62,168 research outputs found
The One-Armed Spiral Instability in Neutron Star Mergers and its Detectability in Gravitational Waves
No full text<p>We distribute complete gravitational-wave signals in the Advanced LIGO band (10 Hz - 8192 Hz) of the inspiral and merger of two neutron stars. These waveforms been constructed by hybridizing numerical-relativity data obtained with the WhiskyTHC code [1] with tidal effective-one-body waveforms [2,3]. More details on the procedure used to generate these waveforms are given in [4]. </p>
<p>The waveforms are distributed as HDF5 files containing the amplitude and phase of the -2 spin-weighted spherical harmonics multipoles of the strain:</p>
<p><span class="math-tex"></span></p>
<p>where <span class="math-tex"></span> is the distance in cm from the source.</p>
<p>The data files include a machine readable "/metadata" group with:</p>
<ul>
<li>/metadata/EOS: name of the equation of state</li>
<li>/metadata/M_{A|B}: mass in isolation of star A (or B) in grams</li>
<li>/metadata/R_{A|B}: radius of star A (or B) in cm</li>
<li>/metadata/k2T: tidal coupling constant of the binary (see [3])</li>
<li>/metadata/kl_{A|B}: l=2,3,4 dimensionless Love numbers of star A (or B)</li>
</ul>
<p>We store amplitude and phase for multipoles modes up to l=4 as time series sampled at 16384 Hz.</p>
<p>We make these waveforms freely available in the hope that they will be useful. We kindly ask you to cite [3] and [4] in any publication resulting from the use of these waveforms.</p>
<p>---<br />
[1] http://www.tapir.caltech.edu/~david_e/whiskythc.html<br />
[2] https://eob.ihes.fr/<br />
[3] S. Bernuzzi, A. Nagar, T. Dietrich, T. Damour; Modeling the Dynamics of Tidally Interacting Binary Neutron Stars up to the Merger; Phys.Rev.Lett. 114 (2015) 16, 161103.<br />
[4] D. Radice, S. Bernuzzi, C. D. Ott; The One-Armed Spiral Instability in Neutron Star Mergers and its Detectability in Gravitational Waves; arXiv:1603.05726.</p>
Arauchemus graudo Ott & Brescovit, 2012, sp. nov.
No full textArauchemus graudo sp. nov. Figs 1 A, B; 2; 4; 5; 7 A; 8 A; 9 Type material. Holotype: male from CPCN Pró-Mata, Potreiro Velho, São Francisco de Paula, Rio Grande do Sul, Brazil, 07.IV. 2001, R. Ott leg. (MCN 47641). Paratypes: 1 male, 3 females, 07.IV. 2001 (MCN 47643); 1 female, 09.VIII. 2001 (MCN 47644); 2 females, 13.XI. 2001 (MCN 47645); 2 females, 14.IV. 2002 (MCN 47646); 2 males, 01.V. 2001 (MCN 47647); 2 males, 07.IV. 2001 (MCN 47648); 2 females, 25.XI. 2000 (MCN 47649); 1 females, 25.X. 2000 (MCN 47658); 1 male, 14.IV. 2002 (IBSP 160963); 1 male, 07.IV. 2001 (IBSP 160964); 1 female, data as holotype, 02.I. 2001 (IBSP 160965); 1 female, 02.I. 2001 (IBSP 160966); 2 males, 14.IV. 2002 (MCTP 30060); 2 females, 18.V. 2002 (MCTP 30061); all same locality and collector as holotype. Other material examined: BRAZIL. Rio Grande do Sul: 13 males, 10 females, CPCN Pró-Mata, São Francisco de Paula, 25.X. 2000 – 18.V. 2002, R. Ott leg. (MCN 47661 –47680); 51 males, 81 females, same data above (MCTP 8976–8981; 30069–30117); 12 males, 10 females, same data above (IBSP 161021 – 161032). Etymology. The specific name is an adjective which in Brazilian slang means “large, well developed”. Diagnosis. Males can be recognized by the short, curved and stout embolus (Figs. 1 A, B; 4 B, C). Females by the epigynal plate as long as wide with short posterior septum (Figs. 2 F–G). Description. Male (holotype). Carapace, chelicerae, endites, labium, sternum and legs orange-brown. Abdomen grayish with darker anterodorsal scutum; pale orange spinnerets. Total length 6.3. Carapace 2.7 long, 2.2 wide. Clypeus 0.12 high. Eye diameters and interdistances: AME 0.16, ALE 0.16, PME 0.14, PLE 0.16; AME–AME 0.04, AME–ALE touching, PME–PME 0.08, PME–PLE 0.08, ALE–PLE 0.06. Abdomen with oval anterior dorsal scutum. Leg measurements: I – femur 2.2 / patella 1.5 / tibia 2.1 / metatarsus 1.7 / tarsus 1.1 / total 8.6 / II – 1.9 / 1.2 / 1.5 / 1.4 / 1.0/ 7.0/ III – 1.8 / 1.0/ 1.3 / 1.4 / 0.8 / 6.3 / IV – 2.3 / 1.0/ 1.8 / 2.2 / 0.8 / 8.1. Leg spination: femur I d 1 - 1 -0, p0- 0-1, II d 1 - 1 -0, p0- 0-1, III d 1 - 1 - 1, p0- 0-1, r 1 - 1 - 1, IV d 0-1 - 1, p0- 0-1, r0- 0-1; patela III r 1, IV r 1, tibia I v 1 p- 1 p- 1 p, II v 0-2 - 1 p, III d 1 - 1 -0, p 1-2 - 1 - 1 - 1, r 1 - 1 - 1, v 2-3 - 3 - 2; IV d 1- 2 - 1 - 1, p 1 - 1 -0, r 1 - 1 -0, v 1 p- 3 - 2 - 2, metatarsus I v 0-2 -0, II v 0-2 -0, III d 0-2 - 2, p 2 - 2 - 1 - 1 - 1, r 1 - 1 - 1, v 2 - 2 -0, IV d 0-2 - 2, p 1 - 1 - 1 - 1, r 1 - 1-2 - 1 - 1-2, v 0-2 - 1-2. Palp with short, robust embolus with distal, small, thorn-like processes (Figs 4 A–C); small triangular process at dorsal base of retrolateral tibial apophysis (Fig. 2 C). Female (paratype MCN 47658). Coloration as in male. Total length 7.5. Carapace 4.8 long, 2.8 wide. Clypeus 0.12 high. Eye diameters and interdistances: AME 0.16, ALE 0.14, PME 0.14, PLE 0.14; AME–AME 0.04, AME–ALE touching, PME–PME 0.10, PME–PLE 0.08, ALE–PLE 0.06. Abdomen dorsal scutum absent. Leg measurements: I – femur 2.4 / patella 1.6 / tibia 1.8 / metatarsus 1.5 / tarsus 1.0/ total 8.30 / II – 2.3 / 1.5 / 1.6 / 1.6 / 1.0/ 8.0/ III – 1.8 / 1.0/ 1.1 / 1.6 / 0.8 / 6.3 / IV – 2.6 / 1.4 / 2.0/ 2.3 / 1.0/ 9.3. Leg spination: femur I d 1 - 1 -0, p 1 - 1 -0, II d 0-1 - 1, d 1 - 1 -0, III d 1 - 1-2, p 0-1 - 1, r 0-1 - 1, IV d 1 - 1 - 1, p0- 0-1, r0- 0-1, tibia I v 0-1 p-0, II v 0-2 - 1 p, III p 1 - 1 - 1, r 0-1 -0, 1p- 2 - 2, d 1 -0-0, IV p 1 - 1 -0, r 1-2 - 2, v 2 - 2 - 2, metatarsus I –II v 0-2 -0, III p 1-2 - 2, r 1 - 1-2; v 0-2 -0, IV p 1 - 1 - 1, r 2 - 2 - 2, v 2 - 2 -0. Pedipalp: femur I d 1 - 1, p 1, patella p 1, tíbia p 1, r 1 - 1, tarsus d 1, p 1 - 1, r 1. Epigynum with small anterior hood and short median posterior septum (Fig. 2 F). Rounded spermathecae separated from each other around 1 / 3 of their diameter (Fig. 2 F); copulatory ducts coiled forming large oval sections; fertilization ducts in anterior half of spermathecae (Fig. 2 G). Variation. Males (72 specimens): total length 4.5–7.6; carapace 1.9–3.2; femora I 1.7–2.9. Females (10 specimens): total length 6.2–7.7; carapace 2.4–3.8; femora I 1.8–2.4. Distribution. Known only from the type locality in the state of Rio Grande do Sul, Brazil.Published as part of Ott, Ricardo & Brescovit, Antonio Domingos, 2012, Arauchemus, a new spider genus of the Echemus group (Araneae: Gnaphosidae: Echeminae) from Araucaria Forest areas in southern Brazil, with notes on habitat preferences and phenology, pp. 44-56 in Zootaxa 3339 on pages 47-49, DOI: 10.5281/zenodo.20977
"Closing the R&D Gap, Evaluating the Sources of R&D Spending"
No full textBoth spending and tax policies have been implemented in the United States with the goal of stimulating private sector research and development (R&D). Karier questions whether current R&D policy, especially the research and experimentation tax credit, can contribute to closing the gap between nondefense expenditures on R&D in the United States and such expenditures in other countries, such as Japan and Germany. He also explores possible changes to our current R&D policy to make it more effective.
Letter from C. D. Dawson, Tusayan Copper Mining and Smelting, to Carl Hayden
No full textLetter from C. D. Dawson to Carl Hayden urging him to consider the rights of miners and farmers when drawing up the boundaries for the proposed park
Arauchemus Ott & Brescovit, 2012, gen. nov.
No full textArauchemus gen. nov. Type species. Arauchemus graudo sp. nov. Etymology. Arauchemus is a contraction between Araucaria and Echemus. Gender is masculine. Diagnosis. Species of this genus can be recognized as belonging to the “ Echemus group” (Murphy, 2007) by the pale abdomen, presence of abdominal dorsal scuta in males, the typical dentition with three teeth at PM and one at RM (Fig. 6 E) and by the larger AME (Figs 2 A, 3 A). Males of Arauchemus differ from those of all other genera of the Echemus group by the presence of several thorn-like processes at distal portion of a very robust male embolus (Figs 4 C, 6 C); females by the small and rounded spermathecae with copulatory ducts posterior to the atrium and to the copulatory openings, forming some 2–3 large rounded to oval sections almost as large as the spermathecae in diameter (Figs. 2 G; 3 G). Note. The placement into Echeminae (sensu Platnick & Shadab, 1976) is justified by the pectinate tarsal claws (Figs 4 G, 5 G), toothed cheliceral promargin (Fig. 6 E) and procurved posterior eye row (Figs 2 A, D; 3 A, D). Platnick & Shadab (1976) would consider for Echeminae only the genera with strong procurved eye row (not exactly the case of Arauchemus species, which presents less conspicuously procurved eye rows) but we considered the placement into this subfamily as the more adequate option. Based on a recent definition of Murphy (2007: 50) there is no doubt that the herein proposed new genus can be regarded as belonging to the Echemus group, since this species posses pale abdomen and developed scutum at males. The new genus is very close to Echemus by the presence of an anterior hood on the female epigynum (Figs 2 F, 3 F), small spermathecae and copulatory ducts of almost the same diameter as spermathecae (Figs 2 G; 3 G). However, the placement of the spermathecae closer to the median body line in Arauchemus (Figs 2 F, G; 3 F, G) is different from the type species of Echemus, E. angustifrons (Westring 1961), in which the spermathecae are located far apart from each other (see Platnick, 1976: 3, figs 3, 4; Murphy, 2007: 349). In E. angustifrons, also differing from Arauchemus, the bulb of male palp present a clear division, with the median apophysis placed well distally. The widely different morphologies of the male palpal bulb in Echemus species suggests that it does not constitute a monophyletic group as currently delimited (e.g., the very divergent morphology of palp in E. angustifrons and E. giaii Gerschman & Schiapelli 1948). Otherwise the embolus in the Echemus group is usually very slender (except in the genus Micythus Thorell 1897; see Murphy, 2007: 365, but in this one the female external genitalia is quite different from Arauchemus). Description. Total length 3.45–7.40. Yellowish-brown to orange-brown colored spiders. Cephalothorax oval, sulcated posteriorly, covered with weak setae (denser and stronger at area between pars cephalica and pars thoracica); thoracic grove short and narrow, longitudinal, at level of second and third coxae. Anterior eye row recurved, posterior eye row slightly procurved; AME largest, surrounded by darker tegument; AME, ALE and PLE rounded, PME smaller and slightly oval (Figs 2 A, D; 3 A, D). Clypeus low, around AME radius. Chelicerae with three teeth at PM and one at RM. Endites longer than wide. Labium triangular, slightly elongated, truncated distally. Sternum broad and rounded anteriorly, narrowing posteriorly, not extending posterior of coxae IV (Fig. 3 E). Leg formula 1423; all femora with dorsal spines; tibia and metatarsus of legs III and IV heavily spinose, same segments of legs I and II much less spinose; tarsal scopula inconspicuous; preening brush distoventral at metatarsi III and IV (Figs 2 B, 3 B, 4 H, 5 H); plumose setae present on leg and palp articles (Fig. 4 D). Trichobotria base with 4–6 ridges (Figs 4 E, 5 C). Tasal organ rounded, slightly elevated and with oval aperture (Figs 5 B, 6 H). Claws pectinate, with long teeth; claw tuffs formed by elongated and flattened hairs (Figs 4 G; 5 A, G). Abdomen grayish, elongated; frontal area covered with longer setae; anterodorsal scutum in males covered with needle-like and branched plumose setae (Fig. 6 F), scutum absent in females, needle-like and plumose setae present at same area. Posterior median spinnerets with large ampullar fusulas (Figs 5 D, E). Male palp with small triangular retrolateral apophysis (Figs 1 B, 1 D, 2 C, 3 C, 4 F, 6 D); robust and somewhat flattened embolus, distally covered with thorn-like processes, conductor lamellar and membranous, median apophysis hook-shaped (Figs 1 A–D; 4 A–C; 6 A–C). Female palp with pectinate claw (Fig. 5 F). Epigynum with single anterior atrial hood, copulatory openings oblique, slit-like, atrium widened anteriorly (Figs. 2 F, 3 F); spermathecae and copulatory ducts posterior to the atrium and copulatory openings; spermathecae small, rounded, very closed together; copulatory ducts coiled, forming some 2–3 large rounded to oval sections which are almost as large as spermathecae in diameter (Figs. 2 G; 3 G). Composition. Two species: Arauchemus graudo sp. nov. and Arauchemus miudo sp. nov.Published as part of Ott, Ricardo & Brescovit, Antonio Domingos, 2012, Arauchemus, a new spider genus of the Echemus group (Araneae: Gnaphosidae: Echeminae) from Araucaria Forest areas in southern Brazil, with notes on habitat preferences and phenology, pp. 44-56 in Zootaxa 3339 on pages 45-47, DOI: 10.5281/zenodo.20977
Short answer assessment: Establishing links between research strands
No full textZiai, R., N. Ott & D. Meurers (2012). Short answer assessment: Establishing links between research strands. In J. Tetreault, J. Burstein & C. Leacock (eds.), Proceedings of the 7th Workshop on Innovative Use of NLP for Building Educational Applications (BEA-7) at NAACL-HLT 2012, 190–200. Montreal: Association for Computational Linguistics
Arauchemus miudo Ott & Brescovit, 2012, sp. nov.
No full text<i>Arauchemus miudo</i> sp. nov. <p>Figs 1C, D; 3; 6; 7B; 8B; 9</p> <p> <b>Type material. Holotype:</b> male from CPCN Pró-Mata, Potreiro Velho, São Francisco de Paula, Rio Grande do Sul, Brazil, 07.IV.2001, R. Ott leg. (MCN 47642). <b>Paratypes:</b> 1 female, 07.VII.2001 (MCN 47650); 1 female, 02.II.2001 (MCN 47651); 5 males, 07.IV.2001 (MCN 47652); 1 female, 25.X.2000 (MCN 47653); 2 females, 14.IV.2001 (MCN 47654); 4 males, 07.IV.2001 (MCN 47655); 2 females, 02.II.2002 (MCN 47656); 1 female, 02.I.2001 (MCN 47657); 1 female, 02.I.2001 (MCN 47659); 5 males, 07.IV.2001 (MCN 47660); 2 males, 14.IV.2002 (IBSP 160962); 1 male, 14.IV.2002 (IBSP 160961); 1 female, 23.XI.2000 (IBSP 160960); 1 female, 23.XI.2000 (IBSP 160959); 2 males, 14.IV.2002 (MCTP 30062); 1 female, 23.XI.2000 (MCTP 30063); 1 female, 02.I.2001 (MCTP 30064); all same locality and collector as holotype.</p> <p> <b>Other material examined:</b> BRAZIL. <i>Rio Grande do Sul</i>: 62 males, 39 females, CPCN Pró-Mata, São Francisco de Paula, 25.X.2000 – 18.V.2002, R. Ott leg. (MCN 47693–47734); 172 males, 23 females, same data above (MCTP 30118–30162); 13 males, 8 females same data above (IBSP 161009 – 161020).</p> <p> <b>Etymology.</b> The specific name is an adjective which in Brazilian slang means “small, less developed”.</p> <p> <b>Diagnosis.</b> Males can be recognized by the long and coiled embolus (Figs 1C, D; 6A, B). Females by a wider than long epigynal plate with T-shaped atrium. (Fig. 3F).</p> <p> <b>Description. Male</b> (<b>holotype</b>). Coloration as in <i>A. graudo</i>, but abdomen paler with brownish scutum and yellowish spinnerets. Total length 4.90. Carapace 2.10 long, 1.60 wide. Clypeus 0.10 high. Eye diameters and interdistances: AME 0.12, ALE 0.12, PME 0.10, PLE 0.12; AME–AME 0.04, AME–ALE touching, PME–PME 0.06, PME–PLE 0.06, ALE–PLE 0.04. Abdomen with anterodorsal scutum. Leg measurements: I – femur 1.90/ patella 1.20/ tibia 1.70/ metatarsus 1.50/ tarsus 0.80/ total 7.10/ II – 1.60/ 0.90/ 1.10/ 1.10/ 0.70/ 5.40; III – 1.50/ 0.60/ 0.90/ 1.10/ 0.60/ 4.70; IV – 1,70/ 0.70/ 1.20/ 1.70/ 0.70/ 6;00. Leg spination: femur I d0-1-1, p0-0-1, II d0-1-2, p0- 0-1, III d0-1-1, p0-0-1, r0-1-1, IV d0-1-1, p0-0-1, r0-0-1; patela III r1, IV r1, tibia II v0-1p-1p, III p1-1-0, r1-1-0, v1 p-2-2; IV p1-1-1, r1-1-1, v1 p-2-2, metatarsus I v1 v-0-0, II v1 r-0-0, III p1-1-1, r1-1-1-1, v0-2-0, IV p1-2-2, r1-2- 2, v2-2 -0. Embolus distally with large number of thorn-like processes (Figs 6A–C); small retrolateral triangular process at distal half of tibia (Fig. 3C).</p> <p> <b>Female</b> (<b>paratype MCN 47659</b>). Coloration as in male. Total length 5.10. Carapace 1.80 long, 1.50 wide. Clypeus 0.08 high. Eye diameters and interdistances: AME 0.10, ALE 0.10, PME 0.10, PLE 0.10; AME–AME 0.04, AME–ALE touching, PME–PME 0.06, PME–PLE 0.06, ALE–PLE 0.04. Abdomen dorsal scutum absent. Leg measurements: I – femur 1.60/ patella 0.90/ tibia 1.10/ metatarsus 1.00/ tarsus 0.70/ total 5.30/ II – 1.20/ 0.70/.00/ 0.80/ 0.60/ 4.30/ III – 1.30/ 0.60/ 0.70/ 0.90/ 0.50/ 4.00/ IV – 1.50/ 0.70/ 1.10/ 1.30/ 0.60/ 5.20. Leg spination: femur I d1-1-1p, II d1-1-0, III d1-1-2, IV d1-1-1r, tibia II v0-1p-1p, III-IV p1-1-0, r 1-1-10, v1p-2-2, metatarsus II v2 -0-0, III p1-1-2, r1-1-2; v0-2-0, IV p1-1-2, r1-1-2, v1 p-2-0. Pedipalp: femur I d1-1, p1, patella p1, tíbia p1, r1-1. Tarsus d1, p1-1, r1, with ventral tuft of setae. Epigynum wider than long, with wide hood and conspicuous slit-like openings “Y” shaped copulatory opening areas (Figs 3F, G). Rounded and contiguous spermathecae (Figs 3F, G); copulatory ducts coiled forming large rounded sections; fertilization ducts very short in posterior half of spermathecae (Fig. 3G).</p> <p> <b>Variation.</b> Males (72 specimens): total length 3.7–6.1; carapace 1.5–2.6; femora I 1.3–2.3. Females (10 specimens): total length 5.1–4.2; carapace 1.5–1.8; femora I 1.3–1.6.</p> <p> <b>Distribution.</b> Known only from the type locality in the state of Rio Grande do Sul, Brazil.</p>Published as part of <i>Ott, Ricardo & Brescovit, Antonio Domingos, 2012, Arauchemus, a new spider genus of the Echemus group (Araneae: Gnaphosidae: Echeminae) from Araucaria Forest areas in southern Brazil, with notes on habitat preferences and phenology, pp. 44-56 in Zootaxa 3339</i> on pages 49-54, DOI: <a href="http://zenodo.org/record/209775">10.5281/zenodo.209775</a>
Measurement of the D+/- production asymmetry in 7 TeV pp collisions
No full textThe asymmetry in the production cross-section \sigma of D+/- mesons, A_P = (\sigma(D+) - \sigma(D-))/(\sigma(D+) + \sigma(D-)), is measured in bins of pseudorapidity \eta and transverse momentum p_T within the acceptance of the LHCb detector. The result is obtained with a sample of D+ -> K_S pi+ decays corresponding to an integrated luminosity of 1.0 fb^-1, collected in pp collisions at a centre of mass energy of 7 TeV at the Large Hadron Collider. When integrated over the kinematic range 2.0 K_S pi+ decay is negligible. No significant dependence on \eta or p_T is observed
Predatoroonops blain Brescovit, Rheims, and Ott 2012, new species
No full textPredatoroonops blain Brescovit, Rheims, and Ott, new species Figures 17, 153–176; map 2 TYPES: Male holotype and female paratype from Parque da Cidade Joventino Silva, 12 ° 599570S 38 ° 289160W, Salvador, Bahia, Brazil (Aug. 22–Sept. 03, 2008; C. Queiróz and D. Mendes) deposited in IBSP 125541 (PBI _ OON 11097). ETYMOLOGY: The specific name refers to the character Blain Cooper, played by Jesse Ventura, in the movie ‘‘Predator’’; he often chews tobacco and wears a battered old slouch hat. DIAGNOSIS: Males of Predatoroonops blain differ from those of the remaining species by the chelicerae with large, triangular subdistal furrow (figs. 17, 156), short lateral subdistal apophysis short and truncated; short, bifid distal projections (fig. 17). Females can be easily distinguished from those of the remaining species by the very long anterior receptaculum with globose tip, short with sinuous posterior receptaculum (figs. 174– 176). MALE (PBI_ OON 10997): Total length 1.99. Carapace 0.90 long, 0.60 wide. ALE 0.10, PLE 0.10, PME 0.12, ALE-ALE 0.06. Carapace orange, without any pattern, anterolateral corners with slightly sclerotized triangular projections (figs. 155, 158). Sternum yellow-brown. Chelicerae, endites, and labium orange-brown. Clypeus with very small needlelike setae (fig. 17). Chelicerae anterior face with small median furrow, subdistal narrow furrow large triangular, lateral subdistal apophysis short and truncated, short and bifid distal projections, condylar projection absent (fig. 17). Abdomen dorsum pale orange. Legs orange, femur I 0.80 long. Leg spination: femur I d1-0-0; v2- 2-1; II d1-0-0; v0-2-2; III d1-0-0; IV d1-0-1; tibia I v2-2-2-2-2, II v2-2-2-2-2, III p0-0-1; v0-1-2; r0-0-1; IV p0-1-1; v0-1-2; r0-1-1; metatarsus I v2-2-2-2, II v2-2-2-2, III v0-1- 2; r0-0-1; IV d0-1-0; p0-0-1; v1-0-2; r0-0-1. Male palp proximal segments orange-brown; cymbium pale orange, bulb yellow, slender hyaline process narrow and twisted with laminar hyaline process (figs. 161–163). FEMALE (PBI_OON_0011097): Total length 2.35. Carapace 0.95 long, 0.75 wide. ALE 0.12, PLE 0.10, PME 0.12, ALE-ALE 0.06. Abdomen dorsum orange. Legs: femur I 0.80 long. Leg spination: femur I v2-2-1; II v0-2-2; III d1-0-0; IV d1-1-0; tibia I v2-2-2-2-2, II v2- 2-2-2-2, III p1-1-0; v0-2-2; r1-1-0; IV p1-1-0; v1-0-2; r1-1-0; metatarsus I v2-2-2-2, II v2-2- 2-2, III v0-1-1; r1-1-0; IV d0-1-0; p1-1-1; v1-0- 2; r1-1-1. Internal genitalia with very long anterior receptaculum with globose tip and short and sinuous posterior receptaculum (figs. 174–176); long and semicircular apodema plate with elongated and sinuous apodema process (figs. 175–176). OTHER MATERIAL EXAMINED: BRAZIL: Bahia: Salvador, Parque da Cidade Joventino Silva, 12 ° 58960S, 38 ° 319W, Aug. 22–Sept. 03, 2008, pitfall (C. Queiróz and D. Mendes, IBSP 125537–125540, PBI _ OON 11091– 11092, 11094, 11096; IBSP 125542–125543, PBI _ OON 11093, 11095), 78 1♀; Cachoeira, Comunidade de São Francisco de Paraguaçu, Reserva de Peninha, 13 ° 4590S, 40 ° 1290W, pitfall (M. Peres et al., IBSP 120280, PBI _ OON 10997), 18. DISTRIBUTION. Known only from the state of Bahia, Brazil (map 2).Published as part of Brescovit, Antonio D., Bonaldo, Alexandre B., Santos, Adalberto J., Ott, Ricardo & Rheims, Cristina A., 2012, The Brazilian Goblin Spiders Of The New Genus Predatoroonops (Araneae: Oonopidae), pp. 1-68 in Bulletin of the American Museum of Natural History 2012 (370) on pages 31-32, DOI: 10.1206/766.1, http://zenodo.org/record/461131
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