Hydraulic architecture and water relations of Spartium junceum branches affected by a mycoplasm disease

Plant water relations, xylem anatomy and the hydraulic architecture of 1‐year‐old twigs of Spartium junceum, both healthy and affected by a phytoplasm disease, were studied. The disease causes twigs to be either shortened (witches broom disease, WBD) or flat (fasciate disease, FD). WBD twigs show a sevenfold increase in total leaf area, smaller and shorter xylem conduits, a higher stomatal conductance (g_l) and a decline of minimum leaf water potentials ( Ψ _l) below the turgor loss point. FD twigs had nearly twice the leaf area of the healthy controls as well as high g_l values and Ψ _l values below the turgor loss point. Moreover, significant differences between healthy and affected twigs in stem stomatal conductance (g_s) and in the total stem area were recorded. Affected twigs die back under drought stress, which is explained by a pronounced loss of hydraulic conductivity of the infected stems (40 and 60%) in FD and WBD as well as by the unfavourable ratio of weighted conduit radius ( Σ r⁴) to total surface area (A_t), so that the efficiency of the stem in supplying the whole transpiring area with water is strongly reduced.     

Changes in the composition of volatile compounds of Spartium junceum induced by the phytoplasmal disease,Spartium witches’‐broom

Abstract

In southern Italy, Spartium junceum (Spanish broom) is severely affected by a phytoplasmal disease, Spartium witches’‐broom (SpaWB). The volatile fractions extracted from flowers of healthy and diseased plants, examined by gas chromatography and gas chromatography–mass spectrometry, appeared to be quantitatively and qualitatively different. In both the healthy and the diseased plants, the main components were n‐alkanes, which occurred at a rate of 55.2% and 38.8%, respectively. The level of aliphatic acids was considerably lower in flowers of the diseased plants than in those of the healthy plants (4.5% vs. 18.7%). Sesquiterpenes were detected only in the diseased plants. It is possible that the changes in the composition of secondary metabolites of diseased plants can be related to plant defense responses.

Abbreviations: AP, apple proliferation; EY, elm yellows; SpaWB, Spartium witches’‐broom     

The ratio of leaf to total photosynthetic area influences shade survival and plastic response to light of green-stemmed leguminous shrub seedlings

Different plant species and organs within a plant differ in their plastic response to light. These responses influence their performance and survival in relation to the light environment, which may range from full sunlight to deep shade. Plasticity, especially with regard to physiological features, is linked to a greater capacity to exploit high light and is usually low in shade-tolerant species. Among photosynthetic organs, green stems, which represent a large fraction of the total photosynthetic area of certain species, are hypothesized to be less capable of adjustment to light than leaves, because of biomechanical and hydraulic constraints. The response to light by leaves and stems of six species of leguminous, green-stemmed shrubs from dry and high-light environments was studied by growing seedlings in three light environments: deep shade, moderate shade and sun (3, 30 and 100 % of full sunlight, respectively). Survival in deep shade ranged from 2 % in Retama sphaerocarpa to 74 % in Ulex europaeus. Survival was maximal at moderate shade in all species, ranging from 80 to 98 %. The six species differed significantly in their ratio of leaf to total photosynthetic area, which influenced their light response. Survival in deep shade increased significantly with increasing ratio of leaf to total photosynthetic area, and decreased with increasing plasticity in net photosynthesis and dark respiration. Responses to light differed between stems and leaves within each species. Mean phenotypic plasticity for the variables leaf or stem specific mass, chlorophyll content, chlorophyll a/b ratio, and carotenoid to chlorophyll ratio of leaves, was inversely related to that of stems. Although mean plasticity of stems increased with the ratio of leaf to total photosynthetic area, the mean plasticity of leaves decreased. Shrubs with green stems and a low ratio of leaf to total photosynthetic area are expected to be restricted to well-lit habitats, at least during the seedling stage, owing to their inefficient light capture and the low plasticity of their stems.     

The influence of water stress on leaf and stem photosynthesis in Spartium junceum L.

Stem and leaf photosynthetic responses to environmental parameters were studied in Spartium junceum L., a legume with chlorophyllous stems. Stem net photosynthesis (P_n) was consistently lower than leaf P_n. The low stem P_n was due to lower quantum yield, lower mesophyll conductance and lower CO₂-saturated P_n than that of leaf P_n. Stomatal limitations to leaf and stem P_n were similar (25%). Water stress caused a greater reduction in leaf P_n than that of stems. Leaf P_n was also reduced in water-stressed plants following rehydration. The reduced leaf P_n was associated with a reduced photon saturated P_n rate and a reduced CO₂ saturated P_n rate. Apparent quantum yield, mesophyll conductance and stomatal limitation of leaves were unaffected by water-stress. Stem P_n following rehydration was not influenced by the water-stress treatment. In general, leaf P_n was more responsive to environmental parameters and more sensitive to water stress than stem P_n. These data support the hypothesis that stem P_n has greater tolerance of water stress, but is limited to low P_n by biochemical means compared to leaves.     

Adaptive longitudinal growth of first-order lateral roots of a woody species (Spartium junceum) to slope and different soil conditions—upward growth of surface roots

First-order lateral roots originating in the upper part of the taproot of a woody species, usually termed surface roots, grow close beneath the soil surface, even on irregular or sloping ground. In slope condition, in fact, the surface roots can assume upward as well as downward growth. Existing knowledge on the controls over root direction does not fully explain these field observations.

Two different soil types and sloping conditions were selected in field condition to explore the behaviour of the surface roots in the woody species Spartium junceum L. The root system 3D architecture was measured with a 3D digitizer and the angle of growth (0° = vertically downwards) and the radial direction (0° = horizontally downslope or northwards) of all root segments measured.

Surface roots were more numerous in clay soil than in loam soil, independently from the slope inclination. They had initial angles larger than 90°, i.e. they grew upwards only in clay soil. The subsequent angles of growth maintained this value only in steep-slope condition, showing a clear soil type x slope inclination interaction. The initial angle of all first-order lateral roots decreased linearly with depth of origin on the taproot always in relation to the soil type, with this relationship being stronger in clay soil.

These findings showed that the liminal angle (the preferred angle of growth) of surface roots was mainly affected by the soil type rather than the soil surface inclination. Thus, upward growth must stand in the plasticity of the plagiotropic response of these secondary laterals rather than in a strong internal control.     

The response of Spartium junceum roots to slope: anchorage and gene factors

BACKGROUND AND AIMS: Plant anchorage is governed by complex, finely regulated mechanisms that occur at a morphological, architectural and anatomical level. Spanish broom (Spartium junceum) is a woody plant frequently found on slopes--a condition that affects plant anchorage. This plant grows throughout the Mediterranean area where it plays an important role in preventing landslides. Spanish broom seedlings respond promptly to slope by altering stem and root morphology. The aim of this study was to investigate the mechanisms whereby the root system of Spanish broom seedlings adapts to ensure anchorage to the ground. METHODS: Seedlings were grown in tilted and untilted pots under controlled conditions. The root apparatus was removed at different times of growth and subjected to morphological, biomechanical and molecular analyses. KEY RESULTS: In slope-grown seedlings, changes in root system morphology, pulling strength and chemical lignin content, all features related to plant anchorage in the soil, were related to seedling age. cDNA-AFLP analysis revealed changes in the expression of several genes in root systems of slope-grown plants. BLAST analysis showed that some differentially expressed genes are homologues of genes induced by environmental stresses in other plant species, and/or are involved in the production of strengthening materials. CONCLUSION: Plants use various mechanisms/strategies to respond to slope depending on their developmental stage.     

Invasive legumes can associate with many mutualists of native legumes,but usually do not

Mutualistic interactions can strongly influence species invasions, as the inability to form successful mutualisms in an exotic range could hamper a host's invasion success. This barrier to invasion may be overcome if an invader either forms novel mutualistic associations or finds and associates with familiar mutualists in the exotic range. Here, we ask (1) does the community of rhizobial mutualists associated with invasive legumes in their exotic range overlap with that of local native legumes and (2) can any differences be explained by fundamental incompatibilities with particular rhizobial genotypes? To address these questions, we first characterized the rhizobial communities naturally associating with three invasive and six native legumes growing in the San Francisco Bay Area. We then conducted a greenhouse experiment to test whether the invasive legume could nodulate with any of a broad array of rhizobia found in their exotic range. There was little overlap between the Bradyrhizobium communities associated with wild‐grown invasive and native legumes, yet the invasive legumes could nodulate with a broad range of rhizobial strains under greenhouse conditions. These observations suggest that under field conditions in their exotic range, these invasive legumes are not currently associating with the mutualists of local native legumes, despite their potential to form such associations. However, the promiscuity with which these invading legumes can form mutualistic associations could be an important factor early in the invasion process if mutualist scarcity limits range expansion. Overall, the observation that invasive legumes have a community of rhizobia distinct from that of native legumes, despite their ability to associate with many rhizobial strains, challenges existing assumptions about how invading species obtain their mutualists. These results can therefore inform current and future efforts to prevent and remove invasive species.