scholarly journals Local environment, not local adaptation, drives leaf-out phenology in common gardens along an elevational gradient in Acadia National Park, Maine

2018 ◽  
Vol 105 (6) ◽  
pp. 986-995 ◽  
Author(s):  
Caitlin McDonough MacKenzie ◽  
Richard B. Primack ◽  
Abraham J. Miller-Rushing
2013 ◽  
Vol 177 ◽  
pp. 116-124 ◽  
Author(s):  
Sait C. Sofuoglu ◽  
Aysun Sofuoglu ◽  
Thomas M. Holsen ◽  
Colleen M. Alexander ◽  
James J. Pagano

2019 ◽  
Author(s):  
Yan Liu ◽  
Caitlin McDonough MacKenzie ◽  
Richard B. Primack ◽  
Michael J. Hill ◽  
Xiaoyang Zhang ◽  
...  

Abstract. Greenup dates of the mountainous Acadia National Park, were monitored using remote sensing data (including Landsat 8 surface reflectances (at a 30 m spatial resolution) and VIIRS reflectances adjusted to a nadir view (gridded at a 500 m spatial resolution)) during the 2013–2016 growing seasons. Ground-level leaf-out monitoring in the areas alongside the north-south-oriented hiking trails on three of the park's tallest mountains (466 m, 418 m, and 380 m) was used to evaluate satellite derived greenup dates in this study. While the 30 m resolution would be expected to provide a better scale for phenology detection in this mountainous region than the 500 m resolution, the daily temporal resolution of the 500 m data would be expected to offer vastly superior monitoring of the rapid variations experienced during vegetation greenup along elevational gradients. Therefore, the greenup dates derived from the Landsat 8 Enhanced Vegetation Index (EVI) data, augmented with Spatial and Temporal Adaptive Reflectance Fusion Model (STARFM) simulated EVI values, does provide more spatial details than VIIRS data alone and agree well with field monitored leaf out dates. Satellite derived greenup dates from the 30 m of Acadia National Park vary among different elevational zones, although the date of greenup is not always the most advanced at the lowest elevation. This indicates that the spring phenology is not only determined by microclimates associated with different elevations in this mountainous area, but is also possibly affected by the species mixture, localized temperatures, and other factors in Acadia.


Author(s):  
Monica Turner ◽  
Rebecca Reed ◽  
William Romme ◽  
Gerald Tuskan

An unexpected consequence of the 1988 Yellowstone fires was the widespread establishment of seedlings of quaking aspen (Populus tremuloides) in the burned forests, including areas outside the previous range of aspen (Kay 1993; Romme et al. 1997). Although aspen is the most widely distributed tree species in North America (Powells 1965), it is relatively uncommon and localized in distribution within Yellowstone National Park (Despain 1991). Most aspen stands in Yellowstone are found in the lower elevation landscapes in the northern portion of the park, and the species was absent - prior to 1988 -- across most of the high plateaus that dominate the southern and central park area. Aspen in the Rocky Mountain region reproduces primarily by means of vegetative root sprouting. Although viable seeds are regularly produced, establishment of seedlings in the wild is apparently a rare event due to the limited tolerance of aspen seedlings for desiccation or competition (e.g., Pearson 1914; McDonough 1985). In the immediate aftermath of the 1988 Yellowstone fires, there was a brief "window of opportunity" for aspen seedling establishment, as a result of abundant aspen seed production, moist weather conditions in spring and summer, and bare mineral soil and reduced plant competition within extensive burned areas (Jelinski and Cheliak 1992; Romme et al. 1997). We initiated this 3-year study in 1996 to address four questions about the aspen seedlings now growing in burned areas across the Yellowstone Plateau: (1) What are the broad-scale patterns of distribution and abundance of aspen seedlings across the subalpine plateaus of Yellowstone National Park? (2) What is the morphology and population structure -- e.g., proportions of genets (genetic individuals that developed from a single seed) and ramets (vegetative root sprouts produced by a genet) of various ages - in aspen seedling populations? (3) What are the mechanisms leading to eventual persistence or extirpation of seedling populations along an elevational gradient, particularly with respect to ungulate browsing and plant competition? (4) What is the genetic diversity and relatedness of the seedling populations along gradients of elevation and substrate?


Author(s):  
Sergio Perez-Limón ◽  
Meng Li ◽  
G Carolina Cintora-Martinez ◽  
M Rocio Aguilar-Rangel ◽  
M Nancy Salazar-Vidal ◽  
...  

Abstract Generations of farmer selection in the central Mexican highlands have produced unique maize varieties adapted to the challenges of the local environment. In addition to possessing great agronomic and cultural value, Mexican highland maize represents a good system for the study of local adaptation and acquisition of adaptive phenotypes under cultivation. In this study we characterize a recombinant inbred line population derived from the B73 reference line and the Mexican highland maize variety Palomero Toluqueño. B73 and Palomero Toluqueño showed classic rank-changing differences in performance between lowland and highland field sites, indicative of local adaptation. Quantitative trait mapping identified genomic regions linked to effects on yield components that were conditionally expressed depending on the environment. For the principal genomic regions associated with ear weight and total kernel number, the Palomero Toluqueño allele conferred an advantage specifically in the highland site, consistent with local adaptation. We identified Palomero Toluqueño alleles associated with expression of characteristic highland traits, including reduced tassel branching, increased sheath pigmentation and the presence of sheath macrohairs. The oligogenic architecture of these three morphological traits supports their role in adaptation, suggesting they have arisen from consistent directional selection acting at distinct points across the genome. We discuss these results in the context of the origin of phenotypic novelty during selection, commenting on the role of de novo mutation and the acquisition of adaptive variation by gene flow from endemic wild relatives.


2006 ◽  
Vol 126 (1-3) ◽  
pp. 69-80 ◽  
Author(s):  
S. J. Nelson ◽  
K. B. Johnson ◽  
J. S. Kahl ◽  
T. A. Haines ◽  
I. J. Fernandez

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