Size-dependent Sex Ratios in the Monoecious, Wind-pollinated Annual, Xanthium strumarium

1989 ◽  
Vol 121 (2) ◽  
pp. 209 ◽  
Author(s):  
Bruce Peary Solomon
1990 ◽  
Vol 68 (6) ◽  
pp. 1364-1368 ◽  
Author(s):  
Marcelo A. Aizen ◽  
Alejandra Kenigsten

We measured floral sex ratios (number of male inflorescences:number of female flowers) and height of stems (= ramets) of monoecious scrub oak (Quercus ilicifolia) growing along a topographic gradient on the slope of a 20 m deep depression. Stems lower in the gradient experienced increasingly severe conditions in terms of a shorter growing season and a higher incidence of killing frosts. At the top of the gradient, floral sex ratios of tall stems were male biased; however, sex allocation patterns at the bottom showed no such size-dependent relationship. With decreasing elevation (greater stress), the production of male flowers declined more rapidly than that of female flowers. Tall stems reduced overall resource allocation to flower production proportionately more with decreasing elevation than did short stems, but this reduction was again more marked in the male flowering function than in the female. These differential patterns of sex investment explain, at least in part, the variation in size-related gender relationships along this gradient. The more stressful environmental conditions prevailing at the bottom of the depression and the relative costs of the male and prezygotic female function may combine to produce these flowering patterns.


Author(s):  
M. A. Listvan ◽  
R. P. Andres

Knowledge of the function and structure of small metal clusters is one goal of research in catalysis. One important experimental parameter is cluster size. Ideally, one would like to produce metal clusters of regulated size in order to characterize size-dependent cluster properties.A source has been developed which is capable of producing microscopic metal clusters of controllable size (in the range 5-500 atoms) This source, the Multiple Expansion Cluster Source, with a Free Jet Deceleration Filter (MECS/FJDF) operates as follows. The bulk metal is heated in an oven to give controlled concentrations of monomer and dimer which were expanded sonically. These metal species were quenched and condensed in He and filtered to produce areosol particles of a controlled size as verified by mass spectrometer measurements. The clusters were caught on pre-mounted, clean carbon films. The grids were then transferred in air for microscopic examination. MECS/FJDF was used to produce two different sizes of silver clusters for this study: nominally Ag6 and Ag50.


Author(s):  
Lawrence W. Ortiz ◽  
Bonnie L. Isom

A procedure is described for the quantitative transfer of fibers and particulates collected on membrane filters to electron microscope (EM) grids. Various Millipore MF filters (Millipore AA, HA, GS, and VM; 0.8, 0.45, 0.22 and 0.05 μm mean pore size) have been used with success. Observed particle losses have not been size dependent and have not exceeded 10%. With fibers (glass or asbestos) as the collected media this observed loss is approximately 3%.


2020 ◽  
Vol 64 (2) ◽  
pp. 383-396
Author(s):  
Lara K. Krüger ◽  
Phong T. Tran

Abstract The mitotic spindle robustly scales with cell size in a plethora of different organisms. During development and throughout evolution, the spindle adjusts to cell size in metazoans and yeast in order to ensure faithful chromosome separation. Spindle adjustment to cell size occurs by the scaling of spindle length, spindle shape and the velocity of spindle assembly and elongation. Different mechanisms, depending on spindle structure and organism, account for these scaling relationships. The limited availability of critical spindle components, protein gradients, sequestration of spindle components, or post-translational modification and differential expression levels have been implicated in the regulation of spindle length and the spindle assembly/elongation velocity in a cell size-dependent manner. In this review, we will discuss the phenomenon and mechanisms of spindle length, spindle shape and spindle elongation velocity scaling with cell size.


1990 ◽  
Vol 78 (4) ◽  
pp. 519-525 ◽  
Author(s):  
T. Kannangara ◽  
J. P. Durkin ◽  
J. ApSimon ◽  
F. Wightman
Keyword(s):  

1977 ◽  
Vol 38 (C1) ◽  
pp. C1-267-C1-269 ◽  
Author(s):  
C. M. SRIVASTAVA ◽  
M. J. PATNI ◽  
N. G. NANADIKAR
Keyword(s):  

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