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142 results for “mating behaviour”
FIG. 8 in Mating behaviour of Staminodeus vectoris (Coleoptera: Curculionidae), and the value of systematics in behavioural studies
FIG. 8. Phylogenetic relationships among the seven species of Staminodeus, with Not. basalis, Per. carludovicae and Sys. costaricensis as outgroup taxa; behaviourally relevant characters are mapped (according to fast optimization), homology is indicated by black rectangles and homoplasy by white rectangles; character numbers and state transformations (table 2) are displayed above and below each rectangle, respectively. Adapted from Franz (2001), with permission of The Coleopterists Bulletin.
FIG. 6 in Mating behaviour of Staminodeus vectoris (Coleoptera: Curculionidae), and the value of systematics in behavioural studies
FIG. 6. Linear regression of morphological characteristics of S. vectoris in comparison to length of metepisternum; values are transformed to log, r2 and regression coefficient are indicated: (a) length of male protibia; (b) length of female spine.
FIG. 5 in Mating behaviour of Staminodeus vectoris (Coleoptera: Curculionidae), and the value of systematics in behavioural studies
FIG. 5. Males of S. vectoris, conflict behaviour; dotted lines indicate alternative positions of body parts during sequence of movement, arrows indicate directions of movements: (a) intimidation behaviour, two males are opposed on staminode, their abdomens moving horizontally; (b) fighting behaviour, two males execute fast blows with their prothoracic legs, sustained by prothoracic movements, until their protibiae cling (dotted ring) and dislodge inferior male.
FIG. 4 in Mating behaviour of Staminodeus vectoris (Coleoptera: Curculionidae), and the value of systematics in behavioural studies
FIG. 4. Female of S. vectoris, transport of staminode, sequence of behaviours from 1. to 4. (iteratively); ends of staminode are drawn, dotted lines represent intermediate (omitted) sections of staminode, arrows indicate direction of movement of female, legs, and staminode, respectively: (a) female underneath staminode, using her frontal spine as a 'barb' against substrate and transporting staminode with her legs; (b) female returning to end of staminode.
FIG. 2 in Mating behaviour of Staminodeus vectoris (Coleoptera: Curculionidae), and the value of systematics in behavioural studies
FIG. 2. Inflorescence of A. uncinata, pistillate phase: (a) at 03:30 a.m., approximately two hours before arrival of S. vectoris, spathes are deflected, staminodes are extended and fragrant; (b) at 06:30 a.m., approximately one hour after arrival of S. vectoris, staminodes have been detached by females, some individuals feed and attempt to copulate on remains.
FIG. 3 in Mating behaviour of Staminodeus vectoris (Coleoptera: Curculionidae), and the value of systematics in behavioural studies
FIG. 3. Female of S. vectoris, detachment of staminode: (a) female searching and probing staminode of A. uncinata, note damage by previous visitors; (b) female detaching staminode with her mandibles, rocking back and forth and using her rostrum to tear final connections, before falling to ground.
FIG. 1 in Mating behaviour of Staminodeus vectoris (Coleoptera: Curculionidae), and the value of systematics in behavioural studies
FIG. 1. Staminodeus vectoris, habitus: (a) male; (b) protibia of male; (c) spine on frons of female.
Fig. 2 a–g in When dwarf males and hermaphrodites copulate: first record of mating behaviour in a dwarf male using the androdioecious barnacle Scalpellum scalpellum (Crustacea: Cirripedia: Thoracica)
Fig. 2 a–g Penis structure in dwarf males of Scalpellum scalpellum. A hermaphrodite photographed in vivo and carrying dwarf males in the receptacle area on either side of the brood chamber (mantle cavity). b One of the males in close up, revealing the tube-like penis still inside its body. c Another male with the penis already extended for mating; note the length of the penis relative to the small male body; another deeply buried male situated close by. d SEM of dwarf male with penis almost fully extended and showing the side branches. e Tip of the penis furnished with sensory setae; note the central opening. f SEM of dwarf males located symmetrically on either side of the brood chamber; one male with penis extended; note in both d and f how the males are located outside the brood chamber when the mantle valves are fully closed. g SEM of dwarf male fixed when the penis is extended into the brood chamber for mating; the cirri of the hermaphrodite hovering over the male
Fig. 1 in New information on the evolution of mating behaviour in Sepsidae (Diptera) and the cost of male copulations in Saltella sphondylii
Fig. 1 Evolution of behavioural characters modified from Puniamoorthy et al. (2009) on the phylogenetic tree of Sepsidae based on the molecular data from Puniamoorthy et al. (2008) and Su et al. (2008) (ACCTRAN: black symbols non-homoplasious; open symbols homoplasious changes)
Figure 5 in Mating behaviour in ageing Teratorhabditis palmarum (Nematoda: Rhabditida)
Figure 5. Duration of mating of 2- and 10-day-old males with different age groups of females. Significant differences are indicated with an asterisk (p <.05).
Figure 4 in Mating behaviour in ageing Teratorhabditis palmarum (Nematoda: Rhabditida)
Figure 4. Duration of different phases of mating behaviour of 10-day-old males with 2- and 10-day-old females. Significant differences are indicated with an asterisk (p <.05).
Figure 3 in Mating behaviour in ageing Teratorhabditis palmarum (Nematoda: Rhabditida)
Figure 3. Duration of different phases of mating behaviour of 2-day-old males with 2- and 10-day-old females. Significant differences are indicated with an asterisk (p <.05).
Figure 2 in Mating behaviour in ageing Teratorhabditis palmarum (Nematoda: Rhabditida)
Figure 2. Sub-behaviours in mating and post-mating phases of T. palmarum: copulating (adhering, ejaculating and detaching) and enduring (sluggish and strolling).
Figure 1 in Mating behaviour in ageing Teratorhabditis palmarum (Nematoda: Rhabditida)
Figure 1. Sub-behaviours in pre-mating phases of T. palmarum: searching (crawling, accessing and encountering) and contacting (touching, coiling and positioning).
Figure 4 in Mating behaviour, territoriality and natural history notes of Phyllomedusa ayeaye Lutz, 1966 (Hylidae: Phyllomedusinae) in south-eastern Brazil
Figure 4. Interactions among males of Phyllomedusa ayeaye: (a) a second male successfully interrupts an ongoing oviposition, adopting a posture similar to an amplexus over the amplectant male; (b) physical combat among two territorial males: the attacked male tries to release himself from the grasp of another male, by adopting a hanging posture over the branch; (c) the attacker male further clasps the attacked male and both engage in a ventral position similar to an embrace, hanging over the vegetation by their legs.
Figure 1 in Mating behaviour, territoriality and natural history notes of Phyllomedusa ayeaye Lutz, 1966 (Hylidae: Phyllomedusinae) in south-eastern Brazil
Figure 1. (a) Geographic location of the study site in the southern portion of the Espinhaço Mountain Range in the state of Minas Gerais, south-eastern Brazil. (b) One of the temporary meadows which were sampled in the present study, showing the structure of riparian vegetation used for vocalisation and oviposition by individuals of Phyllomedusa ayeaye.
Figure 2 in Mating behaviour, territoriality and natural history notes of Phyllomedusa ayeaye Lutz, 1966 (Hylidae: Phyllomedusinae) in south-eastern Brazil
Figure 2. Boxplots showing values of snout-vent length (SVL) (a) and body mass (b) for males and females (n = 116), SVL (c) and body mass (d) for amplectant and non-amplectant males (n = 94) of Phyllomedusa ayeaye. Solid boxes contain 50% of data variation and vertical bars the remaining 50% of data distribution. Horizontal lines inside each box are medians.
Figure 2 in Mating behaviour, nympho-imaginal development and description of a new Mesabolivar species (Araneae: Pholcidae) from the Brazilian dry forest
Figure 2. Diagram of the sexual repertoire displayed by the Mesobolivar delclaroi sp. nov. spider. The behaviours are divided into four steps: Step I, Courtship; Step II, Pre-copulation – note in the arrow the early introduction of the copulatory bulb into the female's genitalia; Step III, Copulation, (a) lateral view, (b) ventral view – note the arrows indicating the pedipalp bristles rubbing the abdominal region of the female; Step IV, Post-copulation.
Figure 1 in Mating behaviour, nympho-imaginal development and description of a new Mesabolivar species (Araneae: Pholcidae) from the Brazilian dry forest
Figure 1. Mesabolivar delclaroi sp. nov. (A, B) Male chelicerae, (A) frontal, (B) lateral; (C) male left palp, retrolateral; (D–F) procursus tip, (D) prolateral, (E) dorsal, (F) retrolateral; (G) bulb, prolateral; (H–J) epigynum, (H) ventral, (I) lateral, (J) dorsal. Scale bar 0.5 mm.
Figure 1 in Mating behaviour and maternal care in the tropical savanna funnel-web spider Aglaoctenus lagotis Holmberg (Araneae: Lycosidae)
Figure 1. Experimental set-up to evaluate the role of chemical cues on female webs. (A) General view of arena, the arrow shows the diameter of tube entrance; (B) test comparing the attraction of virgin or mated female webs to males; (C) comparison between old and recent webs used by females.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
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