Extracted Eucalyptus globulus Bark Fiber as a Potential Substrate for Pinus radiata and Quillaja saponaria Germination.

This study aimed to explore alternative substrates for growing forest species using eucalyptus bark. It evaluated the potential of extracted Eucalyptus globulus fiber bark as a substitute for commercial growing media such as coconut fiber, moss, peat, and compost pine. We determined the physicochemical parameters of the growing media, the germination rate, and the mean fresh and dry weights of seedlings. We used the Munoo-Liisa Vitality Index (MLVI) test to evaluate the phytotoxicity of the bark alone and when mixed with commercial substrates. Generally, the best mixture for seed growth was 75% extracted eucalyptus bark fiber and 25% commercial substrates. In particular, the 75E-25P (peat) mixture is a promising substitute for seedling growth of Pinus radiata, achieving up to 3-times higher MLVI than the control peat alone. For Quillaja saponaria, the best growth substrate was the 50E-50C (coconut fiber) mixture, which had the most significant MLVI values (127%). We added chitosan and alginate-encapsulated fulvic acid phytostimulants to improve the performance of the substrate mixtures. The fulvic acid, encapsulated or not, significantly improved MLVI values in Q. saponaria species and P. radiata in concentrations between 0.05 and 0.1% w/v. This study suggests that mixtures with higher levels of extracted fiber are suitable for growing forest species, thus promoting the application of circular economy principles in forestry.

Sirex noctilio infestation led to inevitable pine death despite activating pathways involved in tolerance.

Defense-related metabolome traits in pine species after infestation by Sirex noctilio are largely unknown, despite, in most cases, trees being overwhelmed. Using LC-MS-based untargeted metabolomics, we revealed the systemic metabolic changes induced by this insect in 14-year-old Pinus radiata trees, the most affected species worldwide. An immediate metabolome alteration was expressed in needles after infestation, including the up-regulation of flavonols, flavan-3-ols, oxyneolignans, auxins, proline, and tryptophan, among others. The flavan-3-ols (catechin and procyanidin B1) suggested a rapidly induced photoprotection mechanism aided by diverting proline as an alternative substrate for respiration to compensate for the progressive chlorosis that degrades photosystems. Meanwhile, glutathione, glutamate, and ascorbate levels significantly dropped in needles, which may indicate the critical oxidative stress that trees had to face since the onset of the infestation. They were not fully replenished after long-term infestation, and redox homeostasis was probably not achieved, compromising tree survival. Nevertheless, a huge auxins overexpression detected in needles throughout the infestation may reflect tolerance against the premature senescence caused by the woodwasp venom. In contrast, the metabolome of wood tissues remained initially unchanged, although it seems to collapse after three months. Overall, the metabolomics strategy adopted in this work evidenced its usefulness in uncovering the fundamental roles of plants' chemical defense that govern interactions with specific stressors.

Intra-annual nutrient flux in Pinus taeda.

Intra-annual nutrient (nitrogen, phosphorus, potassium, calcium and magnesium) flux was quantified for Pinus taeda L. at a nutrient-poor, well-drained sandy site in Scotland County, NC, USA where a 2 × 2 factorial of irrigation and nutrition was applied in four replications in a 10-year-old stand with 1200 stems ha(-1). Treatments were applied with the goal of providing optimum nutrition (no nutritional deficiencies) and water availability. Component (foliage, branch, stem and root) nutrient content was estimated monthly for 2 years using nutrient concentration and phenology assessments combined with destructive harvests. Positive flux values indicated nutrient accumulation in the trees while negative values indicated nutrient loss from the trees. Fertilization significantly increased nitrogen, phosphorus, potassium, calcium and magnesium flux 140%, on average, over non-fertilized. Irrigation significantly increased calcium flux 28% while there was no significant irrigation effect on nitrogen, phosphorus, potassium or magnesium. Maximum nutrient fluxes (kg ha(-1) day(-1)) for non-fertilized and fertilized stands were 0.36 and 1.05 for nitrogen, 0.042 and 0.095 for phosphorus, 0.13 and 0.51 for potassium, 0.27 and 0.42 for calcium, and 0.04 and 0.12 for magnesium, respectively. Maximum flux was coincident with ephemeral tissue (foliage and fine root) development and likely would be higher in stands with more foliage than those observed in this study (projected leaf area indices were 1.5 and 3.0 for the non-fertilized and fertilized stands). Minimum nutrient fluxes (kg ha(-1) day(-1)) for non-fertilized and fertilized stands were -0.18 and -0.42 for nitrogen, -0.029 and -0.070 for phosphorus, -0.05 and -0.18 for potassium, -0.04 and -0.05 for calcium, and -0.02 and -0.03 for magnesium, respectively. Minimum fluxes were typically observed in the dormant season and were linked to foliage senescence and branch death. Foliage and branch component nutrient contents were out of phase for nitrogen, phosphorus, potassium and magnesium, indicating nutrient retranslocation and storage in branches prior to foliage development and after foliage senescence. In contrast to current operational fertilizer programs which often target winter application these data suggest the best application times would be during foliage development.