Shade avoidance in plants involves rapid shoot elongation to grow toward the light. Cell wall-modifying mechanisms are vital regulatory points for control of these elongation responses. Two protein families involved in cell wall modification are expansins and xyloglucan endotransglucosylase/hydrolases. We used an alpine and a prairie ecotype of Stellaria longipes differing in their response to ...

Utilization efficiency (LUE) of lightflecks by leaves increases with decreasing duration of the lightfleck, and depends on photosynthetic induction. Sun and shade leaves differ with respect to photosynthetic induction. Shade leaves may become fully induced by a series of light pulses, whereas photosynthetic induction of leaves from partial shade or full sun depends on continuous light. Addition...

STATEMENT OF PROBLEM Production of a ceramic dental restoration that matches a target shade is dependent on porcelain thickness. Even when adequate porcelain thickness exists, clinical shade matches are difficult to achieve. PURPOSE This study predicted the thickness of dentin porcelain required to obtain a clinical shade match (</=3 DeltaE units) for a variety of dental porcelain systems and...

Shade from neighboring plants limits light for photosynthesis; as a consequence, plants have a variety of strategies to avoid canopy shade and compete with their neighbors for light. Collectively the response to foliar shade is called the shade avoidance syndrome (SAS). The SAS includes elongation of a variety of organs, acceleration of flowering time, and additional physiological responses, wh...

In June 1993, net photosynthetic rates, stomatal conductance and isoprene emission rates of sweetgum leaves (Liquidambar styraciflua L.) were measured at the top of the forest canopy (sun leaves) and within the canopy at a height of 8-10 m above ground level (shade leaves). Large differences in net photosynthetic rates and stomatal conductance were found between sun and shade leaves. Mean rates...

A field experiment was conducted to determine the optimum shade level and nitrogen fertilizer for quality Bangladhonia (Eryngium foetidum L.) production at the Bangahandhu Sheikh Mujibar Rahman Agricultural University (BSMRAU) Research Farm during December 2002 to May 2003. The treatments consisted of four shade levels (0, 25, 50, and 75% shades) and five nitrogen rates (0, 115, 138, 161, and 1...

The molecular basis behind shade tolerance in plants is not fully understood. Previously, we have shown that a connection may exist between shade tolerance and dwarfism, however, the mechanism connecting these phenotypes is not well understood. In order to clarify this connection, we analyzed the transcriptome of a previously identified shade-tolerant mutant of perennial ryegrass (Lolium perenn...

Above- and belowground tissues of co-occurring saplings (0.1-1 m height) of Acer saccharum Marsh. (very shade tolerant), Acer rubrum L. (shade tolerant), Fraxinus americana L. (intermediate shade tolerant), and Prunus serotina Ehrh. (shade intolerant) were harvested from a forest understory to test the hypothesis that the pattern of biomass allocation varied predictably with shade-tolerance ran...

Light-related plasticity of crown morphology and within-crown characteristics were investigated in understory sun and shade saplings of three codominant subalpine conifers, Abies mariesii M.T. Mast., Abies veitchii Lindl. and Picea jezoensis var. hondoensis (Mayr) Rehd. Compared with those of sun saplings, current-year shoots of shade saplings allocated less biomass to needles, resulting in les...

AIM The aim of this study was to investigate the influence of light curing method, composite shade, and depth of cure on composite microhardness. METHODS AND MATERIALS Forty-eight specimens with 4 mm of depth were prepared with a hybrid composite (Filtek Z-100, 3M ESPE); 24 with shade A1 and the remaining with shade C2. For each shade, two light curing units (LCUs) were used: a quartz-tungste...