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1 ragers in coastal California from 1999, when feral A. mellifera populations were low due to Varroa de
2  encompassing 12 horticultural groups, and 1 feral accession was sequenced using a combination of sho
3                                              Feral adult female cynomolgus macaques were ovariectomiz
4 ing habits, and mite-biting behavior between feral Africanized honey bees (genomically verified Apis
5    Our analyses indicate that adaptations to feral and domestic environments involve different genomi
6 ses a contagious and often lethal disease of feral and domestic swine.
7 ly reported seroprevalence in SIVsm-infected feral and household pet sooty mangabeys.
8 infections in rural Sierra Leone, where both feral and pet sooty mangabeys harbor divergent members o
9 er as drinking source for poultry, access of feral and wild animals to poultry houses) were associate
10    We analyzed sera from 35 client-owned, 20 feral, and 30 specific pathogen-free (SPF) cats for pre-
11 g genetic data for over 4,000 domestic, semi-feral, and wild canids and behavioral survey data for ov
12  Sequencing and heteroduplex analysis of one feral animal-derived SIV showed a mosaic genome containi
13                                              Feral animals represent an important problem in many eco
14 ttings, studying the brains and behaviors of feral animals, and comparative analyses of feral populat
15 rom exposure to Brucella-infected livestock, feral animals, or wildlife or frequently via consumption
16 ting for two-thirds of the MHC haplotypes in feral animals.
17                          Captive monkeys and feral apes have been reported to only rarely "spontaneou
18 at equids, even those that are introduced or feral, are able to buffer water availability, which may
19 ent blood cultures from a woman and from two feral barn cats.
20 structure, and cannabinoid profile of the US feral Cannabis collection provides critical information
21                 To maximize the potential of feral Cannabis germplasm, determining the genetic struct
22             To resolve this, a collection of feral Cannabis, comprising 760 plants across twelve US s
23 t litter, keeping cats indoors, reducing the feral cat population, and protecting the play areas of c
24 tion by introduced species, particularly the feral cat, Felis catus, and European red fox, Vulpes vul
25                                 Five trapped feral cats were euthanized, four diagnosed with advanced
26                                A total of 40 feral cats were trapped, 20 males and 20 females, mostly
27  example of dwarfing of a large mammal - the feral cattle of Amsterdam Island, southern Indian Ocean,
28                The origins and uniqueness of feral cattle on Chirikof Island, Alaska, are uncertain.
29  possibility of introgression events between feral chickens and the wild chickens in areas surroundin
30 We have previously shown that Kauai Island's feral chickens are a highly variable and admixed populat
31        Previous studies have shown these now feral chickens are an admixed population between Red Jun
32 nments involve different genomic regions and feral chickens show some evidence of adaptation at genes
33  intestinal tract of free-range, broiler and feral chickens.
34 ed to reconstruct in vitro the microbiota of feral chickens.
35 he cannabinoid genotyping assay resolved the feral collections into Type I - B2/B2 (6%), Type II - B2
36  ecological changes in weedy environments if feral crop plants or hybrids formed with compatible weed
37  salmonids could favour admixed over wild or feral crosses if an inbreeding avoidance mechanism is pr
38 of bovine origin, but isolates from badgers, feral deer, sheep, humans, and a pig were included.
39 hirsutum are challenging to distinguish from feral derivatives, and truly wild populations are uncomm
40 3.7%; P=.0005), suggesting that they are not feral descendants of hospital isolates.
41  an infectious cell line circulating in many feral dog populations.
42      Homologous DRB exon 2 sequences from 36 feral domestic cats throughout the world plus from three
43 ed from 35 genera of animals that were wild, feral, domesticated, or otherwise held captive in the Un
44 ar predation corresponds with differences in feral donkey behaviour and associated effects on desert
45                                Focusing on a feral donkey population in the Death Valley National Par
46 n the first documented predation of juvenile feral donkeys Equus africanus asinus by cougars Puma con
47  reveal a trophic cascade involving cougars, feral equids and vegetation.
48 , digging of 2-meter wells to groundwater by feral equids increased the density of water features, re
49                                              Feral fish outnumber wild populations, leading to a poss
50 enic activity measured in water extracts and feral fish that have been shown to be in population decl
51                              Weedy rice is a feral form of rice that infests paddies worldwide and ag
52 nd the challenge of distinguishing them from feral forms.
53                  Here we show that in female feral fowl most copulations are coerced, and that female
54 investigated male reproductive senescence in feral fowl, Gallus gallus domesticus, where socially dom
55 n, artificial selection, and gene flow shape feral genomes, traits, and fitness.
56                     Notably, the Montecristo feral goat showed the highest number of HRR islands desp
57 ction and spatial memory affect space use of feral hogs (Sus scrofa).
58                                       Though feral hogs may not be of conservation concern, these ani
59 riments, and mathematical models to show how feral hogs reduce resilience in southeastern US salt mar
60 or mite is a parasitic threat to managed and feral honey bee colonies around the world.
61                                 In contrast, feral honey bees have developed multiple ways to counter
62 were positively associated with proximity to feral honeybee (Apis mellifera) hives, suggesting potent
63                     Therefore, the resulting feral honeybee population of south Texas was best viewed
64                                  We followed feral horses (Equus caballus) in three populations for a
65 chanisms which may underlie such patterns in feral horses, and perhaps, wild herbivores more generall
66 s, fruit flies, pipefish, wild mallards, and feral house mice.
67 SA SSTI at SUH were more likely to represent feral isolates of nosocomial origin.
68              Here we map selective sweeps in feral Kauai chickens using whole-genome sequencing.
69                                              Feral livestock may harbor genetic variation of commerci
70 Analysis of gag region sequences showed that feral mangabeys in one small troop harbored four distinc
71 e present in free-living barn populations of feral mice and pet store mice with diverse microbial exp
72                               Cohousing with feral mice changed the bacterial colonization of laborat
73 germ-free mice, a complete lack of data from feral mice, and an unclear relationship between AIMT cel
74                            MMMol, a Japanese feral mouse cell line, is an exception in that these cel
75 re, Hampshire, breeds of Chinese origin, and feral Pacific Island populations were identified.
76  community over a ~25 year chronosequence of feral pig removal in tropical montane wet forests on the
77 s the need for localized strategies based on feral pig social behaviour to enhance global control eff
78  color variants of their principal prey, the feral pigeon Columba livia, presumably because targeting
79 reeds have made substantial contributions to feral pigeon populations.
80           Several plumage types are found in feral pigeons (Columba livia), but one type imparts a cl
81 nd oropharyngeal swabs of clinically healthy feral pigeons captured in Durban, KwaZulu-Natal Province
82 e detection of novel gammacoronaviruses from feral pigeons in South Africa and propose revisions to t
83 wild rock dove, the ancestor of domestic and feral pigeons.
84 ect of plumage coloration on the survival of feral pigeons.
85                          Nonnative, invasive feral pigs (Sus scrofa) modify habitats by disturbing so
86 NA was amplified from one farmed pig and two feral pigs and characterized by nucleotide sequencing to
87 g the social interactions of 146 GPS-tracked feral pigs in Australia using a proximity-based social n
88                    As such, we conclude that feral pigs influence overall bacterial community diversi
89                                              Feral pigs threaten biodiversity in 54 countries and cau
90 ty, which decreases following the removal of feral pigs, was a useful predictor of dissimilarity amon
91 ancestral gene pool currently represented by feral plants and landraces in China.
92 mporal changes in the genetic structure of a feral population from the southern United States undergo
93 n gut microbiome variation and survival in a feral population of horses under natural food limitation
94 estes size) is associated with T levels in a feral population of Soay sheep, resident on St. Kilda, S
95  the time of the admixture event between the feral population on the island and the RJF to 1981, coin
96 o determine the most plausible source of the feral population.
97 nal hypothesis surrounding the origin of the feral populations and draws attention to the possibility
98 f feral animals, and comparative analyses of feral populations and taxa.
99 re and differences among 19 pig populations (feral populations from Pacific islands, continental US,
100          These have occasionally established feral populations in nature, often with devastating ecol
101                                     Eighteen feral populations of B. napus also showed a strong tende
102 tentionally, leading to the establishment of feral populations through escapees.
103 istory strategies (often reported in wild or feral populations) relating to parental investment were
104 haped by the varied and complex histories of feral populations, and by novel selection pressures.
105 rge groups of monkeys randomly selected from feral populations, suggesting that the capacity for depr
106                                              Feral populations, those which successfully persist outs
107 l genome sequences representing domestic and feral populations.
108 utions from a racing breed to North American feral populations.
109 c, hybrid, and transgenic plants in wild and feral populations.
110                                New data from feral rats point to the regulatory influences on mesocor
111 y rats with rodent hepacivirus isolated from feral Rattus norvegicus (RHV-rn1) mirrors key aspects of
112                              Weedy rice is a feral relative of rice that infests paddies and causes s
113 gh November) of colony nest defensiveness in feral scutellata-hybrid and a popular lineage of Europea
114 rs that limit extensive gene transfer in the feral setting.
115 g an env gene that was homologous with other feral SIVsm env genes in the troop but having a gag gene
116 Polymorphisms among inbred mouse strains and feral species suggest that mutations responsible for the
117                                        Since feral strains of S. cerevisiae are dimorphic and have a
118 8, 0.6%), farmed swine (267/648, 41.2%), and feral swine (9/306, 2.9%).
119 tified the overlap between seropositivity of feral swine and human Q fever incidence.
120 S.A., which has an established population of feral swine and is a popular destination for water-based
121                                              Feral swine are globally known as one of the most destru
122                                              Feral swine are invasive in the United States and a rese
123 i'i and Texas, respectively, indicating that feral swine cannot be ruled out as a potential reservoir
124                When pre-emergence culling of feral swine caused population declines, it was effective
125 re possible hotspots for visitor exposure to feral swine contaminants.
126                                              Feral swine could contribute to the spread of Coxiella b
127 ffective at reducing passerine attendance at feral swine feeders, but their effectiveness when direct
128  history of Marfan syndrome and recreational feral swine hunting.
129                              The increase in feral swine population and the geographic range are a co
130 tions at many national and state parks where feral swine populations are established, and thus are po
131 risk of C. burnetii exposure associated with feral swine populations in Hawai'i and Texas.
132 terized the seroprevalence of C. burnetii in feral swine populations of Hawai'i and Texas, which have
133                                              Feral swine rooting commonly exceeds 20 cm in depth, esp
134  early response to the FMDV-like pathogen in feral swine was unwarranted while response to the CSFV-l
135 ife-histories in hypothetical populations of feral swine with different contact structures (homogenou
136  phylogenetic relationship between VACV-IOC, feral VACV established in nature, and the ancestor-like
137  hypothesis that CTGV-like viruses represent feral VACV that evolved in parallel with VACV-IOC after
138 (3) rice (Oryza sativa), often infested with feral weedy rice, which interbreeds with the crop; and (

 
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