The historically known avifauna of Jamaica is unusual among the Greater Antilles for its dearth of raptorial birds. The only endemic species is the Jamaican Owl Pseudoscops grammicus. The Barn Owl (Tyto alba furcata) found on Jamaica is the same subspecies as found in Cuba, Isle of Pines, Grand Cayman, and Cayman Brac (König et al. 1999). Barn owls in Jamaica may have been derived from Cuba following the European introduction of rats of the genus Rattus (S. Olson unpubl. data). The only resident falcon is the American Kestrel (Falco sparverius), which is nearly ubiquitous in the New World, and the only hawk is the eponymous but very widely distributed Red-tailed Hawk (Buteo jamaicensis). In the fossil record, an eagle-sized accipitrid, much larger than B. jamaicensis, is known from a single incomplete claw from a cave deposit in Trelawny Parish (Olson and Steadman 1977).
I report here two bones from a cave deposit in the southernmost part of Jamaica that are identified as Rufous Crab-Hawk Buteogallus aequinoctialis and that presumably indicate a resident population that has become extinct. This is an extraordinary range extension with some interesting implications.
Modern comparative skeletons were examined in the Division of Birds, Department of Vertebrate Zoology, National Museum of Natural History, Smithsonian Institution, Washington, DC (USNM). Fossils are in the collections of the Department of Paleobiology of the same institution. The following catalog numbers are all USNM (M = male, F = female): Accipiter cooperii 18855 F Maryland, 501627 M West Virginia, 614361 F New Mexico; A. striatus 554770 F North Carolina; Busarellus nigricollis 345772 F Brazil; Buteo albicaudatus 622367 F Guyana; B. albonotatus 621010 M Guyana; B. brachyurus 50938 unsexed partial Brazil, 291403 M partial Florida; B. j. jamaicensis 289619 F Haiti; B. j. borealis 561859 M Maryland; B. platypterus platypterus 613957 F Panama; B. p. brunnescens 500678 unsexed partial Puerto Rico; B. p. insulicola 554967 M Antigua; B. poecilochrous 346398 M captive; B. polyosoma 319437 M Argentina; B. regalis 320771 M New Mexico; B. ridgwayi 318882 F Haiti; B. swainsoni 321986 M California, 614363 F Colorado; B. ventralis 400056 M partial Chile; B. magnirostris 562526 M Panama, 630135 F Uruguay; Buteogallus aequinoctialis 621054 F, 621849 M, 621850 M, 621851 M, 621944 F—all Guyana; B. anthracinus 344052 F Venezuela, 562529F, 562530 M, 611554 M, 611555M, 612260 M 612261 F, 613358 M—all Panama; B. gundlachii 323421 M partial Cuba; B. meridionalis 622379 M Guyana; Chondrohierax uncinatus 611557 F Panama; Circus cyaneus 291684 M Maryland; Elanus leucurus 19603 unsexed California; Elanoides forficatus 621940 F Guyana; Geranospiza caerulescens 3455774 M Brazil; Harpagus bidentatus 612259 F Panama; Ictinia plumbea 613357 M Panama; Leptodon cayanensis 613953 M Panama; Leucopternis plumbea 4321154 M partial Panama; L. semiplumbea 613395 F Panama; L. albicollis 611558 M Panama; L. princeps 613281 M Panama; Parabuteo unicinctus 630259 M Uruguay; Rostrhamus sociabilis 227376 M Argentina.
Genus Buteogallus Lesson
Rufous Crab-Hawk Buteogallus aequinoctialis (Gmelin)
Complete right humerus (USNM 531488) lacking most of the internal tuberosity and with the entepicondyle abraded; complete left tibiotarsus (USNM 531489). Collected by Ross MacPhee and Donald A. McFarlane in 1995.
Locality and Age of Fossils
Both bones were collected in Clarendon Parish, Jamaica, on Portland Ridge Peninsula at Jacksons Bay Caves (ca. 17° 44′N, 77° 3′W), Lloyd's Cave (McFarlane et al. 2002, Figs. 1–2; MacPhee and Horovitz 2004). The tibiotarsus came from Calcite Passage of Mantrap entrance. Details of where within Lloyd's Cave the humerus was found were not recorded but the preservation (very fresh-appearing but with reddish stains) was identical to that of the tibiotarsus and the size would be compatible with both specimens being from a single individual. All Calcite Passage specimens were surface-collected (R. MacPhee pers. comm.). In a passage nearby, equally fresh-looking cranial remains of the extinct platyrrhine monkey Xenothrix mcgregori were discovered (MacPhee and Horovitz 2004). Surface guano at another point in Lloyd's Cave gave a date of 1750 ± 80 radiocarbon years BP (McFarlane et al. 2002), so it is highly likely that the hawk fossils are Holocene in age.
Comparisons were made with virtually all possible taxa of New World Accipitridae except eagle-sized species that would obviously be too large. All kites had proportionately smaller hindlimbs and most were absolutely too small to agree with the Jamaican fossils. In Accipiter the humerus had the pectoral crest larger, more triangular, with the apex situated more distally, the shaft more sigmoid, and the distal end relatively wider. That of Circus differed in about the same way and the tibiotarsus was much more elongate and gracile. These may be relatively closely related genera (Olson 2006) and the Jamaican fossils lacked other osteological features by which Circus and Accipiter may be recognized (Olson and James 1991).
The fossils were very similar in size to Leucopternis albicollis, in which, however, the shafts of the humerus and tibiotarsus were much less robust. The other species of Leucopternis examined were either too small (L. plumbea and L. semiplumbea) or too large (L. princeps) to agree with the fossils. In Parabuteo the proportions were very different with the humerus shorter and tibiotarsus longer than in the fossils and the pectoral crest of humerus much more triangular.
The Jamaican fossils came from a species considerably smaller than Buteo jamaicensis, the only hawk in Jamaica today, and larger than B. ridgwayi or any of the forms of B. platypterus, the only other species of the genus now present in the West Indies (Raffaele et al. 1998). The humerus would fall in the size range of B. lineatus, a mainland species now known from fossils in the Bahamas and Cuba (Olson 2000, Suárez and Olson 2003). In all species of Buteo, however, the tibiotarsus was proportionately shorter and more robust than the Jamaican fossil.
An elongated tibiotarsus was characteristic of the species of Buteogallus. There was no overlap in skeletal measurements between B. anthracinus and the smaller species B. aequinoctialis, and the Jamaican fossils fell squarely on the mean of values for the latter (Table 1). Although the Cuban Black-Hawk (B. gundlachii) was stated to be smaller than B. anthracinus and judged to be specifically distinct from that species (Wiley and Garrido 2005), bones removed from a study skin were still considerably larger than in the Jamaican fossils (Table 1), which were in every respect identical with B. aequinoctialis and are assigned to that species.
Skeletal measurements (range and mean in mm) of Jamaican fossil and modern Buteogallus. Length of tibiotarsus includes the cnemial crest.
The Rufous Crab-Hawk Buteogallus aequinoctialis occurs in coastal mangroves from southern Brazil (Paraná) to the Gulf of Paria in Venezuela (Hilty 2003). Mangrove habitats are scattered around coastal Jamaica but the largest area is around the Portland Ridge Peninsula and extending NE to near Kingston (Asprey and Robbins 1953). The Jamaican fossil locality is very close (0.5 km or less) to the southern coast of the Portland Ridge Peninsula near areas of mangrove extending to the NW. Only about 5 km across the peninsula are the even more extensive mangrove forests around West Harbour and Portland Bight (Asprey and Robbins 1953), where there are about 80 km2 of mangrove habitat extending continuously for about 48 km. It is doubtless not a coincidence that the fossils of Rufous Crab-Hawk were found in the one area of Jamaica with the most suitable habitat for the species.
Because the range of the Rufous Crab-Hawk does not now extend into the Caribbean basin at all, its occurrence some 1760 km to the WNW in Jamaica seems all the more extraordinary. This suggests that its distribution in the Holocene included mainland shores of the Caribbean from which it would have been better able to colonize Jamaica. The nearest point of Colombia to southern Jamaica is about 750 km, which differs little from the ca. 700 km to the nearest point of Central America. Present distributions suggest rather strongly that B. aequinoctialis may be in the process of being replaced by the larger Common Black-Hawk B. anthracinus, as their ranges overlap only in easternmost Venezuela and Guyana. Thus, they are not mutually exclusive, but occur in sympatry only in a very limited part of the ranges of either species, as might be expected if one were gradually replacing the other. Field observations of the interactions of these two species where they occur together and long-term monitoring of the relative abundance of each may clarify this possibility.
What caused the extinction of the Rufous Crab-Hawk in Jamaica is unknown, as there is no species now occupying the niche of a large avian predator of coastal invertebrates in southern Jamaica. Habitat loss due to rising sea-levels and cutting of mangroves for charcoal, perhaps in combination with human-introduced predators, may have been factors.
I am most grateful to Ross MacPhee for supplying fossil material from Jamaica and providing information on it. The figure is by Brian Schmidt, Division of Birds, Smithsonian Institution.