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The prevailing hypothesis posits that this spike may be, at least in part, a passive mathematical artifact: removing primary-head contributions collapses signal variance in the residual stream, which triggers LayerNorm scaling changes. These LayerNorm-induced changes can raise a target token’s attention probability when competing logits shift downward or shift less favorably. Disentangling this passive denominator effect from target-directed pre-softmax logit changes has remained methodologically elusive under standard causal tracing.\n\nWe introduce the Frozen Attention Logit Intervention, a surgical counterfactual technique that isolates the dynamic, ablation-induced pre-softmax logit of a single target token while simultaneously freezing all non-target pre-softmax logits to their clean-run baseline values. This construction eliminates the confound of background denominator inflation, yielding a counterfactual attention probability that reflects target-logit attention contributions. We apply this method to GPT-2 Small on a cohort of 200 Indirect Object Identification (IOI) prompts, evaluating all 144 attention heads across 12 layers.\n\nOur principal finding is that in GPT-2 Small on a 200-example mixed-template IOI cohort, ablating L9H9 and L10H0 induces a robust L10H10 increase in IO-directed attention. This effect survives zero, mean, and resample ablation controls. Path-stable FALI/Shapley decomposition shows that the attention increase is dominated by the IO-target attention-logit contribution, while background-logit changes oppose the spike on average. QK decomposition suggests the IO-target score increase is primarily query-driven and largely cosine-alignment-driven. Output mediation shows that the L10H10 attention-pattern change causally contributes to IO-S logit recovery under this intervention, explaining about 43.6% of L10H10’s zero-ablation degradation by aggregate ratio of means. We keep this evidence separate from the LayerNorm-scale freezing diagnostic, which shows that under the Layer-10 clean-scale intervention, 24.3% of the observed L10H10 attention spike is removed (reducing L10H10's attention delta from +0.1893 to +0.1433). 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We apply this method to GPT-2 Small on a cohort of 200 Indirect Object Identification (IOI) prompts, evaluating all 144 attention heads across 12 layers.\n\nOur principal finding is that in GPT-2 Small on a 200-example mixed-template IOI cohort, ablating L9H9 and L10H0 induces a robust L10H10 increase in IO-directed attention. This effect survives zero, mean, and resample ablation controls. Path-stable FALI/Shapley decomposition shows that the attention increase is dominated by the IO-target attention-logit contribution, while background-logit changes oppose the spike on average. QK decomposition suggests the IO-target score increase is primarily query-driven and largely cosine-alignment-driven. Output mediation shows that the L10H10 attention-pattern change causally contributes to IO-S logit recovery under this intervention, explaining about 43.6% of L10H10’s zero-ablation degradation by aggregate ratio of means. We keep this evidence separate from the LayerNorm-scale freezing diagnostic, which shows that under the Layer-10 clean-scale intervention, 24.3% of the observed L10H10 attention spike is removed (reducing L10H10's attention delta from +0.1893 to +0.1433). 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The findings provide insight into the way judges interact with expert information.","descriptionType":"Abstract"}],"geoLocations":[],"fundingReferences":[],"url":"https://dataverse.harvard.edu/citation?persistentId=doi:10.7910/DVN/JMARDN","contentUrl":null,"metadataVersion":1,"schemaVersion":"http://datacite.org/schema/kernel-4","source":"mds","isActive":true,"state":"findable","reason":null,"viewCount":0,"downloadCount":0,"referenceCount":0,"citationCount":0,"partCount":0,"partOfCount":0,"versionCount":0,"versionOfCount":0,"created":"2026-05-01T17:47:12Z","registered":"2026-05-20T22:41:06Z","published":null,"updated":"2026-05-20T22:41:06Z"},"relationships":{"client":{"data":{"id":"gdcc.harvard-dv","type":"clients"}}}},{"id":"10.5281/zenodo.13699602","type":"dois","attributes":{"doi":"10.5281/zenodo.13699602","identifiers":[],"creators":[{"name":"Medina, Iliana","nameType":"Personal","givenName":"Iliana","familyName":"Medina","affiliation":[{"name":"The University of 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L.","nameType":"Personal","givenName":"Kate D. L.","familyName":"Umbers","affiliation":[{"name":"Western Sydney University","schemeUri":"https://ror.org","affiliationIdentifier":"https://ror.org/03t52dk35","affiliationIdentifierScheme":"ROR"}],"nameIdentifiers":[]},{"name":"Venton, Molly","nameType":"Personal","givenName":"Molly","familyName":"Venton","affiliation":[{"name":"Swansea University","schemeUri":"https://ror.org","affiliationIdentifier":"https://ror.org/053fq8t95","affiliationIdentifierScheme":"ROR"}],"nameIdentifiers":[]},{"name":"Vitosovich, Mackenzie","nameType":"Personal","givenName":"Mackenzie","familyName":"Vitosovich","affiliation":[{"name":"University of Auckland","schemeUri":"https://ror.org","affiliationIdentifier":"https://ror.org/03b94tp07","affiliationIdentifierScheme":"ROR"}],"nameIdentifiers":[]},{"name":"Wang, Lu-Yi","nameType":"Personal","givenName":"Lu-Yi","familyName":"Wang","affiliation":[{"name":"The University of Melbourne","schemeUri":"https://ror.org","affiliationIdentifier":"https://ror.org/01ej9dk98","affiliationIdentifierScheme":"ROR"}],"nameIdentifiers":[]},{"name":"Weil, Sarah-Sophie","nameType":"Personal","givenName":"Sarah-Sophie","familyName":"Weil","affiliation":[{"name":"Swansea University","schemeUri":"https://ror.org","affiliationIdentifier":"https://ror.org/053fq8t95","affiliationIdentifierScheme":"ROR"}],"nameIdentifiers":[]},{"name":"Allen, William L.","nameType":"Personal","givenName":"William L.","familyName":"Allen","affiliation":[{"name":"Swansea University","schemeUri":"https://ror.org","affiliationIdentifier":"https://ror.org/053fq8t95","affiliationIdentifierScheme":"ROR"}],"nameIdentifiers":[]}],"titles":[{"title":"Data from: Global selection on insect antipredator coloration"}],"publisher":"Dryad","container":{},"publicationYear":2026,"subjects":[{"subject":"camouflage"},{"subject":"aposematism"},{"subject":"crypsis"},{"subject":"Predation","schemeUri":"https://github.com/PLOS/plos-thesaurus","subjectScheme":"PLOS Subject Area Thesaurus"},{"subject":"strategy"},{"subject":"FOS: Biological sciences","schemeUri":"https://web-archive.oecd.org/2012-06-15/138575-38235147.pdf","subjectScheme":"fos"},{"subject":"FOS: Biological sciences","schemeUri":"http://www.oecd.org/science/inno/38235147.pdf","subjectScheme":"Fields of Science and Technology (FOS)"}],"contributors":[{"name":"Australian Research Council","affiliation":[],"contributorType":"Sponsor","nameIdentifiers":[]},{"name":"ARC Centre for Nanoscale BioPhotonics","affiliation":[],"contributorType":"Sponsor","nameIdentifiers":[]}],"dates":[{"date":"2024-09-06T00:18:14Z","dateType":"Created"},{"date":"2025-07-14T14:27:40Z","dateType":"Submitted"},{"date":"2026-05-20T00:00:00Z","dateType":"Issued"},{"date":"2026-05-20T00:00:00Z","dateType":"Available"}],"language":"en","types":{"ris":"DATA","bibtex":"misc","citeproc":"dataset","schemaOrg":"Dataset","resourceType":"dataset","resourceTypeGeneral":"Dataset"},"relatedIdentifiers":[{"relationType":"IsCitedBy","relatedIdentifier":"10.1126/science.adr7368","relatedIdentifierType":"DOI"},{"relationType":"IsDerivedFrom","relatedIdentifier":"10.5281/zenodo.13699591","relatedIdentifierType":"DOI"},{"relationType":"IsDerivedFrom","relatedIdentifier":"10.5281/zenodo.13699591","relatedIdentifierType":"DOI"},{"relationType":"IsSourceOf","relatedIdentifier":"10.5281/zenodo.13699603","relatedIdentifierType":"DOI"},{"relationType":"IsSourceOf","relatedIdentifier":"10.5281/zenodo.13699603","relatedIdentifierType":"DOI"}],"relatedItems":[],"sizes":["5420746 bytes"],"formats":[],"version":"9","rightsList":[{"rights":"Creative Commons Zero v1.0 Universal","rightsUri":"https://creativecommons.org/publicdomain/zero/1.0/legalcode","schemeUri":"https://spdx.org/licenses/","rightsIdentifier":"cc0-1.0","rightsIdentifierScheme":"SPDX"}],"descriptions":[{"description":"Natural selection has repeatedly led to the evolution of two alternative\n antipredator color strategies – camouflage to avoid detection and\n aposematism to advertise unprofitability – but we lack understanding of\n how ecological context favors one strategy over the other. We conducted a\n globally replicated predation experiment at 21 sites on six continents to\n test how predator community, prey community, and visual environment\n influenced predation risk of 15,018 paper ‘moth’ artificial prey with\n cryptic or warning coloration. Results indicated that aposematic\n strategies fare better in low predation intensity environments, while\n camouflage strategies are advantaged when other camouflaged prey species\n are rare and when light levels are low. This study demonstrates how\n multiple mechanisms shape antipredator strategies, helping explain the\n evolution and global distribution of camouflaged and aposematic animals.","descriptionType":"Abstract"},{"description":"We used a standard and well-established field predation paradigm\n where triangular paper ‘moths’ printed with different color patterns and\n attached to a mealworm prey are exposed to free-living predators in\n natural conditions. We deployed three treatments: 1.) typical warning\n color pattern consisting of orange and black stripes surrounded by a black\n border, 2.) atypical warning color pattern that was identically patterned\n and equally conspicuous (see Stimuli) but with the orange replaced by a\n turquoise color atypical of warning coloration, and 3.) a cryptic pattern\n consisting of a fine orange and black checkerboard with the same average\n color and lightness as the typical warning treatment, but having a brown\n appearance. To ensure all predators globally would be required to make\n similar generalizations about the warning treatments’ potential defenses,\n the warning color pattern was designed to have some general features\n typical of many aposematic lepidopteran species found globally, but not\n closely mimic any specific species. Based on effect sizes of previous\n experiments using this paradigm, anticipated predator learning rates, and\n how many targets could be placed and checked by experimenters in the time\n available, at each location, 720 targets (240 per treatment, 90 per day)\n were tested.","descriptionType":"Methods"},{"description":"# Data from: Global selection on insect antipredator coloration\n [https://doi.org/10.5061/dryad.8931zcs0j](https://doi.org/10.5061/dryad.8931zcs0j) Predation dataset for global experiment across 21 locations using three types of palatable targets (mealworms). We also present an alternative version of the experiment using unpalatable prey. All analyses are attached in the code.  ## Description of the data and file structure **Main dataset:**  dataset_survival_tot_2026_excel_dryad.xlsx This dataset contains all the raw predation data on whether targets were attacked or censored and the survival times (15,018 targets). All locations are included and description of each of the columns has been added in a metadata sheet and below. The datafile contains **empty cells** because not all targets were photographed, only the photographed targets have values in photo-dependent measurements and only targets with multiple photos through the day have data on variation in photo measurements between photos. | Variable | Description | | :------------------------------- | :------------------------------------------------------------------------------------------------------------------------------------ | | **id** | Unique identification for each target with location and block information | | **Location** | Location were the experiment was performed | | **TargetID** | Individual target ID that was created by the local team | | **Treatment** | Treatment colour of the target: A= Aposematic, B=Atypical warning colour, C=Camouflage | | **BlockNumber** | Day that the event data was collected | | **SurvTime** | Time of the day when the target was either taken or considered to be censored | | **Status** | 1= taken, 0= censored | | **Censored\\_Streamlined** | Few categories for censoring: Survived or whether taken by a non-avian predator | | **Censored\\_Original** | Original information that came with each target | | **date** | Date when the block was run | | **PhotoID\\_start** | ID of photo at beginning | | **illum\\_start** | Illumination of start photo | | **sal\\_NS\\_start** | Salience of start photo | | **PhotoID\\_noon** | ID of photo at noon | | **illum\\_noon** | Illumination at noon photo | | **sal\\_NS\\_noon** | Salience at noon photo | | **PhotoID\\_sunset** | ID of photo at sunset | | **illum\\_sunset** | Illumination at sunset photo | | **sal\\_NS\\_sunset** | Salience at sunset photo | | **PhotoID\\_sunrise** | ID of photo at sunrise | | **illum\\_sunrise** | Illumination at sunrise photo | | **sal\\_NS\\_sunrise** | Salience at sunrise photo | | **predation\\_rate** | Predation rate calculated from last mealwork block | | **temp\\_seasonality** | Temperature seasonality calculated from bioclim variable | | **blue\\_species\\_count** | Number of species categorised as blue | | **blue\\_species\\_percentage** | Percentage of species categorised as blue | | **cryptic\\_species\\_count** | Number of species categorised as cryptic | | **cryptic\\_species\\_percentage** | Percentage of species categorised as cryptic | | **warning\\_species\\_count** | Number of species categorised as warning | | **warning\\_species\\_percentage** | Percentage of species categorised as warning | | **ratioCrypticWarning** | Number of species categorised as cryptic divided by species classified as warning | | **ratioWarningCryptic** | Number of species categorised as warning divided by species classified as cryptic | | **log\\_mean\\_illum** | Log of the mean of the illumination at start photos for each location | | **sd\\_log\\_illum** | standard deviation across photos at noon for each location | | **mean\\_sal** | mean of the salience at noon photos for each location | | **sd\\_sal** | standard deviation of salience across photos at noon for each location | | **n** | Number of photos used to calculate the mean values of illumination and salience per location | | **log\\_mean\\_illum\\_noon** | Log of the mean of the illumination at noon photos for each location. THIS IS THE VARIABLE THAT WAS USED | | **local\\_cv\\_illum** | standard deviation across photos at noon for each location | | **TransectLenghtKm** | Transect length for each location | | **InsectivoreAbundance** | Abundance but only for species classified as insectivores | | **InsectivoresPerKm** | Insectivore species standarised for transect length. We use this variable as density of insectivorous predators. | | **InsectivoreSpeciesNumber** | Number of insectivore species | | **InsectivoreShannonDiversity** | Shannon diversity index for insectivore species only. We use this variable as predator diversity. | | **Latitude** | Latitude of location | | **Sp60ProIndiv** | Specialisation index where species are considered specialists with 60% of insect prey in diet but considering the individuals | | **cv\\_illum\\_time** | variation in illumination across photos for each target | | **log\\_cv\\_sal\\_time** | variation in salience across photos for each target (log transformed) | | **match\\_illum** | value of illumination for the last photo before the target was taken (i.e. if target taken at noon, then it would be the start photo) | | **match\\_sal** | value of salience for the last photo before the target was taken (i.e. if target taken at noon, then it would be the start photo) | | **minutes** | Minute of the day when the status check was done and when target was considered taken or censored | **Second dataset:** dataset_unpalatable_experiment_2026.xlsx This dataset contains the raw predation data for the alternative experiment in the Czech Republic that used unpalatable mealworms. The column description is the same as in the main dataset (variables described above). The data file contains **empty cells** because not all targets were photographed; only the photographed targets have values in photo-dependent measurements, and only targets with multiple photos through the day have data on variation in photo measurements between photos. *code_times* Concatenated value of location and time of check  *location* location and type of experiment (CZ_unpalatable is the unpalatable version and Czech_Republic, with palatable prey, same value as in large dataset).  *Palatability* U - Unpalatable P- Palatable *TargetID* ID of the target (treatment and number) *Treatment* Treatment colour of the target: A= Aposematic, B=Atypical warning colour, C=Camouflage *BlockNumber* Day that the event data was collected *Survtime* Time of the day when the target was either taken or considered to be censored *Status* 1= Taken 0=Censored *StatusB* Censoring those targets that had been taken during night *minutes* Minute of the day when the status check was done and when the target was considered taken or censored **Third dataset:**  Location_level_data_GACN_2025.csv This dataset contains the location-level information for each of the 21 locations. Latitude and longitude used for the plots is also included (lat*_b, Lon_b).* Column description is the same as in the metadata sheet in the main dataset (also presented above), and values are also the same but summarised per locality. **Fourth dataset:**  BirdSurveyLocations_2026.xls This dataset compiles all the information from the bird surveys in each location and the indices and variables calculated from the bird survey data that were used in posterior analyses. The column description is in a second sheet in the same file, and below: *Location*: Location names. *TransectLenghtKm*: Lengths of transects as reported by location teams. *TotalBirdAbundance*: Total abundances of all birds recorded at particular locations calculated following the BTO Breeding Bird Survey protocol (Newson et al. 2008) as maximum total counts of each species from the two bird surveys carried out. *TotalBirdSpeciesNumber*: Numbers of all bird species recorded at particular locations. *PredatorAbundance*: Total abundances of birds recorded at particular locations that are classicied as at least partly insectivorous predators. The classification is based on the Elton Traits database (Wilman et al. 2014). This metric filters out the species that are unlikely to be predators of experimental targets (such as specialised granivores or aerial hawkers). *PredatorSpeciesNumber*: Numbers of at least partly insectivorous bird species recorded at particular locations. *PredatorsPerKm*: Abundances of at least partly insectivorous birds recorded at particular locations standardised per 1 km of the transect. *PredatorShannonDiversity*: Shannon Diversity Index based on abundances of at least partly insectivorous species. *Insectivore60ProIndiv*: Proportions of bird individuals recorded at particular locations that belong to specialist insectivorous species based on the criterion of having at least 60% of the diet consisting of invertebrates according to Elton Traits database (Wilman et al. 2014). *Team Experience*: Team experience with bird identification in the field based on self-assessment (four-grade scale: 1 = highly expert, 4 = familiar with common species). *SurveyObservers*: Number of observers that carried out the bird survey. **Fifth dataset:**  SuppDataLocationsMaxNumSpecGen_2025B.xls This dataset contains the raw information from the bird survey experiments with the names of all species detected in each of the locations. The column description is in a second sheet in the same file and below: *Location*: Location names. *BinomialName*: EltonTraits Binomial names of species as they appear in the Elton Traits database (Wilman et al. 2014). The species names are unified across all locations, with synonyms included in brackets. *MaxNumber*: Total species abundances at each location calculated following the BTO Breeding Bird Survey protocol (Newson et al. 2008) as maximum total counts from the two bird surveys carried out. *AvianPredator*: Classification of avian species as at least partly insectivorous predators based on the Elton Traits database (Wilman et al. 2014) to filter out the species that are unlikely to be responsible for the predation of experimental targets (such as specialised granivores or aerial hawkers). *Insectivore60*: Classification of species as insectivorous specialists based on the criterion of having at least 60% of the diet consisting of invertebrates according to Elton Traits database (Wilman et al. 2014). **Mealworm analysis:** mealworm_analysis.csv Supplementary dataset with descriptive information on the size of the mealworms used per block and the weather description.  *location*: Location where data was collected *block*: Number of day of data collection *date*: Date of data collection *sunrise*: Sunrise time *sunset*: Sunset time *mealworm_length*: average length of mealworms for that block in mm *start_time*: time of first deployment *start_weather*: weather at first deployment *start_orig_weather*: weather in detail (original) *noon_time*: time of check at noon *noon_weather*: weather at second check *noon_orig_weather*: weather at second check (original) *sunset_time*: time of check at sunset *sunset_weather*: weather at third check *sunset_orig_weather*: weather at third check (original) *sunrise_time*: time of last check at sunrise *sunrise_weather*: weather at last check *sunrise_orig_weather*: weather at last check (original) ## Code/Software R markdown files with the description of the analyses and the instructions to build the plots are presented.  Main analyses were generated using the GACN_final_code_streamlined.rmd ## Additional files: Videos of predators attacking and consuming mealworms from the targets presented.","descriptionType":"TechnicalInfo"}],"geoLocations":[],"fundingReferences":[{"schemeUri":"https://ror.org","funderName":"Australian Research Council","awardNumber":"DE200100500","funderIdentifier":"https://ror.org/05mmh0f86","funderIdentifierType":"ROR"},{"schemeUri":"https://ror.org","funderName":"Coordenação de Aperfeicoamento de Pessoal de Nível Superior","funderIdentifier":"https://ror.org/00x0ma614","funderIdentifierType":"ROR"},{"schemeUri":"https://ror.org","funderName":"The University of Melbourne","funderIdentifier":"https://ror.org/01ej9dk98","funderIdentifierType":"ROR"},{"schemeUri":"https://ror.org","funderName":"National Research Foundation of Korea","awardNumber":"RS-2024-00333709","funderIdentifier":"https://ror.org/013aysd81","funderIdentifierType":"ROR"},{"schemeUri":"https://ror.org","funderName":"Australian Research 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Engineering Research Council","funderIdentifier":"https://ror.org/01h531d29","funderIdentifierType":"ROR"},{"schemeUri":"https://ror.org","funderName":"Natural Environment Research Council","funderIdentifier":"https://ror.org/02b5d8509","funderIdentifierType":"ROR"},{"schemeUri":"https://ror.org","funderName":"Czech Science Foundation","funderIdentifier":"https://ror.org/01pv73b02","funderIdentifierType":"ROR"},{"schemeUri":"https://ror.org","funderName":"Coordenação de Aperfeicoamento de Pessoal de Nível Superior","funderIdentifier":"https://ror.org/00x0ma614","funderIdentifierType":"ROR"},{"schemeUri":"https://ror.org","funderName":"Seoul National University","funderIdentifier":"https://ror.org/04h9pn542","funderIdentifierType":"ROR"}],"url":"https://datadryad.org/dataset/doi:10.5061/dryad.8931zcs0j","contentUrl":null,"metadataVersion":0,"schemaVersion":"http://datacite.org/schema/kernel-4","source":"mds","isActive":true,"state":"findable","reason":null,"viewCount":0,"downloadCount":5,"referenceCount":0,"citationCount":0,"partCount":0,"partOfCount":0,"versionCount":0,"versionOfCount":0,"created":"2026-05-20T08:28:06Z","registered":"2026-05-20T08:28:07Z","published":null,"updated":"2026-05-20T08:28:07Z"},"relationships":{"client":{"data":{"id":"dryad.dryad","type":"clients"}}}},{"id":"10.5061/dryad.47d7wm3vc","type":"dois","attributes":{"doi":"10.5061/dryad.47d7wm3vc","identifiers":[],"creators":[{"name":"Turner, Mark","nameType":"Personal","givenName":"Mark","familyName":"Turner","affiliation":[{"name":"Oklahoma State University","schemeUri":"https://ror.org","affiliationIdentifier":"https://ror.org/01g9vbr38","affiliationIdentifierScheme":"ROR"}],"nameIdentifiers":[{"schemeUri":"https://orcid.org","nameIdentifier":"https://orcid.org/0009-0002-7844-4018","nameIdentifierScheme":"ORCID"}]}],"titles":[{"title":"Influence of temperature, landscape, and fine-scale forage availability on ungulate morphometrics"}],"publisher":"Dryad","container":{},"publicationYear":2026,"subjects":[{"subject":"FOS: Biological sciences","schemeUri":"https://web-archive.oecd.org/2012-06-15/138575-38235147.pdf","subjectScheme":"fos"},{"subject":"FOS: Biological sciences","schemeUri":"http://www.oecd.org/science/inno/38235147.pdf","subjectScheme":"Fields of Science and Technology (FOS)"},{"subject":"white-tailed deer"},{"subject":"antler size"},{"subject":"harvest data"}],"contributors":[],"dates":[{"date":"2026-02-13T18:00:46Z","dateType":"Created"},{"date":"2026-02-13T18:01:12Z","dateType":"Submitted"},{"date":"2026-03-11T00:00:00Z","dateType":"Issued"},{"date":"2026-03-11T00:00:00Z","dateType":"Available"}],"language":"en","types":{"ris":"DATA","bibtex":"misc","citeproc":"dataset","schemaOrg":"Dataset","resourceType":"dataset","resourceTypeGeneral":"Dataset"},"relatedIdentifiers":[{"relationType":"IsCitedBy","relatedIdentifier":"10.1002/ecs2.70632","relatedIdentifierType":"DOI"}],"relatedItems":[],"sizes":["9543 bytes"],"formats":[],"version":"1","rightsList":[{"rights":"Creative Commons Zero v1.0 Universal","rightsUri":"https://creativecommons.org/publicdomain/zero/1.0/legalcode","schemeUri":"https://spdx.org/licenses/","rightsIdentifier":"cc0-1.0","rightsIdentifierScheme":"SPDX"}],"descriptions":[{"description":"Abiotic and biotic variables strongly influence morphological variation in\n wildlife, but there is disagreement on the relative importance of various\n factors. Primary competing hypotheses regarding drivers of interpopulation\n animal morphology include those related to heat regulation and those\n related to forage availability. Despite data to support both hypotheses in\n various systems, few have considered fine-scale forage availability data\n across a large geographic area. White-tailed deer (Odocoileus virginianus)\n body and antler size vary widely across their geographic distribution,\n with larger deer often associated with landscapes providing large amounts\n of high-quality forage. However, there is limited information on the\n influence of temperature, landscape, and site-specific forage availability\n on deer morphology across a wide geographic area. We collected body mass,\n antler size, and site-specific growing-season forage availability from 35\n locations across 21 eastern U.S. states. Average female body mass\n increased by 1.4 kg for every 1˚C decrease in average annual temperature\n and increased by 1.6 kg for every 10% increase in landscape crop coverage.\n Mature male antler size also correlated with temperature and crop\n coverage, with antler size increasing 4.9 cm for every 1˚C decrease in\n average annual temperature and increasing 7.1 cm for every 10% increase in\n landscape crop coverage. After controlling for landscape effects, adult\n female mass was correlated with site-specific nutritional carrying\n capacity based on a 0.3% phosphorus constraint (P NCC), with average\n female body mass increasing 0.15 kg for every 1 deer day/ha increase in P\n NCC. Male antler size was marginally correlated with P NCC as well, with\n antler size increasing 0.7 cm for every 1 deer day/ha increase in P NCC.\n Our results support the Resource Rule at the local scale, but temperature\n and landscape factors contribute to interpopulation variation in\n morphology across broad spatial scales.","descriptionType":"Abstract"},{"description":"# Influence of temperature, landscape, and fine-scale forage availability\n on ungulate morphometrics Dataset DOI:\n [10.5061/dryad.47d7wm3vc](https://doi.org/10.5061/dryad.47d7wm3vc) ##\n Description of the data and file structure These deer harvest and forage\n availability data were collected on 35 properties across the eastern U.S.\n ### Files and variables #### File: Deer_morphology_analysis.R\n **Description:**  #### File: Deer_morphology_data.csv **Description:** \n ##### Variables * Site: Site number * cpNCCha: Deer nutritional carrying\n capacity in deer days per ha using a 14% crude protein constraint *\n pNCCha: Deer nutritional carrying capacity in deer days per ha using a\n 0.3% phosphorus constraint * energyperha: Deer nutritional carrying\n capacity in deer days per ha using a 1.96 kcal digestible energy\n constraint * biomassperha: Deer forage biomass in kg per ha *\n Adultdoeweightkg: Average adult doe live (whole) weight *\n Estimatedmaturescorecm: Average antler score of mature (5.5+) males in cm\n * Forested10: Percent forested NLCD landcover within 10 km of the property\n * Pasture10: Percent pasture NLCD landcover within 10 km of the property *\n Crop10: Percent cropland NLCD landcover within 10 km of the property *\n Average temp: Average annual temperature in C * Region3: Assignment into\n three regions: North, Middle, and South * Ha: Property size in ha * crop2:\n Assignment into 2 crop coverage groups: High and Low ## Code/software\n Excel and R","descriptionType":"TechnicalInfo"}],"geoLocations":[],"fundingReferences":[],"url":"https://datadryad.org/dataset/doi:10.5061/dryad.47d7wm3vc","contentUrl":null,"metadataVersion":1,"schemaVersion":"http://datacite.org/schema/kernel-4","source":"mds","isActive":true,"state":"findable","reason":null,"viewCount":13,"downloadCount":3,"referenceCount":0,"citationCount":0,"partCount":0,"partOfCount":0,"versionCount":0,"versionOfCount":0,"created":"2026-03-11T22:40:54Z","registered":"2026-03-11T22:40:55Z","published":null,"updated":"2026-05-19T13:40:48Z"},"relationships":{"client":{"data":{"id":"dryad.dryad","type":"clients"}}}},{"id":"10.6084/m9.figshare.12880592.v14","type":"dois","attributes":{"doi":"10.6084/m9.figshare.12880592.v14","identifiers":[],"creators":[{"name":"Chao, Shiaoman","givenName":"Shiaoman","familyName":"Chao","affiliation":[{"name":"United States Department of 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P","givenName":"Stephen P","familyName":"Baenziger","affiliation":[{"name":"University of Nebraska–Lincoln","schemeUri":"https://ror.org/","affiliationIdentifier":"https://ror.org/043mer456","affiliationIdentifierScheme":"ROR"}],"nameIdentifiers":[]},{"name":"Matnyazov, Rustam","givenName":"Rustam","familyName":"Matnyazov","affiliation":[{"name":"Kansas State University","schemeUri":"https://ror.org/","affiliationIdentifier":"https://ror.org/05p1j8758","affiliationIdentifierScheme":"ROR"},{"name":"Institute of Biochemistry and Genetics of Ufa Scientific Centre","schemeUri":"https://ror.org/","affiliationIdentifier":"https://ror.org/02a9vnt59","affiliationIdentifierScheme":"ROR"}],"nameIdentifiers":[]},{"name":"Clark, Dale R","givenName":"Dale R","familyName":"Clark","affiliation":[],"nameIdentifiers":[]},{"name":"Talbert, Luther E","givenName":"Luther E","familyName":"Talbert","affiliation":[{"name":"Montana State University","schemeUri":"https://ror.org/","affiliationIdentifier":"https://ror.org/02w0trx84","affiliationIdentifierScheme":"ROR"}],"nameIdentifiers":[]},{"name":"Anderson, James A","givenName":"James A","familyName":"Anderson","affiliation":[{"name":"University of Minnesota","schemeUri":"https://ror.org/","affiliationIdentifier":"https://ror.org/017zqws13","affiliationIdentifierScheme":"ROR"}],"nameIdentifiers":[]},{"name":"Dreisigacker, Susanne","givenName":"Susanne","familyName":"Dreisigacker","affiliation":[{"name":"International Maize and Wheat Improvement Center","schemeUri":"https://ror.org/","affiliationIdentifier":"https://ror.org/03gvhpa76","affiliationIdentifierScheme":"ROR"}],"nameIdentifiers":[]},{"name":"Glover, Karl","givenName":"Karl","familyName":"Glover","affiliation":[{"name":"South Dakota State University","schemeUri":"https://ror.org/","affiliationIdentifier":"https://ror.org/015jmes13","affiliationIdentifierScheme":"ROR"}],"nameIdentifiers":[]},{"name":"Chen, Jianli","givenName":"Jianli","familyName":"Chen","affiliation":[{"name":"University of Idaho","schemeUri":"https://ror.org/","affiliationIdentifier":"https://ror.org/03hbp5t65","affiliationIdentifierScheme":"ROR"}],"nameIdentifiers":[]},{"name":"Campbell, Kim","givenName":"Kim","familyName":"Campbell","affiliation":[{"name":"Washington State University","schemeUri":"https://ror.org/","affiliationIdentifier":"https://ror.org/05dk0ce17","affiliationIdentifierScheme":"ROR"}],"nameIdentifiers":[]},{"name":"Bruckner, Phil L","givenName":"Phil L","familyName":"Bruckner","affiliation":[],"nameIdentifiers":[]},{"name":"Rudd, Jackie C","givenName":"Jackie C","familyName":"Rudd","affiliation":[],"nameIdentifiers":[]},{"name":"Haley, Scott","givenName":"Scott","familyName":"Haley","affiliation":[{"name":"Colorado State University","schemeUri":"https://ror.org/","affiliationIdentifier":"https://ror.org/03k1gpj17","affiliationIdentifierScheme":"ROR"}],"nameIdentifiers":[]},{"name":"Carver, Brett F","givenName":"Brett F","familyName":"Carver","affiliation":[{"name":"Oklahoma State University","schemeUri":"https://ror.org/","affiliationIdentifier":"https://ror.org/01g9vbr38","affiliationIdentifierScheme":"ROR"}],"nameIdentifiers":[]},{"name":"Perry, Sid","givenName":"Sid","familyName":"Perry","affiliation":[],"nameIdentifiers":[]},{"name":"Sorrells, Mark E","givenName":"Mark E","familyName":"Sorrells","affiliation":[{"name":"Cornell University","schemeUri":"https://ror.org/","affiliationIdentifier":"https://ror.org/05bnh6r87","affiliationIdentifierScheme":"ROR"}],"nameIdentifiers":[]},{"name":"Akhunov, Eduard D","givenName":"Eduard D","familyName":"Akhunov","affiliation":[{"name":"Kansas State University","schemeUri":"https://ror.org/","affiliationIdentifier":"https://ror.org/05p1j8758","affiliationIdentifierScheme":"ROR"}],"nameIdentifiers":[]}],"titles":[{"title":"Additional file of Population- and genome-specific patterns of linkage disequilibrium and SNP variation in spring and winter wheat (Triticum aestivum L.)"}],"publisher":"figshare","container":{},"publicationYear":2020,"subjects":[{"subject":"Genetics"},{"subject":"FOS: Biological sciences","schemeUri":"http://www.oecd.org/science/inno/38235147.pdf","subjectScheme":"Fields of Science and Technology 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