Relevant bibliographies by topics / Plastochrone interval

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'Plastochrone interval'

Author: Grafiati
Published: 4 June 2021
Last updated: 13 February 2022

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Journal articles on the topic "Plastochrone interval"

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Cebrián, Just, Nuria Marbà, and Carlos M. Duarte. "Estimating leaf age of the seagrass Posidonia oceanica (L.) Delile using the plastochrone interval index." Aquatic Botany 49, no. 1 (1994): 59–65. http://dx.doi.org/10.1016/0304-3770(94)90006-x.

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Brouns, Joop J. W. M. "The plastochrone interval method for the study of the productivity of seagrasses; possibilities and limitations." Aquatic Botany 21, no. 1 (1985): 71–88. http://dx.doi.org/10.1016/0304-3770(85)90097-x.

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Hibara, Ken-ichiro, Masayuki Miya, Sean Akira Benvenuto, et al. "Regulation of the plastochron by three many-noded dwarf genes in barley." PLOS Genetics 17, no. 5 (2021): e1009292. http://dx.doi.org/10.1371/journal.pgen.1009292.

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The plastochron, the time interval between the formation of two successive leaves, is an important determinant of plant architecture. We genetically and phenotypically investigated many-noded dwarf (mnd) mutants in barley. The mnd mutants exhibited a shortened plastochron and a decreased leaf blade length, and resembled previously reported plastochron1 (pla1), pla2, and pla3 mutants in rice. In addition, the maturation of mnd leaves was accelerated, similar to pla mutants in rice. Several barley mnd alleles were derived from three genes—MND1, MND4, and MND8. Although MND4 coincided with a cyto
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Jin, Jung-Kang, Hui-Ling Chen, Chih-Wen Yu, and Chin-Ho Lin. "Establishment of a plastochron index for growth assessment of Phalaenopsis." Canadian Journal of Botany 83, no. 1 (2005): 47–53. http://dx.doi.org/10.1139/b04-150.

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A plastochron index was established for four commercial cultivars of Phalaenopsis: Phalaenopsis 'Taisuco Carol' × (Doritaenopsis 'New Cinderella' × P. 'Isaribi') (Taiwan Sugar Corp., code No. S88-41); Phalaenopsis 'Taisuco Swan' × (P. 'Casablanca Dream' × (P. 'Hohoemi' × P. 'Grace Palm')) (code No. S88-89); Doritaenopsis 'I-Hsin Dreamer' × Phalaenopsis 'Taisuco Harmonylip' (code No. S88-104), and Phalaenopsis aphrodite. The plastochron was based on a 20-mm reference leaf length. Semilogarithmical plots of ln-transformed leaf lengths versus time and linear regression analysis were used to evalu
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Russin, W. A., M. K. Clayton, and R. D. Durbin. "Modeling nonexponential growth of a short-cycling plant, Tagetes erecta (Asteraceae)." Canadian Journal of Botany 69, no. 2 (1991): 316–20. http://dx.doi.org/10.1139/b91-043.

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A method for establishing a plastochron index was developed as part of an analysis of the growth pattern of Tagetes erecta 'Moonshot' plants. Both log-linear and log-quadratic equations were fitted to balanced sets of leaf-length data. Although the log-linear model fit the data, the log-quadratic model consistently provided a better fit. Slope values and length of plastochron from both models were compared versus leaf and plant number. An analysis of variance showed that overall, the leaves grew at different rates and were initiated at different intervals. However, leaves 2–4 on each plant ful
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Solana-Arellano, E., H. Echavarria-Heras, and E. Franco-Vizcaíno. "A dynamical model for characterising seasonality effects on eelgrass plastochron intervals." Annals of Applied Biology 157, no. 1 (2010): 99–110. http://dx.doi.org/10.1111/j.1744-7348.2010.00414.x.

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Ceulemans, R., I. Impens, and V. Steenackers. "Genetic variation in aspects of leaf growth of Populusclones, using the leaf plastochron index." Canadian Journal of Forest Research 18, no. 8 (1988): 1069–77. http://dx.doi.org/10.1139/x88-162.

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Leaf growth characteristics of seven clones of Populustrichocarpa, P. nigra, and interspecific hybrids with P. deltoides were examined on 1-year-old cuttings grown in a controlled-environment growth chamber. The plastochron index, a morphological time scale that is a linear function of time and correlated with other morphogenetic and physiological developmental processes, was applied to this development and growth study. Uniformity of leaf initiation was studied; new leaves were initiated at regular time intervals, at least under the controlled conditions of this study. Clones with a high leaf
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Gould, Kevin S., Elizabeth G. Cutter, and J. Peter W. Young. "Does growth rate determine leaf form in Pisum sativum?" Canadian Journal of Botany 67, no. 9 (1989): 2590–95. http://dx.doi.org/10.1139/b89-334.

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We have examined the long-standing hypothesis that leaves are morphologically more complex following prolonged proximity to the shoot apical meristem. Growth rates of the petiole and rachis of conventional and mutant pea leaves were compared for successive nodes of insertion in seedling plants. Leaves were longer at higher nodes, though the relative growth rate did not vary. Mature afila leaves were longer than those of conventional and tendril-less genotypes. The afila leaf alone exhibited a transient, highly significant rise in relative growth rate during the plastochron interval P4.5–P5.5.
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Dengler, Nancy G. "The shoot apical meristem and development of vascular architectureThis review is one of a selection of papers published on the Special Theme of Shoot Apical Meristems." Canadian Journal of Botany 84, no. 11 (2006): 1660–71. http://dx.doi.org/10.1139/b06-126.

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The shoot apical meristem (SAM) functions to generate external architecture and internal tissue pattern as well as to maintain a self-perpetuating population of stem-cell-like cells. The internal three-dimensional architecture of the vascular system corresponds closely to the external arrangement of lateral organs, or phyllotaxis. This paper reviews this correspondence for dicotyledonous plants in general and in Arabidopsis thaliana (L.) Heynh., specifically. Analysis is partly based on the expression patterns of the class III homeodomain-leucine zipper transcription factor ARABIDOPSIS THALIAN
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Vincent, Coral A., and Enrico S. Coen. "A temporal and morphological framework for flower development in Antirrhinum majus." Canadian Journal of Botany 82, no. 5 (2004): 681–90. http://dx.doi.org/10.1139/b04-042.

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The entire course of flower development in Antirrhinum majus L., from initiation to maturity, is described in terms of regular time intervals. Floral meristem and bud morphology was determined by scanning electron microscopy for a sequence of 58 plastochrons. These can be grouped to define 15 stages or 7 phases of development, providing a temporal framework for gene expression and key morphological events, such as the formation of the complex corolla. The time course is also used to estimate overall growth rates of sepals and petals. Sepals initially grow at a constant rate, but growth rate gr
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Dissertations / Theses on the topic "Plastochrone interval"

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Meads, Michael Vearl. "Effects of Short Shoot Number and Presence of an Apical Meristem on Rhizome Elongation, New Short Shoot Production, and New Rhizome Meristem Production of Thalassia Testudinum Banks and Solander Ex König Planting Units in Tampa Bay." Scholar Commons, 2012. http://scholarcommons.usf.edu/etd/4157.

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Thalassia testudinum Banks and Solander ex König is the dominant seagrass in the Gulf of Mexico, Caribbean and the West Coast of Florida, yet little rhizome elongation, new short shoot production, or new rhizome meristem production data has been collected via direct measurement. A study of the rhizome growth of T. testudinum was completed in December 2004 in southern Tampa Bay that determined growth after 26.5 months. Two PVC planting frames each containing four rhizomes with 2 short shoots, two rhizomes with 4 short shoots, and two rhizomes with 8 short shoots were planted next to existing T.
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