diff --git a/data/31/57/E0/3157E00AFFF2FFC6FDA40999FAA2DBF1.xml b/data/31/57/E0/3157E00AFFF2FFC6FDA40999FAA2DBF1.xml
new file mode 100644
index 00000000000..b2bd4524748
--- /dev/null
+++ b/data/31/57/E0/3157E00AFFF2FFC6FDA40999FAA2DBF1.xml
@@ -0,0 +1,767 @@
+
+
+
+On new genera and species of crack-leg spiders (Araneae, Udubidae) from Madagascar
+
+
+
+Author
+
+Henrard, Arnaud
+E1B02E6E-D91C-43FE-8D8C-CD102EFEE3B4
+Royal Museum for Central Africa, Leuvensesteenweg 13, B- 3080 Tervuren, Belgium.
+arnaud.henrard@africamuseum.be
+
+
+
+Author
+
+Griswold, Charles
+51E9CD73-DB08-49B6-9B2C-843B27B38B48
+Arachnology Lab, California Academy of Sciences, 55 Music Concourse Drive, San Francisco, CA 94118, USA.
+cgriswold@calacademy.org
+
+
+
+Author
+
+Jocqué, Rudy
+CF15016C-8CD1-4C9D-9021-44CA7DC7A5D5
+Royal Museum for Central Africa, Leuvensesteenweg 13, B- 3080 Tervuren, Belgium.
+rudy.jocque@africamuseum.be
+
+text
+
+
+European Journal of Taxonomy
+
+
+2024
+
+2024-10-23
+
+
+966
+
+
+1
+
+
+1
+80
+
+
+
+
+https://europeanjournaloftaxonomy.eu/index.php/ejt/article/download/2697/12453
+
+journal article
+10.5852/ejt.2024.966.2697
+2118-9773
+14001790
+FFE41347-8B55-4CF1-B10B-53EBB4CF0E26
+
+
+
+
+Family
+
+Udubidae
+Griswold &
+Polotow, 2015
+
+
+
+
+
+Udubidae Griswold & Polotow
+in
+
+Polotow
+et al.
+, 2015: 151
+
+.
+
+
+
+
+
+
+Type
+genus
+
+
+
+
+
+Uduba
+Simon, 1880: 343
+
+(
+Type
+species by monotypy:
+
+Olios madagascariensis
+Vinson, 1863
+
+=
+
+Uduba madagascariensis
+(
+Vinson, 1863
+))
+
+.
+
+
+
+
+
+Diagnosis
+
+
+
+Udubidae
+are entelegyne RTA-clade spiders with three tarsal claws (
+Fig. 21A–B
+), multiple rows of tarsal trichobothria of about equal length (
+Figs 13F
+,
+20E–F
+), eight eyes in 2 nearly straight rows (
+Figs 3C, F
+, 8A–B, 13C–D, 17A, 22A, C, 24A, C), indirect eyes with canoe-shaped tapeta and the cheliceral fang with interior serrula weak to absent. Males may or may not have a subbasal crack or line of autospasy on the leg tibiae (
+Fig. 24B
+, arrow;
+Griswold 1993
+: figs 3–4). All species have a hyaline conductor (C = the “Sierwald conductor” of
+
+Polotow
+et al.
+2015
+
+), which is relatively small, transverse, hyaline and fan-shaped, prolaterally extending from narrow base to wide flattened tip (
+Figs 5A–C
+,
+6D–F
+,
+9A–C
+,
+11A–C
+,
+12E
+,
+14D, F
+,
+15D–F
+). Most have an additional tegular process accompanying the embolus that is a narrow membranous or sclerotized extension inserted between the tegulum and the base of the median apophysis (MA), running backward to MA and ending with fattened fan-shaped tip accompanying the embolus: this is the paraconductor (Pc = the “MTP” and “STP” of
+Griswold 1993
+) (
+Figs 5A–C
+,
+6D–F
+,
+9A–C
+,
+11A–C
+,
+12E
+,
+14D
+,
+15D–F
+). The paraconductor is found in other members of the Oval Calamistrum (OC) clade (the “TA” in
+
+Griswold
+et al.
+2005
+
+: figs 186B–C, 195B–C), and the Sierwald conductor (C) occurs widely among the OC clade and Dionycha
+Petrunkevitch, 1928
+(
+
+Polotow
+et al.
+2015
+
+: figs. 13E–F, 15A–B, E–F).
+
+
+Udubidae
+may be distinguished from most other araneomorph spider families found in
+Madagascar
+by the form of their tarsi. The presence of tarsal trichobothria distinguishes udubids from the
+
+Filistatidae
+Ausserer, 1867
+
+, Synspermiata
+Michalik & Ramírez, 2014
+,
+Palpimanoidea
+
+Forster &
+Platnick
+, 1984
+
+, Araneoidea
+Latreille, 1806
+,
+Eresidae C.L. Koch, 1845
+(in
+Berendt 1845
+),
+
+Hersiliidae
+Thorell, 1869
+
+and
+
+Oecobiidae
+Blackwall, 1862
+
+,
+
+Phyxelididae
+Lehtinen, 1967
+
+and
+
+Titanoecidae
+Lehtinen, 1967
+
+. Multiple rows of tarsal trichobothria distinguish
+Udubidae
+from taxa with only a single row of tarsal trichobothria including
+
+Agelenidae C.L.
+Koch, 1837
+
+,
+
+Dictynidae O.
+Pickard-Cambridge, 1871
+
+,
+
+Hahniidae
+Bertkau, 1878
+
+and most
+
+Zodariidae
+Thorell, 1881
+
+and
+
+Thomisidae
+Sundevall, 1833
+
+. Among taxa with multiple rows of tarsal trichobothria udubids may be distinguished from
+
+Lycosidae
+Sundevall, 1833
+
+,
+
+Pisauridae
+Simon, 1890
+
+and
+
+Oxyopidae
+
+Thorell,
+1869
+
+
+in that these latter families have at least one eye row strongly curved, whereas
+Udubidae
+have both eye rows nearly straight. Udubids have at least a rudiment of the inferior tarsal claw and lack claw tufts, characters that distinguish them from
+
+Sparassidae
+Bertkau, 1872
+
+and the Dionycha (
+
+Cheiracanthiidae
+Wagner, 1887
+
+,
+
+Clubionidae
+Simon, 1878
+
+,
+
+Corinnidae
+Karsch, 1880
+
+,
+
+Gallieniellidae
+Millot, 1947
+
+,
+
+Gnaphosidae
+Banks, 1892
+
+,
+
+Liocranidae
+Simon, 1897
+
+,
+
+Philodromidae
+Thorell, 1869
+
+,
+
+Salticidae
+Blackwall, 1841
+
+,
+
+Selenopidae
+Simon, 1897
+
+,
+
+Trachelidae
+Simon, 1897
+
+,
+
+Trochanteriidae
+Karsch, 1879
+
+and
+
+Viridasiidae
+Lehtinen, 1967
+
+). Finally, like
+Udubidae
+, the lone genus of
+
+Desidae
+Pocock, 1895
+
+from
+Madagascar
+,
+
+Desis
+Walckenaer, 1837
+
+, has numerous tarsal trichobothria and straight eye rows but the latter is quite distinct in having elongate chelicerae, a dense cover of fine hairs and the posterior tracheal spiracle on the abdomen advanced.
+
+
+
+Composition
+
+
+
+
+Campostichomma
+Karsch, 1892
+
+(
+Sri Lanka
+),
+
+Raecius
+Simon, 1892
+
+(Africa), and
+
+Tabiboka
+
+gen. nov.
+,
+
+Uduba
+Simon 1880
+
+,
+
+Zorascar
+
+gen. nov.
+and
+
+Zorodictyna
+Strand, 1907
+
+(
+Madagascar
+).
+
+
+
+
+
+
+Key to
+Udubidae
+of
+Madagascar
+
+
+
+
+
+
+
+1. Male palp without process between tibia and patella; cymbium with retrobasal extension (CE), short to as long as rest of cymbium (
+Figs 5B–C
+,
+6A–C
+,
+9B–C
+,
+11B–C
+,
+12B–D
+,
+14A–C
+,
+15A–B
+,
+16A–B
+,
+23B–C
+,
+25C
+); embolus broad and flat to slender, cylindrical, firmly attached to point of origin on retromargin of tegulum (
+Figs 5A–B
+,
+6D–E
+, 8F, 9A–B, 11A–B, 12E, 14E–F, 15B, D–F, 23A–B, 25A–B); tegulum oval apically; conductor hyaline, fan-shaped crest arising from middle to apex of tegulum; female endogyne with spermathecal ducts short, stout, not making loops, at most twisted (
+Figs 5E
+,
+7C–E
+,
+9E
+,
+11E
+,
+12H
+,
+16D
+,
+18B–D
+,
+19C–F
+,
+23E
+,
+25E
+) ..................................................... 2
+
+
+
+
+– Male palp with small ventral process at base of tibia between tibia and patella (“
+UTA
+” in
+
+Griswold
+et al.
+2022
+
+: figs 27A–B, 39A–C, 40A–C, 41B); cymbium rounded retrobasally; embolus flexibly attached to large, swollen base, embolus elongate and extending behind tegulum and subtegulum to emerge from alveolus near bulb apex (
+
+Griswold
+et al.
+2022
+
+: figs 27A–B, 32C, 41F, 51A); tegulum trilobed apically, with retrolateral (TA1), median (TA2) and prolateral (TA3) processes interacting apically (
+
+Griswold
+et al.
+2022
+
+: figs 27A–B, 29A–I, 51A–C); conductor rectangular hyaline crest arising along apical margin of prolateral tegular lobe near TA3; female endogyne with spermathecal ducts elongate, making at least one (to as many as five) loops (
+
+Griswold
+et al.
+2022
+
+: figs 68B–D, 80B–D, F–G, I–J) ............................................................................................................................... .........
+
+Uduba
+Simon, 1880
+
+(the key to
+
+Uduba
+species
+
+is amply detailed in
+
+Griswold
+et al.
+2022: 13
+
+)
+
+
+
+
+
+
+2. With entire cribellum or vestige; PLS and ALS equal in length; strong scopulae beneath leg tarsi and most of length of metatarsi; males with crack-suture on leg tibiae just anteriad of basalmost pair of ventral spines (
+Fig. 24B
+) ........................................................................3.
+
+Zorodictyna
+Strand, 1907
+
+
+
+
+– Ecribellate; PLS much smaller than ALS; scopulae absent or only with weak scopulae beneath leg tarsi; most males without crack-suture on leg tibiae ........................................................................ 5
+
+
+
+
+
+3. Male palpal cymbium with rounded retrolateral paracymbial process (PP) (
+Figs 23B–C
+,
+25B–C
+); cymbial retrobasal extension (CE) extending at least one-third length of tibia (
+Figs 23B–C
+,
+25B–C
+); female epigyne lateral lobes (LL) lacking teeth (
+Figs 23D
+,
+25D
+) .................................................... 4
+
+
+
+
+– Male palpal cymbium evenly convex retrolaterally, without paracymbial process (
+Griswold 1993
+: figs 20–21); cymbial retrobasal extension, short, extending only to tibial apex (
+Griswold 1993
+: figs 20–21); female epigyne lateral lobes with short teeth (
+Griswold 1993
+: fig. 24) ......................... ......................................................................................................
+
+Zorodictyna oswaldi
+(
+Lenz, 1891
+)
+
+
+
+
+
+
+
+4. Male palp with basal embolic process (EBP) nearly triangular, embolus lacking crest, tegulum with retromedian longitudinal ridge that extends for most of tegulum length (
+Fig. 23A–C
+); female epigyne lateral lobes (LL) parallel, median sector (MS) rectangular (
+Fig. 23D
+); female endogyne with copulatory ducts (CD) larger than spermathecae (
+Fig. 23E
+) ..........
+
+Zorodictyna almae
+
+sp. nov.
+
+
+
+
+– Male palp with basal embolic process (EBP) slender, crescentic, embolus with subapical distal crest, and tegulum retromedian longitudinal ridge weak, short, extending for less than one-half tegulum length (
+Figs 25A–C
+); female epigyne lateral lobes (LL) converging posteriorly, median sector (MS) triangular (
+Fig. 25D
+); female endogyne with copulatory ducts (CD) and spermathecae equal in size (
+Fig. 25E
+) .......................................................................................
+
+Zorodictyna silvadavilae
+
+sp. nov.
+
+
+
+
+
+
+5. Male palp with cymbial retrobasal extension (CE) elongate, extending most of length of tibia, palpal tibia with RTA only, lacking VTA (
+Figs 14A–B
+,
+15A–B
+,
+16A–B
+); female epigyne median lobe (ML) short, concave medially, not extending to posterior margin, copulatory openings (CO) exposed (
+Figs 16C, E
+,
+18A
+) ............................................................................................6.
+
+Zorascar
+
+gen. nov.
+
+
+
+
+– Male palp with cymbial retrobasal extension (CE) shorter, extending to or just past tibial apex, palpal tibia with both VTA and RTA (
+Figs 5A–C
+,
+6A–C
+,
+9A–C
+,
+11A–C
+,
+12A–D
+); female epigyne median lobe (ML) extends to posterior margin, separating lateral lobes (LL) and covering copulatory openings (CO) (
+Figs 4B
+,
+5D
+,
+7A–B
+,
+9D
+,
+11D
+,
+12G
+) .......................................................7.
+
+Tabiboka
+
+gen. nov.
+
+
+
+
+
+
+6. Female epigyne median lobe (ML) broad and shallowly concave medially, copulatory openings (CO) exposed anteromedially (
+Fig. 16C
+), spermathecae elongate, curved, eggplant-shaped (
+Fig. 16D
+); male palp as in figures (
+Figs 14A–F
+,
+15A–F
+,
+16A–B
+) .....................
+
+Zorascar pasunepipe
+
+gen. et sp. nov.
+
+
+
+
+– Female epigyne median lobe (ML) narrow and deeply concave medially, copulatory openings (CO) exposed laterad of median lobe (
+Figs 16E
+,
+18A
+,
+19A–B
+), spermathecae stout, rounded, reniform (
+Figs 18B–D
+,
+19C–F
+); male unknown ................................
+
+Zorascar pasunepomme
+
+gen. et sp. nov.
+
+
+
+
+
+
+7. Male palp with conductor base originating anteriorly, hidden behind embolus or paraconductor (Pc), embolus short, arising retrolaterally near 270° (
+Figs 5A–C
+;
+6D–F
+, 8F, 9A–C); female epigyne median lobe (ML) heart-shaped, sides rounded (
+Figs 4B
+,
+5D
+,
+7A
+,
+9D
+) ....................................................... 8
+
+
+
+
+– Male palp conductor originating medially, near embolus base, not hidden, embolus elongate, arising retrobasally near 200° (
+Figs 11A–C
+,
+12A–C, E
+); female epigyne median lobe (ML) rectangular, narrowest in middle or with sides straight (
+Figs 11D
+,
+12G
+) ......
+
+Tabiboka polotowae
+
+gen. et sp. nov.
+
+
+
+
+
+
+8. Male palpal tibia with elongate retrobasal process (RTA), embolus broad, median apophysis (MA) short, apex far proximad of embolus apex (
+Figs 5A–C
+,
+6D–F
+); female epigyne median lobe (ML) narrow anteriorly, anterior width less than one-half total width (
+Figs 4B
+,
+5D
+,
+7A
+), endogyne with each spermatheca as broad as long (
+Figs 5E
+,
+7C–E
+) ......................
+
+Tabiboka milleri
+
+gen. et sp. nov.
+
+
+
+
+– Male palpal tibia with short, blunt retromedian process (RTA), embolus slender; median apophysis (MA) elongate, cruciform, apex extends to embolus apex (Figs 8C–F, 9A–C); female epigyne median lobe (ML) broad anteriorly, anterior width greater than one-half total width (
+Fig. 9D
+), endogyne with each spermatheca narrow, longer than broad (
+Fig. 9E
+) ...................
+
+Tabiboka milloti
+
+gen. et sp. nov.
+
+
+
+
+
+
+
\ No newline at end of file
diff --git a/data/31/57/E0/3157E00AFFF6FFDDFDF10CBEFD20D971.xml b/data/31/57/E0/3157E00AFFF6FFDDFDF10CBEFD20D971.xml
index 39d7e1667a4..67c321e20b6 100644
--- a/data/31/57/E0/3157E00AFFF6FFDDFDF10CBEFD20D971.xml
+++ b/data/31/57/E0/3157E00AFFF6FFDDFDF10CBEFD20D971.xml
@@ -1,68 +1,68 @@
-
-
-
-On new genera and species of crack-leg spiders (Araneae, Udubidae) from Madagascar
+
+
+
+On new genera and species of crack-leg spiders (Araneae, Udubidae) from Madagascar
-
-
-Author
+
+
+Author
-Henrard, Arnaud
-E1B02E6E-D91C-43FE-8D8C-CD102EFEE3B4
-Royal Museum for Central Africa, Leuvensesteenweg 13, B- 3080 Tervuren, Belgium.
-arnaud.henrard@africamuseum.be
+Henrard, Arnaud
+E1B02E6E-D91C-43FE-8D8C-CD102EFEE3B4
+Royal Museum for Central Africa, Leuvensesteenweg 13, B- 3080 Tervuren, Belgium.
+arnaud.henrard@africamuseum.be
-
-
-Author
+
+
+Author
-Griswold, Charles
-51E9CD73-DB08-49B6-9B2C-843B27B38B48
-Arachnology Lab, California Academy of Sciences, 55 Music Concourse Drive, San Francisco, CA 94118, USA.
-cgriswold@calacademy.org
+Griswold, Charles
+51E9CD73-DB08-49B6-9B2C-843B27B38B48
+Arachnology Lab, California Academy of Sciences, 55 Music Concourse Drive, San Francisco, CA 94118, USA.
+cgriswold@calacademy.org
-
-
-Author
+
+
+Author
-Jocqué, Rudy
-CF15016C-8CD1-4C9D-9021-44CA7DC7A5D5
-Royal Museum for Central Africa, Leuvensesteenweg 13, B- 3080 Tervuren, Belgium.
-rudy.jocque@africamuseum.be
+Jocqué, Rudy
+CF15016C-8CD1-4C9D-9021-44CA7DC7A5D5
+Royal Museum for Central Africa, Leuvensesteenweg 13, B- 3080 Tervuren, Belgium.
+rudy.jocque@africamuseum.be
-text
-
-
-European Journal of Taxonomy
+text
+
+
+European Journal of Taxonomy
-
-2024
-
-2024-10-23
+
+2024
+
+2024-10-23
-
-966
+
+966
-
-1
+
+1
-
-1
-80
+
+1
+80
-
-https://europeanjournaloftaxonomy.eu/index.php/ejt/article/download/2697/12453
+
+https://europeanjournaloftaxonomy.eu/index.php/ejt/article/download/2697/12453
-journal article
-10.5852/ejt.2024.966.2697
-2118-9773
-14001790
-FFE41347-8B55-4CF1-B10B-53EBB4CF0E26
+journal article
+10.5852/ejt.2024.966.2697
+2118-9773
+14001790
+FFE41347-8B55-4CF1-B10B-53EBB4CF0E26
-
+
@@ -71,54 +71,68 @@
gen. et sp. nov.
+
+
urn:lsid:zoobank.org:act:
33C8C4F1-A241-41E2-9B38-1D31AFBF4BE4
-
-
Figs 3–7
,
26
+
+
+
Zorocratidae
gen. Talatakely sp. Talatakely –
+
Morphbank 2023
+
: images [476092–509952] SpiderAToL,
March 3, 2008
, https://www.morphbank.net/?id=218853 [accessed
20 Oct. 2023
].
+
+
Zorodictyna
sp. 2
–
+
Polotow
et al.
2015
+
.
+
+
Zorodictyna
sp.
CG300 –
+
Wheeler
et al.
2017
+
.
+
@@ -220,7 +234,7 @@ Miller
-
+
MADAGASCAR
–
@@ -231,7 +245,7 @@ Miller
;
Ranomafana National Park
,
-Talatakely
+Talatakely
;
21°15′ S
,
@@ -253,7 +267,9 @@ a.s.l.
S. Larcher
and
R. Andriamasamanana
-leg.; CASENT_9016094;
+leg.;
+CASENT_9016094
+;
CAS
.
@@ -264,7 +280,7 @@ leg.; CASENT_9016094;
-
+
MADAGASCAR
–
@@ -272,17 +288,11 @@ leg.; CASENT_9016094;
•
1 ♀
-; same collection data as for holotype; [
-Standard
-view preparations and images for AToL-Spiders project; SEM preparations
-Box
-79-8, 10, 11, 19,
-Box
-81, 1, 2]; CASENT_9016094;
-CAS
+; same collection data as for holotype; [Standard view preparations and images for AToL-Spiders project; SEM preparations Box 79-8, 10, 11, 19, Box 81, 1, 2]; CASENT_9016094;
+CAS
•
-
+
1 ♂
,
1 ♀
@@ -306,33 +316,36 @@ leg.; general collecting; [habitus photos, stacked images,
Apr. 2005
-]; CASENT_9016098;
-CAS
+];
+CASENT_9016098
+;
+CAS
•
-
+
1♂
,
1 ♀
; same data as for preceding; [
♂
-palp drawn]; CASENT_9016086;
-CAS
+palp drawn];
+CASENT_9016086
+;
+CAS
•
-
+
1 ♂
,
1 ♀
-; Parc National
-Ranomafana
+;
+Parc National Ranomafana
,
Talatekely forest
,
42.3 km
-58° NE of
-Fianarantsoa
+58° NE of Fianarantsoa
;
21°15′28.0″ S
@@ -361,13 +374,17 @@ a.s.l.
E. Rajeriarison
,
V. Andriamananony
-leg.; montane rainforest; general collecting; [AToL DNA
-Voucher
-ARACG0300] [HW009/RNAlater: Mad-052]; CASENT_9024004;
-CAS
+leg.;
+montane rainforest
+; general collecting; [AToL DNA Voucher
+ARACG0300
+] [HW009/RNAlater: Mad-052];
+CASENT_9024004
+;
+CAS
•
-
+
1 ♂
;
Ranomafana
@@ -387,14 +404,16 @@ leg.; general collecting; [stacked images, HMW,
April-2005
-]; CASENT_9016097;
-CAS
+];
+CASENT_9016097
+;
+CAS
•
-
+
1 ♀
-; Parc National
-Ranomafana
+;
+Parc National Ranomafana
,
Vohiparara
,
@@ -427,13 +446,15 @@ a.s.l.
N. Scharff
and
H. Wood
-leg.; primary montane rainforest; general collecting day and night; [
-NS Photo
-voucher 893-897; GH photos 5659-5666]; CASENT_9029871;
-CAS
+leg.;
+primary montane rainforest
+; general collecting day and night; [NS Photo voucher 893-897; GH photos 5659-5666];
+CASENT_9029871
+;
+CAS
. –
-
+
Mahajanga Province
@@ -443,8 +464,8 @@ voucher 893-897; GH photos 5659-5666]; CASENT_9029871;
Ampijoroa
,
National Park Ankarafantsika
-, near
-Lake Ravelobe
+,
+near Lake Ravelobe
;
16°17′48″ S
,
@@ -459,10 +480,14 @@ voucher 893-897; GH photos 5659-5666]; CASENT_9029871;
A. Saucedo
,
H. Wood
-leg.; [SEM female epigyne + used for DNA voucher DP-2014c - “
+leg.; [SEM female epigyne + used for DNA voucher
+DP-2014c
+- “
Zorodictyna sp. 2
-”]; CASENT_9035866;
-CAS
+”];
+CASENT_9035866
+;
+CAS
.
@@ -472,7 +497,7 @@ leg.; [SEM female epigyne + used for DNA voucher DP-2014c - “
-
+
MADAGASCAR
–
@@ -483,7 +508,7 @@ leg.; [SEM female epigyne + used for DNA voucher DP-2014c - “
;
Tsinjoarivo Forest
,
-Mahatsinjo
+Mahatsinjo
;
19°40′47.496″ S
,
@@ -499,37 +524,49 @@ a.s.l.
;
B.L. Fisher
-leg.; montane rainforest; BLF35410; CASENT_9065708;
+leg.;
+montane rainforest
+; BLF35410;
+CASENT_9065708
+;
CAS
•
-
+
1 ♂
-; same data as for preceding; CASENT_9065709;
-CAS
+; same data as for preceding;
+CASENT_9065709
+;
+CAS
•
-
+
1 ♂
-; same data as for preceding; CASENT_9065678;
-CAS
+; same data as for preceding;
+CASENT_9065678
+;
+CAS
•
-
+
1 ♂
-; same data as for preceding; CASENT_9065579;
-CAS
+; same data as for preceding;
+CASENT_9065579
+;
+CAS
•
-
+
4 ♂♂
,
5 ♀♀
-; same data as for preceding; CASENT_9017817;
-CAS
+; same data as for preceding;
+CASENT_9017817
+;
+CAS
•
-
+
2 ♀♀
;
Tsinjoarivo Forest
@@ -551,11 +588,17 @@ a.s.l.
;
B.L. Fisher
et al.
-leg.; montane rainforest, sifted litter; BLF33370; CASENT_9064661;
-CAS
+leg.;
+montane rainforest
+,
+sifted litter
+; BLF33370;
+CASENT_9064661
+;
+CAS
. –
-
+
Fianarantsoa Province
@@ -569,9 +612,10 @@ leg.; montane rainforest, sifted litter; BLF33370; CASENT_9064661;
SSW of Ambositra
,
+
4.7 km
-SW of
-Ambalamanakana
+SW of Ambalamanakana
+
;
20°47′ S
,
@@ -587,37 +631,49 @@ a.s.l.
;
S. Goodman
-, SG0001 leg.; disturbed upper montane forest;
+, SG0001 leg.;
+disturbed upper montane forest
+;
pitfall traps
-#1–3; CASENT_9016064;
-FMNH
+#1–3;
+CASENT_9016064
+;
+FMNH
•
-
+
9 ♀♀
-; same data as for preceding; CASENT_9016065;
-FMNH
+; same data as for preceding;
+CASENT_9016065
+;
+FMNH
•
-
+
1 ♀
-; same data as for preceding; CASENT_9016066;
-FMNH
+; same data as for preceding;
+CASENT_9016066
+;
+FMNH
•
-
+
9 ♀♀
-; same data as for preceding; CASENT_9016067;
-FMNH
+; same data as for preceding;
+CASENT_9016067
+;
+FMNH
•
-
+
1 ♂
-; same data as for preceding; CASENT_9016068;
-FMNH
+; same data as for preceding;
+CASENT_9016068
+;
+FMNH
•
-
+
1 ♂
;
Ankazomivady
@@ -641,13 +697,17 @@ a.s.l.
;
B.L. Fisher
-leg.; forest; EBD10
+leg.;
+forest
+; EBD10
pitfall trap
-; BLF1592b; CASENT_9016087;
-CAS
+; BLF1592b;
+CASENT_9016087
+;
+CAS
•
-
+
1 ♀
;
Ambatofitorahana
@@ -666,15 +726,15 @@ S of Ambositra
;
A. Pauly
-leg.; natural forest; BE_
-RMCA
-_ARA.
-Ara.
-201626;
-RMCA
+leg.;
+natural forest
+;
+BE_ RMCA_ARA.Ara.201626
+;
+RMCA
•
-
+
24 ♂♂
,
5 ♀♀
@@ -703,22 +763,28 @@ a.s.l.
E. Elsom
and
F. Vargas
-leg.; mixed tropical forest;
+leg.;
+mixed tropical forest
+;
pitfall traps
-#4–16; COL-DHK-2001-001TN; CASENT_9003432;
-CAS
+#4–16; COL-DHK-2001-001TN;
+CASENT_9003432
+;
+CAS
•
-
+
1 ♀
-; same data as for preceding; CASENT_9003534;
-CAS
+; same data as for preceding;
+CASENT_9003534
+;
+CAS
•
-
+
1 ♀
-; Parc National
-Ranomafana
+;
+Parc National Ranomafana
,
Talatakely
;
@@ -745,20 +811,24 @@ and
D. Ubick
leg.;
pitfall traps
-; CASENT_9006115;
-CAS
+;
+CASENT_9006115
+;
+CAS
•
-
+
1 ♂
-; same data as for preceding; CASENT_9016084;
-CAS
+; same data as for preceding;
+CASENT_9016084
+;
+CAS
•
-
+
1 ♂
-; Parc National
-Ranomafana
+;
+Parc National Ranomafana
,
Talatakely
;
@@ -783,23 +853,31 @@ leg.;
J. Schweikert
,
D. Ubick
-leg.;general collecting; CASENT_9016082;
-CAS
+leg.;
+general collecting
+;
+CASENT_9016082
+;
+CAS
•
-
+
2 ♀♀
-; same data as for preceding; CASENT_9016088;
-CAS
+; same data as for preceding;
+CASENT_9016088
+;
+CAS
•
-
+
6 ♂♂
-; Parc National
-Ranomafana
+;
+Parc National Ranomafana
,
Talatakely
-, trail F;
+,
+trail F
+;
21°16′ S
,
47°25′ E
@@ -818,26 +896,32 @@ and
K.J. Ribardo
leg.;
pitfall trap
-; CASENT_9016089;
-CAS
+;
+CASENT_9016089
+;
+CAS
•
-
+
2 ♂♂
-; same data as for preceding; CASENT_9016090;
-CAS
+; same data as for preceding;
+CASENT_9016090
+;
+CAS
•
-
+
1 ♂
-; same data as for preceding; CASENT_9016093;
-CAS
+; same data as for preceding;
+CASENT_9016093
+;
+CAS
•
-
+
2 ♀♀
-; Parc National
-Ranomafana
+;
+Parc National Ranomafana
,
Vatoharanana
;
@@ -867,14 +951,20 @@ a.s.l.
J. Schweikert
,
D. Ubick
-leg.; primary forest; CEG-MA-1998-03; CASENT_9016080;
-CAS
+leg.;
+primary forest
+;
+CEG-MA-1998-03
+;
+CASENT_9016080
+;
+CAS
•
-
+
1 ♀
-; Parc National
-Ranomafana
+;
+Parc National Ranomafana
,
Vatoharanana
, trail K;
@@ -896,20 +986,24 @@ and
K.J. Ribardo
leg.;
pitfall trap
-; VFL-KJR-02; CASENT_9016091;
-CAS
+; VFL-KJR-02;
+CASENT_9016091
+;
+CAS
•
-
+
1 ♀
-; same data as for preceding; CASENT_9016092;
-CAS
+; same data as for preceding;
+CASENT_9016092
+;
+CAS
•
-
+
1 ♀
-; Parc National
-Ranomafana
+;
+Parc National Ranomafana
,
Vatoharanana River
,
@@ -932,17 +1026,23 @@ a.s.l.
;
Fisher-Griswold Arthropod Team
-leg.; montane rainforest; general day collecting; BLF8394; CASENT_9017837;
-CAS
+leg.;
+montane rainforest
+;
+general day collecting
+; BLF8394;
+CASENT_9017837
+;
+CAS
•
-
+
1 ♀
-; Parc National
-Ranomafana
+;
+Parc National Ranomafana
,
-Vohiparara
-Piste Touristique;
+Vohiparara Piste Touristique
+;
21°14′ S
,
47°24′ E
@@ -971,14 +1071,20 @@ a.s.l.
J. Schweikert
,
D. Ubick
-leg.; running in litter; general collecting; CEG-MA-1998; CASENT_9016081;
-CAS
+leg.;
+running in litter
+;
+general collecting
+; CEG-MA-1998;
+CASENT_9016081
+;
+CAS
•
-
+
6 ♂♂
;
-Ranomafana National Park
+Ranomafana National Park
,
Vohiparara
;
@@ -1002,14 +1108,18 @@ a.s.l.
E. Elsom
,
F. Vargas
-leg.; mixed tropical forest; general collecting; COL- DHK-2001-004; CASENT_9003479;
-CAS
+leg.;
+mixed tropical forest
+; general collecting; COL- DHK-2001-004;
+CASENT_9003479
+;
+CAS
•
-
+
6 ♀♀
-; Parc National
-Ranomafana
+;
+Parc National Ranomafana
,
2.3 km
@@ -1044,23 +1154,27 @@ a.s.l.
J. Schweikert
,
D. Ubick
-leg.; CASENT_9016083;
-CAS
+leg.;
+CASENT_9016083
+;
+CAS
•
-
+
6♀♀
-; same data as for preceding; CASENT_9016085;
-CAS
+; same data as for preceding;
+CASENT_9016085
+;
+CAS
•
-
+
2 ♀♀
;
Ranomafana
N.P.,
-Trail
-F;
+Trail F
+;
21°12′ S
,
47°27′ E
@@ -1074,17 +1188,23 @@ for
Kariko
,
Roth
-leg.; sifting #1; CASENT_9030889;
-MCZ
+leg.;
+sifting
+#1;
+CASENT_9030889
+;
+MCZ
•
-
+
1 ♀
;
Ranomafana
N.P.,
Maharira
-, summit;
+,
+summit
+;
21°12′ S
,
47°27′ E
@@ -1098,17 +1218,19 @@ for
Kariko
,
Roth
-leg.; cryptic #2; CASENT_9030890;
-MCZ
+leg.; cryptic #2;
+CASENT_9030890
+;
+MCZ
•
-
+
1 ♂
;
Ranomafana
N.P.,
-Trail
-M;
+Trail M
+;
21°12′ S
,
47°27′ E
@@ -1122,17 +1244,21 @@ for
Kariko
,
Roth
-leg.; sifting 1hr. samples #2; CASENT_9030891;
-MCZ
+leg.;
+sifting 1hr
+. samples #2;
+CASENT_9030891
+;
+MCZ
•
-
+
1 ♀
;
Ranomafana
N.P.,
-Trail
-M;
+Trail M
+;
21°12′ S
,
47°27′ E
@@ -1146,17 +1272,21 @@ for
Kariko
,
Roth
-leg.; sifting; CASENT_9030892;
-MCZ
+leg.;
+sifting
+;
+CASENT_9030892
+;
+MCZ
•
-
+
3 ♀♀
;
Ranomafana
N.P.,
-Trail
-B;
+Trail B
+;
21°12′ S
,
47°27′ E
@@ -1175,17 +1305,23 @@ for
Kariko
,
Roth
-leg.; sifting, #1; CASENT_9030893;
-MCZ
+leg.;
+sifting
+, #1;
+CASENT_9030893
+;
+MCZ
•
-
+
1 ♀
;
Ranomafana
N.P.,
Maharira
-, summit;
+,
+summit
+;
21°12′ S
,
47°27′ E
@@ -1199,11 +1335,15 @@ for
Kariko
,
Roth
-leg.; sifting #3; CASENT_9030894;
-MCZ
+leg.;
+sifting
+#3;
+CASENT_9030894
+;
+MCZ
•
-
+
2 ♀♀
;
Ranomafana
@@ -1219,17 +1359,27 @@ N.P.;
V. and B. Roth
,
S. Kariko
-leg.; forest; general collecting from foliage; Ranomafana-1000-92; CASENT_9016099;
-CAS
+leg.;
+forest
+;
+general collecting from foliage
+; Ranomafana-1000-92;
+CASENT_9016099
+;
+CAS
•
-
+
1 ♂
,
1 ♀
;
Ranomafana
-N.P., trail F, secondary forest;
+N.P.,
+trail F
+,
+secondary forest
+;
21°12′ S
,
47°27′ E
@@ -1243,11 +1393,15 @@ for
Kariko
,
Roth
-leg.; sifting #3; MCZ-VBR-0116; CASENT_9016100;
-MCZ
+leg.;
+sifting
+#3; MCZ-VBR-0116;
+CASENT_9016100
+;
+MCZ
•
-
+
4 ♂♂
,
7 ♀♀
@@ -1265,14 +1419,18 @@ N.P.;
V. and B. Roth
leg.;
can traps
-; MCZ-VBR-02; CASENT_9016101;
-MCZ
+; MCZ-VBR-02;
+CASENT_9016101
+;
+MCZ
•
-
+
1 ♂
-; same data as for preceding; CASENT_9016102;
-CAS
+; same data as for preceding;
+CASENT_9016102
+;
+CAS
.
@@ -1376,7 +1534,7 @@ SEM of female genitalia, A–B, E–F = female paratype (CASENT_9016094; CAS); C
. Idem, detail. Abbreviations: CD = copulatory duct; CO = copulatory opening; FD = fertilisation duct; LL = lateral lobe; ML = median lobe; S = spermatheca. Scale bars: A–E = 0.1 mm; F = 20 µm. SEM images by Diana Silva Dávila.
-
+
Description
@@ -1687,6 +1845,8 @@ Wheeler
(CASENT_9024004).
+
+
Natural history