On ant-like Synemosyna Hentz, 1846 spiders from Bolivia, with indirect evidence for polymorphic mimicry complexes (Araneae: Salticidae: Simonellini)
Author
Perger, Robert
1019F079-5C55-4467-80BE-DBB75A50F10F
Colección Boliviana de Fauna, La Paz, Bolivia. National Research Council of Argentina (CONICET), Experimental Station of Agriculture (EEA-INTA), R 14, Km 1085, Cerro Azul, Misiones, Argentina. Dept of Zoology & Entomology, University of the Free State, P. O. Box 339, Bloemfontein 9300, South Africa.
robertperger@hotmail.com
Author
Rubio, Gonzalo D.
07433A47-CD98-4C62-83D1-0568B6C98A24
National Research Council of Argentina (CONICET), Experimental Station of Agriculture (EEA-INTA), R 14, Km 1085, Cerro Azul, Misiones, Argentina.
gonzalodrubio@gmail.com
Author
Haddad, Charles R.
417ED537-9B99-48BD-B2AB-CC27E762C850
Dept of Zoology & Entomology, University of the Free State, P. O. Box 339, Bloemfontein 9300, South Africa
haddadcr@ufs.ac.za
text
European Journal of Taxonomy
2021
2021-05-05
748
1
67
88
http://dx.doi.org/10.5852/ejt.2021.748.1343
journal article
7029
10.5852/ejt.2021.748.1343
1b930930-c0cc-41e6-88dc-b26fe4a89992
2118-9773
4745113
F089DD5A-288C-40E2-B6E1-CCDEDD5A6760
Synemosyna nicaraguaensis
Cutler, 1993
Figs 3C, F
,
4C, F
,
5C–F
,
9A–D
Synemosyna nicaraguaensis
Cutler, 1993: 2
, figs 1–2.
Type deposit
Holotype
♀
in
MEL
(examined).
Fig. 5.
Genitalia of
Synemosyna
spp.
A
–B
.
S. myrmeciaeformis
(
Taczanowski, 1871
)
.
A
. Epigyne.
B
. Spermatheca and copulatory duct.
C–F
.
S. nicaraguaensis
Cutler, 1993
.
C
. Epigyne.
D
. Spermatheca and copulatory duct.
E
. Palp, retrolateral view.
F
. Idem, ventral view.
Diagnosis
Bulb small (60% of cymbium length) (
Fig. 5F
); tibial apophysis bifurcate, ventral lobe larger; epigyne with complete, sclerotized transverse hood with strongly procurved anterior margin; female spermathecae large (width of each 35–45% of maximum width of epigyne between sclerotized rims), pear-shaped, and accessory glands as long as spermatheca diameter (
Fig. 5D
).
Material examined
Holotype
NICARAGUA
–
♀
;
Río San Juan
,
El Castillo
[El Castillo de Concepción,
11°01′ N
,
84°25′ W
];
30 Jul. 1989
;
F. Reinboldt
leg.;
MEL
.
Other material
BOLIVIA
–
Santa Cruz
Dept
•
25 ♂♂
,
37 ♀♀
;
La Guardia
;
17.883º S
,
63.317º W
;
Sep. 2015
–
Aug. 2017
;
R. Perger
leg.;
CBF
• •
2 ♂♂
,
2 ♀♀
; same collection data as for preceding;
IBSI-Ara 0724
•
1 ♀
;
Buena Vista
;
17.465º S
,
63.696º W
;
21 Jan. 2016
;
R. Perger
leg.;
IBSI-Ara 0725
•
2 ♀♀
; same collection data as for preceding;
CBF
•
5 ♂♂
,
8 ♀♀
;
Santa María La Antigua
;
17.3719° S
,
63.6563° W
;
10–11 Apr. 2018
;
R. Perger
leg.;
CBF
. –
La Paz
Dept
•
2 ♂♂
,
6 ♀♀
;
Villa Teresa
;
16.201º S
,
67.829º W
;
17 Jan. 2018
;
R. Perger
leg.;
IBSI-Ara 1023
•
3 ♂♂
,
8 ♀♀
; same collection data as for preceding;
16–18 Jan. 2018
;
R. Perger
leg.;
CBF
.
Comparisons
The bifurcated tibial apophysis is only shared with
S. maddisoni
Cutler, 1985
and
S. paraensis
Galiano, 1967
. However, both species can be separated from
S. nicaraguaensis
by a larger bulb (65% of cymbium length in
S. maddisoni
and 80% in
S
.
paraensis
) and the different size and shape of the lobes of the retrolateral tibial apophysis (cf.
Fig. 5F
with
Chamé-Vázquez
et al.
2020
: figs 14–15). The female habitus (
Fig. 4C
) and the almost round spermathecae (
Fig. 5D
) are shared with the female of
S. maddisoni
.
Females of
S. maddisoni
can be distinguished from those of
S. nicaraguaensis
by an epigyne with a U-shaped flap, which is wide and short in
S. nicaraguaensis
(compare
Fig. 5C
with
Chamé-Vázquez
et al.
2020
: fig. 11).
The habitus of females of
S. nicaraguaensis
resembles that of
S. hentzi
Peckham & Peckham, 1892
(
Peckham & Peckham 1892
: pl. 7 fig. 2).
Synemosyna hentzi
was described very briefly based on a single female that was collected in Chapada dos Guimarães, close to Cuiabá,
Mato Grosso state
,
Brazil
, and maintained in the Herbert H. Smith collection (
Peckham & Peckham 1892
), but the
type
specimen appears to be lost (
Galiano 1971
). No description or illustration of the genitalia was provided, and no further specimens of this species were recorded in subsequent works. Considering the original description (
Peckham & Peckham 1892
),
S. hentzi
differs from
S. nicaraguaensis
by a broader, less elongated carapace, 2 times longer than wide (
2.5 in
S. nicaraguaensis
), with the lateral borders parallel (with a slightly narrower constriction in
S. nicaraguaensis
) and without a dorsal constriction (present in
S. nicaraguaensis
), the AER only slightly curved (strongly in
S. nicaraguaensis
), and the ALE and AME touching each other (separated in
S. nicaraguaensis
).
Description
Male
(IBSI-Ara 0724)
Total BL: 4.60. Carapace length 2.05; width: 0.81. Integument smooth, shiny, with simple, separate white setae, denser and longer on cephalic area (particularly around AME), posterior constriction of thoracic area, and on transverse area of anterior part of abdomen. Carapace slender and elongated, cephalic portion slightly longer than wide, followed by slightly narrower constriction, slight impression behind cephalic area (resembling anterior pronotal margin); dense white scales posterolateral of cephalic area, thoracic part about as long as cephalic part, of same width, globose, posteriorly constricted, constriction concave in lateral view. Row of AME and ALE recurved, AME touching each other, separated from ALE, ALE at anterior edges of cephalic area, rectangle of ALE and PE 1.5 times as wide as long. Chelicerae with 2 promarginal and 5 retromarginal teeth. Sternum dark brown. Coxae and trochanters translucent whitish; legs relatively long, 4312; femora stout, remaining segments slender, femora I–III translucent yellowish, I and III somewhat darker distally, IV proximally and distally as in anterior part of abdomen, central half translucent yellowish; tibia I simple, with moderately long setae.
Abdomen length: 2.50; width: 0.70, proximal half broadening in distal direction in dorsal view, proximal and distal half of abdomen separated by concave constriction, distal part of abdomen acuminate oval. Dorsal scutum almost extending along the whole length of abdomen, rectangular proximally, merging into disc-shaped, heavily sclerotized plate on distal half of anterior abdominal part, proximal part of plate surrounded by band of short white setae; scutum narrowing at level of abdominal constriction and widening again on distal half of abdomen, terminating shortly before abdominal apex; epigastric scutum folded over dorsolateral border of anterior part of abdomen, covering somewhat lateral sides of scutum.
Fig. 6. A–D
. Color variants and potential model ants for
Synemosyna aurantiaca
(
Mello-Leitão, 1917
)
.
A
. Orange female, Santiago de Chiquitos, Santa Cruz Dept.
B
. Reddish brown female, Cotoca, Santa Cruz Dept.
C
. Reddish brown male, Bermejo, Santa Cruz Dept.
D
. Dark brown male, Arambulo, Tarija Dept.
E
.
Pseudomyrmex simplex
(Smith, 1877)
.
F
.
P. filiformis
(Fabricius, 1804)
.
G
.
P
.
elongatus
(Mayr, 1870)
.
H
.
P. gracilis
(Fabricius, 1804)
.
Bulb about 60% of the cymbium length, ovoid, narrowing proximally, tibial apophysis bifurcate, ventral tooth larger; embolus thin, arising from the basal side of the bulb, without complete circular revolution, angular, surrounding bulb prolaterally towards the apical cymbial groove.
Variation
Four different color morphs were observed in males (
Fig. 9B–D
,
Table 1
), with no apparent ontogenetic change in body color. The forms included orange-reddish, completely light brown or dark brown forms (all locations), and variants with dark orange carapace and black abdomen (La Guardia and Villa Teresa). In a sample of
51 females
, 92% were orange with a pair of black spots on the posterior half of the abdomen (
Fig. 9A
), and 8% dark brown. Orange males with dark spots on their abdomen were not observed. The comparably even distribution of color forms among males, the high number of orange females, and the lack of orange forms with black abdominal spots in males indicate sex-specific polychromatism.
Geographical and ecoregion distribution
(
Fig. 7
)
Synemosyna nicaraguaensis
is known from
Nicaragua
(
type
location) and
Bolivia
(present study). In
Bolivia
, it was collected in the following forest
types
: Bolivian Yungas forest (Villa Teresa), Sub-Andean Southwest Amazon moist forest (Buena Vista), and Sub-Andean subhumid semi-deciduous Chiquitano forest (La Guardia, Santa María la
Antigua
).
Fig. 7.
Ecoregion distribution of
Synemosyna
spp.
Orange circle =
S. nicaraguaensis
Cutler, 1993
; red star =
S. myrmeciaeformis
(
Taczanowski, 1871
)
; blue diamond =
S. aurantiaca
(
Mello-Leitão, 1917
)
.
Table 1.
Co-occurrence pattern of Bolivian
Synemosyna
Hentz, 1846 species
and potential model species of
Pseudomyrmex
Lund, 1831
(only localities with a sample size higher than n = 12 were considered):
S. aurantiaca
(
Mello-Leitão, 1917
)
(I) 2.5–5.5 mm (orange-reddish); (II) 4.6–6.4 mm (light brown); (III) 5.8–7.0 mm (dark brown/blackish);
S. myrmeciaeformis
(
Taczanowski, 1871
)
(I) 3.1–6.7 mm (orange); (II) 6.0–8.0 mm (dark brown or orange with black cephalic part);
S. nicaraguaensis
Cutler, 1993
(I) male 2.65–5.85 mm (orange-reddish); (II) male 3.45–5.85 mm (brownish); (III) male 3.84–5.05 mm (orange carapace and blackish abdomen); (IV) female 3.45–5.2 mm (orange). Abbreviations: A = Arambulo; C = Cotoca; L = La Guardia; S = Santa María La Antigua; V = Villa Tunari; VT = Villa Teresa. Please note that orange and brown forms of
Pseudomyrmex triplarinus
(Weddell, 1850)
were observed. Body length of
Pseudomyrmex
spp.
:
P. simplex
(Smith, 1877) BL
3.7–4.5 mm;
P
. cf.
pallidus
(Smith, 1855) BL
3.3-3.95 mm;
P. triplarinus
(Weddell, 1850)
(BL 4.8–6.7 mm);
P. sericeus
(Mayr, 1870) BL
4.4– 5.05 mm;
P. elongatus
(Mayr, 1870) BL
2.9–3.8 mm;
P. phyllophilus
(Smith, 1858) BL
4.9–5.1 mm;
P
. cf.
filiformis
(Fabricius, 1804) BL
4.6–5.2 mm;
P. peruvianus
(Wheeler, 1925)
(BL 3.0–3.5 mm);
P. gracilis
(Fabricius, 1804) BL
6.7–11.0 mm;
P. tenuis
(Fabricius, 1804) BL
5.3–7.0 mm.
S. aurantiaca
|
S. myrmeciaeformis
|
S. nicaraguaensis
|
Potential ant model
|
I
|
II
|
III
|
I
|
II
|
I
|
II
|
III
|
IV
|
Orange forms
|
P. simplex
(Smith, 1877)
|
A, C |
VT, R, V |
L, VT, S |
P.
cf.
pallidus
(Smith, 1855)
|
L, VT, S |
P. triplarinus
(Weddell, 1850)
|
L, S |
Brownish forms
|
P. sericeus
(Mayr, 1870)
|
L, VT, S |
P. elongatus
(Mayr, 1870)
|
A, C |
L, VT, S |
P. phyllophilus
(Smith, 1858)
|
A, C |
L |
P.
cf.
filiformis
(Fabricius, 1804)
|
A, C |
L, VT |
P. peruvianus
(Wheeler, 1925)
|
VT |
P. triplarinus
(Weddell, 1850)
|
VT |
VT |
P. gracilis
(Fabricius, 1804)
|
A, C |
VT |
Orange body/black head
|
P. tenuis
(Fabricius, 1804)
|
R, V |
Remarks
The localities in
Nicaragua
and
Bolivia
are more than
3500 km
apart, which is remarkable for such a small arthropod, and would suggest a certain degree of reproductive isolation between both populations. However, the epigyne (examined from drawings by
Cutler 1993
) and external morphology (examined from photographs of the
type
) are similar in the
type
specimen of
S. nicaraguaensis
and the Bolivian material. Another species with a wide distributional range,
S. americana
, occurs from
Mexico
to
Venezuela
(
Cutler 1981b
). The other two Bolivian species of
Synemosyna
have also comparably wide distribution ranges (
Fig. 7
). The widest collection locations of
S. aurantiaca
are about
2200 km
apart, and of
S
.
myrmeciaeformis
about
3100 km
. Molecular studies are needed to test whether the low grade of morphological differentiation in these species represents a high gene flow.