Pair‐bonded primates have uniquely enduring relationships and partners engage in a suite of behaviors to maintain these close bonds. In titi monkeys, pair bond formation has been extensively studied, but changes across relationship tenure remain unstudied. We evaluated differences in behavioral indicators of pair bonding in newly formed (~6 months paired,
- Award ID(s):
- 1836650
- NSF-PAR ID:
- 10167451
- Author(s) / Creator(s):
- ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; more »
- Date Published:
- Journal Name:
- SciPost Physics
- Volume:
- 7
- Issue:
- 1
- ISSN:
- 2542-4653
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Abstract n = 9) compared to well‐established pairs (average 3 years paired,n = 8) of titi monkeys (Callicebus cupreus ) as well as sex differences within the pairs. We hypothesized that overall males would contribute more to maintenance than females, but that the pattern of maintenance behaviors would differ between newly formed and well‐established pairs. Each titi monkey (N = 34) participated in a partner preference test (PPT), where the subject was placed in a middle test cage with grated windows separating the subject from the partner on one side and an opposite‐sex stranger on the other side. During this 150‐min behavioral test, we quantified four key behaviors: time in proximity to the partner or stranger as well as aggressive displays toward the partner or stranger. Overall, we found different behavioral profiles representing newly formed and well‐established pair‐bond relationships in titi monkeys and male‐biased relationship maintenance. Males spent ∼40% of their time in the PPT maintaining proximity to the female partner, regardless of relationship tenure. Males from well‐established bonds spent less time (14%) near the female stranger compared to males from newly formed bonds (21%) at the trend level. In contrast, females from well‐established bonds spent less (23%) time near the male partner in the PPT compared to females from newly formed bonds (47%). Aggressive displays were more frequent in newly formed bonds compared to well‐established bonds, especially for females. Scan sampling for homecage affiliation showed that newly formed pairs were more likely to be found tail twining than well‐established pairs. -
These data are from four separate projects undertaken between 1997 and 2017. The first of these are two snow manipulation (freeze) projects: 1) In 1997, as part of a study of the relationships between snow depth, soil freezing and nutrient cycling, we established eight 10 x 10-m plots located within four stands; two dominated (80%) by sugar maple (SM1 and SM2) and two dominated by yellow birch(YB1 and YB2), with one snow reduction (shoveling) and one reference plot in each stand. 2) In 2001, we established eight new 10-m x 10-m plots (4 treatment, 4 reference) in four new sites; two high elevation, north facing and (East Kineo and West Kineo) two low elevation, south facing (Upper Valley and Lower Valley) maple-beech-birch stands. To establish plots, we cleared minor amounts of understory vegetation from all (both treatment and reference) plots (to facilitate shoveling). Treatments (keeping plots snow free by shoveling through the end of January) were applied in the winters of 1997/98, 1998/99, 2002/2003 and 2003/2004. The Climate Gradient Project was established in October 2010. Here we evaluated relationships between snow depth, soil freezing and nutrient cycling along an elevation/aspect gradient that created variation in climate with little variation in soils or vegetation. We established 6 20 x 20-m plots (intensive plots) and 14 10 x 10-m plots (extensive plots), with eight of the plots facing north and twelve facing south. The Ice Storm project was designed to evaluate the damage and changes ice storms cause to northern hardwood forests in forest structure, nutrient cycling and carbon storage. Ten 20x30 meter plots were established in a predominately sugar maple stand, with 4 icing treatments and 2 control plots. The treatments are as follows: Low (0.25"), Mid (0.5"), Midx2 (0.5") 2 Years in a row, High: (0.75"), Control. The icing treatment was conducted in the winter of 2015-2016, with a second year of icing on the Midx2 treatments plots in the winter of 2016-2017. The treatments are as follows: Low (0.25"), Mid (0.5"), Midx2 (0.5") 2 Years in a row, High: (0.75"), Control.more » « less
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Abstract Since the first Spanish settlers brought horses to America centuries ago, several local varieties and breeds have been established in the New World. These were generally a consequence of the admixture of the different breeds arriving from Europe. In some instances, local horses have been selectively bred for specific traits, such as appearance, endurance, strength, and gait. We looked at the genetics of two breeds, the Puerto Rican Non-Purebred (PRNPB) (also known as the “Criollo”) horses and the Puerto Rican Paso Fino (PRPF), from the Caribbean Island of Puerto Rico. While it is reasonable to assume that there was a historic connection between the two, the genetic link between them has never been established. In our study, we started by looking at the genetic ancestry and diversity of current Puerto Rican horse populations using a 668 bp fragment of the mitochondrial DNA D-loop (HVR1) in 200 horses from 27 locations on the island. We then genotyped all 200 horses in our sample for the “gait-keeper”
DMRT3 mutant allele previously associated with the paso gait especially cherished in this island breed. We also genotyped a subset of 24 samples with the Illumina Neogen Equine Community genome-wide array (65,000 SNPs). This data was further combined with the publicly available PRPF genomes from other studies. Our analysis show an undeniable genetic connection between the two varieties in Puerto Rico, consistent with the hypothesis that PRNPB horses represent the descendants of the original genetic pool, a mix of horses imported from the Iberian Peninsula and elsewhere in Europe. Some of the original founders of PRNRB population must have carried the “gait-keeper”DMRT3 allele upon arrival to the island. From this admixture, the desired traits were selected by the local people over the span of centuries. We propose that the frequency of the mutant “gait-keeper” allele originally increased in the local horses due to the selection for the smooth ride and other characters, long before the PRPF breed was established. To support this hypothesis, we demonstrate that PRNPB horses, and not the purebred PRPF, carry a signature of selection in the genomic region containing theDMRT3 locus to this day. The lack of the detectable signature of selection associated with theDMRT3 in the PRPF would be expected if this native breed was originally derived from the genetic pool of PRNPB horses established earlier and most of the founders already had the mutant allele. Consequently, selection specific to PRPF later focused on allels in other genes (includingCHRM5, CYP2E1, MYH7, SRSF1, PAM, PRN and others) that have not been previously associated with the prized paso gait phenotype in Puerto Rico or anywhere else. -
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Multivariable models for prediction or estimating associations with an outcome are rarely built in isolation. Instead, they are based upon a mixture of covariates that have been evaluated in earlier studies (eg, age, sex, or common biomarkers) and covariates that were collected specifically for the current study (eg, a panel of novel biomarkers or other hypothesized risk factors). For that context, we present the multistep elastic net (MSN), which considers penalized regression with variables that can be qualitatively grouped based upon their degree of prior research support: established predictors vs unestablished predictors. The MSN chooses between uniform penalization of all predictors (the standard elastic net) and weaker penalization of the established predictors in a cross‐validated framework and includes the option to impose zero penalty on the established predictors. In simulation studies that reflect the motivating context, we show the comparability or superiority of the MSN over the standard elastic net, the Integrative LASSO with Penalty Factors, the sparse group lasso, and the group lasso, and we investigate the importance of not penalizing the established predictors at all. We demonstrate the MSN to update a prediction model for pediatric ECMO patient mortality.
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Abstract We consider the dynamics of a virus spreading through a population that produces a mutant strain with the ability to infect individuals that were infected with the established strain. Temporary cross-immunity is included using a time delay, but is found to be a harmless delay. We provide some sufficient conditions that guarantee local and global asymptotic stability of the disease-free equilibrium and the two boundary equilibria when the two strains outcompete one another. It is shown that, due to the immune evasion of the emerging strain, the reproduction number of the emerging strain must be significantly lower than that of the established strain for the local stability of the established-strain-only boundary equilibrium. To analyze the unique coexistence equilibrium we apply a quasi steady-state argument to reduce the full model to a two-dimensional one that exhibits a global asymptotically stable established-strain-only equilibrium or global asymptotically stable coexistence equilibrium. Our results indicate that the basic reproduction numbers of both strains govern the overall dynamics, but in nontrivial ways due to the inclusion of cross-immunity. The model is applied to study the emergence of the SARS-CoV-2 Delta variant in the presence of the Alpha variant using wastewater surveillance data from the Deer Island Treatment Plant in Massachusetts, USA.
- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.21468/SciPostPhys.7.1.014
