@inproceedings{2053,
  abstract     = {In contrast to the usual understanding of probabilistic systems as stochastic processes, recently these systems have also been regarded as transformers of probabilities. In this paper, we give a natural definition of strong bisimulation for probabilistic systems corresponding to this view that treats probability distributions as first-class citizens. Our definition applies in the same way to discrete systems as well as to systems with uncountable state and action spaces. Several examples demonstrate that our definition refines the understanding of behavioural equivalences of probabilistic systems. In particular, it solves a longstanding open problem concerning the representation of memoryless continuous time by memoryfull continuous time. Finally, we give algorithms for computing this bisimulation not only for finite but also for classes of uncountably infinite systems.},
  author       = {Hermanns, Holger and Krčál, Jan and Kretinsky, Jan},
  booktitle    = {Lecture Notes in Computer Science (including subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics)},
  editor       = {Baldan, Paolo and Gorla, Daniele},
  location     = {Rome, Italy},
  pages        = {249 -- 265},
  publisher    = {Schloss Dagstuhl - Leibniz-Zentrum für Informatik},
  title        = {{Probabilistic bisimulation: Naturally on distributions}},
  doi          = {10.1007/978-3-662-44584-6_18},
  volume       = {8704},
  year         = {2014},
}

@article{2056,
  abstract     = {We consider a continuous-time Markov chain (CTMC) whose state space is partitioned into aggregates, and each aggregate is assigned a probability measure. A sufficient condition for defining a CTMC over the aggregates is presented as a variant of weak lumpability, which also characterizes that the measure over the original process can be recovered from that of the aggregated one. We show how the applicability of de-aggregation depends on the initial distribution. The application section is devoted to illustrate how the developed theory aids in reducing CTMC models of biochemical systems particularly in connection to protein-protein interactions. We assume that the model is written by a biologist in form of site-graph-rewrite rules. Site-graph-rewrite rules compactly express that, often, only a local context of a protein (instead of a full molecular species) needs to be in a certain configuration in order to trigger a reaction event. This observation leads to suitable aggregate Markov chains with smaller state spaces, thereby providing sufficient reduction in computational complexity. This is further exemplified in two case studies: simple unbounded polymerization and early EGFR/insulin crosstalk.},
  author       = {Ganguly, Arnab and Petrov, Tatjana and Koeppl, Heinz},
  journal      = {Journal of Mathematical Biology},
  number       = {3},
  pages        = {767 -- 797},
  publisher    = {Springer},
  title        = {{Markov chain aggregation and its applications to combinatorial reaction networks}},
  doi          = {10.1007/s00285-013-0738-7},
  volume       = {69},
  year         = {2014},
}

@inproceedings{2057,
  abstract     = {In the past few years, a lot of attention has been devoted to multimedia indexing by fusing multimodal informations. Two kinds of fusion schemes are generally considered: The early fusion and the late fusion. We focus on late classifier fusion, where one combines the scores of each modality at the decision level. To tackle this problem, we investigate a recent and elegant well-founded quadratic program named MinCq coming from the machine learning PAC-Bayesian theory. MinCq looks for the weighted combination, over a set of real-valued functions seen as voters, leading to the lowest misclassification rate, while maximizing the voters’ diversity. We propose an extension of MinCq tailored to multimedia indexing. Our method is based on an order-preserving pairwise loss adapted to ranking that allows us to improve Mean Averaged Precision measure while taking into account the diversity of the voters that we want to fuse. We provide evidence that this method is naturally adapted to late fusion procedures and confirm the good behavior of our approach on the challenging PASCAL VOC’07 benchmark.},
  author       = {Morvant, Emilie and Habrard, Amaury and Ayache, Stéphane},
  booktitle    = {Lecture Notes in Computer Science (including subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics)},
  location     = {Joensuu, Finland},
  pages        = {153 -- 162},
  publisher    = {Springer},
  title        = {{Majority vote of diverse classifiers for late fusion}},
  doi          = {10.1007/978-3-662-44415-3_16},
  volume       = {8621},
  year         = {2014},
}

@inproceedings{2058,
  abstract     = {We present a method for smoothly blending between existing liquid animations. We introduce a semi-automatic method for matching two existing liquid animations, which we use to create new fluid motion that plausibly interpolates the input. Our contributions include a new space-time non-rigid iterative closest point algorithm that incorporates user guidance, a subsampling technique for efficient registration of meshes with millions of vertices, and a fast surface extraction algorithm that produces 3D triangle meshes from a 4D space-time surface. Our technique can be used to instantly create hundreds of new simulations, or to interactively explore complex parameter spaces. Our method is guaranteed to produce output that does not deviate from the input animations, and it generalizes to multiple dimensions. Because our method runs at interactive rates after the initial precomputation step, it has potential applications in games and training simulations.},
  author       = {Raveendran, Karthik and Wojtan, Christopher J and Thuerey, Nils and Türk, Greg},
  booktitle    = {ACM Transactions on Graphics},
  location     = {Vancouver, Canada},
  number       = {4},
  publisher    = {ACM},
  title        = {{Blending liquids}},
  doi          = {10.1145/2601097.2601126},
  volume       = {33},
  year         = {2014},
}

@article{2059,
  abstract     = {Plant embryogenesis is regulated by differential distribution of the plant hormone auxin. However, the cells establishing these gradients during microspore embryogenesis remain to be identified. For the first time, we describe, using the DR5 or DR5rev reporter gene systems, the GFP- and GUS-based auxin biosensors to monitor auxin during Brassica napus androgenesis at cellular resolution in the initial stages. Our study provides evidence that the distribution of auxin changes during embryo development and depends on the temperature-inducible in vitro culture conditions. For this, microspores (mcs) were induced to embryogenesis by heat treatment and then subjected to genetic modification via Agrobacterium tumefaciens. The duration of high temperature treatment had a significant influence on auxin distribution in isolated and in vitro-cultured microspores and on microspore-derived embryo development. In the “mild” heat-treated (1 day at 32 °C) mcs, auxin localized in a polar way already at the uni-nucleate microspore, which was critical for the initiation of embryos with suspensor-like structure. Assuming a mean mcs radius of 20 μm, endogenous auxin content in a single cell corresponded to concentration of 1.01 μM. In mcs subjected to a prolonged heat (5 days at 32 °C), although auxin concentration increased dozen times, auxin polarization was set up at a few-celled pro-embryos without suspensor. Those embryos were enclosed in the outer wall called the exine. The exine rupture was accompanied by the auxin gradient polarization. Relative quantitative estimation of auxin, using time-lapse imaging, revealed that primordia possess up to 1.3-fold higher amounts than those found in the root apices of transgenic MDEs in the presence of exogenous auxin. Our results show, for the first time, which concentration of endogenous auxin coincides with the first cell division and how the high temperature interplays with auxin, by what affects delay early establishing microspore polarity. Moreover, we present how the local auxin accumulation demonstrates the apical–basal axis formation of the androgenic embryo and directs the axiality of the adult haploid plant.},
  author       = {Dubas, Ewa and Moravčíková, Jana and Libantová, Jana and Matušíková, Ildikó and Benková, Eva and Zur, Iwona and Krzewska, Monika},
  journal      = {Protoplasma},
  number       = {5},
  pages        = {1077 -- 1087},
  publisher    = {Springer},
  title        = {{The influence of heat stress on auxin distribution in transgenic B napus microspores and microspore derived embryos}},
  doi          = {10.1007/s00709-014-0616-1},
  volume       = {251},
  year         = {2014},
}

@article{2061,
  abstract     = {Development of cambium and its activity is important for our knowledge of the mechanism of secondary growth. Arabidopsis thaliana emerges as a good model plant for such a kind of study. Thus, this paper reports on cellular events taking place in the interfascicular regions of inflorescence stems of A. thaliana, leading to the development of interfascicular cambium from differentiated interfascicular parenchyma cells (IPC). These events are as follows: appearance of auxin accumulation, PIN1 gene expression, polar PIN1 protein localization in the basal plasma membrane and periclinal divisions. Distribution of auxin was observed to be higher in differentiating into cambium parenchyma cells compared to cells within the pith and cortex. Expression of PIN1 in IPC was always preceded by auxin accumulation. Basal localization of PIN1 was already established in the cells prior to their periclinal division. These cellular events initiated within parenchyma cells adjacent to the vascular bundles and successively extended from that point towards the middle region of the interfascicular area, located between neighboring vascular bundles. The final consequence of which was the closure of the cambial ring within the stem. Changes in the chemical composition of IPC walls were also detected and included changes of pectic epitopes, xyloglucans (XG) and extensins rich in hydroxyproline (HRGPs). In summary, results presented in this paper describe interfascicular cambium ontogenesis in terms of successive cellular events in the interfascicular regions of inflorescence stems of Arabidopsis.},
  author       = {Mazur, Ewa and Kurczyñska, Ewa and Friml, Jiří},
  journal      = {Protoplasma},
  number       = {5},
  pages        = {1125 -- 1139},
  publisher    = {Springer},
  title        = {{Cellular events during interfascicular cambium ontogenesis in inflorescence stems of Arabidopsis}},
  doi          = {10.1007/s00709-014-0620-5},
  volume       = {251},
  year         = {2014},
}

@article{2062,
  abstract     = {The success story of fast-spiking, parvalbumin-positive (PV+) GABAergic interneurons (GABA, γ-aminobutyric acid) in the mammalian central nervous system is noteworthy. In 1995, the properties of these interneurons were completely unknown. Twenty years later, thanks to the massive use of subcellular patch-clamp techniques, simultaneous multiple-cell recording, optogenetics, in vivo measurements, and computational approaches, our knowledge about PV+ interneurons became more extensive than for several types of pyramidal neurons. These findings have implications beyond the “small world” of basic research on GABAergic cells. For example, the results provide a first proof of principle that neuroscientists might be able to close the gaps between the molecular, cellular, network, and behavioral levels, representing one of the main challenges at the present time. Furthermore, the results may form the basis for PV+ interneurons as therapeutic targets for brain disease in the future. However, much needs to be learned about the basic function of these interneurons before clinical neuroscientists will be able to use PV+ interneurons for therapeutic purposes.},
  author       = {Hu, Hua and Gan, Jian and Jonas, Peter M},
  journal      = {Science},
  number       = {6196},
  publisher    = {American Association for the Advancement of Science},
  title        = {{Fast-spiking parvalbumin^+ GABAergic interneurons: From cellular design to microcircuit function}},
  doi          = {10.1126/science.1255263},
  volume       = {345},
  year         = {2014},
}

@inproceedings{2063,
  abstract     = {We consider Markov decision processes (MDPs) which are a standard model for probabilistic systems.We focus on qualitative properties forMDPs that can express that desired behaviors of the system arise almost-surely (with probability 1) or with positive probability. We introduce a new simulation relation to capture the refinement relation ofMDPs with respect to qualitative properties, and present discrete graph theoretic algorithms with quadratic complexity to compute the simulation relation.We present an automated technique for assume-guarantee style reasoning for compositional analysis ofMDPs with qualitative properties by giving a counterexample guided abstraction-refinement approach to compute our new simulation relation. We have implemented our algorithms and show that the compositional analysis leads to significant improvements.},
  author       = {Chatterjee, Krishnendu and Chmelik, Martin and Daca, Przemyslaw},
  location     = {Vienna, Austria},
  pages        = {473 -- 490},
  publisher    = {Springer},
  title        = {{CEGAR for qualitative analysis of probabilistic systems}},
  doi          = {10.1007/978-3-319-08867-9_31},
  volume       = {8559},
  year         = {2014},
}

@article{2064,
  abstract     = {We examined the synaptic structure, quantity, and distribution of α-amino-3-hydroxy-5-methylisoxazole-4-propionic acid (AMPA)- and N-methyl-D-aspartate (NMDA)-type glutamate receptors (AMPARs and NMDARs, respectively) in rat cochlear nuclei by a highly sensitive freeze-fracture replica labeling technique. Four excitatory synapses formed by two distinct inputs, auditory nerve (AN) and parallel fibers (PF), on different cell types were analyzed. These excitatory synapse types included AN synapses on bushy cells (AN-BC synapses) and fusiform cells (AN-FC synapses) and PF synapses on FC (PF-FC synapses) and cartwheel cell spines (PF-CwC synapses). Immunogold labeling revealed differences in synaptic structure as well as AMPAR and NMDAR number and/or density in both AN and PF synapses, indicating a target-dependent organization. The immunogold receptor labeling also identified differences in the synaptic organization of FCs based on AN or PF connections, indicating an input-dependent organization in FCs. Among the four excitatory synapse types, the AN-BC synapses were the smallest and had the most densely packed intramembrane particles (IMPs), whereas the PF-CwC synapses were the largest and had sparsely packed IMPs. All four synapse types showed positive correlations between the IMP-cluster area and the AMPAR number, indicating a common intrasynapse-type relationship for glutamatergic synapses. Immunogold particles for AMPARs were distributed over the entire area of individual AN synapses; PF synapses often showed synaptic areas devoid of labeling. The gold-labeling for NMDARs occurred in a mosaic fashion, with less positive correlations between the IMP-cluster area and the NMDAR number. Our observations reveal target- and input-dependent features in the structure, number, and organization of AMPARs and NMDARs in AN and PF synapses.},
  author       = {Rubio, Maía and Fukazawa, Yugo and Kamasawa, Naomi and Clarkson, Cheryl and Molnár, Elek and Shigemoto, Ryuichi},
  journal      = {Journal of Comparative Neurology},
  number       = {18},
  pages        = {4023 -- 4042},
  publisher    = {Wiley-Blackwell},
  title        = {{Target- and input-dependent organization of AMPA and NMDA receptors in synaptic connections of the cochlear nucleus}},
  doi          = {10.1002/cne.23654},
  volume       = {522},
  year         = {2014},
}

@article{2080,
  abstract     = {Spinning tops and yo-yos have long fascinated cultures around the world with their unexpected, graceful motions that seemingly elude gravity. We present an algorithm to generate designs for spinning objects by optimizing rotational dynamics properties. As input, the user provides a solid 3D model and a desired axis of rotation. Our approach then modifies the mass distribution such that the principal directions of the moment of inertia align with the target rotation frame. We augment the model by creating voids inside its volume, with interior fill represented by an adaptive multi-resolution vox-elization. The discrete voxel fill values are optimized using a continuous, nonlinear formulation. Further, we optimize for rotational stability by maximizing the dominant principal moment. We extend our technique to incorporate deformation and multiple materials for cases where internal voids alone are insufficient. Our method is well-suited for a variety of 3D printed models, ranging from characters to abstract shapes. We demonstrate tops and yo-yos that spin surprisingly stably despite their asymmetric appearance. },
  author       = {Bächer, Moritz and Whiting, Emily and Bickel, Bernd and Sorkine Hornung, Olga},
  issn         = {1557-7368},
  journal      = {ACM Transactions on Graphics},
  number       = {4},
  publisher    = {ACM},
  title        = {{Spin-It: Optimizing moment of inertia for spinnable objects}},
  doi          = {10.1145/2601097.2601157},
  volume       = {33},
  year         = {2014},
}

@inproceedings{2081,
  abstract     = {We propose an interactive, optimization-in-the-loop tool for designing inflatable structures. Given a target shape, the user draws a network of seams defining desired segment boundaries in 3D. Our method computes optimally-shaped flat panels for the segments, such that the inflated structure is as close as possible to the target while satisfying the desired seam positions. Our approach is underpinned by physics-based pattern optimization, accurate coarse-scale simulation using tension field theory, and a specialized constraint-optimization method. Our system is fast enough to warrant interactive exploration of different seam layouts, including internal connections, and their effects on the inflated shape. We demonstrate the resulting design process on a varied set of simulation examples, some of which we have fabricated, demonstrating excellent agreement with the design intent.},
  author       = {Skouras, Mélina and Thomaszewski, Bernhard and Kaufmann, Peter and Garg, Akash and Bickel, Bernd and Grinspun, Eitan and Gross, Markus},
  number       = {4},
  publisher    = {ACM},
  title        = {{Designing inflatable structures}},
  doi          = {10.1145/2601097.2601166},
  volume       = {33},
  year         = {2014},
}

@article{10382,
  abstract     = {Protein oligomers have been implicated as toxic agents in a wide range of amyloid-related diseases. However, it has remained unsolved whether the oligomers are a necessary step in the formation of amyloid fibrils or just a dangerous byproduct. Analogously, it has not been resolved if the amyloid nucleation process is a classical one-step nucleation process or a two-step process involving prenucleation clusters. We use coarse-grained computer simulations to study the effect of nonspecific attractions between peptides on the primary nucleation process underlying amyloid fibrillization. We find that, for peptides that do not attract, the classical one-step nucleation mechanism is possible but only at nonphysiologically high peptide concentrations. At low peptide concentrations, which mimic the physiologically relevant regime, attractive interpeptide interactions are essential for fibril formation. Nucleation then inevitably takes place through a two-step mechanism involving prefibrillar oligomers. We show that oligomers not only help peptides meet each other but also, create an environment that facilitates the conversion of monomers into the β-sheet–rich form characteristic of fibrils. Nucleation typically does not proceed through the most prevalent oligomers but through an oligomer size that is only observed in rare fluctuations, which is why such aggregates might be hard to capture experimentally. Finally, we find that the nucleation of amyloid fibrils cannot be described by classical nucleation theory: in the two-step mechanism, the critical nucleus size increases with increases in both concentration and interpeptide interactions, which is in direct contrast with predictions from classical nucleation theory.},
  author       = {Šarić, Anđela and Chebaro, Yassmine C. and Knowles, Tuomas P. J. and Frenkel, Daan},
  issn         = {1091-6490},
  journal      = {Proceedings of the National Academy of Sciences},
  keywords     = {multidisciplinary},
  number       = {50},
  pages        = {17869--17874},
  publisher    = {National Academy of Sciences},
  title        = {{Crucial role of nonspecific interactions in amyloid nucleation}},
  doi          = {10.1073/pnas.1410159111},
  volume       = {111},
  year         = {2014},
}

@article{10383,
  abstract     = {We use numerical simulations to compute the equation of state of a suspension of spherical self-propelled nanoparticles in two and three dimensions. We study in detail the effect of excluded volume interactions and confinement as a function of the system's temperature, concentration, and strength of the propulsion. We find a striking nonmonotonic dependence of the pressure on the temperature and provide simple scaling arguments to predict and explain the occurrence of such anomalous behavior. We explicitly show how our results have important implications for the effective forces on passive components suspended in a bath of active particles.},
  author       = {Mallory, S. A. and Šarić, Anđela and Valeriani, C. and Cacciuto, A.},
  issn         = {1550-2376},
  journal      = {Physical Review E},
  number       = {5},
  publisher    = {American Physical Society},
  title        = {{Anomalous thermomechanical properties of a self-propelled colloidal fluid}},
  doi          = {10.1103/physreve.89.052303},
  volume       = {89},
  year         = {2014},
}

@inproceedings{10793,
  abstract     = {The Hanani–Tutte theorem is a classical result proved for the first time in the 1930s that characterizes planar graphs as graphs that admit a drawing in the plane in which every pair of edges not sharing a vertex cross an even number of times. We generalize this classical result to clustered graphs with two disjoint clusters, and show that a straightforward extension of our result to flat clustered graphs with three or more disjoint clusters is not possible.

We also give a new and short proof for a related result by Di Battista and Frati based on the matroid intersection algorithm.},
  author       = {Fulek, Radoslav and Kynčl, Jan and Malinović, Igor and Pálvölgyi, Dömötör},
  booktitle    = {International Symposium on Graph Drawing},
  issn         = {0302-9743},
  pages        = {428--436},
  publisher    = {Springer Nature},
  title        = {{Clustered planarity testing revisited}},
  doi          = {10.1007/978-3-662-45803-7_36},
  volume       = {8871},
  year         = {2014},
}

@book{10811,
  abstract     = {Auxin is an important signaling compound in plants and vital for plant development and growth. The present book, Auxin and its Role in Plant Development, provides the reader with detailed and comprehensive insight into the functioning of the molecule on the whole and specifically in plant development. In the first part, the functioning, metabolism and signaling pathways of auxin in plants are explained, the second part depicts the specific role of auxin in plant development and the third part describes the interaction and functioning of the signaling compound  upon stimuli of the environment. Each chapter is written by international experts in the respective field and designed for scientists and researchers in plant biology, plant development and cell biology to summarize the recent progress in understanding the role of auxin and suggest future perspectives for auxin research.},
  editor       = {Zažímalová, Eva and Petrášek, Jan and Benková, Eva},
  isbn         = {9783709115251},
  pages        = {444},
  publisher    = {Springer Nature},
  title        = {{Auxin and Its Role in Plant Development}},
  doi          = {10.1007/978-3-7091-1526-8},
  year         = {2014},
}

@article{10814,
  abstract     = {We review recent progress towards a rigorous understanding of the excitation spectrum of bosonic quantum many-body systems. In particular, we explain how one can rigorously establish the predictions resulting from the Bogoliubov approximation in the mean field limit. The latter predicts that the spectrum is made up of elementary excitations, whose energy behaves linearly in the momentum for small momentum. This property is crucial for the superfluid behavior of the system. We also discuss a list of open problems in this field.},
  author       = {Seiringer, Robert},
  issn         = {1869-7135},
  journal      = {Jahresbericht der Deutschen Mathematiker-Vereinigung},
  keywords     = {General Medicine},
  pages        = {21--41},
  publisher    = {Springer Nature},
  title        = {{The excitation spectrum for Bose fluids with weak interactions}},
  doi          = {10.1365/s13291-014-0083-9},
  volume       = {116},
  year         = {2014},
}

@article{10815,
  abstract     = {In the last several decades, developmental biology has clarified the molecular mechanisms of embryogenesis and organogenesis. In particular, it has demonstrated that the “tool-kit genes” essential for regulating developmental processes are not only highly conserved among species, but are also used as systems at various times and places in an organism to control distinct developmental events. Therefore, mutations in many of these tool-kit genes may cause congenital diseases involving morphological abnormalities. This link between genes and abnormal morphological phenotypes underscores the importance of understanding how cells behave and contribute to morphogenesis as a result of gene function. Recent improvements in live imaging and in quantitative analyses of cellular dynamics will advance our understanding of the cellular pathogenesis of congenital diseases associated with aberrant morphologies. In these studies, it is critical to select an appropriate model organism for the particular phenomenon of interest.},
  author       = {Hashimoto, Masakazu and Morita, Hitoshi and Ueno, Naoto},
  issn         = {0914-3505},
  journal      = {Congenital Anomalies},
  keywords     = {Developmental Biology, Embryology, General Medicine, Pediatrics, Perinatology, and Child Health},
  number       = {1},
  pages        = {1--7},
  publisher    = {Wiley},
  title        = {{Molecular and cellular mechanisms of development underlying congenital diseases}},
  doi          = {10.1111/cga.12039},
  volume       = {54},
  year         = {2014},
}

@article{7598,
  author       = {Tan, Shutang and Xue, Hong-Wei},
  issn         = {2211-1247},
  journal      = {Cell Reports},
  number       = {5},
  pages        = {1692--1702},
  publisher    = {Elsevier},
  title        = {{Casein kinase 1 regulates ethylene synthesis by phosphorylating and promoting the turnover of ACS5}},
  doi          = {10.1016/j.celrep.2014.10.047},
  volume       = {9},
  year         = {2014},
}

@article{7699,
  author       = {Sweeney, Lora Beatrice Jaeger and Kelley, Darcy B},
  issn         = {0959-4388},
  journal      = {Current Opinion in Neurobiology},
  number       = {10},
  pages        = {34--41},
  publisher    = {Elsevier},
  title        = {{Harnessing vocal patterns for social communication}},
  doi          = {10.1016/j.conb.2014.06.006},
  volume       = {28},
  year         = {2014},
}

@inbook{7743,
  abstract     = {Experimental studies have demonstrated that environmental variation can create genotype‐environment interactions (GEIs) in the traits involved in sexual selection. Understanding the genetic architecture of phenotype across environments will require statistical tests that can describe both changes in genetic variance and covariance across environments. This chapter outlines the theoretical framework for the processes of sexual selection in the wild, identifying key parameters in wild systems, and highlighting the potential effects of the environment. It describes the proposed approaches for the estimation of these key parameters in a quantitative genetic framework within naturally occurring pedigreed populations. The chapter provides a worked example for a range of analysis methods. It aims to provide an overview of the analytical methods that can be used to model GEIs for traits involved in sexual selection in naturally occurring pedigreed populations.},
  author       = {Robinson, Matthew Richard and Qvarnström, Anna},
  booktitle    = {Genotype-by-Environment Interactions and Sexual Selection},
  editor       = {Hunt, John and Hosken, David},
  isbn         = {9780470671795},
  pages        = {137--168},
  publisher    = {Wiley},
  title        = {{Influence of the environment on the genetic architecture of traits involved in sexual selection within wild populations}},
  doi          = {10.1002/9781118912591.ch6},
  year         = {2014},
}

