INDUCED APOGAMY IN DIPLOID GAMETOPHYTES OF PTERIDIUM

1966 ◽  
Vol 44 (12) ◽  
pp. 1717-1721 ◽  
Author(s):  
D. P. Whittier
Keyword(s):  
Weight Basis ◽  
Sterile Culture ◽  
Self Fertilization ◽  
Induced Apogamy

Diploid gametophytes were produced via self-fertilization and apospory from a strain of haploid gametophytes which underwent apogamy in sterile culture. These diploid gametophytes of the fern, Pteridium, demonstrated quantitative differences from the haploid prothalli. The diameters of the rhizoids and antheridia were larger on the diploid prothalli. The diploid gametophytes grew slightly faster than the haploids. Under conditions which induced apogamy in the haploid prothalli, the diploids produced more apogamous sporophytes on a culture or on a weight basis than did the haploid prothalli.

FURTHER STUDIES ON INDUCED APOGAMY IN FERNS

1962 ◽  
Vol 40 (11) ◽  
pp. 1525-1531 ◽  
Author(s):  
D. P. Whittier ◽  
T. A. Steeves
Keyword(s):  
Carbohydrate Metabolism ◽  
Osmotic Potential ◽  
Culture Medium ◽  
General Applicability ◽  
Sterile Culture ◽  
The One ◽  
Induced Apogamy ◽  
Fern Gametophytes

Apogamous sporophyte formation has been induced in 14 strains of seven species of normal fern gametophytes using a technique similar to the one reported earlier (Whittier and Steeves, Can. J. Bot. 38, 925–930 (1960)). These gametophytes were supplied with suitable concentrations of sugar in the sterile culture medium for certain lengths of time which resulted in the formation of apogamous sporophytes. This investigation demonstrated that sucrose is more effective in inducing apogamy probably because it produces about half the osmotic potential as an equivalent percentage of glucose. Therefore more sugar can be made available to gametophytes before the osmotic potential deleteriously affects the prothallial growth and apogamy. This confirms the work carried out previously using sugar in the medium and it demonstrates that this method has general applicability for inducing apogamy in ferns. The sugar in the medium is felt to modify the carbohydrate metabolism enabling the prothalli to undergo a thickened growth and develop apogamous sporophytes.

Effects of carbamylcholine on chick embryo aggregate retina cell cultures

1988 ◽  
Vol 46 ◽  
pp. 350-351
Author(s):  
Glenn M. Cohen ◽  
Radharaman Ray
Keyword(s):  
Cell Cultures ◽  
Single Cells ◽  
Retinal Cell ◽  
Cell Aggregates ◽  
High Concentration ◽  
In Ovo ◽  
Sterile Culture ◽  
Retinal Tissue ◽  
Synaptic Junctions ◽  
And Control

Retinal,cell aggregates develop in culture in a pattern similar to the in ovo retina, forming neurites first and then synapses. In the present study, we continuously exposed chick retinal cell aggregates to a high concentration (1 mM) of carbamylcholine (carbachol), an acetylcholine (ACh) analog that resists hydrolysis by acetylcholinesterase (AChE). This situation is similar to organophosphorus anticholinesterase poisoning in which the ACh level is elevated at synaptic junctions due to inhibition of AChE, Our objective was to determine whether continuous carbachol exposure either damaged cholino- ceptive neurites, cell bodies, and synaptic elements of the aggregates or influenced (hastened or retarded) their development.The retinal tissue was isolated aseptically from 11 day embryonic White Leghorn chicks and then enzymatically (trypsin) and mechanically (trituration) dissociated into single cells. After washing the cells by repeated suspension and low (about 200 x G) centrifugation twice, aggregate cell cultures (about l0 cells/culture) were initiated in 1.5 ml medium (BME, GIBCO) in 35 mm sterile culture dishes and maintained as experimental (containing 10-3 M carbachol) and control specimens.

Neutralisation of Heparan Sulphate and Low Molecular Weight Heparin by Protamine

1985 ◽  
Vol 53 (01) ◽  
pp. 086-089 ◽  
Author(s):  
A R Hubbard ◽  
C A Jennings
Keyword(s):  
Molecular Weight ◽  
Plasma Proteins ◽  
Low Molecular Weight Heparin ◽  
Heparan Sulphate ◽  
Activated Partial Thromboplastin Time ◽  
Weight Basis ◽  
Low Molecular Weight ◽  
Protamine Sulphate ◽  
At Iii ◽  
Reference Preparation

SummaryThe neutralisation by protamine sulphate (PS) of heparan sulphate (HS), a low molecular weight heparin (LMWH), and a reference preparation of unfractionated heparin (UH), was studied by activated partial thromboplastin time (APTT) and anti-Xa clotting assays. UH was most easily neutralised in the APTT assay by PS (on a weight for weight basis), followed by LMWH and HS. The neutralisation of APTT activity by PS closely followed the loss of activity in the anti-Xa clotting assay, when plasma was used as the source of At III. When the anti-Xa clotting assay was carried out using purified At III in place of plasma, HS and LMWH were neutralised by much lower amounts of PS and resembled UH neutralisation more closely. Resistance of HS anti-Xa activity to PS neutralisation decreased with increasing plasma dilution. The presence of bovine albumin with purified At III concentrate increased the resistance of HS to PS neutralisation. It is concluded that PS binding to UH, HS and LMWH is probably related more to their degree of sulphation than molecular weight and that non-specific interactions between PS and plasma proteins inhibit the binding of PS to HS and LMWH.

ERRORS ASSOCIATED WITH HERBAGE DISSECTION ANALYSES 2. Problems of species identification

1976 ◽  
pp. 213-225
Author(s):  
I.M. Ritchie ◽  
C.C. Boswell ◽  
A.M. Badland
Keyword(s):  
New Zealand ◽  
Dry Weight ◽  
Analytical Tool ◽  
Species Level ◽  
Weight Basis ◽  
Plant Identification ◽  
Leaf Fragment ◽  
Research Division ◽  
Or Groups ◽  
Botanical Analysis

HERBACE DISSECTION is the process in which samples of herbage cut from trials are separated by hand into component species. Heavy reliance is placed on herbage dissection as an analytical tool ,in New Zealand, and in the four botanical analysis laboratories in the Research Division of the Ministry of Agriculture and Fisheries about 20 000 samples are analysed each year. In the laboratory a representative subsample is taken by a rigorous quartering procedure until approximately 400 pieces of herbage remain. Each leaf fragment is then identified to species level or groups of these as appropriate. The fractions are then dried and the composition calculated on a percentage dry weight basis. The accuracy of the analyses of these laboratories has been monitored by a system of interchanging herbage dissection samples between them. From this, the need to separate subsampling errors from problems of plant identification was, appreciated and some of this work is described here.

Polycyclic Aromatic Hydrocarbons (PAHs) in Sediments of the Brisbane River (Australia) – Preliminary Results

1989 ◽  
Vol 21 (2) ◽  
pp. 161-165 ◽  
Author(s):  
S. I. Kayal ◽  
D. W. Connell
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Aromatic Hydrocarbons ◽  
River Estuary ◽  
Dry Weight ◽  
Weight Basis ◽  
Sediment Samples ◽  
Preliminary Results ◽  
Treated Sewage ◽  
Polycyclic Aromatic ◽  
Petroleum Refineries

Results of the analysis of twenty-three composite sediment samples revealed that PAHs are widely distributed in the Brisbane River estuary. Mean concentrations for individual compounds, on a dry weight basis, ranged from 0.03 µg/g for dibenz [ah] anthracene to 2.34 µg/g for fluoranthene. Observed PAH assemblages were rich in compounds having pyrolytic origins. However, the presence of petroleum derived compounds was indicative of the importance of petroleum as a PAH source in the estuary. Petroleum refineries, a coal loading terminal and a major treated sewage outfall located at the mouth were not indicated as major contributing sources of PAH pollution in the estuary.

Yield Performance of Calocybe indica on Different Agricultural Subatrate

2016 ◽  
Vol 2 (3) ◽  
pp. 105
Author(s):  
Pinkal Patel ◽  
Ratna Trivedi
Keyword(s):  
Wheat Straw ◽  
Maximum Yield ◽  
Weight Basis ◽  
Biological Efficiency ◽  
Fresh Weight ◽  
Paddy Straw ◽  
Yield Performance ◽  
Fresh Weight Basis ◽  
Temperature And Humidity ◽  
Calocybe Indica

The Milky mushroom, Calocybe Indica was cultivated on different agricultural substrate, paddy straw, wheat straw, sugarcane trace and mango dry leaves. The spawning was done by sterilization of all the four substrate. The bags were kept in mushroom growing room with the maintenance of temperature and humidity 30̊ c-35̊ c and 70-80 % respectively. The minimum days requires for completion of spawn run (18.4 days), primordial formation (25.2 days) and days for first harvest (32.4 days) was first observed on cultivation with Paddy straw.  The maximum yield on fresh weight basis and biological efficiency (134.86 %) was also found to be as the same treatment with the Paddy straw as a substrate. The biological efficiency of wheat straw was at par with Sugarcane trace as substrate which was 85.07 % and 85.02 % respectively.

Mineral nutrition, dinitrogen fixation, and growth of Alnuscrispa and Alnusglutinosa

1985 ◽  
Vol 15 (5) ◽  
pp. 855-861 ◽  
Author(s):  
G. Prégent ◽  
C. Camiré
Keyword(s):  
Mineral Nutrition ◽  
Dry Weight ◽  
Optimal Growth ◽  
Maximum Growth ◽  
Dinitrogen Fixation ◽  
Weight Basis ◽  
Critical Levels ◽  
N Status

Invitro cultures of Alnuscrispa (Ait.) Pursh and Alnusglutinosa (L.) Gaertn. were used to estimate critical foliage levels of selected nutrients for optimal growth and dinitrogen (N2) fixation. For A. crispa to obtain 90% of maximum growth and N2 fixation, foliar levels of 0.12% P, 0.13% Mg, <0.31% K, and <0.04% Ca on a dry weight basis were needed. For A. glutinosa, the critical levels were 0.138% P, 0.10% Mg, 0.29% Ca, and ~0.20% K. From all the deficiencies observed, P had the more pronounced effects on N status of both species.

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