A New Method of Estimating Risk-Adjusted Reserves and Economic Potential of Exploratory Prospects

1985 ◽  
Author(s):  
Michael Holmes ◽  
Wayne Beeks ◽  
Tom Major ◽  
Robin Storey
2017 ◽  
Vol 13 (30) ◽  
pp. 96
Author(s):  
Boye Mambé Auguste Denise ◽  
Soko Dago Faustin ◽  
Lolo Akiapo Landry Joël ◽  
Akaffou Eric Tangui ◽  
Kouadio Yatty Justin

Plantain is an easy plant to grow. There are many varieties directly exploitable which makes it a plant with economic potential. Banana is one of the most consumed foods by the inhabitants of Côte d'Ivoire. However, banana production in this region remains insufficient. The possibility of creating a banana plantation remains a major problem due to the low availability of "seeds". The introduction of a new method under the name DESHYPIF could both reduce the vegetative cycle and the production cycle while allowing the vegetative propagation of the buds. The aim of our study was to show that the production of banana plants by DESHYPIF technique is possible with the use of buds suckers. The study focused on two types of buds, traditional bayonet discharges and buds suckers. The results showed that buds suckers lose more water (39.34 ± 0.52) than the bayonet (27.15 ± 1.03) in the dehydration phase, however, the water level in the phase of physiological awakening remained the same (5.23 ± 0.01). The rehydration rate was 100 %. For the number of young plants emitted in germination, the buds suckers dehydrated gave a number of individuals (77 ± 2) comparable to those of the bayonets (80±1).


Author(s):  
C. C. Clawson ◽  
L. W. Anderson ◽  
R. A. Good

Investigations which require electron microscope examination of a few specific areas of non-homogeneous tissues make random sampling of small blocks an inefficient and unrewarding procedure. Therefore, several investigators have devised methods which allow obtaining sample blocks for electron microscopy from region of tissue previously identified by light microscopy of present here techniques which make possible: 1) sampling tissue for electron microscopy from selected areas previously identified by light microscopy of relatively large pieces of tissue; 2) dehydration and embedding large numbers of individually identified blocks while keeping each one separate; 3) a new method of maintaining specific orientation of blocks during embedding; 4) special light microscopic staining or fluorescent procedures and electron microscopy on immediately adjacent small areas of tissue.


1960 ◽  
Vol 23 ◽  
pp. 227-232 ◽  
Author(s):  
P WEST ◽  
G LYLES
Keyword(s):  

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