Find research datasets worth reusing

opencc-by-4.0Jun 2018View details →

Fig. 6 in Reproductive biology of the eyespot skate Atlantoraja cyclophora (Elasmobranchii: Arhynchobatidae) an endemic species of the Southwestern Atlantic Ocean (34ºS - 42ºS)

Fig. 6. Seasonal variation in gonadosomatic (GSI) and hepatosomatic (HSI) indexes for a.-b. males and c.-d. females of Atlantoraja cyclophora. The number of samples analyzed is between parentheses. The boxes represent the interquartile range between Q1 and Q3 with the 50% of data, the central line represents the median value and whiskers extend to the maximum and minimum values

Fig. 8 in Reproductive biology of Poecilia sphenops Valenciennes, 1846 (Cyprinidontiformes: Poeciliidae) at the Emiliano Zapata Reservoir in Morelos, Mexico

Fig. 8. Seasonal variation of chlorophyll a concentration (mg/m³), water temperature (°C) and dissolved oxygen (mg/L) at Emiliano Zapata Reservoir.

Fig. 7 in Reproductive biology of Poecilia sphenops Valenciennes, 1846 (Cyprinidontiformes: Poeciliidae) at the Emiliano Zapata Reservoir in Morelos, Mexico

Fig. 7. Seasonal variation of the condition index (K) of P. sphenops in the Emiliano Zapata Reservoir.

Fig. 6 in Reproductive biology of Poecilia sphenops Valenciennes, 1846 (Cyprinidontiformes: Poeciliidae) at the Emiliano Zapata Reservoir in Morelos, Mexico

Fig. 6. Seasonal variation of the gonadosomatic index (GSI) for Poecilia sphenops females (a) and males (b).

Fig. 1 in Reproductive biology of Poecilia sphenops Valenciennes, 1846 (Cyprinidontiformes: Poeciliidae) at the Emiliano Zapata Reservoir in Morelos, Mexico

Fig. 1. Map showing location of the study area in Mexico where Poecilia sphenops samples were collected.

Fig. 2 in Reproductive biology of Poecilia sphenops Valenciennes, 1846 (Cyprinidontiformes: Poeciliidae) at the Emiliano Zapata Reservoir in Morelos, Mexico

Fig. 2. Length frequency distribution by sex for Poecilia sphenops at Emiliano Zapata Reservoir, Mexico.

Fig. 3 in Reproductive biology of Poecilia sphenops Valenciennes, 1846 (Cyprinidontiformes: Poeciliidae) at the Emiliano Zapata Reservoir in Morelos, Mexico

Fig. 3. Monthly sex ratio for Poecilia sphenops in the Emiliano Zapata Reservoir. Asterisks indicate not significant differences.

Fig. 4 in Comparative Biology Of Cave-Dwelling Spitting Spiders (Araneae: Scytodidae): Parental Care, Cooperative Prey-Capture, Cannibalism, Natal Dispersal And Reproductive Behaviour

Fig. 4. Scytodid egg-sac. (A) Typical egg-sac of Scytodes cavernarum, S. fusca and the Philippines Scytodes sp. 2; and (B) Scytodes magna egg-sac. Note the denser silk surrounding the eggs of S. magna.

Fig. 8 in Comparative Biology Of Cave-Dwelling Spitting Spiders (Araneae: Scytodidae): Parental Care, Cooperative Prey-Capture, Cannibalism, Natal Dispersal And Reproductive Behaviour

Fig. 8. Reproductive traits of five cave species of scytodids. (A) Mean (± S.E.) total number of spiderlings per female; (B) mean (± S.E.) egg hatching time (d); (C) mean (± S.E.) interval (d) between clutches; (D) mean (± S.E.) interval (d) between hatching and the next egg-sac production; (E) mean (± S.E.) number of clutches; and (F) mean (± S.E.) number of spiderlings per clutch. Different lower cases indicate significant differences.

Fig. 3 in Comparative Biology Of Cave-Dwelling Spitting Spiders (Araneae: Scytodidae): Parental Care, Cooperative Prey-Capture, Cannibalism, Natal Dispersal And Reproductive Behaviour

Fig. 3. Maternal care of egg-sacs in spitting spiders. (A) Scytodes fusca female carrying her egg-sac in her chelicerae. (B) Guangxi Scyloxes sp. 1 female on the surface of the outer cave walls, staying close to her egg-sac. The egg-sac is suspended by two to three threads. (C) Web constructed by S. magna female. Her egg-sac is suspended by a few threads at the centre of the web.

Fig. 2 in Comparative Biology Of Cave-Dwelling Spitting Spiders (Araneae: Scytodidae): Parental Care, Cooperative Prey-Capture, Cannibalism, Natal Dispersal And Reproductive Behaviour

Fig. 2. The 'cage within a cage' set-up for studying the natal dispersal patterns of scytodid spiders. Modified from Ruttan (1990).

Fig. 1 in Comparative Biology Of Cave-Dwelling Spitting Spiders (Araneae: Scytodidae): Parental Care, Cooperative Prey-Capture, Cannibalism, Natal Dispersal And Reproductive Behaviour

Fig. 1. Four species of cave scytodid spiders. (A) female and (B) male Scytodes magna, body length = 10.5 mm; (C) female and (D) male S. fusca, body length = 5.8 mm; (E) female Philippines Scytodes sp. 2, body length = 5.6mm; and (F) female S. cavernarum, body length = 5.3 mm.

Fig. 6 in Comparative Biology Of Cave-Dwelling Spitting Spiders (Araneae: Scytodidae): Parental Care, Cooperative Prey-Capture, Cannibalism, Natal Dispersal And Reproductive Behaviour

Fig. 6. Newly emerged Guangxi Scyloxes sp. 1 spiderlings spread out on the sparse silk nest, and female feeding on house fly alone. Body length of adult female = 11.5 mm.

Fig. 7 in Comparative Biology Of Cave-Dwelling Spitting Spiders (Araneae: Scytodidae): Parental Care, Cooperative Prey-Capture, Cannibalism, Natal Dispersal And Reproductive Behaviour

Fig. 7. Relationship between the days in which spiderlings dispersed and spiderling mass in five cave scytodid species. (A) Scytodes fusca; (B) S. carvernarum; (C) Philippines Scytodes sp. 2.; (D) S. magna; and (E) Guangxi Scyloxes sp. 1.

Figure 1 in Are fisheries regulations influencing the biology and reproduction of the surmullet Mullus surmuletus Linnaeus, 1758 on the south-eastern coasts of France (NW Mediterranean)?

Figure 1. – Sampling sites in West, AMA (Adjacent Marine Protected Area of Hyères Bay) and East zones on the south-eastern coast of France, NW Mediterranean Sea.

Figure 4 in Are fisheries regulations influencing the biology and reproduction of the surmullet Mullus surmuletus Linnaeus, 1758 on the south-eastern coasts of France (NW Mediterranean)?

Figure 4. – Percentages of both sexes and females:males sex-ratio of Mullus surmuletus by zone (A) and season (B).

Figure 3 in Are fisheries regulations influencing the biology and reproduction of the surmullet Mullus surmuletus Linnaeus, 1758 on the south-eastern coasts of France (NW Mediterranean)?

Figure 3. – Mean (± SE) total length (TL, cm) of Mullus surmuletus in West, AMA and East zones. N: number of analyzed individuals per sex in zones. Values with the same post-hoc letters (red for females, blue for males) are not significantly different (p> 0.05).

Figure 2 in Are fisheries regulations influencing the biology and reproduction of the surmullet Mullus surmuletus Linnaeus, 1758 on the south-eastern coasts of France (NW Mediterranean)?

Figure 2. – Percentage of individuals of Mullus surmuletus analyzed by two-cm size class (total length in cm) and by sex. N: number of individuals, F: females, M: males, Undet.: unidentified group includes immature individuals and those whose sex could not be identified.

Figure 8 in Are fisheries regulations influencing the biology and reproduction of the surmullet Mullus surmuletus Linnaeus, 1758 on the south-eastern coasts of France (NW Mediterranean)?

Figure 8. – Mean percentages of gonadal development stages (GDS) of Mullus surmuletus. A: By zone for females; B: By zone for males; C: By season for females; D: By season for males. N: number of individuals.

Figure 6 in Are fisheries regulations influencing the biology and reproduction of the surmullet Mullus surmuletus Linnaeus, 1758 on the south-eastern coasts of France (NW Mediterranean)?

Figure 6. – Mean gonado-somatic index (GSI, %) of males and females of Mullus surmuletus by (A) zone and (B) season. Values with the same post-hoc let-letters (red for females, blue for males) are not significantly different (p> 0.05).