Carbon Dioxide Assimilation, Photosynthetic Efficiency, and Respiration of a Chesapeake Bay Salt Marsh

1981 ◽  
Vol 69 (2) ◽  
pp. 405 ◽  
Author(s):  
Bert G. Drake ◽  
Michael Read
1941 ◽  
Vol 139 (1) ◽  
pp. 365-376 ◽  
Author(s):  
H.G. Wood ◽  
C.H. Werkman ◽  
Allan Hemingway ◽  
A.O. Nier

1990 ◽  
Vol 82 (3) ◽  
pp. 451-459 ◽  
Author(s):  
H. F. Schnier ◽  
M. Dingkuhn ◽  
S. K. De Datta ◽  
K. Mengel ◽  
E. Wijangco ◽  
...  

2020 ◽  
Author(s):  
Branimir Trifunovic ◽  
Alma Vázquez-Lule ◽  
Margaret Capooci ◽  
Angelia Lyn Seyfferth ◽  
Carlos Moffat ◽  
...  

2021 ◽  
Vol 9 ◽  
Author(s):  
Grace D. Molino ◽  
Zafer Defne ◽  
Alfredo L. Aretxabaleta ◽  
Neil K. Ganju ◽  
Joel A. Carr

Coastal salt marshes, which provide valuable ecosystem services such as flood mitigation and carbon sequestration, are threatened by rising sea level. In response, these ecosystems migrate landward, converting available upland into salt marsh. In the coastal-plain surrounding Chesapeake Bay, United States, conversion of coastal forest to salt marsh is well-documented and may offset salt marsh loss due to sea level rise, sediment deficits, and wave erosion. Land slope at the marsh-forest boundary is an important factor determining migration likelihood, however, the standard method of using field measurements to assess slope across the marsh-forest boundary is impractical on the scale of an estuary. Therefore, we developed a general slope quantification method that uses high resolution elevation data and a repurposed shoreline analysis tool to determine slope along the marsh-forest boundary for the entire Chesapeake Bay coastal-plain and find that less than 3% of transects have a slope value less than 1%; these low slope environments offer more favorable conditions for forest to marsh conversion. Then, we combine the bay-wide slope and elevation data with inundation modeling from Hurricane Isabel to determine likelihood of coastal forest conversion to salt marsh. This method can be applied to local and estuary-scale research to support management decisions regarding which upland forested areas are more critical to preserve as available space for marsh migration.


1997 ◽  
Vol 122 (6) ◽  
pp. 837-840 ◽  
Author(s):  
Matej Stopar ◽  
Brent L. Black ◽  
Martin J. Bukovac

The effects of NAA, BA, or Accel on CO2 assimilation of shoot leaves of mature bearing Redchief `Delicious' and `Empire' apple (Malus ×domestica Borkh.) trees were evaluated over two seasons. BA at 50 mg·L-1 did not significantly affect any of the gas-exchange parameters measured. NAA (15 mg·L-1) consistently suppressed CO2 assimilation rate (from ≈10% to 24% below that of the control). This suppression was NAA-concentration dependent, continued for >15 days after treatment, and was completely overcome in `Empire', but only partially or not at all in `Delicious' when BA was combined with NAA. These results are discussed in relation to fruit thinning and NAA-induced inhibition of fruit growth in spur-type `Delicious'. Chemical names used: 2-(1-napthyl) acetic acid (NAA); N-(phenyl)-1H-purine-6-amine (BA); BA + gibberellin A (GA)4+7 (Accel).


1991 ◽  
Vol 21 (2) ◽  
pp. 207-216 ◽  
Author(s):  
P. M. Miller ◽  
L. E. Eddleman ◽  
J. M. Miller

Plants are balanced systems that integrate processes of carbon fixation and uptake of water and nutrients to optimize resource acquisition. Response of Juniperusoccidentalis Hook. to reductions in above- and below-ground tissue was measured to determine effects on carbon dioxide assimilation, leaf conductance, intercellular carbon dioxide, xylem water potential, foliage nutrient concentration, aboveground growth, water-use efficiency, and potential photosynthetic nitrogen-use efficiencies. Approximately 50% of the old foliage was removed and lateral roots were severed at the canopy edge in early April 1988; physiological processes were measured during three periods in the summer of 1988. Foliage removal increased rates of carbon dioxide assimilation and photosynthetic nitrogen-use efficiency, but neither increased growth nor improved water status or nitrogen concentration of remaining foliage. Cutting lateral roots reduced assimilation, leaf conductance, foliage nitrogen concentration, branchlet elongation, water-use efficiency, and photosynthetic nitrogen-use efficiency. By late August, juvenile and small-adult J. occidentalis in the cut-top treatment had compensated for foliage removal by reestablishing patterns of water-use efficiencies similar to those of control plants, which may indicate that an overall metabolic control was functioning to regulate the balance between carbon dioxide assimilation and water loss. Cutting lateral roots had a more lasting effect on efficiencies; by late August, juveniles and small adults still had significantly lower water-use efficiencies than controls.


Sign in / Sign up

Export Citation Format

Share Document