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The problem of average potentials filtration in the case of periodic stimulation is discussed in the paper. Some considerations proving the correctness of Wiener filtering processes suggested by Doyle are presented here. The basic assumtion of the proof is an approximation of the noise power density by means of a step function.  相似文献   

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Chromosome number determinations were made from 407 wild or transplanted individuals and seedlings representing 65 taxa and hybrids inEuthamia andSolidago. The following are first reports:Euthamia remota, 2n=9II;Solidago leavenworthii, 2n=54;S. mollis, 2n=36;S. mollis var.angustata, 2n=36;S. rigida var.glabrata, 2n=9II;S. sempervirens var.azorica, 2n=9II; andS. sparsiflora, 2n=54. Most species have been sampled only a few times or are consistently of one cytotype. Sufficient counts have been made to indicate some general patterns of cytotype distribution in the following species complexes:S. gigantea, S. canadensis, S. flexicaulis, S. rugosa, andS. uliginosa.  相似文献   

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Metatherian remains from Punta Peligro (Chubut Province, Argentina; Salamanca Formation, early Paleocene) are scarce, but at present, there are at least four different taxa known by dental remains. We describe here an incomplete petrosal showing metatherian affinities. Among the dentally known taxa from the same stratigraphic levels, the overall size of the petrosal fits that predicted for Derorhynchus , which in turn was assigned to the order Didelphimorphia. The features of the petrosal we describe do not correspond with the morphology observed among didelphoid marsupials, the only members of Didelphimorphia with well known basicrania, suggesting that if the association of petrosal and dental remains is correct, then referral of Derorhynchus to the Didelphimorphia has to be revised. The taxonomic content of this group of marsupials, as presently interpreted, represents a paraphyletic or polyphyletic grouping of metatherians.  相似文献   

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The present note consists of two separate but related parts. In the first, a new graphtheoretic proof is presented that an (ℳ,R)-system must always contain a nonreestablishable component. The second considers some questions concerning the relation between re-establishability and the time-lag structure in (ℳ,R)-systems. It is supposed that the reader is familiar with the terminology of the author's previous work on (ℳ,R)-systems, particularly R. Rosen,Bull. Math. Biophysics,20, 245–260, 1958.  相似文献   

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