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CONSERVATION OF ARABIAN GAZELLES - Nwrc.gov.sa

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By branch-swapping, using Macelade, three trees were found with a length of 125, one step<br />

than the first three, but with the <strong>sa</strong>me consistency index. The first of these (Figure 2.6d)<br />

the asymmetry of the shorter trees, but returns i<strong>sa</strong>bella to the stem leading to the gazella<br />

p p. and makes pelzelni the sister taxon to the entire dorcas / gazella clade. The second (Figure<br />

Ue) places the bilkis / arabica branch as sister-group to all the C. gazella group except erlangeri,<br />

lid unites cora with muscalensis, gazella with the Thumamah taxon. The third (Figure 2.6f) puts<br />

To reunite pelzelni with other subspecies of C. dorcas requires an increased tree length of<br />

126. and a slightly lower consistency index. When this is done. either cora is the sister species to the<br />

1t.!t of the gazella group. and C. g. gazella is part of the bilkis / arabica clu ster (Figure 2.6g), or it<br />

falls within the C. dorcas cluster. as sister group to i<strong>sa</strong>bella (Figure 2.6h). In either case, Thumamah<br />

can be added to the gazella / bilkis / arabica cluster at no extra cost.<br />

Interestingly. C. subgUlluro<strong>sa</strong>. with a low chromosome number like C. dorcas and C.<br />

gazella. cannot be added to their branch with a tree length below 127. Placing C. bennetti and C.<br />

<strong>sa</strong>udiya on a branch together requires a tree length of at least 128. though the consistency index is<br />

still 40.<br />

• Body Build: C. bilkis appears more sturdily built than other Arabian gazelles, and C. g.<br />

cora more slenderly; but in the absence of extensive external measurements it is difficult to quantify<br />

this. Harrison and Bates (1991) and Mendelssohn and Yom-Tov (1987) give some measurement data<br />

(Table 2.6). For their size C. <strong>sa</strong>udiya, and to a lesser extent C. s. marica. clearly have extremely<br />

large ears; they appear to be short-legged, but the above measurements suggest that the difference is<br />

in the hind limbs. which are elongated in C. gazella (as represented by C. g. muscalensis) but not in<br />

the other two species. C. s. marica also has a relativel y longer tail.<br />

Table 2,6 Body build measurements for Arabian gazelles (data for both sexes combined). <br />

Data from Harrison and Bates (199 1) and Mendelssohn and Yom-Tov (1987). <br />

Head+B ody Tail Hindfoot Ear Shoulder<br />

length length length length height<br />

gazelia (19-20) 101 6.5 105 • 117.5<br />

cora (I) 1041 120 610<br />

muscalens;s (2) 943 .5 105.5 276.5 114.1 559<br />

<strong>sa</strong>udiya (1) 928 90 255 123 600<br />

mariea (1-2) 966.5 152 272 125<br />

• Note: hindfoot iengths given by Mendelssohn and Yom-Tov are not comparable to those given by Harrison<br />

and Bates.<br />

Skeletal postcranial measurements are available only for C. g. gazella. C. dorcas i<strong>sa</strong>bella, C.<br />

s. subgulluro<strong>sa</strong> and a single reputed C. <strong>sa</strong>udiya (author's data). The last of these is in the collection<br />

of AI-Areen Wildlife Park. Bahrain. These data are given in Table 2.7 (sexes combined). As far as<br />

these measurements can be extended to the Arabian peninsula repr~sentatives of their respective<br />

groups. this appears to confirm that C. gazel/a have elongated hindlimbs compared to forelimbs. but<br />

shorter distal segments; C. <strong>sa</strong>udiya is generally short-legged; C. subgulluro<strong>sa</strong> has elongated<br />

metapodials but not an elongated tibia.<br />

31

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