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Record W6969447861 · doi:10.5281/zenodo.6818945

Tamias alpinus Merriam 1893

2016· article· en· W6969447861 on OpenAlexaboutno aff

Bibliographic record

VenueZenodo (CERN European Organization for Nuclear Research) · 2016
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicGenetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Canadian institutionsnot available
Fundersnot available
KeywordsDeer mouseExtinction (optical mineralogy)Sympatric speciationEyespot

Abstract

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187. Alpine Chipmunk Tamias alpinus French: Tamia de montagne / German: Sierra-Nevada-Backenhornchen / Spanish: Ardilla listada alpina Taxonomy. Tamias alpinus Merriam, 1893, “Big Cottonwood Meadows,...just south of Mount Whitney, altitude 3,050 meters or 10,000 feet,” Tulare County, California, USA. This species is monotypic. Distribution. Higher elevations of the Sierra Nevada in SC California, from Tuolumne to Tulare counties (USA). Descriptive notes. Head-body mean 104-6 mm (males) and 106-4 mm (females), tail mean 69-5 mm (males) and 75-5 mm (females); weight mean 35-8 g. Pelage of the Alpine Chipmunk is pale, with four whitish stripes on dorsum and an orangish venter. Lateral stripes are wide and white, but sometimes pale. The Alpine Chipmunk is smaller than almost all sympatric (or parapatric) species, such as the Yellow-pine Chipmunk (7. amoenus), the Colorado Chipmunk (7. quadrimaculatus), the Shadow Chipmunk (7. senex), the Lodgepole Chipmunk (7. speciosus), and the Uinta Chipmunk (7. wmbrinus). The only exception is the Least Chipmunk (7. minimus). The Alpine Chipmunk can be distinguished from the Least Chipmunk by its shorter tail, larger ears, and skull. Chromosome complement of the Alpine Chipmunk is 2n = 38, FN = 48. Karyotypeis type B for Tamias and consists offive pairs of metacentric autosomes, six pairs of submetacentric autosomes, seven pairs of acrocentric autosomes, a submetacentric X chromosome, and an acrocentric Y chromosome. Habitat. Elevations of ¢.2300-3900 m, primarily in alpine biotic zone but also Hudsonian and Canadian biotic zones. The Alpine Chipmunk is a highly insular species, whose prevalence and occurrence probably depends on the physical structure ofits habitat, which consists primarily of meadows, talus slopes, boulderfields, open stands of lodgepole pine (Pinus contorta, Pinaceae), and small patches of whitebark pine (P. albicaulis). Habitat is generally xeric, as it is exposed to full sun, but maximum daily temperatures do not exceed 20°C. Food and Feeding. Diet of the Alpine Chipmunk consists heavily of small seeds of sedges, grasses, and forbs, with a small amount of pine seeds. Most information on its diet is based on cheek-pouch contents, which can contain up to ¢.5000 seeds, in extreme cases. [tis assumed that the Alpine Chipmunk is a larderhoarder,like other chipmunk species; however, early natural-history observations also suggest scatterhoarding behavior. It is a predator of avian eggs and nestlings, and has been suggested to have limited the breeding distribution of the Asian rosy-finch (Leucosticte arctoa). Breeding. Breeding occurs in early summer, with young becoming active by late July to early August, and reaching adult size by October.Litter size appears to be 4-5 young. Activity patterns. The Alpine Chipmunk is diurnal, and spends a considerable amount of time in rocky areas, which may allow a quick and efficient escape from predators. It is reported to enter hibernacula in late October and emerge in June, when its habitat is still covered in snow. This early emergence allows time for territorial establishment and subsequent foraging during the short growing season in its habitat. Movements, Home range and Social organization. Distribution of the Alpine Chipmunk overlaps with those of five other Tamas species, but only the Lodgepole Chipmunk is fully sympatric with the Alpine Chipmunk. It is territorial, and performs variable aggressive displays toward conspecifics, including vertical tail displays and vocalizations described as high-pitched calls, lower-pitched “chucks” and “chips.” Distribution of the Alpine Chipmunk is limited at lower elevations by territorial exclusion by the larger Lodgepole Chipmunk, which is reported to be more aggressive, more successful in territorial disputes in the wild, and more efficient at foraging in dense vegetation where the two species are sympatric. However, the Alpine Chipmunk in captivity appears more aggressive and dominant over the Lodgepole Chipmunk, which suggests that the outcome of aggressive encounters in the wild is partially influenced by habitat structure. Status and Conservation. Classified as Least Concern on The IUCN Red List. The Alpine Chipmunk can be locally common in some areas but population levels vary. Current population trend is stable. There are no major threats to the Alpine Chipmunk; however, it is restricted to a small area of highlands, which could make it vulnerable to habitat loss and climate change. Bibliography. Clawson et al. (1994a), Davis et al. (2008), Hayssen (2008a, 2008b, 2008c¢), Linzey & Nature-Serve (Hammerson) (2008ai), Piaggio & Spicer (2000), Thorington et al. (2012).

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Not applicable · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: none
Teacher disagreement score0.016
Threshold uncertainty score0.054

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0010.000
Science and technology studies0.0010.000
Scholarly communication0.0000.001
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0160.006

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.023
GPT teacher head0.249
Teacher spread0.226 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designNot applicable
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations0
Published2016
Admission routes1
Has abstractyes

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