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Fig. 1. Texas map showing 14 in Seroprevalence of Borrelia burgdorferi antibodies in white-tailed deer from Texas

Fig. 1. Texas map showing 14 counties in which white-tailed deer (WTD) were sampled for Borrelia burgdorferi antibodies from 2001 to 2015. Blue counties: samples negative by ELISA and standardized western immunoblot; Gray counties: negative control samples; Yellow counties: samples sero-reactive by standardized western immunoblot assay (Travis and Williamson counties). (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

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Fig. 2 in Comparison of natural and artificial odor lures for nilgai (Boselaphus tragocamelus) and white-tailed deer (Odocoileus virginianus) in South Texas: Developing treatment for cattle fever tick eradication

Fig. 2. Locations of nilgai lure transects (red bars) at the Santa Rosa Ranch near Riviera, TX. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

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Fig. 5 in Comparison of natural and artificial odor lures for nilgai (Boselaphus tragocamelus) and white-tailed deer (Odocoileus virginianus) in South Texas: Developing treatment for cattle fever tick eradication

Fig. 5. Nilgai cow visiting lure site (A) and (B) nilgai bull defecating at offal lure site at the East Foundation's Santa Rosa Ranch, near Riviera, TX.

Fig. 4 in Molecular identification and characterization of partial COX1 gene from caecal worm (Aulonocephalus pennula) in Northern bobwhite (Colinus virginianus) from the Rolling Plains Ecoregion of Texas

Fig. 4. Molecular Phylogenetic analysis by Maximum Likelihood method. The evolutionary history was inferred using the ML method based on the General Time Reversible model. The phylogenetic tree illustrates COX1 gene sequences of nematodes related to A. pennula. Bootstrap values above 50 are shown in the tree. The tree is drawn to scale, with branch lengths measured in the number of substitutions-per-site. All positions containing gaps and missing data were eliminated. Evolutionary analyses were conducted in MEGA7.

Fig. 1. A in Molecular identification and characterization of partial COX1 gene from caecal worm (Aulonocephalus pennula) in Northern bobwhite (Colinus virginianus) from the Rolling Plains Ecoregion of Texas

Fig. 1. A. Caecum of the wild quail B. Morphology of male and female caecal worm. All the parts of male and female caecal worm Aulonocephalus pennula are marked in Fig. 1B.

Fig. 3 in Molecular identification and characterization of partial COX1 gene from caecal worm (Aulonocephalus pennula) in Northern bobwhite (Colinus virginianus) from the Rolling Plains Ecoregion of Texas

Fig. 3. Pairwise alignment of the sequences of A. pennula and H. gallinarum. Sequence variations between A. pennula and H. gallinarum are highlighted in red. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

Fig. 2. A in Molecular identification and characterization of partial COX1 gene from caecal worm (Aulonocephalus pennula) in Northern bobwhite (Colinus virginianus) from the Rolling Plains Ecoregion of Texas

Fig. 2. A. PCR amplification of COX1 gene using nematode primers. Lane M: 100 bp DNA ladder (Fermentas); lane 1‾4 COX1 gene amplicon (750 bp). B. PCR amplification of partial COX1 gene using gene specific primers. Lane M: 100 bp DNA Marker (Fermentas); lane 1‾4 partial COX1 amplified products (405bp).

Fig. 2 in Predicting seasonal infection of eyeworm (Oxyspirura petrowi) and caecal worm (Aulonocephalus pennula) in northern bobwhite quail (Colinus virginianus) of the Rolling Plains Ecoregion of Texas, USA

Fig. 2. Scatterplot of predicted eyeworm reproduction with temperature 60 days prior to collection date with upper and lower 95% confidence intervals.

Fig. 1 in Predicting seasonal infection of eyeworm (Oxyspirura petrowi) and caecal worm (Aulonocephalus pennula) in northern bobwhite quail (Colinus virginianus) of the Rolling Plains Ecoregion of Texas, USA

Fig. 1. Contour and scatterplot of relationships between temperature and precipitation on parasite worm burdens and egg shedding. a) Predicted caecal worm intensity against temperature and precipitation contour plot. b) Scatterplot of predicted caecal worm reproduction against precipitation. d) Predicted eyeworm reproduction against temperature and precipitation contour plot.

Fig. 4 in A new species of Cavernocypris (Ostracoda) from Texas (U.S.A.) with a taxonomic key

Fig. 4. Male: A, T2; B, T3; C; Hemipenis; D, Zenker Organ; E, Female: Antenna (A2); F, T1; G, Uropod of female with genital organ. Scale: 100 μm.

Fig. 3 in A new species of Cavernocypris (Ostracoda) from Texas (U.S.A.) with a taxonomic key

Fig. 3. Male: A, Antennule (A1); B, Antenna (A2); C, Mandible (Md); D, Maxillule (Mx1); E, Rake-like organ; F, Hypostome; G, Right clasping organ; H, Left clasping organ. Scale: 100 μm.

Fig. 2. Cavernocypris reddelli n in A new species of Cavernocypris (Ostracoda) from Texas (U.S.A.) with a taxonomic key

Fig. 2. Cavernocypris reddelli n. sp. Male: A, RV external view; B, LV external view; C, dorsal view; D, LV internal view; E, RV internal view; F, posterior detail of LV; G, anterior detail of LV; H, muscle scars; I, ventral view of female. Arrows point the list. Scale: A-E, I = 100 μm; F, G = 25 μm; H = 10 μm.

Figure 6-7 in Rhopalocera (Lepidoptera) prey records of Asilidae (Diptera) in eastern New Mexico and western Texas, United States of America

Figure 6-7. Triorla interrupta male feeding on Phyciodes picta. / Triorla interrupta macho alimentándose de Phyciodes picta.

Figure 3 in Rhopalocera (Lepidoptera) prey records of Asilidae (Diptera) in eastern New Mexico and western Texas, United States of America

Figure 3. New Mexico, nr. jct. 480 and Roos. Rd. AG (20.v.2017). / Nuevo México, cerca jct. 480 y Roos. Calle AG (20.v.2017).

Figure 2 in Rhopalocera (Lepidoptera) prey records of Asilidae (Diptera) in eastern New Mexico and western Texas, United States of America

Figure 2. New Mexico, field just NE of Floyd (15.vii.2017). / Nuevo México, campo al NE de Floyd (15.vii.2017).

Figure 1 in Rhopalocera (Lepidoptera) prey records of Asilidae (Diptera) in eastern New Mexico and western Texas, United States of America

Figure 1. New Mexico, Portales, nr. softball complex (28.viii.2021). / Nuevo México, Portales, cerca del complejo de softbol (28.viii.2021).

Figure 4 in Rhopalocera (Lepidoptera) prey records of Asilidae (Diptera) in eastern New Mexico and western Texas, United States of America

Figure 4. Texas, Bailey Co., Muleshoe Nat. Wildlife Refuge nr. Goose Lake (10.vii.2022). / Texas, Bailey Co., Muleshoe Nacional. Refugio de vida silvestre cerca del lago del Ganso (10.vii.2022).

Figure 3 in Comalcandona gibsoni sp. nov. (Ostracoda, Candonidae) from Comal Spring, Texas, USA

Figure 3. Comalcandona gibsoni sp. nov. Male: A) RV close view of posterodorsal horn-like structure. B) Pore opening with seta, external view. C) RV inside view of anterior margin. D) LV inside view of anterior margin. E) Comalcandona tressleri; male LV external view (modified from Külköylüoğlu and Gibson, 2018). Scale bar: A, B, 10 µm; C, D, 100 µm; E, 150 µm.

Figure 2 in Comalcandona gibsoni sp. nov. (Ostracoda, Candonidae) from Comal Spring, Texas, USA

Figure 2. Comalcandona gibsoni sp. nov. A) RV external view. B) LV external view. C) Dorsal view. D) Ventral view. E) Detailed view of anterodorsal margin. F) Detailed view of posterodorsal margin. G) Detailed view of horns and muscle scars on LV, external view. A, D, female; B, C, E–G, male. Scale bar: A, B, C, D, G, 100 µm. E, F, 50 µm.

Fig. 4 in Molecular screening for rickettsial bacteria and piroplasms in ixodid ticks surveyed from white-tailed deer (Odocoileus virginianus) and nilgai antelope (Boselaphus tragocamelus) in southern Texas

Fig. 4. Phylogentic analysis of sca0 (rompA) sequences from putative Rickettsia sp. endosymbionts of Amblyomma maculatum and Ixodes scapularis ticks collected from white-tailed deer in southern Texas. This is a maximum-likelihood tree that is rooted at midpoint. Branch support was assessed with 10,000 replicates of UFBoot bootstrap replication, and bootstrap percentages are indicated at each branch point in the tree. Sequences from GenBank used in the comparative analysis were annotated as rickettsial endosymbionts. Accession numbers and tick species from which sequence was identified are included on the branch label.