Entomobrya linda Soto-Adames, 2002
publication ID |
https://doi.org/ 10.11646/zootaxa.5452.1.1 |
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lsid:zoobank.org:pub:093738EB-2BEE-4DFA-B930-FAC1FBF08FA4 |
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https://treatment.plazi.org/id/062587E9-C70F-FE58-FF7C-C229FA60258D |
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Plazi |
scientific name |
Entomobrya linda Soto-Adames, 2002 |
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Entomobrya linda Soto-Adames, 2002 View in CoL
Figs 71–72 View FIGURE 71 View FIGURE 72 , Table 1
Entomobrya linda Soto-Adames, 2002: 82 View in CoL , figs 21–47, United States, Virgin Islands, Saint Thomas.
Examined material. Two females on slides and 1 specimen in alcohol ( INPA): Brazil, Roraima state, Caracaraí municipality, National Park of “Viruá”, 01°29’23”N, 61°00’12”W ( Fig. 72 View FIGURE 72 ), 86 m, 01–15.iii.2016, malaise-trap, JA Rafael & R Boldrini coll. GoogleMaps Four females on slides and 9 specimens in alcohol ( INPA): idem, except L1-500 grid, 01°29’12”N, 61°00’57”W, 66 m, 21–29.v.2015, SS Gadelha & DRR Fernandes coll. GoogleMaps Fourteen specimens in alcohol ( INPA): idem, except L2-2500 grid, 01°28’39”N, 61°01’29”W, 75 m, SS Gadelha coll. GoogleMaps One specimen in alcohol ( INPA): idem, except L4-500 grid, 01°27’34”N, 61°00’24”W, 65 m, 16.i–06.ii.2013, pitfall-trap, IPS Santos coll. GoogleMaps Two females on slides ( INPA): Amajari municipality, “Serra do Tepequém”, “Manancial” inn, 03°46’55”N, 61°43’48”W, 623 m, 15–30.vi.2015, malaise-trap, PCS Barroso & Boldrini coll. GoogleMaps Two females on slides and 11 specimens in alcohol ( INPA): idem, except 15–31.v.2015 GoogleMaps . One specimen in alcohol ( INPA): idem, except 01– 15.vi.2015 GoogleMaps .
Remarks. Entomobrya linda Soto-Adames, 2002 from the Virgin Islands and Entomobya barbata Siqueira & Bellini, 2020 from Brazil are compared due to their similarity in body color pattern, body proportion, dorsal macrochaetotaxy reduced, ventral tube anterior face with 3 mac, trochanteral organ with similar number of spine-like chaetae (9–12 in E. barbata and 9–11 in E. linda ), and mucro teeth subequal ( Soto-Adames 2002; Santos et al. 2020; Viana et al. 2022). As mentioned in Viana et al. (2022), the differences between these species are very narrow, and for this reason, a paratype of E. barbata deposited in INPA (INPA-CLL 0000256) was analyzed and compared with specimens of E. linda obtained in the present study from Roraima State ( Figs 71A–C View FIGURE 71 ). In the original description of E. barbata ( Santos et al. 2020) , it is reported that the labral papillae have multiple projections, but we observed a single conical projection (similar to Fig. 44A View FIGURE 44 ), diverging from E. linda by the rounded projections (see Soto-Adames 2002: 83, fig. 23), although the latter author does mention in the original description that he sometimes saw it in a conical shape ( Soto-Adames 2002). Another observed difference is the length of labial papilla E l.p. surpassing the base of a.a. in E. linda and not reaching the base of a.a. in E. barbata (as observed by Santos et al. 2020). Furthermore, both species on both sides of Th II have two chaetae as mes (m4 and m5), which eventually may have m4 as mac in E. linda , while m5 is a mac in E. barbata . In this context, although authors may interpret these chaetae (mac or mes) differently, it is evident that this characteristic can be supplementary and occasionally help in species identification.
Distribution. Known from Caribbean Islands ( Virgin Islands, Saint Kitts, and Nevis), Colombia ( Soto-Adames 2002; Soto-Adames & Anderson 2017; Cipola 2024) and now for the first time in the Roraima state, Brazil ( Fig. 72 View FIGURE 72 ). This record indicates that E. linda probably has a wide distribution in the northern region of the Amazon biome.
Postembryonic development of the dorsal chaetotaxy in E. egleri
The dorsal chaetotaxy of the head and Th II to Abd V in 1 st, 4 th, 5 th instars (in part) and adults of E. egleri are herein provided and compared to other Entomobrya spp. (except head) and Homidia jordanai Pan & Zhang, 2011 ( Jordana & Baquero 2005; Pan et al. 2011; Zhang et al. 2019). The final pattern of adults of E. egleri is also compared with other Entomobryinae genera ( Zhang et al. 2009; Pan et al. 2011, 2012; Cipola & Bellini 2016; Cipola et al. 2016a, 2018b; Jin et al. 2017), aiming to improve the chaetae homology recognition between taxa. The nomenclature of the dorsal chaetotaxy herein provided in the descriptions of Entomobrya species were compared and supported by the study of the postembryonic development of E. egleri .
Head dorsal chaetotaxy ( Figs 15D View FIGURE 15 , 73A–B View FIGURE 73 , Table 4). The 1 st instar of E. egleri is similar to H. jordanai , except for the absence of the primary chaetae: A4, M0, S0’, S4 and S6 (named as S 5 in Pan et al. 2011: 30, fig. 29). From the 1 st to the 4 th instar, the An, M and S series show an increase of secondary chaetae, with the addition of Pi, Pmp and Ppe series. In the 5 th instar, An3a2 and S2e (present or absent) mac and three interocular secondary chaetae appears (q, s, r), and even the adult has mac additions in An series. Besides, most mic or mes transform into mac in M, S, Pi, Pmp and Ppe series. The development of H. jordanai also shows increasing numbers of mac in all series, except for A4, M0 and S0’, which disappear or change to mic (see Pan et al. 2011 Fig.5 View FIGURE 5 ). Therefore, such additions, with the exception of A4, M0 and S0’ can be a shared feature in Entomobryinae .
The sutural series in the 1 st instar of Entomobryinae may contain 8 primary chaetae (S0–7), as in Homidia ( Pan et al. 2011) . Therefore, three chaetae traditionally named as S4i, S5 and S5i ( Jordana & Baquero 2005) are here named respectively as primary chaetae: S5, S6 and S7 ( Fig. 73A View FIGURE 73 , Table 4). Even though, two of these chaetae (S4, S6) appear secondarily in Entomobrya and at least in Sinhomidia Zhang, 2009 (in Zhang et al. 2009) (see Pan et al. 2019: 49), and are likely homologous to the Homidia chaetae, so should named accordingly for a better comparison between different taxa.
Still on the head, based on the pattern of development of E. egleri , we propose a new interpretation for some posterior series of the head (Pi, Pmp and Ppe), which can be applied and compared with other Entomobrya species and Entomobryoidea in general ( Cipola et al. 2014, 2016b, 2018b, 2020, 2022; Bellini et al. 2015; Cipola & Bellini 2016; Pan 2015; Pan et al. 2019; Cipola & Greenslade 2022), as this region (named as Gr. II in Chen & Christiansen 1993) is often not labeled in descriptions due to a difficult interpretation (e.g. Chen & Christiansen 1993; Zhang et al. 2009; Pan et al. 2012, 2019). The original proposal for the dorsal macrochaetotaxy of the genus provided by Jordana & Baquero (2005) was based on observations of adults, and therefore some primary and secondary chaetae were mistakenly named, which is understandable given the difficulty of tracing the homology (e.g. position of Pa1 mac in relation to the ‘Pi’ series) ( Fig. 73B View FIGURE 73 , Table 4). Consequently, such misconceptions were replicated in descriptions of Entomobrya spp. (like in Bellini et al. 2015), and some Entomobryinae genera, as Acanthocyrtus Handschin, 1925 , Amazhomidia , Coecobrya Yosii, 1956 , Homidia , Sinella Brook, 1882 and Sinhomidia ( Zhang 2009, Pan et al. 2011, 2012; Cipola & Bellini 2016; Cipola et al. 2016a, 2018b; Jin et al. 2017).
Th II dorsal chaetotaxy ( Figs 17A View FIGURE 17 , 73A–B View FIGURE 73 , Table 4). The 1 st instar of E. egleri is the same of Entomobrya nivalis ( Linnaeus, 1758) , but the pattern at this stage may have small differences between species, like E. proxima Folsom, 1924 with 4 chaetae (a1, m4, p1 and p2) as mic (see Zhang et al. 2019: 260). The 4 th instar has the addition of secondary chaetae (11 in a series, 8 in m series, and 7 p series), plus m1 modified into mac ( Fig. 73B View FIGURE 73 , Table 4). Entomobrya nivalis also shows an increasing pattern of secondary chaetae in a, m and p series (see Zhang et al. 2019, fig. S1C). On the other hand, in the 5 th instar ( Fig. 73B View FIGURE 73 ), three mes interchange into mac (a2e, a5i2, a5p), while two new mac arise (p1i, p2p). After the 5 th instar, as well as in the adult ( Figs 17A View FIGURE 17 , 73B View FIGURE 73 , Table 4), numerous mac appear in all series. This developmental pattern is similar to E. nivalis , including an extra chaeta which does not appear in the final stages until the adult (named here as p 2ei). In this context, the posterior region is generally ignored in some descriptions (Fulgol 2017; Baquero & Jordana 2018; Jordana & Greenslade 2020), possibly due to complexity of variations and/or interpreting of chaetae homology.
Th III dorsal chaetotaxy ( Figs 17A View FIGURE 17 , 73A–B View FIGURE 73 , Table 4). The 1 st instar has a, m and p series with 7 (a1–7), 5 (m1, m4–7) and 7 (p1–6) primary chaetae, respectively. The Entomobrya species (and other Entomobryinae ) have the same primary pattern (see Zhang et al. 2019: 260–261), but E. egleri differs by 8 mac (a2, a4, a6, m6–7, p1–3). Therefore, this can be a unique condition of the species, or even represent a pattern shared by other taxa from the Brazilian Amazon.
In the 4 th instar three chaetae change to mac (a5, m5 and p5) and nine secondary chaetae emerge, two of which as mac (p2a and m6e). Some of these chaetae (e.g. m5i, m6e, m6p) may have arisen before the 4 th instar, as seen in E. nivalis (see Zhang et al. 2019: S12). However, the 4 th instar of E. nivalis has more secondary chaetae. This may be characteristic of this species, because in E. egleri (and perhaps in the other species of the Brazilian Amazon) about half of the chaetae change to mac (a1, a3, a5i, p1i, p1p, p2e) and/or appear (a5e, p1ip, p1p2, p6e) only in the final stages (after 5 th instar) ( Figs 17A View FIGURE 17 , 25A View FIGURE 25 , 32A View FIGURE 32 , 39A View FIGURE 39 , 64A View FIGURE 64 , 69A View FIGURE 69 , Table 4).
Abd I dorsal chaetotaxy ( Figs 17B View FIGURE 17 , 74A–B View FIGURE 74 , Table 4). The 1 st instar has a, m and p series with 5 (a1–3, a5–6), 5 (m2–6) and 2 (p5–6) primary chaetae, respectively, the same pattern seen in other Entomobrya species, except E. proxima which has two chaetae as mes/mic (m2–3). In the 4 th instar (or before), two secondary chaetae arise (m2i, m4i), forming a pattern of four mac (m2, m3, m4i, m4) in which another secondary mac emerges in the 5 th instar, resulting in a similar pattern shared between other species herein studied (except E. bicyana sp. nov.). However, this pattern differs from E. nivalis because m4i and m4ia mac only appear in adults (named respectively as m4p and m4i in Zhang et al. 2019: S14). On the other hand, Entomobrya sp. ( Zhang et al. 2019: S14) shows three extra mac in the 3 rd instar (a3, m2i, “ m4p ” = m4i) and two more in 4 th instar (a3, a5), but such mac appears only in adults of E. egleri ( Fig. 17B View FIGURE 17 , Table 4). This development pattern is not generic. Note that two secondary chaetae traditionally named as m4ip (or m4p) and m4i ( Jordana & Baquero 2005; Zhang et al. 2019) are renamed here (m4i and m4ia respectively) as they are internally positioned in relation to their primary chaetae (m4) ( Fig. 74B View FIGURE 74 , Table 4).
Abd II dorsal chaetotaxy ( Figs 17B View FIGURE 17 , 74A–B View FIGURE 74 , Table 4). The 1 st instar has a, m and p series with 6 (a1–3, a5–7), 6 (m2–7) and 4 (p4–7) primary chaetae (plus el), respectively, the same pattern seen in other Entomobrya species, except E. proxima with 1 primary mac (m3) ( Zhang et al. 2019: 260). The 4 th instar has numerous secondary chaetae which arise at this stage, as seen in E. nivalis , except for m3e mac which appears during the 2 nd instar, but this overall pattern is observed in many Entomobryinae (see Zhang et al. 2019: S16 and S17). The m3ep mac is a chaeta which may emerge at different stages, as observed in 5 th instar of E. egleri , 2 nd in Entomobrya huangi Chen & Ma, 1998 , 3 rd in Entomobrya sp. , and only in the adult of E. nivalis . In this sense, the other secondary mac (a2–3, m6, p6–7) of E. egleri also arise at the end of the development, and probably show a specific configuration to each species ( Table 4), or perhaps this may be a development pattern shared between species from the Brazilian Amazon.
Abd III dorsal chaetotaxy ( Figs 17B View FIGURE 17 , 74A–B View FIGURE 74 , Table 4). The 1 st instar has a, m and p series with 6 (a1–3, a5–7), 7 (m2–5, m7, am6, pm6) and 4 (p3, p5–7) primary chaetae, respectively, plus 5 chaetae of uncertain homology, similar to other Entomobrya species ( Zhang et al. 2019: 261). Although the initial pattern of E. egleri resembles other taxa of the genus, it differs by m3 as mic and Pm6 as mac, the latter being also observed in E. nivalis . In the 4 th instar, numerous secondary chaetae of uncertain homology emerge, and three chaetae change to mac (am6, p6, p7), but at least two of them (am6, p6) probably arise during the 2 nd or the 3 rd instar, as seen in E. nivalis ( Zhang et al. 2019: S18). In adults, five mac may be present ( Table 4).
Abd IV dorsal chaetotaxy ( Figs 17C View FIGURE 17 , 74A–B View FIGURE 74 , Table 4). The 1 st instar of E. egleri is similar to other Entomobrya species, with three primary mac (B4, B5, E3) plus three chaetae from the B series (B4–6), near the posterior region ( Zhang et al. 2019: 261). Furthermore, two primary chaetae (Be3, C4a) which were never observed in the 1 st instar of Entomobrya are present in E. egleri , and are probably present in all the species of the Brazilian Amazon (except for E. bicyana sp. nov.), given their presence in adults as well ( Figs 25C View FIGURE 25 , 32C View FIGURE 32 , 39C View FIGURE 39 , 57C View FIGURE 57 , 64C View FIGURE 64 , 69C View FIGURE 69 , Table 4). However, this will need to be better investigated to confirm whether this primary pattern is unique to E. egleri . In the 4 th instar, numerous secondary chaetae emerge, including four series (Ae, Ce, Ee, Fe), which likely appeared in the 2 nd instar, as seen in E. nivalis ( Zhang et al. 2019: S20). In this stage, there are 14 extra mac (A2, A5, A6, Si, B3, B6, Sm, D3, E2–2p, E4, F1, F2, F3), some of which were previously mic/mes (e.g. A2, A5, A6), while others likely appeared in the 2 nd instar (e.g. Si, Sm), as with Entomobryoidea in general ( Zhang et al. 2019). In the 5 th instar, Be3 mac arises on the inner region, and then, in the subadult/adult, some chaetae change to mac, forming two irregular transverse rows, an anterior (A2, Ae2, B1, Be2, C1) and another subsequent row (A3–3p, Si, B3, Be3, Sm, C1p), plus extra mac clusters which emerge in the posterior region (A6a, A6p, A6p2). This pattern of anterior and posterior regions is similar to Entomobrya koreana Yosii, 1965 ( Zhang et al. 2019: S21), as well as other Entomobryinae , as Acanthocyrtus , Amazhomidia , Lepidocyrtoides Schött, 1917 , Homidia and Sinhomidia , although in the latter two there is only one transverse row ( Zhang et al. 2009; Pan et al. 2011, 2012; Cipola et al. 2016a, 2017, 2018b; Jin et al. 2017). The lateral region of E. egleri is also similar to E. koreana ( Zhang et al. 2019: S21), but compared with adults of other species from the Brazilian Amazon it is still confusing to determine the homology of some mac ( Figs 25C View FIGURE 25 , 32C View FIGURE 32 , 39C View FIGURE 39 , 57C View FIGURE 57 , 64C View FIGURE 64 , 69C View FIGURE 69 , Table 4).
Abd V dorsal chaetotaxy ( Figs 17C View FIGURE 17 , 74A–B View FIGURE 74 , Table 4). The 1 st instar has a, m and p series with 4 (a1, a3, a5–6), 3 (m2–3, m5) and 5 (p1, p3–6) primary chaetae (plus el), similar to other Entomobrya species (see Zhang et al. 2019: 261), except in p series laterally, which has three chaetae with uncertain homologies. The 4 th instar has five chaetae which change to mac (a5, p1, p3–5), four more secondary chaetae (a5a, a6a, m3a, p0) and two extra secondary series of p (pa and pp) ( Table 4), which probably occurred in the 3 rd instar, as seen in E. nivalis (see Zhang et al. 2019: S25). The pattern observed in the 4 th instar of E. egleri is similar to the adult, except for a6a as mac, but this difference may probably occur in other species of Entomobrya as well.
Key to Brazilian species of Entomobrya View in CoL
1 Unguiculus ai lamella clearly excavate ( Fig. 65D View FIGURE 65 )........................................................... 2
- Unguiculus ai lamella acuminate or slightly truncate ( Figs 18E View FIGURE 18 , 33G View FIGURE 33 )........................................... 7
2 Abd IV anteriorly with two small longitudinal dark stripes (see Arlé 1959: 203)................... E. aipatse Arlé, 1959 View in CoL
- Abd IV color pattern different........................................................................... 3
3 Ant IV apical bulb present ( Fig. 49A View FIGURE 49 )..................................................................... 4
- Ant IV apical bulb absent ( Figs 30A View FIGURE 30 , 43A View FIGURE 43 )................................................................. 6
4 Ant IV apical bulb unilobed; body all pigmented or only with Abd IV–VI depigmented (see Arlé 1959: 201)............................................................................................. E. ataquensis Arlé, 1959 View in CoL
- Ant IV apical bulb bilobed ( Fig. 49A View FIGURE 49 ); body color pattern different............................................. 5
5 Head with M4i, Ppe3 and Pe6 mac (see Viana et al. 2022: 265).......................... E. uai Viana & Cipola, 2022 View in CoL
- Head without M4i, Ppe3 and Pe6 mac ( Fig. 50A View FIGURE 50 )............................................ E. bicyana sp. nov.
6 Head with S4i and Pe6 mac ( Fig. 68A View FIGURE 68 ); unguiculus pe lamella serrated ( Fig. 70D View FIGURE 70 )........... E. pseudomaculata sp. nov.
- Head without S4i and Pe6 mac ( Fig. 62D View FIGURE 62 ); unguiculus pe lamella smooth ( Fig. 65D View FIGURE 65 )............... E. idenilzae sp. nov.
7 Ant IV apical bulb present ( Fig. 49A View FIGURE 49 )..................................................................... 8
- Ant IV apical bulb absent ( Fig. 30A View FIGURE 30 ).................................................................... 17
8 Unguiculus III ai lamella slightly truncate ( Fig. 33G View FIGURE 33 )........................................................ 9
- Unguiculus III ai lamella acuminate ( Fig. 26E View FIGURE 26 )............................................................ 10
9 Labral papillae with 3 projections......................................... E. juneae Santos-Costa & Bellini, 2020 View in CoL
- Labral papillae with 1 conical projection ( Fig. 44A View FIGURE 44 )................................. E. wasmanni Handschin, 1924 View in CoL
10 Unguiculus III pe lamella serrate or with at least 3 teeth ( Figs 18E View FIGURE 18 , 58E View FIGURE 58 )........................................ 11
- Unguiculus III pe lamella smooth ( Fig. 33G View FIGURE 33 ).............................................................. 13
11 Unguiculus III pe lamella with 3 teeth ( Fig. 58E View FIGURE 58 ); Abd IV with transversal bands of pigment........................ 12
- Unguiculus III pe lamella serrate ( Fig. 18E View FIGURE 18 ); Abd IV with a U-shaped dark spot (see Katz et al. 2015: 53)............................................................................................. E. nivalis ( Linnaeus, 1758) View in CoL 12 Labral papillae conical ( Fig. 44A View FIGURE 44 ); labial papilla E l.p. surpassing the base of a.a ...... E. barbata Siqueira & Bellini, 2020
- Labral papillae rounded ( Fig. 50B View FIGURE 50 ); labial papilla E l.p. not reaching the base of a.a .......... E. linda Soto-Adames, 2002 View in CoL
13 Mucro proximal tooth subequal or larger than the distal one.................................................. 14
- Mucro proximal tooth shorter than the distal one........................................................... 16
14 Dorsal head with 1 posterior thin longitudinal dark stripe (see Arlé, 1939: 27).................... E. tupiana Arlé, 1939 View in CoL
- Dorsal head with different color pattern.................................................................. 15
15 Th II–Abd III with a longitudinal dark stripe (see Bonet 1933:132)......................... E. decora ( Nicolet, 1847) View in CoL
- Th II–III with a transversal dark band (see Bonet 1933:137)............................... E. inaequalis Denis, 1924 View in CoL
16 Ant IV apical bulb bilobed or trilobed; central head with a dorsal V-shaped dark spot (see Christiansen 1958b: 466).................................................................................. E. griseoolivata ( Packard, 1873) View in CoL
- Ant IV apical bulb unilobed; central head without a dorsal V-shaped dark spot ( Bellini et al. 2015:8)............................................................................................ E. bahiana Bellini & Cipola, 2015 View in CoL
17 Body with two dorsal longitudinal stripes on the median region ( Fig. 21 View FIGURE 21 )............. E. paroara Arlé & Guimarães, 1978 View in CoL
- Body color pattern different........................................................................... 18
18 Th II–Abd III with a transverse dark band ( Figs 12–14 View FIGURE 12 View FIGURE 13 View FIGURE 14 , 29 View FIGURE 29 , 54 View FIGURE 54 ), if absent, the body is mostly depigmented ( Figs 14B and G View FIGURE 14 )................................................................................................... 19
- Body almost completely pigmented, without clear spot patterns ( Figs 36 View FIGURE 36 , 42 View FIGURE 42 ).................................... 21
19 Central head without pigment ( Fig. 54B View FIGURE 54 ); head with Ps5, Pp4 and Pe6 mac ( Fig. 55C View FIGURE 55 )................ E. elizeuli sp. nov.
- Central head color pattern variable ( Figs 29A–F View FIGURE 29 ); head without Ps5, Pp4 and Pe6 mac ( Fig. 30E View FIGURE 30 ).................... 20
20 Labial papilla E l.p. not reaching the base of a.a ( Fig. 16B View FIGURE 16 ); collophore anterior region with 3–4 distal mac ( Fig. 19A View FIGURE 19 ); Abd IV with 19 posterior mes ( Fig. 17C View FIGURE 17 ); unguiculus III pe lamella serrated ( Fig. 18E View FIGURE 18 ).......... E. egleri Arlé & Guimarães, 1978 View in CoL
- Labial papilla E l.p. surpassing the base of a.a ( Fig. 31B View FIGURE 31 ); collophore anterior region with 6 distal mac ( Fig. 34A View FIGURE 34 ); Abd IV with 16 posterior mes ( Fig. 32C View FIGURE 32 ); unguiculus III pe lamella smooth ( Fig. 33G View FIGURE 33 )....................... E. uambae Arlé, 1959 View in CoL
21 Labral inner papillae with 2–3 projections, outer with 2 ( Fig. 38A View FIGURE 38 ); Abd IV with 15 posterior mes ( Fig. 39C View FIGURE 39 ); manubrial plate with 2 psp ( Fig. 41C View FIGURE 41 )................................................................ E. acreanensis sp. nov
- Labral inner and outer papillae only with 1 projection each ( Fig. 44A View FIGURE 44 ); Abd IV with 19 posterior mes ( Fig. 45C View FIGURE 45 ); manubrial plate with 3 psp ( Fig. 47C View FIGURE 47 )........................................................... E. albitrigona sp. nov.
INPA |
Instituto Nacional de Pesquisas da Amazonia |
R |
Departamento de Geologia, Universidad de Chile |
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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Entomobrya linda Soto-Adames, 2002
Viana, Stéphanie Dos Santos, Morais, José Wellington De & Cipola, Nikolas Gioia 2024 |
Entomobrya linda
Soto-Adames, F. N. 2002: 82 |