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Home , Pale chanting goshawk, Tent tortoise

S. Afr. I. Zoo!. 1992.27(1) 33 Short Communications tent census ratio for the total study area was 18 : 1. Leopard ( pardalis) were rare in the study area. and only three individuals were seen over a period of 17 months (January 1988-March 1989. Septem­ Predation on and leopard ber-December 1989). two in dense SBV and one in KBV. The diet of M. canorus was studied by collecting pellets tortoise hatchlings by the pale chanting on a monthly basis from April 1988 to February 1989 goshawk in the Little beneath pre-selected perches. Pellets found beneath perches before the monthly collections started were labelled pre­ April. and no predation date could be associated with these G. Malan· prey remains. The pellets were dissolved in water and the FitzPatrick Institute. University of Cape Town. Rondebosch. macroscopic remains visually identified. A total of 742 pel­ noo Republic of lets was collected, of which 48 contained tortoise remains. W.R. Branch Only the scutes and occasionally the limbs of tortoises were Curator of Herpetology. Port Elizabeth Museum. P.O. Box identifiable, as diurnal raptors are known to be able to digest 13147, Humewood. 6013 bone (Newton 1986). Tortoise remains comprised 45% (by number) of the diet of the goshawk. Received 26 June 1991; accepted 9 September 1991 Results indicate that, of the three tortoise occur­ ring in the study area. P. tentorium was preferred as prey by Predation by the canorus on the goshawks. The remains of 36 tent tortoises were recov­ tentorius and Geoche/one pardalis hatchlings ered from the pellets. This was determined by: (a) the oorrelates with the habitat preference of these tortoise spe­ presence of 19 first vertebral (VI) scutes (characterized by cies as well as with the breeding pattern of P. tentorius. It is the anterior constriction in the scute where it makes contact not known why the particularly abundant Chersina angu/ata with the small nuchal scute) in the pellets; (b) the presence was not preyed upon. in some pellets of more scutes than could be present on a Predasie op pasuitgebroeide Psammobates tentorius en single tortoise (i.e .• more than five large vertebrals. more G90che/one parda/is skilpadjies deur die bleek-singvalk than two large abdominals. etc.). No pellet was positively Melierax canorus. het sterk ooreengekom met die skilpaaie determined to contain the remains of more than two se habitatvoorkeure asook met P. tentorius se seisoenale broeipatroon. Oit is onduidelik waarom die besonder volop tortoises. The scutes ranged in length from 5-8 mm. There are no Chersina angu/ata nie geroof word nie. . ) hatchling tent tortoises in the Port Elizabeth Museum 0

1 • To whom correspondence should be addressed herpetological collection, but a regression of plastron length 0 2

to VI scute length was prepared from preserved material d e (see Appendix I). A significant positive correlation exists t Aspects of the ecology of the widespread and common. but a (If = 0,72404; p < 0,001; df = 22; t test) between the d

( poorly known. pale chanting goshawk (Melierax canorus) measurements and there is no evidence of allometric change r

e (Steyn 1982). were investigated by means of a quantitative related to differential growth. Extrapolation of the regression h s study of the species's diet. The study area is situated in the i l into the region covered by the VI scute length of prey items b Little Karoo. just east of Calitzdorp (33"32'S /21°42'E).

u (5-8 mm) indicates that they originated from tortoises with

P Three veld types occur. namely Spekboomveld (SBV). plastron lengths of 16-30 mm. This corresponds to tortoises e Karroid Broken Veld (KBV) and Succulent Karoo (SK). h

t of 20-35 mm total length, which is similar to that of

y These veld types lie in parallel bands. from the SBV in the hatchlings (25-30 mm; Branch 1988). b north to the SK in the south (Acocks 1975). There is a d Half of all P. tentorius hatchlings were caught by two e t reduction in the rainfall of approximately 40 mm from the pairs of occupying territories incorporating KBV and n a wetter north to the drier south (landowners pers. comm.; SK. The border between the KB V and SK is clearly defmed r g annual mean 241 mm). The study area is primarily used = (Acocks 1975) and this dividing line ran through the e c for ostrich farming. Although part of a much wider study of territories of both pairs, and therefore the source of the prey n e the spatial. temporal and social variation in the diet of the c could not be attributed to a specific veld type. Out of a total i l pale chanting goshawk, in this note we report on predation of 38 reptilian prey items obtained from pellets of these r e on tortoise hatchlings. pairs, 18 were tent tortoises. In the whole study area, in d n The relative abundance of tortoise species in the study cases where capture month is known, tent tortoises were u

y area was determined by counting all observed tortoises caught as follows: four in April, three in May, seven in June a while driving (on a motor-cycle) or walking on a circular w and a single record in September. Tent tortoise are laid e t route (73 km) through the study area. The from September to January and the 'incubation' period is a

G (Chersina angulata) occurs in highest densities in the SBV given as 220 days (7-8 months; Branch 1988). Therefore the t e (0.36 tortoise/km), with densities then dropping off towards eggs are expected to hatch from April to August. Although n i the KBV (0,24 tortoise/km) and SK (0,14 tortoise/km). The no hatchling weights have been recorded for this species, b a tent tortoise (psammobates tentorius) in this census was hatchlings of the closely related (Psam­ S

y only observed in the border regions between the KBV and mobates geometricus) weigh approximately 6-8 g, and b

d SK (0,06 tortoise/km), and in casual observations in the SK, measure 35-40 mm (P. tentorius hatchlings measure 25-30 e c with no individuals seen in the SBV. The angulate tortoise: mm; Branch 1988). It is thus probable that tent tortoise u d o r p e R 34 S.-Afr. Tydskr. Dierk. 1992.27(1)

hatchlings will weigh approximately 5 g and that predation tortoise species render them more vulnerable to different occurs soon after hatching. Excluding the hatchling avian predators. predation of the above-mentioned pairs, five tent tortoises Given the habitat preference, calculated densities and were caught in the Spekboomveld, six in the Karroid Broken seasonal breeding pattern of the tent tortoises, they do Veld and seven in the Succulent Karoo. appear to form an important food source for the opportunis­ Scutes of 12 leopard tortoises were found in the pellets. tic pale chanting goshawk. However, as only three adult Seven were from pre-April pellets and the others were found leopard tortoises were seen in the study area, it would in the following months: one each in February and May, two appear that hatchlings may suffer higher in June and one in October. Leopard tortoises may lay from predation pressures. Compared with the hatchling tent 3-6 clutches comprising 6-15 eggs per season, with an incu­ tortoise, the larger hatchling leopard tortoise will possibly be bation period of 10-15 months (Branch 1988). Hatchlings easier to detect and will certainly provide a higher energy measure 40-50 mm and weigh 23-50 g (Branch 1988), and return. may emerge over a longer period than tent tortoises. Most leopard tortoise prey items were hatchlings with no evidence Acknowledgements of growth on the scutes. However, at least two sets of tor­ This research was supported in part by grants (for G.M.) toise scutes had growth rings, indicating that they came from the Foundation for Research Development, the Frank from juveniles up to 12 months of age. Under natural condi­ M. Chapman Memorial Fund (American Museum of Natural tions tortoise growth is slow during the first year and History), the Bob Blundell Memorial Scholarship, the Leslie juvenile weight may have only increased to 50-80 g after 12 Brown Memorial Grant, and the FitzPatrick Institute. We months (patterson, Boycott & Morgan 1989). This is possi­ thank Tim Crowe, Gay Palmer, Andre Boshoff, Rob Davis bly reaching the upper limit of prey size taken by goshawks, and Ernst Beard for their constructive comments on this as ossification of the hatchling shell will have increased its note. protection. Seven leopard tortoise hatchlings (58%) were preyed upon in the SBV, one in the KBV, three by the two References pairs on the border of the KBV and SK, and one in the SK. ACOCKS, J.P.H. 1975. Veld types of South Africa. Mem. Bot. The numbers of hatchling tortoises caught in the study Surv. S. Afr. No. 40. area correlates with the abundance of the different species, ANON. 1989. Ravens prey heavily on juvenile tortoises in the except that there was no predation on the super-abundant California Desert. In: Voice of the 18: 6 (Reprinted angulate tortoise. Elsewhere, adults and juveniles of this from Tortoise Tracks, Fall 1988).

species are readily preyed on by a variety of avian predators .

) BOSHOFF, A.F., PALMER, N.B: & AVERY B.1990. Regional

0 (see below). As the angulate tortoise prefers wetter habitats

1 variation in the diet of the martial eagles in the Cape

0 (Branch 1988), it may be that they did not breed in 1987 and

2 Province, South Africa. S. Afr. J. Wildl. Res. 20: 57--68. 1988, both years of below average rainfall in the region d BRANCH, W.R. 1988. Bill Branch's field guide to snakes and e t (1987: 181 mm; 1988: 183 mm; mean = 241 mm) (N.B. a other of . Struik Publishers, Cape d Palmer pers. comm.). (

Town, 328 pp. r Very little comparative quantitative data is available on e BRANCH, W.R. 1991. Chersina angulala: Avian predation. J. h

s predation of tortoises, and more specifically hatchlings, by i Herpetol.Assoc.Afr. 39: 27. l

b birds. The black eagle (Aquila verreauxit) is known to take BRANCH. W.R. & ELS, S.F. 1990. Predation on the angulate u the angulate tortoise (Steyn 1984; Fraser 1985; Branch & P

tortoise Chersina angulata by the kelp gull Larus e Els 1990). Shells of five juvenile G. partialis, two adult P. h dominicanus on Dassen Island, Western Cape. S. Afr. J. Zool. t

telllorius, and 53 (17 juveniles) greater padlopers ( y 25: 235-237. b

femoralis) were found below nests of an average of 18 pairs FRASER, M.W. 1985. Black eagle dropping tortoise.Promerops d e of black eagles between 1986-89, all in the Karoo National t .168: 9. n Park (R.A.G. Davies in Iill.). The (Polemaetus a NEWTON, 1.1986. The sparrowhawk. T. & A.D. Poyser, r bellicosus), is also known to take P. tenlOrius (Boshoff, g

Calton. e Palmer & Avery 1990). On Dassen Island kelp gulls (lArus c PATTERSON, R., BOYCOTT, R.C. & MORGAN, D. 1989. n dominicanus) preyed mainly on juvenile angulate .tortoises e

c Reproduction and husbandry of the leopard tortoise i l and the absence of hatchling shells was attributed to their (Geochelone pardalis) in an alien habitat. In: Proceedings of r

e soft shells which can be torn apart and eaten at the capture

d the FirstH. A. A. Conference, (ed.) W.R. Branch. J. Herpetol.

n site (Branch & Els 1990). Branch (1991) noted a record of Assoc.Afr. 36: 75. u predation on the angulate tortoise by the black-headed heron y STEYN, P. 1982. Birds of Prey of Southern Africa. David a (Ardea melanocephala). Elsewhere there are few records of w Phillips, Cape Town. e

t avian predation on hatchling or juvenile tortoises. In certain STEYN, P. 1984. Black eagle (R133) dropping tortoises. a areas in California the common raven (Corvus corax), may G

Promerops 162: 12. t prey heavily on juvenile desert tortoises ( agassizi e n i [Anon 1989]). The common raven, like the pale chanting b

a goshawk, is a generalist feeder (Anon 1989; G.M. unpub­ S

y lished records). As the above mentioned are all records of b adult or juvenile predation, it is unclear how the variation in d e

c size and weight of the shell, and the habits of the various u d o r p e R s. Afr. J. Zoo1. 1992,27(1) 35

Appendix 1 was listed under the restricted category in the updated SA Material examined: (PEM = Port Elizabeth Museum) RDB (Branch 1988). After the description of the new spe­ Psammobates tentorius: PEM X 574, Abbotsbury, Graaff cies, private collection material of a similar cordylid collec­ Reinet; PEM X 162, Fann Request. Somerset East District; ted during 1975 in the Nieuwoudtville and Clanwilliam PEM X 590, between Steytierville and Willow more; PEM districts, 200 kIn to the north of. the type locality of C. X 576, Valk River, near Lake Mentz, Eastern Cape; PEM X mclachlani, came to light. A preliminary analysis of this 54, x 161, x 186, x 193 Adendorp, Graaff Reinet; PEM x additional material showed that these specimens display 208, Fann Mayfair, Albany District; PEM x 588, Droge­ most of the diagnostic characters of C. mclachlani, but that kloof near Klaastroom, Prince Albert District; PEM x 136, there are also some distinct differences. The limited Nelspoort, Beaufort West District; PEM x 207, Fish River material, however, did not allow any firm conclusions Valley near Fort Brown, Eastern Cape; PEM x 211, x 29, regarding the taxonomic status of the northern population to Fann Moedersonskraal, Jansenville District; PEM x 248, be reached. This prompted a more intensive survey of the Carlisle Bridge, Grahamstown; PEM x 338, x 573, x 591 area between the two localities which resulted in additional Graaff Reinet; PEM x 60, Fann Hopewell, Louisvale, Ken­ material from several new localities. hardt District; PEM x 575 and x 572, no locality; three A detailed analysis of geographical variation was now uncatalogued specimens without locality data. possible. The purpose of this study was to detennine whe­ ther the geographical variation in C. mclachlani is categori­ calor clinal in nature. This is seen as a prerequisite for any taxonomic decision. Furthennore, the additional material allowed elaboration of the descriptive character set supplied Morphological variation in the girdled for the species by Mouton (1986). lizard C ordylus mclachlani Mouton 1986 Forty-two specimens from ten localities (Figure 1) were investigated for 15 meristic, 11 two-state and seven morpho­ P.le F.N. Mouton·, J.D. Visser and J.H. van Wyk metric characters. These are the external morphological J. Ellerman Museum, Department of Zoology, University of characters which discriminate either among populations of Stellenbosch, Stellenbosch, 7600 Republic of South Africa C. mclachlani or between C. mclachlani and other Cordylus species Mouton (1986). The considerations followed in Received 18 October 1990; accepted 3 October 1991 taking measurements and scale counts were the same as

.

) those followed by Mouton & Van Wyk (1989). 0

1 The girdled lizard Cordy/us mc/ach/ani. previously known 0

2 only from the type locality in the south-western Cape, South

d Africa, was found at several new localities as far north as e t Nieuwoudtville. The external morphology of the 32 additional a d specimens thus obtained was investigated to establish the (

r nature of geographical variation. Specimens from the type e locality, which lies on the southern periphery of the known h s i distribution range, differ from the rest in the number of l o Nieuwoudlville b suboculars, the shape of the interparietal scale and in the u presence of a post-interparietal scale. Because of some P

e overlap in these characters, separate taxonomic status for h t the specimens outside the type locality is not considered.

y The diagnostic character set for the species is updated and b additional ecological information is supplied. d e t n Die gordelakkedis Cordy/us mc/ach/ani, voorheen slags a r bekend vanaf die tipelokalitelt in die suidwes-Kaap, Suid­ g

e Afrika, is by verskeie nuwe Iokaliteite, so ver ncord as c Nieuwoudtville, gevind. Die uitwendige morfologie van die 32 n e

c bykomende eksemplare wat so verkry is, is ondersoek om i l

die omvang van geografiese variasie te bepaal. Eksemplare r

e vanaf die tipelokaliteit. wat die suidelike grens van die d bekende verspreidingsgebied uitmaak. verskil van die ander n u

eksemplare in die aantal subokulere skubbe, die vorm van y die interparietale skub en in die teenwoordigheid van 'n a

w postinterparietale skub. A.g.v. corvleueling in hierdie eien­ e t skappe word aparte taksonomiese status vir eksemplare a buite die tipelokaliteit nie oorweag nie. Die stel diagnostiese G

• t eienskappe vir die spesie word op datum gebring en aanvul­ e n lende ekologiese inligting word verskaf. o i

b 33~~-1~~~------~------4~------~--~ a S

y Mouton (1986) described a new girdled lizard, Cordylus Figure 1 Localities in the south-western Cape where Cordylus b

d mclachlani, from the Koue Bokkeveld in the Cape Province. mclachlal'li has been collected to date (the 300 m contour line is e c It was believed to have a very limited range and accordingly indicated). u d o r p e R