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Protocols for Micropropagation of Woody Trees and Fruits

Protocols for Micropropagation of Woody Trees and Fruits

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CHAPTER 27<br />

MICROGRAFTING OF PISTACHIO<br />

(PISTACIA VERA L. CV. SIIRT)<br />

A. ONAY*, E. TILKAT, C. ISIKALAN AND S. NAMLI<br />

Department <strong>of</strong> Biology, Faculty <strong>of</strong> Science <strong>and</strong> Literature The University <strong>of</strong> Dicle,<br />

21280 Diyarbakır/TURKEY. *E-mail: ahmeto@dicle.edu.tr<br />

1. INTRODUCTION<br />

Pistacia vera L. is a dioecious tree species cultivated widely in the Mediterranean<br />

regions <strong>of</strong> Europe <strong>and</strong> North Africa, the Middle East, China <strong>and</strong> Cali<strong>for</strong>nia, USA.<br />

Development <strong>of</strong> pistachio plantations is limited by the absence <strong>of</strong> adequate nursery<br />

stock due to the difficulty <strong>of</strong> propagating Pistacia plants by conventional methods,<br />

such as cutting <strong>and</strong> grafting. Consequently, many ef<strong>for</strong>ts have focused on establishing<br />

in vitro propagation procedures <strong>for</strong> Pistacia vera <strong>and</strong> several other Pistacia<br />

species (Hansman & Owens, 1986; Barghchi & Alderson, 1989; Onay & Jeffree,<br />

2000; Onay, 2003; Onay et al., 2004a,b,c; Onay, 2005).<br />

The initiation <strong>of</strong> cultures from mature material usually involves pruning, grafting<br />

as well as BA <strong>and</strong> GA3 spray treatments that stimulate new growth <strong>of</strong> shoots<br />

(Barghchi, 1986; Gonzales & Frutos, 1990). There has been some success in establishment<br />

<strong>of</strong> mature pistachios by direct organogenesis (Yang & Lüdders, 1993; Dolcet-<br />

Sanjuan & Claveria, 1995; Onay, 2000) <strong>and</strong> somatic embryogenesis (Onay et al.,<br />

1995, 1996, 1997, 2000; Onay et al., 2004a). Onay (2000) harvested 3–4 cm long<br />

terminal lignified stem sections from 30-year-old pistachio trees <strong>and</strong> immersed the<br />

cut ends in plant growth regulator solutions, be<strong>for</strong>e placing them in a greenhouse<br />

medium. New, s<strong>of</strong>twood shoots were <strong>for</strong>ced in the greenhouse under a 24 h photo-<br />

period until they were sufficiently large to excise, surface disinfest <strong>and</strong> place<br />

in vitro. However, despite this progress, establishment <strong>and</strong> multiplication <strong>of</strong> field-<br />

grown mature P. vera clones remain problematic. In vitro micrografting can<br />

overcome these limitations. The first attempts to rejuvenate mature materials by micrografting<br />

in vitro mature scion shoot tips onto juvenile P. vera rootstocks were<br />

reported by Barghchi (1986). However, the growth <strong>of</strong> scion was very slow <strong>and</strong><br />

elongation did not occur. Micrografting was investigated in vitro as well as in vivo<br />

by Abousalim & Mantell (1992), but rejuvenation was not reported when mature<br />

289<br />

S.M. Jain <strong>and</strong> H. Häggman (eds.), <strong>Protocols</strong> <strong>for</strong> <strong>Micropropagation</strong> <strong>of</strong> <strong>Woody</strong> <strong>Trees</strong> <strong>and</strong> <strong>Fruits</strong>, 289–298.<br />

© 2007 Springer.

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