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Fig. 21. Lacunipotamon panda n in Fig. 20 in Lanternflies (Hemiptera: Fulgoridae) of Taiwan.

Fig. 21. Lacunipotamon panda n. sp., paratype female (36.8 × 25.6 mm) (ZRC 2022.0707), Vietnam. A, overall dorsal habitus; B, dorsal view of carapace; C, pleon; D, sternopleonal cavity showing vulvae.

Fig. 19. Lacunipotamon panda n in Fig. 20 in Lanternflies (Hemiptera: Fulgoridae) of Taiwan.

Fig. 19. Lacunipotamon panda n. sp. A–E, holotype male (38.3 × 27.4 mm) (ZRC 2022.0706), Vietnam; F, G, paratype male (38.6 × 27.3 mm) (ZRC 2022.0707), Vietnam. A, anterior half of thoracic sternum and pleon; B, sternopleonal cavity; C, left fourth ambulatory leg; D, pleonal somites 1–4; E, G, pleon; F, right major chela.

Fig. 17. Lacunipotamon panda n in Fig. 20 in Lanternflies (Hemiptera: Fulgoridae) of Taiwan.

Fig. 17. Lacunipotamon panda n. sp., colour in life. A, paratype female (34.7 × 25.1 mm) (ZRC 2022.0707), Vietnam; B, paratype male (38.6 × 27.3 mm) (ZRC 2022.0707), Vietnam; C–F, holotype male (38.3 × 27.4 mm) (ZRC 2022.0706), Vietnam.

Fig. 18. Lacunipotamon panda n in Fig. 20 in Lanternflies (Hemiptera: Fulgoridae) of Taiwan.

Fig. 18. Lacunipotamon panda n. sp., holotype male (38.3 × 27.4 mm) (ZRC 2022.0706), Vietnam. A, overall dorsal habitus; B, dorsal view of carapace; C, right third maxilliped; D, frontal view of cephalothorax; E, antennules, antennae and epistome; F, right major chela; G, left minor chela.

opencc-by-4.0Apr 2019View details →

Fig. 1 in Evidence of red panda as an intermediate host of Toxoplasma gondii and Sarcocystis species

Fig. 1. Sarcocysts and Toxoplasma gondii cysts in red panda or mice. A: Tissue cysts, leg muscle, red panda. Two oval cysts (arrow) were observed in the skeletal muscle cell. The walls of the two cysts (arrowhead) were deeply stained by eosin. Red panda, H&E. B: Partial magnification of figure A. a, The wall of the cyst was clearly and deeply stained by eosin. b, The bradyzoites were like cresent or banana, they were arranged in packets (arrowhead). c, Necleus of host cell. C: Tissue cyst (arrow) was cross reacted with T. gondii, the cysts were separated by septa and formed many compartments (arrowhead), leg muscle. T. gondii antibody, red panda, IHC. D: Tissue cysts of T. gondii in brain of mouse (arrows), brain squash, unstained, 75DPI. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

opencc-by-4.0Aug 2020View details →

Fig. 2 in MHC-associated Baylisascaris schroederi load informs the giant panda reintroduction program

Fig. 2. Effects of MHC genotypes on (a–b) infection probability, (c–d) EPG of B. schroederi using important predictors. The Bars show the 95%CI.

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Fig. 3 in MHC-associated Baylisascaris schroederi load informs the giant panda reintroduction program

Fig. 3. Effects of MHC alleles on infection probability (a and b) and EPG (c and d) of B. schroeder.i. The bars show the 95%CI.

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Fig. 1 in Review on parasites of wild and captive giant pandas (Ailuropoda melanoleuca): Diversity, disease and conservation impact

Fig. 1. Distribution of wild giant pandas in six mountain regions (Qinling, Minshan, Qionglai, Liangshan, Daxiangling and Xiaoxiangling) in three Provinces (Gansu, Shaanxi, and Sichuan) of China. Adapted from Wang et al. (2018).

opencc-by-4.0Aug 2022View details →

Fig. 1 in Comparison of a commercial ELISA and indirect hemagglutination assay with the modified agglutination test for detection of Toxoplasma gondii antibodies in giant panda (Ailuropoda melanoleuca)

Fig. 1. Receiver operating characteristics (ROC) analysis of the ELISA. ROC analysis shows an area under the curve (AUC) of 0.861 (95% CI: 0.712–1.000) for ELISA (a), 0.894 (95% CI: 0.791–0.997) for ELISA (b), and 0.902 (95% CI: 0.799–1.000) for ELISA (c).

Fig. 3 in A snapshot of climate drivers and temporal variation of Ixodes ovatus abundance from a giant panda living in the wild

Fig. 3. Boxplot of tick abundance, female-to-male ratio and important climate factors change by months. A: Tick daily abundance; B: Daily female-to-male ratio of ticks; C: Daily temperature; D: Daily air pressure. Variables sharing the same letters among months were not significantly different. The five-day-rolling average values were calculated for all the variables that change by months.

Fig. 6 in A snapshot of climate drivers and temporal variation of Ixodes ovatus abundance from a giant panda living in the wild

Fig. 6. Daily average tick abundance, daily average air pressure and daily average temperature with standard deviations by months. All the values are calculated with five-day-rolling average values.

Fig. 2. Ixodes. ovatus collected from the giant panda. A in A snapshot of climate drivers and temporal variation of Ixodes ovatus abundance from a giant panda living in the wild

Fig. 2. Ixodes. ovatus collected from the giant panda. A: Dorsal of the adult female I. ovatus; B: Ventral of the adult female I. ovatus; C: Dorsal of the adult male I. ovatus; D: Ventral of the adult male I. ovatus.

Fig. 5 in A snapshot of climate drivers and temporal variation of Ixodes ovatus abundance from a giant panda living in the wild

Fig. 5. The correlation plot of daily tick abundance and the daily air pressure with trending line. The five-day-rolling average values were calculated for tick abundance and the air pressure.

Fig. 1 in A snapshot of climate drivers and temporal variation of Ixodes ovatus abundance from a giant panda living in the wild

Fig. 1. Experimental site was located in Daxiangling Natural Reserve, which is a part of the Giant Panda National Park in China. The orange area indicates the range of the Giant Panda National Park. The blue star is the location of this experimental site. Continents outline maps by Vemaps.com. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

Fig. 4 in A snapshot of climate drivers and temporal variation of Ixodes ovatus abundance from a giant panda living in the wild

Fig. 4. The correlation plot of daily tick abundance and the daily temperature with the trending line. The five-day-rolling average values were calculated for tick abundance and temperature.

Fig. 2. Pancola ailurus n in Morphological and molecular evidence reveals a new species of chewing louse Pancola ailurus n. sp. (Phthiraptera: Trichodectidae) from the endangered Chinese red panda Ailurus styani

Fig. 2. Pancola ailurus n. sp. (A) Male Pancola ailurus n. sp., habitus (dorsal morphology to the left of the midline, ventral morphology to the right) (B) Female Pancola ailurus n. sp., habitus (dorsal morphology to the left of the midline, ventral morphology to the right) (C) Meso-metasternal plate of Pancola ailurus n. sp. (D) Male genitalia (E) Female genitalia.

Fig. 3 in Morphological and molecular evidence reveals a new species of chewing louse Pancola ailurus n. sp. (Phthiraptera: Trichodectidae) from the endangered Chinese red panda Ailurus styani

Fig. 3. Phylogenetic trees based on the partial mitochondrial (cox1 and 12S rRNA) sequences of Trichodectidae and Bovicoliidae species using Maximum Likelihood (ML). The bootstrap frequencies (Bf) were shown on each node.

Fig. 4 in Morphological and molecular evidence reveals a new species of chewing louse Pancola ailurus n. sp. (Phthiraptera: Trichodectidae) from the endangered Chinese red panda Ailurus styani

Fig. 4. Divergence time and Bayesian analysis based on the partial cox1 sequence of Trichodectidae and Bovicoliidae species using Beast v.1.10.4 with Liposcelis bostrichophila as the outgroup.

Fig. 1 in Morphological and molecular evidence reveals a new species of chewing louse Pancola ailurus n. sp. (Phthiraptera: Trichodectidae) from the endangered Chinese red panda Ailurus styani

Fig. 1. Chinese red panda Ailurus styani and the lice collected from its surface. (A) the Chinese red panda from Chengdu Research Base of Giant Panda Breeding, Chengdu County, Sichuan Province, China (N30.743◦, E104.150◦) (B) the abdomen of male Pancola ailurus (C) the back of male P. ailurus (D) the back of female P. ailurus (E) the abdomen of female P. ailurus.