Alvarezsauroidea (from the Argentine historian, writer and physician Gregorio Álvarez) is a group of small . The group was first formally proposed by Choiniere and colleagues in 2010, to contain the family Alvarezsauridae and non-alvarezsaurid alvarezsauroids, such as Haplocheirus,
Description
Fossils of alvarezsauroids were described since the 1990s, with many alvarezsauroids being found in Asia and other members also known from North America, South America and possibly Europe.
The body length of the derived members of Alvarezsauroidea range between , but some members may have been larger.
, for example, was among the largest member of the Alvarezsauroidea. Because of the size of
Haplocheirus and its basal phylogenetic position, a pattern of miniaturization for the Alvarezsauroidea is suggested. Miniaturizations are very rare in dinosaurs, but convergently evolved in
Paraves.
Hand morphology and dietary shift
The differences in the morphology of the hand of basic Alvarezsauroidea and the derived members are characterized by digit reduction. In the evolution of
theropod dinosaurs, modifications of the hand were typical. The digital reduction, for instance, is a striking evolutionary phenomenon that is clearly exemplified in
theropod dinosaurs.
The enlargement of the manual digit II in alvarezsauroids and the concurrent reduction of the lateral digits, created one functional medial digit and two very small, and presumably vestigial, lateral digits. These morphological changes have been interpreted as adaptations for digging.
One possible interpretation suggests that alvarezsauroids fed on insects, using their hands to search beyond the tree bark. This interpretation is consistent with their long, elongate snout and small teeth. Another interpretation suggests that they used their claws to break into ant and termite colonies, though the arm anatomy of an alvarezsaurid would require the animal to lie on its chest against a termite nest.
In contrast to the digit reduction of the hand of derived alvarezsauroid to a claw used for digging, Haplocheirus was still able to grab things. However, Haplocheirus already shows the enlargement of the second manual digit. Important data on the evolution of the alvarezsauroid hand is also provided by the basal parvicursorine Linhenykus.
In 2025, Wang and colleagues identified hard tissue debris and possible soft tissues in the intestinal contents of the Bannykus holotype (represented by the yellowish conglomerate) based on scanning electron microscopy, which was consistent with further Raman spectroscopy analysis that detected "characteristic peaks indicative of bone-derived material", suggesting that Bannykus probably had a carnivorous diet. The authors concluded that both the forelimb reduction and the dietary shift from carnivory to probably insectivory among alvarezsaurians occurred later in their evolution.
Classification
The phylogenetic placement of Alvarezsauroidea is still unclear. At first, they were interpreted as a sister group of
Avialae (birds) or nested within the group
Avialae and considered to be flightless birds,
because they share many morphological characteristics with them, such as a loosely sutured skull, a keeled
sternum, fused wrist elements, and a posteriorly directed pubis.
But this association was reevaluated after the discovery of the primitive forms like
Haplocheirus,
Patagonykus and
Alvarezsaurus, which do not show all bird-like features as the first discovered species
Mononykus and
Shuvuuia.
[Holtz, R.T. (2007). "Ornithomimosaurs and Alvarezsaurs". Dinosaurs: The Most Complete, Up-to-Date Encyclopedia for Dinosaur Lovers of All Ages. .] This shows that bird-like characteristics were developed multiple times within the
Maniraptora. Furthermore, the Alvarezsauroidea had simplified homogenous dentition, convergent with that of some extant insectivorous
mammals. More recently, they have been placed within the
Coelurosauria basal to the
Maniraptora or as a sister taxon of Ornithomimosauria within the Ornithomimiformes.
The cladogram below is the latest and most comprehensive analysis of alvarezsaurian evolution, following Meso et al. (2024).
Geographical distribution
At first, alvarezsauroids were thought to have been originated in
South America. However, the discovery of
Haplocheirus, and its basal phylogenetic position, as well as its early temporal position, suggests they derived in
Asia rather than
South America. Xu
et al. (2011) suggested that at least three dispersal events of alvarezsauroids took place; one from Asia to
Gondwana, one from
Gondwana to Asia, and one from Asia to
North America. This hypothesis is consistent with faunal interchanges.
On the other hand, some
theropod groups are inconsistent with this
hypothesis. Xu
et al. (2013) used event−based tree−fitting to perform a quantitative analysis of alvarezsauroid biogeography.
Their results showed an absence of statistical support for previous biogeographic hypotheses that favour pure vicariance or pure dispersal scenarios as explanations for the distributions of alvarezsauroids across South America, North America and Asia. They instead found that statistically significant biogeographic reconstructions suggest a dominant role for sympatric events ("within area" ones), combined with a mix of vicariance, dispersal and regional extinction. The Asian origin of alvarezsauroids is also bolstered by the discovery of alvarezsaurid specimens from the Turonian-age Bissekty Formation (some of which were named
Dzharaonyx in 2022
) of Uzbekistan and
Bannykus,
Tugulusaurus, and
Xiyunykus from the Early Cretaceous of China.
Sources
-
Turner, A.H., Nesbit, S.J., Norell, M.A. (2009): "A Large Alvarezsaurid from the Late Cretaceous of Mongolia". American Museum Novitates. Number: 3648.
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Choiniere, J. (2010). Guest Post: Haplocheirus, the Skillful One Dave Hone's Archosaur Musings, April 23, 2011
