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Ripersiella colombiensis
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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
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1 |
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Aphonopelma jacobii
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sp. nov.
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Hamilton, Chris A., Hendrixson, Brent E. & Silvestre Bringas, Karina, 2024, Discovery of a new tarantula species from the Madrean Sky Islands and the first documented instance of syntopy between two montane endemics (Araneae, Theraphosidae, Aphonopelma): a case of prior mistaken identity, ZooKeys 1210, pp. 61-98
: 61-98
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61-98 |
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Aneflomorpha linsleyae
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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
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35 |
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Dipropus reinae
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sp. nov.
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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
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5-6 |
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Strumigenys arizonica
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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
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222 |
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Laemosaccus bimaculatus
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sp. nov.
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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
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918-920 |
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Scatophila pulchra
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|
|
Zatwarnicki, Tadeusz & Mathis, Wayne N., 2024, Revision of the Nearctic Species of the Shore-Fly Genus Scatophila Becker (Diptera: Ephydridae), Zootaxa 5487 (1), pp. 1-100
: 91-94
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91-94 |
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Scatophila hesperia
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|
|
Zatwarnicki, Tadeusz & Mathis, Wayne N., 2024, Revision of the Nearctic Species of the Shore-Fly Genus Scatophila Becker (Diptera: Ephydridae), Zootaxa 5487 (1), pp. 1-100
: 32-35
|
32-35 |
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Triepeolus kathrynae
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|
|
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
: 34-40
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34-40 |
|
Ooencyrtus californicus
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|
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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 |
|
Triepeolus segregatus
|
|
|
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
: 75-87
|
75-87 |
|
Scatophila viridella
|
|
|
Zatwarnicki, Tadeusz & Mathis, Wayne N., 2024, Revision of the Nearctic Species of the Shore-Fly Genus Scatophila Becker (Diptera: Ephydridae), Zootaxa 5487 (1), pp. 1-100
: 45-49
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45-49 |
