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The objective of this study was to quantify the farm gate nitrogen (N) offset potential of perennial ryegrass (Lolium perenne L.; PRG) white clover (Trifolium repens L.; WC) swards by comparing the herbage and milk production from dairy farmlets that were simulations of full farming systems. A study was established where 120 cows were randomly assigned to 4 farmlets of 10.9 ha (stocking rate: 2.75 cow/ha), composed of 20 paddocks each. Cows were fed 526 kg of DM of concentrate on average each year. The 4 grazing treatments were PRG-only at 150 or 250 kg of N/ha and PRG-WC at 150 or 250 kg of N/ha. Cows remained in their treatment group for an entire grazing season and were re-randomized as they calved across treatments each year. As cows calved in the spring as standard practice in Ireland, they were rotationally grazed from early February both day and night (weather permitting) to mid-November, to a target postgrazing sward height of 4.0 cm. Mean sward WC content was 18.1% and 15.4% for the 150 and 250 kg of N/ha PRG-WC treatments, respectively over the 3-yr period. When WC was included, lowering the N rate did not reduce pregrazing yield, pregrazing height, or herbage removed, but those factors decreased significantly when WC was absent. Total annual herbage DM production was 13,771, 15,242, 14,721, and 15,667 kg of DM/ha for PRG-only swards receiving 150 or 250 kg of N/ha and PRG-WC swards receiving 150 or 250 kg of N/ha, respectively. In addition, when WC was present, compressed postgrazing sward heights were lower (4.10 vs. 4.21 cm) and herbage allowance (approximately 17 kg/cow feed allocation per cow per day) higher than the high-N control (+ 0.7 kg of DM/cow per day). There was a significant increase in milk production, both per cow and per hectare, when WC was included in PRG swards. Over the 3-yr study, cows grazing PRG-WC had greater milk (+304 kg) and milk solids (+31 kg of fat + protein) yields than cows grazing PRG-only swards. This significant increase in milk production suggests that the inclusion of WC in grazing systems can be effectively used to increase milk production per cow and per hectare and help offset nitrogen use. This result shows the potential to increase farm gate N use efficiency and reduce the N surplus compared with PRG-dominant sward grazing systems receiving 250 kg of N/ha, without negatively affecting milk solids yield or herbage production, thus increasing farm profit by €478/ha. [ABSTRACT FROM AUTHOR]

α-Ketoglutarate (AKG) is a key intermediate metabolite in the tricarboxylic acid cycle of respiration and a precursor for glutamate, playing important roles in regulating plant growth and stress tolerance. The objectives of this study were to examine effects of AKG on heat tolerance characterized by leaf senescence in a cool-season grass species by foliar application and to determine major metabolites and associated metabolic pathways regulated by AKG for its effects on heat tolerance. Perennial ryegrass (Lolium perenne L.) plants were exposed to heat stress (35/30 °C, day/night) or optimal temperature (25/20 °C, day/night, non-stress control) in controlled-environment growth chambers. The solution containing AKG (5 mM) was applied to leaves by spraying 7 d prior to the initiation of heat stress and every 7 d during the heat stress period. Exogenous application of AKG enhanced heat tolerance in perennial ryegrass, as manifested by significant increases in leaf chlorophyll content, photochemical efficiency, and membrane stability, as well as activities of antioxidant enzymes for H 2 O 2 scavenging in AKG-treated plants relative to untreated control plants exposed to heat stress. Metabolic profiling and pathway analysis demonstrated that exogenous AKG application enhanced metabolite accumulation in four major metabolic pathways, including antioxidant metabolism, amino acid metabolism, glycolysis and tricarboxylic acid cycle of respiration, and pyrimidine metabolism, contributing to AKG-improved heat tolerance in perennial ryegrass. • α-Ketoglutarate (AKG) enhanced heat tolerance in perennial ryegrass. • AKG suppressed heat-induced leaf senescence. • AKG regulated the metabolism of antioxidant, amino acids, pyrimidine, glycolysis, and TCA cycle of respiration. [ABSTRACT FROM AUTHOR]

Perennial ryegrass (Lolium perenne) is a widely used cool season turfgrass with outstanding turf quality and grazing tolerance. High temperature is the key factor restricting the distribution of perennial ryegrass in temperate and sub-tropic regions. In this study, we found that one HEAT SHCOK TRANSCRIPTION FACOTR (HSF) class A gene from perennial ryegrass, LpHSFA3 , was highly induced by heat stress. LpHSFA3 is localized in nucleus and functions as a transcription factor. Ectopic overexpression of LpHSFA3 in Arabidopsis improved thermotolerance and rescued heat sensitive deficiency of athsfa3 mutant. Overexpression of LpHSFA3 in perennial ryegrass enhanced heat tolerance and increased survival rate in summer season as evidenced by decreased EL and MDA, increased number of green leaves and total chlorophyll content. LpHSFA3 binds to the HSE region in LpHSFA2a promoter to constitutively activate the expression of LpHSFA2a and downstream heat stress responsive genes. Ectopic overexpression of LpHSFA2a consequently rescued thermal sensitivity of athsfa3 mutant and enhanced thermotolerance of athsfa2 mutant. Perennial ryegrass protoplasts with overexpression of LpHSFA3 and LpHSFA2a exhibited induction of similar subsets of heat responsive genes. These results indicated that transcription factor LpHSFA3 functions as positive regulator of LpHSFA2a to improve thermotolerance of perennial ryegrass, providing further evidence to understand the regulatory networks of plant heat stress response. • LpHSFA3 and LpHSFA2a were significantly induced by heat stresss. • LpHSFA3 improves plant heat tolerance and survival rate in summer season. • LpHSFA3 directly activates the expression of LpHSFA2a. • LpHSFA2a enhances plant heat tolerance. [ABSTRACT FROM AUTHOR]

• Toxicity threshold for ryegrass staggers is lowered the longer perennial ryegrass is fed. • Sub-chronic (>60 day) threshold for lolitrem B is 1554 µg/kg in Angus beef cattle. • Lolitrem B accumulates in fat tissue in a dose- and time-responsive manner. Lolitrem B is a potent tremorgen responsible for the syndrome known as "ryegrass staggers" in livestock consuming perennial ryegrass (Lolium perenne) infected with the endophyte fungus Epichloë festucae var. lolii. We evaluated clinical signs in cattle continuously fed endophyte-infected perennial ryegrass straw at four concentrations of lolitrem B (LB)/ergovaline (EV) (groups: I-2256/638, II-1554/373, III-1012/259 or IV-<300/0 µg/kg LB/EV, n =5-6 steers/group) over 64 days to establish a sub-chronic threshold of toxicity for this mycotoxin; animals were supplemented with 1 kg grain mix/day. Most animals in groups I and II developed clinical signs consistent with ryegrass staggers by day 64; thus, it is recommended that a threshold level of 1554 µg/kg LB should not be exceeded for extended feeding regimens using endophyte-infected perennial ryegrass feed material alone. This toxicity threshold is lower than that observed with shorter feeding periods, i.e. 1800–2000 µg/kg LB when fed for less than 30 days. No clinical signs associated with ergovaline toxicosis (i.e. decreased weekly weight gain) were observed. As adipose tissue appears to be the main compartment where LB is deposited, the concentration of LB and its metabolic derivatives in fat samples was determined at 37 and 64 days. Lolitrem B and three previously defined metabolites bioaccumulated in a dose- and time-dependent manner throughout the feeding experiment in fat tissue, at levels similar to those found in past research. Ratios of metabolites to LB were consistent across time points and dose groups, indicating that the enzyme(s) responsible for LB metabolism were not saturated. In summary, LB toxicity thresholds are dependent upon specificities of the dietary program including the duration feed material is fed, and should be considered when formulating safe livestock feeding regimens. [Display omitted] [ABSTRACT FROM AUTHOR]