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Figure 5 in Multi-scale patterns in the host specificity of plant-dwelling arthropods: the influence of host plant and temporal variation on species richness and assemblage composition of true bugs (Hemiptera)

Figure 5. Annual cyclic pattern of the proportion of the effectively specialized fauna (squares) and singleton species (circles) for the total number of hemipteran species from each sampling period.

Figure 3 in Multi-scale patterns in the host specificity of plant-dwelling arthropods: the influence of host plant and temporal variation on species richness and assemblage composition of true bugs (Hemiptera)

Figure 3. Mean number of individuals (from SIMPER analysis) of dominant hemipteran species, during each sampling period, for most plant species.

Figure 1 in Multi-scale patterns in the host specificity of plant-dwelling arthropods: the influence of host plant and temporal variation on species richness and assemblage composition of true bugs (Hemiptera)

Figure 1. Interactions between plant species sampled and sampling period for (A) abundance (number of individuals) per plant and (B) species richness per plant (standard error bars are shown).

Figure 6 in Multi-scale patterns in the host specificity of plant-dwelling arthropods: the influence of host plant and temporal variation on species richness and assemblage composition of true bugs (Hemiptera)

Figure 6. Relationship between the effectively specialized fauna (squares) and singleton species (circles) for the number of hemipteran species from each sampling period and for the entire collection. An exponential decay equation is fitted for effectively specialized fauna, y = 2.973∗ exp (−0.00575∗ x) + (−1.478), R2 = 0.7598, and for singleton species, y = 22.53∗exp (−0.08466∗x) + 0.2614, R2 = 0.9873.

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).

Fig. 2. Study site. a in Temporal Occurrence Patterns of Chrysomelidae (Coleoptera) on the Universiti Malaysia Sabah Campus, Borneo

Fig. 2. Study site. a) Secondary forest, b) Ipomoea pes-caprae-dominated land with coconut palms, sea-oak trees, and Singapore almond trees, c) Abandoned crop field with bananas and grass, d) UMS campus.

Fig. 5 in Temporal Occurrence Patterns of Chrysomelidae (Coleoptera) on the Universiti Malaysia Sabah Campus, Borneo

Fig. 5. Monthly occurrence of Type III and Type IV species across the study period. Shaded areas indicate months when at least one adult specimen was collected, and unshaded areas indicate months when no adults were collected.

Fig. 4 in Temporal Occurrence Patterns of Chrysomelidae (Coleoptera) on the Universiti Malaysia Sabah Campus, Borneo

Fig. 4. The proportions of chrysomelid species that appeared once during the study period (Type I), 2−11 times (Type II), 12−29 times (Type III), and 30−34 times (Type IV).

Fig. 1 in Temporal Occurrence Patterns of Chrysomelidae (Coleoptera) on the Universiti Malaysia Sabah Campus, Borneo

Fig. 1. Study site. Dashed line outlines surveyed area. The upper figure is based on an ArcGIS basemap. a = secondary forest; b = area dominated by Ipomoea pes-caprae, coconut palms, sea-oak trees, and Singapore almond trees; c = abandoned crop field with bananas and grass; and d = UMS campus.