The wood properties of Paulownia clones determine their ultimate price and uses. This study selected superior clones with good color and mechanical properties using selection indexes. Variation in 23 5-year-old Paulownia clones was analyzed using genetic parameters, correlation analysis, and a comprehensive assessment of two color characteristics [color difference (ΔE) and whiteness (WH)] and six mechanical properties [density (ρ), hardness of the tangential, radial, and end surfaces (Ht, Hr, and He), and cleavage strength of the tangential and radial surfaces (qt, qr)]. There were significant differences (p < 0.01) in each of the eight traits among the 23 clones. There were significant negative phenotypic and genetic correlations between ΔE and WH. The six mechanical properties were significantly positively correlated genetically, showing significant positive phenotypic correlations with each other, except for ρ, Ht, and qt. With a selection rate of 8.70%, clones MB04 and L01 were selected as superior using the comprehensive selection index. Compared with the control (9501), the genetic gains of clones MB04 and L01 in ΔE, WH, ρ, qr, qt, He, Hr, and Ht were 0.40, 0.21, 10.32, 12.57, 14.81, 26.05, 28.04, and 6.84%, respectively, and the actual gains were 0.59, 0.31, 17.21, 28.45, 28.09, 34.90, 40.08, and 11.12%.

Clonal forestry has developed rapidly in recent years and already plays a significant role in commercial tree plantations worldwide. Clonal breeding requires accurate assessments of genetic parameters, together with measurements of clonal productivity, stability, and adaptably. However, relevant studies for clones of Paulownia spp. genotypes are rare. We therefore conducted clonal tests on twenty Paulownia clones established at three sites in the temperate and subtropical regions of China. Trees were planted in a randomized block design, with four replications in each site, twenty plots in each block, and six to eight individuals of the same clone in each plot. We measured the trunk diameter at breast height (DBH), total trunk height (H_t), and individual stand volume of 7-year-old trees to estimate genetic parameters and analyze genotype–environment interactions. A combined analysis of variance indicated that clonal, site, and clone–site interactions significantly affected the three growth traits. Clonal heritability and individual heritability were 0.35–0.84 and 0.07–0.30, respectively. The phenotypic and genetic correlation coefficients among the growth traits were 0.46–0.93 and 0.85–0.99, respectively. There were extremely significant positive linear relationships between the best linear unbiased predictors for DBH and the original DBH values (R² > 0.98). Clones 10, 2, 18, and 13 were selected for deployment based on a selection intensity of 1.4, GGE biplots, and the relative performance of harmonic means on genotypic values analysis. For these clones, the genetic gains in DBH, H_t, and volume were 18.05%, 21.46%, and 46.03%, respectively. These results provide useful information for the selection of Paulownia clones at the target sites and will provide a sound basis for improving Paulownia clonal breeding programs in the future.

Summary: This study attempted to investigate and validate whether epididymis cold storage could be a suitable alternative for short-term preservation of spermatozoa. Mouse cauda epididymides and spermatozoa were preserved at 4–8°C from 1 day to 6 weeks. From days 1 to 10, motility and fertility were daily examined when motility loss occurred. From week 1, spermatozoa were used for intracytoplasmic sperm injection (ICSI) at weekly intervals to test their fertility, and spermatozoa DNA integrity was determined by comet assay. We found that motility and progressive motility scores gradually decreased with storage time. In nearly all spermatozoa, DNA integrity was maintained from days 1 to 10, but the percentage of spermatozoa with damaged DNA significantly increased from week 2 to week 6. Spermatozoa retained fertility until day 6, although fertility gradually decreased after day 3. From week 1 to week 5, fertilization rates by ICSI were more than 82.69% but decreased gradually after week 3. We found that spermatozoa preserved in the epididymis at 4–8°C had progressively lower motility, fertility and proportion of undamaged DNA, but could still fertilize oocytes. However, all the parameters of cold-preserved spermatozoa were completely inferior to that from cold-preserved cauda epididymides. The results imply that cold storage of cauda epididymides could be conducive to short-term preservation of spermatozoa, and the cold-stored spermatozoa can resist DNA denaturation, which is necessary for maintaining reproductive ability.

Trunk-extension pruning is often used to promote sprouting of latent buds, and therefore extend the vertical growth of the main trunk in young Paulownia plantation in China. However, the biological basis for the technique remains unclear. In this study, we applied two pruning treatments and a control to 120 and 108 three-year-old Paulownia trees in 2015 and 2016, respectively. We observed the latent buds sprouting in 2015, and found that the number of individuals of first sprouting/total number of individuals and number of sprouted buds/total number of sprouted buds both exceeded 50% from 18 to 24 days after pruning.We collected phloem samples from the top of the stem at 7, 14, 21, and 28 d after the pruning in 2016. We then analyzed phytohormones, total C and N, reduced sugar and free amino acid contents of the samples. Results showed that pruning significantly reduced the contents of abscisic acid (ABA) and indole-3-acetic acid (IAA), especially on day 21 as compared with control. This was coincided with the sprouting of latent buds in the two pruned treatments. Therefore reduced IAA, ABA contents in pruned trees promoted the sprouting of latent buds. Our results provide a biological basis for extending the main trunk height. Keywords: Trunk-extension pruning, Latent buds, Phytohormones, Carbon, Nitrogen, Paulownia plantation.

Paulownia trees are grown globally for their robust timber, agroforestry, and effective carbon dioxide drawdown. China possesses rich Paulownia germplasm resources, offering favorable material for the genetic improvement. Understanding the taxonomy and phylogenetic relationships of Paulownia species is essential for the advancement of germplasm innovation. In this study, we re-sequenced 67 typical accessions of 11 species within the Paulownia genus. A total of 16,163,790 high-quality single nucleotide polymorphisms (SNPs) were identified. Based on these markers, these accessions were classified into three groups: P. fortunei and P. lampropylla (Group I); P. tomentosa, P. fargesii, and P. kawakamii (Group II); and P. taiwaniana, P. jianshiensis, P. catalpifolia, P. elongata, P. ichangensis, and P. albiphloea (Group III). Using maximum likelihood estimation, population genetic structure analysis revealed that the 11 species originated from four different ancestral populations. The two predominant breeding species—P. fortunei and P. tomentosa—exhibit divergent origins: P. fortunei arose from hybridization between two ancestral species followed by complex admixture, whereas P. tomentosa retains a predominantly singular ancestral lineage, with traces of P. kawakamii. The genetic diversity (π) of P. tomentosa was 0.002588, which was considerably lower than that of P. fortunei (0.004181) suggesting that P. tomentosa is subjected to a stronger breeding selection during the evolution than P. fortunei. A total of 59 selected regions and 65 genes were identified by selective sweep analysis. These genes may be involved in biological processes such as morphological development and response to abiotic stress and hormonal activity regulation. These findings provide valuable references for further research on the genetic differentiation and adaptive evolutionary mechanisms of Paulownia species, laying a foundation for future germplasm innovation and variety improvement.