Braz. J. Biol., 62(2): 197-210, 2002 SÃO PAULO WOODLOT BIRDS 197 BIRDS OF A CENTRAL SÃO PAULO WOODLOT: 1. CENSUSES 1982-2000 WILLIS, E. O.1,2 and ONIKI, Y.2 1,2 Departamento de Zoologia, Unesp, Campus de Rio Claro, C.P. 199, CEP 13506-900, Rio Claro, SP, Brazil 2 Instituto de Estudos da Natureza, Rua 2, no 2272, CEP 13500-153, Rio Claro, SP, Brazil Correspondence to: Edwin O’Neill Willis, Instituto de Biologia, Departamento de Zoologia, Unesp, C.P. 199, CEP 13506-900, Rio Claro, SP, Brasil, e-mail: ewillis@rc.unesp.br Received July 31, 2000 – Accepted February 5, 2001 – Distributed May 31, 2002 ABSTRACT Some 263 birds were recorded near and in a 230-ha patch of semideciduous forest in cane fields of central São Paulo, Brazil. Subtracting 67 open-area species, 22 of marshes or creeks, 10 vagrants and 12 recorded later, 152 forest and border species were recorded in 1982-86, much like what was observed in a similar woodlot near Campinas. Both woodlots lost species gradually over the years. Some birds avoided hard cane-field edges, preferring soft bushy edges. Of open-area species, 22 seemed to have disappeared by 1997 due to earlier high El Niño rains or rare permanently open habitats in the sugar cane; 17 new species were mostly nocturnal ones not noted earlier, or occasional visitors. Forest and borders lost 31 species, gaining five of dry regions and one winter visitor. Several migrants from the south appeared only in wet years before recent greenhouse effects, some resident birds were hunted, and canopy hummingbirds were perhaps still present. Dry-forest travel-prone or “metapopulational” species moved their centers of distribution, partly concealing loss of moist-forest diversity. Key words: birds, conservation, greenhouse effect, metapopulations, semideciduous forest, sugar cane. RESUMO Aves de uma mata na região central de São Paulo: 1. Censos 1982-2000 Foram listadas 263 aves próximo e dentro de uma mata semidecídua de 230 ha em meio a plantações de cana-de-açúcar, na região central do Estado de São Paulo, Brasil. Subtraindo-se 67 espécies de áreas abertas, 22 de riachos, 10 vagantes e 12 observadas mais tarde, cerca de 152 espécies de mata e de borda foram observadas entre 1982-86, semelhantemente às observadas em uma mata próxima a Campinas. Ambas as matas perderam espécies gradualmente. Algumas aves evitaram as margens “duras” dos canaviais, preferindo as margens “macias” arbustivas. Das espécies de área aberta, parece que 22 desapareceram até 1997, em razão das abundantes chuvas anteriores causadas por El Niño, ou pela raridade de habitats permanentemente abertos nos canaviais; 17 espécies “novas” eram princi- palmente noturnas que não haviam sido checadas anteriormente, ou visitantes ocasionais. A mata e as bordas perderam 37 espécies, ganhando 5 de regiões secas e 1 visitante de inverno. Vários migrantes do sul apareceram somente em anos chuvosos antes do recente efeito estufa; algumas aves residentes foram caçadas, e os beija-flores das copas talvez estivessem presentes ainda. As espécies de zonas secas, prones à movimentação ou “metapopulacionais”, movem os centros de distribuição, camuflando parcialmente a perda de diversidade da mata úmida. Palavras-chave: aves, conservação, efeito estufa, metapopulações, mata semidecídua, cana-de-açúcar. Braz. J. Biol., 62(2): 197-210, 2002 198 WILLIS, E. O. and ONIKI, Y. INTRODUCTION In central São Paulo State, there was once a belt of semideciduous forest between the evergreen coastal and montane forests, and the interior deci- duous woods and savannas (cerrados). Only small patches of the belt persist today, as the region was deforested for agriculture and cities. In 1982, we started studies of birds in a remanescent patch of semideciduous forest, a 230-ha tract (Pagano & Leitão, 1987; Pagano et al., 1987) on watershed between the basins of the Mogi-Guaçu and Tietê Rivers, at the south edge of the Fazenda São José, border of Rio Claro and Araras townships (22o21'S, 47o29'W and 675 m elevation). Studies of birds of other remnant semide- ciduous forests include ones done near Campinas and Anhembi (Willis, 1979; Aleixo & Vielliard, 1995) and northward, near Jardinópolis (Chiarello, 2000). Transitional vegetation approaching the cerrado near São Carlos, just northwest (Marini et al., 1997), has received some study. Two master’s theses (Cândido-Júnior, 1991, published 2000; Gondim, 1995) studied edge effects and fruit- eating birds in Fazenda São José. Here we report our bird censuses in and near the Fazenda São José woodlot. Later parts of the study will analyze bird body masses, measurements, molt cycles, ectoparasites, and include detailed observations for understory species captured and banded. STUDY AREAS AND METHODS An originally large forest area was cut into three fragments about 60 years ago (Pagano & Leitão, 1987). Sugar cane and other agriculture now surround this tract, the southernmost of the fragments. Grassy swales, with ponds in rainy years, cut through the cane fields. A small per- manent farm pond near the main road to Araras occupies part of one grassy swale (22o23'S, 47o27'W, at 650 m). Secondary scrub and woods along the Ribeirão Claro, at 600 m and 22o20'S, 47o30'W on the west edge of the woodlot, partially connect the woodlots. A small side creek, arising in the north edge of the woodlot, provides some wooded swamps on its way west. Just southeast in the forest, an east-west belt of open-understory woods bor- ders another belt of bamboo-crowded understory across the north-south divide of the Mogi-Guaçu and Tietê (border of Rio Claro and Araras town- ships). Flowering and death of this large bamboo in 1994 left little, except for a small species for- ming thickets in the central understory. Dense spiny Celtis vines took over in the southern un- derstory, moving in from the wind-damaged south edge of the woodlot. Tall jequitibá (Cariniana estrellensis Kuntz) trees project over the canopy near the divide. Eastward, a cleared swath along an electric power line and a cat-tail marsh cut off two narrow end stretches of the woodlot. The marsh drains southeast toward the Mogi-Guaçu, not southwest to the Tietê as does the Ribeirão Claro. Several north-south cleared trails, cleared for Pagano’s and later studies, cross the woodlot and were used for censuses, as were the road along the west edge near the Ribeirão Claro and one on the south edge along sugar cane fields of Fazenda São João. In the cane field, a dip collected rain water in the strong El Niño years of 1982-83, and we recorded water birds at that time. We set up trails in a 300 × 200 m forest area (six 100-m squares) on the divide, by the south edge and sugar cane, in 1983-88; the spiny vines took over later. All banding studies were in the 100-m squares and on a botany trail through the squares. We had hoped to locate bird territories and do behavioral studies, but the wind damage and dense spiny vines complicated our and our students’ work. The road along the west edge was closed in 1995; elephant grass grew there, so 13 of 22 later visits were made to the botany trail through the banding area and to the east marsh, rather than to the west road and the botany trail as earlier. Willis recorded birds at any distance on transect counts, ordinarily from just before dawn to just after midday. He usually walked the west road and back, then the botany trail and back, during about 6 hours from dawn to midday. After the west road was closed, an hour or so at dawn was spent in the east marsh and nearby edges; earlier, these were visited only briefly at dawn and midday for around a half hour. In 1982-1984, when other cross trails were open, he occasionally checked them rather than the main botany trail. Here, as in Willis (1979), we record the number of birds per 100 hours of study, to avoid using space-waste Braz. J. Biol., 62(2): 197-210, 2002 SÃO PAULO WOODLOT BIRDS 199 decimals. To determine total numbers of birds actually seen, one only need multiply by the number of hours of study divided by 100. Banding studies involved 8 mist nets (12 m long, of 36 mm mesh) for about 10 hours daily, along one edge of 100-m squares. We banded on 24 days from 6 Aug. 1983 to 17 June 1984, then 36 days from 12 March 1987 to 16 Aug. 1988. In 3 morning visits in 1985-86 and 12 such visits 1989-2000, 3-5 nets were placed along trails near the road, for ornithology classes. B. S. Ataguile, a student, helped with many captures in 1987-1988; other students also helped. Some 4 hours per visit were of transects along the edge to the east marsh, to the depression in the nearby sugar cane, or on the woodland trails. Half-day visits added 2 hours or so of censuses per visit. Oniki measured the captured birds and checked for ectoparasites, molt, brood patches, and defects. RESULTS AND DISCUSSION Species Willis recorded 263 species (Table 1) in the 601.4 hours of censuses (155 visits) 1982-2000. Xiphorhynchus guttatus, listed by Cândido-Jr. (2000), is not a São Paulo species and may have been a Dendrocolaptes platyrostris. Of these, 67 were birds of surrounding open areas (including distant ponds or marshy zones in the open), 22 of marshes or creeks next to the woods, and 63 edge birds. Five birds of edges and 5 of the 111 woodland species were vagrants. Subtracting these vagrants and 67 open-area birds, 186 species were birds of the woodlot itself. Of these, 22 were of marsh and water areas, not present in woods studied by Willis (1979). Of the remaining 164 edge and forest species, 12 were not recorded in 1982-86 (152 early species present), 22 not in 1987-92 (144 species present), 32 not 1992-97 (132 species), and 31 not in 1997-2000 (133 species). Four of the species in 1987-92 were not recorded before or since, two in 1992-97, and six in 1997-2000. Some 62 species (considered in a later part of this report) were captured and banded. Canopy species, vagrants, marsh and water birds, and open-area birds were not captured, so that the banding project captured 38% of the 164 woodlot and border species. TABLE 1 Birds recorded per 100 hours. 1 = 1982-83 plus 2 visits 1986, 2 = 1987-92, 3 = 1992-95, 4 = 1997-2000, a = banding 1983-86, b = 1987-88, c = end 1988-91, d = 1993-97. A = open areas, B = border, C = creek or marsh, n = migrant from north, N = winter from north, s = migrant from south, S = winter from south, T = summer breeder, V = vagrant. Species 1 a b 2 c 3 d 4 Crypturellus obsoletus 22 24 29 27 24 28 50 28 Crypturellus parvirostris – A 7 10 16 20 12 32 20 16 Crypturellus tataupa 9 19 21 25 42 38 28 Rhynchotus rufescens – A 2 1 6 6 10 3 Nothura maculosa – A 4 3 1 1 7 Penelope superciliaris 6 1 1 Dendrocygna viduata – A 22 11 8 1 Cairina moschata – C 21 10 4 3 12 7 10 2 Amazonetta brasiliensis – C 25 16 67 10 6 17 20 Nomonyx dominicus – A 2 4 Tringa solitaria – An 1 1 Bartramia longicauda – An 10 Gallinago paraguayae – A 2 Gallinago undulata – A 8 10 2 Braz. J. Biol., 62(2): 197-210, 2002 200 WILLIS, E. O. and ONIKI, Y. TABLE 1 (Continued) Species 1 a b 2 c 3 d 4 Jacana jacana – A 8 3 3 6 1 10 3 Vanellus chilensis – A 19 31 11 16 36 88 300 107 Rallus nigricans – C 2 4 6 1 3 13 Aramides cajanea – C 1 1 3 1 8 8 Aramides saracura – C 22 3 7 9 13 Porzana albicollis – A 9 9 13 1 12 5 10 7 Laterallus melanophaius – C 9 7 6 9 5 10 16 Porphyriops melanops – AS 1 Gallinula chloropus – A 7 6 4 4 6 21 20 16 Cariama cristata – A 5 4 5 26 6 29 60 43 Tachybaptus dominicus – A 5 8 Ardea alba – A 3 1 7 Bubulcus ibis – A 1 Egretta thula – A 1 Butorides striatus – C 2 1 1 3 Syrigma sibilatrix – A 3 3 2 6 14 50 44 Pilherodius pileatus – C 1 Mesembrinibis cayennensis – C 4 6 Coragyps atratus – B 101 109 42 121 72 59 110 104 Cathartes aura 6 1 Elanus leucurus – A 1 2 Leptodon cayanensis 4 3 5 Accipiter striatus – B 1 Buteo albicaudatus – A 2 Buteo magnirostris – B 19 9 14 23 12 16 10 35 Buteo brachyurus – B 3 3 3 1 Buteogallus meridionalis – A 1 3 5 6 1 2 Micrastur ruficollis 2 3 Micrastur semitorquatus 1 Caracara plancus – B 25 48 21 20 12 37 20 35 Milvago chimachima – A 8 5 4 6 7 10 10 Herpetotheres cachinnans – B 5 8 5 4 7 Falco sparverius – A 1 3 2 3 6 1 10 5 Falco femoralis – A 1 2 6 2 3 Otus choliba – B 7 2 7 1 Glaucidium brasilianum 1 7 15 4 7 Athene cunicularia – A 5 2 5 8 Caprimulgus rufus 1 Caprimulgus parvulus – AT 1 10 Nyctidromus albicollis – B 3 5 5 2 30 24 10 13 Hydropsalis torquata – A 8 16 6 47 30 10 Podager nacunda – A 3 Chordeiles minor – AN 4 3 Braz. J. Biol., 62(2): 197-210, 2002 SÃO PAULO WOODLOT BIRDS 201 TABLE 1 (Continued) Species 1 a b 2 c 3 d 4 Lurocalis semitorquata – T 2 2 9 Chaetura meridionalis – AT 1 1 Phaethornis pretrei 18 15 22 11 12 13 20 28 Eupetomena macroura – B 2 3 1 Florisuga fusca 10 1 2 3 5 10 3 Colibri serrirostris – B 14 8 16 1 6 5 Anthracothorax nigricollis – T 10 Chlorostilbon aureoventris – B 8 2 1 10 20 5 Thalurania glaucopis 11 7 5 14 13 3 Amazilia lactea 34 10 5 7 21 30 13 Amazilia versicolor 21 8 9 20 6 9 3 Aphantochroa cirrochloris 1 1 Leucochloris albicollis – S 1 Heliomaster squamosus 1 1 2 Calliphlox amethystina 2 Aratinga leucophthalmus – S 15 30 48 36 15 Aratinga auricapilla – V 1 Brotogeris chiriri – V 3 Pyrrhura frontalis 17 14 30 12 Forpus xanthopterygius – B 89 15 58 50 84 38 100 77 Pionopsitta pileata – V 1 Pionus maximiliani 109 62 82 50 102 75 80 69 Amazona aestiva – V 1 Coccyzus melacoryphus – BT 4 1 1 Coccyzus euleri – T 1 2 Coccyzus americanus – N 1 Piaya cayana 65 52 45 50 48 75 25 Crotophaga ani – B 64 22 43 20 102 34 60 56 Guira guira – A 8 4 42 8 50 5 Tapera naevia – B 18 6 6 11 6 13 20 10 Dromococcyx pavoninus – T 1 2 1 1 3 Columba cayennensis – B 67 16 33 85 96 102 70 69 Columba picazuro – A 4 5 5 11 6 19 43 Zenaida auriculata – A 134 49 50 27 30 47 5 Columbina talpacoti – B 200 50 36 56 48 47 20 64 Claravis pretiosa – T 13 7 7 1 Leptotila verreauxi 159 67 82 174 120 145 100 115 Leptotila rufaxilla 3 1 11 5 2 Geotrygon violacea 2 1 5 2 Trogon surrucura 31 34 33 21 18 23 25 Ceryle torquata – C 1 1 Chloroceryle amazona – C 1 3 Chloroceryle americana – C 1 3 Braz. J. Biol., 62(2): 197-210, 2002 202 WILLIS, E. O. and ONIKI, Y. TABLE 1 (Continued) Species 1 a b 2 c 3 d 4 Bucco chacuru – A 1 Ramphastos toco 3 2 Picumnus albosquamatus 52 36 46 47 36 31 30 30 Melanerpes candidus – B 5 72 14 30 1 2 Colaptes melanochloros – B 16 11 8 16 10 10 10 Colaptes campestris – A 19 8 19 27 12 35 30 40 Veniliornis passerinus 33 17 31 24 41 30 30 Dryicopus lineatus 22 15 11 26 12 27 10 23 Campephilus robustus 14 5 9 11 12 8 8 Sittasomus griseicapillus 35 29 27 24 24 36 70 43 Dendrocolaptes platyrostris 3 15 4 3 6 8 8 Lepidocolaptes fuscus 10 14 14 1 Furnarius rufus – A 7 7 15 10 30 Phacellodomus ferrugineigula – C 24 5 2 17 12 16 30 41 Automolus leucophthalmus 51 45 23 28 18 40 10 15 Lochmias nematura 1 1 1 2 7 Sclerurus scansor 4 1 1 1 Xenops rutilans 4 5 3 3 12 20 7 Certhiaxis cinnamomea – C 2 5 1 6 2 3 Certhiaxis vulpina – C 3 6 Synallaxis spixi – B 39 5 3 51 56 10 35 Synallaxis albescens – A 1 5 Synallaxis frontalis – B 17 43 44 34 36 40 70 28 Synallaxis ruficapilla 116 146 128 118 78 100 110 86 Psiloramphus guttatus 40 51 34 57 30 36 10 18 Conopophaga lineata 103 147 86 161 66 66 100 48 Hypoedaleus guttatus – V 1 10 Mackenziaena severa 83 95 73 67 60 73 80 68 Taraba major – B 1 5 Thamnophilus caerulescens 98 80 63 103 54 87 70 63 Thamnophilus ruficapillus – A 1 2 Thamnophilus doliatus – B 26 6 12 57 46 20 35 Dysithamnus mentalis 71 105 91 74 24 98 70 92 Herpsilochmus rufimarginatus 128 115 87 121 102 125 50 104 Pyriglena leucoptera 112 210 159 151 132 113 120 112 Drymophila ochropyga 38 66 50 61 72 73 80 72 Drymophila ferruginea 161 135 102 134 144 138 120 91 Phyllomyias fasciatus – BV 1 Capsiempis flaveola 100 81 82 103 54 131 100 77 Myiornis auricularis 4 6 4 24 9 5 Hemitriccus diops 14 32 20 10 18 36 10 30 Hemitriccus nidipendulus – B 1 1 5 Braz. J. Biol., 62(2): 197-210, 2002 SÃO PAULO WOODLOT BIRDS 203 TABLE 1 (Continued) Species 1 a b 2 c 3 d 4 Todirostrum plumbeiceps 1 7 3 3 Todirostrum poliocephalum 37 34 56 53 42 45 50 49 Todirostrum cinereum – B 2 8 8 9 12 9 21 Serpophaga subcristata – B 16 2 2 4 7 3 Myiopagis caniceps 46 43 42 19 36 25 13 Myiopagis viridicata – T 10 16 20 17 12 17 20 5 Elaenia chiriquensis – BV 1 Elaenia flavogaster – B 28 3 9 14 21 20 40 Elaenia spectabilis – CT 8 6 Elaenia obscura – B 4 4 6 Elaenia mesoleuca – s 2 1 2 Elaenia parvirostris – s 1 3 Phaeomyias murina – BV 1 Cnemotriccus bimaculatus – B 4 4 3 17 80 20 Lathrotriccus euleri 71 70 49 63 36 47 110 30 Myiophobus fasciatus – B 40 23 18 31 30 42 60 36 Platyrhynchus mystaceus 1 1 6 5 5 Tolmomyias sulphurescens 66 54 29 67 24 58 48 Contopus cinereus – s 11 9 4 2 2 Camptostoma obsoletum 20 9 11 27 6 32 30 18 Corythopis delalandi 1 Knipolegus cyanirostris – Bs 2 2 1 1 3 Colonia colonus 60 69 56 26 24 22 40 26 Fluvicola leucocephala – C 13 1 11 6 24 12 23 Pyrocephalus rubinus – AS 3 Xolmis velata – A 2 1 3 Xolmis cinerea – A 1 6 12 2 30 8 Satrapa icterophrys – Bs 12 1 10 8 Gubernetes yetapa – A 5 3 30 8 Machetornis rixosus – A 1 2 Tyrannus melancholicus – BT 26 31 44 50 18 36 60 21 Tyrannus savana – As 1 2 7 3 8 Empidonomus varius – BT 10 4 10 23 22 30 7 Myiodynastes maculatus – BT 14 28 17 17 20 30 13 Pitangus sulphuratus – B 40 17 14 33 6 39 10 48 Myiozetetes similis – C 13 3 11 7 18 10 23 Megarynchus pitangua – BT 11 10 13 20 18 Myiarchus swainsoni – T 13 38 19 9 6 30 5 Myiarchus ferox – B 26 14 17 36 6 30 40 18 Leptopogon amaurocephalus 26 29 15 24 21 20 20 Schiffornis virescens 7 3 Pachyramphus polychopterus – BT 14 5 24 13 2 Braz. J. Biol., 62(2): 197-210, 2002 204 WILLIS, E. O. and ONIKI, Y. TABLE 1 (Continued) Species 1 a b 2 c 3 d 4 Pachyramphus viridis – Bs 2 Pachyramphus validus – B 5 2 3 11 12 10 8 Tityra inquisitor – s 2 Tityra cayana – T 1 7 3 2 2 Phibalura flavirostris – Bs 5 1 Antilophia galeata – C 4 3 2 Chiroxiphia caudata 81 44 11 54 24 85 40 51 Manacus manacus 8 3 2 7 12 14 16 Tachycineta leucorrhoa – A 23 92 91 3 66 4 26 Progne tapera – AT 40 11 14 7 19 10 2 Progne subis – AN 17 4 13 19 Progne chalybea – As 2 2 1 Notiochelidon cyanoleuca – A 27 380 194 23 119 80 21 Alopochelidon fucata – As 2 1 2 24 21 Stelgidopteryx ruficollis – B 48 138 107 14 72 73 90 69 Hirundo rustica – AN 4 151 53 1 Petrochelidon pyrrhonota – An 30 3 Cyanocorax cristatellus – B 1 3 Troglodytes aedon – B 16 2 11 3 6 17 10 31 Donacobius atricapillus – C 11 5 5 7 6 8 31 Mimus saturninus – A 10 6 13 6 12 20 16 Turdus nigriceps – s 1 3 2 3 3 10 Turdus amaurochalinus – B 35 1 5 20 6 28 3 Turdus leucomelas – B 2 1 11 11 28 38 Turdus rufiventris – B 4 3 5 30 25 12 Turdus albicollis 10 2 1 Anthus lutescens – A 7 6 2 3 6 1 Cyclarhis gujanensis 78 58 77 83 54 80 80 51 Vireo olivaceus – T 53 83 42 47 42 40 120 26 Hylophilus amaurocephalus – B 14 1 2 Passer domesticus – A 3 Estrilda astrild – A 29 13 12 14 16 Zonotrichia capensis – B 123 98 74 60 66 80 180 41 Myospiza humeralis – A 5 2 9 8 10 21 Emberizoides herbicola – A 2 3 6 6 2 10 Arremon flavirostris 2 4 1 6 10 Arremon semitorquatus 1 1 Donacospiza albifrons – As 1 Coryphospingus cucullatus – B 2 2 2 Haplospiza unicolor – S 2 Tiaris fuliginosa 10 6 3 6 4 2 Volatinia jacarina – B 69 12 30 36 24 6 74 Sporophila leucoptera – A 2 1 Braz. J. Biol., 62(2): 197-210, 2002 SÃO PAULO WOODLOT BIRDS 205 TABLE 1 (Continued) Species 1 a b 2 c 3 d 4 Sporophila lineola – BV 1 Sporophila caerulescens – B 110 65 29 46 20 20 165 Passerina brissoni – BV 1 Passerina glaucocaerulea – BS 1 4 1 6 Pitylus fuliginosus 24 7 3 13 2 10 15 Saltator similis 34 8 5 21 21 10 13 Schistochlamys ruficapillus – A 5 Hemithraupis ruficapilla 42 57 24 34 6 50 70 33 Nemosia pileata 12 18 8 9 10 20 Thlypopsis sordida 58 38 32 43 24 47 20 33 Pyrrhocoma ruficeps – S 2 Trichothraupis melanops 98 104 67 70 54 77 110 71 Tachyphonus coronatus 67 31 24 78 36 63 70 46 Habia rubica 84 89 52 60 30 89 71 Ramphocelus carbo – B 44 4 11 58 54 60 18 Thraupis sayaca – B 59 14 28 60 48 40 28 Tangara cayana – B 42 14 5 48 29 20 3 Pipraeidea melanonota – S 10 3 2 Euphonia chlorotica 14 1 9 6 6 3 8 Euphonia violacea – S 1 1 1 Euphonia musica – S 2 Dacnis cayana 13 6 6 12 10 20 3 Coereba flaveola – B 53 17 8 19 25 60 18 Conirostrum speciosum 53 38 17 37 51 50 12 Parula pitiayumi 16 5 1 Geothlypis aequinoctialis – C 35 13 17 47 18 64 30 61 Basileuterus flaveolus 48 56 62 78 96 77 110 66 Basileuterus leucoblepharus 76 8 41 55 36 Basileuterus hypoleucus 207 252 148 155 126 150 210 143 Basileuterus culicivorus – S 3 1 2 Pseudoleistes guirahuro – A 2 7 30 Agelaius cyanopus – C 4 3 3 18 1 3 Agelaius ruficapillus – A 15 8 66 Molothrus bonariensis – A 34 10 2 2 Cacicus haemorrhous 8 9 Days 34 25* 33* 15 5* 20 3* 12 Hours 166.8 100 132 70.2 16.6 106 10 60.7 Night Hours 0 + + + + 8.3 + 2.0 * Other days, birds not recorded. Hours of banding not counted. Braz. J. Biol., 62(2): 197-210, 2002 206 WILLIS, E. O. and ONIKI, Y. Comparison with Campinas woodlot In size and forest type, the São José woodlot is rather like the Fazenda Santa Genebra semi- deciduous woodlot of Campinas, studied in the 1970s by Willis (1979) and in the 1990s by A. Aleixo (Aleixo & Vielliard, 1995). Considering only the nonvagrant forest and border species, there were 152 species in São José in 1982-86, 144 in 1987-91, 132 in 1992-97, and 133 in 1997-2000. In Santa Genebra, there were 145 such species in the 1970s (147 counting two swifts that fly over) and 117 in the 1990s. Both woodlots lost species gradually. Other than substitution of Picumnus and Veniliornis for coastal species in Campinas, there were few differences between the woodlots. The kite Ictinia plumbea, antshrike Hypoedaleus, and mixed-flock canopy flycatcher Sirystes sibilator persist in Campinas, while in the 1970’s there had been a summering hawk (Harpagus diodon); two owls (Tyto alba, Otus atricapillus); two swifts (Streptoprocne zonaris, Cypseloides fuliginosus); two rare woodcreepers (Dendrocincla turdina, Campylorhamphus falcularius); two flycatchers (open-understory Hemitriccus orbitatus and mi- grant Elaenia albiceps); and rare, possibly vagrant Dendroica striata (migrant from North America) and Icterus cayanensis (an edge species spreading eastward). In the 1990s, Aleixo added the wood- pecker Celeus flavescens plus a possibly vagrant flycatcher (Mionectes rufiventris) and tanager (Tersina viridis), not yet recorded in São José. Campinas gained, much like São José, a few dry- forest fruit-eating Aratinga, Amazona, and Ram- phastos. Probably present but not seen in the 1970s, Colaptes melanochloros and Turdus rufiventris were also new in Campinas. By the 1990s, Campinas seemed to have lost Cryturellus obsoletus, Glaucidium, summer An- thracothorax, winter Leucochloris, Coccyzus eu- leri, Dromococcyx, Sittasomus, Dendrocolaptes, Lepidocolaptes, Automolus, Lochmias, Synallaxis ruficapilla, Mackenziaena, Dysithamnus, Herpsi- lochmus, Drymophila ferruginea, Capsiempis, Hemitriccus diops, Todirostrum poliocephalum, Myiopagis caniceps, migrant Elaenia mesoleuca, Platyrhynchus, Corythopis, Schiffornis, Hemi- thraupis, plus winter Euphonia violacea and Basi- leuterus culicivorus. Several of these were also lost in São José, or no longer reached there in mi- gration. The Campinas woods lacked several bamboo- forest upland species throughout, notably Dry- mophila ochropyga, Psiloramphus, Todirostrum plumbeiceps, and Myiornis. Arremon, Pyriglena, Trogon, and Pyrrhura were also absent, as well as Sclerurus (both the latter disappeared in São José). Several hummingbirds (Aphantochroa, He- liomaster, Calliphlox) although unrecorded in Santa Genebra, were in suburbs there; censusing canopy nectarivores is difficult in Rio Claro and Campinas. Other birds absent in Campinas were Cathartes, Leptodon, Micrastur spp., Herpetotheres (the first two now gone in São José also), and many of the dry-forest species that invaded São José from the northwest (Cyanocorax reached Campinas, as did Ramphastos later). Lost and new species Of 67 open-area species near São José, 22 seemed to disappear in 1997-2000, but open areas were not censused intensively and will very likely still occur with the 45 species recently recorded. Four “lost” species (Thamnophilus ruficapillus, Machetornis, Passer and Schistochlamys) definitely still occur in open areas closer to or in Rio Cla- ro. Cane fields are not suitable for the species of this group, and grassy or bushy swales provide little habitat locally. Progne subis, a northern open-area wintering bird (here present in summer), once roosted in large flocks in city parks in Rio Cla- ro, but has disappeared from the city and region; it was last noted in 1993. A probable southern open-area wintering bird (here present in winter), Donacospiza albifrons, was only noted 8 April 1983 (2 birds together) in marsh scrub near the farm pond, in an El Niño rainy year. In 1983, a flooded pond inside the cane field attracted several water birds not seen since (Ta- chybaptus, Nomonyx, northern migrant Tringa, Gallinago paraguayae, southern winter Porphy- riops). The first three still occur at times on a large permanent pond in a sizeable eucalyptus grove or “Horto”, closer to Rio Claro. The northern migrant Bartramia was spotted in wet cutover cane fields later in 1983, and has not been recorded since. Migrant swallows have been over cane mostly in wet years (Hirundo, Petrochelidon). Dendrocygna was recorded at that time, but later was occasionally seen on the roadside farm pond; hunters probably hunt it there, discouraging recent visits, except at night when we did not visit. During the day, it is Braz. J. Biol., 62(2): 197-210, 2002 SÃO PAULO WOODLOT BIRDS 207 still common on the Horto pond and a city lake, both protected. Hunters probably rarely check the El Niño pond, hidden in the cane and empty except in wet years. The four other species that seem to have disappeared recently have always been uncommon in cane areas near Rio Claro, commoner in savannas to the northwest: Buteo albicaudatus (with cane fires), Bucco chacuru, Synallaxis albescens, and Sporophila leucoptera. Seventeen “new species” of the 67 in open areas probably were not among the 50 species recorded in 1982-86 either because Willis has been checking before dawn mostly in recent years (Rhynchotus, Gallinago undulata, Caprimulgus parvulus, Podager, Chordeiles, Thamnophilus ruficapillus) or because they are rare visitors at the farm pond or just flying over (Ardea spp., Bubulcus, Egretta, Elanus, Buteo albicaudatus, northern migrant Petrochelidon, southern migrant Pyrocephalus, Sporophila leucoptera). The Spo- rophila, Petrochelidon, Thamnophilus, and Buteo are also unrecorded in recent years (above), as are Bubulcus, Egretta, and Chordeiles. Two of the 17 new open-area species were perhaps absent 1982-86. Furnarius definitely moved into the farm pond after 1984, perhaps after the muddy roads dried up, allowing it to walk there. Cane areas provide little forage for the species, though houses with lawns are not far south. Age- laius ruficapillus moved to the farm pond marsh, as it is increasing statewide; but cane fields here are rarely suitable for its open-field foraging. Columba picazuro of dry regions has also invaded São Paulo in recent years (Willis & Oniki, 1987) and has increased even near Fazenda São José, where it finds food in a few open fields but rarely nests in the few scattered trees, hence not being as common as border nesting C. cayennensis. Zenaida of open fields and Columbina of edges seem less usual than during the 1983 El Niño, but both continue common in the city during the last 15 years. As they drink water on open roads in wet years but not in dry, the problem recently may be heat and lack of water at midday in the São José cane fields. Weed seeds may also be less available in dry years. Progne tapera has also become gene- rally less common in recent years and, like other Progne, was perhaps more successful during the wet 1982-84 period; it had roosted in town with P. subis earlier. Creek and marsh birds were usually present both at the start and end of the studies, though Cairina has become less common in recent dry years. It is still frequent on the protected Horto Pond, as are Butorides and Ceryle (both rare in 1982-84). Aramides saracura appeared on roads more in 1982-84. Elaenia spectabilis seemed to disappear after 1989 and Certhiaxis vulpina after 1995, while Pilherodius was only recorded in 1990, but censuses were not frequent on the bushy and hard-to-approach creek; these species may have been overlooked as they had never been recorded at the east marsh. By 1997-2000, some 31 species had disap- peared from the woodlot, including 6 border species. Eleven were birds from the south that migrate or winter in the Rio Claro region. Five southern species (Phibalura, Pyrrhocoma, Pipraeidea, Passerina glaucocaerulea, and Basileuterus culicivorus) were registered in the wet El Niño years of 1982-84, with a few winter records later only for Phibalura and glaucocaerulea. Pyrrhocoma, Pipraeidea, and Basileuterus were recorded in the dense understory or canopy of the Rio Claro Horto also mainly during 1982-84. Euphonia violacea was noted infrequently in 1982-92, Leucochloris only in Aug. 1988, Ha- plospiza only May 1994. They are rare as southern winter visitors in the region. Migrant Pachyramphus viridis, Turdus nigriceps, and Elaenia mesoleuca are also not common locally. Three summer visitors (Claravis, Coccyzus melacoryphus, Tityra inquisitor) and a northern winter bird (Coccyzus americanus) are also unre- corded recently. Tityra and C. americanus are rare in the region, but the other two may have decreased due to recent dry years. Some other forest and border species that have disappeared since 1982-84 may have been affected by low rainfall in the last 15 years. Arremon semitorquatus of the humid east of the state seems to have been replaced by A. flavirostris of the dry interior. Treetop Parula has dropped in numbers both in São José and in eucalyptuses near Rio Claro, though it seems a dry forest bird and should not have disappeared with droughts. Other treetop birds that join mixed flocks, such as Myiopagis caniceps, Hemitriccus, Conirostrum, and Nemosia also seem less frequent recently. Megarynchus continues in the Horto near Rio Claro, however, and in São José may have little edge habitat except for the hard edges along the cane fields (see below). Braz. J. Biol., 62(2): 197-210, 2002 208 WILLIS, E. O. and ONIKI, Y. Glaucidium, Pyrrhura, and five other midlevel to understory moist-forest species seem to have disap- peared due to loss of the few individuals present earlier: Lepidocolaptes, Sclerurus, Corythopis, Schiffornis, and Turdus albicollis. Cacicus was a river-edge forest species that definitely disappeared from near the east marsh after 1987; it did not survive on Fazenda Barreiro Rico, about 100 km west, after river woods were cut (Willis, 1979; Magalhães, 1999). Hummingbirds were common mainly in Inga and Tabebuia flowers along the Ribeirão Claro, hence several upper-level species have seldom been recorded of late. Anthracothorax was rare in mi- gratory periods, and Eupetomena and Heliomaster are just rare (more common in the eucalyptus grove off to the south). Study of flower cycles probably would have provided better records. Understory and midlevel Phaethornis, Thalurania, Amazilia lactea, and versicolor were more successfully sampled. Micrastur ruficollis appeared in 1986-87 and then disappeared. Hunters would not affect these species, although extreme droughts like the La Niña from March to winter of 2000 may have. Cathartes has disappeared from the Rio Claro region, though still present on rather dry escarpments with better updrafts off to the north (where Sar- corhamphus still occurs). Coragyps declined briefly in 1987, partly due to hunters killing large numbers around a few carcasses. They also may have killed the few Cathartes near Rio Claro. Penelope almost certainly was exterminated by hunters or wandering dogs, first near the roadside banding sites and later in the woods. Various hawks that have disappeared (Leptodon, Buteo brachyurus) may have been shot by occasional hunters, or affected by dry years and low populations. Passerina brissoni is a vagrant in the region due to capture for caging (as Oryzoborus angolensis, Gnorimopsar chopi, Sicalis flaveola), the fate of many macaws and parrots formerly found the Rio Claro region. Five new forest and border species (Accipiter, Micrastur semitorquatus, Caprimulgus rufus, Ram- phastos, Cyanocorax) are still rather rare in the Rio Claro region, and like Taraba major have apparently moved in from dryer and more open regions to the north and west. None have yet been as successful as Columba picazuro, which feeds in open fields. Micrastur do seem to move in and out of local woodlots, as for instance M. ruficollis (above). Euphonia musica, a rare winter visitor at forest edges, was recorded only 1997 but was probably present earlier Some new species may yet disappear and lost species reappear, especially if droughts (possibly linked to greenhouse effects) stop. Many species are able to recolonize (travel-prone species of Willis 1979, metapopulations in more recent works). However, nonmetapopulational forest species like Lepidocolaptes or Schiffornis may be unable to reach the woodlot again. Thus, though border and other species seem to appear and take the place of lost species, the regional diversity will probably decrease with loss of forest species partly concealed by local spread of outside species already present. Entry of new dry-forest species merely moves the centers of distribution of these birds, concealing loss of diversity eastward in moist forest. As houses and intensive agriculture invade the region and water supplies get scarce, even the open-area, border, and water birds will vanish. Intervening censuses In the case of Fazenda São José, we checked birds in intervening years, notably 1987-92 (columns b, 2 and c in Table 1). This allowed one to see if birds absent in the intermediate period had reap- peared in the final study periods, rather than being “lost” forever. Eight forest species, seemingly lost in 1987-92, reappeared later: Calliphlox (rare spring), Coccyzus euleri (rare summer), Taraba (invading region), Hemitriccus nidipendulus (rare), Elaenia parvirostris (rare migrant), Satrapa icte- rophrys (uncommon migrant), Turdus albicollis (rare), and Pipraeidea (rare winter). All but Coc- cyzus and Turdus are more frequently found at soft or bushy edges, censused less (2 of Table 1) than earlier. Probably all these species were present in 1987-92, but not recorded; or they were travel- prone metapopulations and reinvaded. This indicates the kind of error one can make in such censuses – 8 of 16 species (50%) seemingly lost in 1987-92 either moved in again or were actually present throughout. Some 4 species, new in 1987-92 (Micrastur ruficollis, winter Leuco- chloris, northern winter Coccyzus americanus, summer or migrant Tityra inquisitor), were not sighted later. Some 20 species present both in 1982- 86 and 1987-92 subsequently disappeared. Braz. J. Biol., 62(2): 197-210, 2002 SÃO PAULO WOODLOT BIRDS 209 In open areas in 1987-92, three uncommon species (Chaetura, Xolmis velata, Gubernetes) of 15 seemingly lost ones (or 20%) reappeared from 1997 on. Nine rare species previously unrecorded turned up, and four (Bubulcus, Egretta, Buteo albicaudatus, and Petrochelidon) were not seen thereafter, while five (Ardea alba, Chordeiles, Thamnophilus ruficapillus, Agelaius ruficapillus, Sporophila leucoptera) were resighted in later years. Only 2 swallows, present in 1982-86 and 1987-92, vanished later; 12 of 67 open-area species had already been lost soon after the 1982-84 El Niño rains. Open-area species, notably aquatic ones, seemed more directly affected by drought than were forest species. Of creek and marsh species, only Chloroceryle amazona seemed gone in 1987-92 (reappearing later), while two other species were not reported from 1992 on (Ceryle, Elaenia spectabilis). Pilhe- rodius in 1987-92 was not recorded later, while Mesembrinibis and Certhiaxis vulpina were. As noted above, it was difficult to check these creekside species. Records of these birds seemed mostly unrelated to drought, as creek and marsh water did not dry up as much as did the cane swales or forest. For the intervening years of 1992-97 (columns 3 and d in Table 1), 8 forest or border species seemingly lost reappeared later: Colibri, Aphan- tochroa, Calliphlox, Coccyzus euleri, Taraba, Elaenia spp., Antilophia, Hylophilus, Arremon flavirostris, and Coryphospingus. Thus, 12 of 19 (63%) of the birds lost from the preceding period (or earlier) reappeared later. Some 15 other species present up to 1992-97 disappeared later (of these, Turdus albicollis and Pipraeidea were also absent just before). Two species (Anthracothorax and Haplospiza) were only recorded in 1992-97, and Ramphastos and Cyanocorax were new species that also appeared later. In open areas in 1992-97, only 2 species that had disappeared (Elanus and Pseudoleistes) were noted later, out of 8 species (25%) seemingly lost after the preceding 5 years. The only new species were Gallinago undulata and Caprimulgus parvulus, noted due to pre-dawn work. Seven species were not seen from 1998 on. After 1992-97, Butorides and Certhiaxis vul- pina seemed to disappear from creeks and marshes. Three species (above) had disappeared by 1992. Hard vs. soft edges The south forest edge was hard, the forest (though much damaged by wind blowdowns and Celtis vines) abruptly ending at the road and cane field of the neighboring ranch. The west and east edges were either soft or gradual, with scrub and grass, plus additional weeds along the eastern power line swath and cat-tails along the nearby creek. Some species showed a clear difference in censuses because of this, for instance Synallaxis spixi of bushes and tall grass: it was rarely recorded on netting days (abcd in Table 1) along the hard south edge, and regularly on census days (1234 in Table 1) when soft east or west edges were checked. S. frontalis inside shady borders and S. ruficapilla in the woods did not show this pattern. Other birds that showed a preference for soft edges were Aramides saracura and a few other water species or flowering-tree hummingbirds near Ribeirão Claro: Buteo magnirostris; Amazilia; Heliomaster; Tapera; Columbina; Leptotila spp.; Dryocopus; Campephilus; Thamnophilus doliatus; Serpophaga; Elaenia flavogaster and E. obscura; Myiophobus; Camptostoma; Satrapa; Empido- nomus; Pitangus; Myiarchus ferox; Pachyramphus (3 spp.); Troglodytes; Turdus amaurochalinus and T. rufiventris; Hylophilus; Volatinia; Sporophila caerulescens; Pitylus (?); Saltator; Thlypopsis; Tachyphonus; Ramphocelus; Thraupis; Tangara; Coereba, and Parula. Some birds were commoner on regular census days with soft edges, but for other reasons. Several species were found more in swampy uncluttered woods near creeks (not visited on banding days) along the north or west edge: Geotrygon, Lochmias, Sclerurus, 3 manakins, and Basileuterus leucoble- pharus. Only the manakins used bushes beyond the forest border. Penelope was absent along the hard cane-field edge due to hunters; it regularly uses similar edges where not hunted. Birds that seemed somewhat more common (Table 1) along the hard edge were Buteo brachyu- rus (soars and dives at high edges), Nyctidromus (road by the wood at night), Melanerpes (using roost hole), Synallaxis frontalis (?), Drymophila ochropyga (mainly due to bamboo there), Myiarchus swainsoni (avoids M. ferox?), and Basileuterus flaveolus (avoids B. leucoblepharus?). Birds of Braz. J. Biol., 62(2): 197-210, 2002 210 WILLIS, E. O. and ONIKI, Y. open areas were often more common there, notably swallows that fly over cane fields. Some forest birds did enter the cane fields, notably B. flaveolus and S. frontalis (see Cândido- Jr., 2000). Cane cutters reported a banded Pyriglena deep into the cane, near the highway. Willis saw a banded Basileuterus hypoleucus 100 m out in the cane, near the El Niño pond. Other birds entered the cane fields near the road in the early morning. We recorded such species as Crypturellus parvi- rostris, Thamnophilus caerulescens, Pyriglena, Conopophaga, Capsiempis, Geothlypis, and Zono- trichia on several occasions. When cane is burned, several hawks, falcons, and caracaras often are present. Bare fields in spring provide a habitat for Vanellus, Syrigma, Xolmis spp., Anthus, and other open-area birds. However, these birds have to leave as the cane grows, and only the Crypturellus regu- larly move in except for aerial swallows. Note added in proof In 16 more visits (28/7/2000 to 12/2/2002) in and near the São José woodlot, we recorded one or a few Dendrocygna, Bartramia, Bubulcus, Me- sembrinibis, Tachybaptus, Cathartes, Leptodon, Buteo brachyurus, Herpetotheres, Glaucidium, Athene, Lurocalis, Caprimulgus parvulus, Chaetura, Eupetomena, Aphantochroa, Calliphlox, Coccyzus melacoryphus, Claravis, Ceryle, Chloroceryle (2 spp.), Thamnophilus ruficapillus, Elaenia obscura and chiriquensis, Megarynchus, Progne chalybea, Turdus nigriceps, Anthus, Passerina glaucocaerulea, Schistochlamys and Sporophila leucoptera and lineola. Thus, instead of 38 species (including 9 border birds) that disappeared from the woodlot in 1997-2000, there were 23 (2) lost in 1997-2002, or 141 species still present. Four new nonforest species (Ardea cocoi flying past, Porphyrula mar- tinica on the cane pond, Myiarchus tyrannulus down Ribeirão Claro, and Sturnella superciliaris near the farm pond) and one hybrid (Sporophila “ardesiaca”) were added, for an area total of 266. Acknowledgments — We thank CEMAVE and IBAMA for bands and permits to work with wild birds. We appreciate equipment from Idea Wild, which made work with data much easier, and field help by students, notably R. Morini and B. S. Ataguile. Publication n. 20 of the Institute for Studies of Nature. REFERENCES ALEIXO, A. & VIELLIARD, J. M. E., 1995, Composição e dinâmica da avifauna da mata de Santa Genebra, Campi- nas, São Paulo, Brasil. Rev. Brasil. Zool., 12(3): 493-511. CÂNDIDO-JÚNIOR, J. F., 1991, Efeito de borda da mata sobre a composição da avifauna em mata residual em Rio Claro, São Paulo. Dissertação de Mestrado, Instituto de Biociências, Unesp, Rio Claro, SP, 110p. CÂNDIDO-JÚNIOR, J. 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