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Fig. 4. Phylogenetic relationship among the S in Fatal hepatic sarcocystosis in three captive and one free-ranging pinniped

Fig. 4. Phylogenetic relationship among the S. canis-like variants from two Hawaiian monk seals (Monachus schauinslandi) and two California sea lions (Zalophus californianus), a Pacific harbor seal (MT460246) compared against S. canis sequences from two black bears (OR336049, MW136927), a polar bear (DQ176645) and various other Sarcocystis spp. at the complete ITS1 locus. Evolutionary distances were computed using the Tamura-Nei genetic distance model. A Neighbor-Joining midpoint rooted bootstrap consensus tree was inferred from 1000 MUSCLE alignment iterations. Bootstrap percentage values are indicated at the branch points.

Fig. 2 in Fatal hepatic sarcocystosis in three captive and one free-ranging pinniped

Fig. 2. TEM of a schizont with protozoa similar to S. canis in the hepatocyte of a California sea lion (Zalophus californianus) "CSL 1". Merozoites contained micronemes (Mn), a conoid (Co), and a prominent nucleus (Nu), but no rhoptries. Bar = 500 nm.

Fig. 1 in Fatal hepatic sarcocystosis in three captive and one free-ranging pinniped

Fig. 1. Histologic liver sections of a California sea lion (Zalophus californianus) "CSL 2" with numerous coalescing foci of acute necrosis. A. Lower magnification of acute necrosis with Sarcocystis schizonts (black arrow). B. Higher magnification of mature protozoal schizonts with a rosette of merozoites (red arrow) and a schizont with greater than 30 free merozoites (black arrow) within a foci of hepatic necrosis.

Fig. 3 in Fatal hepatic sarcocystosis in three captive and one free-ranging pinniped

Fig. 3. Phylogenetic relationship of the S. canis-like variant isolate CSL-2 that infects pinnipeds from a California sea lion (Zalophus californianus) compared against S. canis from a black bear isolate 11–3173 (OR654898) and various other Sarcocystis spp. Within a 994 nucleotide fragment of the 18S rRNA locus. Evolutionary distances were computed using the Tamura-Nei genetic distance model. A Neighbor-Joining bootstrap consensus tree was inferred from 1000 MUSCLE alignment iterations. Bootstrap percentage values are indicated at the branch points. Toxoplasma gondii was used as an outgroup.

Fig. 1 in Size does not matter: molecular phylogeny reveals one of the largest trematodes from vertebrates, the enigmatic Ithyoclinostomum dimorphum, as a species of Clinostomum (Trematoda: Clinostomidae)

Fig. 1. Metacercariae of Clinostomum dimorphum found in the erythrinid fish, Hoplias intermedius from Brazil: (A) Whole view of a paragenophore specimen. B) Detail of reproductive structures of a hologenophore specimen.

Fig. 3 in Adding one more to the list: A new species of Eniochobothrium (Cestoda: Lecanicephalidea) from the Oman cownose ray in South Africa

Fig. 3. Maximum likelihood phylogram based on partial sequences of the large subunit 28S rRNA gene. Nodal support is shown as posterior probability and bootstrap. GenBank accession number precedes species name. Branch length scale bar indicates the number of substitutions per site. (//) Branch length reduced to one time the scale bar; (///) branch length reduced to two times the scale bar. Squares represent Posterior Probability values while circles represent Bootstrap values.

Fig. 4 in Adding one more to the list: A new species of Eniochobothrium (Cestoda: Lecanicephalidea) from the Oman cownose ray in South Africa

Fig. 4. Maximum likelihood phylogram based on partial sequences of the mitochondrial cytochrome oxidase subunit I (mtCOI) gene. Nodal support is shown as posterior probability and bootstrap. GenBank accession number precedes species name. Branch length scale bar indicates the number of substitutions per site. (//) Branch length reduced to one time the scale bar. Squares represent Posterior Probability values while circles represent Bootstrap values.

Fig. 2 in Adding one more to the list: A new species of Eniochobothrium (Cestoda: Lecanicephalidea) from the Oman cownose ray in South Africa

Fig. 2. Scanning electron micrographs of an immature specimen of Eniochobothrium acostae n. sp. from the South-western Indian Ocean off Scottburgh and Richards Bay, KwaZulu-Natal Province, South Africa. A, entire strobila; B, scolex; C, genital pore; D, trough formed by non-reproductive proglottids of the anterior strobila.

Fig. 2 in Size does not matter: molecular phylogeny reveals one of the largest trematodes from vertebrates, the enigmatic Ithyoclinostomum dimorphum, as a species of Clinostomum (Trematoda: Clinostomidae)

Fig. 2. Maximum likelihood phylogram based on the concatenated ITS1-5.8S-ITS2 + 28S + cox1 datasets of Clinostomum dimorphum (in bold) and selected species of the family Clinostomidae. Clade formed by isolates of 'Ithyoclinostomum' yamagutii (incertae sedis) is highlighted in grey. Taxon names are followed by GenBank accession numbers of ITS, 28S, and cox1, respectively, and country of record. Branch length scale bar indicates number of substitutions per site. Abbreviations: HON, Honduras; ITA, Italy; KEN, Kenya; MEX, Mexico; THAI, Thailand; USA, United States of America.

Fig. 1 in Adding one more to the list: A new species of Eniochobothrium (Cestoda: Lecanicephalidea) from the Oman cownose ray in South Africa

Fig. 1. Line drawings of Eniochobothrium acostae n. sp. from the South-western Indian Ocean off Scottburgh and Richards Bay, KwaZulu-Natal Province, South Africa. A, outline of entire cestode; B, mature proglottid; C, early gravid proglottid; D, trough formed by non-reproductive proglottids of the anterior strobila; E, scolex; F, terminal genitalia; G, cocoon with eggs. Abbreviations: c (cirrus); cs (cirrus sac); ex (excretory canal); gp (genital pore); isv (internal seminal vesicle); ot (ootype); ov (ovary); t (testes); u (uterus); vd (vas deferens); vf (vitelline follicle).

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FIGURE 1 in Paleontologia Electronica is still number one for new open access fossil species

FIGURE 1. Eekaulostomus cuevasae, an extinct armored trumpetfish, and the top open access fossil taxon of 2017 (Farke, 2017). Reproduced from Cantalice and Alvarado-Ortega (2016). 2. Illustration of trumpetfish from Brian Engh, http://dontmesswithdinosaurs.com.

Figure 4 in Building capacity to implement conservation breeding programs for frogs in Madagascar: Results from year one of Mitsinjo's amphibian husbandry research and captive breeding facility

Figure 4. Seven species of frogs were included in a husbandry research and technician training program during the first year of the project. The IUCN Red List status, in parenthesis, follows species. A) Heterixalus betsileo (LC). B) Mantidactylus betsileanus, (LC). C) Heterixalus punctatus (LC). D) Blommersia blommersae (LC). E) Guibemantis aff. albolineatus "Andasibe" (DD). F) Stumpffia sp. "Ranomafana" (DD). G) Boophis pyrrhus (LC).

Figure 3 in Building capacity to implement conservation breeding programs for frogs in Madagascar: Results from year one of Mitsinjo's amphibian husbandry research and captive breeding facility

Figure 3. Terraria and aquaria at the breeding facility. A) Terraria setup on shelving and plumbed so wastewater flows into a drain in the floor. B) A terrarium housing a group of Boophis pyrrhus. C) Aquaria for raising tadpoles. D) Boophis pyrrhus tadpoles produced at the facility.

Figure 9 in Building capacity to implement conservation breeding programs for frogs in Madagascar: Results from year one of Mitsinjo's amphibian husbandry research and captive breeding facility

Figure 9. Pilot study and training exercise on the optimal larval diet for Mantidactylus betsileanus.

Figure 1. The facility was constructed between November 2010 and March 2011 in Building capacity to implement conservation breeding programs for frogs in Madagascar: Results from year one of Mitsinjo's amphibian husbandry research and captive breeding facility

Figure 1. The facility was constructed between November 2010 and March 2011 from the foundations of an old abandoned forest station. A) Original abandoned building in January 2009. B) Facility construction November 2010. C) Facility construction December 2010. D) Facility construction January 2011.

Figure 8 in Building capacity to implement conservation breeding programs for frogs in Madagascar: Results from year one of Mitsinjo's amphibian husbandry research and captive breeding facility

Figure 8. Locally-sourced crickets from Andasibe being bred at Mitsinjo's facility. A) Field cricket (Modicogryllus sp.). B) Large field cricket (Modicogryllus sp.). C) Large black cricket (Gryllus sp.). D) Tropical house cricket (Gryllodes sigillatus). E) Cave cricket (Rhaphidophoridae). F) Shelves with boxes housing field crickets and tropical house crickets.

Figure 2 in Building capacity to implement conservation breeding programs for frogs in Madagascar: Results from year one of Mitsinjo's amphibian husbandry research and captive breeding facility

Figure 2. Overview of the biosecure Mitsinjo amphibian captive breeding and husbandry research center as of April 2012.

Figure 5 in Building capacity to implement conservation breeding programs for frogs in Madagascar: Results from year one of Mitsinjo's amphibian husbandry research and captive breeding facility

Figure 5. Lectures and discussions during January-March 2011 helped train Mitsinjo technicians in captive frog husbandry techniques.

Figure 7. A in Building capacity to implement conservation breeding programs for frogs in Madagascar: Results from year one of Mitsinjo's amphibian husbandry research and captive breeding facility

Figure 7. A) Fruit fly cultures on shelves at the facility. B) Fruit flies are cultured in discarded plastic water bottles collected in Andasibe. Fabric is secured in place, over the top with rubber bands, and strips of plastic bag are placed inside (above the media) on which the flies can deposit eggs.