Numerous coccidian stages were found in the kidney tubules of the golden carp (Carassius auratus gibelio). The merogonial and gamogonial stages were localized extracytoplasmally in the microvillous region of the epithelial cells. The host-parasite interface consisted of i) a large area where the parasite was separated from the host cytoplasm by the parasitophorous vacuole membrane only, and ii) a zone of multiple fusions of the host cell membrane investing the parasite to the neighbouring microvilli. The taxonomic status of the extracytoplasmic stages is not clear, however, their possible appurtenance to Eimeria scardimi, which was frequently found in the kidneys of golden carps in the same population, is discussed.
Let $X$ be a complex space of dimension $n$, not necessarily reduced, whose cohomology groups $H^1(X,{\cal O}), \ldots , H^{n-1}(X,{\cal O})$ are of finite dimension (as complex vector spaces). We show that $X$ is Stein (resp., $1$-convex) if, and only if, $X$ is holomorphically spreadable (resp., $X$ is holomorphically spreadable at infinity). \endgraf This, on the one hand, generalizes a known characterization of Stein spaces due to Siu, Laufer, and Simha and, on the other hand, it provides a new criterion for $1$-convexity.
The paper deals with the adaptive mechanisms in differential evolution (DE) algorithm. DE is a simple and effective stochastic algorithm frequently used in solving the real-world global optimization problems. The efficiency of the algorithm is sensitive to setting its control parameters. Several adaptive approaches have appeared recently in order to avoid control-parameter tuning. A new adaptive variant of differential evolution is proposed in this study. It is based on a combination of two adaptive approaches published before. The new algorithm was tested on the well-known set of benchmark problems developed for the special session of CEC2005 at four levels of population size and its performance was compared with the adaptive variants that were applied in the design of the new algorithm. The new adaptive DE variant outperformed the others in several test problems but its efficiency on average was not better.
The present article concentrates on an analysis of the structure of the opening passages and means of address in the Amarna Letters, one of the largest sources of epistolary documents, written during the 2nd half of the 2nd millennium B.C. From the first look at the Amarna corrpus, those familiar with the topic will notice a formal structure very similar to the one found in other letters written in Peripheral Akkadian. However, the discussion on the formal structure usually limits itself to several short statements and general descriptive comments.
For n=2m\geqslant 4, let \Omega\in \mathbb{R}^{n} be a bounded smooth domain and N\subset \mathbb{R}^{L} a compact smooth Riemannian manifold without boundary. Suppose that \left \{ uk \right \}\in W^{m,2}\left ( \Omega ,N \right ) is a sequence of weak solutions in the critical dimension to the perturbed m-polyharmonic maps \frac{{\text{d}}}{{{\text{dt}}}}\left| {_{t = 0}{E_m}({\text{II}}(u + t\xi )) = 0} \right with Ωk → 0 in W^{m,2}\left( \Omega ,N \right )* and {u_k} \rightharpoonup u weakly in W^{m,2}\left( \Omega ,N \right ). Then u is an m-polyharmonic map. In particular, the space of m-polyharmonic maps is sequentially compact for the weak- W^{m,2} topology., Shenzhou Zheng., and Obsahuje seznam literatury