A total of 31 taper functions from 3 different groups of models (single, segmented and variable-form taper functions) were fitted to diameter-height data from 203 Pinus pinaster trees sampled across even-aged stands in Galicia (northwestern Spain). Most of the taper functions analyzed showed problems of multicollinearity as indicated by the condition number. A second-order autoregressive CAR(2) error process was incorporated into the models to minimize the effect of autocorrelation inherent in the longitudinal data used, and to provide valid tests of significance for model parameter estimates. In general, variable-form taper functions provided the most accurate predictions. The flexibility and predictive performance of the variable-form model developed by Kozak (For Chron 80(4):507-515, 2004) indicated its usefulness for estimating diameter at a specific height, merchantable volume, and total volume of Maritime pine in the study area.

Low inorganic phosphate (Pi) availability causes terminal differentiation of the root apical meristem (RAM), a phenomenon known as root meristem exhaustion or determined growth. Here, we report that the CLE14 peptide acts as a key player in this process. Low Pi stress induces iron mobilization in the RAM through the action of LPR1/LPR2, causing expression of CLE14 in the proximal meristem region. CLV2 and PEPR2 receptors perceive CLE14 and trigger RAM differentiation, with concomitant downregulation of SHR/SCR and PIN/AUXIN pathway. Our results reveal multiple steps of the molecular mechanism of one of the most physiologically important root nutrient responses.

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We report the isolation of a bacterium from Galleria mellonella larva and its identification using genome sequencing and phylogenomic analysis. This bacterium was named Alcaligenes faecalis strain MOR02. Microscopic analyses revealed that the bacteria are located in the esophagus and intestine of the nematodes Steinernema feltiae, S. carpocapsae, and H. bacteriophora. Using G. mellonella larvae as a model, when the larvae were injected with 24,000 CFU in their hemocoel, more than 96% mortality was achieved after 24 h. Additionally, toxicity assays determined that 1 μg of supernatant extract from A. faecalis MOR02 killed more than 70% G. mellonella larvae 96 h after injection. A correlation of experimental data with sequence genome analyses was also performed. We discovered genes that encode proteins and enzymes that are related to pathogenicity, toxicity, and host/environment interactions that may be responsible for the observed phenotypic characteristics. Our data demonstrates that the bacteria are able to use different strategies to colonize nematodes and kill insects to their own benefit. However, there remains an extensive group of unidentified microorganisms that could be participating in the infection process. Additionally, a nematode-bacterium association could be established probably as a strategy of dispersion and colonization.

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