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Fig. 6 in Occurrence and characterisation of tongue worms, Linguatula spp., in South Africa

Fig. 6. Scanning electron microscopy of the nymph #8–2 from African buffalo: A) full view of the parasite; B) anterior end of the parasite showing the mouth, hooks, sensillae (the squares at the top of the image) and the sensory papilla (white square); C) & D) magnified view of the right and left sensillae, respectively; E) structure of the surface of the oral papilla; F to H) left anterior, right anterior and right posterior hooks, respectively; I) annular spines on the anterior ventral region; J) tips of the annular spines; K) pores and annular spine in mid body region (ventral); L) posterior end of the parasite (ventral view).

Fig. 3 in Occurrence and characterisation of tongue worms, Linguatula spp., in South Africa

Fig. 3. Scanning electron microscopy of an adult male Linguatula nuttali from Panthera leo. Colours and shapes in images are enlargement of the corresponding areas in the previous images: A) ventral view of the anterior end of the parasite; B) magnified view of the anterior end indicating location of the minute tentacles on the right side of the parasite; C) magnified view of the right tentacles. Note presence of minute structures around tentacles (arrows); D) Tentacles and the minute structures on the left side of the anterior end; E) mouth; F) magnified view of the most anterior right hook; G) magnified view of the posterior right hook; H) magnified view of a sensory papilla located lateral to the genital pore; I) genital pore; J) magnified view of the posterior left hook; K) arrangement of the annuli on the abdominal region of the parasites; L) magnified view of the border of the annuli in the abdominal region showing presence and arrangements of the scale like projections and pores (arrow); Note presence of multiple rows of scale like projections on the posterior of each annulus and a row of pores on the anterior part of each annulus; M) posterior end showing the terminal cleft (ventral view). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

Fig. 1. Linguatula nuttali female specimen collected from Panthera leo. A in Occurrence and characterisation of tongue worms, Linguatula spp., in South Africa

Fig. 1. Linguatula nuttali female specimen collected from Panthera leo. A) Anterior end, ventral surface. B) L. nuttali (on the right) compared to a specimen of L. serrata collected from a Canis familiaris in Australia (on the left). Note the differences in annuli and overall body shape. C) Posterior ends of L. nuttali (on the bottom) compared to a specimen of L. serrata collected from a C. familiaris in Australia (on the top). Note the deep cleft in the posterior end of L. nuttali compared to the posterior end of L. serrata. D) The posterior end of L. nuttali showing the deep cleft.

Fig. 2 in Occurrence and characterisation of tongue worms, Linguatula spp., in South Africa

Fig. 2. Linguatula nuttali female specimen collected from Panthera leo (A to C) and female nymph collected from African buffalo (D to H). A) High magnification of the cuticular annulation. Cuticle taken from near the anterior end. Bottom of annulus has "scales" and a single row of pores across the middle of the annulus. B) Anterior hook and fulcrum. C) Posterior hook and fulcrum. D) Ventral view of the anterior end. E) Magnified view of the buccal cadre and hooks. F) Buccal cadre. G. Anterior hook. H. Posterior hook.

Fig. 4 in Occurrence and characterisation of tongue worms, Linguatula spp., in South Africa

Fig. 4. Scanning electron microscopy of the nymph #7–2 from African buffalo: A) ventral view of the anterior end of the parasite showing the mouth, hooks (including dorsal accessory pieces (and magnified view of the tip of the dorsal accessory piece in the white square at the bottom right of 4A)), sensillae (the white squares at the top of the image); B) view of the outline of the buccal capsule with the oral papilla; C) magnified view of the oral papilla; D) right anterior hook and dorsal accessory piece (arrow) with magnified view of the tip of the latter shown in the white square box; E) dorsal accessory piece of the left anterior hook; F) arrangement of the first row of the annular spines located between the posterior hooks; G) pores and annular spines in mid body region (ventral); H) tips of the annular spines; I) oblique/lateral view of the posterior end of the parasite; J) full view of the parasite.

Fig. 5 in Occurrence and characterisation of tongue worms, Linguatula spp., in South Africa

Fig. 5. Scanning electron microscopy of the nymph #7–5 from African buffalo: A) full view of the parasite; B) ventral view of the anterior end of the parasite showing the mouth, hooks, sensillae (the squares at the top of the image) and the sensory papilla (white square); C) mouth; D to G) right anterior, right posterior, left anterior and left posterior dorsal accessory pieces, respectively; H) arrangement of the first rows of the annular spines located between the posterior hooks; I) annular spines on the anterior ventral region; J) tips of the annular spines; K) rows of annular spines (mid-body region); L) pores and annular spines in mid body region (ventral); M) pores and annular spine in posterior region (ventral); N) posterior end of the parasite (ventral view).

Fig. 8 in Occurrence and characterisation of tongue worms, Linguatula spp., in South Africa

Fig. 8. Phylogenetic analysis of Cox1 and 18sRNA sequences for Linguatula spp., with Armillifer agkistrodontis as an outgroup for Cox1 (a) and 18sRNA (b) sequences, respectively. Bayesian posterior probabilities values are indicated on the branches.

opencc-by-4.0Aug 2024View details →

Codes and source data for "Common occurrences of subsurface heatwaves and cold-spells in ocean eddies"

This repository contains the MATLAB (R2022b) codes (*.m files) and the figure source data (.mat files)  for the paper "Common occurrences of subsurface heatwaves and cold-spells in ocean eddies" (He et al., 2024).  For installation of MatLab, please refer to: https://au.mathworks.com/products/matlab.html For queries about this repository and its contents, please contact Dr. Qingyou He (qyhe@scsio.ac.cn). %% Fig1.m: For plotting main Fig.1. %% Fig2.m: For plotting main Fig.2. %% Fig3.m: For plotting main Fig.3. %% Fig4.m: For plotting main Fig.4. %% Fig5.m: For plotting main Fig.5. %% Fig6.m: For plotting main Fig.6. %% Data Fig1.mat: For main Fig.1. %% Data Fig2.mat: For main Fig.2. %% Data Fig3.mat: For main Fig.3. %% Data Fig4.mat: For main Fig.4. %% Data Fig5.mat: For main Fig.5. %% Data Fig6.mat: For main Fig.6. References: He, Q., W. Zhan, M. Feng, Y. Gong, S. Cai, and H. Zhan (2024), Common occurrences of subsurface heatwaves and cold spells in ocean eddies, Nature, 634, 1111–1117, doi:10.1038/s41586-024-08051-2.

opencc-by-4.0Mar 2018View details →

Fig. 1 in Occurrence of coccinellids that prey on Diaphorina citri (Hemiptera: Liviidae) on Euphorbia heterophylla (Euphorbiaceae) and Chamaecrista fasciculata (Fabaceae) in a south Florida residential area

Fig. 1. Nectary plants monitored for presence of coccinellids. (A) Chamaecrista fascisculata foliage. (B) Euphorbia heterophylla with adult Harmonia axyridis. Arrows show nectaries.

opencc-by-4.0Sep 2018View details →

Fig. 2 in Environmental determinants affecting the occurrence of defoliator caterpillars on Eucalyptus (Myrtaceae) plantations in the Brazilian Amazonian region

Fig. 2. Average annual growth of Eucalyptus urophylla (Myrtaceae) trees (m3 of wood per ha per yr) as a function of the total number of Lepidoptera individuals collected per light trap (Almeirim Municipality, Pará State, and Laranjal do Jari Municipality, Amapá State, Brazil).

opencc-by-4.0Sep 2018View details →

Fig. 3 in Environmental determinants affecting the occurrence of defoliator caterpillars on Eucalyptus (Myrtaceae) plantations in the Brazilian Amazonian region

Fig. 3. Total number of individuals of the 2 Lepidoptera primary pests, Misogada bleura (Lepidoptera: Notodontidae) and Sarsina violascens (Lepidoptera: Lymantriidae), collected with light traps in Eucalyptus urophylla (Myrtaceae) plantations as a function of the distance from the area of native vegetation (Almeirim Municipality, Pará State, and Laranjal do Jari Municipality, Amapá State, Brazil).

opencc-by-4.0Sep 2018View details →

Fig. 1 in Environmental determinants affecting the occurrence of defoliator caterpillars on Eucalyptus (Myrtaceae) plantations in the Brazilian Amazonian region

Fig. 1. Number of Oxydia vesulia (Lepidoptera: Geometridae) and Sarsina violascens (Lepidoptera: Lymantriidae) adults collected with light traps in Eucalyptus urophylla (Myrtaceae) plantations as a function of the number of rotations of this plant in the same area. (Almeirim Municipality, Pará State, and Laranjal do Jari Municipality, Amapá State, Brazil).

opencc-by-4.0Nov 2018View details →

Fig. 1 in Options for managing Antestiopsis thunbergii (Hemiptera: Pentatomidae) and the relationship of bug density to the occurrence of potato taste defect in coffee

Fig. 1. Effects of pest management tactics on the occurrence of potato taste defect in coffee. No Prun(P) & No Pest (No Pruning and No Pesticide), P & No Pest (Pruning and No Pesticide), P & Fastac (Pruning and Fastac), P & Pyr 5EW (Pruning and Pyrethrum 5EW), P & Pyr EWC (Pruning & Pyrethrum EWC), P & Agroblast (Pruning and Agroblast), and P & Imida (Pruning and Imidacloprid). Fastac sprayed in pruned plots had the lowest levels of potato taste defect whereas the control had the highest. Bars represent the standard error of means. Means followed with the same letter are not statistically different (P ≤ 0.05, ANOVA and Tukey's test).

Fig. 5. Average and 95 in Larvae occurrences of Rhamdia quelen (Quoy & Gaimard, 1824) (Siluriformes: Heptapteridae) in an area under dam influence in the upper Paraná River region, Brazil

Fig. 5. Average and 95% confidence interval for the mean log (Dens. + 1) observed in the different sampling stations 10 during the period (Different letters indicate significant differences according to the Unequal HSD test).

Fig. 4 in Larvae occurrences of Rhamdia quelen (Quoy & Gaimard, 1824) (Siluriformes: Heptapteridae) in an area under dam influence in the upper Paraná River region, Brazil

Fig. 4. Monthly average values of environmental variables in different spawning periods in Ilha Grande National Park.

Fig. 2 in Larvae occurrences of Rhamdia quelen (Quoy & Gaimard, 1824) (Siluriformes: Heptapteridae) in an area under dam influence in the upper Paraná River region, Brazil

Fig. 2. Average abundance of R. quelen larvae by spawning period (a), month (b), and sampling station (c).

Fig. 3 in Larvae occurrences of Rhamdia quelen (Quoy & Gaimard, 1824) (Siluriformes: Heptapteridae) in an area under dam influence in the upper Paraná River region, Brazil

Fig. 3. Monthly density and per sampling stations of the larval development stages of Rhamdia quelen in Ilha Grande National Park.

Fig. 1 in Larvae occurrences of Rhamdia quelen (Quoy & Gaimard, 1824) (Siluriformes: Heptapteridae) in an area under dam influence in the upper Paraná River region, Brazil

Fig. 1. Location of sampling stations (black dots). (1: Bandeirantes right channel; 2: Amambaí; 3: Triângulo; 4: Porto Santo Antônio; 5: Peruzzi; 6: Paraná/Iguatemi; 7: Iguatemi; 8: Paraná/Saraiva; 9: Saraiva middle; 10: Saraiva channel; 11: Ilha Grande right channel; 12: Bandeirantes left channel; 13: Ilha Grande Pontal; 14: Alvarenga; 15: Esmeralda; 16: Três Coqueiros; 17: São João; 18: Porto Luiz; 19 Porto Cerâmica; 20: Piquiri; 21: Porto Terra Roxa; 22: Ilha Grande left channel).

opencc-by-4.0Oct 2023View details →

Fig. 1 in Short Communication Further evidence of the occurrence of the Atlantic blue crab Callinectes sapidus (Rathbun 1896) (Crustacea: Decapoda: Portunidae) along the central Tyrrhenian coast

Fig. 1 - Map of the study area (Latium, Tyrrhenian central Italy) with record of Atlantic blue crab Callinectes sapidus (Rathbun 1896). Black dots: original data (numbers); white dots: indirect data (letters). See Table 1 for details. / Mappa dell'area di studio (Lazio, Italia centrale tirrenica) con segnalazioni del granchio reale blu Callinectes sapidus (Rathbun 1896). Cerchi neri: dati originali (numeri); cerchi bianchi: dati indiretti (lettere). Si veda Tabella 1 per dettagli.