PubMed · 14940743
The source did not provide an abstract. Follow the original record for more information.
Explore connections, maps & timelines
H LAMS. 1951. [An improved illuminating devise for the microscope].. https://pubmed.ncbi.nlm.nih.gov/14940743/
Cite the original work for its findings. Save a collection to share your selection of sources.
KEEP EXPLORING
In order to reveal any roles played by stems and roots of herbaceous plants in responding to the surrounding light environment, the optical properties of the stem and root tissues of 18 herbaceous species were investigated. It was found that light was able to penetrate through to the interior of the stem and was then conducted towards the roots. Light conduction was carried out within the internodes and across the nodes of the stem, and then in the roots from the tap root to lateral roots. Light conduction in both the stem and root occurred in the vascular tissue, usually with fibres and vessels serving as the most efficient axial light conductors. The pith and cortex in many cases were also involved in axial light conduction. Investigation of the spectral properties of the conducted light made it clear that only the spectral region between 710 nm and 940 nm (i.e. far-red and near infra-red light) was the most efficiently conducted in both the stem and the root. It was also found that there were light gradients in the axial direction of the stem or root, and the light intensity generally exhibited a linear attenuation in accord with the distance of conduction. These results revealed that tissues of the stem and root are bathed in an internal light environment enriched in far-red light, which may be involved in phytochrome-mediated metabolic activities. Thus, it appears that light signals from above-ground directly contribute to the regulation of the growth and development of underground roots via an internal light-conducting system from the stem to the roots.
Aggregate structures of aqueous nonionic Gemini surfactant solutions, alpha,alpha'-[2,4,7,9-tetramethyl-5-decyne-4,7-diyl]bis[omega-hydroxyl-polyoxyethylene] with three different length polyoxyethylenes (i.e., 10, 20, and 30 ethylene oxide monomers, denoted from now on as S-10, S-20, and S-30, respectively), are investigated using small angle neutron scattering, dynamic light scattering, and fluorescence spectroscopy. For S-10 at low surfactant concentrations (Cs < 0.9 wt %), large "clusters", with an average hydrodynamic radius (RH) > 40 nm, are found to coexist with monomers. At intermediate Cs (0.9 < Cs < 2 wt %), some clusters break down forming micelles, with an (RH) approximately 2-3 nm, while the remaining clusters coexist with micelles. Increasing Cs further (>2 wt %) results in a pure micellar phase with little or no clusters present. S-20 and S-30 mixtures, on the other hand, differ from S-10 in that irrespective of surfactant concentration, large clusters and small monomers/dimers are found to coexist, while there is no direct evidence for the presence of micelles.
We describe a method of reductive titration of photosystem I (PSI) density in leaves by generating a known amount of electrons (e-) in photosystem II (PSII) and measuring the resulting change in optical signal as these electrons arrive at pre-oxidized PSI. The method complements a recently published method of oxidative titration of PSI donor side e- carriers P700, plastocyanin (PC) and cytochrome f by illuminating a darkened leaf with far-red light (FRL) [V. Oja, H. Eichelmann, R.B. Peterson, B. Rasulov, A. Laisk, Decyphering the 820 nm signal: redox state of donor side and quantum yield of photosystem I in leaves, Photosynth. Res. 78 (2003) 1-15], presenting a nondestructive way for the determination of PSI density in intact leaves. Experiments were carried out on leaves of birch (Betula pendula Roth) and several other species grown outdoors. Single-turnover flashes of different quantum dose were applied to leaves illuminated with FRL, and the FRL was shuttered off immediately after the flash. The number of e- generated in PSII by the flash was measured as four times O2 evolution following the flash. Reduction of the pre-oxidized P700 and PC was followed as a change in leaf transmittance using a dual-wavelength detector ED P700DW (810 minus 950 nm, H. Walz, Effeltrich, Germany). The ED P700DW signal was deconvoluted into P700+ and PC+ components using the abovementioned oxidative titration method. The P700+ component was related to the absolute number of e- that reduced the P700+ to calculate the extinction coefficient. The effective differential extinction coefficient of P700+ at 810-950 nm was 0.40+/-0.06 (S.D.)% of transmittance change per micromol P700+ m(-2) or 17.6+/-2.4 mM(-1) cm(-1). The result shows that the scattering medium of the leaf effectively increases the extinction coefficient by about two times and its variation (+/-14% S.D.) is mainly caused by light-scattering properties of the leaf.