scholarly journals Freezing temperatures restrict woody plant recruitment and restoration efforts in abandoned montane pastures

2021 ◽  
Vol 26 ◽  
pp. e01462
Author(s):  
Evan M. Rehm ◽  
Stephanie Yelenik ◽  
Carla D’Antonio
2019 ◽  
Vol 444 ◽  
pp. 405-413 ◽  
Author(s):  
Evan M. Rehm ◽  
Miles K. Thomas ◽  
Stephanie G. Yelenik ◽  
Dave L. Bouck ◽  
Carla M. D'Antonio

2017 ◽  
Vol 41 (1) ◽  
Author(s):  
Kate McAlpine ◽  
◽  
Shona Lamoureaux ◽  
Susan Timmins ◽  
Debra Wotton

2019 ◽  
Vol 39 (2) ◽  
pp. 189
Author(s):  
Emily M. Booth ◽  
Greg Creacy ◽  
Norma L. Fowler

2022 ◽  
Vol 12 (01) ◽  
pp. 41-59
Author(s):  
Saran Traoré ◽  
Sébastien Ange Habih Nombré ◽  
Issiaka Keïta ◽  
Hassan Bismarck Nacro ◽  
Brice Sinsin

Plant Ecology ◽  
2020 ◽  
Author(s):  
Evan M. Rehm ◽  
Stephanie G. Yelenik ◽  
Marley Puanani Smith ◽  
Carla M. D’Antonio

2010 ◽  
Vol 9 (1) ◽  
Author(s):  
Lutfi Lutfi

<p><em>Effect of four types of diluents</em><em>s</em><em> and four concentration of DMSO (5%, 10%, 15% and 20%) against the motility of African catfish sperm were evaluated after storage at freezing temperatures. </em><em>The steps in preparation the 16 treatments combination of the diluents</em><em> </em><em>are </em><em>preparation of diluents, mixing </em><em>diluents </em><em>with DMSO, packing </em><em>of semen </em><em>in</em><em>to</em><em> 0.3-ml straw, equilibration of </em><em>semen </em><em>at 4 °C for 30 minutes, freezing </em><em>of </em><em>semen in nitrogen vapor liquid </em><em>at </em><em>a height of 6.5 cm for 10 minutes</em><em>,</em><em> and subsequent</em><em>ly</em><em> storage of </em><em>semen </em><em>in liquid nitrogen (-196</em><em> <sup>0</sup></em><em>C) for further analy</em><em>sis</em><em> </em><em>of </em><em>post-thawing motility (PTM). </em><em>The result showed that t</em><em>he highest level of motility of spermatozoa </em><em>was </em><em>in </em><em>treatment </em><em>P</em><em><sub>1</sub></em><em>D</em><em><sub>15 </sub></em><em>(45.7 ± 4.3%) and the lowest </em><em>was </em><em>in </em><em>treatment </em><em>P<sub>2</sub>D<sub>20</sub> (14.5 ± 13.2%). The best diluent </em><em>in </em><em>this observation </em><em>was </em><em>diluents containing NaCl, KCl, CaCl<sub>2</sub> and NaHCO<sub>3</sub>. The best concentration </em><em>was </em><em>DMSO 15%. While the best interaction between the concentration of DMSO diluents is P<sub>1</sub>D<sub>15</sub> treatments containing NaCl, KCl, CaCl <sub>2</sub> and NaHCO<sub>3</sub> with a combination of 15% DMSO concentration. </em><em>The </em><em>conclusion </em><em>of the research is that </em><em>diluents containing NaCl, KCl, CaCl<sub>2</sub> and NaHCO<sub>3</sub> with a combination of 15% DMSO concentration</em><em> can be used in </em><em>cryopreservation of African catfish semen</em><em>.</em></p>


HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 506a-506
Author(s):  
L.A. Klein ◽  
M.T. Windham ◽  
R.N. Trigiano

Microshoot and callus cultures of Cornus florida (flowering dogwood), which were grown on woody plant medium amended with BA, were inoculated with Microsphaera pulchra (an obligate plant parasite) by gently shaking infected leaves bearing numerous conidia over the tissue. Culture dishes were sealed with parafilm and incubated at 24 °C with 25 mol·m–2·s–1 provided by cool fluorescent bulbs for 15 h. Cultures were examined with a dissecting scope every 24 h and cultures transferred when contaminating fungi were present. Specimens were prepared light microscopy and SEM. The fungus infected individual callus cells, but did not sporulate. In contrast, powdery mildew was well-established (both primary and secondary hyphae) in 70% of the microshoot cultures after 6 days and sporulated on 20% by 7 to 8 days. The cellular relationship between host and pathogen in vitro was similar to that found in greenhouse-grown plants. This technique has possible applications in maintaining fungal culture collections and studying host–pathogen relationships under more stringently controlled conditions.


HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 503c-503
Author(s):  
Paul H. Henry ◽  
John E. Preece

A propagation method is being developed that allows softwood shoots to be generated from stem sections of dormant woody plant species. These shoots, forced in the greenhouse during the winter, are subsequently collected and processed as softwood stem cuttings to produce clonal plant material. Many species in the nursery industry can only be propagated using softwood cuttings, and this technique allows propagation of these species to be initiated several months earlier than what is typically possible. Current studies involve expanded screening of ornamental tree and shrub species to determine if commercial production using this technique is feasible. Results demonstrate that many species may be propagated using this method, but that some species are more prolific than others with respect to number of softwood shoots produced. Additional studies are currently in progress to determine the environmental (light regime, moisture regime) and cultural (type of media) conditions that are optimal when producing clonal plant material via this technique.


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