Stuart V. Nielsen

Dr. Stuart V. Nielsen

Florida Museum of Natural History, University of Florida, Gainesville, FL; USA

Research Focus & Metrics

Academic Career Length

9Years (2018-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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27 October 2020 in ZooKeys
Verified
Journal Article
Open access
PDF file
SNStuart V. Nielsen
Stuart V. Nielsen
WCWerner Conradie
Werner Conradie
LCLuis M. P. Ceríaco
Luis M. P. Ceríaco
ABAaron M. Bauer
Aaron M. Bauer
MHMatthew P. Heinicke
Matthew P. Heinicke
DBDavid C. Blackburn
David C. Blackburn
Recent molecular phylogenetic work has found that Breviceps Merrem, 1820 comprises two major clades, one of which, the B. mossambicus group, is widely distributed across southern sub-Saharan Africa. This group is notable for harboring abundant cryptic diversity. Of the four most recently described Breviceps species, three are members of this group, and at least five additional lineages await formal description. Although Breviceps has long been known to occur in Angola, no contemporary material has been collected until recently. The three most widespread taxa, B. adspersus, B. mossambicus, and B. poweri, may all occur in Angola, but accurate species assignment remains challenging given the rampant morphological similarity between these taxa, and, until recently, the lack of genetic resources. Phylogenetic, morphological, and acoustic analyses of recently collected samples from disparate localities within Angola provide evidence for an undescribed species that is sister to B. poweri. The new species can be diagnosed from its sister taxon by lacking pale spots along the flanks, a pale patch above the vent, and a short, dark band below the nares (all present in B. poweri). Additionally, the male advertisement call differs from the three other Breviceps that might occur in Angola in having both a longer interval between consecutive calls and a higher average dominant frequency. We here describe this lineage as a distinct species, currently only known from Angola, and discuss the presence of other Breviceps taxa within Angola.

18 January 2018 in Journal of Evolutionary Biology
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Journal Article
Open access
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SNStuart V. Nielsen
Stuart V. Nielsen
JBJ. L. Banks
J. L. Banks
RDR. E. Diaz
R. E. Diaz
PTP. A. Trainor
P. A. Trainor
TGTony Gamble
Tony Gamble
Much of our current state of knowledge concerning sex chromosome evolution is based on a handful of ‘exceptional’ taxa with heteromorphic sex chromosomes. However, classifying the sex chromosome systems of additional species lacking easily identifiable, heteromorphic sex chromosomes is indispensable if we wish to fully understand the genesis, degeneration and turnover of vertebrate sex chromosomes. Squamate reptiles (lizards and snakes) are a potential model clade for studying sex chromosome evolution as they exhibit a suite of sex‐determining modes yet most species lack heteromorphic sex chromosomes. Only three (of 203) chameleon species have identified sex chromosome systems (all with female heterogamety, ZZ/ZW). This study uses a recently developed method to identify sex‐specific genetic markers from restriction site‐associated DNA sequence (RADseq) data, which enables the identification of sex chromosome systems in species lacking heteromorphic sex chromosomes. We used RADseq and subsequent PCR validation to identify an XX/XY sex chromosome system in the veiled chameleon (Chamaeleo calyptratus), revealing a novel transition in sex chromosome systems within the Chamaeleonidae. The sex‐specific genetic markers identified here will be essential in research focused on sex‐specific, comparative, functional and developmental evolutionary questions, further promoting C. calyptratus’ utility as an emerging model organism.

1 April 2022 in Journal of Heredity
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Journal Article
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BPBrendan J Pinto
Brendan J Pinto
SKShannon E Keating
Shannon E Keating
SNStuart V. Nielsen
Stuart V. Nielsen
DSDaniel P Scantlebury
Daniel P Scantlebury
JDJuan D Daza
Juan D Daza
TGTony Gamble
Tony Gamble
Sex determination is a critical element of successful vertebrate development, suggesting that sex chromosome systems might be evolutionarily stable across lineages. For example, mammals and birds have maintained conserved sex chromosome systems over long evolutionary time periods. Other vertebrates, in contrast, have undergone frequent sex chromosome transitions, which is even more amazing considering we still know comparatively little across large swaths of their respective phylogenies. One reptile group in particular, the gecko lizards (infraorder Gekkota), shows an exceptional lability with regard to sex chromosome transitions and may possess the majority of transitions within squamates (lizards and snakes). However, detailed genomic and cytogenetic information about sex chromosomes is lacking for most gecko species, leaving large gaps in our understanding of the evolutionary processes at play. To address this, we assembled a chromosome-level genome for a gecko (Sphaerodactylidae: Sphaerodactylus) and used this assembly to search for sex chromosomes among six closely related species using a variety of genomic data, including whole-genome re-sequencing, RADseq, and RNAseq. Previous work has identified XY systems in two species of Sphaerodactylus geckos. We expand upon that work to identify between two and four sex chromosome cis-transitions (XY to a new XY) within the genus. Interestingly, we confirmed two different linkage groups as XY sex chromosome systems that were previously unknown to act as sex chromosomes in tetrapods (syntenic with Gallus chromosome 3 and Gallus chromosomes 18/30/33), further highlighting a unique and fascinating trend that most linkage groups have the potential to act as sex chromosomes in squamates.

20 June 2019 in Developmental Dynamics
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Journal Article
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AGAaron H. Griffing
Aaron H. Griffing
TSThomas J. Sanger
Thomas J. Sanger
JDJuan D. Daza
Juan D. Daza
SNStuart V. Nielsen
Stuart V. Nielsen
BPBrendan J. Pinto
Brendan J. Pinto
TGTony Gamble
Tony Gamble

1 December 2019 in Molecular Phylogenetics and Evolution
Verified
Journal Article
Open access
BPBrendan J. Pinto
Brendan J. Pinto
SNStuart V. Nielsen
Stuart V. Nielsen
TGTony Gamble
Tony Gamble
Gecko lizards are a species-rich clade of primarily-nocturnal squamate reptiles. In geckos, adaptations to nocturnality have dramatically reshaped the eye. Perhaps the most notable change is the loss of rod cells in the retina and subsequent "transmutation" of cones into a rod-like morphology and physiology. While many studies have noted the absence of some rod-specific genes, such as the visual pigment Rhodopsin (RH1), these studies have focused on just a handful of species that are nested deep in the gecko phylogeny. Thus, it is not clear whether these changes arose through convergence, are homologous and ubiquitous across geckos, or restricted to a subset of species. Here, we used de novo eye transcriptomes from five gecko species, and genomes from two additional gecko species, representing the breadth of extant gecko diversity (i.e. 4 of the 7 gecko families, spanning the deepest divergence of crown Gekkota), to show that geckos lost expression of almost the entire suite of necessary rod-cell phototransduction genes in the eye, distinct from all other squamate reptiles. Geckos are the first vertebrate group to have lost their complete rod-cell expression pathway, not just the visual pigment. In addition, all sampled species have also lost expression of the cone-opsin SWS2 visual pigment. These results strongly suggest a single loss of rod cells and subsequent cone-to-rod transmutation that occurred prior to the diversification of extant geckos.

2 July 2018 in Journal of Biogeography
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Journal Article
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SNStuart V. Nielsen
Stuart V. Nielsen
SDSavel R. Daniels
Savel R. Daniels
WCWerner Conradie
Werner Conradie
MHMatthew P. Heinicke
Matthew P. Heinicke
BNBrice P. Noonan
Brice P. Noonan