28.12.2013 Views

1985 - Mycological Society of America

1985 - Mycological Society of America

1985 - Mycological Society of America

SHOW MORE
SHOW LESS

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

26<br />

and seasonal study (450 soil samples), Dictvostelium<br />

sohaerocephalum showed a positive response to pasturing<br />

when adjacent woods or old field are used for comparis011.<br />

A similar but less pronounced response was<br />

noted for 2. mucoroides. Polysphondilium violaceum had<br />

an opposite response. Polysphondilium pallidurn was<br />

found more frequently in the survey from pastures and<br />

old fields than from tilled fields, hay fields or<br />

woods. Both Dictvostelium discoideun and 2. polyceph-<br />

- alum were restricted to the undisturbed forest sites,<br />

while D. aureo-stipes and D. puroureum showed little<br />

or no response to agricultural treatment. Forest soil<br />

had the greatest diversity <strong>of</strong> dictyostelid species,<br />

followed by old fields, pastures, tilled fields and<br />

hay fields. The seasonal study indicated that fluctuations<br />

in total dictyostelid density closely follow<br />

fluctuations in the soil moisture through time and<br />

were most pronounced in soils <strong>of</strong> the woods and old<br />

field. The results demonstrate a possible role for the<br />

cellular slime molds as indicators <strong>of</strong> soil conditions<br />

which may be relevant for enhancing soil biological<br />

input into agricultural systems.<br />

T. M. HAMMILL, S. W. BEATTIE, and R. A. GRASSUCCI.<br />

SUNY-Oswego Laboratory for Ultrastructural Studies,<br />

SUNY College <strong>of</strong> Arts and Science, Oswego, NY 13126.<br />

Scanning electron microscopy <strong>of</strong> zyqosporogenesis in<br />

Mucor mucedo .<br />

--<br />

Mated cultures <strong>of</strong> Mucor mucedo L. :Fr., NRRL 3634 (-)<br />

X NRRL 3635 (+), w - r m 10 C with a photoperiod<br />

<strong>of</strong> 12 h light alternatinq with 12 h darkness.<br />

Primary fixation for SEF! was done for 3 h in an unbuffered<br />

mixture <strong>of</strong> 2% ql utaraldehyde and 2% formal dehyde.<br />

Postfixation was in unbuffered 1% 0s04. Dehydration<br />

in ethanol was followed by transition to<br />

acetone and critical point drying in a Sorvall CPD<br />

System.<br />

The position <strong>of</strong> gametangial septa, formed after fusion<br />

<strong>of</strong> progametangial tips, was determined easily in<br />

SEM images. Suspensors, delimited as a result <strong>of</strong><br />

gametangial septation, contained unequal amounts <strong>of</strong><br />

protoplasmic contents, sugqesting that gametangia<br />

contribute disproportionately to zygospores. Branched<br />

micronyphae were observed commonly over the surface<br />

<strong>of</strong> developing zygospores. The outer wall <strong>of</strong> gametangia<br />

became ruptured and torn as the warty projections,<br />

characteristic <strong>of</strong> mature zygospores, developed from<br />

the underside, initially at the position <strong>of</strong> the fusion<br />

septum. Enlargement <strong>of</strong> zygospore initials was<br />

radial in the plane <strong>of</strong> the fusion septum. Then,<br />

zygospores enlarged toward gametangial septa. As a<br />

result , developing zygospores changed shape from<br />

oblong-ell iptical to spherical. Warty projections on<br />

zyqospores were conical with lonqi tudinal ridges.<br />

They commonly had remnants <strong>of</strong> ruptured wall material<br />

on their tips.<br />

T. M. HAMMILL, S. W. BEATTIE, R. A. GRASSUCCI, D. A.<br />

USSMAN, and C. T. WARE. SUNY-Oswego Laboratory for<br />

Ultrastructural Studies. SUNY Colleae <strong>of</strong> Arts and Science,<br />

Oswego, NY 13126. - ~ransmission electron microscopy<br />

<strong>of</strong> zygosporogenesis in Mucor mucedo. I. Early<br />

stages.<br />

Mated cultures <strong>of</strong> M. mucedo were grown as described<br />

above. Fixation fTr m s according to procedures<br />

published elsewhere by the senior author. Gametangia1<br />

septa, which divided programetangia into gametangia<br />

and suspensors, contained numerous plasmodesmata connecting<br />

suspensors and gametangia. Gametangial septa<br />

developed an electron-opaque layer on the suspensor<br />

side. They also showed a variety <strong>of</strong> swellings. At<br />

the margins <strong>of</strong> gametangial septa, conspicuously thick-<br />

ened areas were formed, suggestive <strong>of</strong> a support function.<br />

The conical "warts," which ornament mature zygospores,<br />

were electron-opaque. They initiated as e-<br />

lectron-opaque thickenings in the developing zygospore<br />

wall,. "Mart" initials appeared on fusion septa, and<br />

it appears that fusion septa may only partially dissolve<br />

and then evaginate rather than dissolve completely.<br />

More work should clarify this. Zygospore<br />

wal! layers are deposited beneath qametangial wall<br />

layers which rupture as a zygospore inflates. "Wart"<br />

initials become confluent at their bases. Protoplasmic<br />

projections into regions between developing<br />

"warts" contained numerous vesicles, consistent with<br />

developmental models for wall deposition. Karyogamy<br />

appears to occur shortly after plasmogamy. Nuclei in<br />

prozygospores <strong>of</strong>ten were seen to have variable shapes<br />

and to contain microtubules. Zygospores developed<br />

numerous lipid qlobules. There is no evidence to date<br />

which supports a zygospore/zygosporangium dichotomy.<br />

Hammons, T. H., see Ellzey, (1. T., et. al.<br />

Harding, K., ,ee Pommerville, J., et. al.<br />

S. D. HARRIS and D. A. COTTER, Department <strong>of</strong> Biology,<br />

University <strong>of</strong> Windsor, Windsor, Ontario, Canada<br />

N9B 3P4. Characterization <strong>of</strong> Saccharmyces<br />

cerevisiae mutants unable to grow in trehalose<br />

containing media.<br />

Haploid vegetative cells <strong>of</strong> the yeast Saccharomyces<br />

cerevisiae contain two trehalase activities. The<br />

activity located in the cytoplasm has a neutral pH<br />

optimum and is responsible for the breakdown <strong>of</strong><br />

endogenously synthesized trehalose. The activity<br />

located in the vacuole is active at an acidic pH<br />

value and has not been assigned a cellular function.<br />

We have found that growth <strong>of</strong> vegetative cells on<br />

exogenous trehalose induces the trehalase activity<br />

which functions at the acidic pH value. Cells grown<br />

on maltose, as well as stationary phase glucose<br />

grown cells also express this activity. We have<br />

isolated a mutant that does not grow on trehalose<br />

or maltose, and fails to express this enzyme activity.<br />

The mutant grows well on glucose and sucrose,<br />

but enters the stationary phase earlier than wildtype<br />

cells. Preliminary evidence indicates that the<br />

mutant is not impaired in trehalose transport.<br />

Arrested mutant cells appear to accumulate carbohydrate<br />

material in the vacuole. These results<br />

suggest that this vacuolar trehalase activity has a<br />

degradative function in glucose depleted cells,<br />

while being specifically induced by growth on<br />

trehalose or maltose.<br />

Harrison, J. A,, see Jaworski, A. J.<br />

Haskins, E. F., see McGuinness, M. D.<br />

E. F. HASKINS and M. D. McGUINNESS. Department o f<br />

Botany, University <strong>of</strong> Washington, Seattle, WA 98195.<br />

Light and electron microscopical studies on Semimorula<br />

liquescens.<br />

Semimorula 1 iquescens is a protoplasmodial slime mold<br />

which produces sessile fruiting bodies. We have<br />

recently discovered the occurrence <strong>of</strong> synaptonemal<br />

complexes during sporulation in this species. The<br />

possible taxonomic affinity <strong>of</strong> this organism with the<br />

Myxomycetes and Protostelia will be discussed.<br />

Heath, M. C., see Meyer, S. L. F.

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!