The Effect of Growth Conditions and Origin of Tissue 5Phaseolus vulgaris L.)

Callus cultures isolated from various somatic tissues and anthertissue of Phaseolus vulgaris seedlings on a defined growth mediumcontained few diploid cells. The proportion of diploid cellsdid not alter as cultures lost their ability to form vasculartissue. Meristematic cells of roots initiated after transferto induction medium were diploid. All cultures lost their morphogeneticpotential after five to seven subcultures except anther calluswhich formed vascular tissue over a prolonged period of cultureon maintenance medium. After six subcultures anther callus containedmore polyploid cells than somatic cultures. Callus isolated from bean hypocotyl tissue in the presence ofcoconut milk consisted mainly of diploid cells and retainedits morphogenetic potential for a greater number of subculturesthan callus grown on defined medium. Transfer of callus isolatedon the defined medium to medium containing coconut milk increasedthe proportion of diploid cells and prevented further loss ofinorphogenetic potential. An equivalent concentration of cytokininto that in coconut milk prevented the loss of potential butdid not affect the ploidy of the cultures.     

Modelling climate‐change‐induced nonlinear thresholds in cephalopod population dynamics

A significant global challenge lies in our current inability to anticipate, and therefore prepare for, critical ecological thresholds (i.e. tipping points in ecosystems). This deficit stems largely from an inadequate understanding of the many complex interactions between species and the environment at the ecosystem level, and the paucity of mechanistic models relating environment to population dynamics at the species level. In marine ecosystems, abundant, short‐lived and fast‐growing species such as anchovies or squids, consistently function as ‘keystone’ groups whose population dynamics affect entire ecosystems. Increasing exploitation coupled with climate change impacts has the potential to affect these ecological groups and consequently, the entire marine ecosystem. There are currently very few models that predict the impact of climate change on these keystone groups. Here we use a combination of individual‐based bioenergetics and stage‐structured population models to characterize the fundamental capacity of cephalopods to respond to climate change. We demonstrate the potential for, and mechanisms behind, two unfavourable climate‐change‐induced thresholds in future population dynamics. Although one threshold was the direct consequence of a decrease in incubation time caused by ocean warming, the other threshold was linked to survivorship, implying the possibility of management through a modification of fishing mortality. Additional substantive changes in phenology were also predicted, with a possible loss in population resilience. Our results demonstrate the feasibility of predicting complex nonlinear dynamics with a reasonably simplistic mechanistic model, and highlight the necessity of developing such approaches for other species if attempts to moderate the impact of climate change on natural resources are to be effective.     

The effect of date of haulm destruction and harvest on the development of dry rot caused by Fusarium solani var. coeruleum on potato tubers

Over 3 yr, the development of dry rot, caused by Fusarium solani var. coeruleum, and the efficacy of treating potato tubers with imazalil was examined in relation to the date of haulm destruction and harvest, and the interval between haulm destruction using diquat dibromide and harvest. The effect of these factors on skin set was also assessed. Planting inoculated seed tubers bearing small rots produced more dry rot on the daughter tubers than planting naturally contaminated seed tubers in 1992. The incidence of dry rot was higher on daughter tubers wounded by a standardised method than on those passed over a reciprocating riddle (riddling). The relationship between the two assessment methods was significantly (P<0.05) correlated in 2 out of 3 yr. Overall, the interval between haulm destruction and harvest had less effect on the incidence of dry rot on daughter tubers after riddling than the date of harvest. In 2 out of 3 yr, the incidence of dry rot on riddled tubers was least on those harvested in August and was much greater on September‐harvested tubers. On tubers harvested in October, the pattern was variable, with the incidence declining in 1 yr but increasing in the other. In the third year, the development of dry rot was similar on August‐ and September‐harvested tubers and was least on those harvested in October. Dipping tubers in imazalil gave significant reductions in dry rot although the amount of the reduction was variable and not affected by time of treatment or the amount of fungicide deposited within the range 6.7 to 19.4 mg imazalil kg^?1. Skin set at harvest, as measured by skin strength or the amount of scuff damage, increased the later the tubers were harvested but did not appear to be affected by the interval between haulm destruction and harvest.