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1 chiatric emergency with risk for suicide and infanticide.
2  within groups, triggering hidden threats of infanticide.
3 nd the presence of female counter-tactics to infanticide.
4 ation for the appearance of monogamy is male infanticide.
5 logic underlying pup recognition and ensuing infanticide.
6  offspring would otherwise be susceptible to infanticide.
7 from multiple men and may reduce the risk of infanticide.
8 e treatment of mentally ill women who commit infanticide.
9 a male should be less likely to benefit from infanticide.
10 onistic interactions, and protection against infanticide.
11 erentiating sudden infant death syndrome and infanticide.
12  in subordinates via aggression, eviction or infanticide.
13 quently less likely to lose their infants to infanticide.
14 fter delivery and a high risk of suicide and infanticide.
15  fertility as an adaptive counterstrategy to infanticide.
16 the infant loss and maternal injury was male infanticide.
17 ion toward subordinates [23] and even commit infanticide [24-26].
18                                              Infanticide and adoption have been attributed to sexual
19 and contemporary psychiatric perspectives on infanticide and discusses ways in which the psychiatric
20 ce of age and dominance on the occurrence of infanticide and infant defence.
21           The neural mechanisms that mediate infanticide and its switch to maternal behaviours during
22 nd another 23% of stepfathers exhibited both infanticide and long-term care.
23 chiatric community can improve prevention of infanticide and promote appropriate treatment of mentall
24 imal strategy for the females that minimizes infanticide and that infanticide confers advantage to th
25 sites was a primary cause of eviction-driven infanticide, and 2) attacks occurred less frequently at
26 ave been associated with a high risk of male infanticide, and paternal care is a consequence rather t
27  prostitutes; sex selective abortion, female infanticide, and the deliberate neglect of girls; and ra
28 end well beyond the systems in which acts of infanticide are common.
29                                              Infanticide as a male reproductive tactic is widespread
30 le response correlated with the risk of male infanticide, as +/+ and +/t males did not differ in thei
31                                              Infanticide attacks occurred at 256 nests in two distinc
32                                              Infanticide attacks per nest were positively correlated
33 uccessful at using paternity confusion as an infanticide avoidance tactic, thus increasing the likeli
34             New observations of coalitionary infanticide by female chimpanzees in Uganda shed light o
35                                              Infanticide by newly immigrated or newly dominant males
36  has never been observed in wild orangutans, infanticide by non-sire males has been predicted to occu
37                                              Infanticide by primate males was considered rare if grou
38 s, but that females can escape the threat of infanticide by synchronizing birth to the same day as ol
39                                 Adoption and infanticide conferred similar fitness benefits to stepfa
40  females that minimizes infanticide and that infanticide confers advantage to the males only in certa
41                                              Infanticide did not emerge as a recurrent male strategy
42 frequent and often lead to sexually selected infanticide, exacting high costs on lactating females.
43          In general, the strategies to avoid infanticide exhibited by male lions supported the territ
44         Lower aggressiveness, lower risks of infanticide from female kin and greater protection of te
45 c conditions, with high risks of suicide and infanticide if untreated.
46 y, sufficient and naturally activated during infanticide in female mice.
47 el to explain the presence and prevalence of infanticide in primate groups.
48 d by recent evidence for strong variation of infanticide in primate multi-male groups, we modelled th
49 llustrate society's complicated reactions to infanticide in the context of postpartum mental illness.
50 phylogenetic analyses support a key role for infanticide in the social evolution of primates, and pot
51 ghting the role of brood size regulation via infanticide in this genus.
52        Although our simulations confirm that infanticide increases the risk of population extinction,
53                 These findings indicate that infanticide is a consequence, rather than a cause, of co
54                            Although maternal infanticide is a rare event, a high proportion of cases
55 been given to carnivores and primates, where infanticide is a sexually selected strategy of males to
56 lti-male groups and offer an explanation why infanticide is common in some multi-male groups and rare
57 ed States, the complexity of the response to infanticide is demonstrated by the judicial system's rea
58 del scenarios fit the conditions under which infanticide is known to occur in primate multi-male grou
59                                 Non-parental infanticide is mediated by territorial cues and presumab
60                      While sexually selected infanticide is well known, evidence for sexually selecte
61 t for mothers with mental illness who commit infanticide, "killer mothers" may face the death penalty
62                            Whereas England's Infanticide Law provides probation and mandates psychiat
63 n of males defending probable offspring from infanticide, male primates living in multi-male, multi-f
64  woman with postpartum psychosis who commits infanticide needs treatment rather than punishment and t
65 ry mice show a mating-induced suppression of infanticide (normally observed in virgins) and onset of
66 , within a single species and mating system, infanticide occurred in multiple contexts due to multipl
67                           We have shown that infanticide occurs during turbulent changes accompanying
68 erarchy within the group, we have shown that infanticide occurs only in primate groups where the chan
69 ce tactic, thus increasing the likelihood of infanticide of their first-born infants.
70                                   Systematic infanticide of unrelated young has been reported in seve
71 ecision making, by suggesting that selective infanticide of unrelated young may generally become adap
72 d one female and show that the strategies of infanticide on the males' part and polyandrous mating on
73 g females are the most profitable targets of infanticide or feticide, because their offspring have hi
74    We used comparative analyses to show that infanticide primarily evolves in social mammals in which
75 itters after shorter times and have a higher infanticide rate.
76  relative lactation length, thereby reducing infanticide risk and increasing reproductive rates.
77  groups, we modelled the conditions for when infanticide should occur for a group with a resident and
78                   It is only the presence of infanticide that reliably increases the probability of a
79  socially dominant females use the threat of infanticide to deter selfish reproduction by younger fem
80                         The benefits of such infanticide to males, and its costs to females, probably
81 ally cause male replacements (and associated infanticide) to become sufficiently common to prevent cu
82 gs adjust their parental responses - care or infanticide - towards unrelated clutches according to th
83 odel predicts that increasing the impacts of infanticide will increase the length of the female recep