Leaves absorbed high amounts of clopyralid (3,6-dichloro-2-pyridinecarboxylic acid) as foliar sprays on honey mesquite (Prosopis glandulosa Torr. # PRCJG) as indicated by concentrations of 10 μg/g fresh wt or more in basal stem phloem by 4 days after treatment. Small quantities of clopyralid (< 1 μg/g) were detected in basal stem phloem after spray applications of clopyralid to defoliated plants or roots treated by soil application. When applied to foliated plants, the 0.56 kg/ha of clopyralid killed 60% or more plants, but none were killed when clopyralid sprays were applied to defoliated plants or when 2.2 kg/ha of clopyralid was applied to the soil. Water, diesel oil plus water, or water plus surfactant were equally effective as clopyralid carriers as foliar sprays.

Leaves of greenhouse-grown honey mesquite [Prosopis juliflora (Swartz) DC var. glandulosa (Torr.) Cockerell # PRCJG] initially absorbed more triclopyr {[(3,5,6-trichloro-2-pyridinyl)oxy] acetic acid} from application of the ester than the amine salt. After 24 h, however, honey mesquite had absorbed 66% of the applied ester formulation and 72% of the amine formulation. Triclopyr was rapidly transported from the treated leaf to other plant parts. Triclopyr concentrations recovered 4 h after treatment in the upper canopy, lower canopy, and roots averaged 0.12, 0.19, and 0.09 μg, respectively. Concentrations of triclopyr recovered after 24 h were not significantly different than after 4 h in the canopy. No ester from ester application was recovered in the canopy, other than that in the treated leaf. Triclopyr recovered from stems of honey mesquite in the field ranged from 0.16 to 0.72 μg/g in phloem and from 0.04 to 0.20 μg/g in xylem from a broadcast spray application of the butoxyethanol ester at 1.12 kg/ha. Concentrations of triclopyr were usually not significantly different in either the upper or lower stems whether sampled 3 or 30 days after treatment.

The addition of surfactant I (trimethylnonylpolyethoxyethanol) or surfactant II (4-isopropenyl-1-methyl cyclohexane) at 0.5% (v/v) to the spray solution or 1:1 mixtures of benazolin [4-chloro-2-oxo-3(2H)-benzothiazole-aceticacid], picloram (4-amino-3,5,6-trichloro-2-pyridinecarboxylic acid), or triclopyr {[(3,5,6-trichioro-2-pyridinyl) oxy] acetic acid} with clopyralid (3,6-dichloro-2-pyridinecarboxylic acid) each at 0.28 kg ae/ha enhanced the phytotoxicity of clopyralid on honey mesquite (Prosopis glandulosa Torr. # PRCJG) compared to clopyralid applied alone. Addition of surfactant I, surfactant II, picloram, or triclopyr to clopyralid enhanced its absorption into leaves by 4 h after treatment and movement into upper-stem phloem by all additives by 1 day after treatment. When combined at equal rates, more clopyralid than picloram was transported into stems.

In order to clarify the translocation and metabolism of glyphosate in lead tree, a mixture of glyphosate (0.5 mmol) and 14C-glyphosate was injected into mini tree plants (1.5-cm trunk diameter and 120 cm tall), simulating a grown lead tree in a greenhouse experiment. Within 6 d after treatment (DAT), all leaves on the lead tree plants dropped. Analysis of nonlabeled glyphosate in both xylem and phloem every 15 d showed that glyphosate residues accumulated mainly in phloem, similar to the findings in established lead tree. In this experiment, glyphosate concentration in the phloem of three parts of the trunk, i.e., upper (15 cm above the upper injection hole), middle (between the two injection holes), and lower (15 cm below the lower injection hole) parts, increased rapidly within 45 DAT, and decreased thereafter. Obviously, significant glyphosate metabolism occurred during the latter period. Further 14C radioactivity measurement also exhibited similar time-course changes of glyphosate dissipation, except that a low level of radioactivity in the phloem of the upper part and a high level of radioactivity in the lower part were detected from 45 to 90 DAT, suggesting that more glyphosate metabolites in the phloem of the upper part might have translocated with photosynthetic assimilates and reallocated to the lower part of the mini tree. Thin-layer chromatography (TLC) analysis of metabolites derived from 14C-glyphosate also revealed that about 70% of the radioactivity recovered in the phloem of the lower part comprised the unknown metabolites M1 (retention factor [Rf] : 0.83) and M2 (Rf : 0.94), with nearly 28% of the radioactivity from sarcosine (Rf : 0.76), and less than 2% of the radioactivity from aminomethylphosphoric acid (AMPA) (Rf : 0.49) and glyphosate (Rf : 0.36). It is concluded that active metabolism of glyphosate in this 90-d simulation experiment occurred mainly from 45 to 90 DAT, and the primary metabolism was modulated by C-P lyase.

Continuous ingestion of the phloem sap of plants by aphids can remove a significant amount of photoassimilates. Based on our earlier works, we hypothesized that due to the reduced aphid feeding time caused by antibiosis, wheat plants may achieve growth tolerance to aphids. We tested this hypothesis using three wheat cultivars, XY22 (Xiaoyan22), AK58 (Bainongaikang58) and XN979 (Xinong979) and the grain aphid, Sitobion avenae. In the choice test, S. avenae did not show any preference among the three wheat cultivars. However, S. avenae had a lower body weight and a lower intrinsic rate of increase when feeding on XY22 than on AK58 and XN979. The electrical penetration graph results indicated that S. avenae had significantly shorter mean and total phloem ingestion periods on XY22 than on AK58 or XN979. The aphids required a similar time to reach the phloem sap on the three wheat cultivars, but required more time to establish sustained phloem ingestion on XY22. These results suggest that the resistance factors of XY22 may be phloem based. Moreover, XY22 suffered less biomass loss in response to aphid infestation compared with XN979, suggesting that XY22 also had a better growth tolerance to S. avenae than XN979. Wheat resistance level to S. avenae was partially correlated with plant photosynthetic rates, and peroxidase activities. These results confirmed that the limitation in aphid feeding from plant phloem in wheat cultivar XY22 was related to antibiosis but not antixenosis, which caused XY22 tolerance to S. avenae.

The aim of this study was to determine which Arabidopsis thaliana (L.) genes had significantly altered expression following 2–36 h of infestation by the aphid Myzus persicae (Sulzer). Six biological replicates were performed for both control and treatment at each time point, allowing rigorous statistical analysis of any changes. Only two genes showed altered expression after 2 h (one up- and one down-regulated) while two were down-regulated and twenty three were up-regulated at 36 h. The transcript annotation allowed classification of the significantly altered genes into a number of classes, including those involved in cell wall modification, carbon metabolism and signalling. Additionally, a number of genes were implicated in oxidative stress and defence against other pathogens. Five genes could not currently be assigned any function. The changes in gene expression are discussed in relation to current models of plant-insect interactions.

Axial and radial transport and the accumulation of photoassimilates in carrot taproot were studied using 14C labelling and autoradiography. Axial transport of the 14C labelled assimilates inside the taproot was rapid and occurred mainly in the young phloem found in rows radiating from the cambium. The radial transport of the assimilate inward (to cambium, xylem zone and pith) and outward (to phloem zone and periderm) from the conducting phloem was an order of magnitude slower than the longitudinal transport and was probably mainly diffusive. The cambial zone of the taproot presented a partial barrier in the inward path of the assimilate to the xylem zone. We suggest that this is due to the cambium comprising a strong sink for the assimilate on the basis that our previous work has shown that it contains very low concentrations of free sucrose. By contrast, a high accumulation of nonsoluble 14C was found in the cambium region in good agreement with the active growth of this zone. Autoradiography following the feeding of 14C labelled sugars to excised sections of taproot indicated that only a ring of cells at and/or just within the cambium take up sugars from the apoplast. This indicates that radial movement in the phloem and pith must be symplastic. An apoplastic step between phloem and xylem is possible. The rapid uptake of sugars from the apoplast at this point might represent a mechanism for keeping photoassimilates away from the transpiration stream and re-location back to the leaves.

We review four hypotheses for the control of carbon acquisition by roots, and conclude that the functional equilibrium hypothesis can offer a good description of C acquisition by roots relative to shoots, but is deficient mechanistically. The hypothesis that import into roots is solely dependent on export from the shoot, itself determined by features of the shoot alone (the ‘push’ hypothesis), is supported by some but not all the evidence. Similarly, the idea that root demand, a function of the root alone, determines import into it (the ‘pull’ hypothesis), is consonant with some of the evidence. The fourth, general, hypothesis (the ‘shared control’ hypothesis) – that acquisition of C by roots is controlled by a range of variables distributed between root and shoot – accords with both experiment and theory. Top-down metabolic control analysis quantifies the control of C flux attributable to root relative to source leaf. We demonstrate that two levels of mechanistic control, short-term regulation of phloem transport and control of gene expression by compounds such as sugars, underlie distributed control. Implications for the impact of climate change variables are briefly discussed.

This work explored whether the natural abundances of carbon and nitrogen isotopes could be used to describe the movement of C and N within wheat plants; we also considered whether isotopic analyses of aphids or their honeydew would substitute for direct analysis of phloem exudate.

The δ13C of ears and roots (sinks) most closely matched those of the sugars+organic acids fraction (sources) in both growth stages; phloem δ13C matched that of leaf blade sugars. Xylem exudate δ13C matched no other putative (and measured) source in the ear-forming stage and matched that of whole roots and ears in the grain-filling stage. The δ15N of grain and roots (sinks) resembled that of leaf amino acids (sources) in the ear-forming stage. In the grain-filling stage, ear δ15N continued to resemble that of leaf amino acids, and δ15N of roots most closely resembled that of whole leaves. In the grain-filling stage, phloem δ15N fell between that of leaf blade amino acids and that of whole leaves and was 15N-depleted relative to internal and external NO3−-N. In both growth stages, xylem exudate δ15N was less than that of soil NO3−-N and and more than that of residual soil N after mineral N extraction. The isotopic values are generally in agreement with data from other approaches, such as isotope labelling; they show NO3−-N reduction in both shoots and roots of wheat and significant N recycling (root-shoot-phloem-root) and C movement.

Aphids might serve as a substitute for isotopic analysis of phloem δ15N, having the same value as their food source. Their excreta was 15N-enriched relative to phloem.

Plants of gymnospermous affinities are the most important component of the flora at East Kirkton. Four genera of anatomically preserved gymnosperm stems with well developed secondary xylem are interpreted as arborescent. The largest specimens (trunks up to 50 cm in diameter) are attributed to the genus Pitus. Features of the wood, including ray size, are characteristic of the species Pitus withamii Lindley & Hutton which has long been described from the Strathclyde (former Oil-Shale) Group of Scotland. Decorticated axes of Eristophyton fasciculare are more common; their study has enlarged our concept of the species with regard to maximum diameter, internode length and phloem organisation. Similarly, the decorticated specimens of Bilignea solida Kidston found at East Kirkton exceed in diameter the original material described from Ayrshire. The fourth taxon is Stanwoodia recently described by Galtier and Scott (1991). In all these plants, features of leaf traces suggest that leaves were relatively large and densely borne on ultimate branches. These leaves were shed ultimately, prior to a later phase of wood development; they certainly correspond to (? most of) the compression foliage commonly found in association: Sphenopteridium, Adiantites and Spathulopteris.

A new taxon of probable early gymnosperms is described from permineralised specimens showing excellent preservation of the tissues, from the late Lower Carboniferous (Dinantian), Brigantian, deposits of the Midland Valley of Scotland. Stanwoodia gen. nov., represented by the single species S. kirktonensis sp. nov., shows the combination of a primitive protostelic organisation with a dense secondary wood. It closely compares to the enigmatic genus Bilignea which was formerly referred with some reservations to the Cordaitales. Another interest of the new plant concerns the excellent preservation of the phloem with at least three different types of constituent cells including fibres. Stanwoodia also exhibits the oldest well-documented evidence of a sequent periderm or rhytidome in fossil plants.