The Initiation and Development of Secondary Xylem in Axillary Branches of Populus deltoides

1982 ◽  
Vol 49 (2) ◽  
pp. 149-163 ◽  
Author(s):  
JENNIFER H. RICHARDS ◽  
P. R. LARSON
1983 ◽  
Vol 61 (4) ◽  
pp. 1040-1051 ◽  
Author(s):  
Philip R. Larson ◽  
David G. Fisher

The vasculature of elongating lateral branches was examined to determine how vessels produced in the branch unite with those produced in the main stem axis to form a continuous transport system. In a previous study it was found that differentiation of both primary and secondary xylem in a lateral bud or branch is independent of that in the main axis; i.e., xylem does not differentiate into the bud or branch from the main axis. When serial sections of the nodal region are followed downward, the bud vascular cylinder merges with that of the main axis and the adaxially situated bud traces (those nearest the stem) enter the bud gap margin first. The primary vessels of these bud traces differentiate in an oblique downward path along the margins of the bud gap, and they form radial files of primary vessels that lie adjacent to primary xylem of leaf traces in the stem. Traces situated more abaxially in the bud (those farther from the stem) contribute to other radial files of primary vessels, each of which lies progressively closer to the bud gap. Secondary xylem is initiated in the stem before it is in the branch. Consequently, the last-formed metaxylem vessels of the bud traces are continuous with secondary vessels of the stem. These latter vessels lie in the stem secondary xylem immediately external to primary xylem from the bud. Secondary xylem in the branch is initiated when foliage leaves and internodes mature. Secondary vessels formed in the branch traces are continuous with secondary vessels in the stem; these vessels are embedded in a matrix of fibers. Because cambial activity is more vigorous in the stem than in the branch, two vessels that are radially adjacent in the branch may be widely separated by fibers in the stem. The central trace of the axillant leaf enters the gap immediately below the last branch traces; at this level in the stem the leaf trace vasculature is entirely primary. The stem secondary xylem that overlies the leaf trace is continuous with that in the axillary branch.


2020 ◽  
Vol 45 (4) ◽  
pp. 833-838
Author(s):  
Lamarck Rocha ◽  
Patrícia Luz Ribeiro ◽  
Maria Mercedes Arbo

Abstract—We present a new species, Turnera fasciculifolia, from the Jalapão region, the largest continuous protected area of Cerrado in Tocantins State, in central Brazil. The new species belongs to Turnera series Leiocarpae, and it can be recognized by the linear ericoid leaves with revolute margin, generally without extrafloral nectaries, and the basal leaves of the young axillary branches gathered in fascicles. We provide a description, illustrations, a distribution map, and a comparison with T. genistoides and T. revoluta, which also have ericoid leaves.


Forests ◽  
2021 ◽  
Vol 12 (7) ◽  
pp. 869
Author(s):  
Solomon B. Ghezehei ◽  
Alexander L. Ewald ◽  
Dennis W. Hazel ◽  
Ronald S. Zalesny ◽  
Elizabeth Guthrie Nichols

We evaluated the productivity and profitability of four highly productive poplars including Populus deltoides × P. deltoides (DD ‘140’ and ‘356’), P. deltoides × P. maximowiczii (DM ‘230’), and P. trichocarpa × P. deltoides (TD ‘185’) under two densities (2500 and 5000 trees ha−1), and three fertilization treatments (0, 113, 225 kg nitrogen ha−1) at three sandy coastal sites varying in soil quality. Green stem biomass (GSB) was estimated from the sixth-year stem diameter. Leaf-rust (Melampsora castagne) and beetle damage (by Chrysomela scripta Fabricius), the leaf area index (LAI) and foliar nitrogen, were measured in year two. At all sites, DD and DM had higher survival (>93%) than TD (62–83%). DD produced greater GSB (92.5–219.1 Mg ha−1) than DM (54–60.2 Mg ha−1) and TD (16.5–48.9 Mg ha−1), and this was greater under the higher density (85.9–148.6 Mg ha−1 vs. 55.9–124.9 Mg ha−1). Fertilization significantly increased GSB on fertile soil but not marginal soils; a higher rate did not significantly enhance GSB. Leaf rust was higher for fertile soil (82%) than marginal soils (20–22%), and TD ‘185’ (51% vs. others 34%). C. scripta damage was higher for the higher density (+42%) than lower density, and TD ‘185’ (50% vs. others >38%). LAI was higher on fertile soil (1.85 m2 m−2) than marginal soils (1.35–1.64 m2 m−2), and under the lower density (1.67 m2 m−2 vs. 1.56 m2 m−2). The high GSB producer DD ‘356’ had the lowest LAI (1.39 m2 m−2 vs. 1.80 m2 m−2). Foliar nitrogen varied among genomic groups (DD ‘140’ 1.95%; TD ‘185’ 1.80%). Our plots were unprofitable at a 27 USD Mg−1 delivered price; the biggest profitability barriers were the high costs of higher density establishment and weed control. The best-case treatment combinations of DD (‘140’, ‘356’) would be cost-effective if the price increased by 50% (USD 37.54 Mg−1) or rotations were 12 years (fertile-soil) and longer (marginal soils). The requirement for cost-effectiveness of poplars includes stringent and site-specific weed control which are more important than fertilizer applications.


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