-85.35027, 10.3133335: 12 Treatments

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Scybalocanthon moniliatus     Silva, Fernando A. B. & Valois, Marcely, 2019, A taxonomic revision of the genus Scybalocanthon Martínez, 1948 (Coleoptera Scarabaeidae: Scarabaeinae: Deltochilini), Zootaxa 4629 (3), pp. 301-341 : 327-328 327-328
Leptohyphes zalope     Baumgardner, D. E. & Mccafferty, W. P., 2010, Revision of the genus Leptohyphes Eaton (Ephemeroptera: Leptohyphidae) in North and Central America, Zootaxa 2360 (1), pp. 1-33 : 28-30 28-30
Xylocopa (Neoxylocopa) fimbriata     Mérida-Rivas, Jorge A., Hinojosa-Díaz, Ismael A., Ayala-Barajas, Ricardo, Pozo, Carmen & Vandame, Rémy, 2022, Revision of carpenter bees of the subgenus Neoxylocopa Michener (Hymenoptera: Apidae) from Mexico and Mesoamerica, Zootaxa 5158 (1), pp. 1-67 : 7-16 7-16
Roddenberryus kirk   gen. et sp. nov.  Sánchez-Ruiz, Alexander & Bonaldo, Alexandre B., 2023, Strange new spiders: on Roddenberryus, a new and unusual caponiid genus (Araneae, Caponiidae), European Journal of Taxonomy 891 (1), pp. 1-25 : 8-13 8-13
Leptohyphes mandibulus     Baumgardner, D. E. & Mccafferty, W. P., 2010, Revision of the genus Leptohyphes Eaton (Ephemeroptera: Leptohyphidae) in North and Central America, Zootaxa 2360 (1), pp. 1-33 : 16-19 16-19
Tricorythodes sordidus     Baumgardner, David E. & Ávila, Socorro, 2006, Cabecar serratus, a new genus and species of leptohyphid mayfly from Central America, and description of the imaginal stages of Tricorythodes sordidus Allen (Ephemeroptera: Leptohyphidae), Zootaxa 1187 (1), pp. 47-59 : 54-57 54-57
Lineostethus acuminatus   sp. nov.  Garbelotto, Thereza de Almeida, Kochenborger, Ana Paula Leite & Campos, Luiz Alexandre, 2018, Revision of Lineostethus (Heteroptera: Pentatomidae: Discocephalini), Zoologia (e 21232) 35, pp. 1-24 : 16-18 16-18
Laemosaccus texanus     Hespenheide, Henry A., 2019, A Review of the Genus Laemosaccus Schönherr, 1826 (Coleoptera: Curculionidae: Mesoptiliinae) from Baja California and America North of Mexico: Diversity and Mimicry, The Coleopterists Bulletin (MIMICRY AND LAEMOSACCUS In an earlier paper (Hespenheide 1996), I presented the hypothesis that species of Laemosaccus of the L. nephele group with red humeral spots on the elytra were Batesian mimics of members of the Chrysomelidae in the subfamily Clytrinae. There is no evidence that Laemosaccus species are distasteful, and what is either L. nephele and / or L. obrieni have been reported as prey items of birds (Beal 1912). In Cave Creek Canyon, Cochise County, Arizona, 21 forms (species and “ subspecies ”) of Clytrinae were hypothesized to be the primary models of 22 species of mimics in the families Anthribidae (one species), Bruchidae (two species), Buprestidae (four species), Chrysomelidae, subfamily Cryptocephalinae (three species), Coccinellidae (six species), Curculionidae, subfamily Baridinae (one species), and Laemosaccus (five species). Of these, the coccinellids and the cryptocephaline chrysomelids are probably distasteful Mullerian co-mimics. Ecologically, the species of Laemosaccus co-occurred with their clytrine models on both desert legumes and canyon oaks, although more clytrine species occurred in the desert and more Laemosaccus species occurred in the canyons. Species of clytrines showing the mimetic pattern are common throughout Mexico (Bellamy 2003, who renamed the Mexican buprestid genus Acherusia Laporte and Gory, 1837 as Mimicoclytrina Bellamy to reflect their resemblance to clytrines), but decline in numbers of species and in the proportion of the clytrine fauna through Central America to Panama (Hespenheide 1996, fig. 2). Laemosaccus seems to follow a similar pattern. Mimicry is more common in large faunas, especially in wet tropical areas (Hespenheide 1986, 1995); because the largest clytrine fauna is in Mexico, the clytrine mimicry complex is also larger there (Hespenheide 1996). This complex has more members than I first enumerated and deserves further study. The evolution of mimicry produces resemblances between unrelated species (Laemosaccus and other putative mimics, with clytrines and perhaps other Chrysomelidae and Coccinellidae as models; see Hespenheide 1976, 1996) and selects against the divergence of related species. In Batesian mimicry - hypothesized to be the form of relationship between Laemosaccus and clytrines - the selection for precision of mimicry is stronger on the mimic (Laemosaccus), so that resemblances among them should be closer, regardless of ancestry. Close morphological resemblances based on ecology rather than ancestry may be termed mimetic homoplasy (Hespenheide 2005) and can make recognition of species difficult (as in Laemosaccus) or complicate phylogenetic analyses. I have speculated (Hespenheide 1996) that the sympatric “ subspecies ” of the clytrine models (Moldenke 1970) may in fact be reproductively isolated sibling species. It will be interesting to see whether or not genomic studies show the closeness of relationships among Laemosaccus species that the morphology suggests) 73 (4), pp. 905-939 : 934 934
Azteca beltii     Longino, J. T., 2007, A taxonomic review of the genus Azteca (Hymenoptera: Formicidae) in Costa Rica and a global revision of the aurita group., Zootaxa 1491, pp. 1-63 : 21-22 21-22
Apiomerus pipil     Masonick, Paul & Weirauch, Christiane, 2022, Taxonomic revision of the Apiomerus maya species group (Heteroptera: Reduviidae: Harpactorinae), Zootaxa 5154 (5), pp. 537-556 : 549 549
Triepeolus mexicanus     Onuferko, Thomas M. & Rightmyer, Molly G., 2024, A revision of the simplex species group of the cleptoparasitic bee genus Triepeolus Robertson, 1901 (Hymenoptera: Apidae), European Journal of Taxonomy 950 (1), pp. 1-106 : 40-47 40-47
Cheiloneurus omorus   sp. nov.  Noyes, John Stuart, 2023, ENCYRTIDAE OF COSTA RICA (HYMENOPTERA: CHALCIDOIDEA), 4 Subfamily Encyrtinae: tribes Arrhenophagini, Habrolepidini, Cerapterocerini, Cheiloneurini, Trechnitini, Cercobelini, Polaszekiini, Protyndarichoidini, Gahaniellini and Syrphophagini (part), mainly primary parasitoids and hyperparasitoids of Coccoidea and Psylloidea (Hemiptera), Taxonomic Monographs on Neotropical Hymenoptera (Oxford, England) 2 (11), pp. 1-921 : 453-455 453-455