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"The death of the Emperor Frederick Il in 1250 marked a tuming point in German affairs. When in 1212 the young King of Sicily had taken Germany by storm, driving north his Welf rival Otto IV of Brunswick and securing the support of the German princes, it had seemed that a new golden age had begun. Walther von der Vogelweide at last received his "lêhen", and praised his new patron as "der edel künec, der milte künec". ln Aachen a crusade was proclaimed for the liberation of Jerusalem. Comparisons were made with the Emperor's grandfather, Frederick Barbarossa. The house of Hohenstaufen was again in the ascendency. But these high expectations were always unrealistic. Frederick's crusading vows became a thom in his flesh; his enemies held him to them, but obstructed him as he sought to fulfil them. Much of his energy was taken up in a dual struggle against insurgency in his restive Lombard states, and against the bitter invective of the papal propagandists. Although Innocent lll had been the prime sponsor of the young Emperor, Honorius III became alan·ned at the prospect of a union of the crowns of Sicily and the Empire, and Gregory IX and Innocent IV became determined to break the power of the Hohenstaufen dynasty once and for all. The popes did not have it all their own way. For the most part, the German princes remained loyal, pleased to have an emperor who interfered so little in their affairs. Frederick‘s policy of diplomacy and compromise attracted more sympathy than that of the Pope who refused to meet and treat with him. His early death, however, left his son Conrad IV in a weak position from which he was unable to recover, and within twenty years the last Hohenstaufen rulerwas deposed. The impact of these events on the intellectual climate in Germany was immense. After Frederick's death, there was an upsurge in apocalyptic preaching, and much of the literature of the period was diffused with a sense of nostalgia. It is in this light that we must read the account of the life of Frederick II which is offered by the Viennese patrician, Jansen Enike. Enikel‘s Universal Chronicle ('Weltchronik') recounts the history of the world from Adam to Frederick. It was written about 1272, just four years after the death of Conradin, the last of the Staufen line. Enikel was probably born in the 1230s, and his own lifespan exactly coincided with the years of Hohenstaufen decline. His account ol Frederick's life has limited value as history, but casts an interesting sidelight on the confusion of impressions which had gathered in popular lore. In keeping with the rest of his chronicle, it is anecdotal, falling naturally into ten sections of differing lengths, most of which are to some extent self-contained units. Together, these fill over thirteen hundred lines, making Frederick Enikel's most comprehensively treated post-biblical protagonist; only Moses and David are dealt with at greater length."
Wunschkonzert
(1994)
One of the most interesting domains of feedforward networks is the processing of sensor signals. There do exist some networks which extract most of the information by implementing the maximum entropy principle for Gaussian sources. This is done by transforming input patterns to the base of eigenvectors of the input autocorrelation matrix with the biggest eigenvalues. The basic building block of these networks is the linear neuron, learning with the Oja learning rule. Nevertheless, some researchers in pattern recognition theory claim that for pattern recognition and classification clustering transformations are needed which reduce the intra-class entropy. This leads to stable, reliable features and is implemented for Gaussian sources by a linear transformation using the eigenvectors with the smallest eigenvalues. In another paper (Brause 1992) it is shown that the basic building block for such a transformation can be implemented by a linear neuron using an Anti-Hebb rule and restricted weights. This paper shows the analog VLSI design for such a building block, using standard modules of multiplication and addition. The most tedious problem in this VLSI-application is the design of an analog vector normalization circuitry. It can be shown that the standard approaches of weight summation will not give the convergence to the eigenvectors for a proper feature transformation. To avoid this problem, our design differs significantly from the standard approaches by computing the real Euclidean norm. Keywords: minimum entropy, principal component analysis, VLSI, neural networks, surface approximation, cluster transformation, weight normalization circuit.
The North Arnerican species of the genus Cremastocheilus are reviewed. These belong to 5 subgenera, Macropodina, Trinodea, Anatinodia, Mymcotonus, and Cremastocheilus. Taxonomie changes are: She inclusion of Crernastocheilus nitens and C. chapini in the subgenus Cremastocheilus rather than Myrmecotonus. Also Anatinodia is elevated to subgeneric status. A key to the subgenera is provided, as is a key to the species of the 5 subgenera, recognizing that the 35 species in the subgenus Cremastocheilus are in need of revision. A critical review of the host records, geographic distribution, and ecology of the Tribe Crernastocheilini (Family Scarabaeidae. subfamily Cetoniinae) is provided. This contains enormous numbers of new records for both the genera Genuchinus and CremastocheiLus both from the literature and from the extensive field work that is reported here for the first time. A Summary of the host records is presented in tabular form. This table shows the association of all species of Cremastocheilus with ants as adults and the larvae either associated with the vegetable material of the ant nests or with vegetable material in rodent burrows. Genuchinus is shown to be a general predator on soft bodied insects while the other genera of the Cremastocheilini are associated with plants, particularly bromeliads. A detailed study of the external morphology and sexual dimorphism of the genera Genuchinus and Crernastocheilus is presented. All species of Cremastocheilus can be sexed with the naked eye by the difference in the shapes of the abdominal terminal Segments, wherein males have the posterior border of the last ventral abdominal segment either straight or slightly bowed, while females have this border broadly rounded. There are other microscopic sexual differences in the structure of the legs. The rest of the external morphology is also presented, particularly from the point of view of adaptations to either a predaceous or rnyrmecophilous existente. Particularly adapted for predation are the pointed maxillae which are used for piercing prey. Particularly adapted for myrmecophily are the mentum, the maxillae, the generally thick exoskeleton, trichomes on both the anterior and posterior angles of the pronotum, the elytra, and the legs (which are adapted to the nest substrate of the host ant nests. Exocrine glands are described for Genuchinus ineptus and at least 1 species of each of the 5 subgenera of Cremastocheilus. In general, there are no gland cells nor glandular areas in Genuchinuc that are comparable to those of Cremastocheilus. The gland cells and glandular areas are quite extensive andvariable arnong species of Cremastocheilus. The frontal gland of some Cremastocheilus (strongly developed in C. castaneus and the C. canaliculatus species group, but weakly developed in the C. wheeleri species group) is described for the first time. Because these glands are not found in Genuchinus ineptuc, a species with general predatory habits, it is thought that these play a role, as yet unknown, in interactions with ants. The life cycles of the subgenera of Cremastocheilus are described. The general life cycle entails adult beetles eclosing in ant nests during the summer and then undertaking dispersal flights. The adults then enter ant nests and ovenivinter there, eating ant larvae during the Winter. Another dispersal flight occurs in the spring during which the adults mate and enter ant nests again. The females then lay eggs and the adults die. The eggs hatch and the larvae spend 3 instars feeding upon vegetable material in the nests. The lmae then pupate in typical scarabaeine earthen cells made of fecal material and soil. These eclose in the summer and the cycle is repeated. Variation from species to species is largely in the timing. Leaving the nest in late Summer, mating seems to be triggered by rainfall in all the species studied. Mating of C. (Macropodina) beameri takes place in rodent burrows. Males seem attracted to females from a distance but the mechanism of this remains obscure. In the subgenus Trinodia, mating takes place on sandy washes or roadsides where females land. In the subgenus Myrmecotonus, maüng also takes place in sandy areas. In C. (Cremastocheilus) mating takes place on sand bars along rivers in the southeastern U.S. and in sand dunes in northeastern U.S. The femaies dig down into the sand. Males locate these places by some unknown mechanism and then dig down to copulate with the females. Field experiments showed unequivocaily that males dig only into areas occupied by females. No sex-specific Sex attractant glands have been located in females so far. Dispersal to ant nests occurs after mating except for C. (Macropodina) beameri which lays its eggs in the rodent burrows and then probably disperses to ant nests. Beetle activity going in and out of nests was studied using wire hardware cloth screens over entrances to Mynnecocystus nests. The mesh size was such that the ants could move freely in or out but the beetles got stuck by their thoraces. The direction then could be interpreted by the direction in which they got stuck. By this method, C. stathamae was shown to leave nests from 23 June to 1 September with a peak on 6 July, just after the beginning of the summer rains. Beetles entered nests from June 23 to August 3, however 39% entered on July 16, probably pulsed by the leaving time which was correlated with the rains. Life cycle timing: C. (Macropodina) develop in the nests of Wood rats (Neotoma sp.]. Females lay about 40 eggs each. The 3 larval instars to pupation take about 1 month. Pupae are found from late August to weil into September. In other subgenera as well, larvae are found in parts of the nest devoid of ants, The timing is similar in all the subgenera found with ants. Mortality factors: While ants attack Cremastocheilus adults, there is no evidence that they are ever killed by ants nor is there evidence that ants kill larvae nor hard earthen pupae cases which protect the pupae. During dispersal fiights and mating, the adults are exposed to predation and evidence is presented that shows predation by horned toads, spiders, magpies, and tiger beetles. Probably most mortality occurs in the larval and pupd stages where the beetles are attacked by internal parasites and fungus. Further rnortality is caused by limitation of the food supply during the larval stage. Reentering nests: Females of C. (Macropodina) beameri select specific rodent and other burrows, attract males for rnating. and then enter the burrow for oviposition. C. stathamae are carried into the ants nests from as far away as 25ft. The beetles appear to land spontaneously after flying randomly over M. depilis nesting areas. Then the wander about waiting for the ants to carry them into the nests. Cremastocheilus hirsutus fly low over the ground searching for Pogonomyrrnex barbatus nests, land. and move straight for the nest entrances which they enter unhindered. Among all species, the ants frequently eject beetles but the net rnovement is in. Ants frequently attacked Cremastocheilus in laboratory observation nests when they were introduced. These attacks seldom resulted in the death of the beetles and the beetles were eventually ignored. When the beetles entered brood chambers, where they fed upon larvae, they were mostly ignored and even licked assiduously by the ants. A principle defensive behavior by the beetles is feigning death (letisimulation). The beetles give off an unpleasant "dead fish odor when collected in the I field. Experiments show that this substance functions to fend off some predators but further experiments indicated that these substances were ineffective against both ants and kangaroo rats. Experiments with various species of Cremastocheilus adults indicate that the adults eat only ant larvae. The beetles will eat larvae of non-host ants but show preferences for the larvae of their normal hosts. Under the same experimental conditions. Genuchinus ineptus adults will feed on a variety of insect adults and larvae. Field experiments on the function of trichome secretions did not indicate that they function to attract ants at a distance nor are they involved in worker acceptance. Laboratory experiments in which areas with a high concentration of gland cells were presented to ants showed that no ants were attracted. Laboratory introduction of Cremastocheilus hamisii adults into Fomica schau.si nests yielded many interactions including ants licking the anterior pronotal angles, the mentum area where the frontal glands empty and a carina over the eye with a dense pad of short setae. These are areas of concentration of gland cells and these are the first observations of licking by ants in specific sites containing exocrine glands. Radioisotope experiments showed food exchange among ants but never from ants to beetles. Other experiments showed that ants can pick up radioactivity from the beetles without feeding on trichome secretions. Evolutionary pathways: Adult Cremastocheilini probably followed the evolutionary route from adult predation on soft bodied insects to specialized feeding upon ant brood and the subsequent development of the beetle larvae in vegetable material in the ant colonies. Thus Genuchininseptus makes a logical outgroup in that they are general predators probably feeding mostly on Diptera larvae associated with Sotol plants in the field. The rnajor evolutionary step taken by Cremastocheiluswas to specialize on ant brood. Then the species radiated into ant colonies inhabiting southwestem North Arnenca. Most of the ant hosts invaded have quantities of vegetable material in their nests sufficient to support several developing scarab larvae. Host colonies are large, contain accessible brood, and are usually dominant foragers Evidence supports the idea that the species of Cremastocheilus have differentes in behavior and morphology that reflect adaptation to the behavioral ecology of different species of ants rather than different evolutionary levels of integration into ant colonies.
Observation of enhanced subthreshold K+ production in central collisions between heavy nuclei
(1994)
In the very heavy collision system 197Au+197Au the K+ production process was studied as a function of impact parameter at 1 GeV/nucleon, a beam energy well below the free N-N threshold. The K+ multiplicity increases more than linearly with the number of participant nucleons and the K+/ pi + ratio rises significantly when going from peripheral to central collisions. The measured K+ double differential cross section is enhanced by a factor of 6 compared to microscopic transport calculations if secondary processes (Delta N-->K Lambda N and Delta Delta -->K Lambda N) are ignored.
Until the late 1980s, asset securitisation was an US-American finance technique. Meanwhile this technique has been used also in some European countries, although to a much lesser extent. While some of them have adopted or developed their legal and regulatory framework, others remain on earlier stages. That may be because of the lack of economic incentives, but also because of remaining regulatory or legal impediments. The following overview deals with the legal and regulatory environment in five selected European countries. It is structured as follows: First, this finance technique will be described in outline to the benefit of the reader who might not be familiar with it. A further part will report the recent development and the underlying economic reasons that drive this development. The main part will then deal with international aspects and give an overview of some legal and regulatory issues in five European legislations. Tax and accounting questions are, however, excluded. Concluding remarks follow.
For the German observer the idea of a Company repurchasing its own shares seems to resemble the picture of a snake eating its own tail. It appears to be highly unnatura1 and one wonders how the tail tan possibly be eatable for the snake. Not in the United States. Although repurchases have once been subject to the most stubbornly fought conflict in US Company law only some modest disclosure requirements and safeguards against overt market manipulation exist today. Large repurchases are an almost everyday event and there is an increasing tendency. The aggregate value of shares repurchased by NYSE listed companies has increased from $ 1 .l billion in 1975 to $ 6.3 billion in 1982 to $ 37.1 billion in 1985*. Few examples may illustrate this practice further: Within three years Ford Motor Corp. repurchased 30 million shares for $ 1.2 billion. In 1985 Phillips Petroleum Corp. was faced with two hostile bids and took several defensive Steps, one of which was to tender for 20 million of its own shares at a total tost of $ 1 billion. And by the end of 1988 Exxon Corp. retired 28 percent of its shares that had once been outstanding at an aggregate tost of $ 14.5 billion. The Situation in Germany is completely different. As it will be shown under German law repurchases are severely restricted and do appreciable amount at all. not take place at an In contrast to German law the United Kingdom does not prohibit repurchases but requires companies to comply with such complex rules that US companies would regard simply as limiting their economic freedom. Therefore UK companies very seldom repurchase their own shares, too. This Paper deals with repurchases by quoted companies, in particular the UK public Company and the more or less German equivalent, the Aktiengesellschaft (AG). It seeks to ascertain the reasons why companies might want to engage in those activities. Moreover, it tries to analyse the Problems which may arise from repurchases and the safeguards which the UK and German legal Systems provide for these Problems.This Paper deals with repurchases by quoted companies, in particular the UK public Company and the more or less German equivalent, the Aktiengesellschaft (AG). It seeks to ascertain the reasons why companies might want to engage in those activities. Moreover, it tries to analyse the Problems which may arise from repurchases and the safeguards which the UK and German legal Systems provide for these Problems.