Imaging intracellular fluorescent proteins at nanometer resolution

We introduce a method for optically imaging intracellular proteins at nanometer spatial resolution. Numerous sparse subsets of photoactivatable fluorescent protein molecules were activated, localized (to approximately 2 to 25 nanometers), and then bleached. The aggregate position information from all subsets was then assembled into a superresolution image. We used this method--termed photoactivated localization microscopy--to image specific target proteins in thin sections of lysosomes and mitochondria; in fixed whole cells, we imaged vinculin at focal adhesions, actin within a lamellipodium, and the distribution of the retroviral protein Gag at the plasma membrane.     

Heralded entanglement between widely separated atoms

Entanglement is the essential feature of quantum mechanics. Notably, observers of two or more entangled particles will find correlations in their measurement results that cannot be explained by classical statistics. To make it a useful resource, particularly for scalable long-distance quantum communication, the heralded generation of entanglement between distant massive quantum systems is necessary. We report on the creation and analysis of heralded entanglement between spins of two single rubidium-87 atoms trapped independently 20 meters apart. Our results illustrate the viability of an integral resource for quantum information science, as well as for fundamental tests of quantum mechanics.     

The Potential Effects of Social Interactions on Reproductive Efficiency of Stallions

The reproductive efficiency of stabled domestic stallions is often lower than what could be expected from observations in feral herds. In the wild, stallions typically live with mares in harem bands, with other stallions in bachelor bands, or occasionally in mixed-sex transitional bands. We, therefore, argue that permanent contact with mares may increase reproductive efficiency of stallions suffering from low libido and/or fertility. We also provide a summary of our present knowledge of natural conditions, management, and husbandry of domestic stallions, and of intra- and intersexual behavioral interactions in horses.     

Linking fluorescence induction curve and biomass in herbicide screening

A suite of dose-response bioassays with white mustard (Sinapis alba L) and sugar beet (Beta vulgaris L) in the greenhouse and with three herbicides was used to analyse how the fluorescence induction curves (Kautsky curves) were affected by the herbicides. Bentazone, a photosystem II (PSII) inhibitor, completely blocked the normal fluorescence decay after the P-step. In contrast, fluorescence decay was still obvious for flurochloridone, a PDS inhibitor, and glyphosate, an EPSP inhibitor, which indicated that PSII inhibition was incomplete. From the numerous parameters that can be derived from OJIP-steps of the Kautsky curve the relative changes at the J-step [Fvj = (Fm - Fj)/Fm] was selected to be a common response parameter for the herbicides and yielded consistent dose-response relationships. Four hours after treatment, the response Fvj on the doses of bentazone and flurochloridone could be measured. For glyphosate, the changes of the Kautsky curve could similarly be detected 4 h after treatment in sugar beet, but only after 24 hs in S alba. The best prediction of biomass in relation to Fvj was found for bentazone. The experiments were conducted between May and August 2002 and showed that the ambient temperature and solar radiation in the greenhouse could affect dose-response relationships. If the Kautsky curve parameters should be used to predict the outcome of herbicide screening experiments in the greenhouse, where ambient radiation and temperature can only partly be controlled, it is imperative that the chosen fluorescence parameters can be used to predict accurately the resulting biomass used in classical bioassays.     

Methods for determining the vapour pressure of active ingredients used in crop protection. Part V: Thermogravimetry combined with solid phase microextraction (SPME)

The well-established evaporation rate method for determining the vapour pressure of active ingredients in crop protection down to the order of 10^-12 mbar can be supplemented by the new sample preparation technique of Solid Phase MicroExtraction (SPME). With this technique, it is possible to identify evaporating substances by analysis after partitioning into the polymer coating of a thin fibre in the outlet-gas flow of thermogravimetric equipment. The active ingredients fenpropimorph, kresoxim-methyl, metolachlor, clomazone and (Z)-9-dodecenyl acetate were used in this study, which showed that, despite the relatively small amount of collected material, an analytical identification of the evaporating compound by SPME/GC can be successfully achieved. In particular, the experiments have demonstrated a clear correlation between the linearity of the weight loss curve and the evaporation process of a pure compound. In the case of organic compounds that are unstable to heat, the SPME method can also be utilized to show whether, and at what temperatures, decomposition of the sample into fragments of higher volatility occurs. For example, the insecticide dimethoate showed a clear temperature dependence of both evaporation behaviour and in the SPME/GC analysis. © 1998 SCI