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Fig. 4 in Density dependent variation in the life history traits of mottled emigrant butterfly, Catopsilia pyranthe (Linnaeus, 1758) (Lepidoptera: Pieridae)
Fig. 4. The variations (Mean ± SE) of density impact (DI) on different life history traits of C. pyranthe butterfly species under intraspecific competitions. Shaded bars represent ♀ while nonshaded bars represent ♂. The life history traits are shown in sequence as (a) age at pupation (AP, in days), (b) pupal weight (PW, in mg), (c) adult weight (AW, in mg), (d) adult length (AL, in mm), (e) forewing length (FWL, in mm), (f) forewing breadth (FWB, in mm), (g) hindwing length (HWL, in mm), and (h) hindwing breadth (HWB, in mm). Values less than zero indicates density impact. Рис. 4. Вариации (среднее ± SE) влиЯниЯ плотности (DI) на раЗличные приЗнаки жиЗненного цикла бабочек C. pyranthe в условиЯх внутривидовой конкуренции. ЗаШтрихованные столбцы представлЯют ♀, а неЗаШтрихованные столбцы представлЯют ♂. Параметры жиЗненного цикла покаЗаны в следуюЩей последовательности: (а) воЗраст окукливаниЯ (AP, в днЯх), (b) вес куколки (PW, в мг), (c) вес вЗрослой особи (AW, в мг), (d) вЗрослаЯ особь. длина (AL, в мм), (e) длина переднего крыла (FWL, в мм), (f) Ширина переднего крыла (FWB, в мм), (g) длина Заднего крыла (HWL, в мм) и (h) Ширина Заднего крыла (HWB, в мм). ЗначениЯ меньШе нулЯ укаЗывают на влиЯние плотности.
Fig. 2 in Density dependent variation in the life history traits of mottled emigrant butterfly, Catopsilia pyranthe (Linnaeus, 1758) (Lepidoptera: Pieridae)
Fig. 2. The proportion of survivorship of C. pyranthe in different initial larval rearing density (ranging from 1 through 4). Рис. 2. ДолЯ выживШих C. pyranthe при раЗной начальной плотности выраЩиваниЯ личинок (от 1 до 4).
Fig. 1 in Density dependent variation in the life history traits of mottled emigrant butterfly, Catopsilia pyranthe (Linnaeus, 1758) (Lepidoptera: Pieridae)
Fig. 1. The outline of the experimental design followed for the evaluation of the density dependent effects on the life history traits of the butterfly C. pyranthe. Рис. 1. План Эксперимента, испольЗованный длЯ оценки влиЯниЯ плотности на особенности жиЗненного цикла бабочки C. pyranthe.
Fig. 3 in Density dependent variation in the life history traits of mottled emigrant butterfly, Catopsilia pyranthe (Linnaeus, 1758) (Lepidoptera: Pieridae)
Fig. 3. The differences in the life history traits of C. pyranthe considering male and female separately under intraspecific competitions in minimalist form of density of the individuals The life history traits considered are (a) age at pupation (AP, in days), (b) pupal weight (PW, in mg), (c) adult weight (AW, in mg), (d) adult length (AL, in mm), (e) forewing length (FWL, in mm), (f) forewing breadth (FWB, in mm), (g) hindwing length (HWL, in mm), and (h) hindwing breadth (HWB, in mm). Рис. 3. РаЗличиЯ приЗнаков жиЗненного цикла C. pyranthe с учетом самцов и самок отдельно при внутривидовой конкуренции в минималистской форме плотности особей. (b) масса куколки (PW, в мг), (c) масса вЗрослой особи (AW, в мг), (d) длина вЗрослой особи (AL, в мм), (e) длина переднего крыла (FWL, в мм), (f) Ширина переднего крыла (FWB, в мм), (g) длина Заднего крыла (HWL, в мм) и (h) Ширина Заднего крыла (HWB, в мм).
Figure 2 in Life history bias in endophyte infection of the Antarctic rhodophyte, Iridaea cordata
Figure 2 Percentage of Iridaea cordata life history stages at each site in each season. A, Autumn; W, winter.
Figure 1 in Life history bias in endophyte infection of the Antarctic rhodophyte, Iridaea cordata
Figure 1 Map of collection sites in the archipelago surrounding Palmer Station, Antarctica: (a) the Bahia Paraiso shipwreck, (b) Kristie Cove, (c) Bonaparte Point, (d) southern cove on Shortcut Island, (e) Stepping Stones, and (f) northern cove on Laggard Island. Inset: Antarctic continent, with arrow indicating position of Anvers Island along western Antarctic Peninsula.
Figure 3 in Life history bias in endophyte infection of the Antarctic rhodophyte, Iridaea cordata
Figure 3 Endophyte coverage in different life history stages of Iridaea cordata. Different letters indicate significance at p=0.05 (one-way ANOVA).
Figure 24 in Nereidid polychaetes (Annelida) inhabiting the inside of decaying fronds of the mangrove palm Nypa fruticans in a tropical estuary in Malaysia, with special reference to the life history of the dominant species, Namalycastis sp.
Figure 24. Seasonal change in average salinity and temperature at six sites in Setiu Wetlands, Terengganu, in Malaysia (a), rainfall amount recorded at Bukit Berangan, Setiu, based on data from CHIRPS (Funk et al. 2019) (b), during the sampling period from September 2015 to September 2016.
Figure 21 in Nereidid polychaetes (Annelida) inhabiting the inside of decaying fronds of the mangrove palm Nypa fruticans in a tropical estuary in Malaysia, with special reference to the life history of the dominant species, Namalycastis sp.
Figure 21. Seasonal change in size–frequency histogram of mean diameters of coelomic oocytes of Namalycastis sp. collected from six sites in Setiu Wetlands, Terengganu in Malaysia via seven samplings in the period from September 2015 to September 2016. n: number of females examined.
Figure 19 in Nereidid polychaetes (Annelida) inhabiting the inside of decaying fronds of the mangrove palm Nypa fruticans in a tropical estuary in Malaysia, with special reference to the life history of the dominant species, Namalycastis sp.
Figure 19. Seasonal change in mean body width of females, males, and individuals with sex unknown in pooled samples of Namalycastis sp. collected from six sites in Setiu Wetlands, Terengganu, in Malaysia via seven samplings in the period from September 2015 to September 2016.
Figure 16 in Nereidid polychaetes (Annelida) inhabiting the inside of decaying fronds of the mangrove palm Nypa fruticans in a tropical estuary in Malaysia, with special reference to the life history of the dominant species, Namalycastis sp.
Figure 16. Relationship between body width and body length of 277 complete specimens of Namalycastis sp. collected from September 2015 to September 2016 at six sites in Setiu Wetlands, Terengganu in Malaysia (Table 1).
Figure 7 in Nereidid polychaetes (Annelida) inhabiting the inside of decaying fronds of the mangrove palm Nypa fruticans in a tropical estuary in Malaysia, with special reference to the life history of the dominant species, Namalycastis sp.
Figure 7. Namalycastis sp., NSMT-Pol 113582 (4.2 mm BW, 200 mm BL) collected at Station 4 on 27 November 2015 (a, e, g); NSMT-Pol 113583 (2.5 mm BW, 250 mm BL) collected at Station 3 on 27 November 2015 (b–d); and UMT-Ann 1816 (2.6 mm BW, incomplete) collected from Station 2 on 27 November 2015 (f). (a) Sesquigomph spiniger in upper neurochaetae in posterior body. (b) Heterogomph spiniger with finely serrated blade in lower neurochaetae, chaetiger 5. (c) Heterogomph spinigers having blade with coarse serrations proximally in posterior body. (d) Heterogomph falciger with finely serrated blade, chaetiger 5. (e) Heterogomph falciger with finely serrated blade in posterior body. (f) Heterogomph falcigers having blade with coarse serrations proximally, chaetiger 200. (g) Heterogomph falcigers with finely serrated blade (f), and additional thin sesquigomph spinigers (epitokal chaetae) (ep) located at bottom position of lower neurochaetae in posterior body. Scale bars: a–e, g = 0.1 mm; f = 0.01 mm.
Figure 8 in Nereidid polychaetes (Annelida) inhabiting the inside of decaying fronds of the mangrove palm Nypa fruticans in a tropical estuary in Malaysia, with special reference to the life history of the dominant species, Namalycastis sp.
Figure 8. Percentage distribution of the number of sesquigomph spinigers in upper neurochaetae at chaetiger 35 in nine ranks of body size of Namalycastis sp. collected from Setiu Wetlands, Terengganu, Malaysia. A total of 229 specimens collected from six sites from September 2015 to September 2016 were examined. The number at the top of each bar is the number of individuals examined.
Figure 13 in Nereidid polychaetes (Annelida) inhabiting the inside of decaying fronds of the mangrove palm Nypa fruticans in a tropical estuary in Malaysia, with special reference to the life history of the dominant species, Namalycastis sp.
Figure 13. Perinereis aibuhitensis. (a) UMT-Ann 2191. Dorsal view of anterior end with everted proboscis. (b, c) NSMT-Pol 113581: (b) ventral view of anterior end with everted proboscis; (c) heterogomph falciger in upper neurochaetae, chaetiger 4. Scale bars: a, b = 1 mm; c = 0.01 mm.
Figure 4 in Nereidid polychaetes (Annelida) inhabiting the inside of decaying fronds of the mangrove palm Nypa fruticans in a tropical estuary in Malaysia, with special reference to the life history of the dominant species, Namalycastis sp.
Figure 4. Namalycastis sp., a specimen (UMT-Ann 1741; 4.1 mm BW, 180 mm BL) collected at Station 2 on 27 November 2015. (a) Whole body, dorsal view. (b) Anterior end, dorsal view. (c) Posterior end, dorsal view. (d) Pair of jaws, dorsal view. (e) Parapodium of chaetiger 10, posterior view. (f) Parapodium of chaetiger 65, posterior view. (g) Parapodium of chaetiger 93, posterior view. (h) Parapodium of chaetiger 111, posterior view. (i) Parapodium of chaetiger 142, posterior view. (j) Parapodium of chaetiger 166, posterior view. Scale bars: a = 5 mm; b, c = 1 mm; d–j = 1 mm.
Figure 1 in Nereidid polychaetes (Annelida) inhabiting the inside of decaying fronds of the mangrove palm Nypa fruticans in a tropical estuary in Malaysia, with special reference to the life history of the dominant species, Namalycastis sp.
Figure 1. Landscape of sampling sites in Setiu Wetlands, Terengganu, in Malaysia. (a) Mangrove trees of the palm Nypa fruticans, fringing a slender lagoon on 25 June 2015. (b) Collection of nereidid worms by tearing apart the decaying fronds of Nypa fruticans at Station 1 on 6 August 2015.
Figure 22 in Nereidid polychaetes (Annelida) inhabiting the inside of decaying fronds of the mangrove palm Nypa fruticans in a tropical estuary in Malaysia, with special reference to the life history of the dominant species, Namalycastis sp.
Figure 22. Relationship between the body width of ovigerous females and the mean oocyte diameter in Namalycastis sp. collected from six sites in Setiu Wetlands, Terengganu, in Malaysia via seven samplings in the period from September 2015 to September 2016.
Figure 10 in Nereidid polychaetes (Annelida) inhabiting the inside of decaying fronds of the mangrove palm Nypa fruticans in a tropical estuary in Malaysia, with special reference to the life history of the dominant species, Namalycastis sp.
Figure 10. Namalycastis rhodochorde, UMT-Ann 2270. (a) Anterior end with everted proboscis, dorsal view. (b) Middle body, dorsal view. (c) Posterior end, dorsal view. (d–l) Posterior views of parapodia in chaetigers 10 (d), 36 (e), 51 (f), 101 (g), 201 (h), 301 (i), 401 (j), 501 (k), and 601 (l). Scale bars: 1 mm.
Figure 23 in Nereidid polychaetes (Annelida) inhabiting the inside of decaying fronds of the mangrove palm Nypa fruticans in a tropical estuary in Malaysia, with special reference to the life history of the dominant species, Namalycastis sp.
Figure 23. Relationship between the body width of ovigerous females and the number of oocytes per 10 chaetigers in Namalycastis sp. collected from six sites in Setiu Wetlands, Terengganu, in Malaysia via seven samplings in the period from September 2015 to September 2016.
Figure 20 in Nereidid polychaetes (Annelida) inhabiting the inside of decaying fronds of the mangrove palm Nypa fruticans in a tropical estuary in Malaysia, with special reference to the life history of the dominant species, Namalycastis sp.
Figure 20. Seasonal change in ovigerous rate (%, open circle and solid line) and mean diameter of coelomic oocytes (μm, solid circle with SD bar, and dotted line) in females of Namalycastis sp. collected from six sites in Setiu Wetlands, Terengganu, in Malaysia during seven samplings in the period from September 2015 to September 2016.
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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