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The capital allocation of IVPP V22530 comprises of an abridged partially-articulated larboard dromaeosaurid leg preserved amid a capital slab and counterslab (Fig. 2).

The distal allocation of the femur in IVPP V22530 appears to be arced (Fig. 3) suggesting that the absolute cartilage was apparently bowed, as in best theropods. An ectocondylar bake-apple is present on the after bend of the crabbed condyle (Figs. 3C and 3D; Brusatte et al., 2014: Character 411 accompaniment 0), a affection accepted to theropod dinosaurs. The tibiotarsus is attenuate (length/mid-shaft amplitude arrangement ∼ 18; Fig. 2B), commensurable to those of basal dromaeosaurids, but differs from the able-bodied tibiotarsus of acquired dromaeosaurids such as Deinonychus (ratio ∼ 13, Ostrom, 1969: Table 10), Velociraptor (ratio ∼ 10, Norell & Makovicky, 1999: Fig. 10C) and Linheraptor (ratio ∼ 11, Xu et al., 2010: Fig. 1). The tibial shaft is preserved in anteromedial appearance and is amid biconcave (Figs. 2B, 3A and 3B), as in best theropods including Velociraptor (MPC 100/986, Norell & Makovicky, 1999: Figs. 11A and 11C), Microraptor (CAGS 20-8-001, Hwang et al., 2002: Fig. 28A) and the oviraptorosaur Gigantoraptor (LH V0011, Xu et al., 2007: Fig. 1S). The distal end of the tibiotarsus is missing so annihilation can be said about the analysis of the astragalus and calcaneum. However, the tibiotarsus is estimated to be ∼7 cm long. The adjacent end of the fibula is broadcast and adjacent to its mid-shaft there is an iliofibularis tubercle (Figs. 3A and 3B; Brusatte et al., 2014: Character 820 accompaniment 0) that is anterolaterally projecting, as in added theropods (Rauhut, 2003: Character 211 accompaniment 1; Fig. 48). The closing projects in a agnate administration to Mahakala (MPC 100/1033, Turner, Pol & Norell, 2011: Figs. 32A and 32C), clashing in Rahonavis and ornithurines area this tubercle faces posteriorly (Forster et al., 1998: Fig. 4C). The distal end of the fibula is missing, but it apparently had a complete breadth of beneath than 7 cm.

The metatarsus is attenuate (Fig. 4) and like best added dromaeosaurids it is symmetric (Brusatte et al., 2014: Character 205 accompaniment 0). In contrast, troodontids accept an absurd metatarsus as metatarsal (MT) II is added attenuate than MT IV (Brusatte et al., 2014: Character 205 accompaniment 1). The metatarsus is ∼60% of the breadth of the tibiotarsus (∼4 cm and ∼7 cm continued respectively), but a added authentic arrangement is bare as the adjacent allocation of the metatarsus and the distal allocation of the tibiotarsus are missing from the case (Fig. 2). MT I is a bargain and broadly triangular cartilage that is absorbed to the centermost ancillary of the distal end of MT II (Figs. 4C and 4D), as in best theropods (Rauhut, 2003: Character 222, accompaniment 2), including troodontids (e.g., Mei continued [IVPP 12733, Xu & Norell, 2004: Fig. 1B] and basal birds (e.g., Archaeopteryx [JM 2257, Wellnhofer, 2009: Fig. 5.85). However, in Microraptor MT I is absorbed medioventrally to the distal end of MT II (Hwang et al., 2002: Fig. 30A; Pei et al., 2014: Fig. 15). MT II, III and IV are carefully appressed distally (Figs. 4C and 4D) as in microraptorines and Buitreraptor (MPCA 245, Makovicky, Apesteguía & Agnolin, 2005: Fig. 3I), admitting in Mahakala (MPC 100/1033, Turner, Pol & Norell, 2011: Figs. 33A and 33C), Rahonavis (UA 8656, Turner, Makovicky & Norell, 2012: Fig. 56A), Velociraptor (MPC 100/985, Norell & Makovicky, 1997: Fig. 7) and Deinonychus (YPM 5205, Ostrom, 1969: Fig. 73) the distal end of the metatarsus is not appressed. This intraclade aberration is additionally apparent in ornithomimids (e.g., appressed in Sinornithomimus [IVPP V11797-23, Kobayashi & Lü, 2003: Fig. 23A]; unappressed in Qiupalong [HGM 41HIII-0106, Xu et al., 2011: Fig. 2D]) and alvarezsauroids (e.g., appressed in Linhenykus [IVPP 17608, Xu et al., 2013: Fig. 12A1; unappressed in Alvarezsaurus [MUCPv 54, Chiappe, Norell & Clark, 2002: Fig. 4.25B]), but to our ability the distal ends of the metatarsals in troodontids are consistently appressed (Makovicky & Norell, 2004: Fig. 9.6). The acutely ginglymus distal end of MT II is analogously preserved to affirm the accompanying dromaeosaurid synapomorphy: a ginglymus distal end that extends assimilate the extensor apparent and gives the distal end a acerb biconcave contour in antecedent appearance (Brusatte et al., 2014: Character 198 accompaniment 1). The distal ends of MT II and IV extend as far as anniversary added (Figs. 4C and 4D; Brusatte et al., 2014: Character 433 accompaniment 0) as in several dromaeosaurids, including Buitreraptor (MPCA 245, Makovicky, Apesteguía & Agnolin, 2005: Fig. 3I), Zhenyuanlong (JPM 0008, Lü & Brusatte, 2015: Fig. 3B) and Sinornithosaurus (IVPP V12811, Xu, Wang & Wu, 1999: Fig. 2). However, in some dromaeosaurids MT II and IV accept altered lengths as in Microraptor (Hwang et al., 2002: Fig. 30A), Graciliraptor (IVPP V13474, Xu & Wang, 2004: Fig. 3E), Deinonychus (YPM 5205, Ostrom, 1969: Table 11, Fig. 71; AMNH 3015, Ostrom, 1969: Table 11), Velociraptor (MPC 100/985, Norell & Makovicky, 1997: Fig. 7) and Adasaurus (MPC 100/20, Turner, Makovicky & Norell, 2012: Fig. 13A). In troodontids, MT II is additionally beneath than MT IV (Makovicky & Norell, 2004: Fig. 9.6). MT III is alone hardly best than MT II (Figs. 4C and 4D) like that of Sinornithosaurus (IVPP V12811, Xu, Wang & Wu, 1999: Fig. 4F) and Buitreraptor (MPCA 245, Makovicky, Apesteguía & Agnolin, 2005: Fig. 3I), admitting abounding added dromaeosaurids appearance a ample aberration in breadth including Graciliraptor (IVPP V13474, Xu & Wang, 2004: Fig. 3E), Microraptor (Hwang et al., 2002: Fig. 30A) and Rahonavis (UA 8656, Forster et al., 1998: Fig. 4E). A audible border (ridge) is developed forth the (latero)ventral bend of MT IV (Figs. 4C and 4D; Brusatte et al., 2014: Character 226 accompaniment 1) which is belted to troodontids and some dromaeosaurids such as Neuquenraptor (MCF PVPH 77, Novas & Pol, 2005: Fig. 1F), Buitreraptor (MPCA 245, Makovicky, Apesteguía & Agnolin, 2005), Bambiraptor (AMNH 30554, Burnham et al., 2000), Velociraptor (MPC 100/986, Norell & Makovicky, 1999: Fig. 16B) and Microraptorinae (e.g., Microraptor [BMNHC PH881, Pei et al., 2014: Fig. 15]; Sinornithosaurus [IVPP V12811, Xu, Wang & Wu, 1999: Fig. 1]; Changyuraptor [HG B016, Han et al., 2014: Fig. 2]). In IVPP V22530 (Figs. 4C and 4D), this border is beneath developed than in Neuquenraptor (MCF PVPH 77, Novas & Pol, 2005: Fig. 1F), Microraptor (BMNHC PH881, Pei et al., 2014: Fig. 15) and Sinornithosaurus (IVPP V12811, Xu, Wang & Wu, 1999: Fig. 4F). MT V is attenuate and elongate—approximately bisected the breadth of MT IV (Figs. 4C and 4D)—as in Microraptorinae (e.g., Microraptor [BMNHC PH881, Pei et al., 2014: Fig. 15]; Sinornithosaurus, [IVPP V12811, Xu, Wang & Wu, 1999: Fig. 1]; Changyuraptor [HG B016, Han et al., 2014: Fig. 2]) and abounding added dromaeosaurids (e.g., Deinonychus [YPM 5205, Ostrom, 1969: Fig. 73]; Velociraptor [MPC 100/985, Norell & Makovicky, 1997: Fig. 7]; Bambiraptor [AMNH FR 30556, Burnham, 2003: Table 3.4]). The alone dromaeosaurid we apperceive of with a analogously abbreviate MT V is Balaur (EME PV 313, Brusatte et al., 2013: Figs. 36 and 37) which is about a third of the breadth of MT IV (but the distal tip of the appropriate MT V is burst [EME PV 313, Brusatte et al., 2013: Fig. 37C]), although a contempo studies altercate that it is absolutely an avialan (Cau, Brougham & Naish, 2015; Foth, Tischlinger & Rauhut, 2014; Godefroit et al., 2013). Thus, a continued MT V is potentially a dromaeosaurid synapomorphy. The preserved distal allocation of MT V is burst forth the crabbed even authoritative it difficult to actuate its cross-sectional appearance (Figs. 4C and 4D). However, its crabbed edges abate distally (Figs. 4C and 4D), like in added theropods (Rauhut, 2003) including Microraptor (LVH 0026, Gong et al., 2012: Fig. 7), Velociraptor (MPC 100/985, Norell & Makovicky, 1997: Fig. 7) and Deinonychus (YPM 5205, Ostrom, 1969: Fig. 73).

Pedal phalanx II-2 has a archetypal deinonychosaurian contour with a audible binding amid the continued adjacent end and the distal condyle (Figs. 4C and 4D; Brusatte et al., 2014: Character 201 accompaniment 1). Saurornitholestes and Microraptorinae are aberant in this attention as the binding is beneath developed (Longrich & Currie, 2009: Figs. 2B and 2D). The oval-shaped, dorsally-offset centermost bond pit of phalanx II-2 is abysmal and its belly allowance is aing to the centre of the angled distal condyle, as in best microraptorines, Saurornitholestes (Longrich & Currie, 2009: Fig. 2B2) and Bambiraptor (AMNH 30554, Burnham et al., 2000). In Rahonavis (UA 8656, Forster et al., 1998: Fig. 4D), Neuquenraptor (MCF PVPH 77, Novas & Pol, 2005: Fig. 1H), Deinonychus (YPM 5205, Ostrom, 1969: Fig. 74), Dromaeosaurus (AMNH FARB 5356, Turner, Makovicky & Norell, 2012: Fig. 40A), Adasaurus (MPC 100/21, Barsd, 1983) and Velociraptor (MPC 100/985, Norell & Makovicky, 1997: Fig. 6B) the pit is similar, but its belly allowance is added dorsally-positioned. The microraptorine Hesperonychus (TMP 1983.67.7, Longrich & Currie, 2009: Fig. 2B2) has a agnate action to the closing taxa, but its pit is added circular-shaped. A proximodorsal lip is developed on phalanx II-3 (Figs. 4C and 4D; Brusatte et al., 2014: Character 731 accompaniment 0), as in best theropods. This phalanx is continued as with all deinonychosaurians (Brusatte et al., 2014: Character 201 accompaniment 1). Phalanx III-1 is beeline and best than duke II-1 and IV-1 (Fig. 4), as in best theropods.

IVPP V22530 additionally includes an abandoned theropod chiral ungual (Fig. 5) which was begin in affiliation with the abridged partially-articulated larboard dromaeosaurid leg. Although ungual analysis is generally undiagnostic, there is evidence, admitting limited, suggesting that these fossils accord to the aforementioned individual. The chiral ungual measures ∼16 mm from the proximodorsal bend to the tip, analogous the leg in admeasurement if they are referable to Microraptorinae. The baby articular surface, the well-developed flexor tubercle and a gracile, heavily-curved profile, in aggregate with a axle backbone present anon after to the articular apparent (‘proximodorsal lip’; Brusatte et al., 2014: Character 150 accompaniment 1), advance that this chiral ungual is referable to Pennaraptora (Foth, Tischlinger & Rauhut, 2014). Furthermore, the ungual is dorsally angled (the after allowance is aloft the adjacent end back the adjacent articular bend is positioned vertically) as in Dromaeosauridae (Senter et al., 2004), admitting not as acerb angled as in the latter, acknowledging the dromaeosaurid affection of the specimen. The ventrodistal allocation of the ungual comprises of a vertical keel that is apparently a fossilised keratinous sheath.

A triangular adjacent end of a audible appropriate rib and the adjacent allocation of its shaft are preserved (Fig. 6). It is not bright if it belongs to the aforementioned dromaeosaurid whose larboard leg is preserved. The capitulum and tuberculum are subequal in size, but the above is added dorsally-positioned than the closing and is accurate by a audible aing that separates it from the blow of the rib’s adjacent admeasurement (Fig. 6). The about breadth of the rib shaft is alien because its distal allocation is missing, but the amount of cone-shaped present in the shaft suggests that it is apparently almost abbreviate (Fig. 6A). The tuberculum, the after and crabbed margins of the rib almost anatomy a right-angle, whilst the capitulum makes a ∼45° bend with the crabbed allowance (Fig. 6A). This aggregate of appearance resembles the antecedent after ribs of Deinonychus (YPM 5245, Ostrom, 1969: Fig. 51A; YPM 5204, YPM 5210, Schachner et al., 2011: Fig. 4J) and Microraptor (CAGS 20-7-004, Hwang et al., 2002: Figs. 15B and 15C). This appropriate position forth the back is accurate by the attendance of analytic able bifurcation amid the tuberculum and capitulum because the amount of bifurcation decreases forth the ribcage of theropods (e.g., Allosaurus [Schachner et al., 2011: Fig. 4H], Tyrannosaurus [FMNH PR2081, Schachner et al., 2011: Fig. 4I] and Deinonychus [YPM 5204, YPM 5210, Schachner et al., 2011: Fig. 4J]). Dromaeosaurid antecedent after ribs acquire few taxonomically-informative characteristics and abominably it is not accessible to affirm if there is a abysmal canal forth the antecedent bend of the rib shaft, as empiric in Microraptor (IVPP V12330, Xu, 2002; CAGS 20-8-001, Hwang et al., 2002: Fig. 13; BMNHC PH881, Pei et al., 2014: Fig. 6), because the apparent of the adjacent allocation of the shaft is damaged and because—as mentioned—the distal bisected is missing. Of agenda is a rectangular-shaped action on the antecedent apparent of the rib that is amid ventromedial to the tuberculum (Fig. 6A). The antecedent after ribs of Mahakala (IGM 100/1033, Turner, Pol & Norell, 2011: Fig. 15) and Microraptor (CAGS 20-7-004, Hwang et al., 2002: Fig. 15B) alter from the rib of IVPP V22530 in accepting a dorsoventrally lower and mediolaterally added tuberculum and a abate capitulum on the tip of best and thinner neck. In Velociraptor the antecedent after ribs (MPC-D100/54, Hone et al., 2012: Fig. 1) alter from the rib of IVPP V22530 in accepting a continued and attenuate aing that ends in a abate capitulum. There is no rectangular-shaped action amidst the antecedent after ribs of Mahakala, but this is ambiguous for the added taxa mentioned. Thus, IVPP V22530 is apparently an antecedent after rib, although its exact position forth the vertebral alternation (rib number) is unknown.

The elements that accomplish up IVPP V22530 additionally accommodate an general accumulation of basic that accommodate some tiny ribs (Fig. 7). This awkward accumulation was begin in aing adjacency to the added elements, but does not accommodate any recognisable dromaeosaurid bones. These basic ability be non-dinosaurian so accept been accustomed to accordant experts for added identification.

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form 12 - Kirmi.yellowriverwebsites
form 12 – Kirmi.yellowriverwebsites | da form 705 may 2010 fillable

 

Army Physical Fitness Test Scorecard - da form 705 may 2010 fillable
Army Physical Fitness Test Scorecard – da form 705 may 2010 fillable | da form 705 may 2010 fillable
Army Physical Fitness Test Scorecard - da form 705 may 2010 fillable
Army Physical Fitness Test Scorecard – da form 705 may 2010 fillable | da form 705 may 2010 fillable
da form 12 fillable - Kirmi.yellowriverwebsites
da form 12 fillable – Kirmi.yellowriverwebsites | da form 705 may 2010 fillable
form 12 - Kirmi.yellowriverwebsites
form 12 – Kirmi.yellowriverwebsites | da form 705 may 2010 fillable

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