Acanthotrema hancocki (Martin) (10. Acha; Figs. 1, 41���44) Diagnosis: Parthenitae. Colony comprised of active rediae, densely concentrated in snail gonad region. Rediae translucent white, grey, weak yellow, or colorless; ~ 500���1000 ��m long, elongate (length:width ~4:1 to 10:1), sausage-shaped. Cercaria. Body mostly translucent colorless; oculate; with oral sucker and no ventral sucker; with seven pairs of penetration glands, the bodies of which lie in a relatively compact cluster, anterior to the genital primordium and excretory bladder; body ~ 175 ��m long, much shorter than tail (Cercaria behavior: Fresh, emerged cercariae remain in water column, swim intermittently in short bursts, with periods of resting and slow sinking. Similar species: Acha is most reliably and readily distinguished from Euca [11] by the position of the penetration gland bodies, which are readily observable with flattened cercariae at 100x on a compound scope (and even sometimes at the dissection scope). Although Acha does have wider lateral tail fins than Euca on average, there appears to be overlap; so, tail fin width is not a consistently reliable distinguishing trait. Martin (1972) used the flame cell grouping to distinguish Acha from Euca (groups of 3 versus 2, respectively), but the flame cells are difficult to see, requiring leaving specimens on a slide for a while and 1000x magnification. Remarks: Martin (1950b) documented the life cycle and described this species (as Parastictodora hancocki). He described the mother sporocyst, rediae and cercariae from natural infections, and metacercariae and adults from experimentally infected second intermediate and final hosts. I suspect that cercariae of Acanthotrema hancocki were accidentally pooled with Euhaplorchis californiensis to comprise Maxon and Pequegnat���s (1949) Pleurolophocercous I and pooled with Phocitremoides ovale cercariae to comprise their Pleurolophocercous II. This species has also been referred to as Stictodora hancocki in ecological and evolutionary papers, but, since Lafuente et al. (2000), the appropriate genus has been Acanthotrema. Mature, ripe colonies comprise ~18% the soft-tissue weight of an infected snail (summer-time estimate derived from information in [Hechinger et al. 2009]). Acha infection causes (stolen) snail bodies to grow over 1.5x faster than uninfected snails (Hechinger 2010). This species has a caste of soldier rediae (Garcia-Vedrenne et al. 2017). Using Acha (reported as Euca, see Euca remarks) from Bolinas Lagoon (central California), Koprivnikar et al. (2010) performed laboratory experiments examining the effects of salinity, temperature, and pH on cercaria survivorship and activity., Published as part of Hechinger, Ryan F., 2019, Guide to the trematodes (Platyhelminthes) that infect the California horn snail (Cerithideopsis californica: Potamididae: Gastropoda) as first intermediate host, pp. 459-494 in Zootaxa 4711 (3) on page 478, DOI: 10.11646/zootaxa.4711.3.3, http://zenodo.org/record/3586554, {"references":["Martin, W. E. (1972) An annotated key to the cercariae that develop in the snail Cerithidea californica. Bulletin of the Southern California Academy of Sciences, 71, 39 - 43.","Martin, W. E. (1950 b) Parastictodora hancocki n. gen., n. sp. (Trematoda: Heterophyidae). with observations on its life cycle. Journal of Parasitology, 36, 360 - 370. https: // doi. org / 10.2307 / 3273472","Maxon, M. G. & Pequegnat, W. E. (1949) Cercariae from upper Newport Bay. Journal of Entomology and Zoology, 41, 30 - 55.","Lafuente, M., Roca, V. & Carbonell, E. (2000) Description of Acanthotrema armata n. sp. (Trematoda: Heterophyidae) from Larus audouinii (Aves: Laridae), with an amended diagnosis of the genus Acanthotrema Travassos, 1928. Systematic Parasitology, 45, 131 - 134. https: // doi. org / 10.1023 / A: 1006293611598","Hechinger, R. F., Lafferty, K. D., Mancini III, F. T., Warner, R. R. & Kuris, A. M. (2009) How large is the hand in the puppet? Ecological and evolutionary factors affecting body mass of 15 trematode parasitic castrators in their snail host. Evolutionary Ecology, 23, 651 - 667. https: // doi. org / 10.1007 / s 10682 - 008 - 9262 - 4","Hechinger, R. F. (2010) Mortality affects adaptive allocation to growth and reproduction: field evidence from a guild of body snatchers. BMC Evolutionary Biology, 10 (136), 1 - 14. https: // doi. org / 10.1186 / 1471 - 2148 - 10 - 136","Garcia-Vedrenne, A. E., Quintana, A. C. E., DeRogatis, A. M., Dover, C. M., Lopez, M., Kuris, A. M. & Hechinger, R. F. (2017) Trematodes with a reproductive division of labour: heterophyids also have a soldier caste and early infections reveal how colonies become structured. International Journal for Parasitology, 47, 41 - 50. https: // doi. org / 10.1016 / j. ijpara. 2016.10.003","Koprivnikar, J., Lim, D., Fu, C. & Brack, S. H. M. (2010) Effects of temperature, salinity, and pH on the survival and activity of marine cercariae. Parasitology Research, 106, 1167 - 1177. https: // doi. org / 10.1007 / s 00436 - 010 - 1779 - 0"]}