Demography of an invading forest insect reunited with hosts and parasitoids from its native range

SUPPLEMENTARY MATERIALS : Explanation note: This file includes demographic data from native Sirex nigricornis woodwasps that were collected during our study. TABLE S1. Correlation matrix of bolt-level variables for P. resinosa and P. sylvestris. TABLE S2. Review of 10th and 90th percentile female body mass from insect species estimated from source paper cited, showing comparatively higher female S. noctilio body size variation. FIGURE S1. Examples of S. noctilio oviposition sites, lesion formation and emergence holes in the field. FIGURE S2. Top panels show a typical bolt from P. sylvestris with bark removed and S. noctilio emergence holes and oviposition sites identified. FIGURE S3. The number of S. noctilio emerging per tree was best described by a zero inflated negative binomial distribution (dotted line) with proportion of excess zeroes Φ = 0.32, μ = 75.39 and overdispersion parameter k = 0.35. FIGURE S4. Allometric relationships for S. noctilio in the Central NY data set: number of eggs and adult female mass (a; quantile regression), adult female mass and adult female length (b; fitted power function) and adult length and width of adult head capsule (c; linear regression).The Sirex woodwasp Sirex noctilio Fabricius (Hymenoptera: Siricidae), a widespread invasive pest of pines in the Southern Hemisphere, was first detected in North America in 2004. This study assessed the impacts of life history traits, host resistance and species interactions on the demography of S. noctilio in New York, Pennsylvania and Vermont, then compared key metrics to those found in the native range in Galicia, Spain. Many trees naturally attacked by S. noctilio in North America produced no adult woodwasps, with 5 of 38 infested trees (13%) sampled across six sites yielding 64% of emerging insects. Reproductive success was highest in the introduced host scots pine, Pinus sylvestris, but native red pine, Pinus resinosa, produced larger insects. Sirex noctilio required one or sometimes two years to develop and sex ratios were male biased, 1:2.98 ♀:♂. Body size and fecundity were highly variable, but generally lower than observed in non-native populations in the Southern Hemisphere. Hymenopteran parasitoids killed approximately 20% of S. noctilio larvae and 63% of emerging adults were colonized by the parasitic nematode Deladenus siricidicola, although no nematodes entered eggs. Demographic models suggested that S. noctilio in the northeastern USA have a higher potential for population growth than populations in the native range: estimated finite factor of increase, λ, was 4.17–4.52 (depending on tree species colonized), compared to λ = 1.57 in Spain.USDA Forest Service International Programs and OP RDE.https://neobiota.pensoft.netam2023Forestry and Agricultural Biotechnology Institute (FABI)Zoology and Entomolog

\u3ci\u3eSirex noctilio\u3c/i\u3e in North America: the effect of stem-injection timing on the attractiveness and suitability of trap trees

1 Sirex noctilio Fabricius, an invasive woodwasp responsible for severe economic damage to pine industries in the southern hemisphere, is now established in the northeastern U.S.A. and portions of eastern Canada. 2 Parts of North America are considered to be high risk for S. noctilio invasion. Effective detection tools, including trap trees, are needed to monitor and survey S. noctilio populations. 3 The present study was conducted to determine the optimal time to chemically stress a tree when aiming to attract the most S. noctilio to the host substrate, as well as to determine which timing produced the most adult progeny. Both of these measures (host attraction and host suitability for development) support the main objectives of the study by offering improved methods for monitoring and management of S. noctilio. 4 Red pine (Pinus resinosa) and Scots pine (Pinus sylvestris) were treated withDicamba at three time intervals. Multiple funnel lindgren traps were placed on these trees and, at the end of the flight season, the treatment trees were felled and brought into the laboratory. The number of S. noctilio caught in the traps (host attraction) and the number of S. noctilio emerged from the treated trees (host suitability) were determined. 5 Optimal timing of the chemical girdle was dependent on host species. Significantly more female S. noctilio were captured on trap trees prepared 1 month before flight (red pine and Scots pine) or prepared at flight (Scots pine) compared with other treatments. There were also significantly more females reared from Scots pine trap trees prepared at flight and red pine trap trees prepared 1 month before and/or at flight. 6 By the beginning of August, most (79%) of the S. noctilio for the flight season were caught in the traps at the trap trees. The sex ratio (males : females) was closer to 1 : 1 than previously reported in studies from other countries. 7 The results obtained in the present study demonstrate that timing is important when creating a trap tree with herbicide in North America, whether for the purpose of detection or as part of a biological control effort

Molecular Cloning, Nucleotide Sequence, and Expression of Genes Encoding a Polycyclic Aromatic Ring Dioxygenase from Mycobacterium sp. Strain PYR-1

Mycobacterium sp. strain PYR-1 degrades high-molecular-weight polycyclic hydrocarbons (PAHs) primarily through the introduction of both atoms of molecular oxygen by a dioxygenase. To clone the dioxygenase genes involved in PAH degradation, two-dimensional (2D) gel electrophoresis of PAH-induced proteins from cultures of Mycobacterium sp. strain PYR-1 was used to detect proteins that increased after phenanthrene, dibenzothiophene, and pyrene exposure. Comparison of proteins from induced and uninduced cultures on 2D gels indicated that at least six major proteins were expressed (105, 81, 52, 50, 43, and 13 kDa). The N-terminal sequence of the 50-kDa protein was similar to those of other dioxygenases. A digoxigenin-labeled oligonucleotide probe designed from this protein sequence was used to screen dioxygenase-positive clones from a genomic library of Mycobacterium sp. strain PYR-1. Three clones, each containing a 5,288-bp DNA insert with three genes of the dioxygenase system, were obtained. The genes in the DNA insert, from the 5′ to the 3′ direction, were a dehydrogenase, the dioxygenase small (β)-subunit, and the dioxygenase large (α)-subunit genes, arranged in a sequence different from those of genes encoding other bacterial dioxygenase systems. Phylogenetic analysis showed that the large α subunit did not cluster with most of the known α-subunit sequences but rather with three newly described α subunits of dioxygenases from Rhodococcus spp. and Nocardioides spp. The genes from Mycobacterium sp. strain PYR-1 were subcloned and overexpressed in Escherichia coli with the pBAD/ThioFusion system. The functionality of the genes for PAH degradation was confirmed in a phagemid clone containing all three genes, as well as in plasmid subclones containing the two genes encoding the dioxygenase subunits