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Thermal Optimum (thermal + optimum)
Selected AbstractsGenetic response to rapid climate change: it's seasonal timing that mattersMOLECULAR ECOLOGY, Issue 1 2008W. E. BRADSHAW Abstract The primary nonbiological result of recent rapid climate change is warming winter temperatures, particularly at northern latitudes, leading to longer growing seasons and new seasonal exigencies and opportunities. Biological responses reflect selection due to the earlier arrival of spring, the later arrival of fall, or the increasing length of the growing season. Animals from rotifers to rodents use the high reliability of day length to time the seasonal transitions in their life histories that are crucial to fitness in temperate and polar environments: when to begin developing in the spring, when to reproduce, when to enter dormancy or when to migrate, thereby exploiting favourable temperatures and avoiding unfavourable temperatures. In documented cases of evolutionary (genetic) response to recent, rapid climate change, the role of day length (photoperiodism) ranges from causal to inhibitory; in no case has there been demonstrated a genetic shift in thermal optima or thermal tolerance. More effort should be made to explore the role of photoperiodism in genetic responses to climate change and to rule out the role of photoperiod in the timing of seasonal life histories before thermal adaptation is assumed to be the major evolutionary response to climate change. [source] Dietary strategies to improve the growth and feed utilization of barramundi, Lates calcarifer under high water temperature conditionsAQUACULTURE NUTRITION, Issue 4 2010B. GLENCROSS Abstract Several dietary strategies to ameliorate poorer growth observed to occur at temperatures above the upper thermal optima were examined with juvenile barramundi (Lates calcarifer). A reference (REF) and three experimental diets, one with an increased protein to energy ratio (PRO), another with an increased level of the amino acid histidine (HIS) and a third with supplementation of dietary nucleotides (NUC), were each fed to fish at either 30 °C or 37 °C for a 28-day period. Growth was affected by both temperature and diet. Fish fed the PRO diet at 30 °C grew fastest, but not faster than those fed the NUC diet at the same temperature. The addition of the amino acid histidine to the diet did not improve growth rates at either temperature. At water temperatures of 37 °C, only the fish fed the PRO diet had growth rates equivalent to those of fish at the 30 °C temperatures. Other key factors including feed intake, feed conversion rate, nutrient and energy retention and plasma enzymology were also all affected by temperature and diet. This study shows that the use of a diet with an increased protein to energy ratio provides significant benefits in terms of reducing the impact of growth retardation at higher temperatures. [source] New perspectives on the origin and diversification of Africa's forest avifaunaAFRICAN JOURNAL OF ECOLOGY, Issue 3 2008Jon Fjeldså Abstract The use of DNA sequence data in systematic studies has brought about a revolution in our understanding of avian relationships and when combined with digitized distributional data, has facilitated new interpretations about the origins of diverse clades of the African avifauna including its diversification up through the Tertiary until the present. Here we review recent studies with special reference to Africa's forest avifauna and specifically comment on the putative origins of ,hotspots' of endemism in the Eastern Arc Mountains of Tanzania and in the Cape Region of South Africa. Intriguingly, both these areas appear to have retained populations of relict taxa since the mid-tertiary thermal optimum and at the same time have been centres of recent species differentiation. Résumé L'utilisation des données portant sur la séquence ADN dans les études systématiques représente une révolution dans notre façon de comprendre les relations entre les oiseaux et, combinée avec les données numérisées sur la distribution, elle facilite de nouvelles interprétations concernant les origines de différents clades de l'avifaune africaine, y compris sa diversification tout au long du Tertiaire et jusqu'à nos jours. Nous passons ici en revue des études récentes qui se réfèrent particulièrement à l'avifaune forestière africaine, avec un commentaire spécial sur les origines putatives des hauts lieux d'endémisme dans les montagnes de l'Eastern Arc tanzanien et dans la région du Cap, en Afrique du Sud. Curieusement, ces deux endroits semblent avoir conservé des populations de taxons résiduels depuis l'optimum thermique du milieu du Tertiaire, tout en étant aussi au centre de récentes différenciations entre espèces. [source] The temperature response of photosynthesis in tobacco with reduced amounts of RubiscoPLANT CELL & ENVIRONMENT, Issue 4 2008DAVID S. KUBIEN ABSTRACT The reasons for the decline in net CO2 assimilation (A) above its thermal optimum are controversial. We tested the hypothesis that increasing the ratio of Rubisco activase to Rubisco catalytic site concentration would increase the activation state of Rubisco at high temperatures. We measured photosynthetic gas exchange, in vivo electron transport (J) and the activation state of Rubisco between 15 and 45 °C, at 38 and 76 Pa ambient CO2, in wild-type (WT) and anti- rbcS tobacco. The Rubisco content of the anti- rbcS lines was 30% (S7-1) or 6% (S7-2) of WT, but activase levels were the same in the three genotypes. Anti- rbcS plants had lower A than WT at all temperatures, but had a similar thermal optimum for photosynthesis as WT at both CO2 levels. In WT plants, Rubisco was fully activated at 32 °C, but the activation state declined to 64% at 42 °C. By contrast, the activation state of Rubisco was above 90% in the S7-1 line, between 15 and 42 °C. Both A and J declined about 20% from Topt to the highest measurement temperatures in WT and the S7-1 line, but this was fully reversed after a 20 min recovery at 35 °C. At 76 Pa CO2, predicted rates of RuBP regeneration-limited photosynthesis corresponded with measured A in WT tobacco at all temperatures, and in S7-1 tobacco above 40 °C. Our observations are consistent with the hypothesis that the high temperature decline in A in the WT is because of an RuBP regeneration limitation, rather than the capacity of Rubisco activase to maintain high Rubisco activation state. [source] Low-temperature photosynthetic performance of a C4 grass and a co-occurring C3 grass native to high latitudesPLANT CELL & ENVIRONMENT, Issue 7 2004D. S. KUBIEN ABSTRACT The photosynthetic performance of C4 plants is generally inferior to that of C3 species at low temperatures, but the reasons for this are unclear. The present study investigated the hypothesis that the capacity of Rubisco, which largely reflects Rubisco content, limits C4 photosynthesis at suboptimal temperatures. Photosynthetic gas exchange, chlorophyll a fluorescence, and the in vitro activity of Rubisco between 5 and 35 °C were measured to examine the nature of the low-temperature photosynthetic performance of the co-occurring high latitude grasses, Muhlenbergia glomerata (C4) and Calamogrostis canadensis (C3). Plants were grown under cool (14/10 °C) and warm (26/22 °C) temperature regimes to examine whether acclimation to cool temperature alters patterns of photosynthetic limitation. Low-temperature acclimation reduced photosynthetic rates in both species. The catalytic site concentration of Rubisco was approximately 5.0 and 20 µmol m,2 in M. glomerata and C. canadensis, respectively, regardless of growth temperature. In both species, in vivo electron transport rates below the thermal optimum exceeded what was necessary to support photosynthesis. In warm-grown C. canadensis, the photosynthesis rate below 15 °C was unaffected by a 90% reduction in O2 content, indicating photosynthetic capacity was limited by the capacity of Pi -regeneration. By contrast, the rate of photosynthesis in C. canadensis plants grown at the cooler temperatures was stimulated 20,30% by O2 reduction, indicating the Pi -regeneration limitation was removed during low-temperature acclimation. In M. glomerata, in vitro Rubisco activity and gross CO2 assimilation rate were equivalent below 25 °C, indicating that the capacity of the enzyme is a major rate limiting step during C4 photosynthesis at cool temperatures. [source] Effects of nest temperature and moisture on phenotypic traits of hatchling snakes (Tropidonophis mairii, Colubridae) from tropical AustraliaBIOLOGICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 1 2006GREGORY P. BROWN Previous research on developmentally plastic responses by reptile embryos has paid relatively little attention to tropical species, or to possible interactions between the effects of thermal and hydric regimes. In the present study, eggs of keelback snakes (Tropidonophis mairii), from a tropical area with strong temporal and spatial variation in soil temperatures and moisture levels, were incubated. The phenotypic traits of hatchling snakes (body size, shape, muscular strength) were affected by moisture content of the incubation medium (vermiculite plus 100% vs. 50% water by mass), by mean incubation temperatures (25.7 vs. 27.9 °C) and by diel thermal variation (diel range 6.0 vs. 8.4 °C). Interactions between these factors were negligible. Cooler, more thermostable, moister conditions resulted in larger offspring, a trait under strong selection in this population. Thermal and hydric conditions covary in potential nest-sites (e.g. deeper nests are more thermostable as well as moister). This covariation may influence the evolution of reaction norms for embryogenesis. For example, if moister nests enhance offspring fitness and are cooler, then selection will favour the ability to develop in cool as well as moist conditions. Thus, the evolution of optimal incubation conditions with respect to one variable (e.g. temperature) may be driven by patterns of association with another variable (e.g. soil moisture) among natural nest-sites. Perhaps for this reason, the thermal optimum for incubation is surprisingly low in this tropical species. © 2006 The Linnean Society of London, Biological Journal of the Linnean Society, 2006, 89, 159,168. [source] | ||||||||||