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1 ent species (e.g., song sparrow and chipping sparrow).
2 ng aggressive behavior in the white-throated sparrow.
3 n species, namely chicken and white-throated sparrow.
4 t-fledging survival probability for Brewer's Sparrow.
5 ir species, the American robin and the house sparrow.
6 field sparrow from the more aggressive song sparrow.
7 d cerebrosides in the SC compared with mesic sparrows.
8 ty in RA was not altered by deafening in the sparrows.
9 to some degree pre-encoded in white-crowned sparrows.
10 tion typically removes circulating T in tree sparrows.
11 as occurred in the learned songs of Savannah sparrows.
12 into nests may serve a similar function for sparrows.
13 that controls song behavior in white-crowned sparrows.
14 a pedigreed insular population of wild house sparrows.
15 dial amygdala of field sparrows but not song sparrows.
16 the song system in adult male white-crowned sparrows.
17 ain in breeding-condition male white-crowned sparrows 2 days prior to T withdrawal and shifting them
19 ying neural representations of song in swamp sparrows, a species in which juveniles learn and practic
20 nd for communication between neighbors (song sparrows address or reply to a neighbor with a song they
21 ons for a threatened songbird, the saltmarsh sparrow (Ammodramus caudacutus), in a region where sea l
24 rea, dorsal arcopallium, and optic tectum in sparrow and was essentially undetectable in zebra finch.
26 red sources and pathways of lead exposure in sparrows and children, with strong links to contaminatio
28 issue, we castrated adult male white-crowned sparrows and rapidly shifted them to short-day photoperi
30 peckers excavate holes, storks build stacks, sparrows and swallows build cups (but of different mater
31 phrase types characteristic of white-crowned sparrows and, thus, could contribute to innate song reco
37 he suppression of winter aggression in field sparrows, because similar winter differences were found
38 ely to threaten the persistence of saltmarsh sparrows beyond 2060 and could cause extinction as soon
40 We here confirm earlier findings that swamp sparrows categorically perceive the notes that constitut
42 lts from a 20-year study of free-living song sparrows confirm that attractive males contribute more o
43 easonal changes in the song nuclei, the song sparrows continued to sing the same number of different
44 er quality data analysis, the application of SPARROW controls for confounding factors such as hydrolo
45 d susceptibility to infection we observed in sparrows, coupled with their presence in poultry houses,
48 ion (STI) for 10 min in wild adult male song sparrows during the breeding and non-breeding seasons.
50 t common mammal species captured while house sparrows, European starlings, rock pigeons, swallows, an
51 patial behavior across 10 y, we show that i) sparrows exhibit interannual fidelity to winter home ran
54 ensorimotor neurons in freely behaving swamp sparrows expressed categorical auditory responses to cha
55 analyses further identify groups (New World sparrows, finches, and vireos) disproportionally affecte
57 st recognized, or more subordinate levels - 'sparrow', for example - which require additional percept
58 , M. Hashimoto, K. Nakanishi, J. Dillon & J. Sparrow, for the biosynthesis of A2E: (i) condensation o
59 that a certain class of neurons in the swamp sparrow forebrain displays a precise auditory-vocal corr
61 examined the population genetics of 576 song sparrows from 23 populations using seven microsatellite
64 d lipid composition of the SC of adult house sparrows from two populations, one living in the deserts
65 e a northward shift in current White-crowned sparrow habitat range and a 20-60% increase in their pre
69 Here, we review the natural history of house sparrows, highlight what the study of these birds has me
70 In a field study, we show that a young song sparrow (i) selects his songs from three or four older b
71 d to acute myeloid leukemia expression data, SPARROW identifies an apoptotic biomarker (PYCARD) for a
72 We showed previously that in white-throated sparrows, immediate early gene responses in the auditory
77 ent, but iii) this fidelity is weakened when sparrows lose close flockmates from the previous year.
82 r analyses of three decades of complete song sparrow (Melospiza melodia) pedigree data show that mult
83 We fitted animal models to 38 years of song sparrow (Melospiza melodia) phenology and pedigree data
85 therms, we compare 79 genomes from nine song sparrow (Melospiza melodia) subspecies that vary ~300% i
87 e examine song type representations in swamp sparrows (Melospiza georgiana), a multiple song type spe
88 attributes of Area X in wild adult male song sparrows (Melospiza melodia) captured during the spring
91 ed the hypothesis that free-living male song sparrows (Melospiza melodia) show seasonal changes in en
92 c paternity and pedigree data from wild song sparrows (Melospiza melodia) to partition variance in ea
93 illa), which seasonally flock, and male song sparrows (Melospiza melodia), which are territorial year
98 duals from eight islands in an insular house sparrow metapopulation to examine the generality of inbr
100 does not exceed 20 cm, whereas White-crowned sparrows nested only under shrubs between 20 cm and 1 m
103 f the same species (e.g., two different song sparrows) or different species (e.g., song sparrow and c
104 r and immunity covary among individual house sparrows, particularly in females where those birds that
105 ncreases observed in the abundances of house sparrow (Passer domesticus) and spotted dove (Streptopel
106 lobally ubiquitous and human commensal house sparrow (Passer domesticus) can be used as a sentinel of
107 s France, screening populations of the house sparrow (Passer domesticus) for malaria (Plasmodium reli
108 NP-based pedigree from an insular wild house sparrow (Passer domesticus) metapopulation, was used to
110 ly how the propensity of an individual house sparrow (Passer domesticus) to take foraging risks was r
112 ry Campylobacter spp. than adults, and house sparrows (Passer domesticus) and blackbirds (Turdus meru
113 marked females in eight populations of house sparrows (Passer domesticus) from North America and Euro
114 nths to almost 9 years) of free-living house sparrows (Passer domesticus) in two different island pop
115 Patagonia, and across six continents, house sparrows (Passer domesticus) inhabit most human-modified
116 and corticosteroid physiology in wild house sparrows (Passer domesticus, n = 15) would significantly
117 tion: songs composed of single white-crowned sparrow phrases and songs played in reverse elicited voc
123 enile, long-distance migrating white-crowned sparrows rapidly recognize and correct for a continent-w
124 of the SC in desert and mesic nestling house sparrows reared in low and high humidity and compared ou
125 se inhibitors in vivo in adult white-crowned sparrows rescued neurons within the hormone-sensitive so
127 g circuitry was incompletely developed, male sparrows sang less stereotyped songs than males at day 2
129 the BP neural network is optimized with the Sparrow Search Algorithm (SSA), establishing a detection
131 vergence curve is compared to circle chaotic sparrow search algorithm and tent chaos sparrow search a
132 with the predicted results from the SSA, the sparrow search algorithm based on quantum computations a
133 y wolf optimizer, Harris hawks optimization, sparrow search algorithm, hippopotamus optimization algo
134 and extreme point of hysteresis curves, the sparrow search optimization algorithm (SSA) is adopted t
135 as capable of detecting anti-WN IgM in house sparrow serum samples from laboratory-infected birds but
136 able when wild, adult, free-ranging chipping sparrows sing at dawn than when they sing during the day
138 expression data with a novel method, namely SPARROW ( SPAR: se selected exp R: essi O: n regulators
139 show how a migratory songbird, the chipping sparrow (Spizella passerina), achieves prompt and precis
140 brains in spring and winter from male field sparrows (Spizella pusilla), which seasonally flock, and
141 ing species of sagebrush songbirds (Brewer's Sparrow, Spizella breweri; and Sage Thrasher, Oreoscopte
142 were collected from wild ducks, geese, owls, sparrows, swallows, and starlings and from sentinel duck
144 seasonally breeding adult male white-crowned sparrows, the song system nucleus HVC loses approximatel
145 l U.S. Geological Survey water-quality model SPARROW to investigate whether spatial differences in co
148 the sensorimotor nucleus HVC in anesthetized sparrows to assess neuronal responsiveness to songs in t
149 posed estrogen-primed, female white-throated sparrows to conspecific male song and looked for evidenc
150 Waterborne transmission from inoculated sparrows to contact chickens was absent, while 25% of sp
151 We exposed adult male Gambel's white-crowned sparrows to either short-day photoperiod or long-day pho
157 strildidae and a limited number of emberizid sparrows) using antibodies against 10 neuropeptides and
159 ecifically, studying socially foraging house sparrows, we manipulated competition using depleted or n
161 We show that social groups of white-browed sparrow weavers (Plocepasser mahali) build structures (n
162 heses in cooperatively breeding white-browed sparrow weavers (Plocepasser mahali), using a novel high
166 to contact chickens was absent, while 25% of sparrows were infected via waterborne transmission from
170 modium load in naturally infected wild house sparrows with the antimalarial primaquine to assess the
171 o model songbird species, the white-throated sparrow (Zonotrichia albicollis) and zebra finch (Taenio
172 l behavior and plumage in the white-throated sparrow (Zonotrichia albicollis) is linked to an inversi
173 polymorphism (ZAL2(m)) in the white-throated sparrow (Zonotrichia albicollis) is linked to variation
176 dressed this issue in Gambel's white-crowned sparrow (Zonotrichia leucophrys gambelii), a songbird th
177 rder--is such a feature in the white-crowned sparrow (Zonotrichia leucophrys), the authors tutored ma
178 respiratory performance in the White-crowned Sparrow (Zonotrichia leucophrys), which has a migratory
179 ensory systems in experienced white-throated sparrows (Zonotrichia albicollis) captured in southern O
180 ort-term flocks for wintering golden-crowned sparrows (Zonotrichia atricapilla) across three years an
181 We previously found that golden-crowned sparrows (Zonotrichia atricapilla) show consistent flock
182 e studied two populations of rufous-collared sparrows (Zonotrichia capensis) that breed, only 25 km a
183 ive enzyme plasticity in four populations of sparrows (Zonotrichia capensis) to explore the relations
184 rols song behavior in Gambel's white-crowned sparrows (Zonotrichia leucophrys gambelii) and examined
185 aught wild adult male Gambel's white-crowned sparrows (Zonotrichia leucophrys gambelii) during spring
186 r injected in RA of adult male white-crowned sparrows (Zonotrichia leucophrys gambelii) in breeding o
187 mine into HVC of male Gambel's white-crowned sparrows (Zonotrichia leucophrys gambelii) to block seas
189 arius lapponicus) and Gambel's White-crowned sparrows (Zonotrichia leucophrys gambelii) with modeled
192 rs of the HVC in male Gambel's white-crowned sparrows (Zonotrichia leucophrys gambelii): Nissl staini
193 us, HVC of adult male Gambel's white-crowned sparrows (Zonotrichia leucophrys gambelli) nearly 68,000
194 rds (Anolis cristatellus), and white-crowned sparrows (Zonotrichia leucophrys) acquire gut microbiota
197 ays to show that male mountain white-crowned sparrows, Zonotrichia leucophrys oriantha, must learn to