Propagation for the Conservation of Pityopsis ruthii, an Endangered Species from the Southeastern United States

被引:10
作者
Wadl, Phillip A. [1 ]
Rinehart, Timothy A. [2 ]
Dattilo, Adam J. [3 ]
Pistrang, Mark [4 ]
Vito, Lisa M. [1 ]
Milstead, Ryan [1 ]
Trigiano, Robert N. [1 ]
机构
[1] Univ Tennessee, Dept Entomol & Plant Pathol, Knoxville, TN 37996 USA
[2] USDA ARS, Thad Cochran Southern Hort Res Lab, Poplarville, MS 39470 USA
[3] Tennessee Valley Author, Biol Compliance, Knoxville, TN 37902 USA
[4] USDA ARS, Cherokee Natl Forest, Cleveland, TN 37312 USA
关键词
bonded fiber matrix; ex situ; in vitro; reintroduction; Ruth's golden aster; seed germination; tissue culture; vegetative propagation; IN-VITRO PROPAGATION; PLANT; ASTER; MICROPROPAGATION; REINTRODUCTION; GROWTH;
D O I
10.21273/HORTSCI.49.2.194
中图分类号
S6 [园艺];
学科分类号
0902 ;
摘要
Pityopsis ruthii is an endangered species endemic to the Hiwassee and Ocoee Rivers in Tennessee. As part of a recovery effort focused on P. ruthii, vegetative propagation and in vitro multiplication and seed germination techniques were developed. Plants were vegetatively propagated using greenhouse stock plants and wild-collected stems. Rooting occurred with and without auxin treatments but was greatest when 0.1% indole-3-butyric acid (IBA) talc was applied to the vegetative cuttings; rooting was lowest when flowering stems were used. Pro-Mix BX substrate provided the most consistent rooting. In vitro multiplication was accomplished by the removal of lateral shoots from in vitro-grown plants that were rooted on Murashige and Skoog (MS0) basal medium with 270 clones produced from a single individual after 4 months. Nineteen clones were transplanted and secured with bonded fiber matrix into their natural habitat and 14 survived for 1 year. To avoid genetic swamping of native populations with the introduction of large numbers of genetically identical individuals through clonal propagation, seed-based propagation efforts were explored. Open-pollinated seeds were collected, disinfested and germinated, and seedlings established on MS medium. Seeds were submersed in 70% ethanol for 1 minute and briefly flamed. Seeds were surface-sterilized in a range [10% to 50% (v/v)] Clorox (R) bleach solutions with vigorous shaking for 20 minutes, rinsed three times in sterile water, and germinated on MS0. Removal of pappus from seeds was required for successful disinfestations, but the bleach concentration was not critical. Successful propagation is a step toward the conservation and recovery of P. ruthii and should allow future reintroduction projects.
引用
收藏
页码:194 / 200
页数:7
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