scholarly journals PROCUMBENT GROWTH HABIT CHARACTERIZED IN SEEDLINGS OF `CIPO' ORANGE

HortScience ◽  
1992 ◽  
Vol 27 (6) ◽  
pp. 658g-659
Author(s):  
Kim D. Bowman

`Cipo' sweet orange [Citrus sinensis (L.) Osbeck] is distinctive among citrus selections because of reduced tree height and procumbent growth habit. Open-pollinated seeds were collected from `Cipo' orange and `Pineapple' sweet orange (C. sinensis) at Riverside, California, and grown under cool greenhouse conditions. Seedlings of `Cipo' were relatively uniform in morphology (including drooping shoot habit) and were presumed to be apomicts derived from nucellar embryos. `Cipo' seedlings were distinctly different from `Pineapple' in several characteristics, including smaller shoot altitude/extension ratios (a measure of uprightness) and broader stem-petiole angles (`Cipo' 1.33 radians; `Pineapple' 0.84 radians). The procumbent habit of `Cipo' appeared to be related to a preference for horizontal shoot orientation rather than a weakness of stem structure. Some increased sensitivity to ethylene was observed in the `Cipo' seedlings. `Cipo' is proposed as a resource for hormone research and a potential parent in breeding for unique tree morphology and reduced tree size.

HortScience ◽  
1994 ◽  
Vol 29 (5) ◽  
pp. 505f-505
Author(s):  
Kim D. Bowman

Citrus tree size and growth form are important traits that can be influenced by the genotype of both scion and rootstock cultivars. However, there have been very few reports of size or growth habit traits within Citrus or sexually compatible genera that might be transmitted genetically in breeding programs. A procumbent growth habit has been described for `Cipo' (Citrus sinensis [L.] Osbeck), a unique sweet orange cultivar maintained in the USDA germplasm repository. Sexual hybrids were produced between this selection and four related species, and these progenies were evaluated for two distinct traits associated with the unusual growth habit of `Cipo'. Inheritance of both drooping petiole and horizontal shoot growth were observed among the `Cipo' hybrids. Investigations are continuing on these four populations to verify segregation patterns and identify individuals possessing favorable combinations of growth habit with other desirable tree characteristics.


HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 553d-553
Author(s):  
C.R. Unrath

Historically, most airblast chemical applications to apple orchards used a single “average” water volume, resulting in variability of coverage with tree size and also the greatest variable in chemical thinning. This coverage variability can be eliminated by properly quantifying the tree canopy, as tree row volume (TRV), and relating that volume to airblast water rate for adequate coverge. Maximum typical tree height, cross-row limb spread, and between-row spacing are used to quantify the TRV. Further refinement is achieved by adjusting the water volume for tree canopy density. The North Carolina TRV model allows a density adjustment from 0.7 gal/1000 ft3 of TRV for young, very open tree canopies to 1.0 gal/1000 ft3 of TRV for large, thick tree canopies to deliver a full dilute application for maximum water application (to the point of run-off). Most dilute pesticide applications use 70% of full dilute to approach the point of drip (pesticide dilute) to not waste chemicals and reduce non-target environmental exposure. From the “chemical load” (i.e., lb/acre) calculated for the pesticide dilute application, the proper chemical load for lower (concentrate) water volumes can be accurately determined. Another significant source of variability is thinner application response is spray distribution to various areas of the tree. This variability is related to tree configuration, light, levels, fruit set, and natural thinning vs. the need for chemical thinning. Required water delivery patterns are a function of tree size, form, spacing, and density, as well as sprayer design (no. of nozzles and fan size). The TRV model, density adjustments, and nozzle patterns to effectively hit the target for uniform crop load will be addressed.


2009 ◽  
Vol 25 (2) ◽  
pp. 107-121 ◽  
Author(s):  
Jan H. D. Wolf ◽  
S. Robbert Gradstein ◽  
Nalini M. Nadkarni

Abstract:The sampling of epiphytes is fraught with methodological difficulties. We present a protocol to sample and analyse vascular epiphyte richness and abundance in forests of different structure (SVERA). Epiphyte abundance is estimated as biomass by recording the number of plant components in a range of size cohorts. Epiphyte species biomass is estimated on 35 sample-trees, evenly distributed over six trunk diameter-size cohorts (10 trees with dbh > 30 cm). Tree height, dbh and number of forks (diameter > 5 cm) yield a dimensionless estimate of the size of the tree. Epiphyte dry weight and species richness between forests is compared with ANCOVA that controls for tree size. SChao1 is used as an estimate of the total number of species at the sites. The relative dependence of the distribution of the epiphyte communities on environmental and spatial variables may be assessed using multivariate analysis and Mantel test. In a case study, we compared epiphyte vegetation of six Mexican oak forests and one Colombian oak forest at similar elevation. We found a strongly significant positive correlation between tree size and epiphyte richness or biomass at all sites. In forests with a higher diversity of host trees, more trees must be sampled. Epiphyte biomass at the Colombian site was lower than in any of the Mexican sites; without correction for tree size no significant differences in terms of epiphyte biomass could be detected. The occurrence of spatial dependence, at both the landscape level and at the tree level, shows that the inclusion of spatial descriptors in SVERA is justified.


2021 ◽  
Vol 13 (1) ◽  
pp. 131
Author(s):  
Franziska Taubert ◽  
Rico Fischer ◽  
Nikolai Knapp ◽  
Andreas Huth

Remote sensing is an important tool to monitor forests to rapidly detect changes due to global change and other threats. Here, we present a novel methodology to infer the tree size distribution from light detection and ranging (lidar) measurements. Our approach is based on a theoretical leaf–tree matrix derived from allometric relations of trees. Using the leaf–tree matrix, we compute the tree size distribution that fit to the observed leaf area density profile via lidar. To validate our approach, we analyzed the stem diameter distribution of a tropical forest in Panama and compared lidar-derived data with data from forest inventories at different spatial scales (0.04 ha to 50 ha). Our estimates had a high accuracy at scales above 1 ha (1 ha: root mean square error (RMSE) 67.6 trees ha−1/normalized RMSE 18.8%/R² 0.76; 50 ha: 22.8 trees ha−1/6.2%/0.89). Estimates for smaller scales (1-ha to 0.04-ha) were reliably for forests with low height, dense canopy or low tree height heterogeneity. Estimates for the basal area were accurate at the 1-ha scale (RMSE 4.7 tree ha−1, bias 0.8 m² ha−1) but less accurate at smaller scales. Our methodology, further tested at additional sites, provides a useful approach to determine the tree size distribution of forests by integrating information on tree allometries.


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