Temperature and day length response of some cocksfoot populations

1967 ◽  
Vol 18 (1) ◽  
pp. 1 ◽  
Author(s):  
P BrouT ◽  
CN Williams ◽  
CA Neal-Smith ◽  
L Albrecht

Seedling plants of seven cocksfoot (Dactylis glomerata L.) populations were exposed to day/night temperatures of 20/15, 15/10, 12/7, and 9/4°C at day lengths of either 8 or 16 hr. Leaf size, rate of leaf appearance, and relative growth rate decreased as temperature decreased. At higher temperatures, relative growth rate was greater in long than in short days, but at 9/4° it was greater in short days. Long days increased leaf size but slightly reduced the rate of leaf appearance at higher temperatures; the increased leaf size, however, more than compensated for the slightly lower rate of leaf appearance, so that relative growth rate was greater in long than in short days. At 9/4°, however, greater leaf size did not compensate for the much slower rate of leaf appearance in long days. Growth rates were consequently lower in long than in short days at 9/4°. The populations showed a general similarity in response, although significant differences between populations were recorded for particular treatments. There was no apparent relationship between seedling growth rates at low temperatures in this experiment and winter growth of these populations under field conditions.

1987 ◽  
Vol 33 (9) ◽  
pp. 819-822 ◽  
Author(s):  
Kyo Sato

Pentachlorophenol resistance was investigated in bacteria isolated from glycine- or water-percolated soils where the bacterial flora was modified by the addition of pentachloropenol. The strains isolated from the water-percolated soil amended with PCP had the highest resistance, and the addition of glycine to the percolated soil weakened the resistance. The strains from the glycine-percolated soil without pentachlorophenol had a medium degree of resistance, and the resistance of the strains from the water-percolated soil without PCP was the lowest. The bacterial groups were sorted taxonomically; differences in pentachloropenol resistance were correlated with taxonomic groupings. Relative growth rate in the presence of pentachlorophenol was proposed as a useful means to distinguish among the bacterial species.


1969 ◽  
Vol 5 (3) ◽  
pp. 195-207 ◽  
Author(s):  
A. H. El Nadi

SummaryExperiments were made in glasshouses, growth cabinets and growth rooms to study the differential responses of the broad bean to water stress during the vegetative and flowering phases of growth. Plants in the flowering phase proved to be more sensitive to drought than in the vegetative period, and there were different responses (Relative Growth Rate) to temperature at different stages of plant growth. Day length and temperature influenced the position of the earliest flower initials on the stem, and intensity of flower shedding was aggravated by high temperature.


1986 ◽  
Vol 64 (1) ◽  
pp. 233-237 ◽  
Author(s):  
Susan R. Singer

Growth is the major parameter used to assess novel phenotypes derived from plant tissue cultures. Any quantitative analysis of growth must have an explicit rational basis. Frequently this criterion is not met. For example, the calculation (W2 − W1)/W1(W1 = initial weight; W2 = final weight) approximates neither linear nor exponential growth. Yet, it is a common method of analysis, as is the related calculation W2/W1. When absolute growth values provide insufficient information, meaningful relative growth rate equations can be utilized. Relative growth rates should be evaluated as ln (W2/W1)/(t2 − t1) for t = time, thereby yielding a constant growth rate for exponentially growing cell lines. Linear growth (root growth, for example) can be approximated by 2(W2 − W1)/((W1 + W2)(t2 − t1)). All methods of analysis we have encountered assume that relative growth at a given instant depends on total mass. The possibility exists that growth may actually be proportional to mass raised to some power less than one. For example, growth could be limited to a thin outer shell of a spherical callus. Then the relative growth rate would equal 3(W21/3 − W11/3)/(t2 − t1). Data can be seriously distorted when inappropriate calculations are used. Such distortions are exacerbated when comparisons are made. In all cases an adequate assessment of growth kinetics for each cell line and each treatment is essential.


1994 ◽  
Vol 12 (1) ◽  
pp. 43-46
Author(s):  
Jeff S. Kuehny ◽  
Dennis R. Decoteau

Abstract Exclusion of nitrogen and light from existing leaves at initiation of an episode of shoot growth decreased shoot and root relative growth rate. The combination of both nitrogen and light exclusion synergistically impacted relative growth rate for shoot (RGRs) and relative growth rate for root (RGRr). The next episode of shoot growth provided sufficient leaf area for carbohydrate assimilation and maintaining shoot and root growth rates when light was excluded from mature leaves. A better understanding of the developmental and biochemical changes of this episodic species provided useful information for timing of fertilizer application and transplanting of Ligustrum and other episodic species.


2009 ◽  
Vol 34 (2) ◽  
pp. 91-96
Author(s):  
Jesaja A. Pattikawa ◽  
Elizabeth Ferdinandus

Study on growth of mangrove cockle (Anadara antiquata) was conducted in the intertidal area of Passo, Inner Ambon Bay. Three size-classes of 25 individual cockles were cultured in 1 m3 cage. Length increment data was collected every two weeks for seven periods of observation. Relative growth rate, length-weight relationship and condition factor were estimated using formula proposed by Effendie, Pauly and King, respectively. The results showed that the small size had the highest length increment and relative growth rates while the large size had the best condition factor. Length-weight relationship showed isometric growth for all categories.


1967 ◽  
Vol 18 (1) ◽  
pp. 15 ◽  
Author(s):  
P BrouT ◽  
S Kawanabe

Growth rates of vegetative seedling plants of 15 cocksfoot (Dactylis glomerata L.) populations were measured in long days at near optimum temperature. Relative growth rate of the plant tops was greater in populations from high than in those from low latitudes of origin (r = 0.85; P < 0.001). In a second experiment, the populations from low latitudes were found to initiate inflorescences earlier than those from high latitudes. It is suggested that environmental conditions which maximize population differences in time of floral initiation also maximize differences in growth rates during the vegetative phase of growth.


2009 ◽  
Vol 52 (6) ◽  
pp. 1341-1348 ◽  
Author(s):  
Adriane Schio Silva ◽  
Valdemir Antônio Laura ◽  
Liana Jank

The soil flood tolerance of seven genotypes of Panicum maximum Jacq. (PM11, PM34, PM40 and PM45, and the commercial cultivars Massai, Mombaça and Tanzânia) was evaluated in plants subjected to two conditions: flooded and not flooded, during a period of 14 days. Flooding significantly decreased the total and above ground biomass of PM40 and PM45. For cultivar Tanzânia, flooding decreased these two variables and also root biomass. The root, total and above ground relative growth rates were significantly reduced by flooding in cultivar Tanzânia, while in PM45 only the above ground relative growth rate was reduced. Cultivar Tanzânia showed significant differences for all variables analyzed, thus was not flood tolerant, as well as PM40 and PM45. It could be concluded that Massai, PM34, Mombaça and PM11 were the most flood tolerant genotypes.


Weed Science ◽  
1984 ◽  
Vol 32 (2) ◽  
pp. 206-213 ◽  
Author(s):  
Carol N. Somody ◽  
John D. Nalewaja ◽  
Stephen D. Miller

Twenty-nine wild oat (Avena fatuaL. ♯3AVEFA) andAvena sterilisL. ♯ AVEST accessions having various areas of origin and/or growth characteristics were grown to maturity in controlled environmental chambers. The four environments consisted of a 16-h photoperiod until 3 weeks after emergence, when the photoperiod was decreased (DP) 1 h per week for 8 weeks at a constant 14, 20, or 26 C (DP 14, DP 20, or DP 26); and an 8-h photoperiod until 3 weeks after emergence, when the photoperiod was increased (IP) 1 h per week for 8 weeks at a constant 20 C (IP 20). The relative growth rate of the accessions was similar in each environment. The length of the second leaf was up to 15 cm greater under 8- than 16-h day length at 20 C for some accessions, but was similar under both day lengths for other accessions. The width of the second leaf was greater under 14 than 20 C and was narrower with a 16-h than an 8-h photoperiod. Tiller initiation was slower in the DP 14 and IP 20 than in the DP 20 and DP 26 environments. Days to panicle emergence for individual accessions ranged from 10 to 57 days higher in the DP 14 than in the DP 20 environment. Seed produced on plants grown at 14 C had lower germination in water and 1500 ppm gibberellic acid than seed from plants grown at 20 C. Wild oat accessions varied in morphological characteristics, days to panicle emergence, and dormancy, and responded differently to changes in photoperiod and temperature. Wild oat morphological characteristics, days to panicle emergence, and dormancy did not consistently relate to species or area of origin.


2018 ◽  
Vol 444 ◽  
pp. 11-27 ◽  
Author(s):  
Arijit Pal ◽  
Amiya Ranjan Bhowmick ◽  
Farhana Yeasmin ◽  
Sabyasachi Bhattacharya

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