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142 results for “mating behaviour”
Figure 2 in Mating behaviour and maternal care in the tropical savanna funnel-web spider Aglaoctenus lagotis Holmberg (Araneae: Lycosidae)
Figure 2. Schematic drawings of the male behavioural repertoire of Aglaoctenus lagotis (Araneae: Lycosidae). The sequence (courtship to mating) presents three stages: I – courtship; II – pre-mating; III – mating. Courtship shows five other possible stages: (A) vibration of palps and first legs; (B) vibration of palps and first legs under the web; (C) vibration of palps and first legs alternating with leg rubbing; (D) vibration of palps; (E) moving straight to female's position, tapping the palps on the web.
FIG. 7 in Diurnal mating behaviour of a Nisitrus sp. cricket (Orthoptera: Gryllidae) from Sumatra
FIG. 7. In response to the male's`leg-wave' signal the female (right) bends inwards and eats the spermatophore.
FIG. 4 in Spatial and temporal patterns of territorial mate locating behaviour in Hypolimnas bolina (L.) (Lepidoptera: Nymphalidae)
FIG. 4. The relationship between counts of territorial males and the minimum vegetative corridor width in 10 m segments along both transect 1 (solid triangles) and transect 2 (open squares).
FIG. 2 in Spatial and temporal patterns of territorial mate locating behaviour in Hypolimnas bolina (L.) (Lepidoptera: Nymphalidae)
FIG. 2. Diel patterns of territorial male residence along transect 1 (open squares, solid line) and transect 2 (solid squares, dotted line). The error bars represent Ô1 standard error of sample means, and the ®tted lines are weighted least squares approximations calculated by the STATISTICATM computer program. Sample sizes are given above each hourly point.
FIG. 5 in Spatial and temporal patterns of territorial mate locating behaviour in Hypolimnas bolina (L.) (Lepidoptera: Nymphalidae)
FIG. 5. Representation of hypothetical population-level activity curves derived from simple models of the timing of individual behaviour. Curve A (solid line) represents a population of individuals that arrive at 0900 h and stay for 6 h, curve B (dashed line) represents a population of individuals that arrive at 0900 h and stay for varying times, whilst curve C (dotted line) represents a population of males that arrive at various times but each stay for 3 h.
FIG. 3 in Spatial and temporal patterns of territorial mate locating behaviour in Hypolimnas bolina (L.) (Lepidoptera: Nymphalidae)
FIG. 3. Spatial distribution of territorial males along the length of both transects, with the distribution of the larval food plant species C. cyanea (a), I. triloba (b) and S. nodiXora (c) indicated in the bars above each plot. Transect segments that contained outcrops of ¯owering W. trilobata are indicated by arrows (n 579 for all transect segments).
Figure 3 in First detailed observations on tardigrade mating behaviour and some aspects of the life history of Isohypsibius dastychi Pilato, Bertolani & Binda 1982 (Tardigrada, Isohypsibiidae)
Figure 3. Posterior half of male body. In all structures (indicated by arrows) spermatozoa are visible. A, testis; B, spermatic duct (second one not visible); C and D, seminal vesicles in the two spermatic ducts; E, cloaca.
Figure 2 in First detailed observations on tardigrade mating behaviour and some aspects of the life history of Isohypsibius dastychi Pilato, Bertolani & Binda 1982 (Tardigrada, Isohypsibiidae)
Figure 2. Mating position of Isohypsibius dastychi. The male (left) held the female (right) in the moulting stage, with eggs (in this case three) clearly visible in her ovary.
Figure 4 in First detailed observations on tardigrade mating behaviour and some aspects of the life history of Isohypsibius dastychi Pilato, Bertolani & Binda 1982 (Tardigrada, Isohypsibiidae)
Figure 4. Cloaca (indicated by arrow) of two individuals of Isohypsibius dastychi. The cuticle opens anteriorly. A, cuticle covering the cloaca is pushed towards posterior end of the animal. B, cuticle in the natural state. Scale bar = 10 µm.
Figure 1. A in First detailed observations on tardigrade mating behaviour and some aspects of the life history of Isohypsibius dastychi Pilato, Bertolani & Binda 1982 (Tardigrada, Isohypsibiidae)
Figure 1. A, average procedure of life events and generation time of Isohypsibius dastychi at two different temperatures, 12 and 20 °C (N12 °C = 21, N20 °C = 25). Squares and dotted lines indicate average hatching events at 12 and 20 °C, respectively. B, cumulative events of individual tardigrades becoming adults in dependence of age (days after egg deposition) at two different temperatures, 12 and 20 °C (N12 °C = 21, N20 °C = 25). C, comparison of age at sexual maturity of males and females from different clutches at two different temperatures (12 and 20 °C). Each dot stands for one animal reaching sexual maturity.
Disentangling the effects of male age and mating history: contrasting effects of mating history on pre-copulatory mating behaviour and paternity success
<p>Many studies ask whether older males are better at acquiring mates. Even so, how age affects reproductive success is still poorly understood because male age and mating history are confounded in most studies: older males usually have more mating experience. To what extent does mating history rather than age explain variation in male mating success? And how do mating history and male age determine paternity when there is also post-copulatory sexual selection? Here we experimentally manipulated the mating history of old and young males in the eastern mosquitofish (Gambusia holbrooki). We then recorded male mating behaviour and share of paternity (1259 offspring from 232 potential sires) when they competed for mates and fertilizations. Old males, and males with no mating experience, spent significantly more time approaching females, and attempting to mate, than did young males and those with greater mating experience. Male age and mating history interacted to affect paternity: old males benefited from having previous mating experience, but young males did not. Our results highlight that the age-related changes in male reproductive traits and in paternity that have been described in many taxa, may be partly attributable to male mating history and not simply to age itself.</p>
Using positive-to-negative behavioural responses to evaluate treefrog mate choice
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Data from: Fighting and mating success in giant Australian cuttlefish is influenced by behavioural lateralization
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Data from: The heritability of mating behaviour in a fly and its plasticity in response to the threat of sperm competition
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Data from: The mating behaviour of the seed shrimp Parapolycope spiralis (Ostracoda: Cladocopina), with insight into the evolution of mating systems in cryptic interstitial habitats
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Data from: Evolution of mating behaviour between two populations adapting to common environmental conditions
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Raw data for: Plastic male mating behaviour evolves in response to the competitive environment
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Data from: Does mating behaviour affect connectivity in marine fishes? Comparative population genetics of two protogynous groupers (Family Serranidae)
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Disentangling the effects of male age and mating history: contrasting effects of mating history on pre-copulatory mating behaviour and paternity success
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playback used for "Can vibrational playbacks either disrupt mating or influence other relevant behaviours in Bactericera cockerelli (Triozidae: Hemiptera)?"
<p>Playbacks used for manipulating the behaviour of the insect pest <em>Bactericera cockerelli.</em> </p> <p>For further information see "Can vibrational playbacks either disrupt mating or influence other relevant behaviours in <em>Bactericera cockerelli</em> (Triozidae: Hemiptera)?" by Avosani et al., submitted for publication. </p>
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International Brain Laboratory public data
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OpenNeuro
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