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191 results for “adaptive potential”

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zenodo44/100

Infant N290 event-related potentials and stimulus-specific adaptation to face stimuli

<p>Data for publication:&nbsp; &quot;Neural specialization to human faces at the age of 7 months&quot;.</p> <p>Further details will be available at: https://github.com/yrttiahoS/ssa/</p> <p>&nbsp;</p> <p>Metadata:</p> <p>I. Event-related potentials</p> <p>The current study investigated both cortical sensitivity and categorical specificity through event-related potentials (ERPs) previously implicated in face processing in 7-month-old infants (N290) and adults (N170). Using a category-specific repetition/adaptation paradigm, cortical specificity to human faces, or control stimuli (cat faces), was operationalized as changes in ERP amplitude between conditions where a face probe was alternated with categorically similar or dissimilar adaptors. In adults, increased N170 for human vs. cat faces and category-specific release from adaptation for face probes alternated with cat adaptors was found. In infants, a larger N290 was found for cat vs. human probes. Category-specific repetition effects were also found in infant N290 and the P1-N290 peak-to-peak response where latter indicated category-specific release from adaptation for human face probes resembling that found in adults.</p> <p>*Dataset files: N290_P1_infant, N170_P1_adult.sav</p> <p>&nbsp;</p> <p>*EEG data in EEGLAB&rsquo;s format,</p> <p>Filenames indicate type of data with:</p> <p>1) Initial numerical code indicating (anonymized) participant number, &quot;adult/infant&quot; indicating participant group</p> <p>2) f1/c2/f3/c3 indicating stimulus conditions probe:face, adaptor:face / probe:cat, adaptor:cat / probe:face, adaptor:cat / probe:cat,adaptor:face, respectively</p> <p>&nbsp;3) Final number _1_ or _2_ indicates block number for adult participants (in the order of presentation)</p> <p>Files with only codes 1) and 2) are continuous data with all triggers included</p> <p>&nbsp;</p> <p>*video-based Quality Control is listed in file: anon_vQC2022-09-22.xlsx*video-based Quality Control is listed in file: anon_vQC2022-09-22.xlsx</p> <p>&nbsp;</p> <p>*Analysis syntax: https://github.com/yrttiahoS/ssa/</p> <p>&nbsp;</p> <p>*Dataset updates: TBA at https://github.com/yrttiahoS/ssa/</p> <p>&nbsp;</p> <p>&nbsp;</p> <p>II. Temperament questionnaire</p> <p>*Data collection: Temperament data were collected from participants of an infant event-related potential (ERP) study as potential correlate of outcome variables and as a descriptor of the participant group. Participants were 7-month-old infants from families volunteering in the brain research study, which were contacted through information from a population registry sample. Infant temperament was assessed by parent-reported IBQ-R short form (Putnam, S. P., Helbig, A., Gartstein, M.A., Rothbart, M.K. &amp; Leerkes, E. M. (2014). <em>Development and assessment of short and very short forms of the Infant Behavior Questionnaire-Revised.</em> Journal of Personality Assessment, 96, 445-458. Finnish translation: Professor Katri R&auml;ikk&ouml;nen-Talvitie and the Developmental Psychology Research Group University of Helsinki, Finland)</p> <p>*Authors of the dataset: Santeri Yrttiaho, Mikko Peltola, Anneli Kylli&auml;inen, Tiina, Parviainen, Jari Hietanen</p> <p>*Site of data collection: Human Information Processing laboratory, Tampere University, Finland</p> <p>*Funding: Emil Aaltonen Foundation, Tampere University, Academy of Finland</p> <p>*Participant demographics:&nbsp; Participant group is described by age of M(SD) = 30.5(0.5) weeks. Participants were from Tampere metropolitan area, Finland. Data were collected during Fall 2020 (October 16th&nbsp; &ndash; December 7th, 2020).</p> <p>*Data content. Initial data will contain group level statistics and the individual data will be made available as additional files after publication of study results in a peer-reviewed article. Data is anonymized. Individual data contains IBQ-R short form items, scales, and factors as well as participant gender and age in weeks. Data also includes variable indicating whether the participant was included in the final ERP analysis after EEG quality control.</p> <p>*variable names: see &#39;Scale abbreviations.docx&#39; and for full discussion the original article by Putnam et al. (2014).</p> <p>*Dataset files</p> <p>1. IBQ-R-short-Finnish_dataset.sav / data of items, scales, and factors</p> <p>2. SSA_infant_ibq-r_summary.sps / syntax for computing scores</p> <p>3. IBQ-R-short-Finnish_descriptives.spv / output of descriptive statistics</p> <p>4. Scale abbreviations.docx / explanation of variable names</p> <p>&nbsp;</p> <p>&nbsp;</p> <p>&nbsp;</p> <p>&nbsp;</p>

opencc-by-4.0Jul 2022View details →
dryad40/100

Prey diversity constrains the adaptive potential of predator foraging traits

<p>Predators are generally under selective pressure to get better at foraging, leading to steeper functional responses and stronger predator-prey interactions. Yet strong interactions can de-stabilize food webs, and most interactions across ecological communities are thought to be weak. This conflict between evolutionary and community expectations for the strength of predator-prey interactions represents a fundamental gap in our understanding of how the evolution of foraging plays out in food webs. Here we help to resolve the conflict by showing analytically that the expectation for the evolution of steeper functional responses is relaxed in communities with diverse prey types. We simulate communities with varying prey richness and show that increasing prey richness can indeed constrain the adaptive potential of predator foraging traits, but that at low prey richness predators can evolve to have a stronger interaction with prey that have high net energy yields. Our results also indicate that handling time plays a role in determining whether predators may evolve to have a stronger interaction with abundant prey, suggesting that the evolution of keystone predator modules in food webs is most likely when handling times are negligible. Our results also provide a new mechanism predicting more diffuse interactions in diverse tropical communities relative to more species-poor communities at higher latitudes.</p>

opencc-zeroNov 2021View details →
dryad40/100

Potential local adaptation in populations of invasive reed canary grass (Phalaris arundinacea) across an urbanization gradient

<p>Urban stressors represent strong selective gradients that can elicit evolutionary change, especially in non-native species that may harbor substantial within-population variability. To test whether urban stressors drive phenotypic differentiation and influence local adaptation, we compared stress responses of populations of a ubiquitous invader, reed canary grass (Phalaris arundinacea). Specifically, we quantified responses to salt, copper, and zinc additions by reed canary grass collected from four populations spanning an urbanization gradient (natural, rural, moderate urban and intense urban). We measured ten phenotypic traits and trait plasticities, because reed canary grass is known to be highly plastic and because plasticity may enhance invasion success. We tested the following hypotheses: 1) source populations vary systematically in their stress response, with the intense urban population least sensitive and the natural population most sensitive, and 2) plastic responses are adaptive under stressful conditions. We found clear trait variation among populations, with the greatest divergence in traits and trait plasticities between the natural and intense urban populations. The intense urban population showed stress tolerator characteristics for resource acquisition traits including leaf dry matter content and specific root length. Trait plasticity varied among populations for over half the traits measured, highlighting that plasticity differences were as common as trait differences. Plasticity in root mass ratio and specific root length were adaptive in some contexts, suggesting that natural selection by anthropogenic stressors may have contributed to root trait differences. Reed canary grass populations in highly urbanized wetlands may therefore be evolving enhanced tolerance to urban stressors, suggesting a mechanism by which invasive species may proliferate across urban wetland systems generally.</p>

opencc-zeroJul 2022View details →
dryad40/100

Data from: Can extreme climatic events induce shifts in adaptive potential? A conceptual framework and empirical test with Anolis lizards

<p>Multivariate adaptation to climatic shifts may be limited by trait integration that causes genetic variation to be low in the direction of selection. However, strong episodes of selection induced by extreme climatic pressures may facilitate future population-wide responses if selection reduces trait integration and increases adaptive potential (i.e., evolvability). We explain this counter-intuitive framework for extreme climatic events in which directional selection leads to increased evolvability and exemplify its use in a case study. We tested this hypothesis in two populations of the lizard <em>Anolis scriptus</em> that experienced hurricane-induced selection on limb traits. We surveyed populations immediately before and after the hurricane as well as the offspring of post-hurricane survivors, allowing us to estimate both selection and response to selection on key functional traits: forelimb length, hindlimb length, and toepad area. Direct selection was parallel in both islands and strong in several limb traits. Even though overall limb integration did not change after the hurricane, both populations showed a non-significant tendency toward increased evolvability after the hurricane despite the direction of selection not being aligned with the axis of most variance (i.e., body size). The population with comparably lower between-limb integration showed a less constrained response to selection. Hurricane-induced selection, not aligned with the pattern of high trait correlations, likely conflicts with selection occurring during normal ecological conditions that favor functional coordination between limb traits, and would likely need to be very strong and more persistent to elicit a greater change in trait integration and evolvability. Future tests of this hypothesis should use G-matrices in a variety of wild organisms experiencing selection due to extreme climatic events. </p>

opencc-zeroOct 2022View details →
zenodo40/100

Fig. 5 in A non-avian dinosaur with a streamlined body exhibits potential adaptations for swimming

Fig. 5 Life reconstruction of Natovenator polydontus (Artwork by Yusik Choi). The reconstruction shows the proposed swimming behaviour of Natovenator polydontus.

opencc-by-4.0Nov 2022View details →
zenodo40/100

Fig. 4 in A non-avian dinosaur with a streamlined body exhibits potential adaptations for swimming

Fig. 4 Body plan of Natovenator polydontus (MPC-D 102/114, holotype) and dorsal rib morphology of various diving birds and terrestrial taxa. a Dorsal series of Natovenator in ventral view. b Reconstruction of dorsal vertebrae and ribs of Natovenator in left lateral view. c Skeletal reconstruction of Natovenator with missing parts in dark grey. d–i Dorsal rib morphology of Natovenator (d), diving birds (e–i), common ostrich (j), and Shri devi, a likely terrestrial dromaeosaurid from the Baruungoyot Formation (k) in ventral view (not to scale). l Reconstruction of the fourth dorsal vertebra with corresponding ribs in anterior view. d2 second dorsal vertebra, r2 second dorsal rib, r3 third dorsal rib, r4 fourth dorsal rib.

opencc-by-4.0Nov 2022View details →
zenodo40/100

Fig. 3 in A non-avian dinosaur with a streamlined body exhibits potential adaptations for swimming

Fig. 3 Postcranial elements and phylogenetic position of Natovenator polydontus (MPC-D 102/114, holotype). a Anterior cervical vertebrae in left lateral view. b Axis and third cervical vertebra in dorsal view. c Fourth cervical vertebra in dorsal view. d Posterior cervical vertebrae in right lateral view. e Dorsal series in right lateral view. f Anterior caudal vertebrae in right lateral view. g Left forearm elements in medial view and manus in ventral view. h Right foot in ventral view. i Phylogenetic position of Natovenator in Dromaeosauridae. Numbers at each node indicate Bremer support values. at atlas, c3 third cervical vertebra, c4 fourth cervical vertebra, c7 seventh cervical vertebra, c9 ninth cervical vertebra, ch chevron, d7 seventh dorsal vertebra, fem femur, mc I metacarpal I, mt III metatarsal III, mt IV metatarsal IV, poz postzygapophysis, prz prezygapophysis, r radius, r7 seventh dorsal rib, ul ulna, I-2 pedal phalanx I-2.

opencc-by-4.0Nov 2022View details →
zenodo40/100

Fig. 2 in A non-avian dinosaur with a streamlined body exhibits potential adaptations for swimming

Fig. 2 Skull of Natovenator polydontus (MPC-D 102/114, holotype). a–d Skull in left lateral (a), right lateral (b), dorsal (c), and ventral (d) views. e µCTrendered image sliced at the point marked on a, showing a cross-section of the premaxillary and anterior maxillary teeth in dorsal view. f Micro-computed tomography (µCT) rendered image of the occipital region in posterior view. g µCT-rendered image of the pterygoid and quadrate.?bm possible bite mark, d dentary, f frontal, h humerus, l lacrimal, m5 5th maxillary tooth, mx maxilla, na nasal p parietal, p13 13th premaxillary tooth, pl palatine, pm premaxilla, pop paroccipital process, pt pterygoid, q quadrate, rt replacement tooth, sq squamosal, so supraoccipital.

opencc-by-4.0Nov 2022View details →
dryad40/100

Data to support: Moving beyond heritability in the search for coral adaptive potential

<p><span>Global environmental change is happening at unprecedented rates. Coral reefs are among the ecosystems most threatened by global change. For wild populations to persist, they must adapt. Knowledge shortfalls about corals' complex ecological and evolutionary dynamics, however, stymie predictions about potential adaptation to future conditions. Here, we review adaptation through the lens of quantitative genetics. We argue that coral adaptation studies can benefit greatly from "wild" quantitative genetic methods, where traits are studied in wild populations undergoing natural selection, genomic relationship matrices can replace breeding experiments, and analyses can be extended to examine genetic constraints among traits. Individuals with advantageous genotypes for anticipated future conditions can be identified. Finally, genomic genotyping supports simultaneous consideration of how genetic diversity is arrayed across geographic and environmental distances, providing greater context for predictions of phenotypic evolution at a metapopulation scale.</span></p>

opencc-zeroApr 2023View details →
dryad40/100

Semipermeable species boundaries create opportunities for gene flow and adaptive potential

<p><span>Hybridisation and gene flow can have both deleterious and adaptive consequences for natural populations and species. To better understand the extent of hybridisation in nature and the balance between its beneficial and deleterious outcomes in a changing environment, information on naturally hybridising non-model organisms is needed. This requires the characterisation of the structure and extent of natural hybrid zones. Here we study natural populations of five keystone mound-building wood ant species in the <em>Formica</em> <em>rufa</em> group across Finland. No genomic studies across the species group exist, and the extent of hybridisation and genomic differentiation in sympatry is unknown. Combining genome-wide and morphological data, we demonstrate more extensive hybridisation than was previously detected between all five species in Finland. Specifically, we reveal a mosaic hybrid zone between <em>F. aquilonia, F. rufa </em>and<em> F. polyctena</em>, comprising further generation hybrid populations. Despite this, we find that <em>Formica rufa, F. aquilonia, F. lugubris, </em>and<em> F. pratensis</em> form distinct gene pools in Finland. We also find that hybrids occupy warmer microhabitats than the non-admixed populations of cold-adapted F. aquilonia, and suggest that warm winters and springs, in particular, may benefit hybrids over <em>F. aquilonia</em>, the most abundant <em>F. rufa</em> group species in Finland. In summary, our results indicate that extensive hybridisation may create adaptive potential that could promote wood ant persistence in a changing climate. Additionally, they highlight the potentially significant ecological and evolutionary consequences of extensive mosaic hybrid zones, within which independent hybrid populations face an array of ecological and intrinsic selection pressures.</span></p>

opencc-zeroMay 2023View details →
dryad40/100

Data from: Can extreme climatic events induce shifts in adaptive potential? A conceptual framework and empirical test with Anolis lizards

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publicOct 2022View details →
dryad40/100

Semipermeable species boundaries create opportunities for gene flow and adaptive potential

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publicMay 2023View details →
dryad40/100

Data to support: Moving beyond heritability in the search for coral adaptive potential

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publicApr 2023View details →
dryad40/100

Comparative genomic analysis identifies potential adaptive variation in Mycoplasma ovipneumoniae

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publicJun 2024View details →
dryad40/100

Prey diversity constrains the adaptive potential of predator foraging traits

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publicNov 2021View details →
dryad40/100

Range-wide climate risk and adaptive potential in an iconic cold-water species (Part 2/2)

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publicOct 2025View details →
dryad40/100

Range-wide climate risk and adaptive potential in a cold-water fish species (Part 1/2)

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publicOct 2025View details →
dryad40/100

Potential local adaptation in populations of invasive reed canary grass (Phalaris arundinacea) across an urbanization gradient

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publicSep 2022View details →
dryad36/100

Adaptation potential of the copepod Eurytemora affinis to a future warmer Baltic Sea

<p>To predict effects of global change on zooplankton populations, it is important to understand how present species adapt to temperature and how they respond to stressors interacting with temperature. Here we ask if the calanoid copepod <i>Eurytemora affinis</i> from the Baltic Sea can adapt to future climate warming. Populations were sampled at sites with different temperatures. Full sibling families were reared in the lab and used in two common garden experiments (1) populations crossed over 3 temperature treatments 12, 17 and 22.5°C and (2) populations crossed over temperature in interaction with salinity and algae of different food quality.<br> Genetic correlations of the full siblings' development time were not different from zero between 12°C and the two higher temperatures 17 °C and 22.5°C, but positively correlated between 17 °C and 22.5°C. Hence, a population at 12 °C is unlikely to adapt to warmer temperature, while a population at ≥ 17 °C can adapt to an even higher temperature, i.e. 22.5 °C. In agreement with the genetic correlations, the population from the warmest site of origin had comparably shorter development time at high temperature than the populations from colder sites, that is, a co-gradient variation. The population with the shortest development time at 22.5°C had in comparison lower survival on low quality food, illustrating a cost of short development time. Our results suggest that populations from warmer environments can at present indirectly adapt to a future warmer Baltic Sea, whereas populations from colder areas show reduced adaptation potential to high temperatures, simply because they experience an environment that is too cold.</p>

opencc-zeroMar 2021View details →
dryad36/100

Data from: Substantially adaptive potential in polyploid cyprinid fishes: evidence from biogeographic, phylogenetic and genomic studies

<p>Whole genome duplication is commonly believed to play key roles in vertebrate evolution. However, nowadays polyploidy exists in a few fish, amphibian, and reptile groups only, and seems to be an evolutionary dead-end in vertebrates. We investigate the evolutionary significance of polyploidization in Cyprinidae – a fish family that contains more polyploid species than any other vertebrate groups with integrating biogeographic, phylogenetic, and genomic analyses. First, polyploid species are found to be significantly frequent in higher altitude and lower mean annual temperature areas compared to diploid species in Cyprinidae. Second, a polyploidy-related diversification rate shift is observed in Cyprinidae. It is that increased net diversification rate is only seen in three polyploid lineages, and other polyploid lineages have similar net diversification rate as well as diploid lineages in Cyprinidae. Interestingly, significant 'lag-times' existed between polyploidization and radiation in Cyprinidae. Multiple polyploid lineages were established ~15 Mya through recurrent allopolyploidization events but net diversification rate did not start to increase until ~5 Mya – long after polyploidization events. Environmental changes associated with the continuous uplift of Tibetan Plateau and climate change have likely promoted the initial establishment and subsequent radiation of polyploidy in Cyprinidae. Finally, unique retention of duplicated genes in polyploid cyprinids adapted to harsh environments is found. Taken together, our results suggest that polyploidy in Cyprinidae is far more than an evolutionary dead-end, but rather shows substantially adaptive potential. Polyploid cyprinids thus constitute an ideal model system for unveiling largely unexplored consequences of whole genome duplication in vertebrates, from genomic evolution to species diversification.</p>

opencc-zeroApr 2020View details →

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allen-brain-atlas
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Last verified 2026-04-30Open record

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abode-home-cage
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Last verified 2026-04-30Open record

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dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

OpenNeuro

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openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record