Home About us Contact
|
Home About us Contact | ||
|
|
||
Subsequent Evolution (subsequent + evolution)
Selected AbstractsGeneralized-onset seizures with secondary focal evolutionEPILEPSIA, Issue 7 2009Randy Williamson Summary The international seizure classification recognizes that partial-onset seizures can become secondarily generalized, but generalized-onset seizures are expected to remain generalized. We report six patients who had recorded seizures with generalized onset, but subsequent evolution into a focal discharge. The clinical seizure onset was generalized absence or myoclonic, and the most common subsequent clinical pattern was prolonged behavioral arrest with mild automatisms, and then postictal confusion. The ictal discharge started with generalized spike-and-wave activity and then acquired a focal predominance. Interictal epileptiform activity was generalized. There were no focal magnetic resonance imaging abnormalities. Four patients were misdiagnosed with complex partial seizures. All patients were initially refractory, but three became seizure-free and three improved after treatment with antiepileptic medications appropriate for absence or myoclonic seizures. Generalized-onset seizures that acquire focal features are easily misdiagnosed as complex partial. These seizures have a more favorable response to medications effective against generalized absence and myoclonic seizures. [source] MODULARITY OF THE ANGIOSPERM FEMALE GAMETOPHYTE AND ITS BEARING ON THE EARLY EVOLUTION OF ENDOSPERM IN FLOWERING PLANTSEVOLUTION, Issue 2 2003William E. Friedman Abstract The monosporic seven-celled/eight-nucleate Polygonumtype female gametophyte has long served as a focal point for discussion of the origin and subsequent evolution of the angiosperm female gametophyte. In Polygonumtype female gametophytes, two haploid female nuclei are incorporated into the central cell, and fusion of a sperm cell with the binucleate central cell produces a triploid endosperm with a complement of two maternal and one paternal genomes, characteristic of most angiosperms. We document the development of a four-celled/four-nucleate female gametophyte in Nuphar polysepala (Engelm.) and infer its presence in many other ancient lineages of angiosperms. The central cell of the female gametophyte in these taxa contains only one haploid nucleus; thus endosperm is diploid and has a ratio of one maternal to one paternal genome. Based on comparisons among flowering plants, we conclude that the angiosperm female gametophyte is constructed of modular developmental subunits. Each module is characterized by a common developmental pattern: (1) positioning of a single nucleus within a cytoplasmic domain (pole) of the female gametophyte; (2) two free-nuclear mitoses to yield four nuclei within that domain; and (3) partitioning of three uninucleate cells adjacent to the pole such that the fourth nucleus is confined to the central region of the female gametophyte (central cell). Within the basal angiosperm lineages Nymphaeales and Illiciales, female gametophytes are characterized by a single developmental module that produces a four-celled/four-nucleate structure with a haploid uninucleate central cell. A second pattern, typical of Amborella and the overwhelming majority of eumagnoliids, monocots, and eudicots, involves the early establishment of two developmental modules that produce a seven-celled/eight-nucleate female gametophyte with two haploid nuclei in the central cell. Comparative analysis of onto-genetic sequences suggests that the seven-celled female gametophyte (two modules) evolved by duplication and ectopic expression of an ancestral Nuphar- like developmental module within the chalazal domain of the female gametophyte. These analyses indicate that the first angiosperm female gametophytes were composed of a single developmental module, which upon double fertilization yielded a diploid endosperm. Early in angiosperm history this basic module was duplicated, and resulted in a seven-celled/eight-nucleate female gametophyte, which yielded a triploid endosperm with the characteristic 2:1 maternal to paternal genome ratio. [source] A cyberenvironment for crystallography and materials science and an integrated user interface to the Crystallography Open Database and Predicted Crystallography Open DatabaseJOURNAL OF APPLIED CRYSTALLOGRAPHY, Issue 2 2008Jacob R. Fennick With the advent and subsequent evolution of the Internet the ways in which computational crystallographic research is conducted have dramatically changed. Consequently, secure, robust and efficient means of accessing remote data and computational resources have become a necessity. At present scientists in computational crystallography access remote data and resources via separate technologies, namely SSH and Web services. Computational Science and Engineering Online (CSE-Online) combines these two methods into a single seamless environment while simultaneously addressing issues such as stability with regard to Internet interruption. Presently CSE-Online contains several applications which are useful to crystallographers; however, continued development of new tools is necessary. Toward this end a Java application capable of running in CSE-Online, namely the Crystallography Open Database User Interface (CODUI), has been developed, which allows users to search for crystal structures stored in the Crystallography Open Database and Predicted Crystallography Open Database, to export structural data for visualization, or to input structural data in other CSE-Online applications. [source] Biodiversity and biogeography of the islands of the Kuril ArchipelagoJOURNAL OF BIOGEOGRAPHY, Issue 9 2003Theodore W. Pietsch Abstract Aim Based on seven consecutive seasons of biotic survey and inventory of the terrestrial and freshwater plants and animals of the 30 major islands of the Kuril Archipelago, a description of the biodiversity and an analysis of the biogeography of this previously little known part of the world are provided. Location The Kuril Archipelago, a natural laboratory for investigations into the origin, subsequent evolution, and long-term maintenance of insular populations, forms the eastern boundary of the Okhotsk Sea, extending 1200 km between Hokkaido, Japan, and the Kamchatka Peninsula of Russia. A chain of more than 56 islands, the system is only slightly smaller than the Hawaiian Islands, covering an area of 15,600 km2 and providing 2409 km of coastline. Methods Collections of whole specimens of plants and animals, as well as tissue samples for future molecular studies, were made by teams of scientists from Russia, Japan, and the USA, averaging 34 people for each of the seven annual summer expeditions (1994,2000). Floral and faunal similarities between islands were evaluated by using Sorensen's coefficient of similarity. The similarity matrix resulting from pair-wise calculations was then subjected to UPGMA cluster analysis. Results Despite the relatively small geographical area of all islands combined, the Kuril Island biota is characterized by unusually high taxonomic diversity, yet endemism is very low. An example of a non-relict biota, it originated from two primary sources: a southern source, the Asian mainland by way of Sakhalin and Hokkaido, and a northern source by way of Kamchatka. The contribution of the southern source biota to the species diversity of the Kurils was considerably greater than the northern one. Main conclusion The Bussol Strait, lying between Urup and Simushir in the central Kurils, is the most significant biogeographical boundary within the Archipelago. Of lesser importance are two transitional zones, the De Vries Strait or ,Miyabe Line', which passes between Iturup and Urup in the southern Kurils, and the fourth Kuril Strait, between Onekotan and Paramushir in the northern Kurils. [source] Sectoral Sources of the Massachusetts Miracle and Other Turning PointsJOURNAL OF REGIONAL SCIENCE, Issue 4 2001N. Edward Coulson Previous analyses of the Massachusetts Miracle and the subsequent evolution of employment in the area have centered in part on sectoral explanations. In this paper these explanations are evaluated with the use of a sectoral-based VAR model of the Boston economy, developed to identify local and national sectoral shocks. The relative importance of these shocks is estimated both for the overall sample and at several turning points in aggregate Boston employment, the latter using historical decompostions. [source] Evolution rampant: house mice on MadeiraMOLECULAR ECOLOGY, Issue 21 2009R. J. BERRY House mice are extra-ordinary animals ,extra -ordinary in the literal sense of that word. They are pests , but also a valued laboratory animal. They are generalized rodents , and successful in habitats from tundra to tropics and from sea-level to high altitudes. They have differentiated into a perplexity of taxa, yet differ little in their general morphology. They were long scorned by ecologists as recently arrived commensals, but are increasingly illuminating evolutionary processes as new techniques are applied to their study. Local forms, once valued only by taxonomists, are proving ever more interesting as their genetics are probed. In 1992, Mathias & Mira described the apparently unexciting characteristics of mice living on the two main islands of the Madeira group, 600 km west of continental Portugal. Then in 2000, Britton-Davidian et al. discovered that there were at least six chromosomal (Robertsonian) races on the main island. In the past decade, studies of molecular and mitochondrial genomes have shown an array of variables and posed questions about the origins and subsequent evolution of these island mice. In this issue of Molecular Ecology, Förster et al. report on the mtDNA haplotypes found on the island and in mainland Portugal, discuss the probable source of the island colonizers, and consider data which might give information about the timing of the colonizing event(s). [source] Chemical enrichment of the intracluster medium by FR II radio sourcesMONTHLY NOTICES OF THE ROYAL ASTRONOMICAL SOCIETY, Issue 3 2007D. Heath ABSTRACT We present 2D axisymmetric hydrodynamic simulations investigating the long-term effect of Fanaroff,Riley type II radio galaxies on the metal distribution of the surrounding intracluster medium (ICM). A light jet is injected into a cooling flow atmosphere for 10,30 Myr. We then follow the subsequent evolution for 3 Gyr on a spherical grid spanning 3 Mpc in radius. A series of passive tracer particles were placed in an annulus about the cluster core to simulate metal carrying clouds in order to calculate the metallicity (Z) as a function of time and radial distance from the cluster centre. The jet has a significant effect on the ICM over the entire 3-Gyr period. By the end of the simulations, the jets produced metallicities of ,10 per cent of the initial metallicity of the cluster core throughout much of the cluster. The jets transport the metals not only in mixing regions, but also through upwelling ICM behind the jet, enriching the cluster over both long and short distances. [source] Neo-liberalism and the Decline of Democratic Governance in Australia: A Problem of Institutional Design?POLITICAL STUDIES, Issue 1 2005Ian Marsh This paper is a preliminary attempt to evaluate changing patterns of democratic governance, at least in Westminster-style parliamentary settings, and possibly more generally. It has two specific purposes: first, to propose a paradigm for evaluating the empirical evolution of democratic governance; and second, to illustrate the explanatory potential of this paradigm through a mini-case study of changing patterns of governance in one particular polity. The conceptual framework is drawn from March and Olsen's eponymous study (1995) from which polar (,thick' and ,thin') forms of democratic governance are derived. Four conjectures about its evolution are then explored. First, in its mass party phase, the pattern of democratic governance approximated the ,thick' pole. Second, the subsequent evolution of democratic politics has been in the direction of the ,thin' (minimalist or populist) pole. Third, the cause of this shift was a failure to adapt political institutions to changing citizen identities, which was masked by the ascendancy amongst political elites of the neo-liberal account of governance. Fourth, the paper considers the means by which democratic governance might be renewed. The approach is applied to explain changes in Australian politics over recent decades. [source] A Hierarchical View of Convergent Evolution in Microbial Eukaryotes,THE JOURNAL OF EUKARYOTIC MICROBIOLOGY, Issue 2 2008BRIAN S. LEANDER ABSTRACT. Distinguishing convergent evolution from other causes of similarity in organisms is necessary for reconstructing phylogenetic relationships, inferring patterns of character evolution, and investigating the forces of natural selection. In contrast to animals and land plants, the pervasiveness and adaptive significance of convergent evolution in microbes has yet to be systematically explored or articulated. Convergent evolution in microbial eukaryotes, for instance, often involves very distantly related lineages with relatively limited repertoires of morphological features. These large phylogenetic distances weaken the role of ancestral developmental programs on the subsequent evolution of morphological characters, making convergent evolution between very distantly related lineages fundamentally different from convergent evolution between closely related lineages. This suggests that examples of convergence at different levels in the phylogenetic hierarchy offer different clues about the causes and processes of macroevolutionary diversification. Accordingly (and despite opinions to the contrary), I recognize three broad and overlapping categories of phenotypic convergence,"parallel", "proximate" and "ultimate",that represent either (1) subcellular analogues, (2) subcellular analogues to multicellular systems (and vice versa), or (3) multicellular analogues. Microbial eukaryotes living in planktonic environments, interstitial environments, and the intestinal environments of metazoan hosts provide compelling examples of ultimate convergence. After describing selected examples in microbial eukaryotes, I suggest some future directions needed to more fully understand the hierarchical structure of convergent evolution and the overall history of life. [source] | |||||||||||||