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Figure 4 in Abundance variations and life history traits of two sympatric species of Neotropical annual fish (Cyprinodontiformes: Rivulidae) in temporary ponds of southern Brazil
Figure 4. Sex ratio for Austrolebias minuano (A) and Cynopoecilus fulgens (B) sampling in temporary ponds of Lagoa do Peixe National Park, southern Brazil, in 2008 and 2009.
Figure 5 in Abundance variations and life history traits of two sympatric species of Neotropical annual fish (Cyprinodontiformes: Rivulidae) in temporary ponds of southern Brazil
Figure 5. Length–weight relationship for Austrolebias minuano (A) and Cynopoecilus fulgens (B) sampled in temporary ponds of Lagoa do Peixe National Park, southern Brazil, in 2008 and 2009.
Figure 6 in Abundance variations and life history traits of two sympatric species of Neotropical annual fish (Cyprinodontiformes: Rivulidae) in temporary ponds of southern Brazil
Figure 6. Condition factor (K) ± SE of Austrolebias minuano (A) and Cynopoecilus fulgens (B) sampled in temporary ponds of Lagoa do Peixe National Park, southern Brazil, in 2008 and 2009.
Figure 2 in Abundance variations and life history traits of two sympatric species of Neotropical annual fish (Cyprinodontiformes: Rivulidae) in temporary ponds of southern Brazil
Figure 2. Mean abundances ± SE of Austrolebias minuano (A) and Cynopoecilus fulgens (B) sampled in temporary ponds of Lagoa do Peixe National Park, southern Brazil, in 2008 and 2009.
Figure 3 in Abundance variations and life history traits of two sympatric species of Neotropical annual fish (Cyprinodontiformes: Rivulidae) in temporary ponds of southern Brazil
Figure 3. Mean standard length (LS) ± SE of Austrolebias minuano (A) and Cynopoecilus fulgens (B) sampled in temporary ponds of Lagoa do Peixe National Park, southern Brazil, in 2008 and 2009.
Figure 7 in The life history and host-searching behaviour of the aquatic parasitoid wasp Apsilops japonicus (Hymenoptera: Ichneumonidae), a parasitoid of the aquatic moth Neoshoenobia testacealis (Lepidoptera: Crambidae)
Figure 7. Mean number of ovipositor probes into leaf petioles by Apsilops japonicus females for the three types of leaves. There were no significant differences among the three leaf types (n = 36, F = 0.75, P = 0.48, one-way analysis of variance).
Figure 4 in The life history and host-searching behaviour of the aquatic parasitoid wasp Apsilops japonicus (Hymenoptera: Ichneumonidae), a parasitoid of the aquatic moth Neoshoenobia testacealis (Lepidoptera: Crambidae)
Figure 4. Frequency of Apsilops japonicus females entering the water from the three types of leaves (n = 36).
Figure 5 in The life history and host-searching behaviour of the aquatic parasitoid wasp Apsilops japonicus (Hymenoptera: Ichneumonidae), a parasitoid of the aquatic moth Neoshoenobia testacealis (Lepidoptera: Crambidae)
Figure 5. Mean submergence time for Apsilops japonicus females entering the water from the three types of leaves. There were no significant differences among the three leaf types (n = 36, F = 0.45, P = 0.64, one-way analysis of variance).
Figure 2 in The life history and host-searching behaviour of the aquatic parasitoid wasp Apsilops japonicus (Hymenoptera: Ichneumonidae), a parasitoid of the aquatic moth Neoshoenobia testacealis (Lepidoptera: Crambidae)
Figure 2. An Apsilops japonicus larva beside a mature host larva in the petiole. The white bar indicates a parasitoid larva.
Figure 3 in The life history and host-searching behaviour of the aquatic parasitoid wasp Apsilops japonicus (Hymenoptera: Ichneumonidae), a parasitoid of the aquatic moth Neoshoenobia testacealis (Lepidoptera: Crambidae)
Figure 3. Frequency of host stages at oviposition by Apsilops japonicus females. Unknown (n = 3: parasitoid pupa) indicates that we could not discriminate the host stage because the hosts were dead and probably decomposed in the petioles.
Figure A1 in Life-history traits of a common Caribbean coral-excavating sponge, Cliona tenuis (Porifera: Hadromerida)
Figure A1. Daily growth rate (linear extension) of Cliona tenuis during the three observational periods described in this manuscript and under constant competition with Lobophora variegata, Dictyota pulchella, coral, and short and long turf algae (more details of the methodology are explained in the methods section of this manuscript and in González-Rivero et al. 2012). Error bars depict standard error.
Figure 8 in Life-history traits of a common Caribbean coral-excavating sponge, Cliona tenuis (Porifera: Hadromerida)
Figure 8. Size structure of Cliona tenuis populations at: (A) Long Caye Wall and (B) Middle Caye Wall.
Figure 7 in Life-history traits of a common Caribbean coral-excavating sponge, Cliona tenuis (Porifera: Hadromerida)
Figure 7. Temporal variation in recruitment (individuals.plot−1) among periods of evaluation and between study sites. Vertical bars depict standard error.
Figure 5 in Life-history traits of a common Caribbean coral-excavating sponge, Cliona tenuis (Porifera: Hadromerida)
Figure 5. Linear growth of Cliona tenuis measured during the studied period. The timeline is represented as ordinal dates in days of the year. Data points out of the 5th and 95th confidence intervals (bars) are represented by dots, and box indicates the interquartile range. The solid line inside the box represents the median, whereas the dotted line represents the mean.
Figure 3 in Life-history traits of a common Caribbean coral-excavating sponge, Cliona tenuis (Porifera: Hadromerida)
Figure 3. Female reproductive elements in Cliona tenuis. (A) Immature oocyte in April 2009; (B) sparse distribution of immature oocytes in the tissue; (C) mature oocyte showing a distinctive nucleolus and nucleus, and the absence of nurse cells; (D) oocyte distribution and abundance in February 2009.
Figure 1 in Life-history traits of a common Caribbean coral-excavating sponge, Cliona tenuis (Porifera: Hadromerida)
Figure 1. Temporal variation of attributes describing the reproductive cycle in Cliona tenuis. (A) Proportion of reproductive sponges (bars) and the total number of individuals sampled (circles); (B) mean propagule size over time; the circles show the number of propagules measured; (C) density of propagules over time. Error bars depict standard error.
Figure 9 in Life-history traits of a common Caribbean coral-excavating sponge, Cliona tenuis (Porifera: Hadromerida)
Figure 9. Seasonal change in sea surface temperature (SST) at the study site over time (ordinal date in days of the year): average temperature over 24 years (grey band) and during the 2009 study year (filled dots). Source: AVHRR pathfinder, NOAA.
Figure 6 in Life history and host utilization pattern of a strepsipteran parasite (Insecta: Strepsiptera) on the Blissine bugs (Hemiptera: Lygaeidae) living under dwarf bamboo leaf sheaths
Figure 6. Comparison of Macropes obnubilus body lengths between sexes and between stylopized and unstylopized bugs. Bar shows SD.
Figure 4 in Life history and host utilization pattern of a strepsipteran parasite (Insecta: Strepsiptera) on the Blissine bugs (Hemiptera: Lygaeidae) living under dwarf bamboo leaf sheaths
Figure 4. Seasonal changes in the number of strepsipterans per host bug compared among larva, male pupa (including exuvia), and female adult.
Figure 5 in Life history and host utilization pattern of a strepsipteran parasite (Insecta: Strepsiptera) on the Blissine bugs (Hemiptera: Lygaeidae) living under dwarf bamboo leaf sheaths
Figure 5. Summarized life cycles of the host dwarf bamboo, Macropes obnubilus, and Blissoxenos esakii. Solid and broken lines indicate major and infrequent occurrences, respectively.
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Allen Brain Atlas
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International Brain Laboratory public data
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OpenNeuro
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