-109.2, 31.883333: 100 Treatments

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Hexurella apachea     Monjaraz-Ruedas, Rodrigo, Mendez, Raymond Wyatt & Hedin, Marshal, 2023, Species delimitation, biogeography, and natural history of dwarf funnel web spiders (Mygalomorphae, Hexurellidae, Hexurella) from the United States / Mexico borderlands, ZooKeys 1167, pp. 109-157 : 109 109
Paraleucopis nigra   sp. nov.  Wheeler, Terry A. & Sinclair, Bradley J., 2019, Systematics of Paraleucopis Malloch with proposal of Paraleucopidae, a new family of acalyptrate Diptera, Zootaxa 4668 (3), pp. 301-328 : 319-320 319-320
Crematogaster   SP. NOV.  Ward, Philip S. & Blaimer, Bonnie B., 2022, Taxonomy in the phylogenomic era: species boundaries and phylogenetic relationships among North American ants of the Crematogaster scutellaris group (Formicidae: Hymenoptera), Zoological Journal of the Linnean Society 194, pp. 893-937 : 927-928 927-928
Glenognatha emertoni     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 : 153-158 153-158
Carpophilus taylori   sp. nov.  Powell, Gareth S., 2020, Four New Species Of Carpophilus (Ecnomorphus) Motschulsky (Coleoptera: Nitidulidae: Carpophilinae) From The New World, The Coleopterists Bulletin 74 (1), pp. 175-180 : 179 179
Aneflomorpha linsleyae     Lingafelter, Steven W., 2022, Revision of Aneflomorpha Casey and Neaneflus Linsley (Coleoptera: Cerambycidae) of the United States with an illustrated key to species, Insecta Mundi 2022 (954), pp. 1-59 : 35 35
Ripersiella colombiensis     Schneider, Scott A. & LaPolla, John S., 2022, A Neotropical complex of Ripersiella species (Hemiptera, Coccomorpha, Rhizoecidae) collected from the nests of Acropyga ants (Hymenoptera, Formicidae), ZooKeys 1123, pp. 1-30 : 1 1
Zagrammosoma headricki   sp. nov.  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 : 54-57 54-57
Brachylinga pavida     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 : 104-108 104-108
Amiota hyalou   sp. nov.  Jones, Lance E. & Grimaldi, David A., 2022, Revision Of The Nearctic Species Of The Genus Amiota Loew (Diptera: Drosophilidae), Bulletin of the American Museum of Natural History 2022 (458), pp. 1-181 : 22-23 22-23
Amiota antitormentum   sp. nov.  Jones, Lance E. & Grimaldi, David A., 2022, Revision Of The Nearctic Species Of The Genus Amiota Loew (Diptera: Drosophilidae), Bulletin of the American Museum of Natural History 2022 (458), pp. 1-181 : 34-40 34-40
Lysilinga aurantiaca     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 : 208-210 208-210
Brachymelecta interrupta     Onuferko, Thomas M., Packer, Laurence & Genaro, Julio A., 2021, Brachymelecta Linsley, 1939, previously the rarest North American bee genus, was described from an aberrant specimen and is the senior synonym for Xeromelecta Linsley, 1939, European Journal of Taxonomy 754, pp. 1-51 : 30-33 30-33
Phylloicus mexicanus     PRATHER, AYSHA L., 2003, Revision of the Neotropical caddisfly genus Phylloicus (Trichoptera: Calamoceratidae), Zootaxa 275 (1), pp. 1-214 : 71-73 71-73
Amiota minor     Jones, Lance E. & Grimaldi, David A., 2022, Revision Of The Nearctic Species Of The Genus Amiota Loew (Diptera: Drosophilidae), Bulletin of the American Museum of Natural History 2022 (458), pp. 1-181 : 74-77 74-77
Lasioglossum (Dialictus) mesillense     Gardner, Joel & Gibbs, Jason, 2020, The ‘ red-tailed’ Lasioglossum (Dialictus) (Hymenoptera: Halictidae) of the western Nearctic, European Journal of Taxonomy 725, pp. 1-242 : 125-136 125-136
Roederiodes lawrencei   sp. nov.  Sinclair, Bradley J., 2023, Revision of New World species of Roederiodes Coquillett (Diptera: Empididae: Clinocerinae), Zootaxa 5301 (3), pp. 336-364 : 345-346 345-346
Amiota incurva   sp. nov.  Jones, Lance E. & Grimaldi, David A., 2022, Revision Of The Nearctic Species Of The Genus Amiota Loew (Diptera: Drosophilidae), Bulletin of the American Museum of Natural History 2022 (458), pp. 1-181 : 44-45 44-45
Roederiodes notialis   sp. nov.  Sinclair, Bradley J., 2023, Revision of New World species of Roederiodes Coquillett (Diptera: Empididae: Clinocerinae), Zootaxa 5301 (3), pp. 336-364 : 347 347
Scaralina aethrinsula   sp. nov.  Yanega, Douglas, Goemans, Geert, Dam, Matthew Van, Gómez-Marco, Francesc & Hoddle, Mark, 2024, Description of a new genus of North and Central American planthoppers (Hemiptera: Fulgoridae) with fourteen new species, Zootaxa 5443 (1), pp. 1-53 : 9-11 9-11
Lasioglossum (Dialictus) gaudiale     Gardner, Joel & Gibbs, Jason, 2023, Revision of the Nearctic species of the Lasioglossum (Dialictus) gemmatum species complex (Hymenoptera: Halictidae), European Journal of Taxonomy 858 (1), pp. 1-222 : 76-86 76-86
Lasioglossum (Dialictus) holzenthali   sp. nov.  Gardner, Joel & Gibbs, Jason, 2023, Revision of the Nearctic species of the Lasioglossum (Dialictus) gemmatum species complex (Hymenoptera: Halictidae), European Journal of Taxonomy 858 (1), pp. 1-222 : 100-108 100-108
Lasioglossum (Dialictus) eremum   sp. nov.  Gardner, Joel & Gibbs, Jason, 2023, Revision of the Nearctic species of the Lasioglossum (Dialictus) gemmatum species complex (Hymenoptera: Halictidae), European Journal of Taxonomy 858 (1), pp. 1-222 : 70-76 70-76
Trachymyrmex pomonae   new species  Rabeling, Ch., Cover, S. P., Johnson, R. A. & Mueller, U. G., 2007, A review of the North American species of the fungus-gardening ant genus Trachymyrmex (Hymenoptera: Formicidae)., Zootaxa 1664, pp. 1-53 : 14-16 14-16
Temnothorax pergandei     Prebus, Matthew M., 2021, Taxonomic revision of the Temnothorax salvini clade (Hymenoptera: Formicidae), with a key to the clades of New World Temnothorax, PeerJ (e 11514) 9, pp. 1-462 : 240-253 240-253
Orchestomerus whiteheadi     Yoshitake, Hiraku & Anderson, Robert S., 2015, A Review Of The Genus Orchestomerus Dietz (Coleoptera: Curculionidae: Ceutorhynchinae: Cnemogonini) Of The Usa, The Coleopterists Bulletin 69 (4), pp. 565-578 : 575-576 575-576
Ooencyrtus californicus     Triapitsyn, Serguei V., Rugman-Jones, Paul F. & Perring, Thomas M., 2021, Re-collection and identity of Ooencyrtus californicus (Hymenoptera: Encyrtidae) and its new synonym, Ooencyrtus lucidus, Zootaxa 4966 (1), pp. 97-100 : 98-100 98-100
Arsapnia decepta     Baumann, Richard W. & Stark, Bill P., 2017, Variation In The Epiproct Of Arsapnia Decepta Banks, 1897 (Plecoptera: Capniidae), With Comments On Arsapnia Coyote (Nelson & Baumann 1987), Illiesia 13 (1), pp. 1-21 : 2-17 2-17
Eulechriops hovorei   sp. nov.  Barman, E. H., Michat, M. C., Alarie, Y. & Wolfe, G. W., 2007, Figs. 16 – 17. 16 in A Description of the First Instar of Hoperius planatus Fall, 1927 (Coleoptera: Dytiscidae: Colymbetinae: Colymbetini), with Phylogenetic Implications, The Coleopterists Bulletin 61 (2), pp. 283-286 : 283-286 283-286
Dipropus reinae   sp. nov.  Johnson, Paul J., 2016, Five new species of Dipropus Germar (Coleoptera: Elateridae) from west-central North America, and a lectotype designation for Elater soleatus Say, Insecta Mundi 2016 (523), pp. 1-27 : 5-6 5-6
Nallachius pulchellus     Bowles, David E., Contreras-Ramos, A, Mariza & Ferro, Michael L., 2015, New distributional records for pleasing lacewings (Neuroptera: Dilaridae, Nallachius spp.) in the Americas, Insecta Mundi 2015 (406), pp. 1-10 : 4-6 4-6
Dipropus yaqui   sp. nov.  Johnson, Paul J., 2016, Five new species of Dipropus Germar (Coleoptera: Elateridae) from west-central North America, and a lectotype designation for Elater soleatus Say, Insecta Mundi 2016 (523), pp. 1-27 : 9-11 9-11
Cyrtopeltocoris huachucae     Wyniger, Denise, Schuh, Randall T. & Henry, Thomas J., 2023, Revision of the North American Hallodapini (Insecta: Hemiptera: Heteroptera: Miridae: Phylinae), American Museum Novitates 2023 (3994), pp. 1-48 : 29-30 29-30
Laemosaccus andersoni   sp. nov.  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 : 916-917 916-917
Lymantes obrieni   sp. nov.  Anderson, Robert S., 2016, A Taxonomic Revision of the GenusLymantesSchönherr, 1838 (Coleoptera: Curculionidae: Molytinae: Lymantini) in the United States Ofamerica, The Coleopterists Bulletin 70 (1), pp. 111-124 : 111-124 111-124
Coniopteryx fitchi     Ferro, Michael L., 2018, New state records for Coniopterygidae (Neuroptera) with an updated list of species in North America north of Mexico, Insecta Mundi 668, pp. 1-20 : 7 7
Pachybrachis gilberti   sp. nov.  Barney, Robert J., 2019, Definition and Revision of the Pubescens Species-Group of North American Pachybrachis Chevrolat (Coleoptera: Chrysomelidae: Cryptocephalinae), Including Descriptions of Three New Species, The Coleopterists Bulletin 73 (4), pp. 1017-1048 : 1037-1041 1037-1041
Strumigenys chiricahua     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 : 223-224 223-224
Coniopteryx     Ferro, Michael L., 2018, New state records for Coniopterygidae (Neuroptera) with an updated list of species in North America north of Mexico, Insecta Mundi 668, pp. 1-20 : 9-10 9-10
Syscia madrensis   sp. nov.  Longino, John T. & Branstetter, Michael G., 2021, Integrating UCE Phylogenomics With Traditional Taxonomy Reveals a Trove of New World Syscia Species (Formicidae: Dorylinae), Insect Systematics and Diversity 5 (2), No. 2, pp. 1-51 : 28 28
Acmaeodera amplicollis     Westcott, Richard L. & Raschko, Mike, 2018, New plant associations for adults of some species of Acmaeodera Eschscholtz (Coleoptera: Buprestidae) occurring in the western United States, Insecta Mundi 644, pp. 1-3 : 2 2
Microctonus portalensis   sp. nov.  Pucci, Thomas M., 2013, Contributions to the classification of North American Microctonus (Braconidae, Euphorinae), Zootaxa 3725 (1), pp. 1-150 : 21-22 21-22
Strumigenys arizonica     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 bimaculatus   sp. nov.  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 : 918-920 918-920
Agrilus paraimpexus   sp. nov.  Hespenheide, Henry A., 2007, The identity of Agrilus impexus Horn, a new species, and taxonomic notes and records for other Agrilus Curtis species (Coleoptera: Buprestidae), Zootaxa 1617 (1), pp. 57-66 : 59-63 59-63
Laemosaccus arizonensis   sp. nov.  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 : 917-918 917-918
Eucelatoria sabroskyi   sp. nov.  Burington, Zelia L., 2022, A taxonomic revision of the Eucelatoria ferox species group (Diptera: Tachinidae), Zootaxa 5143 (1), pp. 1-104 : 38-40 38-40
Scaralina metcalfi   sp. nov.  Yanega, Douglas, Goemans, Geert, Dam, Matthew Van, Gómez-Marco, Francesc & Hoddle, Mark, 2024, Description of a new genus of North and Central American planthoppers (Hemiptera: Fulgoridae) with fourteen new species, Zootaxa 5443 (1), pp. 1-53 : 26-32 26-32
Aneflomorpha cazieri     Lingafelter, Steven W., 2022, Revision of Aneflomorpha Casey and Neaneflus Linsley (Coleoptera: Cerambycidae) of the United States with an illustrated key to species, Insecta Mundi 2022 (954), pp. 1-59 : 28-29 28-29
Dolopomyrmex pilatus   new species  Cover, S. P. & Deyrup, M., 2007, A new ant genus from the southwestern United States., Advances in ant systematics (Hymenoptera: Formicidae): Homage to E. O. Wilson - 50 years of contributions. (Memoirs of the American Entomological Institute 80), pp. 89-99 : 92-94 92-94
Laemosaccus howdenae   sp. nov.  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 : 927-928 927-928
Lasioglossum (Dialictus) clavicorne   sp. nov.  Gardner, Joel & Gibbs, Jason, 2020, The ‘ red-tailed’ Lasioglossum (Dialictus) (Hymenoptera: Halictidae) of the western Nearctic, European Journal of Taxonomy 725, pp. 1-242 : 53-58 53-58
Bothronotoxenus tishechkini   sp. nov.  Eldredge, K. Taro, 2011, Bothronotoxenus Eldredge, A New Genus Of Aleocharinae (Coleoptera: Staphylinidae) From Arizona, U. S. A., The Coleopterists Bulletin 65 (4), pp. 381-386 : 383-384 383-384
Lasioglossum (Dialictus) deludens   sp. nov.  Gardner, Joel & Gibbs, Jason, 2023, Revision of the Nearctic species of the Lasioglossum (Dialictus) gemmatum species complex (Hymenoptera: Halictidae), European Journal of Taxonomy 858 (1), pp. 1-222 : 32-52 32-52
Lasioglossum (Dialictus) clematisellum     Gardner, Joel & Gibbs, Jason, 2020, The ‘ red-tailed’ Lasioglossum (Dialictus) (Hymenoptera: Halictidae) of the western Nearctic, European Journal of Taxonomy 725, pp. 1-242 : 58-69 58-69
Saropogon bryanti     Alberts, Charlotte H. E. & Fisher, Eric M., 2022, A new species of Saropogon Loew, 1847 (Diptera, Asilidae) from Arizona, with a review of the Nearctic species north of Mexico, ZooKeys 1130, pp. 1-63 : 1 1
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
Knightopsallus   gen. nov.  Schuh, Randall T., 2006, Revision, Phylogenetic, Biogeographic, And Host Analyses Of The Endemic Western North American Phymatopsallus Group, With The Description Of 9 New Genera And 15 New Species (Insecta: Hemiptera: Miridae: Phylinae), Bulletin of the American Museum of Natural History 2006 (301), pp. 1-115 : 68-71 68-71
Vaejovis cashi   sp. nov.  Graham, Matthew R., 2007, Sky island Vaejovis: two new species and a redescription of V. vorhiesi Stahnke (Scorpiones: Vaejovidae), Euscorpius 51 (51), pp. 1-14 : 6-9 6-9
Syzeton arizonae   sp. nov.  Gompel, Nicolas, 2022, The genus Syzeton Blackburn, 1891 (Coleoptera, Aderidae) in the United States of America, Zootaxa 5162 (3), pp. 243-267 : 258 258
Hemicrepidius montanus     Etzler, Frank E., 2020, A Revision of the Genus Hemicrepidius Germar, 1839 (Coleoptera: Elateridae) of the New World, with Comments on Global Classification, The Coleopterists Bulletin (mo 18) 74, pp. 1-126 : 63-64 63-64
Eutrichosoma mirabile     Baker, Austin J. & Heraty, John M., 2020, Larval morphology and life history of Eutrichosoma mirabile Ashmead and description of a new species of Eutrichosoma (Hymenoptera, Chalcidoidea), Journal of Hymenoptera Research 75, pp. 67-85 : 67 67
Panthea greyi   sp. nov.  Anweiler, Gary G., 2009, Revision of the New World Panthea Hübner (Lepidoptera, Noctuidae) with descriptions of 5 new species and 2 new subspecies, ZooKeys 9 (9), pp. 97-134 : 115-117 115-117
Laemosaccus vaurieae   sp. nov.  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 : 931 931
Tricholita ferrisi   sp. nov.  Crabo, Lars & Lafontaine, Donald, 2009, A Revision of Lasionycta Aurivillius (Lepidoptera: Noctuidae) for North America and notes on Eurasian species, with descriptions of 17 new species, 6 new subspecies, a new genus, and two new species of Tricholita Grote, ZooKeys 30 (30), pp. 1-156 : 102-104 102-104
Hemicrepidius soccifer     Etzler, Frank E., 2020, A Revision of the Genus Hemicrepidius Germar, 1839 (Coleoptera: Elateridae) of the New World, with Comments on Global Classification, The Coleopterists Bulletin (mo 18) 74, pp. 1-126 : 81-83 81-83
Parasemidalis fuscipennis     Ferro, Michael L., 2018, New state records for Coniopterygidae (Neuroptera) with an updated list of species in North America north of Mexico, Insecta Mundi 668, pp. 1-20 : 11 11
Hydraena (Hydraenopsis) arizonica     Perkins, Philip D., 2023, New Neotropical and Nearctic species of water beetles in the genera Hydraena Kugelann and Ochthebius Leach, a key to North American genera and subgenera of the family, new distribution records, and a synopsis of ecology, behavior and morphology related to aquatic life (Coleoptera: Hydraenidae), Zootaxa 5367 (1), pp. 1-86 : 64 64
Dasysyrphus creper     Locke, Michelle M. & Skevington, Jeffrey H., 2013, Revision of Nearctic <i> Dasysyrphus </ i> Enderlein (Diptera: Syrphidae), Zootaxa 3660 (1), pp. 1-80 : 32-34 32-34
Neuroptera     Lonsdale, Owen & Locke, Michelle M., 2018, Name-bearing type specimens in the Canadian National Collection of Insects, Arachnids & Nematodes (CNC): Blattodea, Dermaptera, Notoptera, Mecoptera, Megaloptera, Myriapoda, Neuroptera, Odonata, Orthoptera, Phthiraptera, Pseudoscorpiones, Psocoptera, Raphidioptera & Siphonaptera, Zootaxa 4526 (2), pp. 101-126 : 108-110 108-110
Brachymelecta californica     Onuferko, Thomas M., Packer, Laurence & Genaro, Julio A., 2021, Brachymelecta Linsley, 1939, previously the rarest North American bee genus, was described from an aberrant specimen and is the senior synonym for Xeromelecta Linsley, 1939, European Journal of Taxonomy 754, pp. 1-51 : 13-23 13-23
Leiobunum silum   sp. nov.  Shultz, Jeffrey W., 2018, A new species of Leiobunum from Arizona, U. S. A. highlights the limits of typological classification in harvestmen (Opiliones: Sclerosomatidae: Leiobuninae), Zootaxa 4370 (1), pp. 67-75 : 69-74 69-74
Charadra oligarchia     Schmidt, Christian & Anweiler, Gary, 2010, The North American species of Charadra Walker, with a revision of the Charadra pata (Druce) group (Noctuidae, Pantheinae), ZooKeys 39 (39), pp. 161-181 : 166-172 166-172
Ptilothrix chiricahua   sp. nov.  Florez-Gomez, Nathalia & Danforth, Bryan, 2023, The North American bees of the genus Ptilothrix Cresson, 1878 (Hymenoptera, Apidae, Emphorini), with the description of two new species, Journal of Hymenoptera Research 95, pp. 275-293 : 275 275
Paramyia nigritarsi   sp. nov.  Levesque-Beaudin, Valerie & Mlynarek, Julia J., 2020, Revision of Nearctic Paramyia Williston (Diptera: Milichiidae), Zootaxa 4732 (1), pp. 1-56 : 24-27 24-27
Pseudomarimatha flava   sp. nov.  Ferris, Clifford & Lafontaine, Donald, 2010, Review of the North American species of Marimatha Walker with descriptions of three new species (Lepidoptera, Noctuidae, Eustrotiinae) and the description of Pseudomarimatha flava (Noctuinae, Elaphriini), a new genus and species confused with Marimatha, ZooKeys 39 (39), pp. 117-135 : 133-134 133-134
Agrostis scabra     Vigosa-Mercado, J. Luis, Delgado-Salinas, Alfonso, Alvarado Cardenas, Leonardo O. & Eguiarte, Luis E., 2023, Revision of the genus Agrostis (Poaceae, Pooideae, Poeae) in Megamexico, PhytoKeys 230, pp. 157-256 : 157 157
Marimatha squala   sp. nov.  Ferris, Clifford & Lafontaine, Donald, 2010, Review of the North American species of Marimatha Walker with descriptions of three new species (Lepidoptera, Noctuidae, Eustrotiinae) and the description of Pseudomarimatha flava (Noctuinae, Elaphriini), a new genus and species confused with Marimatha, ZooKeys 39 (39), pp. 117-135 : 124-126 124-126
Acmaeodera scalaris     Westcott, Richard L. & Raschko, Mike, 2018, New plant associations for adults of some species of Acmaeodera Eschscholtz (Coleoptera: Buprestidae) occurring in the western United States, Insecta Mundi 644, pp. 1-3 : 3 3
Ectrichodiinae     Clem, C. Scott, Swanson, Daniel R. & Ray, Charles H., 2019, The Reduviidae (Hemiptera: Heteroptera) of Alabama, with a morphological key to species, Zootaxa 4688 (2), pp. 151-198 : 173 173
Helina lasiosterna     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 : 64 64
Lasioglossum (Dialictus) julipile   sp. nov.  Gardner, Joel & Gibbs, Jason, 2020, The ‘ red-tailed’ Lasioglossum (Dialictus) (Hymenoptera: Halictidae) of the western Nearctic, European Journal of Taxonomy 725, pp. 1-242 : 105-111 105-111
Lasioglossum (Dialictus) indagator   sp. nov.  Gardner, Joel & Gibbs, Jason, 2023, Revision of the Nearctic species of the Lasioglossum (Dialictus) gemmatum species complex (Hymenoptera: Halictidae), European Journal of Taxonomy 858 (1), pp. 1-222 : 109-115 109-115
Invreiella manleyi   sp. nov.  Waldren, George C., Williams, Kevin A., Cambra, Roberto A. & Pitts, James P., 2020, Systematic revision of the North American velvet ant genus Invreiella Suárez (Hymenoptera: Mutillidae) with description of eleven new species, Zootaxa 4894 (2), pp. 151-205 : 185-186 185-186
Semidalis     Ferro, Michael L., 2018, New state records for Coniopterygidae (Neuroptera) with an updated list of species in North America north of Mexico, Insecta Mundi 668, pp. 1-20 : 12-14 12-14
Agrostis exarata     Vigosa-Mercado, J. Luis, Delgado-Salinas, Alfonso, Alvarado Cardenas, Leonardo O. & Eguiarte, Luis E., 2023, Revision of the genus Agrostis (Poaceae, Pooideae, Poeae) in Megamexico, PhytoKeys 230, pp. 157-256 : 157 157
Lasioglossum (Dialictus) lilianae   sp. nov.  Gardner, Joel & Gibbs, Jason, 2020, The ‘ red-tailed’ Lasioglossum (Dialictus) (Hymenoptera: Halictidae) of the western Nearctic, European Journal of Taxonomy 725, pp. 1-242 : 118-125 118-125
Euarestoides acutangulus     Savaris, Marcoandre, Norrbom, Allen L., Marinoni, Luciane & Lampert, Silvana, 2019, Revision of the genus Euarestoides Benjamin (Diptera: Tephritidae), Zootaxa 4551 (3), pp. 299-329 : 305-307 305-307
Aneflomorpha paralinearis   sp. nov.  Lingafelter, Steven W., 2022, Revision of Aneflomorpha Casey and Neaneflus Linsley (Coleoptera: Cerambycidae) of the United States with an illustrated key to species, Insecta Mundi 2022 (954), pp. 1-59 : 21-24 21-24
Phlegyas annulicrus     Leavengood, John M. Jr., 2020, On the distribution of Phlegyas Stål (Hemiptera: Heteroptera: Pachygronthidae), Insecta Mundi 758, pp. 1-4 : 2 2
Lasioglossum (Dialictus) profundum   sp. nov.  Gardner, Joel & Gibbs, Jason, 2023, Revision of the Nearctic species of the Lasioglossum (Dialictus) gemmatum species complex (Hymenoptera: Halictidae), European Journal of Taxonomy 858 (1), pp. 1-222 : 134-142 134-142
Invreiella cephalargia   comb. nov.  Waldren, George C., Williams, Kevin A., Cambra, Roberto A. & Pitts, James P., 2020, Systematic revision of the North American velvet ant genus Invreiella Suárez (Hymenoptera: Mutillidae) with description of eleven new species, Zootaxa 4894 (2), pp. 151-205 : 182-184 182-184
Notiosorex cockrumi     Russell A. Mittermeier & Don E. Wilson, 2018, Soricidae, Handbook of the Mammals of the World – Volume 8 Insectivores, Sloths and Colugos, Barcelona: Lynx Edicions, pp. 332-551 : 448-449 448-449
Lasioglossum (Dialictus) pallidellum     Gardner, Joel & Gibbs, Jason, 2020, The ‘ red-tailed’ Lasioglossum (Dialictus) (Hymenoptera: Halictidae) of the western Nearctic, European Journal of Taxonomy 725, pp. 1-242 : 155-161 155-161
Agrostis elliottiana     Vigosa-Mercado, J. Luis, Delgado-Salinas, Alfonso, Alvarado Cardenas, Leonardo O. & Eguiarte, Luis E., 2023, Revision of the genus Agrostis (Poaceae, Pooideae, Poeae) in Megamexico, PhytoKeys 230, pp. 157-256 : 157 157
Lasioglossum (Dialictus) minckleyi   sp. nov.  Gardner, Joel & Gibbs, Jason, 2020, The ‘ red-tailed’ Lasioglossum (Dialictus) (Hymenoptera: Halictidae) of the western Nearctic, European Journal of Taxonomy 725, pp. 1-242 : 148-154 148-154
Anelaphus piceus     Lingafelter, Steven W., 2020, Review of species of Anelaphus Linsley and its new synonym Gymnopsyra Linsley from the United States and Canada with description of a new species, synonymies, distributional notes and an illustrated identification key (Coleoptera: Cerambycidae: Elaphidiini), Insecta Mundi 2020 (798), pp. 1-30 : 12-13 12-13
Lasioglossum (Dialictus) eophilus     Gardner, Joel & Gibbs, Jason, 2020, The ‘ red-tailed’ Lasioglossum (Dialictus) (Hymenoptera: Halictidae) of the western Nearctic, European Journal of Taxonomy 725, pp. 1-242 : 78-81 78-81
Lasioglossum (Dialictus) semicaeruleum     Gibbs, Jason, 2010, Revision of the metallic species of Lasioglossum (Dialictus) in Canada (Hymenoptera, Halictidae, Halictini) 2591, Zootaxa 2591 (1), pp. 1-382 : 298-301 298-301
Lasioglossum (Dialictus) pseudotegulare     Gardner, Joel & Gibbs, Jason, 2023, Revision of the Nearctic species of the Lasioglossum (Dialictus) gemmatum species complex (Hymenoptera: Halictidae), European Journal of Taxonomy 858 (1), pp. 1-222 : 143-150 143-150

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