X-Received: by 2002:ac8:4f15:0:b0:400:9629:cfad with SMTP id b21-20020ac84f15000000b004009629cfadmr2833qte.13.1701720203561; Mon, 04 Dec 2023 12:03:23 -0800 (PST) X-Received: by 2002:a4a:d0c6:0:b0:58e:2518:eb49 with SMTP id u6-20020a4ad0c6000000b0058e2518eb49mr2075070oor.1.1701720203240; Mon, 04 Dec 2023 12:03:23 -0800 (PST) Path: ...!news-out.google.com!nntp.google.com!postnews.google.com!google-groups.googlegroups.com!not-for-mail Newsgroups: fr.comp.ordinosaures Date: Mon, 4 Dec 2023 12:03:22 -0800 (PST) Injection-Info: google-groups.googlegroups.com; posting-host=216.131.120.45; posting-account=MBaxOAoAAAA9C-ku9CqLZdzH3hCLKFN5 NNTP-Posting-Host: 216.131.120.45 User-Agent: G2/1.0 MIME-Version: 1.0 Message-ID: <435f6ceb-14c9-42f0-8ac4-1ddfd8319782n@googlegroups.com> Subject: Plant Physiology Taiz And Zeiger 5th Edition Pdf 186 From: Karl Stanforth Injection-Date: Mon, 04 Dec 2023 20:03:23 +0000 Content-Type: text/plain; charset="UTF-8" Content-Transfer-Encoding: quoted-printable Bytes: 3974 Lines: 43 Temperature is the driving force for several chemical reactions occurring i= n plant cells at different stages throughout the life cycle. Decreases in t= emperature below the optimum range generally decrease the rate of chemical = reactions. Sub-optimal temperature increases the probability of early-seaso= n seedling injury from pests and pathogens in peanuts with potential seedli= ng death, ultimately resulting in reduced plant populations and lower yield= potential (Prasad et al., 2006; Bell et al., 1993; Bell, 1986). Leong and = Ong (1983) reported a linear increase in rate of peanut development with in= creasing temperature from 19 to 31 C. Low temperature in the early season c= an also have pronounced effects on the physiology and biochemistry of seedl= ings, resulting in reduced plant growth and development due to lower photos= ynthetic rates (Allen and Ort, 2001). Reduced net assimilation rate under l= ow temperature can be due to stomatal factors, such as stomata closure or n= on-stomatal factors, such as deactivation of Rubisco (Holaday et al. 1992; = 2016). Bagnall et al. (1988) reported 50 to 70% decrease in net photosynthe= sis within the first two d with a change in temperature from 30 to 19 C. Th= e authors further indicated that the decrease in net photosynthesis under s= ub-optimal temperature conditions was due to non-stomatal limitations. Plant Physiology Taiz And Zeiger 5th Edition Pdf 186 DOWNLOAD https://tlniurl.com/2wI9bT Schulte PJ. 2009. Water transport processes in desert succulent plants. In:= De la Barrera E, Smith WK, eds. Perspectives in Biophysical Plant Ecophysi= ology: A tribute to Park S. Nobel. Mexico City: Universidad Nacional Aut=C3= =B3noma de M=C3=A9xico, pp. 39-55. ISBN: 978-0-578-00421-1 Hydraulic traits, phenology, and resources acquisition in desert trees. Mex= ico harbors the richest desert flora in the world, yet the ecophysiology an= d hydraulic features of this widespread Mexican environment have been poorl= y studied. Desert environments are characterized by low and unpredictable p= recipitation. Under these extreme conditions, water stress is a dominant se= lective pressure that may act in different directions, resulting in a diver= sity of plant structural and functional attributes that allow plant surviva= l. For desert plants, the study of plant hydraulic traits, and their relati= onship with resource use, are important to identify different strategies di= splayed by individual plants to enhance survival or reproduction. The fast-= slow plant economics spectrum is a general frame that allows determining th= e use of resources by plants based on the relative carbon costs of tissues = and organs (Reich 2014). In this spectrum, the central concept is that plan= ts face a trade-off between productivity and persistence. eebf2c3492