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Fig. 4 in Tripedalia maipoensis Sun & Tsui & Wong & Cheung & Ng & Or & Qiu 2023, sp. nov.
Fig. 4. Temporal change in the number of females releasing larvae between 1800H and 0200H along with the time of the nighttime high tide for Cardisoma carnifex (A, B) and Epigrapsus notatus (C, D). The total number of female C. carnifex and E. notatus are 311 and 204, respectively.
Fig. 1 in Tripedalia maipoensis Sun & Tsui & Wong & Cheung & Ng & Or & Qiu 2023, sp. nov.
Fig. 1. The location of the study area of the crabs in Chengxi windbreaks of Taijiang National Park, Tainan, Taiwan. Red arrows indicate the start point and end point of the migration survey on the road in 2020. The white line (1450 m) and orange line (950 m) represent the migration survey areas on the embankment flood control road for Cardisoma carnifex and Epigrapsus notatus, respectively, in 2021. The white asterisk (site A, photograph A) and orange asterisk (site B, photograph B) represent the sites for the observation of larval release of C. carnifex and E. notatus, respectively, in 2021. Photograph C is the embankment flood control road where the surveys of crabs took place.
Fig. 2 in Tripedalia maipoensis Sun & Tsui & Wong & Cheung & Ng & Or & Qiu 2023, sp. nov.
Fig. 2. Temporal pattern of migrating ovigerous female Cardisoma carnifex recorded on the embankment flood control road of Chengxi windbreaks between March and November 2020 (A, C) and between June and September 2021 (B). Solid lines (─) and dash lines (---) represent nocturnal (1800- 0559H) and diurnal (0600-1759H) high tides, respectively. The breaks in the lines indicate a lack of data on tidal height for the observation days. Closed and open circles represent new and full moons, respectively. Because few Cardisoma carnifex were found on the road in March, April, May, October and November (n <30), the numbers of female crabs per month were combined (C).
Fig. 7. A in Tripedalia maipoensis Sun & Tsui & Wong & Cheung & Ng & Or & Qiu 2023, sp. nov.
Fig. 7. A, Diameter of the sea urchin host and its relationship with the size of the pinnotherid guest. N = 62. B) Size and wet weight of pinnotherid females according to their reproductive condition. Arrow shows minimum incubation size (1.2 cm). N = 62.
Fig. 6 in Tripedalia maipoensis Sun & Tsui & Wong & Cheung & Ng & Or & Qiu 2023, sp. nov.
Fig. 6. GSI for sea urchins with and without pinnotherids inside the host digestive system, as a function of host test diameter.
Fig. 3. A in Tripedalia maipoensis Sun & Tsui & Wong & Cheung & Ng & Or & Qiu 2023, sp. nov.
Fig. 3. A, Relationship between sea urchin size and its total wet weight for the specimens collected from Calfuco Beach. N = 73. B, Sea urchin wet weight with pinnotherid and without pinnotherids, and C, Relationship between total wet weight of the sea urchin host and the carapace length of the harbored pinnotherid. N = 62.
Fig. 9 in Tripedalia maipoensis Sun & Tsui & Wong & Cheung & Ng & Or & Qiu 2023, sp. nov.
Fig. 9. Sea urchin age as estimated from the sea urchin's test diameter (black circles) based on Gebauer and Moreno (1995). Blue circles correspond to the pinnotherid sizes. Arrow 1 corresponds to the period before the guest arrived inside the sea urchin. Arrow 2 corresponds to the range of sea urchin sizes containing the smallest and largest pinnotherids (approx. 3 and 9 cm diameter of test) found in this study. This size range corresponds to a growth period of 5 years for the sea urchin (estimated according to Gebauer and Moreno 1995) and for the guest crab as well, assuming that infestation by the pinnotherid occurred as a very early juvenile, shortly after metamorphosis. The two circled points (red circles) show the sea urchin that harbored the largest pinnotherid symbionts. Data below the lower dash line shows sizes of sea urchins that were never parasitized by pea crabs. The upper dash line indicates the age of the sea urchins in which the largest parasitic pinnotherid was found.
Fig. 8. A in Tripedalia maipoensis Sun & Tsui & Wong & Cheung & Ng & Or & Qiu 2023, sp. nov.
Fig. 8. A, Diagram of the final section of a sea urchin intestine for a) infested and b) non-infected individuals. Solid arrows indicate the terminal portion of the digestive tract (i.e., the anus). The clear, vertical arrow indicates where the hosted pinnotherid was located. Broken arrows show the area of the digestive tract used for comparison between parasitized and non-parasitized sea urchins. B, Impact of the pinnotherid symbiont on the area of the host sea urchin intestine (rectal section). C, Relationship of the widening of the intestine (rectal section) with the diameter of the pinnotherid guest.
Fig. 5. A in Tripedalia maipoensis Sun & Tsui & Wong & Cheung & Ng & Or & Qiu 2023, sp. nov.
Fig. 5. A, Relationship between the test diameter and dry weight of the non-gonadal tissues of the sea urchins collected at Calfuco Beach. N = 73. B, Relationship between presence or absence of pinnotherid symbionts and the weight of non-gonadal sea urchin tissues. C, Influence of the size of the hosted pinnotherid on the dry non-gonadal tissue weight of the sea urchin specimens collected in the Calfuco Beach. N = 62.
Fig. 4. A in Tripedalia maipoensis Sun & Tsui & Wong & Cheung & Ng & Or & Qiu 2023, sp. nov.
Fig. 4. A, Relationship between the dry gonadal weight and the test diameter of the sea urchins collected on Calfuco Beach in 2021. N = 73. B, sea urchin test diameter and dry gonadal weight in sea urchins with pinnotherid and without pinnotherid symbionts, and C, Relationship between symbiont-harboring sea urchin dry gonadal weight and the length of the pinnotherid carapace. N = 62.
Fig. 1. A in Tripedalia maipoensis Sun & Tsui & Wong & Cheung & Ng & Or & Qiu 2023, sp. nov.
Fig. 1. A, Sea urchin without the upper part of the testa, showing the parasitic pinnotherid. P = pinnotherid, G = sea urchin gonads. B, Intertidal environment from which sea urchins were obtained. C, Map of South America, indicating (arrow) the sampling site of the sea urchin used in the present study.
Fig. 7 in Microphysogobio zhangi Sun & Zhao 2022, n. sp.
Fig. 7. Relationship between the number of ovarian corpora and age from female pilot whales (G. melas edwardii). The dark line corresponds to the linear regression (R2 = 0.4483). © 2017 Academia Sinica, Taiwan
Fig. 6 in Microphysogobio zhangi Sun & Zhao 2022, n. sp.
Fig. 6. Relationship between corpora lutea size and fetal size from female pilot whales (G. melas edwardii). The dark line corresponds to the linear regression (R2 = 0.1506)
Fig. 4 in Microphysogobio zhangi Sun & Zhao 2022, n. sp.
Fig. 4. Body growth models by age. Green line designates data from von Bertalanffy model. Orange line designates data from Gompertz model. Symbols designate observed data.
Fig. 2 in Microphysogobio zhangi Sun & Zhao 2022, n. sp.
Fig. 2. Sexual maturity: number of females (G. melas edwardii) by reproductive status and size. Table 1. Average measurements and weights from both ovaries
Fig. 3 in Microphysogobio zhangi Sun & Zhao 2022, n. sp.
Fig. 3. Percent of mature females (G. melas edwardii) by age class (px: ●) and expected values for the adjustment (-) and its 95% CI (-). Above px according to Smith method (1973) and below px by DeMaster method (1984). © 2017 Academia Sinica, Taiwan
Fig. 1 in Microphysogobio zhangi Sun & Zhao 2022, n. sp.
Fig. 1. Deposition pattern on dentine (a). Deposition pattern on cement (b). In both cases, each point represents a GLG.
Fig. 5 in Microphysogobio zhangi Sun & Zhao 2022, n. sp.
Fig. 5. Total evaporative water loss (TEWL) and share of heat dissipated by evaporation (%He) in non-Passeriformes at TA TA = Tlc and at TA TA = Tuc as function of body mass. © 2017 Academia Sinica, Taiwan
Fig. 3 in Microphysogobio zhangi Sun & Zhao 2022, n. sp.
Fig. 3. (A) total evaporative water loss (TEWL) at TA = 25°C as a function of body mass in all birds (this study and Willams, 1996). (B) total evaporative water loss (TEWL) at TA = 25°C as s function of body mass in Passeriformes and Non-Passeriformes (this study and Willams 1996).
Fig. 1 in Microphysogobio zhangi Sun & Zhao 2022, n. sp.
Fig. 1. Body mass loss per hour as a function of time after feeding for small (upper panel) and large (bottom panel) birds. Data for upper panel were slightly displaced horizontally to prevent overlapping. Body mass was measured every hour and thus body mass loss per hour is a mass difference between two successive measurements.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.