5 research outputs found

    Substantial carbon loss respired from a corn-soybean agroecosystem highlights the importance of careful management as we adapt to changing climate

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    Understanding agroecosystem carbon (C) cycle response to climate change and management is vital for maintaining their long-term C storage. We demonstrate this importance through an in-depth examination of a ten-year eddy covariance dataset from a corn-corn-soybean crop rotation grown in the Midwest United States. Ten-year average annual net ecosystem exchange (NEE) showed a net C sink of -0.39 Mg C ha-1 yr-1. However, NEE in 2014 and 2015 from the corn ecosystem was 3.58 and 2.56 Mg C ha-1 yr-1, respectively. Most C loss occurred during the growing season, when photosynthesis should dominate and C fluxes should reflect a net ecosystem gain. Partitioning NEE into gross primary productivity (GPP) and ecosystem respiration (ER) showed this C \u27burp\u27 was driven by higher ER, with a 51% (2014) and 57% (2015) increase from the ten-year average (15.84 Mg C ha-1 yr-1). GPP was also higher than average (16.24 Mg C ha-1 yr-1) by 25% (2014) and 37% (2015), but this was not enough to offset the C emitted from ER. This increased ER was likely driven by enhanced soil microbial respiration associated with ideal growing season climate, substrate availability, nutrient additions, and a potential legacy effect from drought

    Plot-level rapid screening for photosynthetic parameters using proximal hyperspectral imaging

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    Photosynthesis is currently measured using time-laborious and/or destructive methods which slows research and breeding efforts to identify crop germplasm with higher photosynthetic capacities. We present a plot-level screening tool for quantification of photosynthetic parameters and pigment contents that utilizes hyperspectral reflectance from sunlit leaf pixels collected from a plot (∼2 m×2 m) in c,max, R2=0.79) maximum electron transport rate in given conditions (J1800, R2=0.59), maximal light-saturated photosynthesis (Pmax, R2=0.54), chlorophyll content (R2=0.87), the Chl a/b ratio (R2=0.63), carbon content (R2=0.47), and nitrogen content (R2=0.49). Model predictions did not improve when using two cameras spanning 400-1800 nm, suggesting a robust, widely applicable and more 'cost-effective' pipeline requiring only a single VNIR camera. The analysis pipeline and methods can be used in any cropping system with modified species-specific PLSR analysis to offer a high-throughput field phenotyping screening for germplasm with improved photosynthetic performance in field trials.</p

    The short-term impact of abundant fruit upon deer mouse (Peromyscus maniculatus), red-backed vole (Myodes gapperi), and woodland jumping mouse (Napaeozapus insignis) populations

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    Fruit has been identified as an important and potentially population restricting food for red-backed voles (Myodes gapperi (Vigors, 1830)), deer mice (Peromyscus maniculatus (Wagner, 1845)), and woodland jumping mice (Napaeozapus insignis (Miller, 1891)). We added domestic dried strawberries and currants—which have native analogues and are preferred foods of these rodents—to white spruce-plantations from May through August 2011 and 2012 to test fruit and fruit based carbohydrate’s short-term (1-2 year) impact on these rodent populations. We used mark-recapture to estimate density, percentages of population that were juvenile and breeding female, average home range size, and body weight during spring and summer of both years, and fecundity via placental scars from euthanized females in summer 2012. Fruit enhancement had no apparent effect on our species’, fecundity, proportion of breeding females or juveniles during spring and summer of either year, nor were there differences among these metrics in spring 2012 following 2011 fruit additions. Overall, there were no impacts to the short-term adult population dynamics for any species during fruit addition. We are led to believe that short term pulses of fruit and/or fruit based carbohydrate abundance do little to influence temperate forest small mammal populations.The accepted manuscript in pdf format is listed with the files at the bottom of this page. The presentation of the authors' names and (or) special characters in the title of the manuscript may differ slightly between what is listed on this page and what is listed in the pdf file of the accepted manuscript; that in the pdf file of the accepted manuscript is what was submitted by the author
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