Search results for "VARIATION"
showing 10 items of 2124 documents
Extensive sampling sheds light on species-level diversity in Palearctic Placobdella (Annelida: Clitellata: Glossiphoniiformes)
2022
The bloodfeeding leech genus Placobdella is dominated by North American diversity, with only a single nominal species known from Central America and one from the Palearctic region. This is likely due to considerable underestimation of Palearctic biodiversity, but investigations into potential hidden diversity are lacking. To shed light on this, the present study introduces new data for specimens initially identified as Placobdella costata from Ukraine (close to the type locality), Italy, Germany, Latvia, Montenegro, Bulgaria, Slovenia, Turkey, Azerbaijan, Tunisia, and Algeria, and uses both nuclear (Internal Transcribed Spacer [ITS] region) and mitochondrial (cytochrome c oxidase subunit I …
Physiological,anatomical and biomass partitioning responses to ozone in the Mediterranean endemic plant Lamottea dianae
2011
Ozone effects on the perennial forb Lamottea dianae were studied in an open-top chamber experiment. Ozone was found to induce reductions in CO 2 assimilation and water use efficiency in the leaves of this species. These reductions were mainly related to a decline in the in vivo CO 2 fixation capacity of Rubisco (V c,max), rather than to stomatal limitations or photoinhibitory damage (F v:F m). In addition to chloroplast degeneration, other observed effects were callose accumulation, formation of pectinaceous wart-like cell wall exudates and phloem alterations. Moreover, ozone exposure significantly reduced root dry biomass. The possible relevance of these adverse effects for Mediterranean f…
Colour variation between different lineages of a colour polymorphic lizard
2019
VARIANTS OF A SELECTION PRINCIPLE FOR SEQUENCES OF REGULATED AND NON-REGULATED FUNCTIONS
2008
Let $T$ be a nonempty subset of $\RB$, $X$ a metric space with metric $d$ and $X^T$ the set of all functions mapping $T$ into $X$. Given $\vep>0$ and $f\in X^T$, we denote by $N(\vep,f,T)$ the least upper bound of those $n\in\NB$, for which there exist numbers $s_1,\dots,s_n,t_1,\dots,t_n$ from $T$ such that $s_1\vep$ for all $i=1,\dots,n$ ($N(\vep,f,T)=0$ if there are no such $n$'s). The following pointwise selection principle is proved: {\em If a sequence of functions\/ $\{f_j\}_{j=1}^\infty\subset X^T$ is such that the closure in $X$ of the sequence\/ $\{f_j(t)\}_{j=1}^\infty$ is compact for each $t\in T$ and\/ $\limsup_{j\to\infty}N(\vep,f_j,T)0$, then\/ $\{f_j\}_{j=1}^\infty$ contains …
A reliable incremental method of computing the limit load in deformation plasticity based on compliance : Continuous and discrete setting
2016
The aim of this paper is to introduce an enhanced incremental procedure that can be used for the numerical evaluation and reliable estimation of the limit load. A conventional incremental method of limit analysis is based on parametrization of the respective variational formulation by the loading parameter ? ? ( 0 , ? l i m ) , where ? l i m is generally unknown. The enhanced incremental procedure is operated in terms of an inverse mapping ? : α ? ? where the parameter α belongs to ( 0 , + ∞ ) and its physical meaning is work of applied forces at the equilibrium state. The function ? is continuous, nondecreasing and its values tend to ? l i m as α ? + ∞ . Reduction of the problem to a finit…
A pointwise selection principle for metric semigroup valued functions
2008
Abstract Let ∅ ≠ T ⊂ R , ( X , d , + ) be an additive commutative semigroup with metric d satisfying d ( x + z , y + z ) = d ( x , y ) for all x , y , z ∈ X , and X T the set of all functions from T into X . If n ∈ N and f , g ∈ X T , we set ν ( n , f , g , T ) = sup ∑ i = 1 n d ( f ( t i ) + g ( s i ) , g ( t i ) + f ( s i ) ) , where the supremum is taken over all numbers s 1 , … , s n , t 1 , … , t n from T such that s 1 ⩽ t 1 ⩽ s 2 ⩽ t 2 ⩽ ⋯ ⩽ s n ⩽ t n . We prove the following pointwise selection theorem: If a sequence of functions { f j } j ∈ N ⊂ X T is such that the closure in X of the set { f j ( t ) } j ∈ N is compact for each t ∈ T , and lim n → ∞ ( 1 n lim N → ∞ sup j , k ⩾ N , j…
The influence of preparation methodology on the concentrations of heavy metals in Pleurozium schreberi moss samples prior to use in active biomonitor…
2020
AbstractActive biomonitoring is used to assess environmental pollution of elements such as heavy metals by indicator species such as mosses. They are used, among others, in urbanized areas where no indicator species are found. In such study areas, mosses collected from sites considered to be ecologically clean shall be exposed. In this context, it is very important to prepare the mosses properly before the exposure, so that the information received about the condition of the environment is reliable. In 2018, studies were conducted in the forested areas of southern Poland—in Opolskie Province. Pleurozium schreberi mosses were used in these studies. Atomic absorption spectrometry with flame a…
ISOLATION OF RAT CDNA CLONES CODING FOR THE AUTOANTIGEN SS-B/LA - DETECTION OF SPECIES-SPECIFIC VARIATIONS
1993
Clones of cDNA coding for the autoantigen La (or SS-B) were isolated from a library made from rat liver. A comparison of the rat La cDNA (encoding from nt 38 to 1281 for rat La protein) with the sequences known for human and bovine La protein resulted in the identification of species-specific inserts. The inserts seem to be the result of multiplication of flanking sequences during evolution. In addition to these variations, we observed that rat La cDNAs exhibit non-canonical polyadenylation sites. Finally, a databank search resulted in the identification of a DNA sequence originally termed as TAG or TSG20X (GenBank accession No. X61893) which represents the C terminus of mouse La/SS-B prote…
Systematic Variation of the Degree of Branching (DB) of Polyglycerol via Oxyanionic Copolymerization of Glycidol with a Protected Glycidyl Ether and …
2017
C3 reference typing report and nomenclature revision.
1990
As the result of reference typing, two 'new' variants could be provisionally accepted (C3F045 and C3F015). The list of variants of the C3 polymorphism includes now 2 common and 29 rare variants.