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MUSEU PARAENSE EMÍLIO GOELDI
UNIVERSIDADE FEDERAL DO PARÁ
PROGRAMA DE PÓS-GRADUAÇÃO EM ZOOLOGIA
CURSO DE MESTRADO EM ZOOLOGIA
Revisão do Gênero Neoxyphinus Birabén 1953 (Araneae, Oonopidae)
NAIARA ABRAHIM DOS SANTOS
Dissertação de mestrado apresentada ao Programa de
Pós-graduação em Zoologia, Curso de Mestrado, do
Museu Paraense Emílio Goeldi e Universidade
Federal do Pará como requisito parcial para obtenção
do grau de mestre em Zoologia.
Orientador: Dr. Alexandre Bragio Bonaldo
BELÉM – PARÁ
2009
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NAIARA ABRAHIM DOS SANTOS
Revisão do Gênero Neoxyphinus Birabén 1953 (Araneae, Oonopidae)
Dissertação de mestrado apresentada ao Programa de
Pós-graduação em Zoologia, Curso de Mestrado, do
Museu Paraense Emílio Goeldi e Universidade
Federal do Pará como requisito parcial para obtenção
do grau de mestre em Zoologia
Orientador: Dr. Alexandre Bragio Bonaldo
BELÉM – PARÁ
2009
ads:
NAIARA ABRAHIM DOS SANTOS
Revisão do Gênero Neoxyphinus Birabén 1953 (Araneae, Oonopidae)
________________________________________________
Dr. Alexandre Bragio Bonaldo
Orientador
Departamento de Zoologia, Museu Paraense Emílio Goeldi
________________________________________________
Dr. Arno Antonio Lise
Titular
Instituto de Biociências, Pontifícia Universidade Católica do Rio Grande do Sul
________________________________________________
Dr. Ricardo Ott
Titular
Setor de Invertebrados, Fundação Zoobotânica do Rio Grande do Sul
________________________________________________
Dr. Martín J. Ramírez
Titular
Division de Arachnología, Museo Argentino de Ciencias Naturales
________________________________________________
Dr. Gustavo Hormiga
Titular
Department of Biological Sciences, George Washington University
________________________________________________
Dra. Lara Lopardo
Titular
Department of Biological Sciences, George Washington University
BELÉM – PARÁ
2009
i
“Eu poderia suportar,
embora não sem dor,
que tivessem morrido
todos os meus amores...
mas enlouqueceria
se morressem
todos os meus amigos!”
Vinícius de Moraes
ii
Dedico este trabalho
à José Augusto Pereira Barreiros,
o querido Guto,
por todo ensinamento, apoio e amor
que recebi em sua breve passagem pela Terra.
iii
AGRADECIMENTOS
À José Augusto Pereira Barreiros, ou apenas Guto, como todos o
chamavam, por ter sido o grande incentivador e responsável pela minha
entrada no mestrado, estando sempre ao meu lado, me dando apoio, carinho,
fornecendo bibliografias e até aulas de inglês! Muito obrigada, meu amor, por
você ter acontecido em minha vida!!
Ao meu orientador, Dr. Alexandre Bragio Bonaldo, pelos ensinamentos,
por ter acreditado na realização deste trabalho mesmo quando eu não sabia
nem por onde começar, por me mostrar que eu deveria seguir em frente e dar
continuidade a este trabalho apesar de tudo, e principalmente, agradeço por
toda paciência dedicada a mim.
Ao Programa de Pós-graduação em Zoologia do convênio Universidade
Federal do Pará e Museu Paraense Emílio Goeldi por ter me dado a
oportunidade de agregar conhecimentos através deste mestrado.
Ao CNPq pela bolsa concedida no decorrer deste curso.
À equipe do Projeto “Planetary Biodiversity Inventory of “Globin Spiders”
– PBI Oonopidae”, na pessoa do Coordenandor geral, Dr. Norman I. Platnick
(AMNH), por prover as condições para a realização deste trabalho e
proporcionar minha participação na expedição para Soutpansberg, África do
Sul.
À todos os curadores das instituições de pesquisa que gentilmente me
enviaram material: Antonio Brescovit (IBSP), Luis Pereira (MLP), Martín
Ramírez e Cristian Grismado (MACN), Norman Platnick (AMNH); Erica Buckup
(MCN); Arno Lise (MCTP); Ricardo Pinto da Rocha (MZSP) e Hubert Höefer
(SMNK). Aos pesquisadores Cristina Rheims, por ter feito fotos maravilhosas de
iv
meus bichos, que lhe custaram horas intermináveis na frente do Photoshop, e
Adalberto Santos, por ter me trazido importante material que eu ainda não
havia examinado.
Aos colegas de laboratório do Museu Goeldi, pela convivência agradável e
construtiva ao longo destes anos.
Aos colegas do Laboratório de Artrópodes do Instituto Butantan que me
receberam por duas vezes quando fui visitar a coleção.
Aos amigos que contribuíram de alguma forma para a conclusão deste
trabalho, em especial aqueles que “salvaram minha vida” nos últimos dias,
pois sem eles, tenho plena consciência de que eu não teria conseguido
terminar: Marcela, Nayane, Amanda, Adriano e David.
Aos amigos-companheiros-irmãos da minha turma de mestrado, por
terem estado comigo nos piores e melhores momentos destes últimos dois
anos, me dando colo e motivos para rir quando eu só pensava em chorar:
Amanda, Fernanda, Marcela, Silvia (as quais amo de todo coração e que se
tornaram minhas irmãzinhas, afinal, “nóis semo tudo parênteses”, né Silvia?),
Adriano, Alexandro, Laura, Lincoln, Marcelo, Marina e Pedro. E a todos os
“agregados” da nossa turma, com os quais pude compartilhar histórias para
uma vida.
À mãe e irmão do Guto, dona Consola e Fábio, por terem me confortado
diversas vezes e incentivado meu mestrado proporcionando minha ida ao
Congresso Internacional de Aracnologia em São Paulo.
À minha família, por sempre acreditar em mim e ter me dado apoio e
colo nos momentos mais difíceis. Em especial à minha mãe, Clotilde Abrahim,
que mesmo estando longe sempre foi a pessoa mais presente em minha vida.
E ao Rômulo Souza, por ter trazido o sorriso de volta ao meu rosto e a
paz ao meu coração!
1
Introdução Geral
O presente projeto se insere no contexto de uma grande iniciativa
internacional, o Inventário Planetário da Família Oonopidae (Planetary Biodiversity
Inventory (PBI) – The Megadiverse, Microdistributed Spider Family Oonopidae)
(http://research.amnh.org/oonopidae/). Este projeto, coordenado pelo American
Museum of Natural History e financiado pela National Science Foundation (EUA)
com recursos garantidos até 2010, parte do princípio de que o inventário da
biodiversidade pode ser feito em escala mundial através da escolha de grupos-
alvo de organismos, em oposição à visão corrente de que os inventários biológicos
devem ser baseados em uma determinada área geográfica, ecossistema ou
bioma. As vantagens de tal abordagem em relação aos inventários tradicionais
foram listadas por Platnick (1999), com destaque para o fato de que a
caracterização da biodiversidade de um determinado grupo biológico em uma
escala global fornece um contexto ideal para a compreensão da história evolutiva
dos organismos. O PBI - Oonopidae reúne equipes de cientistas de 19 instituições
na África do Sul, Alemanha, Argentina, Austrália, Bélgica, Brasil, China, Estados
Unidos, Suíça, Finlândia e Holanda, com o objetivo de revisar a taxonomia da
família Oonopidae Simon, 1890 em uma escala planetária, promovendo revisões
de gêneros baseadas em preceitos modernos, descrevendo o maior número
possível de espécies novas, propondo hipóteses robustas de relacionamento
filogenético e procurando compreender padrões biogeográficos.
2
A família Oonopidae Simon 1890 é composta por aranhas distribuídas em
todo o globo, atingindo sua maior diversidade nos trópicos. São animais cursoriais
noturnos, com até quatro milímetros de comprimento total, encontrados tanto na
serapilheira quanto no dossel (Jocqué and Dippenaar-Schoeman, 2006).
Atualmente são conhecidas 512 espécies distribuídas em 75 gêneros (Platnick,
2009). Entretanto, dados preliminares do projeto PBI Oonopidae indicam que as
espécies atualmente conhecidas representam apenas cerca de 20% da
diversidade real da família. Os oonopídeos podem ser reconhecidos pela
combinação dos seguintes caracteres: olhos ausentes ou em número de dois ou
seis; duas unhas tarsais denteadas biserialmente, onychium conspícuo; genitália
haplógina, cribelo ausente e aberturas traqueais posteriores posicionadas
anteriormente (Dippenaar-Schoeman & Jocqué, 1997). A presença de escudos
ventral e dorsal sustenta a divisão da família nas subfamílias Oonopinae, onde
estes escudos estão ausentes, e Gamasomorphinae, na qual pelo menos o
escudo ventral está presente. No entanto, o monofiletismo destas subfamílias
ainda não foi testado (Platnick, 2000). A classificação mais antiga, de Simon
(1893), dividia a família em dois grupos, Molles e Loricatæ, os quais são
aproximadamente correspondentes às subfamílias atuais Oonopinae e
Gamasomorphinae, respectivamente.
A taxonomia de Oonopidae é notoriamente repleta de erros e confusões
acerca da validade e posicionamento de seus táxons, tanto em nível específico
como genérico. Diversos gêneros descritos originalmente nesta família foram
transferidos para outras, como por exemplo, Ascuta Forster 1956, Cornifalx
3
Hickman 1979, Duripelta Forster 1956, Pounamua Forster 1956, Subantarctia
Forster 1955 e Tasmanoonops Hickman 1930, transferidos para Orsolobidae
(Foster and Platnick, 1985); Gmogala Keyserling 1890 e Hadrotarsus Thorell 1881,
transferidos para Hadrotarsidae por Roewer (1963), família depois considerada um
sinônimo júnior de Theridiidae (Foster et al., 1990). Um caso extremo foi o do
gênero Brucharachne Mello-Leitão 1925, descrito como um Oonopidae
mirmecófilo e removido da ordem Araneae por se tratar de um ácaro (Krantz and
Platnick, 1995).
Birabén (1953) estabeleceu o gênero Neoxyphinus, que foi assim
denominado por estar, para o autor, claramente vinculado ao gênero asiático
Xyphinus Simon 1893, pela presença de características somáticas semelhantes,
como os quatro grandes tubérculos localizados na região posterior do cefalotórax
(Simon, 1893; Deeleman-Reinhold, 1987). A espécie-tipo N. ogloblini Birabén 1953
foi descrita com base em material proveniente de Loreto, Misiones, Argentina.
Estas aranhas são facilmente reconhecíveis pela presença de quatro curtos e
robustos tubérculos posteriores na carapaça. Birabén (1953) transferiu para
Neoxyphinus a espécie Dysderina xyphinoides Chamberlain and Ivie 1942 que
apresenta 6 tubérculos na região posterior da carapaça. Outra espécie descrita em
Dysderina, D. termitophila Bristowe 1938, apresenta também 4 destes tubérculos,
porém, não foi mencionada pelo autor. No entanto, Brignoli (1983) levantou a
suspeita de que N. ogloblini seja um sinônimo júnior de D. termitophila, já que as
duas espécies têm distribuição geográfica semelhante e possuem igual
ornamentação na carapaça, sendo os tubérculos em mesmo número e tamanho.
4
Esta suposição não foi tratada como uma proposição formal de sinonímia no
catálogo de Platnick (2009).
O gênero Decuana foi proposto por Dumitrescu and Georgescu (1987) para
abrigar a espécie-tipo (por monotipia) D. hispida Dumitrescu and Georgescu 1987,
descrita com base em machos e fêmeas de Rancho Grande, Venezuela. D.
hispida possui minúsculos tubérculos na região posterior da carapaça e espinhos
na região anterior do escudo dorsal do abdômen. Estes processos são mais
robustos nos machos que nas fêmeas (Dumitrescu and Georgescu, 1987).
No decorrer deste trabalho, foram encontradas espécies não descritas de
Neoxyphinus cujos espécimes apresentam tanto os robustos tubérculos da
carapaça quanto os espinhos do dorso do abdômen, características de
Neoxyphinus e Decuana, respectivamente. Esta evidência levou a constatação de
que os minúsculos tubérculos na região torácica de D. hyspida são homólogos aos
grandes tubérculos em formato de espinho presentes em espécies de
Neoxyphinus, Adicionalmente, D. hyspida apresenta outras características
somáticas compartilhadas por espécies de Neoxyphinus: pedicelo longo e
profundamente corrugado; enditos com uma escavação apical retrolateral que
apresenta uma apófise curvada em formato de dente subapical, acompanhados de
uma cerda simples e um sensor tegumentar em fenda; palpo do macho com tégulo
fusionado ao címbio e extremamente inflado; êmbolo em forma de S, sendo
compacto com base escavada e uma projeção apical. Estas características
sustentam a hipótese de que Decuana é um sinônimo júnior de Neoxyphinus e a
sinonímia destes gêneros é proposta no capítulo seguinte.
5
Apresenta-se a revisão taxonômica do gênero Neoxyphinus, formatada de
acordo com as normas do periódico “American Museum Novitates”, com a
redescrição das três espécies conhecidas e a descrição de seis espécies novas,
procedendo-se à transferência de Decuana hyspida e Dysderina termitophila para
Neoxyphinus e a sinonímia de Neoxyphinus ogloblini com N. termitophilus.
Referências Bibliográficas
Birabén, M. 1953. Neoxyphinus. Nuevo género de arañas de la familia Oonopidae.
Physis B. Aires 20: 453-458.
Brignoli, P. M. 1983. A catalogue of the Araneae described between 1940 and
1981. Manchester Univ. Press, 755 pp.
Bristowe, W. S. 1938. Some new Termitophilous Spider frow Brazil. An. And Meag.
Of Nat. Hist., Ser. 11, vol ii. P. 67.
Chamberlin, R. V. and W. Ivie. 1942. A hundred new species of American spiders.
Bull. Univ. Utah 32(13): 1-117.
Deeleman-Reinhold, C. 1987. Revision of the Genus Xyphinus Simon (Araneae:
Oonopidae). Acta Arachnologica, 35 (2): 41-56
Dippenaar-Schoeman, A. S. and Jocqué, R. 1997. African Spiders: An
Identification Manual. Plant Protection Res. Inst. Handbook, no. 9,
Pretoria, 392 pp.
6
Dumitresco, M. and M. Georgesco 1987: Quelques représentants de la famille
Oonopidae (Araneae) du Venezuela. In Fauna hipogea y hemiedáfica
de Venezuela y de otros paises de América del Sur 1: 89-105.
Forster, R. R. and N. I. Platnick 1985. A review of the austral spider family
Orsolobidae (Arachnida, Araneae), with notes on the superfamily
Dysderoidea. Bull. Am. Mus. nat. Hist. 181: 1-230.
Forster, R. R., Platnick N. I. and Coddington, J. 1990.A Proposal and Review of the
Spider Family of Synotaxidae (Araneae, Araneoidea), with Notes on
Theridiid Interrelationships. Bull. Am. Mus. nat. Hist.193: 116 p.
Jocqué, R and Dippenaar-Schoeman, A. S. 2006. Spider Families of the World.
Royal Museum for Central Africa, Tervuren, 336 pp.
Krantz, G. W. and Platnick, N. I. 1995. On Brucharachne, The Spider That Wasn't
(Arachnida, Acari, Dermanyssoidea). Americam Museum Novitates
3151: 1-8.
Platnick N I. 1999. Dimensions of Biodiversity: Targeting Megadiverse Groups.
Pages 33–52 in The Living Planet: Biodiversity Science and Policy,
edited by J Cracraft and F T Grifo. New York: Columbia University
Press.
Platnick, N. I. 2000. On Coxapopha, a New Genus of Spider Family Oonopidae
from Panama (Araneae Haplogynae). Mem. Soc. Entomol. Ital. 78(2):
403-410.
7
Platnick, N. I. 2009. The world spider catalog, version 9.5. American Museum of
Natural History, online at
http://research.amnh.org/entomology/spiders/catalog/index.html
Roewer, C. Fr. 1963: Roewer, C. F. 1963. Araneina: Orthognatha, Labidognatha.
Insects Micronesia 3: 104-132.
Simon, E. 1893. Histoire naturelle des araignées. Paris, 1: 257-488.
8
“Clap! Snap! The black crack!
Grip, grab! Pinch, nab!
And down down to goblin-town
You go, my lad!”
From J. R. R. Tolkien’s “The Hobbit”
9
A Review of the Neotropical Goblin Spider Genus Neoxyphinus Birabén 1953
(Araneae, Oonopidae)
ABSTRACT
The Neotropical genus Neoxyphinus Birabén 1953 is revised, comprising
nine species found from Venezuela to northern Argentina. The monotypic genus
Decuana Dumitrescu and Georgescu 1987 is synonymized with Neoxyphinus and
its type species, D. hyspida Dumitrescu and Georgescu 1987, is transferred to this
genera. Confirming suspicions rose in literature, Dysderina termitophila Bristowe
1938 is transferred to Neoxyphinus and recognized as senior synonym of N.
ogloblini Birabén 1953. Six new species are described, all of which known from
both sexes: N. petrogoblin, from Amazonas, Brazil and Huanuco, Peru; N.
gregoblin, from Andres Bello, Venezuela; N. axe, from Bahia, Brazil; N. barreirosi,
from north Brazil; N. brega, from Brazil, Colombia, Guyana and Venezuela and N.
caterete, from São Paulo, Brazil.
10
INTRODUCTION
The present contribution is part of the Goblin Spider Planetary Biodiversity
Inventory (PBI Oonopidae), which aims to advance the taxonomic and
phylogenetic knowledge of the family Oonopidae in a world-wide basis
(http://research.amnh.org/oonopidae/; see also Platnick, 1999, for an account of
the advantages of the PBI approach over traditional area-based multi-taxonomic
inventories).
Perhaps because their small size (up to 4 mm in length; Tong and Li, 2008)
oonopids are among the poorest known spiders and are often difficult to identify to
the species level. This is especially true for South American oonopids, which are
currently known by only 75 species (see Platnick, 2009). A quick review of recent
papers reporting area-based inventories of Brazilian spiders (e. g. Bonaldo et al.,
2007; Dias and Bonaldo, in press; Brescovit, et al., 2004), shows that the current
level of taxonomic understanding of South American oonopids is particularly poor.
The faunistic lists provided by these papers have extremely low taxonomic
resolution regarding Oonopidae, which are at best identified to genus. One of the
few genera which are readily identified and almost always present in such lists is
Neoxyphinus, proposed by Birabén (1953) to include two South American
Gamasomorphinae species, both with a striking set of large posterior spine-like
tubercles (spikes) in the carapace. The generic name is a reference to the Asian
genus Xyphinus Simon 1893, which presents similarly modified tubercles. In X.
hystrix Simon 1893, for instance, there are two long, curved spikes in the posterior
11
margin of the carapace and two shorter ones at the middle of the posterior surface
(Simon, 1893; Deeleman-Reinhold, 1987). Although hypotheses of phylogenetic
relationship between Oonopidae genera are yet unavailable, these two groups
might not be closely related since the genitalic structures are completely different.
The phylogenetic knowledge of Oonopidae is still superficial and despite the
recent findings supporting monophyly of the family (Burger and Michalik, in press),
the monophyly of the two classical oonopid subfamilies (Oonopinae and
Gamasomorphinae) is yet to be tested (Platnick and Dupérré, in press). This
scenario prevents accurate statements about the placement of Neoxyphinus.
However, the genitalic morphology and even the posterior ornamentation of the
carapace suggest a close relationship to another neotropical genus, Dysderina
Simon 1891.
The type species of Neoxyphinus, N. ogloblini Birabén 1953, from Loreto
(Misiones, Argentina), has four similarly sized spikes in the posterior surface of the
carapace. Dysderina termitophila Bristowe 1938, a species found in termite nest
galleries of Nasutitermes arenarius (Hagen and Bates), in Santa Catarina (Brazil),
also has four carapace spikes, but was overlooked by Birabén. Brignoli (1983)
suspected that N. ogloblini could be a synonym of D. termitophila, probably due to
the geographic proximity of the type localities and by the similar carapace spikes.
This assumption was not treated as a formal synonymy proposition (Platnick,
2009). The single additional species described in the genus so far, N. xyphinoides
(Chamberlin and Ivie, 1942), from Kartabo (British Guyana) transferred from
12
Dysderina by Birabén (1953), has six spikes: two pairs of marginal ones joined
together by the base and one additional pair at the middle of the posterior surface.
An additional generic name is also relevant to the present study. The
monotypic genus Decuana was proposed by Dumitrescu and Georgescu (1987) to
include D. hispida Dumitrescu and Georgescu 1987, described from males and
females from Rancho Grande, Venezuela. This species has small, undeveloped
posterior carapace tubercles and the anterior half of the abdominal dorsal scutum
has several projecting denticles, features which lead the authors to propose the
genus. These denticles are more robust in males than in females (Dumitrescu and
Georgescu, 1987) and, just as the carapace tubercles, are modifications of hair
sockets.
In the course of this study, specimens presenting both large carapace
spikes and projected abdominal denticles were found (Figs. 1 - 4). This is a strong
evidence that Decuana is a junior synonym of Neoxyphinus. The carapace
tubercles are clearly homologous in D. hispida and in the typical Neoxyphinus
species, regardless its development level (small, low, as in Figs 5 - 8 or large,
spine-like, as in Fig. 9 - 12). Besides, scanning electronic microscope surveys
showed that most forms of Neoxyphinus, including its type species, present more
or less modified hair sockets on anterior half of the abdominal dorsal scutum (Figs.
78, 143, 205). On the other hand, some of the species newly described below do
not present either abdominal dorsal denticles or carapace spikes and are assigned
to Neoxyphinus based solely in genitalic and male endites characters.
13
The posterior carapace ornamentation, represented by a procurve arch of
hair-bearing tubercles, appears to be consistent across all Neoxyphinus species,
but it is not restricted to the genus. At least some species of Dysderina present a
similar arched set of hair-bearing tubercles. This feature, in addition to the inflated,
completely fused bulbus and the large epigynal atrium, could even support a claim
for the synonymy of Neoxyphinus with Dysderina. However, the genitalic
morphology of Dysderina, including that of its type species, D. principalis
(Keyserling 1881) (see Chickering, 1968), is different from that presented by
Neoxyphinus species. In Dysderina, the embolus is prominent, often bearing
additional pieces, and the epigynal atrium has rounded laterals, while in
Neoxyphinus the embolus is a compact single piece, with a large ejaculatory
opening, and the epigynal atrium has angled laterals. Notwithstanding, it is not
clear at this point if the maintenance of Neoxyphinus turns Dysderina, as presently
constituted, a paraphyletic group. This is a question to be addressed in the context
of a yet to be done phylogenetic analysis of Gamasomorphinae genera.
In the present paper, the genus Neoxyphinus is revised and diagnosed
based mostly on genitalic morphology. Neoxyphinus is considered the senior
synonym of Decuana and nine species are included, six of them newly described.
14
MATERIAL AND METHODS
Specimens were examined using a Zeiss Stemi SV 11 and LEICA MZ16
stereomicroscopes at Museu Paraense Emílio Goeldi, Belém (MPEG). Compound
photographic images of body parts were produced using a Leica MZ16A motorized
stereomicroscope with a DFC500 camera and assembled with the Leica
Application Suite software package at Instituto Butantan, São Paulo (IBSP).
Female genitalia were prepared following the digesting protocol by Álvarez-Padilla
and Hormiga (2007). Detached male palpi and female genitalia were observed in
temporary slide-mounts (Coddington, 1983), with a compound microscope.
Specimen parts were prepared for scanning electron microscopy (SEM) by
cleaning in an ultrasonic digital washer SoniClean 2P for few seconds, dehydrated
through stages of 80% to 100% ethanol and exposed to gently warm light for
drying. SEM images were taken with a LEO 1450VP scanning electronic
microscope at MPEG. Descriptions were generated through the goblin spider PBI
descriptive database and shortened where possible. Maps were generated with
ArcMap version 9.2 from ArcGis 9. All measurements are in millimeters and were
made upon photographs taken at MPEG with a DFC420 camera in a Leica MZ16
stereomicroscope, using the Leica IM50 software. Total body length variation was
taken from up to ten specimens of both sexes whenever possible. The specimens
examined for this study belong to the following collections: American Museum of
Natural History, New York (AMNH, N. I. Platnick); Instituto Butantan, São Paulo
(IBSP, A. D. Brescovit); Museo Argentino de Ciencias Naturales "Bernardino
15
Rivadavia", Buenos Aires (MACN-Ar, C.L. Scioscia); Museu de Ciências Naturais,
Fundação Zoobotânica do Rio Grande do Sul, Porto Alegre (MCN, E. H. Buckup);
Museu de Ciência e Tecnologia da PUCRS, Porto Alegre (MCTP, A. A. Lise);
Museu Paraense Emílio Goeldi, Belém (MPEG, A. B. Bonaldo); Museo de La Plata
(MLP, L. A. Pereira); Museu de Zoologia, Universidade de São Paulo, São Paulo
(MZSP, R. Pinto da Rocha) and Staatliches Museum für Naturkunde Karlsruhe,
Karlsruhe (SMNK, H. Höefer).
SYSTEMATICS
Neoxyphinus Birabén
Neoxyphinus Birabén 1953:454 (type species by original designation, Neoxyphinus
ogloblini Birabén 1953).
Decuana Dumitrescu and Georgescu 1987: 92 (type species by original
designation, Decuana hispida Dumitrescu and Georgescu 1987). NEW
SYNONYMY.
DIAGNOSIS: Species of Neoxyphinus differ from all other Gamasomorphinae
genera by the combination of the following features: carapace posterior surface
with a procurve set of hairs, which are originated from small, low tubercles (Figs. 5
– 8) or from large spikes (Figs. 9 -12); ribbed pedicel tube (Figs. 13 – 18); male
16
endites with an apical, retrolateral excavation bearing a sub-apical teeth-like,
curved apophysis, accompanied by a single hair and a slit sensilla (Figs. 25 – 30);
males with unarmed femora (Fig. 32); palpal bulb strongly inflated, completely
fused to cymbium (Figs. 37 – 44); embolus a compact, “s”-shaped sclerite, with an
excavated basis and an apical projection (Figs. 45 – 53); ejaculatory opening large,
round, located prolaterally (Fig. 53, 68, 233, 270), or apically (Fig. 303); epyginal
atrium large, ellipsoid, strongly rebordered, with angular laterals (Fig. 54, 181, 217,
288).
D
ESCRIPTION: Total length 1.49-3.33. CEPHALOTHORAX: Carapace without
any color pattern, ovoid in dorsal view (Fig. 11, 309), pars cephalica slightly
elevated in lateral view (Fig. 1, 3, 124), narrowed to between 0.5 and 0.75 times its
maximum width, with rounded posterolateral corners (Figs. 57, 155, 275),
posterolateral edge without pits, posterior margin not bulging below posterior rim,
anterolateral corners without extension or projections, posterolateral surface
without spikes (N. hispidus, N. barreirosi, N. brega, N. caterete, Figs. 5 – 8, 102,
260, 294); 2 pairs of spikes (N. termitophilus, N. petrogoblin, N. gregoblin, Figs. 9 –
11, 61, 149, 177) or 3 pairs of spikes (N. xyphinoides, N. axe, Figs. 12, 89, 186,
187, 207), surface and sides of elevated portion of pars cephalica smooth (N.
hispidus, N. petrogoblin, N. gregoblin, N. axe, N. brega, Figs. 116, 140, 170, 209,
275), reticulate (N. barreirosi, Fig. 240) or granulate (N. termitophilus, N. caterete,
Fig. 74, 309), carapace without depressions, fovea absent, without radiating rows
of pits; lateral margin straight, rebordered, generally with blunt denticles (Figs. 139,
170, 203), except in N. barreirosi and N. caterete (Figs. 240, 308); plumose setae
17
near posterior margin of pars thoracica absent; non-marginal pars cephalica setae
light, needle-like, scattered; non-marginal pars thoracica setae light, needle-like;
marginal setae light, needle-like. Clypeus margin unmodified (N. hispidus, N.
brega, N. caterete, Figs. 101, 276, 293) or slightly rebordered, high, straight in front
view (Fig. 171), vertical in lateral view (Fig. 210); ALE separated from edge of
carapace by their radius or more, median projection absent; setae present, light,
needle-like. Chilum absent. Six eyes, well developed, ALE largest, circular, PME
squared, PLE circular, posterior eye row straight from above, recurved from front;
ALE separated by less than their radius (but by their radius to diameter in N. axe
and N. caterete), ALE-PLE juxtaposed, PME touching throughout most of their
length, PLE-PME juxtaposed. Sternum generally as long as wide, longer than wide
in N. xyphinoides, N. petrogoblin, N. gregoblin and N. axe, color uniform, fused to
carapace, median concavity generally absent (present only in N. xyphinoides, Fig.
90), with radial furrows between coxae I-II, II-III, III-IV, furrows generally smooth
(wrinkled in N. caterete, Fig. 310 and with row of large pits in N. gregoblin, Fig.
156), radial furrow opposite coxae III absent, surface smooth, without pits,
microsculpture generally absent (present medially and on furrows in N. caterete
and N. gregoblin), sickle-shaped structures absent, anterior margin with continuous
transverse groove or unmodified (as in N. hispidus, N. barreirosi and N. brega,
Figs. 117, 244, 277), posterior margin not extending posteriorly of coxae IV,
anterior corner unmodified, lateral margin without infra-coxal grooves, distance
between coxae approximately equal, extensions of pre-coxal triangles present,
lateral margins unmodified, without posterior hump; setae sparse, light, needle-like,
18
evenly scattered, originating from small pits, without hair tufts. Chelicerae slightly
divergent, anterior face unmodified; with one tooth on both promargin and
retromargin, distal region unmodified, posterior surface unmodified, promargin with
row of flattened setae, paturon inner margin with a field of medial denticles (Figs.
20 – 22, 173), laminate groove absent, setae light, needle-like, evenly scattered,
also with some plumose setae; fang without tooth-like projections, directed
medially, shape normal, without prominent basal process, tip unmodified (Figs. 19,
23, 24). Labium rectangular, not fused to sternum, anterior margin not indented at
middle, same as sternum in sclerotization; with 6 or more setae on anterior margin,
subdistal portion with unmodified setae (Fig. 31, 208). Labrum triangular (Fig. 171).
Endites distally excavated in males (Figs. 25 – 30), with single slit sensilla on the
base of distal excavation and a retrolateral sub-apical teeth-like, curved apophysis;
a single modified hair generally inserted in the base of apophysis (but in the middle
of apophysis in N. axe and N. caterete, Figs. 28, 30), serrula absent, anteromedian
tip and posteromedian part unmodified, same as sternum in sclerotization.
ABDOMEN: ovoid, without long posterior extension, rounded posteriorly (Figs. 62,
191, 227, 252, 296), inter-scutal membrane rows of small sclerotized platelets
absent posteriorly; dorsum soft portions pale orange, without color pattern. Book
lung covers large, generally ovoid (elliptical in N. termitophilus and N. xyphinoides),
without setae, anterolateral edge unmodified. Posterior spiracles connected by
groove. Pedicel tube medium to long, ribbed (Figs. 13 – 18), scuto-pedicel region
unmodified, scutum extending far dorsal of pedicel, plumose hairs absent, matted
setae on anterior ventral abdomen in pedicel area absent, cuticular outgrowths
19
near pedicel absent. Dorsal scutum strongly sclerotized, without color pattern,
covering full length of abdomen, no soft tissue visible from above, not fused to
epigastric scutum, middle surface and sides smooth (but reticulate in N. barreirosi,
Figs. 241, 242); anterior half projecting denticles present in N. termitophilus, N.
hispidus, N. petrogoblin and N. gregoblin (Figs. 78, 120, 143, 174). In N. axe,
anterior hair sockets blunt (Fig. 205). Epigastric scutum strongly sclerotized,
surrounding pedicel, not protruding, small lateral sclerites absent. Postepigastric
scutum strongly sclerotized, orange-brown, long, semicircular, covering nearly full
length of abdominal length, fused to epigastric scutum, often with blunt hair sockets
(Figs. 78, 121, 206), anterior margin unmodified, with posteriorly directed lateral
apodemes. Spinneret and supra-anal scuta absent. Dorsum, epigastric and
postepigastric setae present, light, needle-like. Dense patch of setae anterior to
spinnerets absent. Interscutal membrane with setae. Colulus absent. Spinneret:
ALS with three or four spigots, PMS with three spigots, PLS with at least six
spigots (only male of N. termitophilus surveyed, Fig. 36). LEGS: without color
pattern; femur IV not thickened, same size as femora I-III, patella plus tibia I
shorter than carapace (or near as long as carapace in N. xyphinoides), tibia I
unmodified, tibia IV specialized hairs on ventral apex absent, tibia IV ventral
scopula absent, metatarsi I and II meso-apical comb absent, metatarsi III and IV
ventral scopula absent. Spines legs present on tibia and metatarsus, but present
on femur only in females of N. barreirosi and N. hispidus (one and two prolateral
spines, respectively). Legs I and II with spines longer than leg segment width (Fig.
32); leg III with spines shorter and thinner than those of legs I and II, present only
20
in females of N. petrogoblin, N. axe, and N. barreirosi ; leg IV without spines. All
metatarsi with one apical trichobothrium, hood covered by numerous low, closely
spaced ridges (Fig. 33, only N. hyspidus surveyed). Tarsal organ a rounded,
rebordered sub-apical depression, with four visible sensilla: two large, well
separated, posteriorly positioned and two small contiguous, anteriorly positioned
(Fig. 34, only N. hyspidus surveyed). GENITALIA: Male epigastric region with
sperm pore small, oval, unmodified, situated between anterior and posterior
spiracles (N. termitophilus, N. hispidus, N. barreirosi, N. gregoblin) or at level of
anterior spiracles; furrow without omega-shaped insertions, without setae. Palp
normal size, not strongly sclerotized, right and left palps symmetrical (Fig. 256);
trochanter normal size, unmodified; femur normal size, two or more times as long
as trochanter, without posteriorly rounded lateral dilation, attaching to patella
basally; patella shorter than femur, not enlarged, without prolateral row of ridges,
setae unmodified; cymbium ovoid in dorsal view, completely fused with bulb, no
seam visible, extending beyond distal tip of bulb, plumose and stout setae absent,
with distal patch of setae; bulb shorter than cymbium, stout, tapering apically,
embolus dark, compact, with a ventral excavation and apical projection (Figs. 45 –
53); male ejaculatory opening large, round, generally located prolaterally (Fig. 53,
270), but located apically in N. caterete (Fig. 303). Sperm duct wide (Figs. 137,
168, 201, 237). Female genitalia with a large elliptical atrium with angled laterals.
Atrial margins strongly rebordered (Fig. 54). Internally with a median elongated
piece and long lateral apodemes (Figs. 87, 152, 181, 217, 255, 288, 320).
21
NATURAL HISTORY: Neoxyphinus specimens are mostly found in forest litter,
being collected with pitfall traps and winkler extraction. N. termitophilus was
reported to be found in termite nest galleries of Nasutitermes arenarius (Hagen and
Bates) and N. gregoblin was collected with carrion traps.
DISTRIBUTION: South America, from Venezuela to Northwestern Argentina
and South Brazil (Map 1).
Neoxyphinus termitophilus (Bristowe), new combination
Figures 9, 25, 31, 32, 36, 37, 45, 53 – 87; Map 1
Dysderina termitophila Bristowe 1938: 67, f. 1-3 (male holotype from Santa
Catarina, Brazil, The Natural History Museum, London, not examined,
probably lost).
Neoxyphinus ogloblini Birabén 1953: 454, f. 1-9 (female holotype and male
paratype from Loreto, Missiones, Argentina, A. Ogloblin col., 1953, in MLP,
examined); Burger and Michalik, in press: figs. 1 – 4 (male genital system).
NEW SYNONYMY.
DIAGNOSIS: Males resemble those of N. hispidus and N. barreirosi by the
short, rounded embolus (Figs. 45, 68 – 70); differs from both by the presence of
four relatively short posterior spikes in the carapace (Figs. 9, 55, 61). Males differ
from other species with four spikes by the anterior end of abdominal dorsal scutum
22
with tiny, undeveloped denticles (Figs. 64, 78). Females can be recognized by the
combination of four relatively short spikes, smooth carapace (Figs. 81, 83) and
wide epigynal atrium, with a posteriorly or centrally positioned conical median piece
(Fig. 87).
DESCRIPTION: MALE (PBI_OON 14616). Total length 2.05. Carapace orange-
brown, anteriorly narrowed to 0.49 times its maximum width or less, posterolateral
surface with 2 pairs of similarly sized small spikes, surface of elevated portion of
pars cephalica and sides finely granulated, lateral margin straight, rebordered, with
blunt denticles. Clypeus margin slightly rebordered, straight in front view. Eyes:
ALE separated by less than their radius. Sternum as long as wide, orange-brown,
median concavity absent, furrow smooth, microsculpture absent, anterior margin
with continuous transverse groove, lateral margin without infra-coxal grooves,
evenly scattered, originating from small pits. Chelicerae, endites and labium
orange-brown. Book lung covers large, elliptical. Pedicel tube long. Dorsal scutum
orange-brown, surface of middle and sides smooth, anterior half with small,
conspicuous projecting denticles. Postepigastric scutum orange-brown. Legs pale
orange. Legs I and II spines present. Spine formula: tibia I v4-4-1, metatarsus I v2-
2-1; tibia II v2-2-2, metatarsus II v2-0-1. Genitalia: Sperm pore small, oval, situated
between anterior and posterior spiracles. Palp proximal segments pale orange,
cymbium and bulb yellow. Embolus without prolateral lamella and with a small,
rounded prolateral prong (fig. 69).
FEMALE (PBI_OON 14615). Total length 2.37. Pedicel tube medium. Dorsal
scutum anterior half without projecting denticles. Leg I and II spines present. Spine
23
formula: tibia I v4-4-2, metatarsus I v2-2-2; tibia II v4-2-2, metatarsus II v2-1-1.
Epigynal median piece conical, placed posteriorly or centrally in our preparations
(Fig. 87).
V
ARIATION: Specimens from Piauí, Brazil, are darker than those from other
localities and the female anterior pair of spikes is larger than the posterior one (Fig.
81). The carapace granulation may be inconspicuous or even absent, being
completely smooth in some specimens. In few males, the abdominal dorsal scutum
is completely devoid of denticles and others may present a small embolar
prolateral lamella (Fig. 68).
D
ISTRIBUTION: Known from north Brazil to north Argentina.
MATERIAL EXAMINED: BRAZIL: Pará: Belém (Bosque Rodrigues Alves -
Jardim Botânico da Amazônia, 01°25'49.0''S 48°27'22.3''W), 2001, J. A. P.
Barreiros (PBI_OON 40114, MPEG 10520; PBI_OON 40115, MPEG 10521) 1♂,
1♀; (Reserva Mocambo, 01°26'28.7''S 48°24'46.2''W), 06-12 Dec 2007, B. V. B.
Rodrigues & J. M. B. Pereira-Filho (PBI_OON 14645, MPEG 14025; PBI_OON
14646, MPEG 14026; PBI_OON 14647, MPEG 14027; PBI_OON 14648, MPEG
14028; PBI_OON 14649, MPEG 14029; PBI_OON 14650, MPEG 14030;
PBI_OON 14651, MPEG 14031; PBI_OON 14652, MPEG 14032; PBI_OON
14653, MPEG 14033; PBI_OON 14654, MPEG 14034; PBI_OON 14655, MPEG
14035; PBI_OON 14656, MPEG 14036; PBI_OON 14657, MPEG 14037;
PBI_OON 14658, MPEG 14038; PBI_OON 14659, MPEG 14039; PBI_OON
14660, MPEG 14040; PBI_OON 14661, MPEG 14041) 15♂, 6♀. Piauí: Brasileira
e Piracuruca (Parque Nacional de Sete Cidades, 04°05'56.3''S 41°05'56.3"W), 22
24
Nov 2003, E. B. O. Marques (PBI_OON 14378, MPEG 10193) 1♀, 28 Mar 2005, F.
M. Oliveira-Neto (PBI_OON 14377, MPEG 10190) 1♀, 28 Oct 2005 (PBI_OON
14367, MPEG 10192) 1♀, 25 Jun 2005, F. N. Oliveira-Marques (PBI_OON 14354,
MPEG 13410) 1♂, 04 Dec 2006, L. S. Carvalho, D. F. Candiani & N. F. Lo Man
Hung (PBI_OON 14376, MPEG 13406) 1♂, 1♀, 06 Dec 2006 (PBI_OON 14365,
MPEG 13423; PBI_OON 14368, MPEG 13427; PBI_OON 14369, MPEG 13431)
3♀, 13 Dec 2006 (PBI_OON 14346, MPEG 13430; PBI_OON 14347, MPEG
13413; PBI_OON 14351, MPEG 13420) 1♂, 3♀, 15 Dec 2006 (PBI_OON 14364,
MPEG 13422) 1♂, 24 Jan 2007, L. S. Carvalho, M. P. Albuquerque & M. T. L.
Avelino (PBI_OON 14355, MPEG 13409; PBI_OON 14360, MPEG 13408;
PBI_OON 14374, MPEG 13429) 1♂, 2♀, 26 Jan 2007 (PBI_OON 14357, MPEG
13426; PBI_OON 14358, MPEG 13407; PBI_OON 14359, MPEG 13415;
PBI_OON 14361, MPEG 13416; PBI_OON 14371, MPEG 13425; PBI_OON
14373, MPEG 13419) 1♂, 5♀, 02 Feb 2007, (PBI_OON 14363, MPEG 13432) 1♀,
29 Jul 2007 (PBI_OON 14375, MPEG 13405) 1♂, 1♀, 03 Feb 2007, L. S.
Carvalho, E. B. O. Marques & M. T. L. Avelino (PBI_OON 14381, MPEG 13414)
2♀, 01 Jun 2007, L. S. Carvalho, F. M. Oliveira-Neto & M. T. L. Avelino (PBI_OON
14345, MPEG 13433; PBI_OON 14353, MPEG 13424; PBI_OON 14380, MPEG
13434) 4♂, 1♀, 29 Jun 2007 (PBI_OON 14350, MPEG 13428; PBI_OON 14379,
MPEG 13435) 3♂, 24 Jun 2007, L. S. Carvalho, M. P. Albuquerque & F. M.
Oliveira-Neto (PBI_OON 14349, MPEG 13411; PBI_OON 14356, MPEG 13417;
PBI_OON 14370, MPEG 13418) 1♂, 2♀, 27 Jun 2007 (PBI_OON 14348, MPEG
13412; PBI_OON 14372, MPEG 13421) 1♂, 1♀. Castelo do Piauí (ECB Rochas
25
Ornamentais LTDA, Fazenda Bonito, 05°13'50.8''S 41°42'01.1''W), Sep 2006, L. S.
Carvalho (PBI_OON 14366, MPEG 10191) 1♀. José de Freitas, (Fazenda
Nazareth, 04°47'38,38''S 42°37'21,59''W), 31 Jan 2004, V. O. Costa (PBI_OON
14352, MPEG 10194) 1♂. Bahia: Central, 11°01' S 41°47'W, 15-31 Jul 2002, E.
Ramos & F. Cunha (PBI_OON 14598, IB 67377; PBI_OON 14724, IB 67408;
PBI_OON 14725, IB 67413; PBI_OON 14726, IB 67382) 2♂, 3♀. Mato Grosso:
Três Lagoas (Três Lagoas), Jun 1964, D. Z. (PBI_OON 14629, MZUSP 12053)
1♂. Mato Grosso do Sul: Brasilandia, (Fazenda Cisalpina, Usina Hidroelétrica
Sergio Motta), 2000, Equipe IBSP (PBI_OON 14586, IB 30458; PBI_OON 14587,
IB 30470; PBI_OON 14588, IB 30469) 5♂, 2♀, Equipe Biota (PBI_OON 14613, IB
30480) 1♀, 08-12 Aug 2000, Equipe IBSP (PBI_OON 14584, IB 30649; PBI_OON
14585, IB 30625) 2♂, 15-19 Aug 2000, J. P. Guadanucci & C. Fukushima
(PBI_OON 14589, IB 35397; PBI_OON 14590, IB 35402; PBI_OON 14591, IB
35540; PBI_OON 14592, IB 35550) 3♂, 1♀; (Usina Hidroelétrica Sergio Motta,
22°30'00'' S 53°00'59'' W), 16-24 Jul 2000, Equipe IBSP (PBI_OON 14594, IB
30651) 1♂, 31 Jul-07 Aug 2000 (PBI_OON 14582, IB 30852; PBI_OON 14583, IB
30828) 2♀, 08-12 Aug 2000 (PBI_OON 14577, IB 30917; PBI_OON 14578, IB
30929; PBI_OON 14579, IB 30919; PBI_OON 14580, IB 30920; PBI_OON 14581,
IB 30902; PBI_OON 14593, IB 30916; PBI_OON 40116, IB 30900) 7♂. Corumbá
(Pantanal, próximo ao Rio Vermelho), Apr 1999, J. Raizer (PBI_OON 14611, IB
68038) 1♀; (Passo do Lontra, 19°00'34'' S 57°39'11'' W), Jan 1998-Nov 1999, J.
Raizer (PBI_OON 14695, IB 69526; PBI_OON 14696, IB 69551; PBI_OON 14697,
IB 69540; PBI_OON 14698, IB 69543; PBI_OON 14699, IB 69530; PBI_OON
26
14700, IB 69529; PBI_OON 14701, IB 69557; PBI_OON 14709, IB 69523;
PBI_OON 14710, IB 69527; PBI_OON 14711, IB 69528; PBI_OON 14712, IB
69532; PBI_OON 14713, IB 69536; PBI_OON 14714, IB 69537; PBI_OON 14715,
IB 69539; PBI_OON 14716, IB 69547; PBI_OON 14717, IB 69550; PBI_OON
14718, IB 69556; PBI_OON 14719, IB 69559; PBI_OON 14720, IB 69560) 5♂,
20♀. Dois Irmãos do Buriti, (Piratupanga, 20°27' S 55°30' W), 30 Jun 1999-06 Jul
1999, A.D. Brescovit et al. (PBI_OON 14595, IB 67457; PBI_OON 14596, IB
67428; PBI_OON 14702, IB 67419; PBI_OON 14703, IB 67432; PBI_OON 14704,
IB 67444; PBI_OON 14705, IB 67445; PBI_OON 14706, IB 67449; PBI_OON
14707, IB 67451; PBI_OON 14708, IB 67460) 7♂, 5♀. Goiás: Campinaçu (Serra
da Mesa, 13°52'S 48°23'W), 18 Feb-02 Mar 1996, Silvestre, Brandao & Yamamoto
(PBI_OON 40128, MZUSP 15676) 3♂. Niquelandia, 14°01'S 48°18'W, 24 Sep-06
Oct 1995, Silvestre, Dietz & Brandao (PBI_OON 14632, MZUSP 15710) 2♂. São
Paulo: Teodoro Sampaio (Parque Estadual Morro do Diabo, 22°31'S 52°18'W),
24-31 Mar 2003, Equipe Biota (PBI_OON 14599, IB 60187; PBI_OON 14600, IB
60194; PBI_OON 14601, IB 60193) 2♂, 1♀. Paraná: Capitão Leônidas Marques
(Salto Caxias, Rio Iguaçu, 25°30'00''S 53°42'00''W), 23 Feb-23 Mar 1993, A. B.
Bonaldo (PBI_OON 14622, MCN 23460) 1♂, 2♀, 20-28 Mar 1993 (PBI_OON
14626, MCN 23467) 2♂, 1♀. Dois Vizinhos (Foz do Chopin, Cruzeiro do Iguaçu,
25°34'28''S 53°05'48''W), 08-15 Oct 1998, Equipe Biota (PBI_OON 14610, IB
21219) 1♀. Foz do Iguaçu (Parque Nacional de Foz do Iguaçu, 25°36'S 54°25'W),
03-12 Mar 2002, Equipe Biota (PBI_OON 14603, IB 60247; PBI_OON 14604, IB
60257; PBI_OON 14605, IB 60254; PBI_OON 14606, IB 60252; PBI_OON 14607,
27
IB 60255) 8♂, 2♀; (Refúgio Biológico de Bela Vista, 25°24'59''S 54°31'59''W), 09-
11 Nov 1991, A. B. Bonaldo (PBI_OON 14617, MCN 21642) 5♂, 2♀. Londrina
(Parque Estadual Mata dos Godoy, 23°27'S 51°15'W, 700 m), 11 Dec 1998, J.
Lopes (PBI_OON 14602, IB 38191) 1♂; 05 Jan 1999 (PBI_OON 14609, IB 38188)
1♀; 17 Feb 1999 (PBI_OON 14608, IB 38255) 1♂; 08 Sep 1999 (PBI_OON 14612,
IB 38196) 1♂. Pinhão (Usina Hidrelétrica Segredo, Rio da Divisa, 25°47'27"S
52°6'50"W), 21 Nov 1991, R. Pinto-da-Rocha & A. P. Barreto (PBI_OON 14631,
MZUSP 14626) 1♀. Três Barras do Paraná (Foz do Córrego Três Barras, Rio
Guarani, 25°32'30''S 53°08'11''W), 20-26 Feb 1993, A. B. Bonaldo (PBI_OON
14625, MCN 23189; PBI_OON 14627, MCN 23142) 1♂, 2♀; 24 Feb-24 Mar 1993
(PBI_OON 14623, MCN 23413) 6♂, 2♀. Santa Catarina: Ita (Rodovia Nova
Teutonia, 27°11'00''S 52°29'01"W), 01 Feb 1996, A. B. Bonaldo, A. Kury & Rocha
(PBI_OON 14628, MCN 27143) 1♀. Nova Teutonia, Aug 1968, F. Plaumann
(PBI_OON 14614, AMNH) 3♂, 2♀. Rio Grande do Sul: Canela (Barragem dos
Bugres, 29°20'35"S 50°41'44"W), 13 Dec 1999, A. B. Bonaldo (PBI_OON 14619,
MCN 32088) 1♀. Eldorado do Sul (Fazenda KRAMM, Parque Estadual Delta do
Jacui, 29°58'59''S 51°18'58''W), 29 Oct 1998, L. A. Moura (PBI_OON 14621, MCN
30303) 1♂, 2♀, 01 Jul 1999, A. B. Bonaldo (PBI_OON 14618, MCN 31316) 4♂,
1♀. São Francisco de Paula (Barragem dos Bugres), 06 Nov 1998, L. A. Moura
(PBI_OON 14620, MCN 31075) 1♀. Viamão (Morro do Coco, 30°04'59''S
51°01'59''W), 25 Jul 1985, A.A. Lise (PBI_OON 14624, MCN 13380) 3♂, 3♀.
PERU: Junin: Chanchamayo (Estancia Naranjal San Ramon, 1000 m), 20-27 Jul
1965, P., B. Wygodzinsky (PBI_OON 40131, AMNH) 1♂. Satipo (San Ramon de
28
Pangoa, 40 km SE Satipo, 750 m), 07 Jun 1972, R. Schuh (PBI_OON 40132,
AMNH) 1♂. ARGENTINA: Misiones: Cainguas (Sendero al Salto Escondido,
Parque Provincial Salto Encantado, 27°07'S 54°48'W), 11-12 Jan 2005, C.
Grismado, L. Lopardo, L. Piacentini, A. Quaglino, G. Rubio (PBI_OON 40105,
MACN-AR 15326) 1♀. General Manuel Belgrano (Parque Provincial Yacuy,
25°50'S 54°10'W), Dec 1972, M. Galiano (PBI_OON 40113, MACN-AR 15317) 1♀.
Iguazú (Area de la Garganta del Diablo, Parque Nacional de Iguazú, 25°42'S
54°27'W), 19-20 Jan 2005, C. Grismado, L. Lopardo, L. Piacentini, A. Quaglino, G.
Rubio (PBI_OON 40103, MACN-AR 15324; PBI_OON 40130, MACN-AR 15316)
8♂, 9♀; (Parque Nacional Iguazú, 25°37'S 54°20'W), Jul 1983, P. Goloboff
(PBI_OON 40099, MACN-AR 15313) 1♂, 08-15 Feb 1995, M. Ramírez (PBI_OON
40101, MACN-AR 15329; PBI_OON 40106, MACN-AR 15319; PBI_OON 40111,
MACN-AR 15330; PBI_OON 40112, MACN-AR 15315) 5♂, 3♀, 23-26 Oct 1995,
M. Ramírez (PBI_OON 40129, MACN-AR 15328) 4♂, 6♀; (Saltos del Uruguai, 10
km M Puerto Libertad), 23-25 Feb 1997, M. Ramírez (PBI_OON 40098, MACN-Ar
15318) 1♂; (Sendero Macuco y Picadas Aledañas, Parque Nacional Iguazú,
25°40'43''S 54°26'57''W), 18-21 Jan 2005, C. Grismado, L. Lopardo, L. Piacentini,
A. Quaglino, G. Rubio (PBI_OON 40108, MACN-AR 15323; PBI_OON 40109,
MACN-AR 15320; PBI_OON 40110, MACN-AR 15321) 2♂,4♀; (Parque Provincial
Urugua-Í Refugio Caa-Porá, 3 km W Deseado), 15 Feb 1995, M. Ramírez
(PBI_OON 40104, MACN-AR 15331) 3♂, 1♀.
29
Neoxyphinus xyphinoides (Chamberlin and Ivie 1942)
Figures 88 -97; Map 1
Dysderina xyphinoides Chamberlin and Ivie 1942: 7, f. 5-7 (male holotype from
Kartabo, British Guyana, 1924, in AMNH, examined).
Neoxyphinus xyphinoides; Birabén, 1953: 458.
DIAGNOSIS: This species can be readily distinguished by the presence of
three pairs of short carapace spikes (Figs. 88, 89) and a strongly modified sternum
that resembles those of Simonoonops Harvey and some Dysderina Simon species,
with a small concave pit in posterior half, well developed radial furrows and anterior
margin with continuous transverse groove (Fig. 90).
DESCRIPTION: MALE (PBI_OON 14576). Total length 2.05. Carapace dark
red-brown, anteriorly narrowed to between 0.5 and 0.75 times its maximum width,
posterolateral surface with 3 pairs of spikes, surface of elevated portion of pars
cephalica and sides smooth, lateral margin straight, rebordered, with blunt
denticles; non-marginal pars thoracica setae light, needle-like. Clypeus margin
unmodified, straight in front view. Eyes: ALE separated by less than their radius.
Sternum longer than wide, orange-brown; median concavity present, a small
concave pit in posterior half of sternum; furrow smooth, microsculpture absent;
anterior margin with continuous transverse groove; setae evenly scattered,
originating from surface. Chelicerae, endites and labium orange-brown. Book lung
covers large, elliptical. Pedicel tube long. Dorsal scutum dark red-brown; surface of
30
middle and sides smooth, anterior half without projecting denticles. Postepigastric
scutum dark red-brown. Legs orange-brown; patella plus tibia I near as long as
carapace. Legs I and II spines present. Spine formula: tibia I v4-4-1, metatarsus I
2-2-1; tibia II v2-4-0, metatarsus II v2-0-2. Genitalia: Sperm pore situated at level of
anterior spiracles. Palp proximal segments, cymbium and bulb yellow. Embolus
with both prolateral prong and prolateral lamella (Fig. 96).
D
ISTRIBUTION: Know only from type locality.
M
ATERIAL EXAMINED: Only the holotype.
Neoxyphinus hispidus (Dumitrescu and Georgescu), new combination
Figures 7, 13, 22, 26, 33, 34, 38, 46, 98 – 121; Map 1.
Decuana hispida (Dumitrescu and Georgescu 1987): 92, pl. 2-3 (two males, one
female syntypes from Rancho Grande, Venezuela, XI.11.1982, T. Orguidan
& V, Decu col., in "Grigore Antipa" National Museum of Natural History,
Bucharest, not examined).
D
IAGNOSIS: Males differ from those of other species without developed
carapace spikes by the combination of smooth carapace (Fig. 100), well developed
denticles on anterior end of dorsal scutum (Fig. 103, 195) and rounded embolus
(Figs. 111) (not elongated as in N. brega). Females differ from those of N.
barreirosi and N. caterete by the smooth carapace and from those of N. brega by
31
the epigynal atrium strongly rebordered anteriorly and median piece with long
accessory prongs (Dumitrescu and Georgescu, 1987: Figs. 3, 4). Females can be
further distinguished by the presence of two prolateral spines on femur I.
D
ESCRIPTION: MALE (PBI_OON 14295). Total length 1.88. Carapace orange-
brown, posterolateral surface without spikes, surface of elevated portion of pars
cephalica and sides smooth, lateral margin straight, rebordered, without denticles;
non-marginal pars cephalica setae light, needle-like, present in u-shaped row.
Clypeus margin unmodified, straight in front view. Eyes: ALE separated by less
than their radius. Sternum as long as wide, orange-brown, median concavity
absent, furrow smooth, microsculpture absent, anterior margin unmodified; setae
evenly scattered, originating from small pits. Chelicerae, endites and labium
orange-brown. Book lung covers large, ovoid. Pedicel tube long. Dorsal scutum
orange-brown, surface of middle and sides smooth, anterior half with projecting
denticles. Postepigastric scutum orange-brown, without posteriorly directed lateral
apodemes. Legs pale orange. Leg I spines present. Spine formula: tibia I v2-4-0,
metatarsus I v2-3-0. Tarsi I to IV superior claws tooth not examined in detail.
Genitalia: Epigastric region with sperm pore small, narrow, slit-like, situated
between anterior and posterior spiracles. Palp proximal segments pale orange,
cymbium and bulb yellow. Embolus rounded, without both prolateral prong and
prolateral lamella (fig. 46, 111).
Female. Described by Dumitrescu and Georgescu (1987): 92, Figs. 3 – 6.
D
ISTRIBUTION: known from the type locality, Rancho Grande, Venezuela, and
from Serra do Cachimbo, Pará State, Brazil.
32
MATERIAL EXAMINED: BRAZIL: Pará: Novo Progresso (Campo de Provas
Brigadeiro Velloso, Serra do Cachimbo, 09°21'39''S 55°02'01''W), 07-17 Sep 2003,
A. B. Bonaldo, D. R. Santos-Souza & D. D. Guimarães (PBI_OON 14295, MPEG
13671; PBI_OON 14538, MPEG 13674; PBI_OON 14540, MPEG 13676;
PBI_OON 14541, MPEG 13677) 4♂, 16-26 Mar 2004, J. Ricetti, D. D. Guimarães
& J. A. P. Barreiros (PBI_OON 14537, MPEG 13673; PBI_OON 14539, MPEG
13675; PBI_OON 14543, MPEG 13672) 3♂, 22-25 Mar 2004, J. Ricetti, D. D.
Guimarães & J. A. P. Barreiros (PBI_OON 14542, MPEG 14145) 1♂.
Neoxyphinus petrogoblin, new species
Figures 3, 4, 10, 15, 19, 20, 40, 48, 122 – 152; Map 1.
TYPES: Male holotype from Base de Operações Geólogo Pedro de Moura,
Coari (Porto Urucu, Urucu River, 04°52'07.6''S 65°15'53.6''W), Amazonas, 11-20
Jul 2003, A. B. Bonaldo, J. D. Dias & D. D. Guimarães (PBI_OON 14296, MPEG
10181). Female allotype from same locality except (04°51'54''S 65°20'02''W), S. C.
Dias, D. F. Candiani & N. F. Lo Man Hung (PBI_OON 14297, MPEG 13809).
E
TYMOLOGY: The specific name is a contraction of “Petroleum Goblin”,
referring to the type locality, which harbors the largest petroleum production facility
in Brazilian Amazonia.
D
IAGNOSIS: The presence of four long carapace spikes (Figs. 124, 140, 147)
and few, well developed denticles on anterior end of abdominal dorsal scutum
33
(Figs. 141-144) separate this species from most other Neoxyphinus species. Both
males and females differ from those of N. gregoblin by the absence of large blunt
tubercles on dorsal and lateral surfaces of carapace (Fig. 139, 140, 146, 147).
Males are further recognized by the upright embolus, with large prolateral lamella
and without prolateral prong (Fig. 133, 134).
DESCRIPTION: MALE (PBI_OON 14296). Total length 2.11. Carapace dark
red-brown, posterolateral surface with 2 pairs of spikes, surface of elevated portion
of pars cephalica and sides smooth, lateral margin straight, rebordered, with blunt
denticles. Clypeus margin slightly rebordered, straight in front view. Eyes: ALE
separated by less than their radius. Sternum longer than wide, orange-brown,
median concavity absent, furrow smooth, microsculpture absent, anterior margin
with continuous transverse groove, setae evenly scattered, originating from small
pits. Chelicerae, endites and labium orange-brown. Book lung covers large, ovoid.
Pedicel tube long. Dorsal scutum orange-brown, surface of middle and sides
smooth, anterior half with projecting denticles. Postepigastric scutum orange-
brown. Legs orange-brown. Leg I and II spines present. Spine formula: tibia I v4-4-
1, metatarsus I v2-3-0; tibia II v2-3-0, metatarsus II v2-2-0. Genitalia: Sperm pore
situated at level of anterior spiracles. Palp proximal segments pale orange,
cymbium and bulb yellow. Upright embolus with large prolateral lamella and
without prolateral prong (Fig. 134).
F
EMALE (PBI_OON 14297). Total length 2.41. Carapace lateral margin with
sharply pointed denticles. Book lung covers elliptical. Dorsal scutum anterior half
without projecting denticles. Leg I, II and III spines present. Spine formula: tibia I
34
v6-2-2, metatarsus I v3-2-1; tibia II v4-4-0, metatarsus II v3-2-0; tibia III p1-1-0, v0-
1-0, metatarsus III p1-1-0, r0-1-0. Epigynal atrium narrow, with tubular median
piece (Fig. 152).
D
ISTRIBUTION: Know from Brazilian Central Amazonia and Huanuco, Peru.
O
THER MATERIAL EXAMINED: BRAZIL: Amazonas: Coari (Base de Operações
Geólogo Pedro de Moura, Urucu, 4°51'36"S 65°06'23"W), 29 Sep 2006, S. C. Dias,
D. F. Candiani, N. F. Lo Man Hung & C. A. C. Santos-Jr (PBI_OON 14528, MPEG
13811) 1♀, 11-20 Jul 2003, A. B. Bonaldo, J. D. Dias, D. D. Guimarães (PBI_OON
14525, MPEG 10164; PBI_OON 14529, MPEG 10185; PBI_OON 14531, MPEG
10159; PBI_OON 14534, MPEG 10187; PBI_OON 14536, MPEG 10156;
PBI_OON 14530, MPEG 10170) 6♂, 1♀, 12-20 Jul 2003 (PBI_OON 14535, MPEG
10168) 1♂, 19-22 Jul 2003 (PBI_OON 14527, MPEG 10162) 1♂, Sep 2006, S. C.
Dias et al. (PBI_OON 14532, MPEG 13812) 1♂; (04°48'23"S 65°02'05"W), 08 Jul
2006, S. C. Dias, L. T. Miglio & C. A. C. Santos Jr (PBI_OON 14533, MPEG
13813) 2♂. Manaus (Igarape Taruma Mirim, 03°06'00''S 60°01'48''W), 13 Apr
1983, J. Adis (PBI_OON 40122, SMNK ARA 220) 1♀, 13 May 1983 (PBI_OON
40121, SMNK ARA 221) 2♂; (Reserva Florestal Adolpho Ducke, 02°55'12''S
59°58'48''W, 100 m), 21 Aug 1991, H. Hofer & T. Gasnier (PBI_OON 40120,
SMNK ARA 4576) 1♂, 04 Sep 1991 (PBI_OON 40118, SMNK ARA 4572) 1♀.
PERU: Huanuco: Huanuco (Panguana Biological Station, 09°37'S 74°56'W), 30
Jul-13 Aug 1984, M. Verhaagh (PBI_OON 40123, SMNK 4647A) 1♂.
35
Neoxyphinus gregoblin, new species
Figures 1, 2, 11, 21, 41, 49, 153 – 181; Map 1.
T
YPES: Male holotype from Andres Bello, Mérida, Venezuela, 20 km SE
Azulita, ULA, Biological Reserve La Carbonera, 08°38'N 71°21'W, 2150 m, 28 Jun
1989, Peck, S., Peck, J. (PBI_OON 14298, AMNH). Female allotype, same locality
and collector, 27 Jul 1989 (PBI_OON 14299, AMNH).
E
TYMOLOGY: The specific name is a contraction of “Great Goblin”, a
character from J. R. R. Tolkien’s “The Hobbit”, in reference to the body size of the
specimens, the biggest known in the genus.
DIAGNOSIS: As in N. petroglobin, this species has four long carapace spikes
(Figs. 154, 176, 178) and few long abdominal dorsal denticles (Figs. 158, 174), but
differs by the presence, in both sexes, of well developed, blunt tubercles on
carapace dorsal surface, forming two longitudinal lines between eye group and first
pair of carapace spikes; these denticles are also present in carapace lateral
margins (Figs. 155, 170, 177).
D
ESCRIPTION: MALE (PBI_OON 14298). Total length 3.15. Carapace brown,
posterolateral surface with 2 pairs of spikes, surface of elevated portion of pars
cephalica and sides smooth, lateral margin straight, rebordered, with blunt
denticles. Clypeus margin slightly rebordered, sinuous in front view. Eyes: ALE
separated by less than their radius. Sternum longer than wide, dark red-brown,
median concavity absent, furrow with row of large pits, microsculpture medially and
in furrows, anterior margin with continuous transverse groove; setae evenly
36
scattered, originating from small pits. Chelicerae, endites and labium dark red-
brown. Book lung covers large, ovoid. Pedicel tube medium. Dorsal scutum dark
red-brown, surface of middle and sides smooth, anterior half with projecting
denticles. Postepigastric scutum dark red-brown. Legs orange-brown. Leg I and II
spines present. Spine formula: tibia I v4-4-1, metatarsus I v2-2-1; tibia II v2-2-2,
metatarsus II v2-0-2. GENITALIA: Sperm pore situated between anterior and
posterior spiracles. Palp proximal segments, cymbium and bulb pale orange.
Embolus with wide prolateral prong, short prolateral lamellae and tooth-like apical
process (Figs. 163 – 165).
FEMALE (PBI_OON 14299). Total length 3.33. Clypeus margin strongly rebordered.
Book lung covers elliptical. Dorsal scutum anterior half without projecting denticles.
Legs I and II spines present. Spine formula: tibia I v4-4-2, metatarsus I 2-2-1; tibia
II v4-4-1, metatarsus II v2-0-2. Epigynal atrium narrow, with wide tubular, centrally
positioned median piece (Fig. 181).
DISTRIBUTION: Known only from Mérida, Venezuela.
OTHER MATERIAL EXAMINED: VENEZUELA: Mérida: Andres Bello, 28 Jun-27
Jul 1989, Peck, S., Peck, J. (PBI_OON 14302, AMNH) 1♂; 27 Jul 1989 (PBI_OON
14300, AMNH) 1♂; (La Azulita, Jaji Road ESE of Merida; nr San Eusebio,
Maricaibo Basin side, 2250 m), 10 Apr 1994, L. Herman (PBI_OON 14303, AMNH)
1♀; (25 km NW Merida, Jaji Road, Chorrera Gonzales, 1800 m), 28 Jun 1989,
Peck, S., Peck, J. (PBI_OON 14573, AMNH) 1♂; (El Valle, 15 km NE Merida, 2400
m), 21-24 Jul 1989, Peck, S., Peck, J. (PBI_OON 14301, AMNH) 1♂.
37
Neoxyphinus axe, new species
Figures 12, 16, 28, 35, 42, 50, 182 – 217; Map 1.
TYPES: Male holotype from Estação Ecológica do Una (15°17'48''S
39°04'28''W), Ilhéus, Bahia, Brazil, 14 Apr 1998, A.D. Brescovit et al. (PBI_OON
14304, IB 18418). Female allotype same locality, Oct 1999-Sep 2000, M. F. Dias
(PBI_OON 14305, IB 64390).
E
TYMOLOGY: The specific name refers to the Axé Music, a popular genre
autochthonous to State of Bahia. Axé is originally an expression from the Afro-
Brazilian religion Candomblé, meaning sacred force from nature.
D
IAGNOSIS: Both males and females can be recognized by the combined
presence of six long carapace spikes and small blunt tubercles in carapace lateral
margins as well as in three transversal rows (Figs. 186-188, 212).
DESCRIPTION: MALE (PBI_OON 14304). Total length 2.44. Carapace dark
red-brown, posterolateral surface with 3 pairs of spikes, surface of elevated portion
of pars cephalica and sides smooth, with radiating rows of blunt denticles; lateral
margin straight, rebordered, with blunt denticles. Clypeus margin slightly
rebordered, straight in front view. Eyes: ALE separated by their radius to diameter.
Sternum longer than wide, dark red-brown, median concavity absent, furrow
smooth, microsculpture absent, anterior margin with continuous transverse groove,
evenly scattered, originating from small pits. Chelicerae, endites and labium
orange-brown. Book lung covers large, ovoid. Pedicel tube long. Dorsal scutum
38
dark red-brown, surface of middle and sides smooth, anterior half with very small,
blunt denticles (Fig. 205). Postepigastric scutum dark red-brown, with blunt
denticles (Fig. 206). Legs orange-brown. Leg I and II spines present. Spine
formula: tibia I v5-3-1, metatarsus I v2-3-0; tibia II v2-3-1, metatarsus II v1-1-2.
Genitalia: Sperm pore situated at level of anterior spiracles. Palp proximal
segments, cymbium and bulb pale orange. Embolus with narrow prolateral prong
and sharp prolateral lamella; apical process indistinct (Figs. 50, 197 – 199).
FEMALE (PBI_OON 14305). Total length 2.65. Book lung covers elliptical,
anterolateral edge with tubercle. Dorsal scutum anterior half without projecting
denticles. Legs I, II and III spines present. Spine formula: tibia I v4-4-2, metatarsus
I v2-2-2; tibia II v4-4-0, metatarsus II v3-3-0; tibia III p1-1-0, v0-1-0, metatarsus III
p1-0-1, v0-1-0. Epigynal atrium narrow, with tubular median piece, placed
anteriorly in our preparations (Fig. 217).
DISTRIBUTION: Known only from western State of Bahia, Brazil.
OTHER MATERIAL EXAMINED: BRAZIL: Bahia: Itabuna (CEPLAC, 14°38'S
39°18'W, 100 m), 26 Jan 1995, D. Agosti (PBI_OON 14575, AMNH) 1♂. Ilhéus
(CEPLAC, 14°47'22'' S 39°02'57'' W), 07 Apr 1998, A.D. Brescovit et al. (PBI_OON
14306, IB 19377) 1♂, 11 Apr 1998 (PBI_OON 14307, IB 19210) 1♀, 12 Apr 1998
(PBI_OON 14338, IB 18887) 1♀; Una (Estação Ecológica do Una, 15°11'46''S
39°3'34''W), 31 Jan 1995, D. Agosti (PBI_OON 14574, AMNH) 1♂; (Estação
Ecológica do Una, 15°17'48''S 39°04'28''W), Oct 1999-Sep 2000, M. F. Dias
(PBI_OON 14308, IB 64345; PBI_OON 14309, IB 64269; PBI_OON 14310, IB
65177; PBI_OON 14311, IB 65427; PBI_OON 14312, IB 65362; PBI_OON 14313,
39
IB 65124; PBI_OON 14314, IB 64508; PBI_OON 14315, IB 64429; PBI_OON
14327, IB 65203; PBI_OON 14544, IB 64242; PBI_OON 14339, IB 18106;
PBI_OON 14316, IB 64321; PBI_OON 14317, IB 65258; PBI_OON 14318, IB
64381; PBI_OON 14319, IB 65224; PBI_OON 14320, IB 66815; PBI_OON 14321,
IB 64336; PBI_OON 14322, IB 64474; PBI_OON 14323, IB 65208; PBI_OON
14324, IB 64391; PBI_OON 14325, IB 64529; PBI_OON 14326, IB 65325;
PBI_OON 14328, IB 65259; PBI_OON 14329, IB 64433; PBI_OON 14330, IB
65166; PBI_OON 14331, IB 65254; PBI_OON 14332, IB 64296; PBI_OON 14333,
IB 64436; PBI_OON 14334, IB 64500; PBI_OON 14335, IB 64502; PBI_OON
14336, IB 65491; PBI_OON 14337, IB 65109; PBI_OON 14341, IB 63933;
PBI_OON 14342, IB 64446; PBI_OON 14344, IB 65161; PBI_OON 14545, IB
64344) 32♂, 19♀, 2003 (PBI_OON 14340, IB 62540; PBI_OON 14343, IB 62532)
1♂, 1♀.
Neoxyphinus barreirosi, new species
Figures 5, 17, 23, 29, 43, 51, 218 – 255; Map 1.
T
YPES: Male holotype from Bosque Rodrigues Alves - Jardim Botânico da
Amazônia (01°25'49.0''S 48°27'22.3''W), Belém, Pará, Brazil, 08 Nov 2001, J. A. P.
Barreiros (PBI_OON 14382, MPEG 10506). Female allotype, same data
(PBI_OON 14383, MPEG 13670).
40
ETYMOLOGY: The specific name is a patronym in honor of the collector of the
holotype, José Augusto Pereira Barreiros (in memoriam), who dedicated his brief
life to the study of soil spiders and was an enthusiast of the goblin spiders.
D
IAGNOSIS: As in N. brega and N. caterete, the specimens of N. barreirosi
are devoid of carapace spikes and abdominal denticles. Both males and females of
this species can be distinguished by the reticulate surface of carapace and dorsal
scutum (Figs. 219, 226, 239 – 242, 248, 251). Males differ from all other species by
presence of a small prolatero-apical lamella (Figs. 233, 234, 237). Females can be
further distinguished by the presence of one prolateral spine on femur I, contrasting
with two in N. hispidus and none in the remaining species.
D
ESCRIPTION: MALE (PBI_OON 14382). Total length 1.98. Carapace orange-
brown, posterolateral surface without spikes, surface of elevated portion of pars
cephalica and sides strongly reticulate, lateral margin straight, rebordered, without
denticles. Clypeus margin slightly rebordered, straight in front view. Eyes: ALE
separated by less than their radius. Sternum as long as wide, orange-brown,
median concavity absent, microsculpture absent, setae evenly scattered,
originating from surface. Book lung covers large, ovoid. Pedicel tube medium.
Dorsal scutum orange-brown, surface of middle and sides reticulate, anterior half
without projecting denticles. Postepigastric scutum orange-brown. Legs pale
orange. Leg I spines present. Spine formula: tibia I v2-4-0, metatarsus I v2-1-2.
Genitalia: Sperm pore situated between anterior and posterior spiracles. Palp
proximal segments, cymbium and bulb yellow. Embolus rounded, without both
41
prolateral prong and prolateral lamella, but with a prolatero-apical lamella (Fig. 51,
233, 234).
FEMALE (PBI_OON 14383). Total length 1.93. Carapace surface of elevated
portion of pars cephalica and sides finely reticulate. Clypeus margin unmodified.
Book lung covers round. Dorsal scutum middle and sides surface finely reticulate.
Epigastric and postepigastric area needle-like. Legs I, II and III spines present.
Spine formula: femur I p0-1-0, tibia I v5-3-2, metatarsus I v2-2-2; tibia II v4-4-0,
metatarsus II v3-2-0; tibia III v1-1-1, metatarsus III v1-1-1. Epigynal atrium wide,
with median piece conical, placed anteriorly in our preparations (Fig. 255).
DISTRIBUTION: Know from north Brazil.
OTHER MATERIAL EXAMINED: BRAZIL: Roraima: Amajari (Reserva Biológica
Ilha de Maracá, 03°22'01''N 61°25'00''W), 31 Jan-14 Feb 1992, A. B. Bonaldo
(PBI_OON 40125, MCTP 1836) 1♀. Amazonas: Manaus, 03°06'07''S 60°01'30''W,
28 Jan 1992, A. B. Bonaldo (PBI_OON 40124, MCTP 1479) 2♀. Pará: Belém
(Bosque Rodrigues Alves - Jardim Botânico da Amazônia, 01°25'49.0''S
48°27'22.3''W), 01 Apr 2001, J. A. P. Barreiros (PBI_OON 14412, MPEG 10501)
1♀, 08 Apr 2001 (PBI_OON 14402, MPEG 10503) 1♀, 12 May 2001 (PBI_OON
14417, MPEG 10490) 1♀, 16 Apr 2001 (PBI_OON 14418, MPEG 10500) 1♀, 22
Apr 2001 (PBI_OON 14387, MPEG 10498; PBI_OON 14401, MPEG 10497;
PBI_OON 14416, MPEG 10499) 3♀, 27 Sep 2001 (PBI_OON 14419, MPEG
10495) 1♀, 18 Oct 2001 (PBI_OON 14404, MPEG 10491; PBI_OON 14428,
MPEG 10496) 2♀, 25 Oct 2001 (PBI_OON 14391, MPEG 10483; PBI_OON
14392, MPEG 10480; PBI_OON 14400, MPEG 10504; PBI_OON 14434, MPEG
42
10482) 7♀, 08 Nov 2001 (PBI_OON 14393, MPEG 10484; PBI_OON 14410,
MPEG 10488; PBI_OON 14429, MPEG 10505; PBI_OON 14435, MPEG 10481;
PBI_OON 14547, MPEG 10486) 9♀, 2001 (PBI_OON 14385, MPEG 10507;
PBI_OON 14389, MPEG 10492; PBI_OON 14397, MPEG 10493; PBI_OON
14408, MPEG 10487; PBI_OON 14413, MPEG 10502; PBI_OON 14414, MPEG
10485; PBI_OON 14415, MPEG 10494; PBI_OON 14427, MPEG 10489) 8♀.
Reserva Mocambo, 01°26'28.7''S 48°24'46.2''W, 06-12 Dec 2007, B. V. B.
Rodrigues & J. M. B. Pereira-Filho (PBI_OON 14633, MPEG 14013; PBI_OON
14635, MPEG 14015; PBI_OON 14636, MPEG 14016; PBI_OON 14637, MPEG
14017; PBI_OON 14638, MPEG 14018; PBI_OON 14640; MPEG 14020;
PBI_OON 14641, MPEG 14021; PBI_OON 14642, MPEG 14022; PBI_OON
14643, MPEG 14023; PBI_OON 14644, MPEG 14024) 10♀, 13-15 Dec 2007
(PBI_OON 14634, MPEG 14014) 1♀, 07 May 2008, B. V. B. Rodrigues, J. M. B.
Pereira-Filho, N. Abrahim & N. C. Bastos (PBI_OON 14639, MPEG 14019) 1♀.
Goianésia (Fazenda Rio Capim, 03°18'50'' S 48°28'54'' W), 30 Jul 2002, Equipe
IPAN (PBI_OON 14388, MPEG 10742, PBI_OON 14398, MPEG 10741; PBI_OON
14421, MPEG 10732) 2♂, 1♀, 30 Aug 2002 (PBI_OON 14409, MPEG 10739) 1♀,
15-29 Jun 2003 (PBI_OON 14394, MPEG 10735, PBI_OON 14439, MPEG 10727)
2♂, 17 Jun 2003 (PBI_OON 14407, MPEG 10730; PBI_OON 14426, MPEG
10743; PBI_OON 14440, MPEG 10715; PBI_OON 14384, MPEG 10744;
PBI_OON 14390, MPEG 10740; PBI_OON 14438, MPEG 10716) 2♀, 5♂. Melgaço
(Estação Científica Ferreira Penna, FLONA Caxiuana, 01°44'15.5''S
51°26'42.0''W), 17 Aug 2003, J. A. P. Barreiros (PBI_OON 14755, MPEG 10372)
43
1♀, 25 Oct 2003 (PBI_OON 14405, MPEG 10345) 1♀, 28 Oct 2003 (PBI_OON
14754, MPEG 10374) 1♂. Novo Repartimento (Fazenda Arataú, 04°19'51'' S
49°47'47)'' W, 19 Jun-12 Aug 2003, Equipe IPAN (PBI_OON 14423, MPEG 10724)
1♀, 25-26 Jun 2003 (PBI_OON 14395, MPEG 10719; PBI_OON 14399, MPEG
10734; PBI_OON 14403, MPEG 10710; PBI_OON 14406, MPEG 10726;
PBI_OON 14411, MPEG 10713; PBI_OON 14424, MPEG 10728; PBI_OON
14430, MPEG 10720; PBI_OON 14431, MPEG 10721; PBI_OON 14436, MPEG
10722; PBI_OON 14546, MPEG 10729) 2♂, 9♀, 11 Aug 2006 (PBI_OON 14425,
MPEG 10745) 1♀. Tailândia (Fazenda Santa Marta), 13-14 May 2003, Equipe
IPAN (PBI_OON 14396, MPEG 10733; PBI_OON 14422, MPEG 10738; PBI_OON
14432, MPEG 10731) 3♀; 10-30 Jul 2003 (PBI_OON 14433, MPEG 10714) 1♀,
19-30 Jul 2003 (PBI_OON 14420, MPEG 10711; PBI_OON 14386, MPEG 10723)
1♂, 1♀. No precise location, (Mata, Varzea), Oct 2005, L. Macambira (PBI_OON
14548, MPEG 10708) 3♀.
Neoxyphinus brega, new species
Figures 8, 14, 27, 39, 47, 256 – 288; Map 1.
TYPES: male holotype from Estação Cientifica Ferreira Penna, FLONA
Caxiuana, (01°44'15.5''S 51°26'42.0''W), 25 Oct 2003, J. A. P. Barreiros (PBI_OON
14441, MPEG 10369). Female allotype same locality and collector, 16 Oct 2003
(PBI_OON 14442, MPEG 10383).
44
ETYMOLOGY: The specific name refers to the Brega Music, a popular genre
autochthonous to State of Pará, Brazil. In other parts of the country the word brega
is used as an adjective, meaning tasteless.
D
IAGNOSIS: Males resemble N. hispidus by the smooth carapace surface,
without developed posterior spikes (Figs.259, 260, 275), but differ by the long and
slender embolus, with pointed apical projection (Figs. 47, 267, 273), and by the
absence of abdominal anterior denticles (Fig. 263, 265, 278). Females resemble
those of N. termitophilus, N. hispidus, N. barreirosi and N. caterete by the wide
epigynal atrium, differing by the unique combination of the posteriorly positioned
median piece (Fig. 288) and absence of carapace spikes (Fig. 282, 283).
D
ESCRIPTION: MALE (PBI_OON 14441). Total length 1.49. Carapace orange-
brown, posterolateral surface without spikes, surface of elevated portion of pars
cephalica and sides smooth, lateral margin straight, rebordered, with blunt
denticles. Clypeus margin unmodified, straight in front view. Eyes: ALE separated
by less than their radius. Sternum as long as wide, orange-brown, median
concavity absent, furrow smooth, microsculpture absent, anterior margin
unmodified, setae evenly scattered, originating from small pits. Book lung covers
large, ovoid. Pedicel tube medium. Dorsal scutum orange-brown, middle and sides
surface smooth, anterior half without projecting denticles. Postepigastric scutum
orange-brown. Legs pale orange. Leg I spines present. Spine formula: tibia I v4-4-
0, metatarsus I v2-2-1. Genitalia: Sperm pore situated at level of anterior spiracles.
Palp proximal segments, cymbium and bulb yellow. Embolus long and slender,
45
with pointed apical projection (Fig. 269, 270), and without prolateral prong and
prolateral lamella (Fig. 47).
FEMALE (PBI_OON 14442). Total length 1.58. Clypeus margin slightly
rebordered. Legs I and II spines present. Spine formula: tibia I v4-4-2, metatarsus
I v2-3-1; tibia II v3-4-0, metatarsus II v3-1-1. Epigynal atrium wide, with posteriorly
positioned median piece (Fig. 288).
D
ISTRIBUTION: This species is known from north of South America.
O
THER MATERIAL EXAMINED: VENEZUELA. Bolivar: Gran Sabana (12 Km N
Luepa, 1500 m), 01-11 Jun 1987, Peck, S., Peck, J. (PBI_OON 14571, AMNH) 1♂.
COLOMBIA. Amazonas: (18 km of Leticia), 24-28 Feb 1974, Peck, S., Peck, J.
(PBI_OON 14570, AMNH) 1♂. GUYANA. Potaro-Siparuni: Tukeit, 21 Jul 1911, F.
Lutz (PBI_OON 14572, AMNH) 1♂. BRAZIL. Amazonas: Manaus (Reserva
Florestal Adolpho Ducke, 02°55'12''S 59°58'48''W, 100 m), 13 Jun 1998, R. Ott
(PBI_OON 40126, MCTP 12628) 2♀. Pará: Juruti (Platô Capiranga, 02°28'22.1''S
56°12'29.4''W), 09-11 Feb 2007, J. A. P. Barreiros & N. F. Lo-Man-Hung
(PBI_OON 14554, MPEG 10056) 1♂; (Sitio Três Irmãos, 02°27'51.4''S
56°00'08.6''W), 08-15 Aug 2006, D. F. Candiani & N. F. Lo-Man-Hung (PBI_OON
14450, MPEG 10882; PBI_OON 14466, MPEG 10884; PBI_OON 14468, MPEG
10886; PBI_OON 14469, MPEG 10887; PBI_OON 14471, MPEG 10889;
PBI_OON 14473, MPEG 10893; PBI_OON 14475, MPEG 10895; PBI_OON
14478, MPEG 10881; PBI_OON 14479, MPEG 10897) 9♂, 2♀, 06-13 Feb 2007, J.
A. P. Barreiros & N. F. Lo-Man-Hung (PBI_OON 14564, MPEG 10112; PBI_OON
14558, MPEG 10141; PBI_OON 14561, MPEG 10063) 3♂, 2♀; (Vale do Igarapé
46
Mutum, Platô do Rio Juruti, 01°36'44.7''S 56°11'39.2''W), 08-15 Aug 2006, D. F.
Candiani & N. F. Lo-Man-Hung (PBI_OON 14449, MPEG 10883 (PBI_OON 14467,
MPEG 10885; PBI_OON 14472, MPEG 10890; PBI_OON 14474, MPEG 10894;
PBI_OON 14476, MPEG 10896; PBI_OON 14477, MPEG 10899; PBI_OON
14480, MPEG 10898; PBI_OON 14481, MPEG 10891) 8♂, 1♀, 13 Aug 2006
(PBI_OON 14470, MPEG 10888) 1♂, 06-13 Feb 2007, J. A. P. Barreiros & N. F.
Lo-Man-Hung (PBI_OON 14557, MPEG 10122; PBI_OON 14568, MPEG 10115;
PBI_OON 14555, MPEG 10135; PBI_OON 14556, MPEG 10107; PBI_OON
14560, MPEG 10127; PBI_OON 14562, MPEG 10061; PBI_OON 14565, MPEG
10085; PBI_OON 14567, MPEG 10093; PBI_OON 14569, MPEG 10070) 9♂, 4♀;
Melgaço, (Estação Científica Ferreira Penna, FLONA Caxiuanã, 01°44'15.5''S
51°26'42.0''W), Apr 2002, Equipe MPEG (PBI_OON 14727, MPEG 10432;
PBI_OON 14729, MPEG 10456; PBI_OON 14731, MPEG 10453; PBI_OON
14732, MPEG 10472; PBI_OON 14734, MPEG 10459; PBI_OON 14736, MPEG
10466; PBI_OON 14737, MPEG 10460; PBI_OON 14740, MPEG 10449;
PBI_OON 14742, MPEG 10469; PBI_OON 14743, MPEG 10463; PBI_OON
14745, MPEG 10437; PBI_OON 14746, MPEG 10458; PBI_OON 14748, MPEG
10465; PBI_OON 14749, MPEG 10442; PBI_OON 14750, MPEG 10471;
PBI_OON 14751, MPEG 10464; PBI_OON 14752, MPEG 10433; PBI_OON
14753, MPEG 10435) 25♂, 3♀, 08-16 Jul 2002 (PBI_OON 14665, MPEG 14047)
1♂, 09 Jul 2002 (PBI_OON 14662, MPEG 14042) 1♂, 11 Jul 2002 (PBI_OON
14664, MPEG 14045) 1♂, Nov 2002 (PBI_OON 14663, MPEG 14043) 1♂, 26 Dec
2002, A. B. Bonaldo & L. F. Montag (PBI_OON 14730, MPEG 9639) 1♂, 09 Mar
47
2003, J. A. P. Barreiros (PBI_OON 14463, MPEG 10392) 1♂, 12 Mar 2003
(PBI_OON 14446, MPEG 10380) 1♀, 19 May 2003 (PBI_OON 14444, MPEG
10376; PBI_OON 14457, MPEG 10391; PBI_OON 14465, MPEG 10395) 2♀, 1♂,
25 May 2003 (PBI_OON 14447, MPEG 10381) 1♂, 28 May 2003 (PBI_OON
14462, MPEG 10389; PBI_OON 14738, MPEG 10343) 2♂, 08 Aug 2003
(PBI_OON 14443, MPEG 10373; PBI_OON 14458, MPEG 10394; PBI_OON
14461, MPEG 10388; PBI_OON 14741, MPEG 10299) 3♂, 1♀, 11 Aug 2003
(PBI_OON 14454, MPEG 10378) 1♂, 14 Aug 2003 (PBI_OON 14464, MPEG
10393) 1♂, 17 Aug 2003 (PBI_OON 14451, MPEG 10382; PBI_OON 14445,
MPEG 10377) 2♂, 20 Aug 2003 (PBI_OON 14460, MPEG 10387) 1♂, 16 Oct 2003
(PBI_OON 14453, MPEG 10386) 1♀, 19 Oct 2003 (PBI_OON 14452, MPEG
10375) 1♂, 21-31 Oct 2003, Equipe MPEG (PBI_OON 14673, MPEG 14057;
PBI_OON 14674, MPEG 14059; PBI_OON 14675, MPEG 14060; PBI_OON
14676, MPEG 14102; PBI_OON 14678, MPEG 14104; PBI_OON 14679, MPEG
14105; PBI_OON 14680, MPEG 14106; PBI_OON 14686, MPEG 14112) 10♂, 2♀,
22 Oct 2003, J. A. P. Barreiros (PBI_OON 14455, MPEG 10390; PBI_OON 14549,
MPEG 10396) 1♂, 3♀, 24 Oct-03 Nov 2003, Equipe MPEG (PBI_OON 14666,
MPEG 14048; PBI_OON 14667, MPEG 14049; PBI_OON 14668, MPEG 14050;
PBI_OON 14669, MPEG 14052; PBI_OON 14671, MPEG 14054; PBI_OON
14681, MPEG 14107; PBI_OON 14682, MPEG 14108; PBI_OON 14683, MPEG
14109; PBI_OON 14684, MPEG 14110; PBI_OON 14685, MPEG 14111) 11♂, 25
Oct 2003, J. A. P. Barreiros, (PBI_OON 14550, MPEG 10371; PBI_OON 14448,
MPEG 10368) 1♂, 1♀, 27-30 Oct 2003, Equipe MPEG (PBI_OON 14670, MPEG
48
14053) 1♀, 28 Oct 2003, J. A. P. Barreiros (PBI_OON 14459, MPEG 10385) 1♂,
31 Oct-03 Nov 2003, Equipe MPEG (PBI_OON 14672, MPEG 14055; PBI_OON
14677, MPEG 14103) 1♂, 1♀. Portel (Parcela PPBio, Igarapé Caquajó, Floresta
Nacional de Caxiuanã, 01°57'38.9''S 51°36'45.3''W), 08-13 May 2005, J. A. P.
Barreiros et al. (PBI_OON 14728, MPEG 10412; PBI_OON 14733, MPEG 10422;
PBI_OON 14735, MPEG 10430; PBI_OON 14739, MPEG 10425; PBI_OON
14744, MPEG 10415; PBI_OON 14747, MPEG 10418) 5♂, 2♀. Santarém
(CEMEX, 02°26'36''S 54°42'29''W), Feb-Apr 1995, L. Vitt et al. (PBI_OON 40127,
MCTP 9810) 1♀.
Neoxyphinus caterete, new species
Figures 6, 18, 24, 30, 44, 52, 289 – 320; Map 1.
TYPES: male holotype from Parque Ilha dos Eucaliptos, Reservatório
Guarapiranga (23°44'1''S 46°44'1''W), 07 Apr 2004 - 13 Apr 2004, I. Cizauskas &
C. R. M. Garcia (PBI_OON 14482, IB 62132). Female allotype, same data
(PBI_OON 14483, IB 62115).
E
TYMOLOGY: Cateretê is a rural music genre, popular in State of São Paulo
countryside.
D
IAGNOSIS: This species is readily recognized by the evenly granulated
carapace surface (Figs. 291, 309, 314) and by the wrinkled sternal furrows (Fig.
315) in both males and females. Males are unique by the embolus with a prolateral
sulcus and apical copulatory opening (Figs. 52, 303). Females resemble those of
49
N. hispidus and N. barreirosi by the wide epigynal atrium, with an anteriorly
positioned median piece (Fig. 320), differing by the carapace micro-sculpture and
by the bilobated epigynal median piece (Fig. 320).
D
ESCRIPTION: MALE (PBI_OON 14482). Total length 2.16. Carapace dark
red-brown, broadly oval in dorsal view, pars cephalica slightly elevated in lateral
view, posterolateral surface without spikes, surface of elevated portion of pars
cephalica and sides granulate, lateral margin straight, rebordered, without
denticles. Clypeus margin unmodified, straight in front view. Eyes: ALE separated
by their radius to diameter. Sternum as long as wide, dark red-brown, median
concavity absent, furrow wrinkled, microsculpture medially and in furrows, anterior
margin with continuous transverse groove, setae evenly scattered, originating from
small pits. Book lung covers large, ovoid. Pedicel tube medium. Dorsal scutum
dark red-brown, middle and sides surface smooth, anterior half without projecting
denticles. Postepigastric scutum dark red-brown. Legs orange-brown. Leg I and II
spines present. Spine formula: tibia I v5-3-2, metatarsus I v2-2-1; tibia II v2-4-1,
metatarsus II v2-2-0. Genitalia: Sperm pore situated at level of anterior spiracles.
Palp proximal segments, cymbium and bulb yellow. Embolus with a prolateral
sulcus and apical copulatory opening, without prolateral prong and prolateral
lamella (Figs. 52, 306).
F
EMALE (PBI_OON 14483). Total length 2.33. Legs I and II spines present.
Spine formula: tibia I v4-4-2, metatarsus I v2-2-1; tibia II v4-4-1, metatarsus II v3-2-
0. Epigynal atrium wide, with an anteriorly positioned, bilobated median piece (Fig.
320).
50
DISTRIBUTION: Known from Southeastern Brazil.
MATERIAL EXAMINED: Paratypes. BRAZIL. Espirito Santo: Linhares (Reserva
Florestal Vale do Rio Doce, 19°23'30'' S 40°04'20'' W), Jun 1997, J. Raizer
(PBI_OON 14692, IB 14881) 1♂. São Paulo: Iporanga (PETAR - Parque Estadual
Turístico do Alto Ribeira, 24°28'30'' S 48°39'30'' W), 02 May 2002, R. Andrade
(PBI_OON 14690, IB 44806) 1♂. Itapevi (Condomínio Residencial TransUrb,
23°32'57'' S 46°56'02'' W), 25 Jun 1999, V. C. Onofrio (PBI_OON 14694, IB 67608)
1♂, 1♀. Peruibe (Estação Ecológica de Juréia - Itatins, 24°18'47'' S 47°00'03'' W),
17-21 Mar 1997, A.D. Brescovit et al. (PBI_OON 14693, IB 9605) 1♂, 2♀. São
Paulo (CUASO, Universidade de São Paulo), 16-23 Aug 1999, D. F. Candiani
(PBI_OON 14691, IB 42180; PBI_OON 14509, IB 42192) 2♂; (Mata da Biologia,
Universidade de São Paulo), 1999, D. F. Candiani (PBI_OON 14485, IB 69007;
PBI_OON 14490, IB 69018; PBI_OON 14516, IB 69010; PBI_OON 14522, IB
69006; PBI_OON 14552, IB 68987) 2♂, 5♀, 11-18 Jun 1999, D. F. Candiani
(PBI_OON 14489, IB 69004; PBI_OON 14502, IB 69019) 1♂, 1♀, 12-19 Dec 1999,
D. F. Candiani (PBI_OON 14521, IB 68998) 2♂; (Parque Ilha dos Eucaliptos,
Reservatório Guarapiranga, 23°44'1''S 46°44'1''W), 07-13 Oct 2003, I. Cizauskas &
C. R. M. Garcia (PBI_OON 14553, IB62152) 1♀, 07-13 Apr 2004 (PBI_OON
14484, IB 62155; PBI_OON 14486, IB 62151; PBI_OON 14487, IB 62105;
PBI_OON 14488, IB 62112; PBI_OON 14491, IB 62131; PBI_OON 14492, IB
62150; PBI_OON 14493, IB 62129; PBI_OON 14508, IB 62149; PBI_OON 14518,
IB 62123; PBI_OON 14520, IB 62107, PBI_OON 14495, IB 62110; PBI_OON
14496, IB 62134; PBI_OON 14497, IB 62158; PBI_OON 14498, IB 62124;
51
PBI_OON 14499, IB 62114; PBI_OON 14500, IB 62142; PBI_OON 14501, IB
62099; PBI_OON 14503, IB 62121; PBI_OON 14504, IB 62162; PBI_OON 14506,
IB 62120; PBI_OON 14507, IB 62104; PBI_OON 14511, IB 62106; PBI_OON
14512, IB 62101; PBI_OON 14513, IB 62130; PBI_OON 14514, IB 62109;
PBI_OON 14515, IB 62156; PBI_OON 14517, IB 62135; PBI_OON 14519, IB
62111; PBI_OON 14523, IB 62139; PBI_OON 14524, IB 62126; PBI_OON 14551,
IB 62113) 23♂, 20♀. São Luis do Paraitinga (Núcleo Santa Virginia, Parque
Estadual Serra do Mar, 23°20'28''S 45°08'49''W), 10 Apr 2005, M. U. Prado
(PBI_OON 14688, IB 58438) 1♀; 22 May 2005 (PBI_OON 14687, IB 58436;
PBI_OON 14689, IB 58439) 2♀.
ACKNOWLEDGEMENTS
This project is part of the Planetary Biodiversity Inventory of “Goblin Spiders”
Oonopidae supported by the U.S. National Science Foundation (NSF grant DEB-
0613754). The author was supported by CNPq (grant 134114/2007-8). Special
thanks to the curators of the collections and others researchers that have supplied
specimens: Antonio Brescovit (IBSP), Luis Pereira (MLP), Cristina Scioscia, Martín
Ramírez (MACN), Norman Platnick (AMNH); Erica Buckup (MCN); Arno Lise
(MCTP); Ricardo Pinto da Rocha (MZSP) and Hubert Höefer (SMNK). I also
thanks to the PBI staff at Butantan for making the automontage pictures of
Neoxyphinus species.
52
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Physis B. Aires 20: 453-458.
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Bristowe, W. S. 1938. Some new termitophilous spider frow Brazil. An. And Meag.
Of Nat. Hist., Ser. 11, vol ii. P. 67.
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Burger, M., and P. Michalik. In press. The male genital system of goblin spiders –
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Museum Novitates.
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Hamburg NP 26:291–292.
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Oonopidae). Acta Arachnologica, 35 (2): 41-56
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in natural and artificial forest gaps at Porto Urucu, Western Brazilian
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Oonopidae (Araneae) du Venezuela. In Fauna hipogea y hemiedáfica de
Venezuela y de otros paises de América del Sur 1: 89-105.
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Platnick, N. I. 2009. The world spider catalog, version 9.5. American Museum of
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http://research.amnh.org/entomology/spiders/catalog/index.html
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55
LEGENDS
Figs. 1-4. Carapace spikes and abdominal denticles, males, lateral view. 1,
2. Neoxyphinus gregoblin new species 3, 4. N. petroglobin new species.
Figs. 5-12. Carapace, posterior view, males. 5. Neoxyphinus barreirosi new
species. 6. N. caterete new species. 7. N. hispidus (Dumitresco and Georgesco).
8. N. brega new species. 9. N. termitophilus (Bristowe). 10. N. petrogoblin new
species. 11. N. gregoblin new species. 12. N. axe new species.
Figs. 13-18. Pedicel, lateral view, males. 13. Neoxyphinus hispidus
(Dumitresco and Georgesco). 14. N. brega new species 15. N. petrogoblin new
species. 16. N. axe new species. 17. N. barreirosi new species. 18. N. caterete
new species.
Figs. 19-24. Chelicerae, posterior view. 19, 20. Neoxyphinus petrogoblin
new species. 21. N. gregoblin new species. 22. N. hispidus (Dumitresco and
Georgesco). 23. N. barreirosi new species. 24. N. caterete new species.
Figs. 25-30. Male endites, ventral view. 25. Neoxyphinus termitophilus
(bristowe). 26. N. hispidus (Dumitresco and Georgesco). 27. N. brega new species.
56
28. N. axe new species. 29. N. barreirosi new species. 30. Neoxyphinus caterete
new species.
Figs. 31-36. 31, 32, 36: Neoxyphinus termitophilus (Bristowe); 33, 34: N.
hyspidus (Dumitresco and Georgesco); 35: Neoxyphinus axe new species. 31.
Labium, ventral view. 32. Leg I, prolateral view. 33. Metatarsus I, apical
Trichobothrium, dorsal view. 34. tarsus II, claw, lateral view. 35. Tarsus I, Tarsal
organ, dorsal view. 36. Spinnerets, posterior view.
Figs. 37-44. Male palpus. 37. Neoxyphinus termitophilus (Bristowe), left
palp, ventral view. 38. N. hispidus (Dumitresco and Georgesco), right palp, ventral
view. 39. N. brega new species, left palp, ventral view. 40. N. petrogoblin new
species, same, retrolateral view. 41. N. gregoblin new species, same, prolateral
view. 42. N. axe new species, same, ventral view. 43. N. barreirosi new species,
same, ventral view. 44. N. caterete new species, same, ventral view.
Figs. 45-50. Left embolus, ventral view. 45. Neoxyphinus termitophilus
(Bristowe) 46. N. hispidus (Dumitresco and Georgesco). 47. N. brega new species.
48. N. petrogoblin new species. 49. N. gregoblin new species. 50. N. axe new
species.
57
Figs. 51 - 54. 51. Neoxyphinus barreirosi new species, left embolus, ventral
view. 52. N. caterete new species, same. 53, 54, Neoxyphinus termitophilus
(Bristowe). 53. Left embolus, apical view. 54. Female epigynum, ventral view.
Figs. 55-64. Neoxyphinus termitophilus (Bristowe), male. 55. Habitus,
dorsal view. 56. Same, lateral view. 57. Carapace, dorsal view. 58. Cephalothorax,
ventral view. 59. Carapace, anterior view. 60. Same, lateral view. 61. Same,
posterior view. 62. Abdomen, dorsal view. 63. Same, ventral view. 64. Same,
lateral view.
Figs. 65--73. Neoxyphinus termitophilus (Bristowe), male, 65. Left palp,
prolateral view. 66. Same, ventral view. 67. Same, retrolateral view. 68, 71.
Embolus, prolateral view. 69, 72. Same, ventral view. 70, 73. Same, retrolateral
view.
Figs. 74-79. Neoxyphinus termitophilus (Bristowe), male. 74. Habitus, lateral
view. 75. Carapace, dorsal view. 76. Cephalothorax, ventral view. 77, 78.
Abdomen, lateral view. 79. Mouthparts, posterior view.
Figs. 80-87. Neoxyphinus termitophilus (Bristowe), female. 80. Habitus,
dorsal view. 81. Same, lateral view. 82. Carapace, anterior view. 83. Same,
posterior view. 84. Abdomen, dorsal view. 85. Same, ventral view. 86.
Cephalothorax, ventral view. 87. Epigynum, dorsal view.
58
Figs. 88-97. Neoxyphinus xyphinoides (Chamberlin and Ivie), male. 88.
Habitus, dorsal view. 89. Same, lateral view. 90. Cephalothorax, ventral view. 91.
Abdomen, ventral view. 92. Left palp, prolateral view. 93. Same, ventral view. 94.
Same, retrolateral view. 95. Left palp, embolus, prolateral view. 96. Same, ventral
view. 97. Same, retrolateral view.
Figs. 98-106. Neoxyphinus hispidus (Dumitresco and Georgesco), male. 98.
Habitus, dorsal view. 99. Same, same view. 100. Same, lateral view. 101.
Carapace, anterior view. 102. Same, posterior view. 103. Abdomen, lateral view.
104. Same, ventral view. 105. Same, anterior view. 106. Cephalothorax, ventral
view.
Figs. 107-115. Neoxyphinus hispidus (Dumitresco and Georgesco), male, 107.
Right palp, prolateral view. 108. Same, ventral view. 109. Same, retrolateral view.
110. Left palp, prolateral view. 111. Right palp, ventral view. 112. Left palp,
retrolateral view. 113. Left palp, embolus, prolateral view. 114. Same, ventral view.
115. Same, retrolateral view.
Figs. 116-121. Neoxyphinus hispidus (Dumitresco and Georgesco), male.
116. Carapace, lateral view. 117. Cephalothorax, ventral view. 118. Mouthparts,
posterior view. 119, 120. Abdomen, lateral view. 121. Same, anterior view.
59
Figs. 122-129. Neoxyphinus petrogoblin new species, male. 122, 123.
Habitus, dorsal view. 124. Same, lateral view. 125. Abdomen, ventral view. 126.
Same, lateral view. 127. Same, anterior view. 128. Cephalothorax, ventral view.
129. Carapace, posterior view.
Figs. 130-138. Neoxyphinus petrogoblin new species, male, 130. Left palp,
prolateral view. 131. Same, ventral view. 132. Same, retrolateral view. 133. Right
palp, embolus, prolateral view. 134. Left palp, embolus, ventral view. 135. Same,
retrolateral view. 136. same, embolus, prolateral view. 137. Same, ventral view.
138. Same, retrolateral view.
Figs. 139-144. Neoxyphinus petrogoblin new species, male. 139.
Cephalothorax, lateral view. 140. same, dorsal view. 141. abdomen, lateral view.
142. same, antero-lateral view. 143, 144. Same, lateral view.
Figs. 145-152. Neoxyphinus petrogoblin new species, female. 145, 146.
Habitus, dorsal view. 147. Same, lateral view. 148. Abdomen, anterior view. 149.
Carapace, posterior view. 150. Abdomen, ventral view. 151. Same, lateral view.
152. Epigynum, dorsal view.
Figs. 153-159. Neoxyphinus gregoblin new species, male. 153. Habitus,
dorsal view. 154. Same, lateral view. 155. Carapace, dorsal view. 156.
60
Cephalothorax, ventral view. 157. Abdomen, ventral view. 158. Same, lateral view.
159. Leg I, prolateral view.
Figs. 160-169. Neoxyphinus gregoblin new species, male. 160. Right palp,
prolateral view. 161. Same, ventral view. 162. Same, retrolateral view. 163. Same,
embolus, ventral view. 164. Left palp, same. 165. Same, prolateral view. 166.
Compound microscope, same, embolus, prolateral view. 167. Same, ventral view,
apices in focus. 168. Same, basis in focus. 169. Same, retrolateral view.
Figs. 170-175. Neoxyphinus gregoblin new species, male. 170.
Cephalothorax, lateral view. 171. Same, frontal view. 172. Carapace spike, lateral
view. 173. Chelicerae, posterior view. 174. Abdomen, lateral view. 175. Epigastric
scutum, ventral view.
Figs. 176-181. Neoxyphinus gregoblin new species, female. 176, 177.
Habitus, dorsal view. 178. Same, lateral view. 179. Abdomen, ventral view. 180.
Same, anterior view. 181. Epigynum, dorsal view.
Figs. 182-193. Neoxyphinus axe new species, male. 182, 183. Habitus,
dorsal view. 184. Same, lateral view. 185. Cephalothorax, anterior view. 186.
Same, lateral view. 187. Same, posterior view. 188. Same, dorsal view. 189.
61
same, ventral view. 190. Abdomen, anterior view. 191. Same, dorsal view. 192.
Same, lateral view. 193. Same, ventral view.
Figs. 194-202. Neoxyphinus axe new species, male, 194. Right palp,
prolateral view. 195. Same, ventral view. 196. Same, retrolateral view. 197. Left
palp, embolus, prolateral view. 198. Same, apical view. 199. Same, retrolateral
view. 200. Left palp, embolus, prolateral view. 201. Same, ventral view. 202.
Same, retrolateral view.
Figs. 203-208. Neoxyphinus axe new species, male. 203, 207.
Cephalothorax, latero-posterior view. 204 – 206. Abdomen, lateral view. 208.
Mouthparts, posterior view.
Figs. 209-217. Neoxyphinus axe new species, female. 209. Habitus, dorsal
view. 210. Same, lateral view. 211. cephalothorax, anterior view. 212. Same,
lateral view. 213. Same, posterior view. 214. Abdomen, ventral view. 215. Same,
lateral view. 216. Same, anterior view. 217. Epigynum, dorsal view.
Figs. 218-229. Neoxyphinus barreirosi new species, male. 218, 219.
Habitus, dorsal view. 220. Same, lateral view. 221. Cephalothorax, anterior view.
222. Same, lateral view. 223. Same, posterior view. 224. Same, dorsal view. 225.
Same, ventral view. 226. Abdomen, anterior view. 227. Same, dorsal view. 228.
Same, lateral view. 229. Same, ventral view.
62
Figs. 230-238. Neoxyphinus barreirosi new species, male, 230. Left palp,
prolateral view. 231. Same, ventral view. 232. Same, retrolateral view. 323, 236.
Left palp, embolus, prolateral view. 234, 237. Same, ventral view. 235, 238. Same,
retrolateral view.
Figs. 239-244. Neoxyphinus barreirosi new species. 239, 240. Male habitus
and carapace, dorsal view. 241. Female Abdomen, frontal view. 242. Male
abdomen, lateral view. 243. Male endite, posterior view. 244. Male cephalotorax,
ventral view.
Figs. 245-255. Neoxyphinus barreirosi new species, female. 245, 246.
Habitus, dorsal view. 247. Same, lateral view. 248. Cephalothorax, dorsal view.
249. same ventral view. 250. same, anterior view. 251. Same, posterior view. 252.
Abdomen, dorsal view. 253. Same, ventral view. 254. Same, lateral view. 255.
Epigynum, dorsal view.
Figs. 256-265. Neoxyphinus brega new species, male. 256, 257. Habitus,
dorsal view. 258. Cephalothorax, anterior view. 259. Same, lateral view. 260.
Same, posterior view. 261. Abdomen, dorsal view. 262. Same, ventral view. 263.
Same, lateral view. 264. Cephalothorax, ventral view. 265. Abdomen, anterior
view.
63
Figs. 266-274. Neoxyphinus brega new species, male, 266. Left palp,
prolateral view. 267. Same, ventral view. 268. Same, retrolateral view. 269. Right
palp, embolus, prolateral view. 270. Left palp, embolus, ventral view. 271. Same,
retrolateral view. 272. Left palp, embolus, prolateral view. 273. Same, ventral view.
274. Same, retrolateral view.
Figs. 275-278. Neoxyphinus brega new species, male. 275. cephalothorax,
dorsal view. 276. Same, lateral view. 277. Sternum, ventral view. 278. Abdomen,
lateral view.
Figs. 279-288. Neoxyphinus brega new species, female. 279. Habitus,
dorsal view. 280. Same, lateral view. 281. Cephalothorax, anterior view. 282.
Same, lateral view. 283. Same, posterior view. 284. Abdomen, dorsal view. 285.
Same, ventral view. 286. Same, lateral view. 287. Cephalothorax, ventral view.
288. Epigynum, dorsal view.
Figs. 289-298. Neoxyphinus caterete new species, male. 289, 290. Habitus,
dorsal view. 291. Cephalothorax, dorsal view. 292. same, ventral view. 293. same,
anterior view. 294. Same, posterior view. 295. Abdomen, anterior view. 296.
Same, dorsal view. 297. Same, ventral view. 298. Same, lateral view.
Figs. 299-307. Neoxyphinus caterete new species, male, 299. Left male
palp, prolateral view. 300. Same, ventral view. 301. Same, retrolateral view. 302.
64
Left palp, embolus, prolateral view. 303. Right palp, apical view. 304. Left palp,
retrolateral view. 305. Left palp, embolus, prolateral view. 306. Same, ventral view.
307. Same, retrolateral view.
Figs. 308-311. Neoxyphinus caterete new species, male. 308. Habitus,
lateral view. 309. Cephalothorax, dorsal view. 310. same, ventral view. 311.
Mouthparts, posterior view.
Figs. 312-320. Neoxyphinus caterete new species, female. 312. Habitus,
dorsal view. 313. Same, lateral view. 314. Cephalothorax, dorsal view. 315. same,
ventral view. 316. Abdomen, dorsal view. 317. Same, lateral view. 318. Same,
ventral view. 319. Cephalothorax, anterior view. 320. Epigynum, dorsal view.
Map 1. Known distribution of Neoxyphinus species.
2
1
3
4
5
6
7
8
9
10
11
12
16
17
18
13
14
15
19
22
21
20
23 24
25
26
27
28
29
30
31 32
33 34
35
36
37 38
39 40
41 42
43 44
45 46
47
48
49
50
53 54
51 52
55 56
57
58
59
60
61
62 63 64
68 69
70
71 72
73
65 66 67
74
75
76
77
78
79
80
81 82
83
84 85 87
86
88 89 91
90
94
979695
9392
98 99
100
102101
105
106
104103
107
108
109
110
111 112
113
114
115
116
117
119
121
120
118
122
123
124
125
126 127
129128
130 131
132
135134133
138137136
139
140
141 142
143
144
145
146
147
148
149
152
151150
153 154
158
157
159
156
155
160 161 162
165
164
166 167
168 169
163
170
172
171
175
174
173
176
177
178
181180
179
182 183 184
185 186 187
188 189
190
193192191
194
195
196
199198197
202201
200
203 204
205
207
208
206
211
212
213
216
217
215
214
209
210
218 219
220
223222221
226
225
224
229228
227
230
231
232
235
234
233
236 237 238
239
240
241
243
242
244
245 246
247
250
251
255254253252
248
249
256 257
260
259
258
261 262 263 265
264
266 267 268
269
270 271
272 273 274
275 276
278277
279 280
281
282
283
287
288284 285 286
289 290
293 294
295
292
291
298297296
299 300 301
304
303
302
305 306 307
308 309
311310
312
313
314
315
319
320
318
317316
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