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1 me structural polymorphism were found within Saccharum.
2                             In autopolyploid Saccharum, 36 significant associations between variation
3 th minor contributions from other species in Saccharum and other genera.
4 by 242 common probes were homologous between Saccharum and Sorghum.
5 c resistance (R(leaf)) for sugar maple (Acer saccharum) and red oak (Quercus rubra) by measuring the
6 ter and fine roots at four sugar maple (Acer saccharum)-dominated hardwood forests in the north-centr
7 experiment with litter of four species (Acer saccharum, Drypetes glauca, Pinus resinosa, and Thuja pl
8 in ongoing molecular analysis of the complex Saccharum genome.
9                      Genetic maps of the six Saccharum genotypes, including up to 72 linkage groups,
10 or large-scale genomic rearrangements in the Saccharum genus after two rounds of whole genome duplica
11 rdeum vulgare]), and ShSUT1 (from sugarcane [Saccharum hybrid]), and results indicate that type I and
12                                   Sugarcane (Saccharum hybrids spp.) is the most important sugar crop
13 in temperature class where cool-adapted Acer saccharum increased and temperature neutral changes wher
14 erability to cavitation of sugar maple (Acer saccharum Marsh.) was quantified by measuring the pressu
15                    This study investigated a Saccharum officinarum (Green German or GG, 2n approximat
16                     Sugarcane is a hybrid of Saccharum officinarum and Saccharum spontaneum, with min
17 ected 2460 loci in F1 progeny of the crosses Saccharum officinarum Green German x S. spontaneum IND 8
18 e (HFO)-treated sugarcane bagasse (SCB-HFO) (Saccharum officinarum L.) was investigated.
19 orghum bicolor) immature embryos, sugarcane (Saccharum officinarum) callus, and indica rice (Oryza sa
20 sses, including maize (Zea mays), sugarcane (Saccharum officinarum), sorghum (Sorghum bicolor), Misca
21 orghum [Sorghum bicolor]), sugar (sugarcane [Saccharum officinarum]), and biofuel (Miscanthus spp.) p
22 al temperatures, growth of species like Acer saccharum, Quercus rubra, and Picea glauca will vary mor
23 ere found to be different in the Pennisetum, Saccharum, Sorghum and Zea lineages.
24       The complex polyploid genomes of three Saccharum species have been aligned with the compact dip
25 Zea and of Leviathan elements in Sorghum and Saccharum species suggests that members of these familie
26 P markers scored on 90 plants of the species Saccharum spontaneum L. was used to illustrate the const
27 chromosomes of a wild relative of sugarcane (Saccharum spontaneum L.) anther culture-derived clone (A
28 ane is a hybrid of Saccharum officinarum and Saccharum spontaneum, with minor contributions from othe
29                                   Sugarcane (Saccharum spp. hybrids) accumulates high concentrations
30 ap of stalk storage parenchyma of sugarcane (Saccharum spp. hybrids) increases by an order of magnitu
31                                   Sugarcane (Saccharum spp.) is currently one of the most efficient c
32 rops such as maize (Zea mays) and sugarcane (Saccharum spp.), and is a logical complement to distantl
33 mays), sorghum (Sorghum bicolor), sugarcane (Saccharum spp.), and rice (Oryza sativa).
34 s probes that foster comparative genomics of Saccharum (sugarcane), Zea (maize), Oryza (rice), Pennis
35 t two different sites with sugar maple (Acer saccharum), we investigated ascending sap (sugar concent

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