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117 results for “misidentifications”
Distribution. Philippines (S Luzon, Catanduanes, Panay, Samar, Leyte, Negros, and Mindanao Is), Peninsular Malaysia, CW Sumatra, N & NW Borneo, Sulawesi, New Guinea and the Bismarck Archipelago (New Ireland and New Britain Is). A record from Java is erroneous, and a record from Bangka I does not appear to be authentic. Previous records from India (Sikkim) and C & E Nepal are misidentifications, now attributable to Joftre's Pipistrelle (Hypsugo joffrer). in Vespertilionidae
Distribution. Philippines (S Luzon, Catanduanes, Panay, Samar, Leyte, Negros, and Mindanao Is), Peninsular Malaysia, CW Sumatra, N & NW Borneo, Sulawesi, New Guinea and the Bismarck Archipelago (New Ireland and New Britain Is). A record from Java is erroneous, and a record from Bangka I does not appear to be authentic. Previous records from India (Sikkim) and C & E Nepal are misidentifications, now attributable to Joftre's Pipistrelle (Hypsugo joffrer).
Subspecies and Distribution. R.m.muscatellumThomas,1903—EArabianPeninsulaatAl-HajarMts(EUnitedArabEmiratesandNEOman). R. m. secanum Thomas, 1913 — W & S Iran, S Afghanistan, and S Pakistan, up to 34° N; perhapsalso India, but records from Genji in Rajasthan and Gingee in Tamil Nadu are doubtful (suspected misidentification). in Rhinopomatidae
Subspecies and Distribution. R.m.muscatellumThomas,1903—EArabianPeninsulaatAl-HajarMts(EUnitedArabEmiratesandNEOman). R. m. secanum Thomas, 1913 — W & S Iran, S Afghanistan, and S Pakistan, up to 34° N; perhapsalso India, but records from Genji in Rajasthan and Gingee in Tamil Nadu are doubtful (suspected misidentification).
Subspecies and Distribution. A.p.phaeotisG.S.Miller,1902—E&SEMexico(fromVeracruztoYucatanPeninsula),NGuatemala,Belize,Honduras,ENicaragua,ECostaRica,PanamaandWColombia. A.p.nanusK.Andersen,1906—W&SWMexico(fromSinaloatoOaxaca). A. p. palatinus W. B. Davis, 1970 — S Mexico (SW Chiapas), S Guatemala, W El Salvador, W Nicaragua, and W Costa Rica. Records from W Ecuador and N Peru are unverified; they could represent the Little Fruit-eating Bat (A. ravus), which was thought to be part of this taxon. Those from Venezuela, N Brazil, and Guyana probably represent misidentifications. in Phyllostomidae
Subspecies and Distribution. A.p.phaeotisG.S.Miller,1902—E&SEMexico(fromVeracruztoYucatanPeninsula),NGuatemala,Belize,Honduras,ENicaragua,ECostaRica,PanamaandWColombia. A.p.nanusK.Andersen,1906—W&SWMexico(fromSinaloatoOaxaca). A. p. palatinus W. B. Davis, 1970 — S Mexico (SW Chiapas), S Guatemala, W El Salvador, W Nicaragua, and W Costa Rica. Records from W Ecuador and N Peru are unverified; they could represent the Little Fruit-eating Bat (A. ravus), which was thought to be part of this taxon. Those from Venezuela, N Brazil, and Guyana probably represent misidentifications.
Distribution. Central America from Honduras to Panama and along coasts of W Colombia and NW Ecuador. In the literature, there have been two isolated records in the Amazonian Basin, including one in SE Peru, and one in Brazil that probably are misidentifications. in Phyllostomidae
Distribution. Central America from Honduras to Panama and along coasts of W Colombia and NW Ecuador. In the literature, there have been two isolated records in the Amazonian Basin, including one in SE Peru, and one in Brazil that probably are misidentifications.
Distribution. NE Brazil, at E border of semiarid Caatinga ecoregion ("sertao") and Caatinga—Atlantic Forest ecotone ("agreste") of Alagoas, Sergipe, and Bahia states. Previous records outside this area could be misidentifications. in Phyllostomidae
Distribution. NE Brazil, at E border of semiarid Caatinga ecoregion ("sertao") and Caatinga—Atlantic Forest ecotone ("agreste") of Alagoas, Sergipe, and Bahia states. Previous records outside this area could be misidentifications.
Subspecies and Distribution. C.h.hoffmanniPeters,1858—fromSHondurasSEtoNW&NColombia,WoftheAndes. C.h.agustinusJ.A.Allen,1913—fromNWVenezuelaSthroughCColombiatoNEcuador. C.h.capitalisJ.A.Allen,1913—SWColombiaandWEcuador. C.h.juruanusLLonnberg,1942—SWBrazilianAmazon(AmazonasandAcrestates),SEPeru,andNBolivia. C.h.pallescensLLonnberg,1928—extremeSColombia(PutumayoDepartment),EEcuador,andEPeru.DistributionofHoffmann'sTwo-toedSlothinBrazilisunclear,andfurthersurveysareneeded.TherearetwodoubtfuloutlyingrecordsfromnorthernMatoGrossoState,Brazil.TheselocalitiesarenearorwithindistributionofLinnaeus'sTwo-toedSloth(C.h. didactylus), suggesting possible misidentification. in Megalonychidae
Subspecies and Distribution. C.h.hoffmanniPeters,1858—fromSHondurasSEtoNW&NColombia,WoftheAndes. C.h.agustinusJ.A.Allen,1913—fromNWVenezuelaSthroughCColombiatoNEcuador. C.h.capitalisJ.A.Allen,1913—SWColombiaandWEcuador. C.h.juruanusLLonnberg,1942—SWBrazilianAmazon(AmazonasandAcrestates),SEPeru,andNBolivia. C.h.pallescensLLonnberg,1928—extremeSColombia(PutumayoDepartment),EEcuador,andEPeru.DistributionofHoffmann'sTwo-toedSlothinBrazilisunclear,andfurthersurveysareneeded.TherearetwodoubtfuloutlyingrecordsfromnorthernMatoGrossoState,Brazil.TheselocalitiesarenearorwithindistributionofLinnaeus'sTwo-toedSloth(C.h. didactylus), suggesting possible misidentification.
Subspecies and Distribution. D.p.pannietensisDeVis,1905—D'Entre-casteauxIs(Goodenough,Fergusson,andNormanby)andLouisiadeArchi-pelago(Misima,Panaeati,Rossel,andVanatinaiIs). D. p. remota Cabrera, 1920 — Trobriand Is (Kiriwina) and Woodlark Is. A record attributed to Bougainville I is a misidentification of the Solomons Nakedbacked Fruit Bat (D. inermas). in Pteropodidae
Subspecies and Distribution. D.p.pannietensisDeVis,1905—D'Entre-casteauxIs(Goodenough,Fergusson,andNormanby)andLouisiadeArchi-pelago(Misima,Panaeati,Rossel,andVanatinaiIs). D. p. remota Cabrera, 1920 — Trobriand Is (Kiriwina) and Woodlark Is. A record attributed to Bougainville I is a misidentification of the Solomons Nakedbacked Fruit Bat (D. inermas).
Distribution. Mt Kenya, Aberdare Range, and Cherangani Hills in WC Kenya, and apparently recorded throughout much of the mountainous regions of Ethiopia (although these specimens need to be further investigated for misidentification). in Soricidae
Distribution. Mt Kenya, Aberdare Range, and Cherangani Hills in WC Kenya, and apparently recorded throughout much of the mountainous regions of Ethiopia (although these specimens need to be further investigated for misidentification).
Distribution. SE Kenya and NE Tanzania, as well as a disjunct record from NW Kenya, although this specimen needs to be further examined for misidentification. in Soricidae
Distribution. SE Kenya and NE Tanzania, as well as a disjunct record from NW Kenya, although this specimen needs to be further examined for misidentification.
Distribution. SE Cameroon, SW Central African Republic, N DR Congo (N of the Congo River, from Ubangi River to the Ituri Forest and the Semliki River), NE Gabon (E of the Ivindo River), and the N of the Republic of Congo (across the Sangha River). A single record from Equatorial Guinea was possibly a misidentification. in Cercopithecidae
Distribution. SE Cameroon, SW Central African Republic, N DR Congo (N of the Congo River, from Ubangi River to the Ituri Forest and the Semliki River), NE Gabon (E of the Ivindo River), and the N of the Republic of Congo (across the Sangha River). A single record from Equatorial Guinea was possibly a misidentification.
Distribution. EC China (25-33° N, 102° 30°-119° 30" E) in E Xizang Autonomous Region (= Tibet), Sichuan, S Gansu, S Shaanxi, Hubei, Anhui, Zhejiang, N Yunnan, Guizhou, Jiangxi, Fujian, N Guangxi, and N Guangdong provinces; W limit in the Yangtze Gorge in W & NW Sichuan and S limit at 23° 48' N, ¢.110° E in Guangxi. The species may range into NE India (Arunachal Pradesh, Assam, and Meghalaya states), although these reports appear to be based on misidentifications. in Cercopithecidae
Distribution. EC China (25-33° N, 102° 30°-119° 30" E) in E Xizang Autonomous Region (= Tibet), Sichuan, S Gansu, S Shaanxi, Hubei, Anhui, Zhejiang, N Yunnan, Guizhou, Jiangxi, Fujian, N Guangxi, and N Guangdong provinces; W limit in the Yangtze Gorge in W & NW Sichuan and S limit at 23° 48' N, ¢.110° E in Guangxi. The species may range into NE India (Arunachal Pradesh, Assam, and Meghalaya states), although these reports appear to be based on misidentifications.
FIGURE 1. Acusilas coccineus Simon, 1895. A in Phonognatha vicitra Sherriffs, 1928 - a taxonomic misidentification of the orb-weaving spider Acusilas coccineus Simon, 1895 (Araneae, Araneidae)
FIGURE 1. Acusilas coccineus Simon, 1895. A, Female guarding spiderlings from Ponmudi, retrolateral. B, Same (after preservation), dorsal. C, Male (after preservation) from Ponmudi, dorsal. D, Female (after preservation) from Charlotte estate/division, dorsal. E, Vulva showing mating plugs (arrows), dorsal. Scale bars: B, D, 2 mm; C, 1 mm; E, 0.2 mm. Photo credit A Jimmy Paul.
FIGURE 3 in Phonognatha vicitra Sherriffs, 1928 - a taxonomic misidentification of the orb-weaving spider Acusilas coccineus Simon, 1895 (Araneae, Araneidae)
FIGURE 3. Distribution records of Acusilas coccineus Simon, 1895 in India. ○ new record, ● record from literature (Sherriffs 1928, Roy et al. 2017).
Figure 3 in Detailed integrative taxonomic analysis reveals large-scale species misidentification of barnacles based on DNA barcoding data
Figure 3. Neighbour-joining tree for the three investigated barcode index numbers. Ŋe coloured sequences in each clade indicate our newly generated sequences of specimens with unequivocal morphological identification.
Figure 2 in Detailed integrative taxonomic analysis reveals large-scale species misidentification of barnacles based on DNA barcoding data
Figure 2. Morphology of unidentified Balanus sp. individuals of clade A (BOLD:AAG0069) (A), Balanus balanus (B), Balanus crenatus
Figure 1 in Detailed integrative taxonomic analysis reveals large-scale species misidentification of barnacles based on DNA barcoding data
Figure 1. Bubble plot of the correspondence between species assignments and the barcode index number (BIN; genetic clade). Ŋe size of the bubbles corresponds to the number of sequences contained in each combination of BIN and species assignment. Vertical lines highlight BINs that contain more than one species assignment, and horizontal lines highlight species assignments that are present in more than one BIN. Grey bubbles indicate a one-to-one match between BIN and species assignment. Coloured bubbles represent the three BINs that were investigated further by integrative taxonomic analysis.
FIGURE 2. Morphological differences between North American and Chinese taxa. A,C,E,G in On the presence of North American clubmoss Huperzia lucidula (Lycopodiaceae) in China: An intercontinental disjunction or misidentification
FIGURE 2. Morphological differences between North American and Chinese taxa. A,C,E,G. Huperzia lucidula from North America (D. E. Boufford 43754). B,D,F,H. H. lucidula from China (PE-NIBR Changbaishan Exped. 230-6). A–B. General habit. C–D. Main branch showing arrangement of leaves. E–F. Single tropophyll. G–H. Magnified view of tropophyll showing leaf serration and apex.
FIGURE 3 in On the presence of North American clubmoss Huperzia lucidula (Lycopodiaceae) in China: An intercontinental disjunction or misidentification
FIGURE 3. Cladogram obtained from the Maximum Likelihood analysis of the combined dataset including sequences of rbcL, matK
Figure 3 in Breeding biology of mimetic species based on secondary data sources should address misidentifications: the case of the lesser kiskadee Philohydor lictor (Aves: Tyrannidae)
Figure 3. Eggs of eight kiskadee-like mimetic species from egg collections. Egg collection reference (institution acronym–catalogue number): (a) NBCN–181942; (b) NBCN–181153; (c) COMB-E165; (d) WFVZ–118541-2; (e) USNM–48256; (f) MHNG–735096; (g) NBCN–181945; (h) ZMB–SN; (i) DMNH– 10519; (j) WFVZ–184215; (k) MNHN–489-490; (l) NBCN–180866; (m) WFVZ–118522.
Figure 2 in Breeding biology of mimetic species based on secondary data sources should address misidentifications: the case of the lesser kiskadee Philohydor lictor (Aves: Tyrannidae)
Figure 2. Egg-laying records of lesser kiskadee (Philohydor lictor) based on citizen science, literature, and museum egg collections in relation to monthly total precipitation.
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