No abstract

Attention to the management of insects that feed on foliar flush growth has increased in Florida citrus as a result of the establishment of invasive plant diseases associated with insects that develop exclusively on flush. Citrus can be monitored to identify peak periods of flush abundance to time insecticide applications for these insects; however, guidelines for quantifying flush abundance are lacking. We therefore investigated sampling procedures for estimating flush abundance. A sampling method was devised to enable a quantitative estimation of flush shoots, defined as any shoot with immature leaves. A sample unit was the area within a 15 × 15 × 15-cm frame slipped into the outer edge of a tree with the end of a branch inside the frame. The number of flush shoots originating within the sample unit was counted. Three sample units were examined per tree in 45 randomly selected trees weekly during 2005 in each of two blocks of trees, one containing young ‘Marsh’ grapefruit (Citrus paradise Macf.) and one containing mature ‘Temple’ orange (tangors) [C. reticulate Blanco × C. sinensis (L.) Osbeck]. A pronounced abundance of flush was generally indicated by means of one or more flush shoots per sample in the particular trees studied. Variation in numbers of flush shoots per sample was similar within and among trees, differed significantly among sample dates, and did not differ significantly between the two blocks of trees overall sample dates. Taylor's power law coefficients indicated that, over all sample weeks, flush shoots were randomly distributed within the young grapefruit trees and only weakly aggregated within the block of mature oranges. Projections indicated that a sampling plan consisting of 40 trees (one sample per tree) would provide density estimates acceptable enough for general estimates at mean densities of one or more shoots per sample. An index of pest abundance based on mean pest density per flush shoot and mean density of flush shoots per sample is proposed.

Cool ambient temperatures (5 to 20 °C) and water deficit are the only factors known to induce flowering in sweet orange (Citrus sinensis). Whereas the effects of cool ambient temperatures on flowering have been described extensively, reports on the mechanisms underlying floral induction by water deficit in sweet orange (and other tropical and subtropical species) are scarce. We report changes in the accumulation of transcripts of four flower-promoting genes, CsFT, CsSL1, CsAP1, and CsLFY, in sweet orange trees in response to water deficit or a combination of water deficit and cool temperatures under controlled conditions. Exposure to water deficit increased the accumulation of CsFT transcripts, whereas transcripts of CsSL1, CsAP1, and CsLFY were reduced. However, when water deficit was interrupted by irrigation, accumulation of CsFT transcripts returned rapidly to pre-treatment levels and accumulation of CsSL1, CsAP1, and CsLFY increased. The accumulation of CsFT transcripts in trees during the combined water deficit and cool temperatures treatment was higher than in trees exposed to either factor separately, and accumulation of CsAP1 and CsLFY transcripts after the combined treatment was also higher. These results suggest that water deficit induces flowering through the upregulation of CsFT and that CsFT is the leaf integrator of flower-inducing signals generated by the exposure to water deficit and cool temperatures in sweet orange.

Foliar-applied urea nitrogen (N) has potential to become an important component in fertilizer programs for citrus in Florida and other citrus growing areas as it can reduce nitrate leaching into ground water. We evaluated seasonal absorption characteristics of three urea formulations, Triazone-urea, liquid urea, and spray grade urea by citrus leaves that were from 2 weeks to 6 months old. The effect of leaf age on 15N absorption by N-deficient and N-sufficient leaves, together with urea absorption over an eight-week period were studied using greenhouse-grown and field-grown plants. All foliar N applications were based on a recommended rate of 34 kg N/ha in 469 L of water. In the field studies, leaf N was increased similarly by the three urea formulations one week after three weekly applications. Young leaves (0.25 month and 1 month old) absorbed a greater percentage of N than the older leaves (3 month and 6 month old). Epicuticular wax concentration increased and 15N absorption declined with leaf age. Nitrogen deficient leaves (1.80% N) had greater wax concentration and lower N absorption than N sufficient leaves (2.60% N). Four to 8 weeks after urea applications, Triazone-urea sprayed leaves had significantly greater leaf N concentration than leaves sprayed with liquid urea or nonsprayed control leaves. The greenhouse studies revealed that the 15N absorption was greater through abaxial leaf surfaces than through adaxial surfaces regardless of leaf N level and application time. Applying foliar 15N-urea during night (2000 hr to 2200 hr) resulted in greater absorption of 15N than in the morning (0800 hr to 1000 hr) or afternoon (1200 hr to 1400 hr). It is clear that maximum N absorption from foliar urea sprays occurred at night through the abaxial surfaces of young leaves with sufficient N. Triazone-urea acted as a slow-release N source that could be exploited in supplying N over an extended period of time.