ON THE LIGHT CONTROLLING FLOWER INITIATION OF SILENE ARMERIA

Silene armeria was cultured on a medium containing 5% sucrose,and subjected to various light conditions. 1. Plants subjected to continuous illumination of far-red radiantenergy exclusive of other spectral regions initiated flowerbuds most readily. Far-red light mixed with other spectral regionswas less effective in promoting flowering than far-red lightalone. 2. The plants subjected to short photoperiods initiated no flowerbuds irrespective of the quality of light in the light period. 3. Red light was more effective in promoting flowering thandaylight fluorescent light but was less effective than the far-redlight. (Received October 8, 1960; )     

EFFECT OF SUCROSE ON FLOWER INITIATION OF PHARBITIS NIL IN ASEPTIC CULTURE

1. Pharbitis plants were cultured on a nutrient medium containing5% sucrose or no sucrose. They were subjected to various lightconditions at temperatures of 10? or 20?.
2. All the plants culturedon the sucrose-medium at 10? initiatedflower buds independentlyof the light to which the plants wereexposed.
3. Plants culturedon the sucrose-free medium at 10? initiatedflower buds undershort photoperiods, but did not under continuousillumination.
4. Plants cultured on the sucrose-medium at 20? initiated flowerbuds in total darkness or under short photoperiods regardlessof the intensity and quality of the light, but those subjectedto continuous illumination did not.
5. Plants cultured on thesucrose-free medium at 20? initiatedflower buds under shortphotoperiods but did not initiate themunder continuous illumination.

(Received June 9, 1960; )     

Metabolism of (--)-kaurene-3H and (--)-kaurenol-3H during the photoperiodic floral induction in Pharbitis nil

(—)-Kaurene-U-³H was metabolized in seedlings of Pharbitisnil, a short-day plant, to labeled ( — )-kaurenol, ( —)-kaurenal, ( — )-kaurenoic acid, and unidentified polarsubstances, in this sequence. No significant effect of photoperiodicfloral induction upon the metabolism of ( — )-kaurene-U-³Hor ( — )-kaurenol-U-³H was observed, which suggests that( — )-kaurene metabolism is not involved in photoperiodicfloral induction ¹This work was supported in part by grants from the Ministryof Education. (Received September 24, 1970; )     

Detection of Mouse Tyrosinase With a Monoclonal Antibody MAT-1 Against Human Tyrosinase

In this study we explored the possible application of MAT-1, which has been established as a monoclonal antibody against human tyrosinase, for detection of mouse tyrosinase. The MAT-1 reacted with B16 mouse melanoma cells, but not with tyrosinase-negative NIH-3T3 mouse fibroblasts. In western blot analysis of the large granule fraction (LGF) of B16 cells, MAT-1 detected a single protein of 80 kDa, whose size was close to that of human tyrosinase detected with MAT-1 in extracts of human melanocytes. Furthermore, the 80 kDa band that was detected with MAT-1 in the LGF of B16 cells was also detected by DOPA reaction. In order to confirm that the protein detected with MAT-1 is tyrosinase, a transient expression assay was carried out. When mouse tyrosinase or mouse tyrosinase-related protein 1, which shares high homology with human tyrosinase, was transiently expressed in tyrosinase-negative K1735 mouse melanoma cells by cDNA transfection, MAT-1 reacted only with the cells expressing mouse tyrosinase. These results indicate that MAT-1 specifically reacts with mouse tyrosinase.     

EFFECT OF TWILIGHT ON PHOTOPERIODIC INDUCTION IN SOME SHORT DAY PLANTS

Light-sensitivity of the first and the last processes in theinductive dark period, and the effect of twilight on photoperiodicinduction were investigated with four short day plants. In Oryza sativa (Akebono), the first and the last processesare relatively light-insensitive, and the photoperiodicallyeffective day length under natural conditions is consideredto be equal to the astronomical day length. In Biloxi soybean and Perilla frutescens, the first processis re latively light-insensitive, but the last process is moresensitive. Effective dark period seems to begin when twilightis 50200 lux in the evening and continue until it is about 10lux in the morning. In Xanthium saccharatum, both the first and the last processesare relatively light-sensitive, but the former is more sensitivethan the latter. Effective dark period seems to begin when twilightis 110 lux in the evening and continue until it is 1050 luxin the morning. ¹Present address: Laboratory of Genetics and Plant Breending,Faculty of Agriculture, University of Osaka Prefecture, Sakai-City,Osaka. (Received February 17, 1961; )     

Monoclonal Antibody MAT-1 Against Human Tyrosinase Can Detect Melanogenic Cells on Formalin-Fixed Paraffin-Embedded Sections

Immunohistochemical localization of tyrosinase was examined with a monoclonal antibody (MoAb MAT-1) against human tyrosinase on routine formalin-fixed paraffin-embedded sections of 3 normal skin specimens, 15 melanocytic tumors (6 pigmented nevi, 3 juvenile melanomas and 6 malignant melanomas) and 3 non-melanocytic tumors. In the melanotic melanomas, almost all tumor cells were clearly stained with the antibody. In the nevocytic nevi, the nevus cells in lower epidermis and upper dermis were positive for MoAb MAT-1, but negative in middle and lower dermis. All three juvenile melanomas, one amelanotic melanoma, and three non-melanocytic tumors were entirely negative for MoAb MAT-1. Thus, MoAb MAT-1 could recognize the cells with melanogenic activity on routine formalin-fixed paraffin-embedded sections. However, the staining quality was not adequate for normal epidermal melanocytes, indicating that small technical innovations in the immunostaining process such as formalin fixation after PBS washing are required. Nevertheless, MoAb MAT-1 can be expected to be very useful for identifying melanogenic cells on paraffin-embedded sections, because we have to date no other antibody available for it.     

Roles of parasitic fungi in aquatic food webs: a theoretical approach

1. Parasites are ubiquitous in ecosystems, but their roles in material transfer are poorly understood. Fungal parasites in freshwater ecosystems are of major importance to small heterotrophic eukaryotes and consume large phytoplankton that are resistant to zooplankton grazing. 2. To evaluate their ecosystem‐level effects, we developed a simple food web model that incorporates competition between small and large phytoplankton for nutrients, zooplankton grazing on small phytoplankton, fungal parasitism on large phytoplankton and includes a newly discovered trophic link from fungal zoospores to zooplankton (F‐Z link). 3. Our model demonstrates the likely occurrence of an indirect mutualism between fungi and zooplankton, in which fungal parasitism increases zooplankton production by reducing the biomass of inedible large phytoplankton. Contradicting the expectation from a previous short‐term experiment that the F‐Z link may benefit zooplankton, the presence of the F‐Z link can reduce material transfer from phytoplankton to zooplankton because of the negative effect of the indirect mutualism. The model indicates that high growth efficiency of fungi on host tissue and their high nutrient status for zooplankton are crucial for the F‐Z link to increase zooplankton production. 4. The model also indicates that the contribution of material transfer via F‐Z link to zooplankton increases with nutrient availability. Our results suggest that parasitic fungi may be a key player in material transfer, especially in eutrophic ecosystems.