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opencc-by-4.0Sep 2017View details →

Fig. 2 in Seasonal abundance and spatial distribution of Diaphania hyalinata (Lepidoptera: Crambidae) on yellow squash in south Florida

Fig. 2. Weekly abundance (mean ± SE per 2 leaves) of total Diaphania hyalinata larvae on yellow squash during 4 planting seasons from 26 May through 30 Dec 2014. Means topped by the same lowercase letter are not significantly different (P> 0.05) (analysis of variance and Waller–Duncan K-ratio test). Bars above and below means represent standard errors.

opencc-by-4.0Jun 2017View details →

Fig. 1. Percival environmental chambers housing Eumaeus atala. A in Life history variations and seasonal polyphenism in Eumaeus atala (Lepidoptera: Lycaenidae)

Fig. 1. Percival environmental chambers housing Eumaeus atala. A) Interior view of fabric housing cages in the Percival chambers and B) plastic 'deli-box' larval cages inside with host plant material and young Eumaeus atala larvae.

opencc-by-4.0Sep 2017View details →

Fig. 1 in Seasonal abundance and spatial distribution of Diaphania hyalinata (Lepidoptera: Crambidae) on yellow squash in south Florida

Fig. 1. Weekly abundance (mean ± SE per 2 leaves) of small (L1 + L2), medium (L3 + L4), large (L5) Diaphania hyalinata larvae on yellow squash from a) 26 May through 16 Jun, b) 18 Jul through 8 Aug, c) 1 Sep through 22 Sep, and d) 9 Dec through 30 Dec 2014. Means topped by the same uppercase letter are not significantly different (P> 0.05) between larval sizes, and means topped by the same lowercase letter are not significantly different (P> 0.05) between sampling dates (analysis of variance and Waller–Duncan K-ratio test). Bars above and below means represent standard errors.

Fig. 4 in Occurrence and seasonality of internal parasite infection in elephants, Loxodonta africana, in the Okavango Delta, Botswana

Fig. 4. The prevalence of fluke (= trematode) eggs in wild elephants of different ages, using sedimentation of FP-samples (formalin-preserved faecal samples).

Fig. 2 in Occurrence and seasonality of internal parasite infection in elephants, Loxodonta africana, in the Okavango Delta, Botswana

Fig. 2. Nematode egg densities found in UP-samples (unpreserved, immediately analysed faecal samples) from wild elephants, categorised into two group types. Group 1 consists of groups with all female elephants and/or male elephants under the age of 15 years, and Group 2 consists of male elephants aged 15 years or more. Error bars show the standard deviation. EPG = eggs per gram of faeces.

Fig. 1 in Occurrence and seasonality of internal parasite infection in elephants, Loxodonta africana, in the Okavango Delta, Botswana

Fig. 1. The prevalence of coccidial oocysts in FP-samples (formalin-preserved faecal samples) from wild elephants, in each month (2008 to 2012 combined).

Fig. 3 in Occurrence and seasonality of internal parasite infection in elephants, Loxodonta africana, in the Okavango Delta, Botswana

Fig. 3. Photomicrographs of typical nematode (A) and trematode (= fluke, B) eggs found in elephant faecal samples. For dimensions see text.

opencc-by-4.0Jan 2018View details →

Fig. 3 in Seasonal, Lunar and Tidal Influences on Habitat Use of Indo-Pacific Humpback Dolphins in Beibu Gulf, China.

Fig. 3. Map of humpback dolphin sightings based on (a) dry and wet seasons, (b) lunar phases and (c) tidal phases for the humpback dolphins in northern Beibu Gulf.

opencc-by-4.0Jan 2018View details →

Fig. 4 in Seasonal, Lunar and Tidal Influences on Habitat Use of Indo-Pacific Humpback Dolphins in Beibu Gulf, China.

Fig. 4. The profile of distance from estuary (a) and water depth (b) of humpback dolphin sightings in northern Beibu Gulf among different seasons, lunar phases and tidal phases, and significance tests (c, d). Note: "*" indicates a significance at P <0.05, "**" indicates a significance at P <0.01.

opencc-by-4.0Jan 2018View details →

Fig. 2 in Seasonal, Lunar and Tidal Influences on Habitat Use of Indo-Pacific Humpback Dolphins in Beibu Gulf, China.

Fig. 2. Definitions for high and low tidal phases in the Beibu Gulf, China, as used in the present study.

Fig. 4 in Physiological and Biochemical Thermoregulatory Responses in Male Chinese Hwameis to Seasonal Acclimatization: Phenotypic Flexibility in a Small Passerine.

Fig. 4. Seasonal variation in dry mass (A), state-4respiration (B), and cytochrome c oxidase (C) in the pectoral muscle, heart, liver and kidneys of hwameis (Garrulaxcanorus) captured in either summer or winter in Wenzhou, China. Data are shown as mean ± SEM, *p <0.05, **p <0.01, ***p <0.001.

Fig. 3 in Physiological and Biochemical Thermoregulatory Responses in Male Chinese Hwameis to Seasonal Acclimatization: Phenotypic Flexibility in a Small Passerine.

Fig. 3. Correlations between body mass and resting metabolic rate (RMR) (A), between body mass and EWL (B), between RMR and EWL (C), and between RMR and thermal conductance (D) in Chinese hwameis (Garrulax canorus) captured in either summer or winter in Wenzhou, China.

Fig. 1 in Physiological and Biochemical Thermoregulatory Responses in Male Chinese Hwameis to Seasonal Acclimatization: Phenotypic Flexibility in a Small Passerine.

Fig. 1. Minimum, maximum and mean ambient daily summer (July to August 2013) and winter (January to February 2014) temperatures in Wenzhou, China. Mean ambient temperature ranged from 31.3 ± 0.2°C in summer to 8.6 ± 0.4°C in winter.

Fig. 2 in Physiological and Biochemical Thermoregulatory Responses in Male Chinese Hwameis to Seasonal Acclimatization: Phenotypic Flexibility in a Small Passerine.

Fig. 2. Seasonal variation in body mass (A), resting metabolic rate (B), evaporative water loss (C) and thermal conductance (D) in Chinese hwamei (Garrulax canorus) captured in either summer or winter in Wenzhou, China. Data are shown as mean ± SEM, **p <0.01.

Fig. 5 in Physiological and Biochemical Thermoregulatory Responses in Male Chinese Hwameis to Seasonal Acclimatization: Phenotypic Flexibility in a Small Passerine.

Fig. 5. Correlations between resting metabolic rate (RMR) and state-4 respiration in the pectoral muscle (A), heart (C), liver (E) and kidneys (G), and between RMR and cytochrome c oxidase activity in the pectoral muscle (B), heart (D), liver (F) and kidneys (H), in Chinese hwameis (Garrulax canorus) captured in either summer or winter in Wenzhou, China.

opencc-by-4.0Dec 2015View details →

Fig. 3 in Seasonal variation in the abundance and distribution of ticks that parasitize Microcebus griseorufus at the BezàMahafaly Special Reserve, Madagascar

Fig. 3. Possible life cycle of H. lemuris. Peak activity for larvae occurs in May, but larvae may be found feeding into June and October. Larvae attach to Microcebus hosts and after a blood meal, fall off and molt into nymphs. Nymphs are active and feed on Microcebus throughout the dry season and likely feed on other lemurs during part of the wet season. Adult-stage ticks remain active during the wet season, feeding on larger-bodied lemurs, such as L. catta, and P. verreauxi. Engorged females fall off and lay eggs in leaf litter. It is possible that all four stages can diapause if no suitable hosts or conditions are found (gray dotted line). Mice or rats may also serve as hosts to larvae during the dry season.

opencc-by-4.0Dec 2015View details →

Fig. 1. Monthly averages for A in Seasonal variation in the abundance and distribution of ticks that parasitize Microcebus griseorufus at the BezàMahafaly Special Reserve, Madagascar

Fig. 1. Monthly averages for A) tick intensity on mouse lemurs as it compares to B) rainfall and C) temperature, during the year-long study season. Shaded area indicates months included in the dry season. Environmental data were collected daily.

opencc-by-4.0Dec 2015View details →

Fig. 2 in Seasonal variation in the abundance and distribution of ticks that parasitize Microcebus griseorufus at the BezàMahafaly Special Reserve, Madagascar

Fig. 2. Differences in infestation rates at Parcel 1 by A) sex B) substrate C) males and substrate and D) females and substrate. * indicates P <0.05, **P <0.01; ***P <0.001 and compares variables on the x-axis.

opencc-by-4.0Dec 2017View details →

Fig. 1. A in Seasonality, richness and prevalence of intestinal parasites of three neotropical primates (Alouatta seniculus, Ateles hybridus and Cebus versicolor) in a fragmented forest in Colombia

Fig. 1. A. Trichuris sp., B. Oxyuridae, C. Ancylostomatidae, D. Strongyloides sp. (larva), E. Ascarididae, F. Gnathostomatidae, G. Trichostrongylidae, H-I. Trematodes, J. Entamoeba sp. (cyst), K. Acanthocephala, L. Balantidiidae.