB1 allele. One might further speculate that other types of behavioral plasticity, such as reversal learning or memory enhancement after unpredicted high temperature exposures in the heat-box might be more sen.

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