Feedback regulation of the alpha electroencephalogram activity through control of the internal and external parameters

Summary Experiments with feedback stimulation triggered from the subject's electroencephalogram result in changing the sequential time series of intervals of occipital alpha and intervals of little or no alpha EEG activity. The rate of recurrence of alpha and no-alpha EEG can be changed by regulating the external feedback stimuli or by asking the subject to change his internal state. Four different paradigms were investigated and the results interpreted in terms of the hypothesis that oculomotor functions regulate the occurrence and nonoccurrence of alpha.This work was supported by NIGMS Grants 5 PO1 GM 14940-04 and GM 15006-03.Most of this research was conducted at the Perception Laboratory, Veterans' Administration Hospital, Bedford, Massachusetts, with the cooperation of Dr. Thomas B. Mulholland.     

Die Schätzung der Varianzkomponenten beim Fixwertmodell der Varianzanalyse

Zusammenfassung Die Schätzung der Varianzkomponenten bei Versuchen mit festen Variabilitätsursachen, z. B. bei der Prüfung von Sorten, Behandlungen usw., ist nur dann sinnvoll, wenn die Varianzkomponenten so definiert sind, daß ihre Summe der Gesamtvarianz gleich ist, d. h. daß sie sich additiv verhalten. Will man die so definierten Varianzkomponenten erwartungstreu schätzen, muß man die Überhöhung der mittleren Quadrate, die durch Division mit Freiheitsgraden statt mit der Gruppenzahl entstanden ist, wieder korrigieren. Diese Korrektion entfällt bei der Schätzung der Varianz von Zufallswirkungen.Die Erwartungswerte der mittleren Quadrate der üblichen varianzanalytischen Zerlegung und die erwartungstreuen Schätzungen der additiv definierten Varianzkomponenten werden am Beispiel eines Versuches mit zwei konstanten Variabilitätsursachen und einer Zufallseinwirkung dargelegt.

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Estimating variance components in a fixed model of variance analysis

Summary The partition of a variance into components in experiments with fixed effects, i.e. experiments with varieties, treatment etc., is meaningful only if components are defined as additive parts of a whole. This also demands that the sum of the components of variance be equal to the total variance. Such additivity of the components of variance is achieved by appropriate definitions of the components of variance. Unbiassed estimates of the additively defined components of variance are obtained by a simple correction which eliminates the influence of degrees of freedom on the calculation of mean squares. This correction is not needed for the estimation of variances of random effects.The expected values of mean squares for the partition of variance and formulas for unbiassed estimates of additively defined components of variance are demonstrated in an experiment with two fixed effects and one random effect.

     

Why do males of the dance flyEmpis borealis refuse to mate? The importance of female age and size

Empis borealisfemales form swarms, and males carrying a nuptial gift come to swarms to mate. Males either mated with one of the females (accepted swarms) or left swarms without mating (refused swarms). Males mated with the younger (low wing-wear) and relatively larger females in accepted swarms. They seemed to be able to judge the relative size of the females but to ignore their absolute size. Visiting males stayed shorter in accepted swarms as female size variation increased. This probably reflects their greater ease in choosing a mate among females of relatively different sizes. Females in accepted swarms tended to be larger and to have less worn wings than females in rejected swarms.     

Food limitation and social regulation in a red fox population

This study evaluates a conceptual model on functional and numerical response to short-term fluctuating vole populations of a red fox ( Vulpes vulpes L.) population in south-central Sweden. The model assumes that this particular population is located in between socially regulated stable populations to the south and direct food-limited populations to the north. The model predicts: (1) food availability as the primary factor for limiting fox numbers, causing reduced rates of reproduction and survival during years of low vole densities, and (2) density-dependent regulation during years of increasing and high vole densities resulting in increased group sizes within territories of fixed dimensions. During 1973–1980 data were obtained from 1216 fox scats, 874 fox carcasses, 63 tagged foxes, nine radio-collared females and from yearly den counts in an area of 130 km², Eight predictions of the model were tested. These concerned the occurrence of small rodents in fox diet, fluctuations in the density of foxes, variations in the number of fox litters, the effect on reproduction of providing supplemental food during January–May, the proportion of vixens bearing a litter different years, dispersal of young males relative to that of young females throughout the vole cycle, and variations in mortality rates of young males and females. All tests were in favour of the conceptual model, and contradictory to alternative models.     

Predation and potential transfer of pollen in a population of Saxifraga hirculus

Body surface pollen load and gut pollen (pollen diet load) of flower visitors in a Danish population of Saxifraga hirculus were analyzed. The four most frequent visitors, Eurimyia lineata (Syrphidae), Neoascia tenur (Syrphidae), Asindulum nigrum (Mycetophilidae), and Zygaena trifolii (Zygaenidae) had total surface loads (and S. hirculus loads) of 1031 (771), 137 (106), 108 (78), and 318 (27) pollen grains, respectively. Other syrphid visitors had on average a load of 407 (192) pollen grains. Males of E. lineata, N. tenur , and A. nigrum carried more surface pollen than the females; females of E. lineata had a lot of pollen from Ranunculus acris and S. hirculus and males had a lot from S. hirculus . Females of N. tenur carried pollen mostly from S. hirculus, Lotus uliginosus and Galium uliginosum ; males carried pollen mostly from S. hirculus . The surface pollen load of A. nigrum was dominated by S. hirculus pollen, whereas that of Z. trifolii was dominated by Cirsium palustre and Lychnis flos-cuculi pollen. The amount and kind of pollen varied enormously both intraspecifically and interspecifically. Eurimyia lineata, N. tenur and other syrphids had total pollen diet loads (and S. hirculus pollen diet loads) of approximately 14900 (657), 3739 (2327) and 17784 (13040). The average syrphid contained pollen from five plant species, only one to two, however, were quantitatively important. The average diet load in females was nine times that in males in both E. lineata and N. tenur. Eurimyia lineata ate a lot of R. acris; N. tenur ate a lot of S. hirculus and G. uliginosum . Generally, no correlation was observed between size or season and the composition of surface load and diet load. Eurimyia lineata made most of the pollen visits. Thus, the seed set from this Danish population of S. hirculus was dependent on a single syrphid species.     

The influence of creosote compounds on the aerobic degradation of toluene

The inhibiting effect of 14 typical creosote compounds on the aerobic degradation of toluene was studied in batch experiments. Four NSO-compounds (pyrrole, 1-methylpyrrole, thiophene, and benzofuran) strongly inhibited the degradation of toluene. When the NSO-compounds were present together with toluene, little or no degradation of toluene was observed during 16 days of incubation, compared with a total removal of toluene within 4 days when the four compounds were absent. Indole (an N-compound) and three phenolic compounds (phenol, o-cresol, and 2,4-dimethylphenol) also inhibited the degradation of toluene, though the effect was much weaker that of the four NSO-compounds. O-xylene, p-xylene, naphthalene and 1-methylnaphthalene seemed to stimulate the degradation even though the influence was very weak. No effects of benzothiophene (an S-compound) and quinoline (an N-compound) were observed. Benzofuran (an O-compound) was identified as the compound that most inhibited the degradation of toluene. An effect could be detected even at low concentrations (40 g/l).Abbreviations bf benzofuran - bt benzothiophene - dmp 2,4-dimethylphenol - GC gas chromatograph - ind indole - mnap 1-methylnaphthalene - MAH monoaromatic hydrocarbons - mpyr 1-methylpyrrole - nap naphthalene - o-cre o-cresol - o-xyl o-xylene - phe phenol - pyr pyrrole - p-xyl p-xylene - tol toluene - thi thiophene - qui quinoline