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Dochtermann, N. A.

Publications and source records attributed to Dochtermann, N. A..

4 recordsLinked to original sources

Flowering cues in a Costa Rican cloud forest: analyzing the effect of climate

The influence of a changing climate on the phenology of organisms in a region is dependent on how regional climate cues or modifies the timing of local life history events and how those cues are changing over time. There is extensive evidence of phenolological shifts in flowering time over the past 50 years in response to increasing temperatures in temperate regions, but far less is known about tropical regions where seasonality is less temperature driven. We examined historical datasets of flowering patterns in two guilds of ornithophilous plants in the montane cloud forests of Monteverde, Costa Rica in order to identify environmental cues for flowering in nine species of plant that are important resources for hummingbirds. Bimonthly censuses of flower production were used to quantify flower production during two sampling periods:1981-1983, 1986-1991., the species studied here appear to cue flowering patterns to either accumulated drought units or a combination of accumulated drought units and chill units prior to flowering. These results have implications for how tropical cloud forest plants will respond to climate change to the extent that drought and chill patterns are changing with time.

ecology↗

Drift on holey landscapes as a dominant evolutionary process

An organisms phenotype has been shaped by evolution but the specific processes have to be indirectly inferred for most species. For example, correlations among traits imply the historical action of correlated selection and, more generally, the expression and distribution of traits is expected to be reflective of the adaptive landscapes that have shaped a population. However, our expectations about how quantitative traits--like most behaviors, physiological processes, and life-history traits--should be distributed under different evolutionary processes is not clear. Here we show that genetic variation in quantitative traits is not distributed as would be expected under dominant evolutionary models. Instead, we found that genetic variation in quantitative traits across 6 phyla and 60 species (including both Plantae and Animalia) is consistent with evolution across high dimensional "holey landscapes". This suggests that the leading conceptualizations and modeling of the evolution of trait integration fail to capture how phenotypes are shaped and that traits are integrated in a manner contrary to predictions of dominant evolutionary theory. Our results demonstrate that our understanding of how evolution has shaped phenotypes remains incomplete and these results provide a starting point for reassessing the relevance of existing evolutionary models. Significance StatementWe found that empirical estimations of how quantitative genetic variation is distributed do not correspond to typical Gaussian representations of fitness landscapes. These Gaussian landscapes underpin major areas of evolutionary biology and how selection is estimated in natural populations. Rather than being consistent with evolution on Gaussian landscapes, empirical estimates of genetic variation are, instead, consistent with evolution on high-dimensional "holey" landscapes. These landscapes represent situations where specific combinations of trait values are either viable or not and populations randomly drift among the viable combinations. This finding suggests that we have substantially misunderstood how selection actually shapes populations and thus how evolution typically proceeds.

evolutionary biology↗

The role of trade-offs and feedbacks in shaping integrated plasticity, behavioral syndromes, and behavioral correlations

How behaviors vary among individuals and covary with other behaviors has been a major topic of interest over the last two decades. Unfortunately, proposed theoretical and conceptual frameworks explaining the seemingly ubiquitous observation of behavioral (co)variation have rarely successfully generalized. Two observations perhaps explain this failure: First, phenotypic correlations between behaviors are more strongly influenced by correlated and reversible plastic changes in behavior than by "behavioral syndromes". Second, while trait correlations are frequently assumed to arise via trade-offs, the observed pattern of correlations is not consistent with simple pair-wise trade-offs. A possible resolution to the apparent inconsistency between observed correlations and a role for trade-offs is provided by state-behavior feedbacks. This is critical because the inconsistency between data and theory represents a major failure in our understanding of behavioral evolution. These two primary observations emphasize the importance of an increased research focus on correlated reversible plasticity in behavior--frequently estimated and then disregarded as within-individual covariances. LAY SUMMARYCorrelations between behaviors are common but observed patterns of these correlations are, at least superficially, inconsistent with expectations of trade-offs. This mismatch is potentially resolved via feedbacks between behaviors and energy availability, suggesting important new research directions. DATA AND MODEL AVAILABILITYModel code, as well as the data associated with Figures 2 & 3, are available at github.com/DochtermannLab/FeedbacksModel. Both code and data will be made available at Dryad if accepted. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=66 SRC="FIGDIR/small/453877v2_fig2.gif" ALT="Figure 2"> View larger version (19K): org.highwire.dtl.DTLVardef@f3814forg.highwire.dtl.DTLVardef@ae702dorg.highwire.dtl.DTLVardef@46be9borg.highwire.dtl.DTLVardef@8be692_HPS_FORMAT_FIGEXP M_FIG O_FLOATNOFigure 2.C_FLOATNO Relationship of within-individual behavioral correlations (rW) with (A) among-individual correlations (rA) and (B) genetic correlations (rG). The sign and magnitude of rA and rG are highly concordant with rW across behaviors and taxa. Diagonal lines indicate 1:1 relationship. Horizontal and vertical dashed lines divide plots into sign mismatches (top left, bottom right) and sign matches (top right, bottom left). Within-individual correlations were the same sign as among-individual and genetic correlations in 62% and 79% of cases respectively. Data in A are from Brommer and Class (2017). Data in B are from Dochtermann (2011). C_FIG O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=102 SRC="FIGDIR/small/453877v2_fig3.gif" ALT="Figure 3"> View larger version (19K): org.highwire.dtl.DTLVardef@ce931dorg.highwire.dtl.DTLVardef@1c8798org.highwire.dtl.DTLVardef@10a418eorg.highwire.dtl.DTLVardef@55e6ae_HPS_FORMAT_FIGEXP M_FIG O_FLOATNOFigure 3.C_FLOATNO (A) Simple model structure combining Sih et al.s (2015) feedback model with Houles (1991) y-model to include feedbacks between behavior and state. TO (the trade-off parameter) is the proportion of state energy (S1 at time t) allocated to behavior B1, making 1-TO the energy allocated to B2. {lambda} is the feedback strength and the conversion rate of a behavior (B1 or B2) into energy that can be used at a later time. (B) Magnitude of among-(purple) and within-individual (green) correlations under feedbacks ({lambda}) of different strength. Shaded regions indicate those feedback strengths that produce correlations of the same sign. Repeatability is not set a priori and is instead an emergent property of the model. Individuals within a population expressed behaviors according to A over ten time steps, with 250 individuals per population. Fifty populations were simulated at each of five levels of feebacks ({lambda} in B). rA and rW were estimated using the MCMCglmm package in R (Hadfield 2010). C_FIG

evolutionary biology↗

Misalignment of selection, plasticity, and among-individual variation: A test of theoretical predictions with Peromyscus maniculatus.

Genetic variation and phenotypic plasticity are predicted to align with selection surfaces, a prediction that has rarely been empirically tested. Understanding the relationship between sources of phenotypic variation, i.e. genetic variation and plasticity, with selection surfaces improves our ability to predict a populations ability to adapt to a changing environment and our understanding of how selection has shaped phenotypes. Here, we estimated the (co)variances among three different behaviors (activity, aggression, and anti-predator response) in a natural population of deer mice (Peromyscus maniculatus). Using multi-response generalized mixed effects models, we divided the phenotypic covariance matrix into among- and within-individual matrices. The among-individual covariances includes genetic and permanent environmental covariances (e.g. developmental plasticity) and is predicted to align with selection. Simultaneously, we estimated the within-individual (co)variances, which include reversible phenotypic plasticity. To determine whether genetic variation, plasticity and selection align in multivariate space we calculated the dimensions containing the greatest among-individual variation and the dimension in which most plasticity was expressed (i.e. the dominant eigenvector for the among- and within-individual covariance matrices respectively). We estimated selection coefficients based on survival estimates from a mark-recapture model. Alignment between the dominant eigenvectors of behavioural variation and the selection gradient was estimated by calculating the angle between them, with an angle of 0 indicating perfect alignment. The angle between vectors ranged from 68{degrees} to 89{degrees}, indicating that genetic variation, phenotypic plasticity, and selection are misaligned in this population. This misalignment could be due to the behaviors being close to their fitness optima, which is supported by low evolvabilities, or because of low selection pressure on these behaviors.

animal behavior and cognition↗