Data from: Conservation genetics of Notelaea lloydii (Oleaceae) in south-eastern Queensland, Australia
Data files
Nov 22, 2023 version files 80.07 MB
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Metadata_N-lloydii_Manawaduge_etal.csv
880 B
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README.md
1.19 KB
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SNP-data_N-lloydii_Manawaduge_etal.csv
80.07 MB
Abstract
Habitat fragmentation can increase the chance of population bottlenecks and inbreeding, and may ultimately lead to reduced fitness and local extinction. Notelaea lloydii is a native olive species endemic to Australia and listed as vulnerable due to its restricted distribution. A recent molecular systematics study has revealed there might be some geographic structuring among the N. lloydii populations. Therefore, we undertook a genome wide Single Nucleotide Polymorphism (SNP) analysis to determine levels and patterns of genetic diversity, inbreeding and gene flow within and among N. lloydii populations in south-eastern Queensland (SE-QLD). Furthermore, as the reproductive phase of a plant’s life history has a profound influence on genetic diversity, life history reproductive traits were also studied. Our SNP analysis revealed low genetic diversity, inbreeding and significant genetic structuring even among proximate populations. Results of a flower and fruit bagging experiment in two consecutive seasons revealed that N. lloydii produced many flowers but only a few fruits survived to maturity. There were no differences in bagged and un-bagged flowering and fruiting rates and therefore, we conclude that the high fruit abortion rate was probably due to inbreeding depression and/or suboptimal conditions, rather than pollinator availability and insect attack. Overall, results of this study indicate that the populations of N. lloydii are small, inbred and genetically isolated and represent unique management units that require local conservation management due to ongoing threats associated with urbanisation.
This is the SNP data set that was used in the manuscript “Conservation genetics of Notelaea lloydii (Oleaceae) in south-eastern Queensland, Australia “
Description of the data and file structure
File Format: SNP 1 Row Mapping Format: “0” = Reference allele homozygote, “1” = SNP allele homozygote, “2”= heterozygote and “-“ = double null/null allele homozygote (absence of fragment with SNP in genomic representation)
Metadata columns:
AlleleID:Unique identifier for the sequence in which the SNP marker occurs
SNP:In 1 row format: contains the base position and base variant details
SnpPosition:The position (zero indexed) in the sequence tag at which the defined SNP variant base occurs
CallRate:The proportion of samples for which the genotype call is either “1” or “0”, rather than “-“
AvgPIC:The average of the polymorphism information content (PIC) of the Reference and SNP allele rows
RepAvg:The proportion of technical replicate assay pairs for which the marker score is consistent
Sharing/Access information
Data was derived from the following sources:
Diversity Arrays Technology Pty Ltd (https://www.diversityarrays.com/)
Genomic DNA of 123 individuals were sent to DArT analysis facility (DArT Pty Ltd., Canberra, Australia) for DArTseq high-density genotyping and the results of the SNP calling were obtained as a matrix.
Data set can be opened and analysed using the DArTR package in the R platform.