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14 SMITHSONIAN CONTRIBUTIONS TO PALEOBIOLOGY TABLE 6.—Dimensions (mm) of the skull and long bones of the extinct Alopochen (Mascarenachen) kervazoi, from Reunion, modem A. aegyptiacus (USNM), and extinct Alopochen sirabensis (MNHN), from Madagascar. (a= maximal width of frontal at level of processus supraorbitalis of prefrontal bone; b= minimal width of frontal above orbits; c=cranium width at level of insertion of postorbital processes; d=bill length, from frontonasal hinge to tip of premaxillae; e=bill depth, from dorsal surface at frontonasal hinge to ventral surface at proximal end of maxillary; f= sternum-keel depth, from dorsal surface of sternum to ventral tip of keel; g= pelvis length, from first synsacral vertebra to last synsacral vertebra; h=length of anterior scapula, from base of glenoid facet to top of acromion; «=number of specimens.) Measurement Skull frontal width (a) frontal width (b) cranium width (c) bill length (d) bill depth (e) ratio e x 100 : d Sternum keel depth (f) Pelvis length (g) Coracoid maximum length internal length proximal width proximal depth stemal-facet length stemal-facet depth midshaft width midshaft depth Scapula anterior length (h) Humerus total length proximal width proximal depth distal width distal depth midshaft width midshaft depth Ulna total length proximal width proximal depth distal width depth external condyle midshaft width midshaft depth Carpometacarpus total length proximal width proximal depth distal width distal depth width metacarpale majus depth metacarpale majus Phalanx 1, major wing digit total length Phalanx 2, major wing digit total length Femur A. (M.) kervazoi mean (n) range 25.3(1) 13.0(1) 30.7(1) 45.1(1) 18.6(1) 41.2(1) 37.20 (2) 100.6(1) -63(1) 56.90 (3) 13.8(1) 12.03 (3) 23.5(1) 5.4(1) 6.87 (3) 4.97 (3) 14.70 (3) 126.0(1) 25.7(1) 14.2(1) 19.2(1) 10.9(1) 9.65 (2) 8.25 (2) -119(1) 13.1(1) 11.9(1) 12.3(1) 10.8(1) 6.65 (2) 6.50 (2) 72.35 (4) 7.70 (4) 19.80(4) 9.05 (4) 6.23 (4) 6.07 (7) 4.78 (6) 31.60(2) 24.1(1) - - - - - - 36.7-37.7 - - 53.7-60.0 - 11.1-13.0 - - 6.2-7.4 4.6-5.2 14.2-15.5 - - - - - 9.0-10.3 8.0-8.5 - - - - - 6.3-7.0 6.0-7.0 70.7-75.7 7.4-8.2 18.3-22.4 8.6-9.5 5.8-6.5 5.3-6.5 4.2-5.3 30.9-32.3 - A. ae mean (n) 24.17(7) 12.58(8) 30.46 (8) 50.91 (8) 19.16(8) 37.66 (8) 37.17(9) 104.71 (9) 67.71 (9) 60.56(11) 14.17(9) 13.71 (9) 25.30 (9) 6.10(9) 7.52(10) 5.33 (9) 17.11(9) 134.10(11) 28.79(10) 14.86(10) 20.63 (10) 11.63(10) 9.62(10) 8.89 (9) 128.92(11) 13.80(10) 12.53(10) 12.01 (10) 11.47(9) 7.13(10) 6.84 (9) 79.06(10) 8.21 (10) 22.61(11) 9.76 (9) 6.92 (9) 6.06 (9) 5.09(8) - 26.06 (7) gyptiacus range 21.8-26.3 11.1-14.2 29.4-32.3 47.6-54.1 17.5-21.0 34.3-39.9 34.1^*0.2 99.0-112.0 62.0-75.1 55.0-65.6 12.4-16.0 12.2-15.1 23.7-27.9 5.0-7.3 6.5-8.8 4.6-6.2 15.7-19.0 122.8-148.4 25.7-32.7 13.2-16.4 18.3-22.5 10.5-12.5 8.6-11.0 8.1-10.0 118.1-144.1 11.8-15.4 11.5-13.7 10.6-13.5 10.2-12.7 6.4-7.9 5.9-7.5 72.0-86.0 7.2-9.0 19.3-27.4 8.8-10.6 6.3-7.5 5.5-6.7 4.5-6.0 - 24.1-28.1 A. sirabensis mean (ri) - - - - - - - - - 63.11 (16) - - - - 7.34(16) - - 140.26(30) - - - - 10.07 (30) - 128.56(10) - - - - 6.96(10) - 80.69(21) - _ _ _ 6.52(21) _ _ - range - - - - - - - - - 56.7-68.3 - - - - 6.6-7.9 - - 127.3-152.4 - - - - 8.8-11.8 _ 119.5-139.1 _ _ _ _ 6.3-7.5 _ 73.2-90.0 _ _ _ _ 5.9-7.1 -

NUMBER 89 15 Measurement total length proximal width proximal depth distal width distal depth midshaft width midshaft depth Tibiotarsus total length proximal width proximal depth distal width distal depth midshaft width midshaft depth Tarsometatarsus total length proximal width proximal depth distal width distal depth midshaft width midshaft depth mean (n) 69.0(1) 18.8(1) 11.8(1) 16.9(1) 12.6(1) 6.9(1) 7.8(1) - - - - - 6.0(1) 5.8(1) 80.5(1) 14.8(1) 13.4(1) -16(1) -11(1) 5.95 (2) 5.30(2) A. (M.) kervazoi range - - - - - - - - - - - - - - - - - - 5.2-6.7 4.8-5.8 Humerus UCB FSL-330517 (Figure li) also shows a slight difference compared with A. aegyptiacus. On the anconal face, below the head, and on the medial side of the pneumatic fossa, there is a proximodistally elongated depression that does not exist in A. aegyptiacus. Moreover, on this humerus, the pneumatic foramen, which opens at the bottom of the pneumatic fossa, has a small surface compared with that of the fossa, whereas in A. aegyptiacus the pneumatic foramen occupies all the surface of the pneumatic fossa. On the whole, because of the great similarities between the Reunion sheldgoose and the living Egyptian goose, we think that Mascarenachen must be considered a subgenus, and that the Reunion form can be designated as Alopochen {Mascarenachen) kervazoi (Cowles), new combination. This subgenus includes only the type species, kervazoi. Although the size of A. aegyptiacus is highly variable (Table 6), the mean dimensions of A. (M) kervazoi are smaller than those of A. aegyptiacus. The size of the Reunion sheldgoose either is at the lower limit of variation in A. aegyptiacus or is slightly smaller. COMPARISON WITH FOSSIL FORMS.—An extinct sheldgoose, Chenalopex sirabensis, was described by Andrews (1897) from Holocene deposits in Madagascar. Because Chenalopex is a synonym of Alopochen, it is now known as Alopochen sirabensis (Brodkorb, 1964). It varies widely in size, so Andrews divided the material into two sets that he attributed to males and females. In a large amount of material at MNHN, the size of the bones also varies according to the locality, the material TABLE 6.—Continued. mean (n) 71.04(11) 17.31(10) 12.01 (10) 17.60(10) 13.38(10) 7.24(10) 7.70 (9) 133.30(11) 14.52 (9) 17.42(9) 14.01 (10) 15.33(10) 7.44(10) 6.14(9) 86.42(11) 15.25(10) 13.23(10) 16.17(10) 11.96(9) 6.13(10) 5.90(10) A. aegyptiacus range 65.0-78.0 14.9-20.6 11.0-13.7 15.5-20.1 12.1-15.0 6.4-7.9 6.1-9.0 124.2-146.2 12.8-17.0 16.0-18.7 12.6-15.6 13.7-17.6 6.5-8.3 5.3-6.9 77.0-96.6 14.3-16.1 12.1-14.6 14.6-18.7 10.9-13.4 5.3-7.0 5.2-6.6 mean (n) 72.64(12) - - - - 8.03(12) - 136.97(19) - - - - 7.55 (19) - 86.03(17) - - - - 6.01 (17) - A. sirabensis range 66.8-78.4 - - - - 7.3-9.0 - 123.7-144.8 - - - - 6.2-8.7 - 76.5-94.3 - - - - 5.3-7.3 - from Antsirabe being larger than that from Ankazoabo. We present measurements of specimens from both sites (Table 6) without trying to separate males and females. Bones of A. sirabensis on average are larger than those of living A. aegyptiacus and are thus distinctly larger than A. (M) kervazoi. Another extinct species, Sarkidiornis mauritianus, was described by Newton and Gadow (1893). The holotype is a left carpometacarpus with a very projecting alular metacarpal ending in a callosity. Andrews (1897) showed that this bone corresponded to the genus Chenalopex and did not differ from the species Chenalopex sirabensis that he was describing from Madagascar (although the former name has priority). The length of this carpometacarpus (77 mm) is within the variation of A. sirabensis (Table 6) and is slightly larger than the largest individuals of A. {M.) kervazoi. The Reunion form shows some characteristics that are probably related to insularity (see below). The Mauritian form also may be an endemic insular form. With more fossil material from Mauritius, it might be possible to discern distinctive characteristics compared with the Madagascar and Reunion forms. The ratio-diagram (Figure 5) drawn for the species Alopochen aegyptiacus, A. sirabensis, and A. (M) kervazoi shows a slight lessening of flying ability in A. sirabensis compared with A. aegyptiacus, as indicated by shortening of the ulna and carpometacarpus and by the slight lengthening of the femur. The curve of A. (M) kervazoi closely parallels that of A. sirabensis, but it also shows a slight reduction of the ulna and carpometacarpus and a slightly longer femur. For comparison, an-

NUMBER 89 15<br />

Measurement<br />

total length<br />

proximal width<br />

proximal depth<br />

distal width<br />

distal depth<br />

midshaft width<br />

midshaft depth<br />

Tibiotarsus<br />

total length<br />

proximal width<br />

proximal depth<br />

distal width<br />

distal depth<br />

midshaft width<br />

midshaft depth<br />

Tarsometatarsus<br />

total length<br />

proximal width<br />

proximal depth<br />

distal width<br />

distal depth<br />

midshaft width<br />

midshaft depth<br />

mean (n)<br />

69.0(1)<br />

18.8(1)<br />

11.8(1)<br />

16.9(1)<br />

12.6(1)<br />

6.9(1)<br />

7.8(1)<br />

-<br />

-<br />

-<br />

-<br />

-<br />

6.0(1)<br />

5.8(1)<br />

80.5(1)<br />

14.8(1)<br />

13.4(1)<br />

-16(1)<br />

-11(1)<br />

5.95 (2)<br />

5.30(2)<br />

A. (M.) kervazoi<br />

range<br />

-<br />

-<br />

-<br />

-<br />

-<br />

-<br />

-<br />

-<br />

-<br />

-<br />

-<br />

-<br />

-<br />

-<br />

-<br />

-<br />

-<br />

-<br />

5.2-6.7<br />

4.8-5.8<br />

Humerus UCB FSL-330517 (Figure li) also shows a slight<br />

difference compared with A. aegyptiacus. On the anconal face,<br />

below the head, and on the medial side of the pneumatic fossa,<br />

there is a proximodistally elongated depression that does not<br />

exist in A. aegyptiacus. Moreover, on this humerus, the pneumatic<br />

foramen, which opens at the bottom of the pneumatic<br />

fossa, has a small surface compared with that of the fossa,<br />

whereas in A. aegyptiacus the pneumatic foramen occupies all<br />

the surface of the pneumatic fossa.<br />

On the whole, because of the great similarities between the<br />

Reunion sheldgoose and the living Egyptian goose, we think<br />

that Mascarenachen must be considered a subgenus, and that<br />

the Reunion form can be designated as Alopochen {Mascarenachen)<br />

kervazoi (Cowles), new combination. This subgenus includes<br />

only the type species, kervazoi.<br />

Although the size of A. aegyptiacus is highly variable (Table<br />

6), the mean dimensions of A. (M) kervazoi are smaller than<br />

those of A. aegyptiacus. The size of the Reunion sheldgoose either<br />

is at the lower limit of variation in A. aegyptiacus or is<br />

slightly smaller.<br />

COMPARISON WITH FOSSIL FORMS.—An extinct sheldgoose,<br />

Chenalopex sirabensis, was described by Andrews (1897) from<br />

Holocene deposits in Madagascar. Because Chenalopex is a<br />

synonym of Alopochen, it is now known as Alopochen sirabensis<br />

(Brodkorb, 1964). It varies widely in size, so Andrews divided<br />

the material into two sets that he attributed to males and<br />

females. In a large amount of material at MNHN, the size of<br />

the bones also varies according to the locality, the material<br />

TABLE 6.—Continued.<br />

mean (n)<br />

71.04(11)<br />

17.31(10)<br />

12.01 (10)<br />

17.60(10)<br />

13.38(10)<br />

7.24(10)<br />

7.70 (9)<br />

133.30(11)<br />

14.52 (9)<br />

17.42(9)<br />

14.01 (10)<br />

15.33(10)<br />

7.44(10)<br />

6.14(9)<br />

86.42(11)<br />

15.25(10)<br />

13.23(10)<br />

16.17(10)<br />

11.96(9)<br />

6.13(10)<br />

5.90(10)<br />

A. aegyptiacus<br />

range<br />

65.0-78.0<br />

14.9-20.6<br />

11.0-13.7<br />

15.5-20.1<br />

12.1-15.0<br />

6.4-7.9<br />

6.1-9.0<br />

124.2-146.2<br />

12.8-17.0<br />

16.0-18.7<br />

12.6-15.6<br />

13.7-17.6<br />

6.5-8.3<br />

5.3-6.9<br />

77.0-96.6<br />

14.3-16.1<br />

12.1-14.6<br />

14.6-18.7<br />

10.9-13.4<br />

5.3-7.0<br />

5.2-6.6<br />

mean (n)<br />

72.64(12)<br />

-<br />

-<br />

-<br />

-<br />

8.03(12)<br />

-<br />

136.97(19)<br />

-<br />

-<br />

-<br />

-<br />

7.55 (19)<br />

-<br />

86.03(17)<br />

-<br />

-<br />

-<br />

-<br />

6.01 (17)<br />

-<br />

A. sirabensis<br />

range<br />

66.8-78.4<br />

-<br />

-<br />

-<br />

-<br />

7.3-9.0<br />

-<br />

123.7-144.8<br />

-<br />

-<br />

-<br />

-<br />

6.2-8.7<br />

-<br />

76.5-94.3<br />

-<br />

-<br />

-<br />

-<br />

5.3-7.3<br />

-<br />

from Antsirabe being larger than that from Ankazoabo. We<br />

present measurements of specimens from both sites (Table 6)<br />

without trying to separate males and females. Bones of A. sirabensis<br />

on average are larger than those of living A. aegyptiacus<br />

and are thus distinctly larger than A. (M) kervazoi.<br />

Another extinct species, Sarkidiornis mauritianus, was described<br />

by Newton and Gadow (1893). The holotype is a left<br />

carpometacarpus with a very projecting alular metacarpal ending<br />

in a callosity. Andrews (1897) showed that this bone corresponded<br />

to the genus Chenalopex and did not differ from the<br />

species Chenalopex sirabensis that he was describing from<br />

Madagascar (although the former name has priority). The<br />

length of this carpometacarpus (77 mm) is within the variation<br />

of A. sirabensis (Table 6) and is slightly larger than the largest<br />

individuals of A. {M.) kervazoi. The Reunion form shows some<br />

characteristics that are probably related to insularity (see below).<br />

The Mauritian form also may be an endemic insular<br />

form. With more fossil material from Mauritius, it might be<br />

possible to discern distinctive characteristics compared with<br />

the Madagascar and Reunion forms.<br />

The ratio-diagram (Figure 5) drawn for the species Alopochen<br />

aegyptiacus, A. sirabensis, and A. (M) kervazoi shows<br />

a slight lessening of flying ability in A. sirabensis compared<br />

with A. aegyptiacus, as indicated by shortening of the ulna and<br />

carpometacarpus and by the slight lengthening of the femur.<br />

The curve of A. (M) kervazoi closely parallels that of A. sirabensis,<br />

but it also shows a slight reduction of the ulna and carpometacarpus<br />

and a slightly longer femur. For comparison, an-

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