scholarly journals Quantification of Seed Dormancy of Deciduous Orchard Species

HortScience ◽  
1995 ◽  
Vol 30 (4) ◽  
pp. 908A-908
Author(s):  
Schuyler D. Seeley
Keyword(s):  
Low Temperature ◽  
Plant Material ◽  
Temperature Response ◽  
Woody Species ◽  
Normal Growth ◽  
Response Curves ◽  
Naturally Occurring ◽  
Breaking Dormancy ◽  
Temporary Growth ◽  
Per Se

Forcing plant material has long been used to determine dormancy intensity (DI) in woody species. Forcing with growth regulators may enhance this ability. Some forcing with naturally occurring hormones may be showing us the actual DI of certain materials. But, measurements of DI that use caustic, near-lethal treatments, or metabolic agents may be all or nothing breaking indicators acting on mechanisms other than the dormancy mechanism and thus not as useful in determining DI. It is possible to cause a meristem to break without completely breaking dormancy. Measurement of normal post-dormancy growth is necessary to determine the effect of a DI agent. DI breaking treatments that act on the dormancy mechanism can cause a temporary growth flush, but, unless the extent of that growth flush is measured and compared with the growth flush of the same normally broken plant material, its true effect remains unknown. In some plant material, the safest way to determine DI is to determine the chilling required to produce normal growth. This assumes that the vernalization requirement and temperature response curves are known for the plant in question. In peach, for instance, vernalization at 2C will cause seeds to germinate, but the resulting seedlings will be physiologically dwarfed. Vernalization at 6C or at 2C cycled with higher temperatures within the vernalization range results in normal seedlings. This indicates that, for chilling to progress normally, vernalization per se must be interspersed or concomitant with growth heat units. Vernalization, therefore, has a low temperature driven component and a heat requiring development and/or growth component. Vernalization driving conditions are slowly being elucidated. Each clarification requires modification of dormancy models. DI does not equal dormancy status!

Metabolic Responses to Thermal Stressors of Altitude-Acclimated Rats

1958 ◽  
Vol 195 (3) ◽  
pp. 739-743 ◽  
Author(s):  
Henry B. Hale ◽  
Roy B. Mefferd
Keyword(s):  
Urine Volume ◽  
Temperature Response ◽  
Ground Level ◽  
Metabolic Responses ◽  
Control Group ◽  
Response Curves ◽  
Level Pressure ◽  
Metabolic Functions ◽  
Per Se ◽  
The Difference

Fasting 24-hour exposures of altitude-acclimated rats (380 mm Hg, 18,000 ft. simulated) to ground level pressure (750 mm Hg) at either cold (3°C), neutral (24°C), or hot (35°C) temperatures seldom resulted in return of their metabolic functions to preacclimative ‘normalcy.’ Although the control and altitude-acclimated groups both were accustomed to neutral temperatures (24° and 26°C), quantitative differences at ground level and altitude occurred in various indices of water, mineral and nitrogen metabolism. Of the 32 physiologic variables studied, only 4 (ratio of urine volume/ water intake, and urinary excretion of potassium, creatinine and glycine) failed to differentiate the responses of the altitude- and ground-accustomed rats. The temperature response curves of the altitude group tended to parallel the corresponding ones for the control group, but most variables were on higher or lower planes. The difference in plane resulted either from the effects of the return to ground level pressure, or from nonreversible effects of acclimation to altitude per se.

scholarly journals Comparative transcriptome analysis of the cold resistance of the sterile rice line 33S

PLoS ONE ◽  
2022 ◽  
Vol 17 (1) ◽  
pp. e0261822
Author(s):  
Hongjun Xie ◽  
Mingdong Zhu ◽  
Yaying Yu ◽  
Xiaoshan Zeng ◽  
Guohua Tang ◽  
...  
Keyword(s):  
Low Temperature ◽  
Cold Resistance ◽  
Temperature Response ◽  
Enrichment Analysis ◽  
Abiotic Factor ◽  
Comparative Transcriptome ◽  
Important Species ◽  
Expression Of Genes ◽  
Nutrient Reserve ◽  
Cold Tolerant

Rice (Oryza sativa L.) is one of the most important species for food production worldwide. Low temperature is a major abiotic factor that affects rice germination and reproduction. Here, the underlying regulatory mechanism in seedlings of a TGMS variety (33S) and a cold-sensitive variety (Nipponbare) was investigated by comparative transcriptome. There were 795 differentially expressed genes (DEGs) identified only in cold-treated 33S, suggesting that 33S had a unique cold-resistance system. Functional and enrichment analysis of these DEGs revealed that, in 33S, several metabolic pathways, such as photosynthesis, amino acid metabolism, secondary metabolite biosynthesis, were significantly repressed. Moreover, pathways related to growth and development, including starch and sucrose metabolism, and DNA biosynthesis and damage response/repair, were significantly enhanced. The expression of genes related to nutrient reserve activity were significantly up-regulated in 33S. Finally, three NAC and several ERF transcription factors were predicted to be important in this transcriptional reprogramming. This present work provides valuable information for future investigations of low-temperature response mechanisms and genetic improvement of cold-tolerant rice seedlings.

scholarly journals Differences in Leaf Temperature between Lianas and Trees in the Neotropical Canopy

2018 ◽  
Author(s):  
J. Antonio Guzmán Q. ◽  
G. Arturo Sánchez-Azofeifa ◽  
Benoit Rivard
Keyword(s):  
Primary Productivity ◽  
Net Primary Productivity ◽  
Temperature Response ◽  
Life Forms ◽  
Leaf Temperature ◽  
Response Curves ◽  
Tropical Environments ◽  
Host Trees ◽  
Temperature Responses ◽  
Photosynthesis And Respiration

Leaf temperature (Tleaf) influences photosynthesis and respiration. Currently, there is a growing interest on including lianas in productivity models due to their increasing abundance, and their detrimental effects on net primary productivity in tropical environments. Therefore, understanding the differences of Tleaf between lianas and trees is important for future of forest on whole ecosystem productivity. Here we determined the displayed leaf temperature (Td= Tleaf – ambient temperature) of several species of lianas and their host trees during ENSO and non-ENSO years to evaluate if the presence of lianas affects the Td of their host trees, and if leaves of lianas and their host trees exhibit differences in Td. Our results suggest that close to midday, the presence of lianas does not affect the Td of their host trees; however, lianas tend to have higher values of Td than their hosts across seasons, in both ENSO and non-ENSO years. Although lianas and trees tend to have similar physiological-temperature responses, differences in Td could lead to significant differences in rates of photosynthesis and respiration based temperature response curves. Future models should thus consider differences in leaf temperature between these life forms to achieve robust predictions of productivity.

Acclimation of leaf dark respiration to nocturnal and diurnal warming in a semiarid temperate steppe

2013 ◽  
Vol 40 (11) ◽  
pp. 1159 ◽  
Author(s):  
Yonggang Chi ◽  
Ming Xu ◽  
Ruichang Shen ◽  
Shiqiang Wan
Keyword(s):  
Dark Respiration ◽  
Temperature Response ◽  
Terrestrial Ecosystems ◽  
Northern China ◽  
Thermal Acclimation ◽  
Nonstructural Carbohydrates ◽  
Temperate Steppe ◽  
Response Curves ◽  
Diurnal Warming ◽  
Leaf Dark Respiration

A better understanding of thermal acclimation of leaf dark respiration in response to nocturnal and diurnal warming could help accurately predict the changes in carbon exchange of terrestrial ecosystems under global warming, especially under the asymmetric warming. A field manipulative experiment was established with control, nocturnal warming (1800–0600 hours), diurnal warming (0600–1800 hours), and diel warming (24 h) under naturally fluctuating conditions in a semiarid temperate steppe in northern China in April 2006. Temperature response curves of in situ leaf dark respiration for Stipa krylovii Roshev. were measured at night (Rn) and after 30 min of darkness imposed in the daytime (Rd). Leaf nonstructural carbohydrates were determined before sunrise and at sunset. Results showed that Rn could acclimate to nocturnal warming and diurnal warming, but Rd could not. The decreases in Q10 (temperature sensitivity) of Rn under nocturnal-warming and diurnal warming regimes might be attributed to greater depletion of total nonstructural carbohydrates (TNC). The real-time and intertwined metabolic interactions between chloroplastic and mitochondrial metabolism in the daytime could affect the impacts of warming on metabolite pools and the distinct response of Rn and Rd to warming. Projection on climate change–carbon feedback under climate warming must account for thermal acclimation of leaf dark respiration separately by Rn and Rd.

XVII.—Utilization of Dietary Purines and Pyrimidines by Drosophila melanogaster

1957 ◽  
Vol 66 (4) ◽  
pp. 339-359 ◽  
Author(s):  
James H. Sang
Keyword(s):  
Drosophila Melanogaster ◽  
Orotic Acid ◽  
De Novo ◽  
Normal Growth ◽  
Energy Utilization ◽  
Good Growth ◽  
Response Curves ◽  
Adenylic Acid ◽  
Multicellular Organisms

SynopsisDrosophila melanogaster larvæ when cultured aseptically on a synthetic diet require exogenous ribose nucleic acid (RNA) for normal growth even though they can synthesize their own endogenous RNA from simple precursors. The optimum dietary supply lies between 0.4 and 0.7 per cent RNA. Individual bases, nucleosides and nucleotides which make up RNA cannot substitute for the whole polynucleotide, but adenine, adenosine, adenylic acid, guanosine and guanylic acid are used and stimulate growth to varying degrees. The pyrimidines and their nucleosides and nucleotides are not used when fed singly.It is shown that the de novo synthesis of purines may be more difficult than that of pyrimidines, and that if a source of purines is supplied (as adenylic acid), then the nucleosides and nucleotides of both cytosine and uracil are utilized by the larvæ, whereas the free bases are not. Cytidylic and uridylic acids seem to be interchangeable, and together with an adequate supply of adenylic acid give as good growth as RNA. Orotic acid and 2—6-diaminopurine are not used by the larvæ under the conditions described, but hypoxanthine and inosine are: xanthine and xanthosine can also be shown to have an effect on growth.Dose-response curves were determined for adenylic, guanylic, cytidylic and uridylic acids under conditions which allow the determination of the optimal supplies of each. These are found to be about 0.110, 0.080, 0.025 and 0.025 per cent, respectively. The requirement of RNA is therefore primarily a requirement of adenylic acid, since more than enough of the other nucleotides should be available when the supply of RNA is optimal. The optimal supply of adenine corresponds almost exactly with the optimal supply of adenylic acid, though a somewhat delayed larval development may be a result of energy utilization in the base-nucleoside-nucleotide conversion.These results are discussed in the light of our knowledge of purine and pyrimidine utilization in other multicellular organisms, particularly the rat, and possible applications of the findings are considered.

scholarly journals Temperature response of photosynthesis and its interaction with light intensity in sweet orange leaf discs under non-photorespiratory condition

2006 ◽  
Vol 30 (4) ◽  
pp. 670-678 ◽  
Author(s):  
Rafael Vasconcelos Ribeiro ◽  
Eduardo Caruso Machado ◽  
Ricardo Ferraz de Oliveira
Keyword(s):  
Sweet Orange ◽  
Photochemical Efficiency ◽  
Temperature Response ◽  
Light Response ◽  
Photon Flux ◽  
O2 Evolution ◽  
Response Curves ◽  
Leaf Discs ◽  
Light Response Curves ◽  
Heat Effects

This study aimed to evaluate the response of photosynthesis (A), given by photosynthetic O2 evolution, to increasing temperature from 25 to 50ºC in sweet orange (Citrus sinensis (L.) Osbeck) leaf discs under non-photorespiring conditions. In order to evaluate the response of gross photosynthesis to temperature and the balance between photosynthetic and respiratory activities, respiration (Rd) rates were also measured, i.e. the O2 uptake in each temperature. In addition, light response curves of photosynthesis were performed by varying the photosynthetic photon flux density (PPFD) from 0 to 1160 µmol m-2 s-1 at 25 and 40ºC. The highest A values were observed at 35 and 40ºC, whereas the highest Rd values were noticed at 50ºC. A higher relationship A/Rd was found at 30 and 35ºC, suggesting an optimum temperature of 35ºC when considering the balance between photosynthesis and respiration under non-photorespiring condition. Overall, heat effects on plant metabolism were more evident when evaluating the relationship A/Rd. In light response curves, higher A values were also found at 40ºC under PPFD higher than 300 µmol m-2 s-1. Light saturation point of photosynthesis was increased at 40ºC, without significant change of quantum efficiency under low PPFD. Respiration was also enhanced at 40ºC, and as a consequence, the light compensation point increased. The better photosynthetic performance at 35-40ºC was supported by higher photochemical efficiency in both light and temperature response curves. The temperature-dependence of photosynthesis was affected by growth temperature, i.e. a high air temperature during plant growth is a probable factor leading to a higher photosynthetic tolerance to heat stress.

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