Out-of-Place Zoologist
Zoologist Reviews Evol Archetype From Yu-Gi-Oh!
updated
*Footage*
Swimming: youtube.com/watch?v=uyf_jjPxZIA
*Timestamps*
0:00 Opening Thought
1:23 Taxonomy and General Information
4:56 Morphology
7:36 Ecology
*References*
MolluscaBase eds. (2026). MolluscaBase. Aplysiidae Lamarck, 1809. Accessed through: World Register of Marine Species at: marinespecies.org/aphia.php?p=taxdetails&id=172
MolluscaBase eds. (2026). MolluscaBase. Aplysia Linnaeus, 1767. Accessed through: World Register of Marine Species at: marinespecies.org/aphia.php?p=taxdetails&id=137654
Golestani, H., Crocetta, F., Padula, V., et al. (2019). The little Aplysia coming of age: from one species to a complex of species complexes in Aplysia parvula (Mollusca: Gastropoda: Heterobranchia). Zoological Journal of the Linnean Society, 187(2): 279-330. doi.org/10.1093/zoolinnean/zlz028
Kicklighter, C. E., Shabani, S., Johnson, P. M., & Derby, C. D. (2005). Sea Hares Use Novel Antipredatory Chemical Defenses. Current Biology, 15(6): p549-554. doi.org/10.1016/j.cub.2005.01.057
Sheybani, A., Nusnbaum, M., Caprio, J., & Derby, C. D. (2009). Responses of the sea catfish Ariopsis felis to chemical defenses from the sea hare Aplysia californica. Journal of Experimental Marine Biology and Ecology, 368(2): 153-160. doi.org/10.1016/j.jembe.2008.09.024
Hawkins, R. D., Clark, G. A., & Kandel, E. R. (2006). Operant conditioning of gill withdrawal in Aplysia. The Journal of neuroscience : the official journal of the Society for Neuroscience, 26(9), 2443–2448. doi.org/10.1523/JNEUROSCI.3294-05.2006
Angeloni, L. & Bradbury, J. (1999). Body size influences mating strategies in a simultaneously hermaphroditic sea slug, Aplysia vaccaria. Ethology Ecology & Evolution, 11(2): 187-195. doi.org/10.1080/08927014.1999.9522836
Cummins, S. F., Nichols, A. E., Schein, C. H., & Nagle, G. T. (2006). Newly identified water-borne protein pheromones interact with attractin to stimulate mate attraction in Aplysia. Peptides, 27(3): 597-606. doi.org/10.1016/j.peptides.2005.08.026
Ludwig, A. N. & Walsh, P. J. (2008). Multiple Mating, Sperm Storage, and Mating Preference in Aplysia californica. The Biological Bulletin, 215(3). doi.org/10.2307/25470710
Lee, C-H., Kaang, B-K., & Lee, Y-D. (2014). Spawning Behavior and Egg Development of Aplysia kurodai Inhabiting the Coastal Waters of Jeju Island, Korea. Development & Reproduction, 18(1): 25-31. doi.org/10.12717/DR.2014.18.1.025
Heyland, A. & Moroz, L. (2006). Signaling mechanisms underlying metamorphic transitions in animals. Integrative and Comparative Biology, 46(6): 743-59. doi.org/10.1093/icb/icl023
*Thumbnail Image*
Aplysia californica - Genny Anderson
*Outro*
Bubbles Drifting in the Morning Breeze - Artificial.Music & Akosmo
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*Timestamps*
0:00 Opening Thought
0:54 Taxonomy and General Information
4:10 Morphology
7:28 Ecology
*References*
Richter, W. and G. M. Kirwan (2020). Guianan Cock-of-the-rock (Rupicola rupicola), version 1.0. In Birds of the World (T. S. Schulenberg, Editor). Cornell Lab of Ornithology, Ithaca, NY, USA. doi.org/10.2173/bow.gcoroc1.01
Snow, D. (2020). Andean Cock-of-the-rock (Rupicola peruvianus), version 1.0. In Birds of the World (J. del Hoyo, A. Elliott, J. Sargatal, D. A. Christie, and E. de Juana, Editors). Cornell Lab of Ornithology, Ithaca, NY, USA. doi.org/10.2173/bow.andcot1.01
Rodríguez-Ferraro, A. & Azpiroz, A. B. (2005). Notes on the natural history of the Andean Cock-of-the-rock (Rupicola peruviana) in western Venezuela. Ornitología Neotropical, 16(1): 105-108. https://digitalcommons.usf.edu/cgi/viewcontent.cgi%3Farticle%3D1522%26context%3Dornitologia_neotropical
Trail, P. W. & Adams, E. S. (1989). Active mate choice at cock-of-the-rock leks: tactics of sampling and comparison. Behav Ecol Sociobiol 25, 283–292. doi.org/10.1007/BF00300055
Trail P. W. (1985). Courtship disruption modifies mate choice in a lek-breeding bird. Science (New York, N.Y.), 227(4688), 778–780. doi.org/10.1126/science.227.4688.778
Zuleta, L., Ocampo, D., Fierro-Calderón, K., Sánchez-Martínez, M. A., Greeney, H., David, S., & Londoño, G. A. (2025). Breeding biology of the Andean cock-of-the-rock (Rupicola peruvianus). Journal of Natural History, 59(9–12), 543–556. doi.org/10.1080/00222933.2025.2454487
BirdLife International. (2025). Rupicola rupicola. The IUCN Red List of Threatened Species 2025: e.T22700971A280999592. dx.doi.org/10.2305/IUCN.UK.2025-2.RLTS.T22700971A280999592.en.
BirdLife International. (2018). Rupicola peruvianus. The IUCN Red List of Threatened Species 2018: e.T22700974A130267257. dx.doi.org/10.2305/IUCN.UK.2018-2.RLTS.T22700974A130267257.en.
Duce, S. & Brannian, J. (1990). Social behavior of the Guianan cock-of-the-rock (Rupicola rupicola) in captivity. Zoo Biology, 9(3): 223-232. doi.org/10.1002/zoo.1430090305
*Outro*
Bubbles Drifting in the Morning Breeze - Artificial.Music & Akosmo
youtube.com/watch?v=wS4hkYXuasE
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*Timestamps*
0:00 Opening Thought
0:52 Taxonomy and General Information
4:46 Morphology
7:15 Ecology
9:08 Which Came First?
*References*
Tsang, L. M., Chan, T. Y., Ahyong, S. T., & Chu, K. H. (2011). Hermit to king, or hermit to all: multiple transitions to crab-like forms from hermit crab ancestors. Systematic biology, 60(5), 616–629. doi.org/10.1093/sysbio/syr063
Karasawa, H., Schweitzer, C. E., Feldmann, R. M., & Luque, J. (2014). Phylogeny and Classification of Raninoida (Decapoda: Brachyura). Journal of Crustacean Biology, 34(2): 216-272. doi.org/10.1163/1937240X-00002216
Ng, P.K., & Guinot, D. (2020). Description of a new genus for Cyrtorhina balabacensis Serène, 1971,with notes on the Cyrtorhininae (Decapoda, Brachyura, Raninidae). Crustacean Research, 49: 237-262. doi.org/10.18353/crustacea.49.0_237
DecaNet eds. (2026). DecaNet. Raninoidea De Haan, 1839. Accessed through: World Register of Marine Species at: marinespecies.org/aphia.php?p=taxdetails&id=106705
Lam-Gordillo, O. & Ardisson, P-L. (2019). The global distribution and richness of frog crabs (Raninoidea). Crustaceana, 92(1): 1-31. doi.org/10.1163/15685403-00003832
Schmidt, M., Hazerli, D., & Richter, S. (2020). Kinematics and morphology: A comparison of 3D-patterns in the fifth pereiopod of swimming and non-swimming crab species (Malacostraca, Decapoda, Brachyura). Journal of morphology, 281(12), 1547–1566. doi.org/10.1002/jmor.21268
Krajangdara, T., & Watanabe, S. (2005). Growth and reproduction of the red frog crab, Ranina ranina (Linnaeus, 1758), in the Andaman Sea off Thailand. Fish Sci, 71: 20–28. doi.org/10.1111/j.1444-2906.2005.00926.x
Baylon, J. C., & Tito, O. D. (2012). Reproductive Biology of the Red Frog Crab, Ranina ranina (Linnaeus, 1758) (Crustacea: Decapoda: Raninidae) from Southwestern Mindanao, Philippines. Asian Fisheries Science, 25(2). doi.org/10.33997%2Fj.afs.2012.25.2.001
Luque, J., Feldmann, R. M., Schweitzer, C. E., Jaramillo, C., & Cameron, C. B. (2012). The Oldest Frog Crabs (Decapoda: Brachyura: Raninoida) from the Aptian of Northern South America. J. of Crustacean Biology, 32(3): 405-420. doi.org/10.1163/193724012X626539
Klompmaker, A. A., Starzyk, N., Fraaije, R. H. B., & Schweigert, G. (2020). Systematics and convergent evolution of multiple reef-associated Jurassic and Cretaceous crabs (Decapoda, Brachyura). Palaeontologia Electronica, 23(2): a32. doi.org/10.26879/1045
*Thumbnail Image*
李博恒
*Outro*
Bubbles Drifting in the Morning Breeze - Artificial.Music & Akosmo
youtube.com/watch?v=wS4hkYXuasE
Join the channel's membership:
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*Timestamps*
0:00 Opening Thought
1:01 Taxonomy and General Information
5:27 Morphology
8:41 Ecology
*References*
Cuff, A. R., & Rayfield, E. J. (2013). Feeding Mechanics in Spinosaurid Theropods and Extant Crocodilians. PLoS ONE 8(5): e65295. doi.org/10.1371/journal.pone.0065295
Rio, J. P., & Mannion, P. D. (2021). Phylogenetic analysis of a new morphological dataset elucidates the evolutionary history of Crocodylia and resolves the long-standing gharial problem. PeerJ, 9, e12094. doi.org/10.7717/peerj.12094
Willis, R. E., McAliley, L. R., Neeley, E. D., & Densmore, L. D., 3rd (2007). Evidence for placing the false gharial (Tomistoma schlegelii) into the family Gavialidae: inferences from nuclear gene sequences. Molecular phylogenetics and evolution, 43(3), 787–794. doi.org/10.1016/j.ympev.2007.02.005
Oaks J. R. (2011). A time-calibrated species tree of Crocodylia reveals a recent radiation of the true crocodiles. Evolution; international journal of organic evolution, 65(11), 3285–3297. doi.org/10.1111/j.1558-5646.2011.01373.x
Piras, P., Colangelo, P., Adams, D. C., Buscalioni, A., Cubo, J., Kotsakis, T., Meloro, C., & Raia, P. (2010). The Gavialis-Tomistoma debate: the contribution of skull ontogenetic allometry and growth trajectories to the study of crocodylian relationships. Evolution & development, 12(6), 568–579. doi.org/10.1111/j.1525-142X.2010.00442.x
Shaney, K., Shwedick, B., Simpson, B.K., Pine, A., Sideleau, B. & Stevenson, C. (2023). Tomistoma schlegelii. The IUCN Red List of Threatened Species 2023: e.T21981A214287051. dx.doi.org/10.2305/IUCN.UK.2023-1.RLTS.T21981A214287051.en.
Charette R. (1995). CITES Identification Guide: Crocodilians. Environment Canada; Ottawa, ON, Canada. publications.gc.ca/site/eng/464832/publication.html
Bezuijen, M. R., Webb, G. J. W., Hartoyo, P., & Samedi. (2001). Peat swamp forest and the false gharial Tomistoma schlegelii (Crocodilia, Reptilia) in the Merang River, eastern Sumatra, Indonesia. Oryx, 35(4), 301–307. doi:10.1046/j.1365-3008.2001.00195.x
Sharney, K, Shwedick, B., Simpson, B. and Stevenson, C. (2019). Tomistoma Tomistoma schlegelii. in Crocodiles. Status Survey and Conservation Action Plan. Fourth Edition, ed. by S.C. Manolis and C. Stevenson. iucncsg.org/365_docs/attachments/protarea/29250d3a4c25ac44646a45ccf2aeebdc.pdf
Staniewicz, A., Foggett, S., McCabe, G., & Holderied, M. (2021). Courtship and underwater communication in the Sunda gharial (Tomistoma schlegelii). Bioacoustics. Advance online publication. doi.org/10.1080/09524622.2021.1967782
Litton, M., Fullerton, W. and Mendyk, R. (2018). Successful Reproduction of the Sunda Gharial (Tomistoma schlegelii) at Audubon Zoo. Crocodile Specialist Group Newsletter 37(4): 21-23. iucncsg.org/365_docs/attachments/protarea/3ab6597756810d7ab30707a91943b1f3.pdf
Mathew, A., Ganesan, M., Majid, R. A. & Beastall, C. (2011). Breeding of False Gharial (Tomistoma schlegelii) at Zoo Negara, Malaysia. https://www.zoonegara.my/RPFalseGharial.pdf.
Latip, M. Q. A., Tengku Azizan, T. R. P., Ahmad, H., Abu Hassim, H., Noor, M. H. M., & Mikail, M. (2021). Blood Profiling of Captive and Semi-Wild False Gharial in Peninsular Malaysia. Animals : an open access journal from MDPI, 11(6), 1481. doi.org/10.3390/ani11061481
*Outro*
Bubbles Drifting in the Morning Breeze - Artificial.Music & Akosmo
youtube.com/watch?v=wS4hkYXuasE
Join the channel's membership:
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*Timestamps*
0:00 Opening Thought
0:57 Taxonomy and General Information
4:48 Morphology
9:26 Ecology
*References*
Hassanin, A., Veron, G., Ropiquet, A., Jansen van Vuuren, B., Lécu, A., Goodman, S. M., Haider, J., & Nguyen, T. T. (2021). Evolutionary history of Carnivora (Mammalia, Laurasiatheria) inferred from mitochondrial genomes. PloS one, 16(2), e0240770. doi.org/10.1371/journal.pone.0240770
Han, J. I., Yang, H., Jeung, E. B., & Na, K. J. (2012). Altered expression of melanocortin-1 receptor (MC1R) in a yellow-coloured wild raccoon dog (Nyctereutes procyonoides). Veterinary dermatology, 23(3), 187–e37. doi.org/10.1111/j.1365-3164.2012.01036.x
Kim, S-I., Oshida, T., Lee, H., Min, M-S., & Kimura, J. (2015). Evolutionary and biogeographical implications of variation in skull morphology of raccoon dogs (Nyctereutes procyonoides, Mammalia: Carnivora). Biological Journal of the Linnean Society, 11(4): 856–872. doi.org/10.1111/bij.12629
Hong, Y., Lee, H., Kim, K.S. et al. (2020). Phylogenetic relationships between different raccoon dog (Nyctereutes procyonoides) populations based on four nuclear and Y genes. Genes Genom 42, 1075–1085. doi.org/10.1007/s13258-020-00972-2
Mae, Y., Nagara, K., Miyazaki, M., Katsura, Y., Enomoto, Y., & Koga, A. (2020). Complex intragene deletion leads to oculocutaneous albinism in tanuki (Japanese raccoon dog). Genome, 63(10), 517–523. doi.org/10.1139/gen-2020-0049
Wooldridge, B., Svenning, JC. & Pagh, S. (2024). Habitat selection and movement patterns of the Raccoon dog (Nyctereutes procyonoides) in Denmark using GPS telemetry data. Eur J Wildl Res 70, 64. doi.org/10.1007/s10344-024-01803-5
Tuomikoski, E., Selonen, V., Merimaa, K., & Laaksonen, T. (2024). Diet of the raccoon dog, an invasive mesopredator, during the breeding season of declining waterbird populations. Global Ecology and Conservation, 51: e02917. doi.org/10.1016/j.gecco.2024.e02917
Kitao, N., Fukui, D., Hashimoto, M. et al. (2009). Overwintering strategy of wild free-ranging and enclosure-housed Japanese raccoon dogs (Nyctereutes procyonoides albus). Int J Biometeorol, 53, 159–165. doi.org/10.1007/s00484-008-0199-7
Wójcicki, A., Kowal, J., Kuchta-Gładysz, M. et al. (2025). The largest litter size in raccoon dog Nyctereutes procyonoides recorded outside its native range. Eur J Wildl Res 71, 134. doi.org/10.1007/s10344-025-02017-z
*Thumbnail Images*
Raccoon Dog: John Witton
Raccoon: Rhododendrites
*Outro*
Bubbles Drifting in the Morning Breeze - Artificial.Music & Akosmo
youtube.com/watch?v=wS4hkYXuasE
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*Timestamps*
0:00 Preface
2:19 Expert and Expertise
5:33 Credibility and Scepticism
7:25 Would experts want to be on YouTube?
15:39 Is expertise even required?
18:08 The Merit of Each Side
24:03 Saturation and Redundancy
26:59 Intent VS Impact
28:50 Target Audience
34:46 When Education is No Longer the Goal
36:38 The World Revolves Around You
39:20 Mitigation and Treatment
40:01 Hate is a Strong Word
41:46 Communication (and the lack of it)
44:51 What Does YouTube need?
Join the channel's membership:
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*Timestamps*
0:00 Opening Thought
1:15 Taxonomy and General Information
4:39 Morphology
7:27 Ecology
*References*
Roubik D. W. (1982). Obligate necrophagy in a social bee. Science (New York, N.Y.), 217(4564), 1059–1060. doi.org/10.1126/science.217.4564.1059
Camargo, J. M. F. & Roubik, D. W. (1991). Systematics and bionomics of the apoid obligate necrophages: the Trigona hypogea group (Hymenoptera: Apidae; Meliponinae). Biological Journal of the Linnean Society, 44 (1): 13–39. doi.org/10.1111/j.1095-8312.1991.tb00604.x
Noll, F. B., Zucchi, R., Jorge, J. A., & Mateus, S. (1996). Food Collection and Maturation in the Necrophagous Stingless Bee, Trigona hypogea (Hymenoptera: Meliponinae). Journal of the Kansas Entomological Society, 69(4), 287–293. http://www.jstor.org/stable/25085725
Figueroa, L. L., Maccaro, J. J., Krichilsky, E., Yanega, D., & McFrederick, Q. S. (2021). Why Did the Bee Eat the Chicken? Symbiont Gain, Loss, and Retention in the Vulture Bee Microbiome. mBio, 12(6), e0231721. doi.org/10.1128/mBio.02317-21
*Thumbnail Image*
Quinn McFrederick
*Outro*
Bubbles Drifting in the Morning Breeze - Artificial.Music & Akosmo
youtube.com/watch?v=wS4hkYXuasE
Join the channel's membership:
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*Timestamps*
0:00 Opening Thought
1:00 Taxonomy & General Information
5:21 Morphology
7:09 Ecology
10:31 Cultural Relevance
*References*
Prum, R., Berv, J., Dornburg, A. et al. (2015). A comprehensive phylogeny of birds (Aves) using targeted next-generation DNA sequencing. Nature, 526, 569–573. doi.org/10.1038/nature15697
Gill F, D Donsker & P Rasmussen (Eds). 2025. IOC World Bird List (v15.1). worldbirdnames.org/new/classification/orders-of-birds-draft
Barbaro, L., Couzi, L., Bretagnolle, V., Nezan, J., Vetillard, F. (2007). Multi-scale habitat selection and foraging ecology of the eurasian hoopoe (Upupa epops) in pine plantations. In: Brockerhoff, E.G., Jactel, H., Parrotta, J.A., Quine, C.P., Sayer, J., Hawksworth, D.L. (eds) Plantation Forests and Biodiversity: Oxymoron or Opportunity? . Topics in Biodiversity and Conservation, vol 9. Springer, Dordrecht. doi.org/10.1007/978-90-481-2807-5_8
Martín-Vivaldi, M., Palomino, J. J., & Soler, M. (2000). Attraction of Hoopoe Upupa epops Females and Males by Means of Song Playback in the Field: Influence of Strophe Length. Journal of Avian Biology, 31(3), 351–359. http://www.jstor.org/stable/3677417
Martín-Vivaldi, M., Martínez, J.G., Palomino, J.J. and Soler, M. (2002), Extrapair paternity in the Hoopoe Upupa epops: an exploration of the influence of interactions between breeding pairs, non-pair males and strophe length. Ibis, 144: 236-247. doi.org/10.1046/j.1474-919X.2002.00044.x
Barón, M. D., Martín-Vivaldi, M., Martínez-Renau, E., & Soler, J. J. (2024). Extra Nestlings That Are Condemned to Die Increase Reproductive Success in Hoopoes. The American Naturalist, 203(4). doi.org/10.1086/728883
*Thumbnail Image*
Lukas Sekelsky from iNaturalist
*Outro*
Bubbles Drifting in the Morning Breeze - Artificial.Music & Akosmo
youtube.com/watch?v=wS4hkYXuasE
Join the channel's membership:
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*Outro*
Bubbles Drifting in the Morning Breeze - Artificial.Music & Akosmo
youtube.com/watch?v=wS4hkYXuasE
Join the channel's membership:
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*Timestamps*
0:00 Opening Thought
0:56 Taxonomy & General Information
3:21 Morphology
5:33 Ecology
*References*
Fouquet, A., Marinho, P., Réjaud, A., Carvalho, T. R., Caminer, M. A., Jansen, M., et al. (2021). Systematics and biogeography of the Boana albopunctata species group (Anura, Hylidae), with the description of two new species from Amazonia. Systematics and Biodiversity, 19(4), 375–399. doi.org/10.1080/14772000.2021.1873869
Tupy, G. S., Cardoso, G. S., Vilanova-Júnior, J. L., et al. (2021). Trophic ecology of Boana albomarginata and Boana pombali (Anura: Hylidae) during the dry season in the Serra de Itabaiana National Park, Northeast Brazil. North-Western Journal of Zoology, 17(2): 220-226. https://biozoojournals.ro/nwjz/content/v17n2/nwjz_e211510_Tupy.pdf
Sabino Martins, A., de Castro Araújo, K., Zochio Fischer, H., Solé, M., Silva Ruas, D., de Mira-Mendes, C. V., & Ribeiro Dias, I. (2026). Dinner Time in the Atlantic Forest: Trophic Niche Partitioning of Two Sympatric Boana Species in the Southern Bahia State, Brazil. Acta Herpetologica. doi.org/10.36253/a_h-18506
Höbel, G. (2008). Plasticity and geographic variation in the reproductive ecology of gladiator frogs, particularly Hypsiboas rosenbergi. Stapfia 88, zugleich Kataloge der oberösterreichischen Landesmuseen Neue Serie 80: 329-334. https://www.zobodat.at/pdf/STAPFIA_0088_0329-0334.pdf
de Assis, V. R., Navas, C. A., Mendonça, M. T., & Gomes, F. R. (2012). Vocal and territorial behavior in the Smith frog (Hypsiboas faber): relationships with plasma levels of corticosterone and testosterone. Comparative biochemistry and physiology. Part A, Molecular & integrative physiology, 163(3-4), 265–271. doi.org/10.1016/j.cbpa.2012.08.002
Candaten, A., Possenti, A.G., Mainardi, Á.A. et al. (2020). Fighting scars: heavier gladiator frogs bear more injuries than lighter frogs. acta ethol 23, 39–44. doi.org/10.1007/s10211-019-00333-7
Dias, T. M., Prado, C. P. A., & Bastos, R. P. (2021). Reproductive ecology and territorial behavior of Boana goiana (Anura: Hylidae), a gladiator frog from the Brazilian Cerrado. Zoologia, 38: 1–12. doi.org/10.3897/zoologia.38.e53004
Kluge, A. G. (1981). The Life History, Social Organization, and Parental Behavior of Hyla rosenbergi Boulenger, a Nest-Building Gladiator Frog. Miscellaneous Publications of the Museum of Zoology University of Michigan, 160: 1–170. http://deepblue.lib.umich.edu/bitstream/handle/2027.42/56404/MP160.pdf?sequence=1
*Outro*
Bubbles Drifting in the Morning Breeze - Artificial.Music & Akosmo
youtube.com/watch?v=wS4hkYXuasE
Join the channel's membership:
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*Timestamps*
0:00 Opening Thought
0:30 Taxonomy and General Information
3:41 Morphology
8:58 Ecology
13:49 Popularity
*References*
Nyegaard, M., Sawai, E., Gemmell, N., Gillum, J., Loneragan, N. R., Yamanoue, Y., & Stewart, A. L. (2017). Hiding in broad daylight: molecular and morphological data reveal a new ocean sunfish species (Tetraodontiformes: Molidae) that has eluded recognition. Zoological Journal of the Linnean Society, 182(3), 631-658. doi.org/10.1093/zoolinnean/zlx040
Chang, C.T., Chih, C.H., Chang, Y.C., Chiang, W.C., Tsai, F.Y., Hsu, H.H., et al. (2018). Seasonal variations of species, abundance and size composition of Molidae in Eastern Taiwan. J. Taiwan Fish. Res. 26: 27–42.
Freedman, J.A. & Noakes, D.L. (2002). Why are there no really big bony fishes? A point-of-view on maximum body size in teleosts and elasmobranchs. Reviews in Fish Biology and Fisheries, 12, 403–416. doi.org/10.1023/A:1025365210414
Sousa, L., Xavier, R., Costa, V. et al. (2016). DNA barcoding identifies a cosmopolitan diet in the ocean sunfish. Sci Rep, 6, 28762. doi.org/10.1038/srep28762
Nyegaard, M., Loneragan, N., & Santos, M. B. (2017). Squid predation by slender sunfish Ranzania laevis (Molidae). Journal of fish biology, 90(6), 2480–2487. doi.org/10.1111/jfb.13315
Nyegaard, M., Andrzejaczek, S., Jenner, C.S. et al. (2019). Tiger shark predation on large ocean sunfishes (Family Molidae) – two Australian observations. Environ Biol Fish, 102, 1559–1567. doi.org/10.1007/s10641-019-00926-y
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*Timestamps*
0:00 Opening Thought
0:30 Taxonomy & General Information
2:53 Morphology
6:40 Ecology
*References*
Schuchert, P. (2010). The European athecate hydroids and their medusae (Hydrozoa, Cnidaria): Capitata Part 2. Revue suisse de zoologie, 117(3):337-555. doi.org/10.5962/bhl.part.117793
Tassara, E., Mikšík, I., Pompach, P., Mariottini, G. L., Xiao, L., Giovine, M., & Pozzolini, M. (2024). Proteomic Analysis and Biochemical Characterization of the Nematocyst Extract of the Hydrozoan Velella velella. Marine drugs, 22(10), 468. doi.org/10.3390/md22100468
Killi, N., Bonello, G., Mariottini, G. L., Pardini, P., Pozzolini, M., & Cengiz, S. (2020). Nematocyst types and venom effects of Aurelia aurita and Velella velella from the Mediterranean Sea. Toxicon : official journal of the International Society on Toxinology, 175, 57–63. doi.org/10.1016/j.toxicon.2019.12.155
Larson, R. J. (1980). The Medusa of Velella velella (Linnaeus, 1758) (Hydrozoa, Chondrophorae). Journal of Plankton Research, 2(3): 183-186. doi.org/10.1093/plankt/2.3.183
Helm, R. R. (2021). Natural history of neustonic animals in the Sargasso Sea: reproduction, predation, and behavior of Glaucus atlanticus, Velella velella, and Janthina spp.. Mar. Biodivers. 51(99). doi.org/10.1007/s12526-021-01233-5
Duarte, I. M., Leandro, S. M., Ferreira, M. et al. (2019). Early development of Velella velella medusae in laboratory. Front. Mar. Sci. Conference Abstract: IMMR'18 | International Meeting on Marine Research 2018. doi: 10.3389/conf.FMARS.2018.06.00080
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Adam Walter
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0:00 Opening Thoughts and Rules
1:46 Commander Yammarck
4:03 Shield Sheldon
8:41 Blizzard Wolfang
10:20 Rainy Turtloid
13:40 Blaze Heatnix
18:35 Metal Shark Player
21:51 Ground Scaravich
25:07 Infinity Mijinion
31:53 Closing Thoughts
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*Timestamps*
0:00 Opening Thought
0:47 Taxonomy and General Information
3:19 Morphology
8:44 Lifestyle and Behaviour
12:35 Evolution
*References*
MolluscaBase eds. (2026). MolluscaBase. Janthina janthina (Linnaeus, 1758). Accessed through: World Register of Marine Species at: marinespecies.org/aphia.php?p=taxdetails&id=140155
Beu, A. G. (2017). Evolution of Janthina and Recluzia (Mollusca: Gastropoda: Epitoniidae). Records of the Australian Museum, 69(3): 119-222. doi.org/10.3853/j.2201-4349.69.2017.1666
Churchill, C. K., Ó Foighil, D., Strong, E. E., & Gittenberger, A. (2011). Females floated first in bubble-rafting snails. Current Biology, 21(19), R802–R803. doi.org/10.1016/j.cub.2011.08.011
Calabrò, C., Rindone, A., Bertuccio, C. et al. (2019). Hermaphroditism in a violet snail, Janthina pallida (Gastropoda, Caenogastropoda): a contribution. Biologia, 74: 509–513. doi.org/10.2478/s11756-018-00177-9
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normfarmerimages
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*Timestamps*
0:00 Opening Thought
0:43 Taxonomy and General Information
2:29 Phacellophora camtschatica
6:21 Cotylorhiza tuberculata
*References*
Straehler-pohl, I., Widmer, C.L., & Morandini, A.C. (2011). Characterizations of juvenile stages of some semaeostome Scyphozoa (Cnidaria), with recognition of a new family (Phacellophoridae). Zootaxa, 2741(1): 1–37. doi.org/10.11646/zootaxa.2741.1.1
Moura, C. J., Ropa, N., Magalhães, B. I., & Gonçalves, J. M. (2022). Insight into the cryptic diversity and phylogeography of the peculiar fried egg jellyfish Phacellophora (Cnidaria, Scyphozoa, Ulmaridae). PeerJ, 10, e13125. doi.org/10.7717/peerj.13125
Motta, G., Voltolini, M., Mancini, L., Dreossi, D., Brun, F., Tirelli, V., Castelletto, L. P., Rogelja, M., Terlizzi, A., & Avian, M. (2025). New advances in jellyfish anatomy: the benefits of endocasts and X-ray microtomography in the investigation of the gastrovascular system of Cotylorhiza tuberculata (Scyphozoa; Rhizostomeae; Cepheidae). PloS one, 20(11), e0336682. doi.org/10.1371/journal.pone.0336682
Enrique-Navarro, A., Huertas, E., Flander-Putrle, V., Bartual, A., Navarro, G., Ruiz, J., Malej, A., & Prieto, L. (2022). Living Inside a Jellyfish: The Symbiosis Case Study of Host-Specialized Dinoflagellates, “Zooxanthellae”, and the Scyphozoan Cotylorhiza tuberculata. Front. Mar. Sci., 9:817312. doi.org/10.3389/fmars.2022.817312
Prieto, L., Astorga, D., Navarro, G., & Ruiz, J. (2010). Environmental control of phase transition and polyp survival of a massive-outbreaker jellyfish. PloS one, 5(11), e13793. doi.org/10.1371/journal.pone.0013793
Enrique-Navarro, A., Huertas, I. E., León Cobo, M. J., & Prieto, L. (2021). Impact of ocean warming and ocean acidification on asexual reproduction and statolith formation of the symbiotic jellyfish Cotylorhiza tuberculata. PloS one, 16(8), e0254983. doi.org/10.1371/journal.pone.0254983
Leone, A., Lecci, R. M., Durante, M., & Piraino, S. (2013). Extract from the zooxanthellate jellyfish Cotylorhiza tuberculata modulates gap junction intercellular communication in human cell cultures. Marine drugs, 11(5), 1728–1762. doi.org/10.3390/md11051728
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Phacellophora camtschatica: pnwdancer
Cotylorhiza tuberculata: Liutauras Dirse
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*Timestamps*
0:00 Opening Thought
1:05 Taxonomy and General Information
3:29 Morphology
5:56 Ecology
*References*
Baizurah, S.N. & Das, I. (2020). Heosemys spinosa (Spiny Hill Turtle). Diet. Herpetological Review, 51(4): 831-832. researchgate.net/publication/350486966_Heosemys_spinosa_Spiny_Hill_Turtle_Diet
Baizurah, S.N. & Das, I. (2021). Sexual Dimorphism in Heosemys spinosa (Testudines: Geoemydidae) from Sarawak, Borneo. Herpetology Notes, 14: 1231-1235. biotaxa.org/hn/article/view/67247
Cota, M., Guntoro, J., Horne, B.D., Kusrini, M.D., Krishnasamy, K. & Shepherd, C. (2021). Heosemys spinosa. The IUCN Red List of Threatened Species 2021: e.T9942A3152508. dx.doi.org/10.2305/IUCN.UK.2021-2.RLTS.T9942A3152508.en.
Goetz, M. (2007). Husbandry and Breeding of the Spiny Turtle Heosemys spinosa (GRAY, 1931) at the Durrell Wildlife Conservation Trust. Radiata, 16(2). researchgate.net/publication/305462838_Husbandry_and_Breeding_of_the_Spiny_Turtle_Heosemys_spinosa_GRAY_1931_at_the_Durrell_Wildlife_Conservation_Trust
Andersen, S. K., Staerk, J., Kalhor, E., Natusch, D. J. D., da Silva, R., Pfau, B., & Conde, D. A. (2020). Economics, life history and international trade data for seven turtle species in Indonesian and Malaysian farms. Data in brief, 34, 106708. doi.org/10.1016/j.dib.2020.106708
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Binturong27
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*Timestamps*
0:00 Opening Thought
0:46 Taxonomy and General Information
3:34 History and Extinction
5:38 Morphology
7:20 Lifestyle and Behaviour
*References*
Heupink, T. H., van Grouw, H., & Lambert, D. M. (2014). The mysterious Spotted Green Pigeon and its relation to the Dodo and its kindred. BMC evolutionary biology, 14, 136. doi.org/10.1186/1471-2148-14-136
Soares, A. E., Novak, B. J., Haile, J., Heupink, T. H., Fjeldså, J., Gilbert, M. T., Poinar, H., Church, G. M., & Shapiro, B. (2016). Complete mitochondrial genomes of living and extinct pigeons revise the timing of the columbiform radiation. BMC evolutionary biology, 16(1), 230. doi.org/10.1186/s12862-016-0800-3
Newton, A. & Newton, E. (1869). VIII. On the osteology of the solitaire or Didine Bird of the Island of Rodriguez, Pezophaps solitaria ( Gmel.). Philosophical Transactions, 159: 327-362. doi.org/10.1098/rstl.1869.0011
Rijsdijk, K. F., Croll, J. C., Hume, J. P., Janoo, A., Aguilée, R., De Groeve, J., Kentie, R., Schilthuizen, M., Warren, B. H., & Claessens, L. P. A. M. (2024). Sea level rise and the evolution of aggression on islands. iScience, 27(11), 111236. doi.org/10.1016/j.isci.2024.111236
Byrkjedal, I., Grønstøl, G., & Lislevand, T. (2016). Possible resource-defence polygyny in the extinct Rodrigues Solitaire Pezophaps solitaria (Columbidae: Raphini). Ibis, 158(1): 199-201. doi.org/10.1111/ibi.12329
Rodríguez-Pontes, M. A. (2016). Digital reconstruction of Rodrigues Solitaire (Pezophaps solitaria) (Aves: Columbidae) physical appearance based on early descriptive observation and other evidence. Historical Biology, 28(3), 398–414. doi.org/10.1080/08912963.2014.954569
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Bubbles Drifting in the Morning Breeze - Artificial.Music & Akosmo
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*Timestamps*
0:00 Opening Thought
1:13 Taxonomy and General Information
3:14 Morphology
6:03 Lifestyle and Behaviour
9:22 Interaction
11:20 Evolution
*References*
Paolo, P. (2021). Checklist of Fishes of the Family Echeneidae. International Journal of Zoological Investigations, 7(2): 566-573. doi.org/10.33745/ijzi.2021.v07i02.036
Britz, R., & Johnson, G. D. (2012). Ontogeny and homology of the skeletal elements that form the sucking disc of remoras (Teleostei, Echeneoidei, Echeneidae). Journal of morphology, 273(12), 1353–1366. doi.org/10.1002/jmor.20063
Kenaley, C. P., Stote, A., Ludt, W. B., & Chakrabarty, P. (2019). Comparative Functional and Phylogenomic Analyses of Host Association in the Remoras (Echeneidae), a Family of Hitchhiking Fishes. Integrative organismal biology (Oxford, England), 1(1), obz007. doi.org/10.1093/iob/obz007
Flammang, B. E., & Kenaley, C. P. (2017). Remora cranial vein morphology and its functional implications for attachment. Scientific reports, 7(1), 5914. doi.org/10.1038/s41598-017-06429-z
Wang, Y., Yang, X., Chen, Y., Wainwright, D. K., Kenaley, C. P., Gong, Z., Liu, Z., Liu, H., Guan, J., Wang, T., Weaver, J. C., Wood, R. J., & Wen, L. (2017). A biorobotic adhesive disc for underwater hitchhiking inspired by the remora suckerfish. Science robotics, 2(10), eaan8072. doi.org/10.1126/scirobotics.aan8072
Gayford J. H. (2024). The multidimensional spectrum of eco-evolutionary relationships between sharks and remoras. Journal of fish biology, 105(1), 4–9. doi.org/10.1111/jfb.15759
Weihs, D., Fish, F. E., & Nicastro, A. J. (2007). MECHANICS OF REMORA REMOVAL BY DOLPHIN SPINNING. Marine Mammal Science, 23(3): 707-714. doi.org/10.1111/j.1748-7692.2007.00131.x
Friedman, M., Johanson, Z., Harrington, R. C., Near, T. J., & Graham, M. R. (2013). An early fossil remora (Echeneoidea) reveals the evolutionary assembly of the adhesion disc. Proceedings. Biological sciences, 280(1766), 20131200. doi.org/10.1098/rspb.2013.1200
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Bubbles Drifting in the Morning Breeze - Artificial.Music & Akosmo
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Kevin Bryant
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*Timestamps*
0:00 Preface
0:41 First Thought
1:15 The Multitude of Failure
3:51 A Lonely Road
6:57 Mediocrity is the Norm
9:08 Opportunity Cost
11:44 Lifeline
12:42 Potential Men & Women
14:24 Knowing Doesn’t Mean Understanding
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*Timestamps*
0:00 Opening Thought
1:04 Taxonomy, Distribution, and Origin
5:01 Morphology
7:06 Ecology
*References*
Maekawa, K., & Nalepa, C. A. (2011). Biogeography and Phylogeny of Wood-feeding Cockroaches in the Genus Cryptocercus. Insects, 2(3), 354–368. doi.org/10.3390/insects2030354
Evangelista, D. A., Nelson, D., Kotyková Varadínová, Z., Kotyk, M., Rousseaux, N., Shanahan, T., Grandcolas, P., & Legendre, F. (2024). Phylogenomic analyses of Blattodea combining traditional methods, incremental tree-building, and quality-aware support. Molecular phylogenetics and evolution, 200, 108177. doi.org/10.1016/j.ympev.2024.108177
Tang, Q., Vargo, E. L., Ahmad, I., Jiang, H., Varadínová, Z. K., Dovih, P., Kim, D., Bourguignon, T., Booth, W., Schal, C., Mukha, D. V., Rheindt, F. E., & Evans, T. A. (2024). Solving the 250-year-old mystery of the origin and global spread of the German cockroach, Blattella germanica. Proceedings of the National Academy of Sciences of the United States of America, 121(22), e2401185121. doi.org/10.1073/pnas.2401185121
Cai, J.-Z., Yao, W.-W., Wang, Z.-Q., & Che, Y.-L. (2025). On the species status of Blattella germanica and Blattella asahinai (Blattodea, Blattellidae), and other morphologically similar species. ZooKeys (1250, 155–188). doi.org/10.3897/zookeys.1250.145981
Latorre, A., Domínguez-Santos, R., García-Ferris, C., & Gil, R. (2022). Of Cockroaches and Symbionts: Recent Advances in the Characterization of the Relationship between Blattella germanica and Its Dual Symbiotic System. Life, 12(2), 290. doi.org/10.3390/life12020290
Lin, L., Wen, J., Li, S., & Liu, F. (2022). Life-History Traits from Embryonic Development to Reproduction in the American Cockroach. Insects, 13(6), 551. doi.org/10.3390/insects13060551
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Bogdan V. Kryzhatyuk
*Outro*
Bubbles Drifting in the Morning Breeze - Artificial.Music & Akosmo
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*BGM*
The Roach Emperor by Studio EIM (Limbus Company OST - Canto IX Boss 8 Battle Theme)
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*Timestamps*
0:00 Opening Thought
0:43 Taxonomy and General Information
4:12 Morphology
7:12 Ecology
*References*
Mead J. G. (2007). Stomach anatomy and use in defining systemic relationships of the Cetacean family Ziphiidae (beaked whales). Anatomical record (Hoboken, N.J. : 2007), 290(6), 581–595. doi.org/10.1002/ar.20536
Quick, N. J., Cioffi, W. R., Shearer, J. M., Fahlman, A., & Read, A. J. (2020). Extreme diving in mammals: first estimates of behavioural aerobic dive limits in Cuvier's beaked whales. The Journal of experimental biology, 223(Pt 18), jeb222109. doi.org/10.1242/jeb.222109
Best, P. B., Smale, M. J., Glass, J., Herian, K., & Von Der Heyden, S. (2014). Identification of stomach contents from a Shepherd’s beaked whale Tasmacetus shepherdi stranded on Tristan da Cunha, South Atlantic. Journal of the Marine Biological Association of the United Kingdom, 94(6), 1093–1097. doi:10.1017/S0025315412001658
Adams, J., Walker, W. A., Burton, E. J., & Harvey, J. T. (2015). STOMACH CONTENTS OF A CUVIER’S BEAKED WHALE (ZIPHIUS CAVIROSTRIS) STRANDED IN MONTEREY BAY, CALIFORNIA. Northwestern Naturalist, 96(1), 93–98. http://www.jstor.org/stable/26382435
Tonay, A. M., Salman, A., Taşkaya, İ., et al. (2025). Stomach Contents of Stranded Goose-Beaked Whales in the Levantine Basin and Aegean Sea. Marine Mammal Science, 42(1): e70075. doi.org/10.1111/mms.70075
Heyning, J.E. & Mead, J. G. (1996). Suction feeding in beaked whales: morphological and observational evidence. Contributions in science, 464, 1-12. doi.org/10.5962/p.226802
Fedutin, I. D., Filatova, O. A., Mamaev, E. G., et al. (2014). Occurrence and social structure of Baird's beaked whales, Berardius bairdii, in the Commander Islands, Russia. Marine Mammal Science, 31(3): 853-865. doi.org/10.1111/mms.12204
Visser, F., Oudejans, M. G., Keller, O. A., Madsen, P. T., & Johnson, M. (2022). Sowerby's beaked whale biosonar and movement strategy indicate deep-sea foraging niche differentiation in mesoplodont whales. The Journal of experimental biology, 225(9), jeb243728. doi.org/10.1242/jeb.243728
*Outro*
Bubbles Drifting in the Morning Breeze - Artificial.Music & Akosmo
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ifonu
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*Timestamps*
0:00 Opening Thought
1:09 Taxonomy and General Information
3:39 Morphology
6:35 Ecology
*References*
Harris, J. M. & Maloney, K. S. (2010). Petauroides volans (Diprotodontia: Pseudocheiridae). Mammalian Species, 42(866), 207-219. doi.org/10.1644/866.1
McGregor, D. C., Padovan, A., Georges, A., Krockenberger, A., Yoon, H. J., & Youngentob, K. N. (2020). Genetic evidence supports three previously described species of greater glider, Petauroides volans, P. minor, and P. armillatus. Scientific reports, 10(1), 19284. doi.org/10.1038/s41598-020-76364-z
Mulley, B., Gracanin, A., & Mikac, K. M. (2024). Population Viability of an Endangered Population of Greater Gliders (Petauroides volans) and Management Implications. Conservation, 4(4), 871-887. doi.org/10.3390/conservation4040052
Johnson, C. & Burbidge, A.A. (2025). Petauroides volans. The IUCN Red List of Threatened Species 2025: e.T40579A217036853. dx.doi.org/10.2305/IUCN.UK.2025-2.RLTS.T40579A217036853.en.
*Outro*
Bubbles Drifting in the Morning Breeze - Artificial.Music & Akosmo
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Josh Bowell
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*Timestamps*
0:00 Opening Thought
0:40 Introduction
3:31 The Experiment
7:13 Aftermath
*References*
Santiago-Rivera, E. & Scheibel, T. (2025). Spider Eye Development Editing and Silk Fiber Engineering Using CRISPR-Cas (RETRACTED). Angewandte Chemie, 64(25): e202502068. doi.org/10.1002/anie.202502068
Ye, R., Yang, X., & Rao, Y. (2022). Genetic Engineering Technologies for Improving Crop Yield and Quality. Agronomy, 12(4), 759. doi.org/10.3390/agronomy12040759
*Outro*
Bubbles Drifting in the Morning Breeze - Artificial.Music & Akosmo
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Common House Spider: sankax
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*References*
Hausmann, A., Toivonen, T., Fink, C., Heikinheimo, V., Tenkanen, H., Butchart, S. H. M., Brooks, T. M., & Di Minin, E. (2019). Assessing global popularity and threats to Important Bird and Biodiversity Areas using social media data. The Science of the total environment, 683, 617–623. doi.org/10.1016/j.scitotenv.2019.05.268
Maple, D.J., Barr, R., & Smith, M. J. (2012). A new record of the Christmas Island Blind Snake, Ramphotyphlops exocoeti (Reptilia:Squamata: Typhlopidae). Records of the Western Australian Museum, 27: 156-160. http://dx.doi.org/10.18195/issn.0312-3162.27(2).2012.156-160
Emery, J-P. Mitchell, N.J., Cogger, H., et al. (2021). The lost lizards of Christmas Island: A retrospective assessment of factors driving the collapse of a native reptile community. Conservation Science and Practice, 3(2): e358. doi.org/10.1111/csp2.358
Andrew, P., Cogger, H., Driscoll, D., et al. (2018). Somewhat saved: a captive breeding programme for two endemic Christmas Island lizard species, now extinct in the wild. Oryx, 52(1), 171–174. doi.org/10.1017/S0030605316001071
*Thumbnail Image*
Christmas Island Pipistrelle (Bottom Right): Lindy Lumsden
Christmas Island Forest Skink (Middle): Biodiversity Heritage Library
The rest are public domain
*Outro*
Silent Night (Youtube Library)
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*Timestamps*
0:00 Opening Thought
0:46 Taxonomy and General Information
3:37 Morphology
9:08 Lifestyle and Behaviour
13:19 Fossil Records
*References*
Bamber, R.N.; El Nagar, A.; Arango, C.P.; Sabroux, R. (Eds) (2025). Pycnobase: World Pycnogonida Database. marinespecies.org/pycnobase. doi:10.14284/360
Ballesteros, J. A., Setton, E. V. W., Santibáñez-López, C. E., Arango, C. P., Brenneis, G., Brix, S., Corbett, K. F., Cano-Sánchez, E., Dandouch, M., Dilly, G. F., Eleaume, M. P., Gainett, G., Gallut, C., McAtee, S., McIntyre, L., Moran, A. L., Moran, R., López-González, P. J., Scholtz, G., Williamson, C., … Sharma, P. P. (2021). Phylogenomic Resolution of Sea Spider Diversification through Integration of Multiple Data Classes. Molecular biology and evolution, 38(2), 686–701. doi.org/10.1093/molbev/msaa228
Wang, J. J., Huang, D. Y., Lin, R. C., & Zheng, X. Q. (2013). A new species of Austrodecus Hodgson, 1907 (Arthropoda, Pycnogonida, Austrodecidae) from the Southwest Indian Ridge. ZooKeys, (349), 73–79. doi.org/10.3897/zookeys.349.6170
Brenneis, G., Frankowski, K., Maaß, L., & Scholtz, G. (2023). The sea spider Pycnogonum litorale overturns the paradigm of the absence of axial regeneration in molting animals. Proceedings of the National Academy of Sciences of the United States of America, 120(5), e2217272120. doi.org/10.1073/pnas.2217272120
Dietz, L., Dömel, J. S., Leese, F., Lehmann, T., & Melzer, R. R. (2018). Feeding ecology in sea spiders (Arthropoda: Pycnogonida): what do we know?. Frontiers in zoology, 15, 7. doi.org/10.1186/s12983-018-0250-4
Richards, P.R. & Fry, W.G. (1978). Digestion in pycnogonids: a study of some polar forms. Zoological Journal of the Linnean Society, 63(1-2): 75-97. doi.org/10.1111/j.1096-3642.1978.tb02091.x
Woods, H. A., Lane, S. J., Shishido, C., Tobalske, B. W., Arango, C. P., & Moran, A. L. (2017). Respiratory gut peristalsis by sea spiders. Current biology : CB, 27(13), R638–R639. doi.org/10.1016/j.cub.2017.05.062
Lehmann, T., Heß, M., & Melzer, R. R. (2014). Common littoral pycnogonids of the Mediterranean Sea. Zoosystematics and Evolution, 90(2): 163–224. doi.org/10.3897/zse.90.7520
Lucena, R. A. & Christoffersen, M. L. (2022). Pycnogonida (Arthropoda) from Museu de Ciências Naturais, Rio Grande do Sul, Brazil. Zoosystematics and Evolution, 98(2): 305–312. doi.org/10.3897/zse.98.83671
Alexeeva, N. & Tamberg, Y. (2023). Ultrastructure of the female pedal gonad in Phoxichilidium femoratum (Chelicerata, Pycnogonida). Arthropod Structure & Development, 76, 101295. doi.org/10.1016/j.asd.2023.101295
Moran, A. L., Lobert, G. T., & Toh, M. W. A. (2024). Spawning and larval development of Colossendeis megalonyx, a giant Antarctic sea spider. Ecology, 105(3), e4258. doi.org/10.1002/ecy.4258
Sabroux, R., Garwood, R. J., Pisani, D., Donoghue, P. C. J., & Edgecombe, G. D. (2024). New insights into the Devonian sea spiders of the Hunsrück Slate (Arthropoda: Pycnogonida). PeerJ, 12, e17766. doi.org/10.7717/peerj.17766
*Outro*
The Soundlings - Silent Night (Youtube Library)
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Danny Lee
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Check out these videos to see them moving around
youtube.com/watch?v=Hjt6VV0qhok
youtube.com/watch?v=dSk3IMpR0nc
*Timestamps*
0:00 Opening Thought
1:03 Taxonomy and General Information
3:00 Morphology
4:37 Eye
6:46 Lifestyle and Behaviour
*References*
Read, G.; Fauchald, K. (Ed.) (2025). World Polychaeta Database. Alciopini Ehlers, 1864. Accessed through: World Register of Marine Species at: marinespecies.org/aphia.php?p=taxdetails&id=932
Lewin, T. D., Liao, I. J., & Luo, Y. J. (2024). Annelid Comparative Genomics and the Evolution of Massive Lineage-Specific Genome Rearrangement in Bilaterians. Molecular biology and evolution, 41(9) , msae172. doi.org/10.1093/molbev/msae172
San Martín, G., Álvarez-Campos, P., Kondo, Y. et al. (2020). New symbiotic association in marine annelids: ectoparasites of comb jellies. Zoological Journal of the Linnean Society, 191(3): 672-694. doi.org/10.1093/zoolinnean/zlaa034
Syomin, V., Kolbasova, G., Semenova, M., & Neretina, T. (2025). A new species of an unusual polychaete genus Ctenophoricola (Phyllodocida, Phyllodocidae, Alciopini) from the Indian Ocean. Zootaxa, 5613(1), 82–98. doi.org/10.11646/zootaxa.5613.1.3
Bok, M. J., Macali, A., & Garm, A. (2024). High-resolution vision in pelagic polychaetes. Current Biology,
*Outro*
The Soundlings - Silent Night (Youtube Library)
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Alison Sweeney
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*Background Music*
Limbus Company Main Menu Theme
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*Timestamps*
0:00 Opening Thought
0:52 Taxonomy and General Information
2:50 Morphology
4:39 Lifestyle and Behaviour
9:43 Tentacle
*References*
Murphy, J., Brooks, S.E. & Bain, R.H. 2010. Erpeton tentaculatum. The IUCN Red List of Threatened Species 2010: e.T176697A7285596. dx.doi.org/10.2305/IUCN.UK.2010-4.RLTS.T176697A7285596.en.
Catania K. C. (2012). Evolution of brains and behavior for optimal foraging: a tale of two predators. Proceedings of the National Academy of Sciences of the United States of America, 109 Suppl 1(Suppl 1), 10701–10708. doi.org/10.1073/pnas.1201885109
Catania K. C. (2010). Born knowing: tentacled snakes innately predict future prey behavior. PloS one, 5(6), e10953. doi.org/10.1371/journal.pone.0010953
Catania, K. C., Leitch, D. B., & Gauthier, D. (2010). Function of the appendages in tentacled snakes (Erpeton tentaculatus). The Journal of experimental biology, 213(3), 359–367. doi.org/10.1242/jeb.039685
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The Soundlings - Silent Night (Youtube Library)
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Catania, 2010 (see the Reference section)
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*Timestamps*
0:00 Opening Thought
1:02 Taxonomy and General Information
3:05 Morphology
4:39 Lifestyle and Behaviour
7:23 Evolutionary Relationship
*References*
IUCN SSC Amphibian Specialist Group. 2022. Myobatrachus gouldii. The IUCN Red List of Threatened Species 2022: e.T41171A78444058. dx.doi.org/10.2305/IUCN.UK.2022-2.RLTS.T41171A78444058.en. Accessed on 20 November 2025.
Emerson S. B. (1976). Burrowing in frogs. Journal of morphology, 149(4), 437–458. doi.org/10.1002/jmor.1051490402
Portik, D. M., Streicher, J. W., & Wiens, J. J. (2023). Frog phylogeny: A time-calibrated, species-level tree based on hundreds of loci and 5,242 species. Molecular phylogenetics and evolution, 188, 107907. doi.org/10.1016/j.ympev.2023.107907
Vertucci, S., Pepper, M., Edwards, D. L., Roberts, J. D., Mitchell, N., & Keogh, J. S. (2017). Evolutionary and natural history of the turtle frog, Myobatrachus gouldii, a bizarre myobatrachid frog in the southwestern Australian biodiversity hotspot. PloS one, 12(3), e0173348. doi.org/10.1371/journal.pone.0173348
*Outro*
The Soundlings - Silent Night (Youtube Library)
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Nick Volpe
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*Timestamps*
0:00 Opening Thought
0:55 Taxonomy and General Information
5:01 Morphology
8:20 Lifestyle and Behaviour
*References*
Scholtz, G. (2014). Evolution of crabs - history and deconstruction of a prime example of convergence. Contributions to Zoology, 83(2): 87-105. doi.org/10.1163/18759866-08302001
Roterman, C. N., Lee, W. K., Liu, X., Lin, R., Li, X., & Won, Y. J. (2018). A new yeti crab phylogeny: Vent origins with indications of regional extinction in the East Pacific. PloS one, 13(3), e0194696. doi.org/10.1371/journal.pone.0194696
Thurber, A. R., Jones, W. J., & Schnabel, K. (2011). Dancing for food in the deep sea: bacterial farming by a new species of Yeti crab. PloS one, 6(11), e26243. doi.org/10.1371/journal.pone.0026243
Rogers, A. D., Tyler, P. A., Connelly, D. P., Copley, J. T., James, R., Larter, R. D., Linse, K., Mills, R. A., Garabato, A. N., Pancost, R. D., Pearce, D. A., Polunin, N. V., German, C. R., Shank, T., Boersch-Supan, P. H., Alker, B. J., Aquilina, A., Bennett, S. A., Clarke, A., Dinley, R. J., … Zwirglmaier, K. (2012). The discovery of new deep-sea hydrothermal vent communities in the southern ocean and implications for biogeography. PLoS biology, 10(1), e1001234. doi.org/10.1371/journal.pbio.1001234
Thatje, S., Marsh, L., Roterman, C. N., Mavrogordato, M. N., & Linse, K. (2015). Adaptations to Hydrothermal Vent Life in Kiwa tyleri, a New Species of Yeti Crab from the East Scotia Ridge, Antarctica. PloS one, 10(6), e0127621. doi.org/10.1371/journal.pone.0127621
Lee, S-H., Lee, W-K., & Won, Y-J. (2016). A New Species of Yeti Crab, Genus Kiwa (Decapoda: Anomura: Kiwaidae), from a Hydrothermal Vent on the Australian-Antarctic Ridge. Journal of Crustacean Biology, 36(2): 238-247. doi.org/10.1163/1937240X-00002418
Liu, X., Lin, J., Mendoza, J.C.E. (2024). A new species of the bathyal yeti crab genus Kiwa Macpherson, Jones & Segonzac, 2005 (Decapoda: Anomura: Kiwaidae) from a hydrothermal vent field in the Eastern Pacific Ocean, with a key to the genus. Journal of Crustacean Biology, 44(2): ruae030. doi.org/10.1093/jcbiol/ruae030
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The Soundlings - Silent Night (Youtube Library)
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*Timestamps*
0:00 Opening Thought
0:47 Wings and Flight
5:20 Insect Wing
13:03 Vertebrate Wing
13:40 Pterosaur Wing
19:04 Bird Wing and Other Non-Avian Theropods
28:05 Bat Wing
*References*
Cho, M., et al. (2018). doi.org/10.1371/journal.pbio.2004405
Alexander D. E. (2018). doi.org/10.1016/j.asd.2017.11.007
Prokop, J., et al. (2019). http://doi.org/10.1098/rsos.190460
Tomoyasu, Y., et al. (2017). doi.org/10.12688/f1000research.10285.1
Prokop, et al. (2017). doi.org/10.1016/j.cub.2016.11.021
Ross A. (2022). doi.org/10.1016/j.cub.2022.06.087
Almudi, et al. (2020). doi.org/10.1038/s41467-020-16284-8
Dehling J. M. (2017). doi.org/10.1371/journal.pone.0189573
Ezcurra, et al. (2020). doi.org/10.1038/s41586-020-3011-4
Zhou, et al. (2020). doi.org/10.5194/fr-23-191-2020
Witton M. P. (2015). doi.org/10.7717/peerj.1018
Bennett, S. C. (2000). doi.org/10.1080/10292380009380572
Kellner, et al. (2010). doi.org/10.1098/rspb.2009.0846
Dyke, et al. (2006). doi.org/10.1111/j.1420-9101.2006.01096.x
Pittman, et al. (2021). doi.org/10.1073/pnas.2107631118
Chatterjee, S., & Templin, R.J. (2004). doi.org/10.1130/SPE376
Witton, M. P., & Habib, M. B. (2010). doi.org/10.1371/journal.pone.0013982
Longrich, et al. (2018). doi.org/10.1371/journal.pbio.2001663
Voeten, et al. (2018). doi.org/10.1038/s41467-018-03296-8
Hone, et al. (2010). doi.org/10.1371/journal.pone.0009223
Liard, et al. (2015). researchgate.net/publication/341039760_Phu_Noi_a_mesozoic_vertebrate_locality_from_the_Jurassic_of_Thailand
Hartman, et al. (2019). doi.org/10.7717/peerj.7247
Tobalske B. W. (2016). doi.org/10.1098/rstb.2015.0383
Rietbergen, et al. (2023). doi.org/10.1371/journal.pone.0283505
Tokita, et al. (2012). doi.org/10.1038/ncomms2298
Cheney, et al. (2017). doi.org/10.1111/joa.12580
Adams, et al. (2012). doi.org/10.1371/journal.pone.0032074
*Outro*
The Soundlings - Silent Night (Youtube Library)
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Pterosaur Wing: Rudolf Hima
(The rest are Public Domain)
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*Timestamps*
0:00 Opening Thought
0:49 Taxonomy and General Information
2:16 Morphology
4:02 Blood and Iron
8:35 Lifestyle and Behaviour
*References*
Corliss, B. A., Delalio, L. J., Stevenson Keller, T. C., 4th, Keller, A. S., Keller, D. A., Corliss, B. H., Beers, J. M., Peirce, S. M., & Isakson, B. E. (2019). Vascular Expression of Hemoglobin Alpha in Antarctic Icefish Supports Iron Limitation as Novel Evolutionary Driver. Frontiers in physiology, 10, 1389. doi.org/10.3389/fphys.2019.01389
Beers, J. M., & Jayasundara, N. (2015). Antarctic notothenioid fish: what are the future consequences of 'losses' and 'gains' acquired during long-term evolution at cold and stable temperatures?. The Journal of experimental biology, 218(Pt 12), 1834–1845. doi.org/10.1242/jeb.116129
Sidell, B. D., & O'Brien, K. M. (2006). When bad things happen to good fish: the loss of hemoglobin and myoglobin expression in Antarctic icefishes. The Journal of experimental biology, 209(Pt 10), 1791–1802. doi.org/10.1242/jeb.02091
Corliss, B. A., Delalio, L. J., Stevenson Keller, T. C., 4th, Keller, A. S., Keller, D. A., Corliss, B. H., Beers, J. M., Peirce, S. M., & Isakson, B. E. (2019). Vascular Expression of Hemoglobin Alpha in Antarctic Icefish Supports Iron Limitation as Novel Evolutionary Driver. Frontiers in physiology, 10, 1389. doi.org/10.3389/fphys.2019.01389
Purser, A., Hehemann, L., Boehringer, L., Tippenhauer, S., Wege, M., Bornemann, H., Pineda-Metz, S. E. A., Flintrop, C. M., Koch, F., Hellmer, H. H., Burkhardt-Holm, P., Janout, M., Werner, E., Glemser, B., Balaguer, J., Rogge, A., Holtappels, M., & Wenzhoefer, F. (2022). A vast icefish breeding colony discovered in the Antarctic. Current biology : CB, 32(4), 842–850.e4. doi.org/10.1016/j.cub.2021.12.022
Froese, R. and D. Pauly. Editors. (2025). FishBase. Channichthyidae Gill, 1861. Accessed through: World Register of Marine Species at: marinespecies.org/aphia.php?p=taxdetails&id=234518
*Outro*
The Soundlings - Silent Night (Youtube Library)
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Blood: Jody M. Beers
Larva: uwe kils
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*Timestamps*
0:00 Opening Thought
1:00 Taxonomy and General Information
3:13 Morphology
6:20 Lifestyle and Behaviour
8:30 Cultural Relevance
*References*
Kryštufek, B. (2010). Glis glis (Rodentia: Gliridae). Mammalian Species, 42(865), 195–206. doi.org/10.1644/865.1
Kryštufek, B., Naderi, M., Janžekovič, F., Hutterer, R., Bombek, D. & Mahmoudi, A. (2021). A taxonomic revision of fat dormice, genus Glis (Rodentia). Mammalia, 85(4), 362-378. doi.org/10.1515/mammalia-2020-0161
Vekhnik, V. A. (2022). Nutrition of the Edible dormouse (Glis glis Linnaeus, 1766) across the distributional range. Journal of Wildlife and Biodiversity, 6(Special issue), 1–23. doi.org/10.5281/zenodo.7154224
Bieber, C., Turbill, C. & Ruf, T. (2018). Effects of aging on timing of hibernation and reproduction. Sci Rep 8, 13881. doi.org/10.1038/s41598-018-32311-7
Amori, G., Hutterer, R., Kryštufek, B., Yigit, N., Mitsainas, G., Muñoz, L., Meinig, H. & Juškaitis, R. 2021. Glis glis (amended version of 2016 assessment). The IUCN Red List of Threatened Species 2021: e.T39316A197292692. dx.doi.org/10.2305/IUCN.UK.2021-1.RLTS.T39316A197292692.en.
*Outro*
The Soundlings - Silent Night (Youtube Library)
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Julien 31
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MBARI Video: youtube.com/watch?v=MszfZriuVVs&t=1s
*Timestamps*
0:00 Opening Thought
0:44 Discovery
1:37 Taxonomy and General Information
3:13 Morphoanatomy
6:49 Lifestyle and Behaviour
9:17 Evolutionary Relationship
*Reference*
Robison, B. H. & Haddock, S. H. D. (2024). Discovery and description of a remarkable bathypelagic nudibranch, Bathydevius caudactylus, gen. et. sp. nov. Deep Sea Research Part I: Oceanographic Research Papers, 214: 104414. doi.org/10.1016/j.dsr.2024.104414
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The Soundlings - Silent Night (Youtube Library)
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Robison & Haddock, 2024 (check the reference section)
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Sandfish Robot: youtube.com/watch?v=Rwoz4WbXxdI
*Timestamps*
0:00 Opening Thought
0:36 Taxonomy and General Information
2:27 Morphology
5:01 Lifestyle and Behaviour
*References*
Els, J., Eid, E.K.A., Al Johany, A.M.H., Amr, Z.S.S., Egan, D.M., Sharifi, M., Papenfuss, T. & Shafiei Bafti, S. 2022. Scincus mitranus (amended version of 2012 assessment). The IUCN Red List of Threatened Species 2022: e.T164651A217762229. dx.doi.org/10.2305/IUCN.UK.2022-1.RLTS.T164651A217762229.en.
Baumgartner, W., Fidler, F., Weth, A., Habbecke, M., Jakob, P., Butenweg, C., & Böhme, W. (2008). Investigating the locomotion of the sandfish in desert sand using NMR-imaging. PloS one, 3(10), e3309. doi.org/10.1371/journal.pone.0003309
Maladen, R. D., Ding, Y., Li, C., & Goldman, D. I. (2009). Undulatory swimming in sand: subsurface locomotion of the sandfish lizard. Science (New York, N.Y.), 325(5938), 314–318. doi.org/10.1126/science.1172490
Wu, W., Lutz, C., Mersch, S., Thelen, R., Greiner, C., Gomard, G., & Hölscher, H. (2018). Characterization of the microscopic tribological properties of sandfish (Scincus scincus) scales by atomic force microscopy. Beilstein journal of nanotechnology, 9, 2618–2627. doi.org/10.3762/bjnano.9.243
Stadler, A. T., Vihar, B., Günther, M., Huemer, M., Riedl, M., Shamiyeh, S., Mayrhofer, B., Böhme, W., & Baumgartner, W. (2016). Adaptation to life in aeolian sand: how the sandfish lizard, Scincus scincus, prevents sand particles from entering its lungs. The Journal of experimental biology, 219(Pt 22), 3597–3604. doi.org/10.1242/jeb.138107
Hetherington, T. E. (1989). Use of vibratory cues for detection of insect prey by the sandswimming lizard Scincus scincus. Animal Behaviour, 37(2): 290-297. doi.org/10.1016/0003-3472(89)90118-8
Zimin, Anna; Zimin, Sean; Shine, Richard et al. (2022). A global analysis of viviparity in squamates highlights its prevalence in cold climates [Dataset]. Dryad. doi.org/10.5061/dryad.kd51c5b6m
Al-Johany, A. M., Al-Sadoon, M. K., & Al-Farraj, S. A. (1997). Reproductive biology of the skinkScincus mitranus(Anderson, 1871) in the central region of Saudi Arabia. Journal of Arid Environments, 36(2), 319–326. doi.org/10.1006/JARE.1996.0241
*Outro*
The Soundlings - Silent Night (Youtube Library)
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dhfischer (iNaturalist)
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*Timestamps*
0:00 Opening Thought
1:01 Taxonomy and General Information
4:41 Morphology and Anatomy
7:51 Behaviour and Physiology
*References*
Sui, Z., Zhao, Z., & Dong, B. (2021). Origin of the Chordate Notochord. Diversity, 13(10), 462. doi.org/10.3390/d13100462
Röttinger, E., & Lowe, C. J. (2012). Evolutionary crossroads in developmental biology: hemichordates. Development (Cambridge, England), 139(14), 2463–2475. doi.org/10.1242/dev.066712
Satoh, N., Tagawa, K., Lowe, C. J., Yu, J. K., Kawashima, T., Takahashi, H., Ogasawara, M., Kirschner, M., Hisata, K., Su, Y. H., & Gerhart, J. (2014). On a possible evolutionary link of the stomochord of hemichordates to pharyngeal organs of chordates. Genesis (New York, N.Y. : 2000), 52(12), 925–934. doi.org/10.1002/dvg.22831
Igawa, T., Nozawa, M., Suzuki, D. G., Reimer, J. D., Morov, A. R., Wang, Y., Henmi, Y., & Yasui, K. (2017). Evolutionary history of the extant amphioxus lineage with shallow-branching diversification. Scientific reports, 7(1), 1157. doi.org/10.1038/s41598-017-00786-5
Wei-Ye, L., Fang, S. H., & Wang, Y. Q. (2014). Complete mitochondrial genome of Epigonichthys cultellus (Cephalochordata: Branchiostomatidae). Zoological science, 31(11), 766–772. doi.org/10.2108/zs130213
Nishikawa T. (2004). A new deep-water lancelet (Cephalochordata) from off Cape Nomamisaki, SW Japan, with a proposal of the revised system recovering the genus Asymmetron. Zoological science, 21(11), 1131–1136. doi.org/10.2108/zsj.21.1131
Kon, T., Nohara, M., Yamanoue, Y., Fujiwara, Y., Nishida, M., & Nishikawa, T. (2007). Phylogenetic position of a whale-fall lancelet (Cephalochordata) inferred from whole mitochondrial genome sequences. BMC evolutionary biology, 7, 127. doi.org/10.1186/1471-2148-7-127
Madrid Concepcion, M. E., Macdonald, K. S., III, Driskell, A. C., Wetzer, R., Di Domenico, M., & Collin, R. (2025). Lots of Lancelets or Not? Diversity of Cephalochordates in the Tropical Eastern Pacific. Diversity, 17(6), 411. doi.org/10.3390/d17060411
Lamb T. D. (2013). Evolution of phototransduction, vertebrate photoreceptors and retina. Progress in retinal and eye research, 36, 52–119. doi.org/10.1016/j.preteyeres.2013.06.001
McDougall, A., Hebras, C., Gomes, I., & Dumollard, R. (2021). Gene Editing in the Ascidian Phallusia mammillata and Tail Nerve Cord Formation. Methods in molecular biology (Clifton, N.J.), 2219, 217–230. doi.org/10.1007/978-1-0716-0974-3_13
Garcia-Fernàndez, J., & Benito-Gutiérrez, E. (2009). It's a long way from amphioxus: descendants of the earliest chordate. BioEssays : news and reviews in molecular, cellular and developmental biology, 31(6), 665–675. doi.org/10.1002/bies.200800110
D'Aniello, S., Bertrand, S., & Escriva, H. (2023). Amphioxus as a model to study the evolution of development in chordates. eLife, 12, e87028. doi.org/10.7554/eLife.87028
Yue, J. X., Holland, N. D., Holland, L. Z., & Deheyn, D. D. (2016). The evolution of genes encoding for green fluorescent proteins: insights from cephalochordates (amphioxus). Scientific reports, 6, 28350. doi.org/10.1038/srep28350
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Chris Isaacs (iNaturalist)
*Outro*
The Soundlings - Silent Night (Youtube Library)
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*Timestamps*
0:00 Opening Thought
0:44 Taxonomy and General Information
3:00 Morphology
5:03 Lifestyle and Behaviour
6:31 Electric Shock
*References*
Jacobsen, I.P. & Lisney, T.J. 2015. Hypnos monopterygius. The IUCN Red List of Threatened Species 2015: e.T41828A68630121. dx.doi.org/10.2305/IUCN.UK.2015-4.RLTS.T41828A68630121.en.
Frost A.-M., Jacobsen I. P., Bennett M. B. (2017) The diet of the coffin ray, Hypnos monopterygius (Shaw, 1795), and predation mode inferred from jaw, dentition and electric organ morphology. Marine and Freshwater Research 68, 1193-1198. doi.org/10.1071/MF16200
McGrouther, M. (2023). Coffin Ray, Hypnos monopterygius (Shaw & Nodder 1795). Australian Museum. https://australian.museum/learn/animals/fishes/numbfish-hypnos-monopterygium-shaw-nodder-1795/
Dulvy, N.K. & Reynolds, J.D. (1997). Evolutionary transitions among egg-Laying, live-bearing and maternal inputs in sharks and rays. Proceedings of the Royal Society B, 264: 1309-1315. http://dx.doi.org/10.1098/rspb.1997.0181
Katona, G., Szabó, F., Végvári, Z., Székely, T., Jr, Liker, A., Freckleton, R. P., Vági, B., & Székely, T. (2023). Evolution of reproductive modes in sharks and rays. Journal of evolutionary biology, 36(11), 1630–1640. doi.org/10.1111/jeb.14231
Blackburn, D. G., & Hughes, D. F. (2024). Phylogenetic analysis of viviparity, matrotrophy, and other reproductive patterns in chondrichthyan fishes. Biological reviews of the Cambridge Philosophical Society, 99(4), 1314–1356. doi.org/10.1111/brv.13070
Tanaka, Y., Funano, Si., Nishizawa, Y. et al. (2016). An electric generator using living Torpedo electric organs controlled by fluid pressure-based alternative nervous systems. Sci Rep 6, 25899. doi.org/10.1038/srep25899
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5:57 Lifestyle and Behaviour
*References*
Herrera, C., Leza, M. & Martínez-López, E. (2020). Diversity of compounds in Vespa spp. venom and the epidemiology of its sting: a global appraisal. Arch Toxicol 94, 3609–3627. doi.org/10.1007/s00204-020-02859-3
Cappa, F., Cini, A., Bortolotti, L., Poidatz, J., & Cervo, R. (2021). Hornets and Honey Bees: A Coevolutionary Arms Race between Ancient Adaptations and New Invasive Threats. Insects, 12(11), 1037. doi.org/10.3390/insects12111037
Ono, M., Terabe, H., Hori, H. et al. (2003). Components of giant hornet alarm pheromone. Nature 424, 637–638. doi.org/10.1038/424637a
Hirano, K., & Tanikawa, A. (2020). Ocular Injury Caused by the Sprayed Venom of the Asian Giant Hornet (Vespa mandarinia). Case reports in ophthalmology, 11(2), 430–435. doi.org/10.1159/000508911
BHOOLA, K. D., CALLE, J. D., & SCHACHTER, M. (1961). Identification of acetylcholine, 5-hydroxy-tryptamine, histamine, and a new kinin in hornet venom (V. crabro). The Journal of physiology, 159(1), 167–182. doi.org/10.1113/jphysiol.1961.sp006799
Gong, Z., Tan, K., & Nieh, J. C. (2019). Hornets possess long-lasting olfactory memories. The Journal of experimental biology, 222(Pt 13), jeb200881. doi.org/10.1242/jeb.200881
Rominiecki, J. (2022). ‘Northern Giant Hornet’ Adopted as Common Name for Vespa mandarinia. Entomological Society of America. entsoc.org/news/press-releases/northern-giant-hornet-common-name-vespa-mandarinia
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8:31 Conservation and Relevance
*References*
Langevin, P. & Barclay, R.M.R. (1990) Hypsignathus monstrosus, Mammalian Species, Issue 357: 1–4, doi.org/10.2307/3504110
Olson, S. H., Bounga, G., Ondzie, A., Bushmaker, T., Seifert, S. N., Kuisma, E., Taylor, D. W., Munster, V. J., & Walzer, C. (2019). Lek-associated movement of a putative Ebolavirus reservoir, the hammer-headed fruit bat (Hypsignathus monstrosus), in northern Republic of Congo. PloS one, 14(10), e0223139. doi.org/10.1371/journal.pone.0223139
Russo, N.J., Takuo, J.M., Tegebong, V. et al. (2025). Spaceborne and UAV-LiDAR reveal hammer-headed bat preference for intermediate canopy height and diverse structure in a Central African rainforest. Mov Ecol 13, 30. doi.org/10.1186/s40462-025-00552-7
Mildenstein, T., Tanshi, I., Racey, P.A. (2016). Exploitation of Bats for Bushmeat and Medicine. In: Voigt, C., Kingston, T. (eds) Bats in the Anthropocene: Conservation of Bats in a Changing World. Springer, Cham. doi.org/10.1007/978-3-319-25220-9_12
Tanshi, I. 2016. Hypsignathus monstrosus (errata version published in 2017). The IUCN Red List of Threatened Species 2016: e.T10734A115098825. dx.doi.org/10.2305/IUCN.UK.2016-3.RLTS.T10734A21999919.en.
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0:38 Taxonomy and General Information
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5:45 Lifestyle and Behaviour
10:02 Fossil Record
10:53 Conservation and Cultural Relevance
*References*
Fraser, R.A., Grün, R., Privat, K., & Gagan, M.K. (2008). Stable-isotope microprofiling of wombat tooth enamel records seasonal changes in vegetation and environmental conditions in eastern Australia. Palaeogeography, Palaeoclimatology, Palaeoecology, 269(1-2), 66-77. doi.org/10.1016/j.palaeo.2008.08.004
Linley, G.D., Geary, W.L., Jolly, C.J., et al. (2024). Wombat burrows are hotspots for small vertebrates in a landscape subject to gigafire. Journal of Mammalogy, 105(4), 752–764. doi.org/10.1093/jmammal/gyae034
Yang, P.J., Lee, A.B., Chan, M., et al. (2021). Intestines of non-uniform stiffness mold the corners of wombat feces. Soft Matter, 17, 475-488. doi.org/10.1039/D0SM01230K
Old, J. M., Vallin, B. L., Thorley, R. K., Casey, F., & Stannard, H. J. (2024). DNA metabarcoding analysis of the bare-nosed wombat (Vombatus ursinus) diet. Ecology and evolution, 14(5), e11432. doi.org/10.1002/ece3.11432
Casey, F., Old, J. M., & Stannard, H. J. (2023). Assessment of the diet of the critically endangered northern hairy-nosed wombat (Lasiorhinus krefftii) using DNA metabarcoding. Ecology and evolution, 13(9), e10469. doi.org/10.1002/ece3.10469
Brewer, P., Archer, M., Hand, S., & Price, G.J. (2018). A new species of Miocene wombat (Marsupialia, Vombatiformes) from Riversleigh, Queensland, Australia, and implications for the evolutionary history of the Vombatidae.
Brewer, P., Archer, M., Hand, S., & Godthelp, H. (2007). A new species of the wombat Warendja from late Miocene deposits at Riversleigh, northwest Queensland, Australia. Palaeontology 50: 811–828. doi.org/10.1111/j.1475-4983.2007.00678.x
Old, J., Stannard, H., Woinarski, J.C.Z. & Burbidge, A.A. (2025). Vombatus ursinus. The IUCN Red List of Threatened Species 2025: e.T40556A258654868. dx.doi.org/10.2305/IUCN.UK.2025-1.RLTS.T40556A258654868.en.
Woinarski, J.C.Z., Burbidge, A.A., Old, J. & Stannard, H. (2025). Lasiorhinus latifrons. The IUCN Red List of Threatened Species 2025: e.T40555A258654451. dx.doi.org/10.2305/IUCN.UK.2025-1.RLTS.T40555A258654451.en.
Taggart, D., Martin, R. & Horsup, A. (2016). Lasiorhinus krefftii. The IUCN Red List of Threatened Species 2016: e.T11343A21959050. dx.doi.org/10.2305/IUCN.UK.2016-2.RLTS.T11343A21959050.en.
Thorley, R.K. & Old, J.M. (2020). Distribution, abundance and threats to bare-nosed wombats (Vombatus ursinus). Australian Mammalogy. 42(3): 249–256. doi.org/10.1071/AM19035
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1:09 Taxonomy and General Information
2:22 Morphology
3:42 Unique Traits and Lifestyle
7:01 Uses and Importance
*References*
Holland, R. A., Wikelski, M., Kümmeth, F., & Bosque, C. (2009). The secret life of oilbirds: new insights into the movement ecology of a unique avian frugivore. PloS one, 4(12), e8264. doi.org/10.1371/journal.pone.0008264
Martin, G., Rojas, L.M., Ramírez, Y. et al. (2004). The eyes of oilbirds (Steatornis caripensis): pushing at the limits of sensitivity. Naturwissenschaften 91, 26–29. doi.org/10.1007/s00114-003-0495-3
Rojas, L. M., Ramírez, Y., McNeil, R., Mitchell, M., & Marín, G. (2004). Retinal morphology and electrophysiology of two caprimulgiformes birds: the cave-living and nocturnal oilbird (Steatornis caripensis), and the crepuscularly and nocturnally foraging common pauraque (Nyctidromus albicollis). Brain, behavior and evolution, 64(1), 19–33. doi.org/10.1159/000077540
BirdLife International. 2021. Steatornis caripensis. The IUCN Red List of Threatened Species 2021: e.T22689633A137757943. dx.doi.org/10.2305/IUCN.UK.2021-3.RLTS.T22689633A137757943.en.
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8:04 Evolution
*References*
Tubelis, D.P. (2020). Breeding biology of the Horned Screamer (Anhima cornuta) in non-protected areas in the Brazilian Cerrado. Ornithol. Res. 28: 115–124. doi.org/10.1007/s43388-020-00015-0
Mayr, G., Pittman, M., Saitta, E., Kaye, T.G., & Vinther, J. (2016). Structure and homology of Psittacosaurus tail bristles. Palaeontology, 59(6): 793-802. doi.org/10.1111/pala.12257
Kurochkin, E. N., Dyke, Gareth, & Karhu, Alexandr A. (2002). A new presbyornithid bird (Aves, Anseriformes) from the late Cretaceous of southern Mongolia. American Museum of Natural History.
De Pietri, V. L., Scofield, R. P., Zelenkov, N., Boles, W. E., & Worthy, T. H. (2016). The unexpected survival of an ancient lineage of anseriform birds into the Neogene of Australia: the youngest record of Presbyornithidae. Royal Society Open Science, 3(2). doi.org/10.1098/rsos.150635
Livezey, B.C. (1997). A phylogenetic analysis of basal Anseriformes, the fossil Presbyornis, and the interordinal relationships of waterfowl, Zoological Journal of the Linnean Society, 121(4): 361–428, doi.org/10.1111/j.1096-3642.1997.tb01285.x
Donne-Goussé, C., Laudet, V., & Hänni, C. (2002). A molecular phylogeny of anseriformes based on mitochondrial DNA analysis. Molecular phylogenetics and evolution, 23(3), 339–356. doi.org/10.1016/s1055-7903(02)00019-2
Houde, P., Dickson, M., & Camarena, D. (2023). Basal Anseriformes from the Early Paleogene of North America and Europe. Diversity, 15(2), 233. doi.org/10.3390/d15020233
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*Timestamps*
0:00 Opening Thought
0:39 Taxonomy and General Information
3:59 Morphology
6:55 Lifestyle and Behaviour
8:58 Invasive Species
*References*
Kawakatsu, M., Ogren, R.E., & Froehlich, E.M. (1998). The Taxonomic Revision of Several Homonyms in the genus Bipalium, Family Bipaliidae (Turbellaria, Seriata, Tricladida, Terricola). Bull. Fuji Women’s College, 36, ser. II: 83-93. fujijoshi.repo.nii.ac.jp/record/1375/files/KJ00006968702.pdf
Ogren, R.E. & Sluys, R. (2001). The genus Humbertium gen. nov., a new taxon of the land planarian family Bipaliidae (Tricladida, Terricola). Belg. J. Zool, 131: 201-204. biblio.naturalsciences.be/associated_publications/bjz/131-1-supplement/volume-131-s1-pp-201-204.pdf
Kawakatsu, M., Ogren, R.E., Froehlich, E.M., Takai, M., & Sasaki, G. (2002). Additions and Corrections of the Previous Land Planarian Indices of the World (Turbellaria, Seriata, Tricladida, Terricola) - 10. Bull. Fuji Women’s College, 40, ser. II: 157-177. fujijoshi.repo.nii.ac.jp/record/259/files/KJ00004724391.pdf
Solà, E., Sluys, R., Riutort, M., & Kawakatsu, M. (2023). Molecular phylogenetics facilitates the first historical biogeographic analysis of the hammerhead worms (Platyhelminthes: Tricladida: Bipaliinae), with the description of twelve new species and two new genera. Zootaxa, 5335(1), 1–77. doi.org/10.11646/zootaxa.5335.1.1
Justine, J. L., Gastineau, R., Gros, P., Gey, D., Ruzzier, E., Charles, L., & Winsor, L. (2022). Hammerhead flatworms (Platyhelminthes, Geoplanidae, Bipaliinae): mitochondrial genomes and description of two new species from France, Italy, and Mayotte. PeerJ, 10, e12725. doi.org/10.7717/peerj.12725
Fourcade, Y., Winsor, L., & Justine, J.-L. (2022). Hammerhead worms everywhere? Modelling the invasion of bipaliin flatworms in a changing climate. Diversity and Distributions, 28, 844–858. doi.org/10.1111/ddi.13489
Justine, J. L., Winsor, L., Gey, D., Gros, P., & Thévenot, J. (2018). Giant worms chez moi! Hammerhead flatworms (Platyhelminthes, Geoplanidae, Bipalium spp., Diversibipalium spp.) in metropolitan France and overseas French territories. PeerJ, 6, e4672. doi.org/10.7717/peerj.4672
Stokes, A. N., Ducey, P. K., Neuman-Lee, L., Hanifin, C. T., French, S. S., Pfrender, M. E., Brodie, E. D., 3rd, & Brodie, E. D., Jr (2014). Confirmation and distribution of tetrodotoxin for the first time in terrestrial invertebrates: two terrestrial flatworm species (Bipalium adventitium and Bipalium kewense). PloS one, 9(6), e100718. doi.org/10.1371/journal.pone.0100718
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*Timestamps*
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0:44 Sea Monkey?
1:32 Sea-Monkeys
5:00 Brine Shrimp
8:59 Usage and Importance
*References*
sea-monkeys.com
Criel, G.R.J., Macrae, T.H. (2002). Artemia Morphology and Structure. In: Abatzopoulos, T.J., Beardmore, J.A., Clegg, J.S., Sorgeloos, P. (eds) Artemia: Basic and Applied Biology. Biology of Aquatic Organisms, vol 1. Springer, Dordrecht. doi.org/10.1007/978-94-017-0791-6_1
Gajardo, G. M., & Beardmore, J. A. (2012). The brine shrimp artemia: adapted to critical life conditions. Frontiers in physiology, 3, 185. doi.org/10.3389/fphys.2012.00185
Kara, M.H. & Amarouayache, M. (2012). Review of the biogeography of Artemia Leach 1819 (Crustacea: Anostraca) in Algeria. International Journal of Artemia Biology, 2(1): 40-50.
University of Utah. Brine Shrimp Life Cycle. https://learn.genetics.utah.edu/content/gsl/artemia/
Blizzard, T. A., Ruby, C. L., Mrozik, H., Preiser, F. A., & Fisher, M. H. (1989). Brine shrimp (Artemia salina) as a convenient bioassay for avermectin analogs. The Journal of antibiotics, 42(8), 1304–1307. doi.org/10.7164/antibiotics.42.1304
Lewan L, Andersson M, & Morales-Gomez P. (1992). The Use of Artemia Salina in Toxicity Testing. Alternatives to Laboratory Animals, 20(2): 297-301. doi.org/10.1177/026119299202000222
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0:47 Taxonomy and Discovery
3:53 Morphology
8:15 Lifestyle and Uncertainties
*References*
Grace, M. A., Doosey, M. H., Bart, H. L., & Naylor, G. J. P. (2015). First record of Mollisquama sp. (Chondrichthyes: Squaliformes: Dalatiidae) from the Gulf of Mexico, with a morphological comparison to the holotype description of Mollisquama parini Dolganov. Zootaxa, 3948(3). doi.org/10.11646/zootaxa.3948.3.10
Denton, J. S. S., Maisey, J. G., Grace, M., Pradel, A., Doosey, M. H., Bart, H. L., Jr, & Naylor, G. J. P. (2018). Cranial morphology in Mollisquama sp. (Squaliformes; Dalatiidae) and patterns of cranial evolution in dalatiid sharks. Journal of anatomy, 233(1), 15–32. doi.org/10.1111/joa.12823
Grace, M. A., Doosey, M. H., Denton, J. S. S., Naylor, G. J. P., Bart, H. L. J., & Maisey, J. G. (2019). A new Western North Atlantic Ocean kitefin shark (Squaliformes: Dalatiidae) from the Gulf of Mexico. Zootaxa, 4619(1), zootaxa.4619.1.4. doi.org/10.11646/zootaxa.4619.1.4
Kyne, P.M. & Herman, K. (2020). Mollisquama mississippiensis. The IUCN Red List of Threatened Species 2020: e.T153198442A153199019. dx.doi.org/10.2305/IUCN.UK.2020-3.RLTS.T153198442A153199019.en.
Kyne, P.M., Ebert, D.A., Concha, F. & Herman, K. (2020). Mollisquama parini. The IUCN Red List of Threatened Species 2020: e.T44515A124432387. dx.doi.org/10.2305/IUCN.UK.2020-3.RLTS.T44515A124432387.en.
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*Timestamps*
0:00 Opening Thought
0:44 Taxonomy and General Information
3:17 Morphology
4:41 Lifestyle and Behaviour
7:08 Pentastomiasis
9:29 Fossil Records
*References*
McAllister, C.T. (2024). Pentastomida: Endoparasitic Arthropods, in S. L. Gardner & S. A. Gardner, eds. Concepts in Animal Parasitology. Zea Books, Lincoln, Nebraska, United States. doi.org/10.32873/unl.dc.ciap059
Kelehear, C., Spratt, D. M., O'Meally, D., & Shine, R. (2013). Pentastomids of wild snakes in the Australian tropics. International journal for parasitology. Parasites and wildlife, 3(1), 20–31. doi.org/10.1016/j.ijppaw.2013.12.003
Wingstrand, K.G. (1972). Comparative spermatology of a pentastomid, Raillietiella hemidactyli, and a branchiuran crustacean, Argulus foliaceus, with a discussion of pentastomid relationships. Det Kongelige Danske Videnskabernes Selskab Biologiske Skrifter. 19(4):1-72.
Lavrov, D. V., Brown, W. M., & Boore, J. L. (2004). Phylogenetic position of the Pentastomida and (pan)crustacean relationships. Proceedings. Biological sciences, 271(1538), 537–544. doi.org/10.1098/rspb.2003.2631
Waloszek, D., Repetski, J. E., & Maas, A. (2005). A new Late Cambrian pentastomid and a review of the relationships of this parasitic group. Transactions of the Royal Society of Edinburgh: Earth Sciences, 96(2), 163–176. doi:10.1017/S0263593300001280
Almeida, W.O., Christoffersen, M. L., Amorim, D. S., & Eloy, E. C. C. (2008). Morphological support for the phylogenetic positioning of Pentastomida and related fossils. Biotemas. 21 (3): 81–90. doi:10.5007/2175-7925.2008v21n3p81
Raele, D. A., Petrella, A., Troiano, P., & Cafiero, M. A. (2022). Linguatula serrata (Fröhlich, 1789) in Gray Wolf (Canis lupus) from Italy: A Neglected Zoonotic Parasite. Pathogens, 11(12), 1523. doi.org/10.3390/pathogens11121523
Chen, S. H., Liu, Q., Zhang, Y. N., Chen, J. X., Li, H., Chen, Y., Steinmann, P., & Zhou, X. N. (2010). Multi-host model-based identification of Armillifer agkistrodontis (Pentastomida), a new zoonotic parasite from China. PLoS neglected tropical diseases, 4(4), e647. doi.org/10.1371/journal.pntd.0000647
Barton, D.P. & Shamsi, S. (2024). Diagnosis of Pentastome Infections and the Need for Increased Awareness Among Medical Practitioners and Diagnosticians in the Developed World. Curr Clin Micro Rpt 11, 79–87. doi.org/10.1007/s40588-024-00225-w
Tappe, D., & Büttner, D. W. (2009). Diagnosis of human visceral pentastomiasis. PLoS neglected tropical diseases, 3(2), e320. doi.org/10.1371/journal.pntd.0000320
Sulyok, M., Rózsa, L., Bodó, I., Tappe, D., & Hardi, R. (2014). Ocular pentastomiasis in the Democratic Republic of the Congo. PLoS neglected tropical diseases, 8(7), e3041. doi.org/10.1371/journal.pntd.0003041
Ioannou, P., & Vamvoukaki, R. (2019). Armillifer Infections in Humans: A Systematic Review. Tropical Medicine and Infectious Disease, 4(2), 80. doi.org/10.3390/tropicalmed4020080
Siveter, D. J., Briggs, D. E., Siveter, D. J., & Sutton, M. D. (2015). A 425-million-year-old silurian pentastomid parasitic on ostracods. Current biology : CB, 25(12), 1632–1637. doi.org/10.1016/j.cub.2015.04.035
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8:49 Fossil Records
*References*
Hévin, N.-C., Kergoat, G.J., Clamens, A.-L., Le Ru, B., Mansell, M.W. & Michel, B. (2023) Evolution, systematics and historical biogeography of Palparini and Palparidiini antlions (Neuroptera: Myrmeleontidae): Old origin and in situ diversification in Southern Africa. Systematic Entomology, 48(4), 600–617. Available from: doi.org/10.1111/syen.12593
Hayashi, T., Hayashi, K., Hayashi, N. et al. (2023). Optimal pit site selection in antlion larvae: the relationship between prey availability and pit maintenance costs. J Ethol 41, 59–72. doi.org/10.1007/s10164-022-00767-w
Badano, D., Engel, M.S., Basso, A. et al. (2018). Diverse Cretaceous larvae reveal the evolutionary and behavioural history of antlions and lacewings. Nat Commun 9, 3257. doi.org/10.1038/s41467-018-05484-y
Haug, C., Posada Zuluaga, V., Zippel, A., Braig, F., Müller, P., Gröhn, C., Weiterschan, T., Wunderlich, J., Haug, G. T., & Haug, J. T. (2022). The Morphological Diversity of Antlion Larvae and Their Closest Relatives over 100 Million Years. Insects, 13(7), 587. doi.org/10.3390/insects13070587
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0:25 Taxonomy and General Information
2:49 Morphology
5:30 Lifestyle and Behaviour
6:51 Speed, Power, Stamina
9:55 Domestication
11:55 Evolution
13:22 Mustang
14:16 Przewalski’s Horse
16:39 Hybrid
*References*
Barrón-Ortiz, C. I., Avilla, L.S., Jass, C.N., et al. (2019). What Is Equus? Reconciling Taxonomy and Phylogenetic Analyses. Front. Ecol. Evol, 7: 00343. doi.org/10.3389/fevo.2019.00343
Bernátková, A., Ceacero, F., Oyunsaikhan, G. et al. (2023). Novel observation of play behaviour between a harem holder and a bachelor group of Przewalski’s horses in the wild. acta ethol 26, 145–150. doi.org/10.1007/s10211-023-00421-9
Menard, C., Duncan, P., Fleurance, G., Georges, J-Y., & Lila, M. (2002). Comparative foraging and nutrition of horses and cattle in European wetlands. Journal of Applied Ecology, 39(1): 120-133. doi.org/10.1046/j.1365-2664.2002.00693.x
Taylor W. T. (2024). When Horse Became Steed: Archaeological and genetic discoveries topple long-standing ideas about the domestication of equines. Scientific American, 331(5), 22. doi.org/10.1038/scientificamerican122024-7qfHkaSxwWOJpTcwY2J0bg
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*Outro*
The Soundlings - Silent Night (Youtube Library)
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