Annual-shoot growth and branching patterns in Nothofagus dombeyi (Fagaceae)

1998 ◽  
Vol 76 (4) ◽  
pp. 673-685 ◽  
Author(s):  
J Puntieri ◽  
D Barthélémy ◽  
P Martinez ◽  
E Raffaele ◽  
C Brion
Keyword(s):  
Growth Rate ◽  
Apical Meristem ◽  
Shoot Growth ◽  
Relative Size ◽  
Growth Dynamics ◽  
Growth Period ◽  
Maximum Growth ◽  
Annual Shoot ◽  
Nothofagus Dombeyi ◽  
Axillary Branches

During the growing seasons 1994-1995 and 1995-1996, weekly measures of length and number of internodes and morphological observations were made on annual shoots of 11- to 21-year-old Nothofagus dombeyi (Mirb.) Blume trees growing in northern Patagonia, Argentina. Growth period and shoot size at the end of the extension period were highly variable. Four main types of annual shoots could be identified according to the death or persistence of the apical meristem and the development or not of axillary branches during the growth season of main stem extension. For all shoots the maximum growth rate took place in late November and was followed by a slower growth rate or cessation of growth in early December to early January. For those shoots with a long growth period, a second growth peak took place in late January-February, and only those shoots with a growth rate higher than 35-40 mm/week developed axillary branches as they elongated. Results from bud dissections suggest that the early growth rate peak corresponded to the development of those structures preformed at the time of bud break. The death of the apical meristem of a shoot affected both the position and the relative size of axillary branching on that shoot.Key words: Nothofagus, annual shoot, growth dynamics, branching pattern.

Phenological and growth response of legume cover crops to shading

2013 ◽  
Vol 152 (6) ◽  
pp. 917-931 ◽  
Author(s):  
R. P. MAURO ◽  
O. SORTINO ◽  
M. DIPASQUALE ◽  
G. MAUROMICALE
Keyword(s):  
Growth Rate ◽  
Cover Crops ◽  
Seedling Emergence ◽  
Growth Period ◽  
Maximum Growth ◽  
Maximum Growth Rate ◽  
Cycle Duration ◽  
Cover Cropping ◽  
Future Attempt ◽  
Annual Medics

SUMMARYAnnual medics and clovers have distinct properties in terms of usage as cover crops in Mediterranean orchards, but little is known of their capacity to adapt to the level of shading encountered on an orchard floor. A 2-year field experiment was conducted in South–Eastern Sicily to investigate the effects of withholding 0·50 of sunlight on the phenology and growth pattern of four medic and five clover accessions, focusing on traits known to be important for cover cropping. Shading delayed both seedling emergence and the onset of flowering (by up to 5 and 9 days, respectively), while it extended both the growth period and the overall life-cycle duration (by up to 5 and 11 days, respectively). It also induced an increase in cover crop height (from 34 to 38 cm) and crop light use (from 0·60 to 0·94 g DW/m2/MJ), but a reduction in soil coverage, above-ground dry biomass, maximum growth rate and maximum relative growth rate (by up to 13, 18, 21 and 7%, respectively), so compromising the competitiveness of cover crops against weeds. The responses to shading varied between genotypes. Medicago polymorpha ecotype S. Rosalia, Medicago rugosa ecotype Piano Lauro and ecotype Zappulla were the strongest competitors against weeds, whereas Trifolium tomentosum ecotype Bucampello was interesting in terms of its biomass yield and crop light use. The performance was unstable over seasons, so any future attempt to improve the species’ performances under shade by breeding will need to focus on reseeding capacity.

The assessment of seasonal yield using some Stylosanthes guyanensis accessions in humid tropical and sub-tropical environments

1977 ◽  
Vol 17 (86) ◽  
pp. 425 ◽  
Author(s):  
LA Edye ◽  
WT Williams ◽  
RL Burt ◽  
B Grof ◽  
SL Stillman ◽  
...  
Keyword(s):  
Growth Rate ◽  
High Growth ◽  
Growth Period ◽  
Maximum Growth ◽  
Maximum Growth Rate ◽  
Growth Patterns ◽  
Seasonal Growth ◽  
Seasonally Dry ◽  
Tropical Environments ◽  
Dry Tropics

The seasonal growth patterns of some S. guyanensis accessions were compared in three humid environments at South Johnstone (extended rainfall tropics), 'Heathlands' (seasonally dry tropics) and Cooroy (humid sub-tropics). The accessions were selected mainly for their productivity in previously described small mown sward experiments over three years at each site. Previous methods of presenting seasonal growth patterns are reviewed, and a new, simpler method of presentation is defined. Growth was highly seasonal at all sites. There was no growth during July to November at 'Heathlands' and Cooroy due to moisture and temperature limitations respectively. At South Johnstone growth was continuous but depressed in August and December with limitations due to both soil moisture and temperature: the maximum growth rate was 22 times the minimum growth rate. The accessions differed markedly in their growth patterns at each site. In general, the yield differences between accessions were greater at the beginning and end of the growing season than during the peak growth period. The highest yielding accessions at each site had high growth rates spread over a long period. The yield distribution and persistence of Q8231 and 46589C seemed superior to existing cultivars in tropical and sub-tropical environments respectively

Annual-shoot growth and branching patterns in Nothofagus dombeyi (Fagaceae)

1998 ◽  
Vol 76 (4) ◽  
pp. 673-685 ◽  
Author(s):  
J. Puntieri ◽  
D. Barthélémy ◽  
P. Martinez ◽  
E. Raffaele ◽  
C. Brion
Keyword(s):  
Shoot Growth ◽  
Annual Shoot ◽  
Branching Patterns ◽  
Nothofagus Dombeyi

Diagnostic nitrogen concentrations for cabbages grown in sand culture

1989 ◽  
Vol 29 (6) ◽  
pp. 883 ◽  
Author(s):  
DO Huett ◽  
G Rose
Keyword(s):  
Growth Rate ◽  
Growth Period ◽  
Maximum Growth ◽  
Maximum Growth Rate ◽  
Sand Culture ◽  
Total N ◽  
Rate Range ◽  
Nitrate N ◽  
N Concentration ◽  
Petiole Sap

The cabbage cv. Rampo was grown in sand culture with 5 nitrogen (N) levels, between 2 and 43 mmol/L, applied as nitrate each day in a complete nutrient solution. The youngest fully opened leaf (YFOL), which became the wrapper leaf at heading, the youngest fully expanded leaf (YFEL) and the oldest green leaf (OL) were harvested at a minimum of 2-week intervals over a 12-week growth period. Standard laboratory leaf total N and nitrate-N determinations and rapid petiole sap nitrate-N determinations were conducted on YFOL, YFEL and OL. Total N was also determined in bulked leaves. The relationship between growth rate relative to the maximum at each sampling time and leaf N concentration was used to derive diagnostic petiole sap nitrate-N, leaf nitrate-N and total N in YFOL, YFEL and OL and bulked leaf total N concentrations. Critical concentration corresponded to 90% maximum growth rate and adequate concentration corresponded to 9 1-1 00% maximum growth rate. Petiole sap nitrate-N concentration, which can be measured rapidly in the field, and leaf nitrate-N concentration were very responsive to N application where positive growth responses were recorded. Critical N concentrations are presented for all leaves at most sampling times throughout the growth period. Critical total N concentrations in YFOL, YFEL and bulked leaves were higher during the pre-heading growth stage (weeks 2-6) than the post-heading growth stage (weeks 8-12). Critical N concentrations were inconsistent over the growth period and it was not possible to present single values to represent the full growth period, with 2 exceptions. A critical petiole sap nitrate-N concentration for OL of 3.0 g/L can be recommended for the full growth period because it represents a percentage of maximum growth rate range of 88-95%. Similarly, for YFEL, a critical total N concentration of 4.10% pre-heading (range 4.10-4.38%) represents a percentage maximum growth rate range of 62-90% and a post-heading critical total N concentration of 3.10% (range 3.10-3.50%) represents a percentage maximum growth rate range of 76-90%. The concentrations of potassium, phosphorus, calcium, magnesium and sulfur in YFOL, YFEL, OL and bulked leaf corresponding to N treatments producing maximum growth rates are also presented.

Saturation mechanism and generated viscosity in gravito-turbulent accretion disks

2020 ◽  
Vol 640 ◽  
pp. A53
Author(s):  
L. Löhnert ◽  
S. Krätschmer ◽  
A. G. Peeters
Keyword(s):  
Growth Rate ◽  
Numerical Simulations ◽  
Accretion Disks ◽  
Gravitational Instability ◽  
Turbulent Viscosity ◽  
Radial Distance ◽  
Maximum Growth ◽  
Wave Number ◽  
Radiative Cooling ◽  
Mixing Length

Here, we address the turbulent dynamics of the gravitational instability in accretion disks, retaining both radiative cooling and irradiation. Due to radiative cooling, the disk is unstable for all values of the Toomre parameter, and an accurate estimate of the maximum growth rate is derived analytically. A detailed study of the turbulent spectra shows a rapid decay with an azimuthal wave number stronger than ky−3, whereas the spectrum is more broad in the radial direction and shows a scaling in the range kx−3 to kx−2. The radial component of the radial velocity profile consists of a superposition of shocks of different heights, and is similar to that found in Burgers’ turbulence. Assuming saturation occurs through nonlinear wave steepening leading to shock formation, we developed a mixing-length model in which the typical length scale is related to the average radial distance between shocks. Furthermore, since the numerical simulations show that linear drive is necessary in order to sustain turbulence, we used the growth rate of the most unstable mode to estimate the typical timescale. The mixing-length model that was obtained agrees well with numerical simulations. The model gives an analytic expression for the turbulent viscosity as a function of the Toomre parameter and cooling time. It predicts that relevant values of α = 10−3 can be obtained in disks that have a Toomre parameter as high as Q ≈ 10.

In-Situ Dual-Wavelength Ellipsometry and Light Scattering Monitoring of Si/Si1−xGex Heterostructures and Multiuantum Wells

1993 ◽  
Vol 324 ◽  
Author(s):  
C. Pickering ◽  
D.A.O. Hope ◽  
W.Y. Leong ◽  
D.J. Robbins ◽  
R. Greef
Keyword(s):  
Growth Rate ◽  
Light Scattering ◽  
Laser Light ◽  
Growth Period ◽  
Laser Light Scattering ◽  
Heterojunction Bipolar Transistor ◽  
Dual Wavelength ◽  
Multi Quantum Well ◽  
Refractive Index Data

AbstractIn-situ dual-wavelength ellipsometry and laser light scattering have been used to monitor growth of Si/Si1−x,Gex heterojunction bipolar transistor and multi-quantum well (MQW) structures. The growth rate of B-doped Si0 8Ge0.2 has been shown to be linear, but that of As-doped Si is non-linear, decreasing with time. Refractive index data have been obtained at the growth temperature for x = 0.15, 0.20, 0.25. Interface regions ∼ 6-20Å thickness have been detected at hetero-interfaces and during interrupted alloy growth. Period-to-period repeatability of MQW structures has been shown to be ±lML.

A note on growth curves of rabbit lines selected on growth rate or litter size

1993 ◽  
Vol 57 (2) ◽  
pp. 332-334 ◽  
Author(s):  
A. Blasco ◽  
E. Gómez
Keyword(s):  
Growth Rate ◽  
Litter Size ◽  
Growth Curves ◽  
Live Weight ◽  
Maximum Growth ◽  
Maximum Growth Rate ◽  
Standard Errors ◽  
Adult Weight ◽  
Weight Growth ◽  
Using Data

Two synthetic lines of rabbits were used in the experiment. Line V, selected on litter size, and line R, selected on growth rate. Ninety-six animals were randomly collected from 48 litters, taking a male and a female each time. Richards and Gompertz growth curves were fitted. Sexual dimorphism appeared in the line V but not in the R. Values for b and k were similar in all curves. Maximum growth rate took place in weeks 7 to 8. A break due to weaning could be observed in weeks 4 to 5. Although there is a remarkable similarity of the values of all the parameters using data from the first 20 weeks only, the higher standard errors on adult weight would make 30 weeks the preferable time to take data for live-weight growth curves.

Reassessment of Maximum Growth Rates for C3 and C4 Crops

1978 ◽  
Vol 14 (1) ◽  
pp. 1-5 ◽  
Author(s):  
J. L. Monteith
Keyword(s):  
Growth Rate ◽  
Growth Rates ◽  
Growing Season ◽  
Maximum Growth ◽  
Maximum Growth Rate ◽  
Crop Growth ◽  
Close Inspection ◽  
Similar Difference ◽  
Photosynthetic Efficiencies

SUMMARYFigures for maximum crop growth rates, reviewed by Gifford (1974), suggest that the productivity of C3 and C4 species is almost indistinguishable. However, close inspection of these figures at source and correspondence with several authors revealed a number of errors. When all unreliable figures were discarded, the maximum growth rate for C3 stands fell in the range 34–39 g m−2 d−1 compared with 50–54 g m−2 d−1 for C4 stands. Maximum growth rates averaged over the whole growing season showed a similar difference: 13 g m−2 d−1 for C3 and 22 g m−2 d−1 for C4. These figures correspond to photosynthetic efficiencies of approximately 1·4 and 2·0%.

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