Cunninghamia lanceolata is one of the most important tree species in China due to its significance both in economy and ecology. The aims of the present study were to construct a high-density genetic map and identify a quantitative trait locus (QTL) for C. lanceolata. In this study, an F1 population comprising 81 individuals was developed. Using specific length amplified fragment sequencing (SLAF-seq) technology, a total of 254,899 loci were found to be polymorphic. After linkage analysis, 2574 markers were used to construct genetic linkage maps. Specifically, 1632 markers were allocated to 11 linkage groups (LGs) for the female map, 1038 for the male map, and 2574 for the integrated map. The integrated map consisted of 4596 single-nucleotide polymorphisms (SNPs) loci, resulting in an average of 1.79 SNP loci per SLAF marker. The marker coverage was 1665.76 cM for the female map, 1436.39 cM for the male map, and 1748.40 cM for the integrated map. The average interval between two adjacent mapped markers was 1.03 cM, 1.40 cM, and 0.68 cM for the female map, male map, and integrated map, respectively. Using the integrated map, we performed interval mapping (logarithm of odds, LOD > 2.0) to detect traits of interest. We identified a total of 2, 1, 2, 5, 1, 2, 1, and 3 QTLs for diameter at breast height, heartwood diameter, heartwood proportion, heartwood a*, heartwood b*, heartwood L*, sapwood a*, and sapwood L*, respectively. The number of markers associated with each QTL ranged from 1 to 14, and each marker explained phenotypic variances ranging from 12.70% to 23.60%. Furthermore, a common QTL was identified for diameter at breast height and heartwood color a*, while another common QTL was observed for heartwood color L* and heartwood color a*. These findings suggest possible pleiotropic effects of the same genes on these traits. In conclusion, we successfully constructed high-density genetic maps for C. lanceolata using the SLAF-seq method with an F1 population. Notably, these linkage maps represent the most comprehensive and densest ones available to date for C. lanceolata and will facilitate future chromosome assignments for C. lanceolata whole-genome sequencing. These identified QTLs will serve as a valuable resource for conducting fine-scale QTL mapping and implementing marker-assisted selection in C. lanceolata, particularly for growth and wood-color traits.

Phoebe bournei is an important economic tree species in China, its large-scale propagation is limited by the difficulty of adventitious root (AR) formation in cuttings. In this study, morphological, physiological, and transcriptomic analyses were conducted to investigate the process of AR formation in P. bournei. The results showed that ARs mainly originated from callus tissue. During AR formation, soluble sugar and soluble protein contents changed significantly. Malondialdehyde (MDA) and oxygen free radicals (OFRs) peaked at first sampling stage (PB0), while the activities of polyphenol oxidase (PPO) and indoleacetic acid oxidase (IAAO) exhibited similar patterns. Lignin content increased during callus induction stage, whereas phenolic content continuously declined throughout rooting. Endogenous hormone levels also changed markedly, and Orthogonal partial least squares discriminant analysis (OPLS-DA) analysis indicated that indole-3-acetic acid (IAA) and abscisic acid (ABA) played dominant roles in this process. KEGG enrichment analysis revealed significant enrichment of the phenylpropanoid biosynthesis pathway in all three comparison groups. A total of 48 differentially expressed genes (DEGs) were enriched in plant hormone signal transduction pathways, with 22 and 14 genes associated with IAA and ABA signaling, respectively. Weighted gene co-expression network analysis (WGCNA) further identified two hub modules related to IAA and ABA contents, including eight hub genes such as D6PKL1 and ISTL1. Correlation analysis revealed that the hub genes D6PKL1 and HSP were significantly positively correlated with IAA4 in the IAA signaling pathway. Overall, this study provides new insights into the mechanisms underlying AR formation in P. bournei cuttings and offers a theoretical basis for optimizing its clonal propagation system.