100 research outputs found

    Antifungal effect and reduction of Ulmus minor symptoms to Ophiostoma novo-ulmi by carvacrol and salicylic acid

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    There are still no effective means to control Dutch elm disease (DED), caused by the vascular fungi Ophiostoma ulmi and O. novo-ulmi. Plant phenolics may provide a new strategy for DED control, given their known antifungal activity against pathogens and their involvement in plant defence mechanisms. The in vitro antifungal activity of salicylic acid, carvacrol, thymol, phenol, o-cresol, m-cresol, p-cresol, and 2,5-xylenol against the DED pathogens was tested. Also, the protective effect of watering Ulmus minor seedlings with these compounds was tested against O. novo-ulmi. Salicylic acid, carvacrol, and thymol showed the strongest antifungal in vitro activity, while carvacrol and salicylic acid provided the strongest in vivo protection against O. novo-ulmi (63 and 46% reduction of leaf wilting symptoms with respect to controls, respectively). The effect of the treatments on tree phenology was low, and a significant negative relation was observed between the number of days to bud burst and the leaf wilting symptoms after inoculation, probably determined by genetic differences among the elm tree progenies used. The treatments with salicylic acid, carvacrol and thymol induced the highest shift in phenolic metabolite profile with respect to control trees. The protective effect of carvacrol and salicylic acid is discussed in terms of their combined activity as antifungal compounds and as inductors of tree defence responses

    Jesús G. MAESTRO, "La filosofía de los poetas". Madrid, Verbum, 2018, 245 pp.

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    Review of Jesús G. MAESTRO, La filosofía de los poetas. Madrid, Verbum, 2018, 245 pp.Reseña de Jesús G. MAESTRO, La filosofía de los poetas. Madrid, Verbum, 2018, 245 pp

    Spatial structure of deciduous forest stands with contrasting human influence in northwest Spain

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    Five contrasting deciduous forest stands were studied to characterize the spatial structural variability in human-influenced forests. These stands are representative of cultural forest types widely represented in western Europe: one plantation, two coppices, one wood-pasture forest and one high forest stand. All stems with DBH > 5 cm were measured and mapped, and stem DBH distributions, spatial structure of DBH, spatial point patterns and spatial associations were analysed. Spatial autocorrelation for DBH was calculated with Moran’s I correlograms and semivariograms. Complete spatial randomness hypothesis for spatial point patterns, and both independence and random labelling hypotheses for spatial associations were analysed using Ripley’s K function. The results showed that tree sizes were conditioned by particular former management systems, which determined unimodal symmetric, positively skewed or compound DBH distributions. Spatial structure was more complex when human influence became reduced. Coppice stands showed clumped spatial patterns and independence among size classes, as a consequence of sexual and vegetative establishment of new stems in open areas. The largest clumping intensity was observed in the wood-pasture with an intermediate disturbance frequency and low inter-tree competition. The high forest stand displayed spatial traits consistent with the gap-dynamics paradigm, such as clumping of smaller trees, random arrangement of larger trees, negative association between juveniles and adults, and high structural heterogeneity. It can be expected that after cessation of human interference, coppices and wood-pastures would evolve to a more heterogeneous structure, probably with a higher habitat and species diversity.This research was partially supported by the Consejería de Medio Ambiente del Principado de Asturias (SV-PA-00-01).Peer reviewe

    Effect of grafting on phenology, susceptibility to Phytophthora cinnamomi and hormone profile of chestnut

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    Ink disease caused by the root-rot pathogen P. cinnamomi (Pc) threatens European sweet chestnut (Castanea sativa Mill.) orchards, and growers increasingly graft susceptible C. sativa traditional varieties on Pc-resistant hybrid commercial rootstocks. The influence of the scion, the rootstock, and grafting per se on the vegetative budburst, growth, susceptibility to Pc and defence-related hormone profile of Castanea spp. are unknown. In a greenhouse experiment, these effects were evaluated by reciprocally grafting two Pc resistant C. crenata x C. sativa clones and two Pc susceptible C. sativa clones. Resistance to Pc and the hormone content of leaves and roots were rootstock-dependent, and survival rates of susceptible chestnuts strongly increased when grafted on resistant rootstocks. The scion had no effect on the resistance to Pc and the hormone profile of leaves and roots of grafted trees, but influenced vegetative budburst and primary growth. Grafting per se increased susceptibility to Pc and altered the defence-related phytohormone content of trees, especially in resistant rootstocks, but did not influence budburst and growth of trees. Grafting-induced alteration of the constitutive defense-related hormone profile could explain the increased susceptibility of resistant rootstocks to Pc. Nine days after infection, a dynamic hormonal response consisting of decreased jasmonates (JA and JA-Ile) in leaves and increased ABA and JA-Ile in roots was observed in resistant chestnuts. This is the first study addressing the role of grafting in modulating resistance to the soil-borne pathogen Pc in chestnut trees

    Densidad y área de los canales resiníferos de "Pinus pinaster" ante tratamientos de fertilización, y su relación con la defensa ante "Hylobius abietis"

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    6 páginas, 3 tablas -- Actas de la I Reunión sobre Sanidad Forestal celebrada en Palencia el 24 y 25 de septiembre de 2007.Las coníferas poseen una estructura de canales resiníferos que actúa como defensa contra el ataque de insectos y patógenos. Varios autores han observado que un aumento en la disponibilidad de nutrientes puede alterar el reparto de energía en las plantas, en detrimento de los sistemas defensivos. El presente estudio tiene como objetivo determinar el efecto de la fertilización de establecimiento sobre el desarrollo del sistema de canales resiníferos en Pinus pinaster. Mediante histología en brinzales de 3 savias sometidos a dos ensayos familia x fertilización se cuantificó la densidad y el área de los canales resiníferos del floema y del xilema tanto en el tallo principal como en ramas laterales en dos ensayos familia x fertilización. Se observó un efecto significativo de la fertilización en el desarrollo de los canales resiníferos del floema (p<0,05), con valores de 0,45 y 0,36 canales.mm-2 para brinzales no fertilizados y sí fertilizados, respectivamente. Este efecto no se observó en las variables del xilema. La densidad de canales resiníferos en el xilema fue significativamente diferente entre las dos parcelas estudiadas, siendo mayor en la atacada por el curculiónido Hylobius abietis. Por último, la relación tallo-rama de las variables cuantificadas no fue lo suficientemente consistente como para utilizar los canales en ramas de P. pinaster como indicadores de los canales en el tronco principal.Este trabajo se ha realizado bajo financiación del proyecto INIA-RTA05-173.Peer reviewe

    Alterations of the resin canal system of Pinus pinaster seedlings after fertilization of a healthy and of a Hylobius abietis attacked stand

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    Abstract Changes in resource availability and biotic and abiotic stress may alter the defensive mechanisms of pine trees. The effect of fertilisation on the resin canal structure of Pinus pinaster seedlings established in two trials in NW Spain, one attacked by Hylobius abietis and the other nonattacked, was studied. The leaders of 50 plants were destructively sampled and the resin canal density, the canal area and its relative conductive area in the phloem and xylem were assessed. Experimentally increased nutrient availability significantly decreased resin canal density in the phloem of the seedlings in the two analysed trials, where unfertilised seedlings presented up to 30% more resin canal density than the fertilised seedlings (mean value ± SEM = 0.32 ± 0.02 resin canals mm -2 in the fertilised plants versus 0.45 ± 0.04 resin canals mm -2 in the control plants). Fertilisation had no effect on the resin canal system in the xylem, but significantly increased tracheid size. Significant differences of resin canals among sites were observed mainly in the xylem; the resin canal density was 1.7-fold greater in the attacked site than in the non-attacked site. The similar structure of phloem resin canals in both sites supports that phloem resin canals are constitutive mechanisms of defence in P. pinaster, whereas xylem resin canals would be constitutive mechanisms but also inducible mechanisms of resistance following the attack of pine weevils or bark beetles

    Holm oak decline is determined by shifts in fine root phenotypic plasticity in response to belowground stress

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    Climate change and pathogen outbreaks are the two major causes of decline in Mediterranean holm oak trees (Quercus ilex L. subsp. ballota (Desf.) Samp.). Crown-level changes in response to these stressful conditions have been widely documented but the responses of the root systems remain unexplored. The effects of environmental stress over roots and its potential role during the declining process need to be evaluated. We aimed to study how key morphological and architectural root parameters and nonstructural carbohydrates of roots are affected along a holm oak health gradient (i.e. within healthy, susceptible and declining trees). Holm oaks with different health statuses had different soil resource-uptake strategies. While healthy and susceptible trees showed a conservative resource-uptake strategy independently of soil nutrient availability, declining trees optimized soil resource acquisition by increasing the phenotypic plasticity of their fine root system. This increase in fine root phenotypic plasticity in declining holm oaks represents an energy-consuming strategy promoted to cope with the stress and at the expense of foliage maintenance. Our study describes a potential feedback loop resulting from strong unprecedented belowground stress that ultimately may lead to poor adaptation and tree death in the Spanish dehesa.This research was mainly funded by the Spanish Government through the IBERYCA project (CGL2017-84723-P), its associated FPI scholarship BES-2014-067971 (ME-V) and SMARTSOIL (PID2020-113244GB-C21). It was further supported by the BC3 María de Maeztu excellence accreditation (MDM-2017-0714; the Spanish Government) and by the BERC 2018–2021 and the UPV/EHU-GV IT-1018-16 programme (Basque Government). Additionally, this research was further supported through the ‘Juan de la Cierva programme’ (MV; IJCI-2017-34640; the Spanish Government) and one project funded by the Romanian Ministry of Research, Innovation and Digitization through UEFISCDI (A-MH; REASONING, PN-III-P1-1.1-TE-2019-1099)

    Genetic variation and heritability estimates of Ulmus minor and Ulmus pumila hybrids for budburst, growth and tolerance to Ophiostoma novo-ulmi

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    Seedlings obtained by crossing Ulmus minor and U. minor × U. pumila clones were assessed for flowering, bark beetle damage, vegetative budburst, height growth and resistance to Ophiostoma novo-ulmi. Ramets and open pollinated seedlings obtained from the parent trees were assessed for the same traits. Most progenies had similar traits to their parents, but some presented heterosis in annual growth or resistance to O. novo-ulmi. Leaf wilting was significantly lower in progenies with U. minor × U. pumila rather than U. minor as female parent (21.5 and 30.6%, respectively; P<0.05). Resistance to O. novoulmi increased significantly as a function of increased amounts of U. pumila germplasm from the female parent, suggesting that resistance to Dutch elm disease is primarily transmitted from the mother. Budburst occurred earlier in seedlings with low rather than high growth rates (P=0.0007) and percentage of wilting was negatively related to early budburst (P<0.0001). Other phenotypic relations included percentage of flowering trees and annual height growth (rp=0.44; P=0.0042), percentage of flowering trees and vegetative budburst (rp=-0.53; P=0.0004) and percentage of beetle-affected trees and annual height growth (rp=0.60; P<0.0001). Heritability estimates obtained from the regression and variance components methods ranged from 0.06 ± 0.04 to 0.64 ± 0.18, 0.10 ± 0.05 to 0.69 ± 0.17, and 0.13 ± 0.32 to 0.71 ± 0.22 for budburst, growth and tolerance to O. novo-ulmi, respectively. Broad- and narrowsense heritability values were higher when estimated 60 days post inoculation (dpi) than 15, 30 or 120 dpi. Heritability estimates and genetic gains reported indicate a high degree of additive genetic control and show the effectiveness of selection for Dutch elm disease resistance and rapid tree growth

    Complexities underlying the breeding and deployment of Dutch elm disease resistant elms

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    Dutch elm disease (DED) is a vascular wilt disease caused by the pathogens Ophiostoma ulmi and Ophiostoma novo-ulmi with multiple ecological phases including pathogenic (xylem), saprotrophic (bark) and vector (beetle flight and beetle feeding wound) phases. Due to the two DED pandemics during the twentieth century the use of elms in landscape and forest restoration has declined significantly. However new initiatives for elm breeding and restoration are now underway in Europe and North America. Here we discuss complexities in the DED 'system' that can lead to unintended consequences during elm breeding and some of the wider options for obtaining durability or 'field resistance' in released material, including (1) the phenotypic plasticity of disease levels in resistant cultivars infected by O. novo-ulmi; (2) shortcomings in test methods when selecting for resistance; (3) the implications of rapid evolutionary changes in current O. novo-ulmi populations for the choice of pathogen inoculum when screening; (4) the possibility of using active resistance to the pathogen in the beetle feeding wound, and low attractiveness of elm cultivars to feeding beetles, in addition to resistance in the xylem; (5) the risk that genes from susceptible and exotic elms be introgressed into resistant cultivars; (6) risks posed by unintentional changes in the host microbiome; and (7) the biosecurity risks posed by resistant elm deployment. In addition, attention needs to be paid to the disease pressures within which resistant elms will be released. In the future, biotechnology may further enhance our understanding of the various resistance processes in elms and our potential to deploy trees with highly durable resistance in elm restoration. Hopefully the different elm resistance processes will prove to be largely under durable, additive, multigenic control. Elm breeding programmes cannot afford to get into the host-pathogen arms races that characterise some agricultural host-pathogen systems
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