Germination in light and darkness was compared after cold stratification of seeds of 54 species known or suspected to accumulate persistent seed banks. Germination became less dependent on light with increasing seed mass. This pattern was clear in a direct correlation of individual species data (P<0.0001) as well as when considering phylogenetically independent contrasts (P<0.001). The latter analysis suggests that light response and seed mass coevolved.

Variation in dormancy level was tested in seeds of four species, each collected from three populations in 1994 and 1995 (experiment 1) Germination was tested in light and darkness on recently-harvested seeds and on those after-ripened in dry storage for one year In addition, seeds from each of eight individual plants within each of eight populations were tested for germination when recently harvested and after warm stratification or cold stratification followed by a drying period (experiment 2) Seeds from the two years differed in dormancy level in Silene noctiflora, Sinapis arvensis and Spergula arvensis Germination percentage differed significantly among populations in Sinapis arvensis and Spergula arvensis in both experiments and in Thlaspi arvense in experiment 2 Furthermore, dormancy level in seeds from different mother plants also varied in the three species tested in experiment 2 Variations at the three levels tested (year, population and mother plant) indicate that these species have a random pattern of variation in dormancy level It is concluded that variation in seed dormancy among mother plants, populations and years must be taken into account when testing the germination characteristics of a species and also when attempting to model weed seed bank dynamics

We investigated the cellular localization and tissue distribution of the glucose transporter protein in the nervous system of the monkey and rat, and in other tissues of the rat, by immunocytochemical methods with monoclonal and polyclonal antibodies to the glucose transporter of human erythrocytes. We found intense immunostaining, indicating a high density of the glucose transporter, in all intraparenchymal blood vessels of the brain and spinal cord, in pial vessels, and in endoneurial capillaries of peripheral nerves, nerve roots, and dorsal root ganglia. Larger blood vessels at the base of the brain and in major fissures did not stain. The only intraparenchymal brain microvessels that did not immunostain were in circumventricular organs. There was no specific immunostaining of neurons or glia, except for tanycytes in the floor of the third ventricle, which immunostained intensely. Vessels of the choroid plexus did not stain, but the choroid epithelium, especially its basal membranes, stained. The only non-neural organ where immunostaining was evident in its microvessels was the testis. In addition to the endothelium of neural and testicular tissues, there was immunostaining in certain epithelial tissues, such as the perineurium of peripheral nerves and nerve roots, the epithelium of the ascending loop of Henle in the kidney, and the epidermis of the skin. Based on these findings, we hypothesize that a high density of the erythroid-type glucose transporter is inherent to many endothelial and epithelial cells that are joined by occluding junctions. However, other epithelial tissues with known occluding intercellular junctions that lack the erythroid-type of glucose transporter may have other types of glucose transporter proteins.

The toxicities of the coplanar polychlorinated biphenyls 3,3',4,4'-tetrachlorobiphenyl (TCB), 3,3',4,4',5-pentachlorobiphenyl (PeCB) and 3,3',4,4',5,5'-hexachlorobiphenyl (HCB) were compared in a 72-h study on chick embryos. The substances were injected into the air sacs of hens' eggs preincubated for 7 days. Mortality was measured 72 h later and corresponding LD50 values were calculated. The rank order of toxicity was PeCB greater than TCB greater than HCB. Using the same injection procedure, the potencies of these chlorobiphenyls with regard to their induction of hepatic 7-ethoxyresorufin O-deethylase activity were compared. The ranking order of the substances as inducers was the same as their order when ranked according to toxicity. The three coplanar chlorobiphenyls were considerably more toxic and potent as inducers than the nonplanar 2,2',4,4',5,5'-hexachlorobiphenyl. In a 2-week toxicity study, PeCB and HCB were injected into the yolks of hens' eggs preincubated for 4 days. PeCB was about 50-fold more potent than HCB in causing embryonic death. Both substances caused abnormalities, including edema, liver lesions, microphthalmia and beak deformities.

We recorded germination in three different light environments (light, dark, and after a short light exposure) in eight annual weed species. Seeds were buried outdoors at the end of November 1994 and exhumed monthly from March 1995 to April 1996. All species exhibited substantial seasonal changes in dormancy level, and the patterns suggest that seeds of Papaver rhoeas germinate strictly in the autumn; Capsella bursa-pastoris, Descurainia sophia, Spergula arvensis, and Urtica urens mainly in the autumn; Chenopodium suecicum strictly in the spring; and Matricaria perforata mainly in the spring. Lapsana communis showed inconsistent dormancy changes over the year. All species had acquired a light requirement for germination after being in the soil, and in many cases the short light exposure (1050 μmol∙m−2) was enough to fulfil this requirement. The demonstrated seasonal changes in light sensitivity in several of the species will have to be taken into account in attempts to photocontrol weeds. By using the short-light treatment, we were able to detect seasonal dormancy changes that would not have been obvious by testing for germination in only light and darkness. Hence, light is not a simple dichotomous factor in its effect on germination. Key words: dormancy, germination, light, seed, Sweden, weed.