Bulletin No. 20: Tidal Marsh Invertebrates of Connecticut

36 pp. 1974. Descriptions and illustrations of over 40 species of mollusks, crustaceans, arachnids and insects found on our tidal marshes

Graded Effects of Social Conformity on Recognition Memory

Previous studies have shown that the opinion of confederates in a group influences recognition memory, but inconsistent results have been obtained concerning the question of whether recognition of items as old and new are affected similarly, possibly because only one or two confederates are present during the recognition phase. Here, we present data from a study where recognition of novel faces was tested in the presence of four confederates. In a long version of this experiment, recognition of items as old and new was similarly affected by group responses. However, in the short version, recognition of old items depended proportionally on the number of correct group responses, while rejection of new items only decreased significantly when all confederates gave an incorrect response. These findings indicate that differential effects of social conformity on recognition of items as old and new occur in situations with an intermediate level of group pressure

Metabolism of gemmules from the freshwater sponge Eunapius fragilis during diapause and post-diapause states

Post-diapause gemmules of the freshwater sponge Eunapius fragilis remained quiescent when maintained at 5°C. Germination occurred within 48 to 72 h following warming to 20°-23°C, culminating with the emergence of a new sponge from the collagenous capsule. Both heat dissipation and oxygen consumption climbed steadily during germination and eventually reached 600% of the starting values. By comparison, energy flow was much lower over the same period of time in diapausing gemmules, clearly demonstrating metabolic depression during diapause. The calorimetric:respirometric (CR) ratio increased significantly from -354 kJ/mol O2 to -541 kJ/mol O2 between hours 3.5 and 56.5 of germination, with an average value across this period of about -495 kJ/mol O2. The low CR ratio at hour 12.5 (-374 ± 21; ± 1 SE, n = 3) was statistically below the oxycaloric equivalent, which suggests that gemmules may have experienced hypoxia during the more than 3 months of storage at 5°C prior to experiments. The increase in metabolism during germination could be blocked by perfusing the gemmules with nitrogen- saturated medium (nominally oxygen free). Developing gemmules were able to survive oxygen limitation for several hours at least; during that time energy flow was depressed to 6% of normoxic values. During germination, the range of values was 3.5 to 4.0 nmol/mg protein for ATP, 0.2 to 0.4 nmol/mg protein for ADP, and 0.5 to 0.8 nmol/mg protein for AMP. Because ATP was high even before gemmules were warmed to room temperature, it is unlikely that levels were severely compromised during the diapause condition

Enhancement of Neocortical-Medial Temporal EEG Correlations during Non-REM Sleep

Interregional interactions of oscillatory activity are crucial for the integrated processing of multiple brain regions. However, while the EEG in virtually all brain structures passes through substantial modifications during sleep, it is still an open question whether interactions between neocortical and medial temporal EEG oscillations also depend on the state of alertness. Several previous studies in animals and humans suggest that hippocampal-neocortical interactions crucially depend on the state of alertness (i.e., waking state or sleep). Here, we analyzed scalp and intracranial EEG recordings during sleep and waking state in epilepsy patients undergoing presurgical evaluation. We found that the amplitudes of oscillations within the medial temporal lobe and the neocortex were more closely correlated during sleep, in particular during non-REM sleep, than during waking state. Possibly, the encoding of novel sensory inputs, which mainly occurs during waking state, requires that medial temporal dynamics are rather independent from neocortical dynamics, while the consolidation of memories during sleep may demand closer interactions between MTL and neocortex

Locally Trivial W*-Bundles

We prove that a tracially continuous W$^*$-bundle $\mathcal{M}$ over a compact Hausdorff space $X$ with all fibres isomorphic to the hyperfinite II$_1$-factor $\mathcal{R}$ that is locally trivial already has to be globally trivial. The proof uses the contractibility of the automorphism group $\mathrm{Aut}({\mathcal{R}})$ shown by Popa and Takesaki. There is no restriction on the covering dimension of $X$.Comment: 20 pages, this version will be published in the International Journal of Mathematic

Construction of Parseval wavelets from redundant filter systems

We consider wavelets in L^2(R^d) which have generalized multiresolutions. This means that the initial resolution subspace V_0 in L^2(R^d) is not singly generated. As a result, the representation of the integer lattice Z^d restricted to V_0 has a nontrivial multiplicity function. We show how the corresponding analysis and synthesis for these wavelets can be understood in terms of unitary-matrix-valued functions on a torus acting on a certain vector bundle. Specifically, we show how the wavelet functions on R^d can be constructed directly from the generalized wavelet filters.Comment: 34 pages, AMS-LaTeX ("amsproc" document class) v2 changes minor typos in Sections 1 and 4, v3 adds a number of references on GMRA theory and wavelet multiplicity analysis; v4 adds material on pages 2, 3, 5 and 10, and two more reference

Noncommutative Lattices and Their Continuum Limits

We consider finite approximations of a topological space $M$ by noncommutative lattices of points. These lattices are structure spaces of noncommutative $C^*$-algebras which in turn approximate the algebra \cc(M) of continuous functions on $M$. We show how to recover the space $M$ and the algebra \cc(M) from a projective system of noncommutative lattices and an inductive system of noncommutative $C^*$-algebras, respectively.Comment: 22 pages, 8 Figures included in the LaTeX Source New version, minor modifications (typos corrected) and a correction in the list of author

Recoil Correction to Hydrogen Energy Levels: A Revision

Recent calculations of the order (Z\alpha)^4(m/M)Ry pure recoil correction to hydrogen energy levels are critically revised. The origins of errors made in the previous works are elucidated. In the framework of a successive approach, we obtain the new result for the correction to S levels. It amounts to -16.4 kHz in the ground state and -1.9 kHz in the 2S state.Comment: 15 pages, Latex, no figure