SANSALONE, Gabriele
 Distribuzione geografica
Continente #
AS - Asia 3.563
NA - Nord America 2.544
EU - Europa 1.013
SA - Sud America 482
OC - Oceania 56
AF - Africa 50
Continente sconosciuto - Info sul continente non disponibili 1
Totale 7.709
Nazione #
US - Stati Uniti d'America 2.470
CN - Cina 1.344
SG - Singapore 932
HK - Hong Kong 452
BR - Brasile 392
IT - Italia 294
KR - Corea 251
VN - Vietnam 224
GB - Regno Unito 183
BD - Bangladesh 128
RU - Federazione Russa 111
SE - Svezia 84
FR - Francia 77
DE - Germania 49
IN - India 46
ID - Indonesia 39
LT - Lituania 35
AR - Argentina 33
FI - Finlandia 31
NZ - Nuova Zelanda 31
CA - Canada 29
NL - Olanda 28
AU - Australia 25
JP - Giappone 25
ES - Italia 22
MX - Messico 22
BE - Belgio 21
IQ - Iraq 18
AT - Austria 17
EC - Ecuador 16
TR - Turchia 16
PK - Pakistan 14
ZA - Sudafrica 14
MA - Marocco 11
CL - Cile 10
CO - Colombia 10
IE - Irlanda 10
UA - Ucraina 9
UZ - Uzbekistan 9
AE - Emirati Arabi Uniti 8
PL - Polonia 8
PY - Paraguay 8
TN - Tunisia 7
JO - Giordania 6
NP - Nepal 6
PH - Filippine 6
RS - Serbia 6
VE - Venezuela 6
CZ - Repubblica Ceca 5
EG - Egitto 5
MY - Malesia 5
PE - Perù 5
HR - Croazia 4
JM - Giamaica 4
KG - Kirghizistan 4
KZ - Kazakistan 4
SI - Slovenia 4
AL - Albania 3
AZ - Azerbaigian 3
BH - Bahrain 3
CR - Costa Rica 3
DO - Repubblica Dominicana 3
IL - Israele 3
SA - Arabia Saudita 3
SV - El Salvador 3
TH - Thailandia 3
TT - Trinidad e Tobago 3
AO - Angola 2
GR - Grecia 2
GT - Guatemala 2
IR - Iran 2
LK - Sri Lanka 2
MD - Moldavia 2
PT - Portogallo 2
QA - Qatar 2
RO - Romania 2
TW - Taiwan 2
BB - Barbados 1
BG - Bulgaria 1
BO - Bolivia 1
BS - Bahamas 1
CG - Congo 1
CH - Svizzera 1
CM - Camerun 1
ET - Etiopia 1
GA - Gabon 1
GM - Gambi 1
IS - Islanda 1
KE - Kenya 1
KH - Cambogia 1
LB - Libano 1
NE - Niger 1
NG - Nigeria 1
NI - Nicaragua 1
OM - Oman 1
PA - Panama 1
SK - Slovacchia (Repubblica Slovacca) 1
SN - Senegal 1
UG - Uganda 1
UY - Uruguay 1
Totale 7.706
Città #
Hefei 913
Santa Clara 814
Singapore 501
Hong Kong 440
San Jose 343
Ashburn 260
Seoul 250
London 133
The Dalles 115
Los Angeles 92
Beijing 67
Ho Chi Minh City 67
Hanoi 62
Kent 55
Modena 51
Lauterbourg 49
Council Bluffs 46
São Paulo 43
Chicago 40
Buffalo 38
Moscow 38
Milan 35
New York 34
Reggio Emilia 33
Columbus 30
Dallas 30
Shanghai 30
Jakarta 29
Boardman 26
Helsinki 21
Rome 21
Amsterdam 19
Tokyo 19
Atlanta 18
Redondo Beach 17
Rio de Janeiro 16
Belo Horizonte 15
Melbourne 15
Salt Lake City 15
Mexico City 13
Da Nang 12
Florence 11
Brussels 10
Dublin 10
Haiphong 10
Lappeenranta 10
Naples 10
Auckland 9
Bologna 9
Elk Grove Village 9
Liège 9
Nuremberg 9
Orem 9
Chennai 8
Guayaquil 8
Hackney 8
Miano 8
Munich 8
Phoenix 8
San Francisco 8
Tashkent 8
Dunedin 7
Kilburn 7
Ninh Bình 7
Stockholm 7
Vienna 7
Amman 6
Barcelona 6
Brasília 6
Campinas 6
Frankfurt am Main 6
Guangzhou 6
Hangzhou 6
North Bergen 6
Philadelphia 6
Santiago 6
Stuttgart 6
Warsaw 6
Albuquerque 5
Bauru 5
Belgrade 5
Birmingham 5
Brooklyn 5
Fairfax 5
Gainesville 5
Johannesburg 5
Montreal 5
Novo Hamburgo 5
Ribeirão Preto 5
Seattle 5
Shenzhen 5
Shijiazhuang 5
Tampa 5
Toronto 5
Wellington 5
Asunción 4
Baghdad 4
Bishkek 4
Bogotá 4
Brisbane 4
Totale 5.256
Nome #
Geometric morphometrics and finite element analyses reveal the Haast's eagle (Harpagornis moorei) to be a mixed predator-scavenger 283
RRmorph—a new R package to map phenotypic evolutionary rates and patterns on 3D meshes 192
Evolution of the vomer and its implications for cranial kinesis in Paraves 189
Evolutionary trends and stasis in carnassial teeth of European Pleistocene wolf Canis lupus (Mammalia, Canidae) 188
Condylura (Mammalia, Talpidae) reloaded: New insights about the fossil representatives of the genus 176
Systematics and macroevolution of extant and fossil scalopine moles (Mammalia, Talpidae) 161
Abdominal contents reveal Cretaceous crocodyliforms ate dinosaurs 154
Marsupial Functional Morphology, Biomechanics, and Feeding Ecology 150
New systematic insights about Plio-Pleistocene moles from Poland 148
Cortical areas associated to higher cognition drove primate brain evolution 146
One among many: The enigmatic case of the Miocene mammal, Kolponomos newportensis 140
UNVEILING THE DIGGING ADAPTATIONS IN PROSCALOPIDAE HUMERUS BY MEANS OF COMPARATIVE 3D FINITE ELEMENT ANALYSIS 138
DIFFERENTIAL RATES OF EVOLUTION WITHIN HIGHLY FOSSORIAL MOLES (TALPINAE) CONSTRAIN TRAJECTORIES AND EVOLUTIONARY ALLOMETRIES OF HUMERAL MORPHOLOGY 135
When moles became diggers: Tegulariscaptor gen. nov., from the early Oligocene of south Germany, and the evolution of talpid fossoriality 130
Examining the effect of feralization on craniomandibular morphology in pigs, Sus scrofa (Artiodactyla: Suidae) 127
Reassessing the earliest Oligocene vertebrate assemblage of Monteviale (Vicenza, Italy) 125
Decoupling Functional and Morphological Convergence, the Study Case of Fossorial Mammalia 124
Macroevolutionary trends of brain mass in Primates 122
Evolution of the sabertooth mandible: A deadly ecomorphological specialization 121
REASSESSING THE (?)EARLY OLIGOCENE VERTEBRATE ASSEMBLAGE OF MONTEVIALE (VICENZA, ITALY) 121
Think Big, Evolutionary Allometry as a Major Factor in Rates, Trajectories and Scaling of Morphological Evolution of the Primate Brain Shape 121
FEEDING BIOMECHANICS INFLUENCES CRANIOFACIAL MORPHOLOGY AMONG EAST AUSTRALIAN PADEMELONS (MACROPODIDAE: THYLOGALE) 121
Basicranium and face: Assessing the impact of morphological integration on primate evolution 119
Digging adaptation in insectivorous subterranean eutherians. The enigma of Mesoscalops montanensis unveiled by geometric morphometrics and finite element analysis 119
UNRAVELING THE MYSTERY OF DIGGING ADAPTATION OF MESOSCALOPS MONTANENSIS BY MEANS OF GEOMETRIC MORPHOMETRICS AND FINITE ELEMENT ANALYSIS 118
Head to head: the case for fighting behaviour in Megaloceros giganteus using finite-element analysis 118
Raptor talon shape and biomechanical performance are controlled by relative prey size but not by allometry 118
Did the Late Pleistocene climatic changes influence evolutionary trends in body size of the red deer? The study case of the Italian Peninsula 118
Small vertebrates from the Late Pleistocene of Avetrana (Apulia, southern Italy) karst filling 116
Relationship between foramen magnum position and locomotion in extant and extinct hominoids 113
Talpa fossilis or Talpa europaea? Using geometric morphometrics and allometric trajectories of humeral moles remains from Hungary to answer a taxonomic debate 113
A method for mapping morphological convergence on three-dimensional digital models: the case of the mammalian sabre-tooth 112
THE ORAL APPARATUS OF MARSUPIALS IS MORE INTEGRATED BUT NOT LESS MORPHOLOGICALLY DIVERSE THAN THAT OF PLACENTAL CARNIVORES 112
Condylura reloaded: a review of fossil star nosed moles 112
How Changes in Functional Demands Associated with Captivity Affect the Skull Shape of a Wild Boar (Sus scrofa) 112
Influence of evolutionary allometry on rates of morphological evolution and disparity in strictly subterranean moles (Talpinae, Talpidae, Eulipotyphla, Mammalia) 110
A new integrated tool to calculate and map bilateral asymmetry on three-dimensional digital models 110
The influence of domestication, insularity and sociality on the tempo and mode of brain size evolution in mammals 110
Trapped in the morphospace: The relationship between morphological integration and functional performance 109
The prodigious alliance: molecular systematics and morphometrics dig out the puzzling origin and diversification of European moles (Soricomorpha: Talpidae) 108
THINK BIG: EVOLUTIONARY ALLOMETRY AS A MAJOR FACTOR IN RATES OF MORPHOLOGICAL EVOLUTION OF THE PRIMATE BRAIN SHAPE 107
EVOLUTIONARY TRENDS AND STASIS IN MOLAR MORPHOLOGY OF RHAGAPODEMUS-RHAGAMYS LINEAGE IN THE PLEISTOCENE OF SARDINIA 107
A NEW CROCODYLIFORM FROM THE WINTON FORMATION (CA 95 MA) OF QUEENSLAND (AUSTRALIA) 107
Human face-off: a new method for mapping evolutionary rates on three-dimensional digital models 107
Homo sapiens and Neanderthals share high cerebral cortex integration into adulthood 107
From Smart Apes to Human Brain Boxes. A Uniquely Derived Brain Shape in Late Hominins Clade 106
Tuning Geometric Morphometrics: an R tool to reduce information loss caused by surface smoothing 106
Skull shape of a widely distributed, endangered marsupial reveals little evidence of local adaptation between fragmented populations 103
Morphological integration and functional modularity in the crocodilian skull 102
Finite element analyses on the skull and talon of Haast's eagle (Harpagornis moorei) 98
Testing convergent and parallel adaptations in talpids humeral mechanical performance by means of geometric morphometrics and finite element analysis 97
Morfometria geometrica dell' omero di specie attuali e fossili del genere Talpa 97
Unexpectedly uneven distribution of functional trade-offs explains cranial morphological diversity in carnivores 97
New Zealand's extinct giant raptor (Hieraaetus moorei) killed like an eagle, ate like a condor 96
Domestication, insularity and sociality. Determinants of brain size evolutionary rate and trends in mammals 95
Morphological integration affects the evolution of midline cranial base, lateral basicranium, and face across primates 94
Variation in the strength of allometry drives rates of evolution in primate brain shape 94
How domestication, feralization and experience-dependent plasticity affect brain size variation in Sus scrofa 92
THE ORAL APPARATUS OF MARSUPIALS IS MORE INTEGRATED BUT NOT LESS MORPHOLOGICALLY DIVERSE THAN THAT OF PLACENTAL CARNIVORES 91
Impact of transition to a subterranean lifestyle on morphological disparity and integration in talpid moles (Mammalia, Talpidae) 90
Reassessing the Eocene-Oligocene Transition vertebrate assemblage of Monteviale (Vicenza, Italy) 89
Palaeoecological significance of the “wolf event” as revealed by skull ecometrics of the canid guilds 86
Evolution of hypsodonty reveals a long-standing ecological separation in the Japanese shrew-moles 86
Feeding Biomechanics Influences Craniofacial Morphology at the Subspecies Scale among Australian Pademelons (Macropodidae: Thylogale) 85
Reassessing the faunal assemblages of the late pleistocene stratified karst filling from avetrana (Apulia, Southern Italy): The BED 8, palaeoenvironment and biochronology 77
Totale 7.775
Categoria #
all - tutte 32.999
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 32.999


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/2024334 0 0 56 18 61 13 20 17 21 35 55 38
2024/20252.912 93 16 14 174 568 436 160 193 296 209 398 355
2025/20264.529 475 489 564 462 299 196 544 158 285 473 349 235
Totale 7.775