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Abstract Effects of global climate change on population persistence are often mediated by life‐history traits of individuals, especially the timing of somatic growth, reproductive development, and reproduction itself. These traits can vary among age groups and between the sexes, a result of differential life‐history tactics and levels of lifetime reproductive investment. Unfortunately, the trait data necessary for revealing sex‐specific breeding behaviors and use of breeding cues over reasonably large geographic areas remain sparse for most taxa. In this study, we assembled and analyzed a new reproductive trait base for the North American deer mouse (Peromyscus maniculatus) from digitized natural history specimens and field censuses. We used the data to reconstruct sex‐specific breeding phenologies and their drivers within and among North American ecoregions. Male and female phenologies varied across the geographic range of this species, with discordance in timing and intensity being highest in regions of lower seasonality (and longer breeding seasons). Reliance on environmental variables as breeding cues also appeared to vary in a sex‐specific manner, being most similar for photoperiod and least similar for temperature (positive male response and negative female response); in addition, model validation indicated that phenological models generalized better for males than for females. Finally, our individual‐level trait data also show that male reproductive investment (quantified as relative testis size) varies across the vastly different abiotic and social (i.e., female breeding) contexts studied here. By harmonizing across a broad set of digital data resources, we demonstrate the potential to uncover drivers of phenological variation within species and inform global change predictions at multiple scales of biological organization.
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An affordable and convenient diagnostic marker to identify male and female hop plants
Abstract Hop production utilizes exclusively female plants, whereas male plants only serve to generate novel variation within breeding programs through crossing. Currently, hop lacks a rapid and accurate diagnostic marker to determine whether plants are male or female. Without a diagnostic marker, breeding programs may take 1–2 years to determine the sex of new seedlings. Previous research on sex-linked markers was restricted to specific populations or breeding programs and therefore had limited transferability or suffered from low scalability. A large collection of 765 hop genotypes with known sex phenotypes, genotyping-by-sequencing, and genome-wide association mapping revealed a highly significant marker on the sex chromosome (LOD score = 208.7) that predicted sex within our population with 96.2% accuracy. In this study, we developed a PCR allele competitive extension (PACE) assay for the diagnostic SNP and tested three quick DNA extraction methodologies for rapid, high-throughput genotyping. Additionally, the marker was validated in a separate population of 94 individuals from 15 families from the USDA-ARS hop breeding program in Prosser, WA with 96% accuracy. This diagnostic marker is located in a gene predicted to encode the basic helix-loop-helix transcription factor protein, a family of proteins that have been previously implicated in male sterility in a variety of plant species, which may indicate a role in determining hop sex. The marker is diagnostic, accurate, affordable, and highly scalable and has the potential to improve efficiency in hop breeding.
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- Award ID(s):
- 2239530
- PAR ID:
- 10474001
- Publisher / Repository:
- Oxford University Press
- Date Published:
- Journal Name:
- G3: Genes, Genomes, Genetics
- ISSN:
- 2160-1836
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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