Magnetic Flux Transport at the Solar Surface

After emerging to the solar surface, the Sun's magnetic field displays a complex and intricate evolution. The evolution of the surface field is important for several reasons. One is that the surface field, and its dynamics, sets the boundary condition for the coronal and heliospheric magnetic fields. Another is that the surface evolution gives us insight into the dynamo process. In particular, it plays an essential role in the Babcock-Leighton model of the solar dynamo. Describing this evolution is the aim of the surface flux transport model. The model starts from the emergence of magnetic bipoles. Thereafter, the model is based on the induction equation and the fact that after emergence the magnetic field is observed to evolve as if it were purely radial. The induction equation then describes how the surface flows -- differential rotation, meridional circulation, granular, supergranular flows, and active region inflows -- determine the evolution of the field (now taken to be purely radial). In this paper, we review the modeling of the various processes that determine the evolution of the surface field. We restrict our attention to their role in the surface flux transport model. We also discuss the success of the model and some of the results that have been obtained using this model.Comment: 39 pages, 15 figures, accepted for publication in Space Sci. Re

Measurements of the unsteady flow field within the stator row of a transonic axial-flow fan. 1: Measurement and analysis technique

This two-part paper presents laser anemometer measurements of the unsteady velocity field within the stator row of a transonic axial-flow fan. The objective is to provide additional insight into unsteady blade-row interactions within high speed compressors which affect stage efficiency, energy transfer, and other design considerations. Part 1 describes the measurement and analysis techniques used for resolving the unsteady flow field features. The ensemble-average and variance of the measured velocities are used to identify the rotor wake generated and unresolved unsteadiness, respectively. (Rotor wake generated unsteadiness refers to the unsteadiness generated by the rotor wake velocity deficit and the term unresolved unsteadiness refers to all remaining contributions to unsteadiness such as vortex shedding, turbulence, mass flow fluctuations, etc.). A procedure for calculating auto and cross correlations of the rotor wake generated and unresolved unsteady velocity fluctuations is described. These unsteady-velocity correlations have significance since they also result from a decomposition of the Navier-Stokes equations. This decomposition of the Navier-Stokes equations resulting in the velocity correlations used to describe the unsteady velocity field will also be outlined in this paper

Requirements Study for System Implementation of an Atmospheric Laser Propagation Experiment Program, Volume II

Program planning, ground support and airborne equipment for laser space communication syste

The Vitamin A Content of Soybean Silage and of A.I.V., Molasses, and Common Corn Silages, and the Effect of Feeding these Materials upon the Vitamin A Content of Milk

A study was made of the vitamin A content of soybean silage, and of A.l.V., molasses, and common corn silage. The silages were fed to groups of cows and the vitamin A content of their milk determined. The vitamin A determinations were made by feeding the silage or the milk to groups of rats whose body stores of this vitamin had been depleted by being fed a vitamin-A-deficient ration. Approximately 780 rats were used in these experiments. There were no apparent ill effects of feeding as much as 3.2 grams of the A.l.V. silage per rat per day for eight weeks. This was 20 to 30 per cent of the food consumed. The A. l.V. silage contained only slightly more vitamin A than did the molasses silage. The ordinary corn silage contained less vitamin A than either the A.I.V. or molasses silage. The soybean silage was inferior to any of the other silages as a source of vitamin A. Milk produced by cows receiving these silages as the only source of roughage ranked in the same order of vitamin A potency as did the silages, namely A.I.V. silage, molasses silage, and common silage. On the other hand when a good g ade of alfalfa hay served as the only source of roughage, the milk produced contained more vitamin A than did the milk produced by cows receiving A.I.V. silage as the only roughage. In another experiment one group of cows was fed both molasses silage and alfalfa hay, while a second group received A.I.V. silage and alfalfa hay. The hay was fed ad libitum and the group which received the molasses silage consumed the most hay. In this instance the milk produced by the group receiving the molasses silage contained more vitamin A than did the milk produced by the A.l.V. silage group, which was probably due to the greater consumption of alfalfa hay

A guanosine 5′-triphosphate-dependent protein kinase is localized in the outer envelope membrane of pea chloroplasts

A guanosine 5-triphosphate (GTP)-dependent protein kinase was detected in preparations of outer chloroplast envelope membranes of pea (Pisum sativum L.) chloroplasts. The protein-kinase activity was capable of phosphorylating several envelope-membrane proteins. The major phosphorylated products were 23- and 32.5-kilo-dalton proteins of the outer envelope membrane. Several other envelope proteins were labeled to a lesser extent. Following acid hydrolysis of the labeled proteins, most of the label was detected as phosphoserine with only minor amounts detected as phosphothreonine. Several criteria were used to distinguish the GTP-dependent protein kinase from an ATP-dependent kinase also present in the outer envelope membrane. The ATP-dependent kinase phosphorylated a very different set of envelope-membrane proteins. Heparin inhibited the GTP-dependent kinase but had little effect upon the ATP-dependent enzyme. The GTP-dependent enzyme accepted phosvitin as an external protein substrate whereas the ATP-dependent enzyme did not. The outer membrane of the chloroplast envelope also contained a phosphotransferase capable of transferring labeled phosphate from [-32P]GTP to ADP to yield (-32P]ATP. Consequently, addition of ADP to a GTP-dependent protein-kinase assay resulted in a switch in the pattern of labeled products from that seen with GTP to that typically seen with ATP

On the Importance of Cycle Minimum in Sunspot Cycle Prediction

The characteristics of the minima between sunspot cycles are found to provide important information for predicting the amplitude and timing of the following cycle. For example, the time of the occurrence of sunspot minimum sets the length of the previous cycle, which is correlated by the amplitude-period effect to the amplitude of the next cycle, with cycles of shorter (longer) than average length usually being followed by cycles of larger (smaller) than average size (true for 16 of 21 sunspot cycles). Likewise, the size of the minimum at cycle onset is correlated with the size of the cycle's maximum amplitude, with cycles of larger (smaller) than average size minima usually being associated with larger (smaller) than average size maxima (true for 16 of 22 sunspot cycles). Also, it was found that the size of the previous cycle's minimum and maximum relates to the size of the following cycle's minimum and maximum with an even-odd cycle number dependency. The latter effect suggests that cycle 23 will have a minimum and maximum amplitude probably larger than average in size (in particular, minimum smoothed sunspot number Rm = 12.3 +/- 7.5 and maximum smoothed sunspot number RM = 198.8 +/- 36.5, at the 95-percent level of confidence), further suggesting (by the Waldmeier effect) that it will have a faster than average rise to maximum (fast-rising cycles have ascent durations of about 41 +/- 7 months). Thus, if, as expected, onset for cycle 23 will be December 1996 +/- 3 months, based on smoothed sunspot number, then the length of cycle 22 will be about 123 +/- 3 months, inferring that it is a short-period cycle and that cycle 23 maximum amplitude probably will be larger than average in size (from the amplitude-period effect), having an RM of about 133 +/- 39 (based on the usual +/- 30 percent spread that has been seen between observed and predicted values), with maximum amplitude occurrence likely sometime between July 1999 and October 2000

On Determining the Rise, Size, and Duration Classes of a Sunspot Cycle

The behavior of ascent duration, maximum amplitude, and period for cycles 1 to 21 suggests that they are not mutually independent. Analysis of the resultant three-dimensional contingency table for cycles divided according to rise time (ascent duration), size (maximum amplitude), and duration (period) yields a chi-square statistic (= 18.59) that is larger than the test statistic (= 9.49 for 4 degrees-of-freedom at the 5-percent level of significance), thereby, inferring that the null hypothesis (mutual independence) can be rejected. Analysis of individual 2 by 2 contingency tables (based on Fisher's exact test) for these parameters shows that, while ascent duration is strongly related to maximum amplitude in the negative sense (inverse correlation) - the Waldmeier effect, it also is related (marginally) to period, but in the positive sense (direct correlation). No significant (or marginally significant) correlation is found between period and maximum amplitude. Using cycle 22 as a test case, we show that by the 12th month following conventional onset, cycle 22 appeared highly likely to be a fast-rising, larger-than-average-size cycle. Because of the inferred correlation between ascent duration and period, it also seems likely that it will have a period shorter than average length

Gauging the Nearness and Size of Cycle Minimum

By definition, the conventional onset for the start of a sunspot cycle is the time when smoothed sunspot number (i.e., the 12-month moving average) has decreased to its minimum value (called minimum amplitude) prior to the rise to its maximum value (called maximum amplitude) for the given sunspot cycle. On the basis (if the modern era sunspot cycles 10-22 and on the presumption that cycle 22 is a short-period cycle having a cycle length of 120 to 126 months (the observed range of short-period modern era cycles), conventional onset for cycle 23 should not occur until sometime between September 1996 and March 1997, certainly between June 1996 and June 1997, based on the 95-percent confidence level deduced from the mean and standard deviation of period for the sample of six short-pei-iod modern era cycles. Also, because the first occurrence of a new cycle, high-latitude (greater than or equal to 25 degrees) spot has always preceded conventional onset of the new cycle by at least 3 months (for the data-available interval of cycles 12-22), conventional onset for cycle 23 is not expected until about August 1996 or later, based on the first occurrence of a new cycle 23, high-latitude spot during the decline of old cycle 22 in May 1996. Although much excitement for an earlier-occurring minimum (about March 1996) for cycle 23 was voiced earlier this year, the present study shows that this exuberance is unfounded. The decline of cycle 22 continues to favor cycle 23 minimum sometime during the latter portion of 1996 to the early portion of 1997