In China, the genus Tulipa L. has been identified as a national second-class protected plant. Due to the complex evolutionary and genetic backgrounds of tulips, the taxonomy of the genus Tulipa and its species remains a matter of dispute. The current study is dedicated to clarifying the taxonomic relationship between two closely related species, T. iliensis and Tulipa thianschanica, by integrating morphological, karyotypic, and molecular evidence—a novel framework for resolving taxonomic ambiguities in closely related species. Morphological analyses showed significant differences in filament shape, pistil length, overall plant height, presence or absence of stem hairs, and perianth length and width, which supports the conclusion that they are distinct species (p < 0.001). Karyotype analysis further verified disparities in their chromosome morphology, and distinct karyotype indices and scatter plot distributions suggest differences between the two species. Molecular phylogenetic analyses using Internal Transcribed Spacer sequences (ITSs) and chloroplast genomes confirmed the genetic differences between T. iliensis and T. thianschanica, and there is evidence indicating the possible occurrence of hybridization events. The research findings demonstrate that T. thianschanica and T. iliensis are independent species, thereby providing valuable insights into the taxonomy of wild tulips and contributing to the conservation of these protected species.

This study systematically investigated the genetic characteristics and germplasm conservation strategies of Xinjiang Thompson Seedless grapes (Vitis vinifera Thompson Seedless) and Munake grapes (Vitis vinifera L. cv. Munake) using SSR molecular markers and whole-genome resequencing technology. A genetic diversity analysis of 165 Thompson Seedless accessions with 16 SSR markers identified 442 alleles (27.63 alleles per locus on average), with the expected heterozygosity (He = 0.76) and observed heterozygosity (Ho = 0.83) indicating moderate-to-low genetic diversity. A molecular variance analysis (AMOVA) further revealed that 96% of the genetic variation originated within populations, with minimal inter-population differentiation (Fst = 0.04). Phylogenetic reconstruction using SSR markers demonstrated significant genealogical associations between the two cultivars, supporting the hypothesis that Thompson Seedless may have originated from a domesticated lineage of Munake. The selected SSR markers exhibited high discriminatory power (PIC = 0.92), enabling the precise differentiation of accessions with closely related genetic backgrounds. Whole-genome resequencing identified 20,074,046 and 69,214,080 high-quality SNPs in 100 Thompson Seedless and 141 Munake accessions, respectively. Core germplasm banks were subsequently established: the Thompson Seedless core collection (25 accessions) captured 94% of genetic variation, reflecting genetic homogenization driven by intensive clonal cultivation, while the Munake core collection (42 accessions) retained 95% of allelic diversity and resolved regional synonym issues through highly polymorphic SNP markers. A comparative analysis revealed that Munake maintains higher genetic diversity due to natural gene flow, whereas Thompson Seedless faces heightened risks of genetic erosion from prolonged asexual propagation. These findings provide a theoretical foundation and technical framework for precise conservation, varietal improvement, and sustainable utilization of grape germplasm resources in Xinjiang.

Various species from the genus Calligonum L. are widely used in erosion control in Northwest China. Their widespread use and breeding efforts highlight the need for the conservation of the high-quality germplasm resources of this genus. To assess genetic diversity, the genome of Calligonum junceum was screened, and 380,328 SSR loci were identified. After further screening, 17 microsatellite markers were identified and transferred to 11 other species of the genus. When analyzed together, the 11 species showed significant discrimination power (PIC = 0.623), and we detected that the mean number of alleles per locus was 2.684, the overall heterozygosity observed value was 0.295, and the expected heterozygosity (He) was 0.373. Genetic diversity in Calligonum mongolicum was the highest at I = 1.305, He = 0.647, and that of Calligonum gobicum was the lowest at I = 0.127, He = 0.072. The results of this study provide reference SSR primers for the genus Calligonum, supporting the improvement of its germplasm conservation efforts.

Ammopiptanthus nanus, a Tertiary-era endangered plant, is of great scientific value. In this research, we focus on A. nanus population dynamics in an effort to bridge the divide between micro genetic variation and a macroscopic ecological pattern of distribution. The population structure of 129 wild specimens of A. nanus from eight populations was analyzed using EST-SSR molecular markers in this research. The Mantel test and RDA analysis have been used in this research to investigate the factors that influence the genetic diversity of A. nanus. Using 15 pairs of SSR primers, a total of 227 alleles were detected in 129 samples from 8 populations. The mean number of alleles was 17, and the average expected heterozygosity was 0.405. It is shown that wild A. nanus is divided into six individual populations. A. nanus are significantly affected by wind speed in terms of the variation of genetics. It is suggested that a nature conservation area for A. nanus be established as soon as possible, based on our results and the current natural distribution of the species. It is necessary to focus on the issue of pests and diseases while simultaneously preventing the continuation of anthropogenic woodcutting and disaster. Manual seedling collection should be employed in regions where the environment permits. Through making use of manual breeding techniques, this will contribute to the growth of the natural population of A. nanus.