Commercial diets for tilapia juveniles contain high levels of plant protein sources. Soybean meal has been utilised due to its high protein content; however, soy-based diets are limited in methionine (Met) and require its supplementation to fulfil fish requirements. dl-Methinone (dl-Met) and Ca bis-methionine hydroxyl analogue (MHA-Ca) are synthetic Met sources supplemented in aquafeeds, which may differ in biological efficiency due to structural differences. The present study evaluated the effect of both methionine sources on metabolism and growth of Nile tilapia. A growth trial was performed using three isonitrogenous and isoenergetic diets, containing plant ingredients as protein sources: DLM and MHA diets were supplemented on equimolar levels of Met, while REF diet was not supplemented. Hepatic free Met and one-carbon metabolites were determined in fish fed for 57 d. Metabolism of dl-Met and MHA was analysed by an in vivo time-course trial using 14C-labelled tracers. Only dl-Met supplementation significantly increased final body weight and improved feed conversion and protein efficiency ratios compared with the REF diet. Our findings indicate that Met in DLM fed fish follows the transsulphuration pathway, while in fish fed MHA and REF diets it is remethylated. The in vivo trial revealed that 14C-dl-Met is absorbed faster and more retained than 14C-MHA, resulting in a greater availability of free Met in the tissues when fish is fed with DLM diet. Our study indicates that dietary dl-Met supplementation improves growth performance and N retention, and that Met absorption and utilisation are influenced by the dietary source in tilapia juveniles.

Although common beans (Phaseolus vulgaris L.) are consumed worldwide, studies on the metabolic fate of phenolic compounds from common beans are still very scarce. The present work aimed to study the bioavailability of phenolic compounds in human plasma and urine, after acute consumption of a single meal of cooked common beans. Blood and urine of seven volunteers were collected before (0 h) and at different time points (1, 2, 4, 6 and 8 h for plasma and 0–2, 2–4, 4–6, 6–8 and 8–24 h for urine) after beans’ intake. Ultra-high performance liquid chromatography-quadrupole-time of flight-MS (UPLC-Q-TOF-MS) was used for quantification. After beans’ intake, 405 (sd 3) g, containing 188 mg of phenolic compounds (expressed as gallic acid equivalents), there was a significant increase (P < 0·05) in the plasma concentration of six metabolites and in the urinary excretion of eleven metabolites. After 1 h post-consumption, metabolites, such as kaempferol-3-O-glucuronide, showed a significant increase in plasma concentration, suggesting kaempferol’s glucuronidation in the upper gastrointestinal tract. More than 50 % of the total amount of metabolites, such as 4-methylcatechol-O-sulphate and dihydrocaffeic acid-3-O-sulphate, were excreted after 8 h post-consumption, indicating colonic bacterial metabolism of the phenolic compounds. Partial least square-discriminant analysis models clearly showed clusters of metabolites, which contributed to extend the list of compounds related to cooked common beans’ human intake at different time points and showed the human inter-individual variability in plasma concentration as well as in urinary excreted metabolites, after cooked common beans’ intake.

Goosegrass is considered one of the worst agricultural weeds worldwide. Understanding its life cycle will provide useful management information. Field experiments with six emergence times (April, May, June, July, August, and September) were conducted at Anyang, China in 2015 and 2017 to clarify the growth and reproduction of goosegrass emerging at different times within a season. The result showed that plant height, dry weight, average weight per inflorescence, total inflorescence weight, average seed number per inflorescence, and total number of seeds per plant were relatively low in the April cohort, peaked with the May or June emergence cohort, and decreased thereafter. However, the earliest emergence of goosegrass in April had the highest total number of inflorescences. The plants of the May cohort produced the greatest number of seeds: 225,954 and 322,501 seeds per plant in 2015 and 2017, respectively. Delayed emergence resulted in less seed production; most plants that emerged in September did not flower or set seed. The 1,000-seed weight did not vary among the emergence cohorts. The reproductive investment was lowest for plants of the May cohort and then increased as emergence time was delayed to June, July, and August. Fresh mature seed of all emergence cohorts was extremely dormant and had low germination only up to 6% from August to November, and high germination (44% to 93%) in December. The information gained from this study indicates that weed management strategies should focus on the early-emerged seedlings such as the April and May cohorts, so as to effectively prevent goosegrass seed production, minimize the weed seed replenishment into the soil seed bank, and reduce the infestation in subsequent seasons.

Crop plants have been used as mimic weeds to substitute for real weeds in competition studies. These mimic weeds have the advantages of availability of seed, uniform germination and growth, and the potential to confer better experimental controllability and repeatability. However, the underlying assumption that the competitive effects of mimic weeds are similar to real weeds has not been tested. We compared a range of morphological traits (plant height, node and leaf number, leaf area, leaf size, and dry weight) between the mimic weeds and real weeds: Japanese millet vs. junglerice, mungbean vs. bladder ketmia, and common sunflower vs. fierce thornapple. The impact of these mimic and real weeds on cotton was also assessed. There were similarities and differences between the mimic and real weeds, but impact on cotton lint yield was most closely associated with weed height and dry weight at mid-season. Mimic weeds may be satisfactorily substituted for real weeds in competition experiments where seasonal and environmental conditions are not limiting, such as with fully irrigated cotton, provided the plants have similar dry weight and height at mid-season. Alternatively, one can account for the differences in dry weight and height. We define here a generalized relationship estimating the yield loss of high-yielding, irrigated cotton from weed competition over a range of weed dry weights and heights, allowing extrapolation from the results with mimic weeds to the competitive effects of a range of weeds.

The influence of ammonium sulfate on the activity of sethoxydim on wild oats and barley was examined under field conditions in 1989 and 1990. A chlorophyll assay, together with plant height and dry weight determinations, was used to quantify the visual ratings for sethoxydim activity. Ammonium sulfate enhanced the activity of 75 and 150 g ai ha-1 sethoxydim in 1989. In 1990, ammonium sulfate increased the activity of the lower rate of sethoxydim only. Of the three quantitative assays, chlorophyll concentration alone differentiated the more rapid development of injury symptoms with added ammonium sulfate that was observed in the visual ratings. The chlorophyll assay was not better than the visual rating assessment, however, and appears to offer no advantages that would justify the time required.

Destructive growth analysis of field replacement series experiments with mayweed chamomile and dry field peas was used to determine the competitive relationship between the two species. Mayweed chamomile produced similar amounts of leaf area and dry weight per plant in a dry year and a wet year. On the other hand, dry field peas produced 20% more leaf area and 100% more dry weight per plant in the wet year compared to the dry year. Height, leaf area, and dry weight of peas reached maximum between bloom and pod-set, and then declined. Height and dry weight of mayweed chamomile increased steadily throughout the growing season. Mayweed chamomile leaf area reached a maximum at the beginning of flower stem elongation. Initially, the relative growth rate of mayweed chamomile was about three times greater than the rate for peas, but by 40 to 48 d after planting, rates were similar for both species. Relative yields and relative crowding coefficients for dry weight showed that peas were 3 to 20 times more aggressive than mayweed chamomile. Results of these experiments show that mayweed chamomile is a weak competitor against peas, but because it continues to grow after peas senesce, it could interfere with crop harvest.

Plants produced by yellow nutsedge (Cyperus esculentus L. # CYPES) tubers planted in a field at the U.S. Cotton Research Station, Shafter, CA, at monthly intervals were harvested 2, 4, or 8 weeks after planting or at the end of a full season that varied from 12 to 37 weeks. In the 2 yr of the study, 1982 and 1983, tubers were slow to sprout in March and April, taking up to 8 weeks. From June through October about 60% of the plants emerged within 2 weeks of the planting date. Parent plants produced daughter plants by the 4-week harvest except for March, April, and October 1982, and March 1983 planting periods. All planting periods had daughter plants by the 8-week harvest. In 1982, plants of the June full-season planting had significantly more daughter plants than plants of other full-season treatments even though the June full season was 12 weeks shorter than the March full season. In 1983, the number of daughter plants produced by plants for the full-season harvest was equal for all monthly plantings regardless of the length of the full season. In 1982, for the May through September plantings, more tubers were produced by plants at the 8-week harvest than the number of tubers originally planted. In 1983, only plants of the June and August plantings produced more tubers by the 8-week harvest than had been planted. In both years, plants that grew for a full season produced more tubers than the number planted, up to 200-fold more.

Field studies were conducted in 1986-87 and 1988-89 to compare chiseling, disking, and skewtreading to no-till and to compare 0.3 and 0.4 kg ai ha−1 pronamide applied before or after fall tillages for weed control in fallow. Chiseling or disking in October 1986 when weeds were emerged reduced the dry weight of volunteer wheat about 90% the following spring; however, only disking reduced the dry weight of downy brome 90%. Disking or skewtreading in October 1988 before weeds germinated reduced the dry weight of volunteer wheat about 95% 6 mo later, but none of the three tillages reduced the dry weight of downy brome. Pronamide applied at 0.3 and 0.4 kg ha−1 to emerged downy brome and volunteer wheat with either chiseling or disking before or after herbicide application reduced the dry weight of both species 90% or more 6 mo later compared with tillage alone. If weeds did not emerge until early November, then only pronamide at 0.4 kg ha−1 applied in no-till or after fall tillage controlled both species at least 90%.

The effects of MT-101 and its herbicidally active form, NOP, on the germination and seedling growth of hemp sesbania and rice were investigated. MT-101 decreased the germination of hemp sesbania by 57 and 90% at 0.05 and 0.5 mM, respectively, 1 d after treatment (DAT) in petri dishes. The germination, however, recovered such that there was no significant difference between treatments 4 to 6 DAT. NOP completely inhibited the germination of hemp sesbania at both 0.05 and 0.5 mM 1 DAT. However, germination also similarly recovered, and there was no difference between treatments 4 to 6 DAT. Neither MT-101 nor NOP decreased the germination of rice 3 to 6 DAT. In greenhouse trials preemergence (PRE) application of MT-101 at 2.25 kg ai ha−1 decreased the density (number of plants pot−1), plant height, and dry weight of hemp sesbania by 85, 67, and 91%, respectively. When applied postemergence (POST), MT-101 at 2.25 kg ha−1 decreased the density, plant height, and dry weight by a maximum of 58, 61, and 82%, respectively, indicating that MT-101 may have greater activity when applied PRE. NOP had greater activity than MT-101 on hemp sesbania. NOP at 2.25 kg ai ha−1 decreased the density, plant height, and dry weight of hemp sesbania 99, 78, and 97%, respectively, with PRE application. A POST application of NOP at 2.25 kg ha−1 decreased the dry weight of hemp sesbania 91 to 94%. A PRE application of NOP at 2.25 kg ha−1 decreased the dry weight of rice by 58%. Rice was not affected by POST applications of MT-101 but was affected slightly by NOP. These results suggest that MT-101 is a possible weed control agent in rice.

Two separate studies were conducted to determine the relative importance of root and shoot competition in dry direct-seeded rice growing with junglerice and ludwigia. By growing rice in pots placed within larger pots such that the roots of the plants were either separated from or free to mingle with those of neighboring weeds, or by growing rice in the same pots but in the absence of weeds, the relative importance of shoot and root competition can be described. When rice was grown together with either weed species, shoot competition reduced the growth and yield of rice more than root competition. Results suggest that shoot competition for light may be the primary mechanism determining competitive outcomes between dry direct-seeded rice and junglerice or ludwigia. Junglerice was more competitive than ludwigia, which may reflect the C4 metabolism efficiency of junglerice compared to the C3 metabolism of ludwigia. Rice grain yield was highly correlated with above- and belowground biomass. The results also suggest the importance of measuring the whole plant when seeking to understand differences in the competitive ability of dry direct-seeded rice.

Volunteer Enlist corn with the AAD-1 (aryloxyalkanoate dioxygenase-1) transgene can become a problem when glyphosate-resistant (GR) soybean follows Enlist corn in the rotation. Field trials were conducted at Ridgetown, Ontario in 2013 and 2014 to evaluate the control of volunteer Enlist corn in GR soybean. Glyphosate plus clethodim at 30 g ai ha−1 provided 75 to 92% control of volunteer Enlist corn at 1, 2, 4, and 8 weeks after treatment application (WAT) and reduced volunteer Enlist corn density and dry weight 95 to 97%. Glyphosate plus clethodim at 60 g ai ha−1 provided 84 to 98% control of volunteer Enlist corn at 1, 2, 4, and 8 WAT and reduced volunteer Enlist corn density and dry weight 97 to 99%. Glyphosate plus sethoxydim at 150 g ai ha−1 provided 66 to 86% control of volunteer Enlist corn at 1, 2, 4, and 8 WAT and reduced volunteer Enlist corn density and dry weight 91 to 97%. Glyphosate plus sethoxydim at 300 g ha−1 provided 84 to 96% control of volunteer Enlist corn at 1, 2, 4, and 8 WAT and reduced volunteer Enlist corn density and dry weight 96 to 98%. Glyphosate plus fenoxaprop-p-ethyl, fluazifop-p-butyl, and quizalofop-p-ethyl applied POST provided 0 to 9% control of volunteer Enlist corn at 1, 2, 4, and 8 WAT and reduced volunteer Enlist corn density and dry weight 18 to 44%. Soybean yields closely reflected the level of volunteer Enlist corn control. Based on these results, the cyclohexanedione herbicides, clethodim and sethoxydim, provide adequate control of volunteer Enlist corn in GR soybean. In contrast, the aryloxyphenoxypropionate herbicides, fenoxaprop-p-ethyl, fluazifop-p-butyl and quizalofop-p-ethyl do not provide control of volunteer Enlist corn in GR soybean.

Field experiments were conducted from 2011 to 2013 near Ridgetown and Exeter, Ontario, Canada to evaluate the tolerance of seven identity-preserved (IP) soybean cultivars to protoporphyrinogen oxidase (PPO)-inhibiting herbicides flumioxazin, saflufenacil/dimethenamid-P, and sulfentrazone applied PRE; fomesafen applied POST; as well as PRE followed by (fb) POST application. Ridgetown sites demonstrated excellent tolerance (< 10% injury) to PRE treatments, whereas PRE sulfentrazone caused up to 36% injury at 1 and 2 wk after application (WAA) at Exeter. Of the PRE fb POST treatments evaluated, those containing saflufenacil/dimethenamid-P and sulfentrazone were most injurious to soybean, with cultivar being a further determinant of injury. At Exeter 1 WAA, cultivars ‘S03W4’ and ‘S23T5’ showed 23 to 27 and 45 to 46% injury for saflufenacil/dimethenamid-P and sulfentrazone when followed by POST fomesafen, respectively. Sulfentrazone application (PRE alone or fb fomesafen) consequently reduced S03W4 yield up to 38% and S23T5 up to 25%, whereas saflufenacil/dimethenamid-P fb fomesafen reduced S03W4 by 18%. In general, PRE fb POST caused more injury than PRE treatments; however, injury diminished over time and no significant reduction to soybean yield could be attributed to adding POST fomesafen. On the basis of this study, the injury from PPO herbicides applied PRE is active ingredient, cultivar, and environment specific. Although PPO herbicides have the potential to cause unacceptable crop injury in some IP soybean cultivars, selecting a tolerant cultivar will minimize yield losses.

Pre-adult development time, dry weight at eclosion, and daily fecundity over the first 10 days of adult life were measured in five species of Drosophila from the melanogaster and immigrans species groups. Overall, the three species of the melanogaster group (D. melanogaster, D. ananassae, D. malerkotliana) developed faster, were lighter at eclosion, and produced more eggs per unit weight at eclosion than the two species of the immigrans group (D. n. nasuta, D. sulfurigaster neonasuta). The degree of sexual dimorphism in dry weight was greater than that in development time, but did not vary significantly among species, and was not correlated with fecundity, contrary to expectations that sexual selection for increased fecundity drives sexual size dimorphism in Drosophila. The degree of dimorphism in development time was significantly correlated with dry weight and fecundity, with lighter species tending to be more dimorphic for development time as well as more fecund, both in absolute terms and in terms of fecundity per unit weight. The results suggest that our understanding of the evolutionary forces maintaining sexual size dimorphism in Drosophila will probably benefit from more detailed studies on the correlates of sexual dimorphism within and among Drosophila species, and on the shape of reaction norms for the degree of sexual dimorphism across different levels of ecologically relevant environmental variables.

We have explored the relationships between specific leaf area calculated for a whole plant and its individual leaves. Barley was grown in hydroponics in controlled environment cabinets. Plants were harvested on the basis of physiological age (defined as the number of days after full expansion of leaves on the main stem) and the area and weight of whole, fully expanded, leaves measured and specific leaf area (SLA) of individual leaves or whole plants calculated. Specific leaf area calculated for individual leaves (SLAL) varied with leaf position and with leaf age after full expansion whereas SLA calculated for whole plants (SLAP) varied with plant age. The same conclusions were reached whether the results were based on total dry weight or dry weight minus soluble carbohydrates (‘structural weight’). Transferring plants to shade on the day of full expansion of the third leaf on the main stem increased the SLAP, and also SLAL of leaves 3 and 4 on the main stem (leaf 4 being the younger leaf of the two), because of a decrease in the ‘structural weight’ of these leaves. However SLAL of leaf 2 (which was older than leaf 3) was not affected by shading; the effect was confined to leaves developing in the new conditions.