-98.28333, 26.033333: 11 Treatments

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Glenognatha foxi     Jimmy Cabra-García & Antonio D. Brescovit, 2016, Revision and phylogenetic analysis of the orb-weaving spider genus Glenognatha Simon, 1887 (Araneae, Tetragnathidae), Zootaxa 4069 (1), pp. 1-183 : 109-116 109-116
Xylocopa (Neoxylocopa) griswoldi     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 : 35-39 35-39
Strumigenys boneti     Booher, Douglas B., 2021, The ant genus Strumigenys Smith, 1860 (Hymenoptera: Formicidae) in western North America North of Mexico, Zootaxa 5061 (2), pp. 201-248 : 222 222
Laemosaccus burkei   new species  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 : 920-923 920-923
Adetus croton   sp. nov.  Heffern, Daniel, Santos-Silva, Antonio & Botero, Juan Pablo, 2019, A new genus and two new species of Apomecynini, a new species of Desmiphorini and new records in Lamiinae and Disteniidae (Coleoptera), Zootaxa 4691 (5), pp. 561-574 : 565-570 565-570
Brachylinga cinerea     Webb, Donald W. & Metz, Mark A., 2006, A Revision of the New World Genera Brachylinga Irwin and Lyneborg and Lysilinga Irwin and Lyneborg (Diptera: Therevidae: Therevinae) with the Description of a New Genus, Elcaribe Webb, Zootaxa 1288 (1288), pp. 1-241 : 63-66 63-66
Lasioglossum (Dialictus) hudsoniellum     Gardner, Joel & Gibbs, Jason, 2020, The ‘ red-tailed’ Lasioglossum (Dialictus) (Hymenoptera: Halictidae) of the western Nearctic, European Journal of Taxonomy 725, pp. 1-242 : 90-99 90-99
Cirrospilus coachellae     Perry, Ryan K. & Heraty, John M., 2021, Read between the lineata: A revision of the tattooed wasps, Zagrammosoma Ashmead (Hymenoptera: Eulophidae), with descriptions of eleven new species, Zootaxa 4916 (1), pp. 1-108 : 103 103
Dolichophaonia Texensis     LÖWENBERG-NETO, PETER & DE CARVALHO, CLAUDIO J. B., 2013, Muscidae (Insecta: Diptera) of Latin America and the Caribbean: geographic distribution and check-list by country, Zootaxa 3650 (1), pp. 1-147 : 60 60
Blapstinus tibialis     Kamiński, Marcin Jan, Lumen, Ryan, Kanda, Kojun & Smith, Aaron Dennis, 2022, Phylogenetic status of some unique species representing Blapstinina Mulsant & Rey (Tenebrionidae: Blaptinae: Opatrini), and implications for continued study of the subtribe, Zootaxa 5093 (5), pp. 519-532 : 527-530 527-530
Xanthocomus concinnus   comb. nov.  Gimmel, Matthew L., 2011, Review of the species described in Leptostilbus Casey in North America (Coleoptera: Phalacridae: Xanthocomus Guillebeau), Insecta Mundi 2011 (188), pp. 1-8 : 6-7 6-7