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Iheringia, Série Zoologia, 107: e2017037
1
Série Zoologia
Fundação Zoobotânica do Rio Grande do Sul
Museu de Ciências Naturais
www.scielo.br/isz
e-ISSN 1678-4766
Iheringia
Iheringia
Breeding biology and conservation of hawk-eagles (Spizaetus spp.)
Aves, Accipitridae) in southern Atlantic Forest, Brazil
Felipe Zilio
Setor de Ornitologia. Seção de Zoologia de Vertebrados, Museu de Ciências Naturais, Fundação Zoobotânica do Rio Grande do Sul, Rua Dr. Salvador França, 1427,
Jardim Botânico, 90690-000 Porto Alegre, RS, Brazil.
Present address: Universidade Federal de Viçosa (UFV) – Campus Rio Paranaíba, Rodovia MG-230, Km 7, s/n, Caixa Postal 22 , 38810-000,
Rio Paranaíba, MG, Brazil. (fzilio@msn.com)
Received 28 September 2016
Accepted 01 August 2017
DOI: 10.1590/1678-4766e2017037
ABSTRACT . Neotropical hawk-eagles (Spizaetus spp.) are large forest raptors, having low population densities and high sensitivity to human disturbance.
The three species of Brazil’s Atlantic forest (S. ornatus, S. melanoleucus, S. tyrannus) are threatened and little is known of many aspects of their biology,
such habitat requirements, nesting behavior, and food habitats. Here I present data about the breeding biology, diet and behavior of the Ornate Hawk-Eagle
(S. ornatus; OHE) and the Black-and-white Hawk-Eagle (S. melanoleucus; BWHW), and estimations of distribution - extent of occurrence (EOO) - and
S. tyrannus;
Spizaetus seems to have very variable breeding cycles and begin breeding in the
Spizaetus require large, unbroken forest areas to live, and my data reinforce the critical situation of hawk-
eagles in southern Atlantic forest. All three species have lost habitat and their distributions have shrunk over the past decades. The estimated population
preserve and limit the disturbance of remaining forests, establish connectivity among fragments and reduce direct threats to raptors (e.g., persecution).
We also need to better understand the ecological requirements of hawk-eagles and establish public policies to protect both species and their habitats.
KEYWORDS.
RESUMO. Biologia reprodutiva e conservação de Spizaetus spp. (Aves, Accipitridae) na porção sul da Mata Atlântica, Brasil. Os gaviões do
gênero Spizaetus
As três espécies que ocorrem na Mata Atlântica (S. ornatus, S. melanoleucus, S. tyrannus
aspectos de sua biologia, como habitat, comportamento reprodutivo e dieta, são pouco conhecidos. Neste trabalho eu apresento dados sobre a biologia
reprodutiva, dieta e comportamento do gavião-de-penacho (S. ornatus, ) e do gavião-pato (S. melanolecus, ), bem como estimativas da
Spizaetus
S. tyrannus, ).
e
para
Spizaetus
Spizaetus
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Iheringia, Série Zoologia, 107: e2017037
e.g.,
PALAVRAS-CHAVE.
Spizaetus hawk-eagles are large top predators in
the forests of the Neotropics. Three of the four species of
Spizaetus occur in Brazil: the Black Hawk-Eagle [Spizaetus
tyrannus Spizatus
ornatus
Eagle [Spizaetus melanoleucus
are widespread over both lowland and montane Neotropical
forests from Mexico to northern Argentina and southern
Brazil (&
Black-and-white Hawk-Eagle, Spizaetus populations of the
Atlantic Forest are disconnected from those of the Amazon
forest (&
species are nationally or globally threatened (
Threatened and all species have decreasing population
et al
&
et al.
populations might be neglected by conservation policies
that assume that the Amazon forest does support healthy
populations.
The three hawk-eagles are syntopic for most of their
distribution, but segregate themselves by nesting habitats,
food and hunting behavior (
& et al.,
km of forest
& ,
feeds mainly upon mammals, hunting from perches in the
lower canopy and captures prey mostly on trees or diurnal
retreats or by making long attacks through the forest. Black
(e.g.,
et al.
Ornate Hawk-Eagles are apparently more abundant
in French
in Tikal Forest
&,
mainly stalk-and-ambush strategy, food being mostly birds
and squirrels and selecting more exposed trees for nesting and
locating the nest on large branches near the trunk (
et al.
The Black-and-white Hawk-Eagle is the least known
of these three species. It is rare or at least uncommon
(&
underestimated because usually soars high (
hunting tactics are poorly described, but it is known to feed
manly upon reptiles and birds caught in the canopy by long
only by observation of few nests ( &
et al.b;
et al.
being sought after by birdwatchers and ornithologists, and
having a widespread distribution, much of the biological
information about these species are scarce (e.g., diet. breeding
biology, habitat requirements), especially for Atlantic
Forest populations for which information on breeding and
nesting biology are basically anecdotal. There is only one
description of a nest of the Black-and-white Hawk-Eagle
(
et al.
and which acquired
much information about their diet, breeding biology, habitat
requirements, territory size, and so on ( et al.,
Eagle is basically unknown (
b&
information about these three species of hawk-eagles at the
southern limits of their distribution in the Atlantic Forest in
southern Brazil. Here I present estimates of the distribution
about the breeding biology, diet and behavior of Ornate and
Black-and-white Hawk-Eagles.
METHODS
Distribution and abundance. The abundance of
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Iheringia, Série Zoologia, 107: e2017037
both anecdotal observations and standardized sampling
i.e.
count per point) from elevated points above the forest canopy
The literature survey included searching in digital
already been compiled to evaluate the threatened status of
et al.
(
duplicate records. All records associated with a geographical
valid. In cases where the name of the municipality was the only
geographical information available, I used the coordinates of
the municipality’s city hall.
The abundance of each species was estimated based
for estimating the number of individuals and territory for
estimating the number of pairs were taken from the literature
(&
pair. The extent of occurrence (EOO) of each species was
excluding historical data, and overlaiding data of Atlantic
www.sosma.org.br) to estimate the area of forest available
of the area available since these species need large areas
of continuous forest ( et
al.
et al
also did a more conservative evaluation to estimate population
( et al.
Breeding biology. Breeding behavior of the Black-
and-white Hawk-Eagle was derived from observations at
a single nest. To Ornate Hawk-Eagle breeding data was
collected by monitoring one nest during an entire breeding
season, and with additional information from another two
nests. The nest was monitored one or twice every month
and taking notes and photos about breeding behavior, nestling
development, and prey remains. Afterwards I visited the local
Diet.
based on prey remains and pellets collected in the nests
and from a direct observation of one adult carrying prey
by comparing the remains (i.e., bones and feathers) with
Weights of prey species were taken from
and
RESULTS
Distribution and abundance.
overlaid with the EOO of Black-and-white Hawk-Eagle,
while the current distribution of Black Hawk-Eagle was
their historical distributions. Black and Ornate Hawk-Eagle
showed greater reduction in their area of occurrence (i.e.,
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Tab. I. Extent of forest remaining within the Extent of Occurrence (EOO) of hawk-eagles’ species in the southern Atlantic Forest, Brazil. The amount
.
Spizaetus species
)
EOO EOO
Black Hawk-Eagle S. tyrannus
Ornate Hawk-Eagle S. ornatus
Black-and-white Hawk-Eagle S. melanoleucus
size for a pair is smaller than for an individual;
&
important for regional evaluation (e.g., state red list), are as
regardless of the isolation of the patch, the forest available to
individuals showed on Tab. II).
Breeding biology
Black-and-white Hawk-Eagle.
found a nest of the Black-and-white Hawk-Eagle built in an
took the prey and the male moved to a nearby tree. After a
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Iheringia, Série Zoologia, 107: e2017037
&
a) Estimated number of individuals
Spizaetus species
EOO EOO
Black Hawk-Eagle S. tyrannus
Ornate Hawk-Eagle S. ornatus
Black-and-white Hawk-Eagle S. melanoleucus
b) Estimated number of pairs
Spizaetus species
EOO EOO
Black Hawk-Eagle S. tyrannus
Ornate Hawk-Eagle S. ornatus
Black-and-white Hawk-Eagle S. melanoleucus
apparently foraging, and sometimes diving into the valley.
Few minutes after the female came back to nest, the male
valley, chasing each other and, sometimes grasping onto
the back of the other. After a while, they separated and I
did not see them during the rest of the day (I ended my
but was not successful.
Ornate Hawk-Eagle.
reservoir (data available in et al
with intense vocalization, the male was performing an
undulating display (series of loops and dives) and chasing the
and sticks. The presence of prey remains, faeces and feather
of Ornate Hawk-Eagle suggested that the nest was still active,
adult carrying a green stick to an Araucaria tree (Araucaria
angustifolia
reservoir in second-growth forest near Pinus sp. plots
male above the female and trying several time to scratch
the female’s back. Twice I observed foot-touching, although
without complete claw bonding, and only for a few seconds.
I lost visual contact when the female dived into the valley,
followed by the male.
deep and decorated with green sticks and leaves of Lithraea
brasiliensis
before climbing to the nest, I observed one adult perched on
nest, other adult (smaller, probably the male) left the nest,
adults were noted to have continued to bring green leaves to
and attacked me several times, both while climbing and when
and I kept all visits short in order to reduce stress on the
nestling nor did I band it. Based on the estimated hatching
et
al.
it outside the nest although its rectrices were not completely
still within its parents’ territory. I found prey remains in the
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(bottom right) of the nest.
Diet – Ornate Hawk-Eagle. I collected bones,
feathers and hair of several prey remains and two pellets
at nest B during two visits and during several visits over
least to genus (Tab. III) with the most abundant prey being
Brown Tinamou [Crypturellus obsoletus
Guerlinguetus
ingrami
adult Ornate Hawk-Eagle carried to the nest. Mean weight
quail-dove; Geotrygon montana
Penelope obscura
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with details of the chamber (with green leaves and sticks).
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Patagioenas cayennensis
Weight (g)
Nest B Total
Tinamidae
Crypturellus obsoletus
Penelope obscura
Gallus gallus -
Patagioenas picazuro -
Patagioenas sp.# -
Leptotila sp. -
Geotrygon montana -
Ramphastos dicolorus -
Colaptes melanochloros
Pionus maximilliani -
Cyanocorax chrysops -
-
Total Aves
Guerlinguetus ingrami -
Total Mammalia
Total 7
DISCUSSION
Distribution and abundance. Hawk-eagles are
threatened in southern Brazil (&
), mostly
because of habitat loss ( et al.
rate of deforestation has been reduced in recent decades,
remaining forests are extremely fragmented (et al.,
&
suggests that they are declining. I did not estimate vegetation
available for historical records, so the real loss is probably
overestimated since species distributions were calculated
which included inappropriate habitats for hawk-eagles
(e.g., grasslands). The past distribution of the Black Hawk-
Eagle, for example, is probably overestimated. In spite of
its occurrence in Misiones, Argentina (&
et al.,
are few recent records, et al
et al
not been recorded at several places at which they occurred
in the past, suggesting true local extinction rather than lack
of surveys. I’d highlight the lack of recent records of Black
Eagles, and even a Harpy Eagle [Harpia harpyja
&
has vanished from the western portion of the state (last
have disappeared from the central and southern forests of
by urban and agricultural expansion. The Black-and-white
Hawk-Eagle, for instance, which historically has occurred
, mentioned in
&
Ihering,
the state.
I have estimated population size based on data from
Amazon and Tikal forests, areas which are better preserved
than the southern Atlantic Forest. et al
summarized data on Spizaetus from the Atlantic Forest and
for the Ornate and Black Hawk-
for the Black-and-white Hawk-
Eagle, estimations that are smaller than those of
&
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Iheringia, Série Zoologia, 107: e2017037
the same situation is true for southern Brazil, where most
( et al.
than half of the estimation based on Amazon and Tikal forests
data (&
and probably more accurate, since the highly fragmented
condition of the Atlantic Forest ( et al.
there are no data about population structure and trends in
southern Brazil, it is reasonable to assume that each possible
based on
Endangered species in the southern Atlantic Forest.
the Black-and-white Hawk-Eagle, which seems to be in a
similar situation to that of the Ornate Hawk-Eagle in terms
The current species risk evaluation for hawk-eagles
and Black-and-white Hawk-Eagle as Endangered and the
that the Black Hawk-Eagle has the smallest population of
the three species and it is possible that the regional risk
evaluation underestimates the risk to this species. Both Black
and Ornate Hawk-Eagle depend on mature forests (
et al.
Black Hawk-Eagle has for second-growth and forest edge
( &
the species is to disturbed landscapes ( et al.,
Black-and-white Hawk-Eagle were downlisted to Endangered
same criteria above, my data suggest that all species should
;
et al.
population size for all species. Although my evaluations are
they should be treated with caution, and I would suggest
Eagle until there is more accurate data. My estimates were
based only on the potential habitat available and probably
Hawk-Eagle also need to be monitored, but risk evaluation for
Breeding biology. Individuals of Spizaetus seems to
have high plasticity in their breeding cycle. The Black-and-
white Hawk-Eagle is the least known species of these three
species of Spizaetus, and the nest reported here is only the
second known for the Atlantic Forest. In southeastern Brazil,
Spizaetus spp.;
et al
that Black-and-white Hawk-Eagle starts it breeding cycle
et al
corresponds with the dry season for most of Brazil.
&
& et
al.
et
al.,
Ornate Hawk-Eagles seems to have the same pattern in the
Amazon basin: nesting in March in Ecuador ( et al.,
et al.
in Manaus, Brazil. In the Atlantic Forest, egg laying by the
Ornate Hawk-Eagle has been reported, or estimated, to be
et al.
(this study). It is unclear why the Ornate Hawk-Eagle and
also the Black-and-white Hawk-Eagle start breeding in the
when starting to breeding; “it is more a matter of avoiding the
worst months” (
Spizaetus species ( et
al.
order to avoid the worst months.
Most nest characteristics and breeding behavior I
observed follow what has been reported for hawk-eagles or
for raptors in general (&
et al.Spizaetus species nest in
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Iheringia, Série Zoologia, 107: e2017037
Black and Ornate Hawk-Eagles are similar ( et
al.
et al
&
development seems similar to the accounts reported by
et al.
The Black-and-white Hawk-Eagle seems to have
a less elaborated courtship display than other species of
Spizaetus. While both Ornate and Black Hawk-Eagle performs
diving, looping, grasping, food-touching and rolling-over
(&
observations of courtship of the Black-and-white Hawk-Eagle
report pairs gliding together, low vocal activity, chasing
and diving culminating with grasping (&
&
this study). et al.
observation of an elaborate courtship by Ornate Hawk-Eagles
and none for the Black Hawk-Eagle in Tikal Forest.
Behavior by the pair before and during copulation of the
behavior of both Black and Ornate Hawk-Eagle. While
et al.
between the pair before copulation for both Black and Ornate
Hawk-Eagle, I did not hear any call from Black-and-white
Hawk-Eagle before or after copulation. Indeed, the Black-and-
white Hawk-Eagle seems to be a very shy species, detected
rather by visualization than vocalization (pers. obs.). I did not
see the female bringing sticks or green leaves materials to the
nest before copulation, as has been reported for other hawk-
eagles ( et al.
the male might represent a gift to reinforce pair bonding or
stimulates copulation, as reported to other raptors (&
&
Black-and-white Hawk-Eagle copulating on the nest is more
similar to the behavior shown by Black Hawk-Eagles than by
Ornate Hawk-Eagles ( et al.
CONCLUSION
&
is required to
maintain a viable population of Black Hawk-Eagle or any
other raptors including the Ornate Hawk-Eagle that have
small home ranges (&
this requirement to the Atlantic Forest, there is only one patch
of continuous forest able to support viable populations of
these three species of Spizaetus:
(
et al.
. Other forested areas are fragments of
et
al.
a breeding pair of Spizaetus
( et al
et al.
Forest fragments might have a breeding pair of hawk-eagle.
In addition to deforestation, fragment isolation adds
to the threat to large raptors. According to et al.
distance between territories of Spizaetus ( et al.,
km ( et al
and isolation of Atlantic Forest remnants suggest a patchy
distribution for Spizaetus, with single birds or pairs limited
to isolated patches of forest.
The conservation of large raptors such as Spizaetus,
Morphnus and Harpyia in the Atlantic Forest it is not a
simple task. Their conservation requires preservation
not only of the best remaining forest fragments, but also
halting deforestation and disturbance of the remained forest
fragments, establishing connectivity among fragments and
reducing direct threats to raptors (e.g., persecution). We also
need to better understand the ecological requirements of the
species in terms of habitat requirements, diet, and breeding
biology, as well as establish public policies to protect both
species and their habitats, as stated in the Brazilian Action
et
al.
guessing about the conservation status of the species, and
barely able for formulate a conservation plan.
Acknowledgements.
Trigo for help in identifying prey items. I appreciate the improvements in
Ornithologists’ program of editorial assistance. I dedicate this paper to
had helped me in several studies.
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Black-and-white Hawk-Eagle; Ornate Hawk-Eagle; Black Hawk-Eagle).
Tree species or family Tree height (m) Nest height (m) Nest external dimensions
(length x wide x height)(cm)
et al. Metoxylon balsamum Tree crown
Cariniana legalis (Mart.) Kuntze 86
Cavanillesia platanifolia (H.& B.) H.B.K.
et al Joannesia sp.
Zeyheria cf. tuberculosa Burman 86
et al Myrocarpus frondosus Fr. Allem
et al Copaifera langsdori 66
This study Myrtaceae
Araucaria angustifolia (Bertol.) Kuntze
et al
Swietenia macrophyla King, Ceiba pentandra
Bucidas buceras Ficus sp.,
Piscidia piscipula Cedrela odorata
Pouteria amygdalina
Calophyllum brasiliensis
A
A
E
E
& Manilkara zapota
Bucida buceras
Ceiba pentandra
Bucida buceras
&
et al
et al.
et al.
Bucida buceras
Brosimum alicastrum
Rehdera penninervia
B
BB
F
F,
Means 86
cm; depth)F
F
all species
A
B
measure of the center depression on the nest
E
F
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