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Context Mungbean (Vigna radiata (L.) Wilczek) is an important grain legume for food, feed, and green manure. Mungbean yield is highly variable due to fluctuating temperature and unpredictable rainfall. Aims To improve yield stability, it is critical to utilise a model that can simulate mungbean phenology, biomass, and yield accurately. Methods A thorough understanding of the physiological determinants of growth and yield is required to advance existing mungbean crop modelling capability. Currently, there is limited understanding of the physiological determinants of canopy and reproductive development and their variation in mungbean germplasm. Two experiments (controlled and field environments) were conducted at Gatton, Queensland, in 2018–19. Six Australian mungbean genotypes and one black gram (Vigna mungo L.) were grown under non-limiting conditions. Plant phenotypic traits (canopy development, time to first, 50% flowering, duration of flowering and podding, flower appearance, pod addition rates) were recorded. Key results Genotypes M10403 and Satin II had significantly higher leaf appearance rate (LAR). Genotypes with a greater LAR had higher number of leaves but lower individual leaf area. Genotypes varied significantly in time to first and 50% flowering, with Onyx-AU (black gram) and Celera II-AU flowering earliest. Flowering and podding rates, and duration of these phenological phases varied among genotypes. Total plant leaf area (TPLA) approached its maximum at mid-podding stage. Implications This study quantified the key phenotypic and physiological relationships associated with canopy and reproductive development, critical for the improvement of mungbean crop modelling required to accurately simulate growth and development and inform possible canopy constraints that are limiting mungbean productivity.

The development of reproductive tissues determines plant fecundity and yield. Loading of resources into the developing reproductive tissue is thought to be under the co-limiting effects of source and sink strength. The dynamics of this co-limitation are unknown, largely due to an inability to measure the flux of resources into a developing sink. Here we use nuclear magnetic resonance (NMR) sensors to measure sink strength by quantifying rates of pod dry matter accumulation (pod loading) in Phaseolus vulgaris at 13-min intervals across the diel period. Rates of pod loading showed contrasting variation across light and dark periods during the onset of water deficit. In addition, rates of pod loading appeared decoupled from net photosynthetic rates when adjusted to the plant scale. Combined, these observations illustrate that the rate of pod development varies under water limitation and that continuous, non-invasive methodologies to measure sink strength provide insight into the governing processes that determine the development of reproductive tissues.

Ninhydrin was implemented as the primary police method of developing latent fingermarks on paper, cardboard and some other porous surfaces from the late 1960s. Some researchers have used individual amino acids, or mixtures of amino acids, as a method of testing the effectiveness of reagent formulations. It was not however known whether simple mixtures of amino acids could effectively emulate latent fingermarks in reactions with reagents such as ninhydrin. The first part of this study compared the effects of ninhydrin fingermark treatments used internationally in various police laboratories on test targets created by inkjet printing graduated concentrations of a representative mixture of amino acids in a series of blocks on paper. Variations in intensity of development were observed between laboratories which used various formulations and heat and humidity post treatment protocols. In a further trial in 2015 several participants in the International Fingerprint Research Group (IFRG) meeting processed test targets in their own laboratories and submitted them for measurement. Again, variation in developed intensity was observed. The depletion of the activity of ninhydrin solutions during use was also investigated in early evaluations of the test targets. An established fingerprint laboratory then processed a number of samples from a batch of targets to examine batch consistency. This was followed by designing a new test target which enabled comparisons between the developed intensity of printed test target blocks alongside depletion series of split, natural donor fingermarks. A panel of 20 donors provided depletion fingermarks and four ninhydrin formulations and treatment protocols were used. The developed test target blocks were scanned, intensity of development measured, and the results compared with the fingermark development which was evaluated by three assessors using two types of scale. Good correlation between the intensity of the developed test targets and latent fingermark quality and intensity scores was observed with the four ninhydrin treatment protocols, including some which used deliberately downgraded ninhydrin concentrations. This type of evaluation was carried out a second time to investigate modified heat and humidity protocols. The use of such test targets for routine reagent quality control and process verification would appear to be far more accurate and reliable than the use of small numbers of donor fingermarks. It is not clear why the different ninhydrin formulations investigated in the latter part of the work have very different optimum post treatment heating regimes.