Construction of Texas coastal foredunes with sea oats (Uniola paniculata) and bitter panicum (Panicum amarum)

1977 ◽  
Vol 21 (3) ◽  
pp. 267-275 ◽  
Author(s):  
B. E. Dahl ◽  
D. W. Woodard
EDIS ◽  
2018 ◽  
Vol 2018 (5) ◽  
Author(s):  
Debbie Miller ◽  
Mack Thetford ◽  
Chris Verlinde ◽  
Gabriel Campbell ◽  
Ashlynn Smith

Sea oats occur throughout Florida on beach dunes and beaches and on coastal areas west to Texas and north to Maryland. Sea oats are vital dune builders that accumulate sand and prevent erosion due to wind, waves, and large storms. As sand is trapped by the long leaves of sea oats, vertical growth is stimulated, and rooting occurs at the buried nodes. This plant is extremely drought- and salt-tolerant, grows up to the high tide line of beaches, and propagates both vegetatively and by seed in the wild (Shadow 2007).https://edis.ifas.ufl.edu/sg186 This publication is derived from information in SGEB-75/SG156, Dune Restoration and Enhancement for the Florida Panhandle, by Debbie Miller, Mack Thetford, Christina Verlinde, Gabriel Campbell, and Ashlynn Smith. https://edis.ifas.ufl.edu/sg156.


HortScience ◽  
1994 ◽  
Vol 29 (5) ◽  
pp. 559d-559 ◽  
Author(s):  
Nancy Phiman ◽  
Michael E. Kane

Beach stabilization by replanting dune species such as Uniola paniculata L. (Sea Oats), is an accepted practice to control erosion in the southeastern United States. Increased restrictions on collection of sea oat seed and plant material for propagation is of increasing concern. Development of micropropagation protocols for establishment and production of sea oats from donor plants of known phenotype would be useful for selecting and producing plants with commercially valuable characteristics. Terminal and lateral shoot tips (3 mm wide and 4 mm high) from containerized plants were surface sterilized and established on Linsmaier & Skoog mineral salts and organics supplemented with 87.6 mM sucrose, 2.2 μM benzyladenine solidified with 0.8% TC® Agar. Terminal tiller shoot tips were more responsive than lateral shoot tips. Four monthly subcultures were. required for stabilized shoot multiplication from culture lines established from terminal tiller shoot tips. Shoot organogenesis frequently occurred from the cut leaf surfaces of subcultured shoot clusters. Microcuttings were established ex vitro in plug cells containing sand or vermiculite.


2005 ◽  
Vol 111 (8) ◽  
pp. 1632-1641 ◽  
Author(s):  
Prasanta K. Subudhi ◽  
Neil P. Parami ◽  
Stephen A. Harrison ◽  
Michael D. Materne ◽  
J. Paul Murphy ◽  
...  

EDIS ◽  
2018 ◽  
Vol 2018 (5) ◽  
Author(s):  
Debbie Miller ◽  
Mack Thetford ◽  
Chris Verlinde ◽  
Gabriel Campbell ◽  
Ashlynn Smith

Bitter panicgrass is important in dune stabilization and building and often grows intermixed with sea oats onforedunes. It is also found spread throughout back dunes, interdunal swales, and coastal grasslands. This plantoccurs throughout coastal Florida, except for the Big Bend coast, west to New Mexico, and along coastal northeast states to Massachusetts. A significant proportion of bitter panicgrass reproduction is by vegetative spread; its seeds are often sterile.https://edis.ifas.ufl.edu/sg178 This publication is derived from information in SGEB-75/SG156, Dune Restoration and Enhancement for the Florida Panhandle, by Debbie Miller, Mack Thetford, Christina Verlinde, Gabriel Campbell, and Ashlynn Smith. https://edis.ifas.ufl.edu/sg156.


HortScience ◽  
2004 ◽  
Vol 39 (4) ◽  
pp. 891B-891 ◽  
Author(s):  
Carmen Valero Aracama* ◽  
Michael E. Kane ◽  
Nancy L. Philman ◽  
Sandra B. Wilson

A sea oats (Uniola paniculata L.) micropropagation protocol was previously developed for 28 genotypes that favored multiplication and rooting of shoots in vitro. However, microcutting size, morphology, and acclimatization ex vitro varied considerably among genotypes. In the present study we evaluated the effect of Stage III duration on in vitro morphology, biomass production, and ex vitro survivability of easy-(EK 16-3) and difficult-to-acclimatize (EK 11-1) sea oats genotypes. After 3, 6, and 9 weeks at Stage III, survivability of microcuttings was 85%, 96% and 98% for EK 16-3, and 2%, 27% and 40% for EK 11-1, respectively. After 9 weeks Stage III, EK 16-3 microcuttings had higher shoot dry weights but lower root dry weights than in EK 11-1. Moreover, roots in EK 11-1 were fewer but longer than in EK 16-3. Leaf production was similar in both genotypes. However, leaf elongation was significantly inhibited in EK 11-1, in which 95% of the leaves were ≤ 15 mm long in contrast with EK 16-3, with 50% leaves ≥ 16 mm long after 9 weeks Stage III. Light microscopy examinations showed anatomical similarities between EK 16-3 in vitro leaves and mature ex vitro leaves. Conversely, short in vitro leaves of EK 11-1 exhibited mesophyll disruption and reduced cuticle development. Conceivably, the short leaves had limited photosynthetic competency, thereby reducing ex vitro survival of rooted EK 11-1 microcuttings.


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