The large Gunnera's (G. tinctoria and G. manicata) in Europe in relation to EU regulation 1143/2014.

Incorrect labelling of plants in the horticultural trade and misidentification is widespread. For the inspection services of the EU member states, correct identification of G. tinctoria has become important since the species was added to the List of Union concern in accordance with EU regulation 1143/2014 in August 2017. In the horticultural trade Gunnera plants are generally of modest dimensions and rarely flowering, so that the major distinguishing morphological characters for the identification of the two large species, G. tinctoria and G. manicata, are missing. As G. tinctoria is included in the EU regulation, its trade is prohibited, although the closely related species, G. manicata is not included on the list. Given that it is often difficult to distinguish between these two large herbaceous species using morphological attributes we used standard chloroplast DNA barcode markers, supplemented at a later stage by ITS markers. Plant material of putative G. tinctoria or G. manicata was obtained from the native and introduced range, both from "wild" sources, botanical gardens, and the horticultural trade. In western Europe plants circulating in the horticultural trade turned out to be predominantly G. tinctoria, with only one plant in cultivation identified as true G. manicata and the G. manicata found in botanical gardens was a hybrid recently described as G. x cryptica.

Enhancing the productivity of ryegrass at elevated CO2 is dependent on tillering and leaf area development rather than leaf-level photosynthesis.

Whilst a range of strategies have been proposed for enhancing crop productivity, many recent studies have focused primarily on enhancing leaf photosynthesis under current atmospheric CO2 concentrations. Given that the atmospheric CO2 concentration is likely to increase significantly in the foreseeable future, an alternative/complementary strategy might be to exploit any variability in the enhancement of growth/yield and photosynthesis at higher CO2 concentrations. To explore this, we investigated the responses of a diverse range of wild and cultivated ryegrass genotypes, with contrasting geographical origins, to ambient and elevated CO2 concentrations and examined what genetically tractable plant trait(s) might be targeted by plant breeders for future yield enhancements. We found substantial ~7-fold intraspecific variations in biomass productivity among the different genotypes at both CO2 levels, which were related primarily to differences in tillering/leaf area, with only small differences due to leaf photosynthesis. Interestingly, the ranking of genotypes in terms of their response to both CO2 concentrations was similar. However, as expected, estimates of whole-plant photosynthesis were strongly correlated with plant productivity. Our results suggest that greater yield gains under elevated CO2 are likely through the exploitation of genetic differences in tillering and leaf area rather than focusing solely on improving leaf photosynthesis.

Resource competition in plant invasions: emerging patterns and research needs.

Invasions by alien plants provide a unique opportunity to examine competitive interactions among plants. While resource competition has long been regarded as a major mechanism responsible for successful invasions, given a well-known capacity for many invaders to become dominant and reduce plant diversity in the invaded communities, few studies have measured resource competition directly or have assessed its importance relative to that of other mechanisms, at different stages of an invasion process. Here, we review evidence comparing the competitive ability of invasive species vs. that of co-occurring native plants, along a range of environmental gradients, showing that many invasive species have a superior competitive ability over native species, although invasive congeners are not necessarily competitively superior over native congeners, nor are alien dominants are better competitors than native dominants. We discuss how the outcomes of competition depend on a number of factors, such as the heterogeneous distribution of resources, the stage of the invasion process, as well as phenotypic plasticity and evolutionary adaptation, which may result in increased or decreased competitive ability in both invasive and native species. Competitive advantages of invasive species over natives are often transient and only important at the early stages of an invasion process. It remains unclear how important resource competition is relative to other mechanisms (competition avoidance via phenological differences, niche differentiation in space associated with phylogenetic distance, recruitment and dispersal limitation, indirect competition, and allelopathy). Finally, we identify the conceptual and methodological issues characterizing competition studies in plant invasions, and we discuss future research needs, including examination of resource competition dynamics and the impact of global environmental change on competitive interactions between invasive and native species.

Is acclimation required for success in high light environments? A case study using Mycelis muralis (L.) Dumort (Asteraceae).

In the field significant differences in maximum photosynthetic O2 -exchange rate (Pm ) were found between leaves of Mycelis muralis (L.) Dumort (Asteraceae) collected from woodland and exposed habitats, with the highest values in the exposed sites- However, there were no differences in the Pm of leaves collected from plants growing in grikes (fissures in the limestone pavement), of exposed limestone pavement, despite a greater than four-fold difference in the integrated daily irradiance. Leaves of plants from the open pavement had lower photon yields (ø1 ) and higher dark respiration rates and light compensation points, in comparison to shaded plants. Under controlled environmental conditions the highest Pm of leaves from plants subjected to variations in irradiance were found at the intermediate (8-6 mol photon m-2 d-1 growth light level used. At the highest growth irradiance 17.3 mol photon m-2 d-1 used in the laboratory both Pm and øl were reduced, although the latest plant biomass was found at this irradiance. No changes were found in the chlorophyll a:b ratio over the same range of irradiances. Examination of plant populations of M. muralis, collected from open or shaded habitats and exposed to growth irradiances that covered the range over which increases in photosynthesis were, observed in the laboratory (0.86-8.6 mol photon m-2 d-1 ), resulted in changes in leaf structure and pigment composition. The chlorophyll a:b ratio was low and largely independent of irradiance or the origin of the plant population. Differences in total chlorophyll content were small with the lowest values m the Durrow woodland populations at both irradiances. No variations were found in a number of chloroplast thylakoid structural features. In particular, the ratio of oppressed to non-appressed membranes was unchanged by growth at the two irradiances, consistent with an invariant chlorophyll a:b ratio. Based on peaks in the difference spectra the woodland populations had mi enhanced in vivo absorption at λlD= 650 and 706 nm when grown at low irradiance. These peaks were absent from the population collected from the open limestone pavement. The significance of the enhanced absorption at low irradiance and the possibility that these peaks represent long-wavelength forms of chlorophyll a (λlD = 706) and b (λlD = 650) is discussed. A particular feature of plants grown at high irradiance was an enhanced anthocyanin content in comparison to those grown at low irradiance. This was associated with an increase in absorptance. particularly in the green region (λlD = 550 nm) of the visible spectrum. Overall these results suggest that complete acclimation of photosynthesis and an ability to modulate light-harvesting is not a prerequisite, for success in a high light environment.

THE MINIMUM PHOTON REQUIREMENT FOR PHOTOSYNTHESIS: AN ANALYSIS OF THE DATA OF WARBURG & BURK (1950) AND YUAN, EVANS & DANIELS (1955).

Variations in the apparent photon requirement for photosynthesis (Φ-1 co 2 ) or (Φ-1 co 2 ) in the data of Warburg & Burk (1950) and Yuan, Evans & Daniels (1955) can be ascribed to changes in O2 uptake and energy-dependent processes which result in aberrant photon requirements in organisms subjected to non-optimal conditions. The increase in Φ-1 co 2 with increases in the gas exchange quotient (γ) in the observations of Yuan et al. (1955) is consistent with increases in photorespiratory production of glycollate, whilst changes in Φ-1 co 2 and Φ-1 co 2 in the results of Warburg & Burk (1950) can be explained by a variable Kok effect associated with nitrate assimilation at low light levels. When these O2 and energy-dependent processes are minimal, the lowest values should be observed. The minimum value obtained when Chlorella is photosynthesizing under optimal conditions is 6 mol photons mol-1 O2 . These results provide direct independent evidence for a photon requirement for photosynthesis of less than 8 mol photons mol-1 O2 . Such a value is not consistent with the Z scheme of photosynthesis.