LAMBERTINI, CARLA
 Distribuzione geografica
Continente #
AS - Asia 2.526
NA - Nord America 2.443
EU - Europa 2.005
SA - Sud America 330
Continente sconosciuto - Info sul continente non disponibili 273
AF - Africa 84
OC - Oceania 27
Totale 7.688
Nazione #
US - Stati Uniti d'America 2.260
SG - Singapore 865
CN - Cina 686
IT - Italia 643
SE - Svezia 284
RU - Federazione Russa 275
HK - Hong Kong 271
BR - Brasile 256
DE - Germania 168
IN - India 138
FR - Francia 132
BD - Bangladesh 129
CA - Canada 116
VN - Vietnam 115
IE - Irlanda 101
GB - Regno Unito 72
ID - Indonesia 70
NL - Olanda 66
TR - Turchia 57
IQ - Iraq 37
FI - Finlandia 34
JP - Giappone 34
KR - Corea 32
ES - Italia 30
CZ - Repubblica Ceca 27
PL - Polonia 26
AR - Argentina 25
ZA - Sudafrica 25
AU - Australia 24
MX - Messico 23
RO - Romania 23
CI - Costa d'Avorio 22
PK - Pakistan 19
CO - Colombia 18
BE - Belgio 13
AT - Austria 12
EC - Ecuador 12
CH - Svizzera 11
MT - Malta 11
PH - Filippine 10
PT - Portogallo 10
UA - Ucraina 10
NP - Nepal 9
HU - Ungheria 8
EG - Egitto 7
IL - Israele 7
NG - Nigeria 7
CL - Cile 6
CR - Costa Rica 6
DK - Danimarca 6
LT - Lituania 6
MY - Malesia 6
TH - Thailandia 6
UZ - Uzbekistan 6
DZ - Algeria 5
GR - Grecia 5
HN - Honduras 5
NI - Nicaragua 5
PR - Porto Rico 5
SK - Slovacchia (Repubblica Slovacca) 5
VE - Venezuela 5
AE - Emirati Arabi Uniti 4
GT - Guatemala 4
HR - Croazia 4
JO - Giordania 4
LU - Lussemburgo 4
MA - Marocco 4
SA - Arabia Saudita 4
BS - Bahamas 3
BY - Bielorussia 3
DO - Repubblica Dominicana 3
EE - Estonia 3
JM - Giamaica 3
ME - Montenegro 3
PE - Perù 3
TN - Tunisia 3
AZ - Azerbaigian 2
BA - Bosnia-Erzegovina 2
BZ - Belize 2
NO - Norvegia 2
NZ - Nuova Zelanda 2
OM - Oman 2
PA - Panama 2
PY - Paraguay 2
SN - Senegal 2
SV - El Salvador 2
SY - Repubblica araba siriana 2
TT - Trinidad e Tobago 2
TW - Taiwan 2
AO - Angola 1
BH - Bahrain 1
BO - Bolivia 1
BW - Botswana 1
CD - Congo 1
CM - Camerun 1
CY - Cipro 1
ET - Etiopia 1
EU - Europa 1
GH - Ghana 1
GP - Guadalupe 1
Totale 7.396
Città #
Singapore 439
Ashburn 293
Hong Kong 242
San Jose 215
Milan 200
Chandler 171
Council Bluffs 171
Santa Clara 114
Beijing 99
Dublin 99
Princeton 98
Dallas 94
Frankfurt am Main 84
Los Angeles 69
Lauterbourg 65
Jakarta 58
Hefei 52
Buffalo 51
Rome 47
Bengaluru 45
Cambridge 45
Ho Chi Minh City 41
Bologna 40
Guangzhou 40
Istanbul 37
Boardman 34
New York 32
Roxbury 32
Medford 31
Berlin 28
Hanoi 28
Moscow 27
São Paulo 26
Cangzhou 24
Abidjan 22
Montreal 22
Helsinki 21
Naples 21
Turin 21
Nuremberg 20
Chicago 19
Kingston 19
Shanghai 18
Tokyo 18
Atlanta 17
Toronto 17
Fairfield 15
Rio de Janeiro 14
Tianjin 13
Baghdad 12
Baton Rouge 12
Shenzhen 11
Florence 10
Lappeenranta 10
Seattle 10
Seoul 10
Basra 9
Belo Horizonte 9
Granada 9
Warsaw 9
Denver 8
Prague 8
San Diego 8
Stockholm 8
Sydney 8
Bucharest 7
Columbus 7
Johannesburg 7
Kathmandu 7
Kent 7
Lagos 7
Manaus 7
Philadelphia 7
Qingdao 7
Thetford 7
Valencia 7
Vienna 7
Wakefield 7
Washington 7
Amsterdam 6
Boston 6
Brno 6
Brussels 6
Cape Town 6
Cesena 6
Chennai 6
Da Nang 6
Des Moines 6
Duisburg 6
Durban 6
Edinburgh 6
Fragagnano 6
Fuzhou 6
Hyderabad 6
Imsida 6
London 6
Manila 6
Melbourne 6
Mexico City 6
Modena 6
Totale 3.823
Nome #
Physiology of a plant invasion : Biomass production, growth and tissue chemistry of invasive and native Phragmites australis populations 523
Ecosistemi da progettare : Esercizi progettuali per la conservazione della biodiversità, il ripristino funzionale degli ecosistemi e l’accessibilità alle risorse naturali 334
La caratterizzazione genetica: La storia della domesticazione del pomodoro registrata nel genoma delle sue varietà 259
Physiological adaptation to water salinity in six wild halophytes suitable for mediterranean agriculture 214
Climate and genome size shape the intraspecific variation in ecological adaptive strategies of a cosmopolitan grass species 168
Genetic diversity of common reed in the southern Baltic Sea region – Is there an influence of disturbance? 166
The c4 atriplex halimus vs. The c3 atriplex hortensis: Similarities and differences in the salinity stress response 145
Nutrient sequestration and biomass production by Phragmites australis and Typha latifolia in European rewetted peatlands 138
Rivisiting Phragmites australis variation in the Danube Delta with DNA molecular techniques 134
Salt tolerance and Na allocation in sorghum bicolor under variable soil and water salinity 130
Preadaptation and post-introduction evolution facilitate the invasion of Phragmites australis in North America 128
Complex responses to climate warming of arctic‐alpine plant populations from different geographic provenance 127
Extensive hybridization in Ranunculus section Batrachium (Ranunculaceae) in rivers of two postglacial landscapes of East Europe 124
Living in two worlds : Evolutionary mechanisms act differently in the native and introduced ranges of an invasive plant 124
Small genome separates native and invasive populations in an ecologically important cosmopolitan grass 124
Invasion trends of aquatic Ludwigia hexapetala and L. peploides subsp. montevidensis (Onagraceae) in Italy based on herbarium records and global datasets 120
Recovery from Salinity and Drought Stress in the Perennial Sarcocornia fruticosa vs. the Annual Salicornia europaea and S. veneta 120
Cosmopolitan species as models for ecophysiological responses to global change: The common reed phragmites australis 116
La dimensione storica delle idrofite invasive: un database condiviso, potenzialità e studi fatti 115
Competition among native and invasive Phragmites australis populations : An experimental test of the effects of invasion status, genome size, and ploidy level 113
Exploring the borders of European Phragmites within a cosmopolitan genus 111
Intraspecific variation in Phragmites australis : Clinal adaption of functional traits and phenotypic plasticity vary with latitude of origin 110
Phylogenetic diversity shapes salt tolerance in Phragmites australis estuarine populations in East China 108
Interactive effects of elevated temperature and CO2 on two phylogeographically distinct clones of common reed (Phragmites australis) 108
The invasion history of Elodea canadensis and E. nuttallii (Hydrocharitaceae) in Italy from herbarium accessions, field records and historical literature 105
Contributo alla conoscenza della flora vascolare del Parco Regionale dell’Abbazia di Monteveglio (Emilia-Romagna, provincia di Bologna) 105
New highlights on Old World giant Phragmites (Poaceae) using leaf and floral bract microscopic characters 105
Expansive reed populations-alien invasion or disturbed wetlands? 104
Assessing nutrient responses and biomass quality for selection of appropriate paludiculture crops 102
Genetic diversity patterns in Phragmites australis populations in straightened and in natural river sites in Lithuania 101
Invasion strategies in clonal aquatic plants: Are phenotypic differences caused by phenotypic plasticity or local adaptation? 98
Genetic diversity patterns in Phragmites australis at the population, regional and continental scales 97
Assessment of Anthropogenic Impacts on the Genetic Diversity of Phragmites australis in Small-River Habitats 95
Evidence does not support the targeting of cryptic invaders at the subspecies level using classical biological control : the example of Phragmites 95
Some like it hot: small genomes may be more prevalent under climate extremes 94
Caratterizzazione morfologica, genetica ed ecologica di popolamenti di Phragmites australis (Cav.) Trin ex Steudel in aree umide della pianura bolognese 94
Gas exchange and growth responses to nutrient enrichment in invasive Glyceria maxima and native New Zealand Carex species 91
Tall-statured grasses: a useful functional group for invasion science 91
Cryptic lineages and potential introgression in a mixed-ploidy species (Phragmites australis) across temperate China 90
Phenotypic traits of phragmites australis clones are not related to ploidy level and distribution range 89
Hybridization of common reed in North America? The answer is blowing in the wind 88
Global networks for invasion science: benefits, challenges and guidelines 85
Genetic diversity patterns of rice (Oryza sativa L.) landraces after migration by Tai Lue and Akha between China and Thailand 84
Photosynthesis of co-existing Phragmites haplotypes in their non-native range: are characteristics determined by adaptations derived from their native origin? 84
Minimum Fe requirement and toxic tissue concentration of Fe in Phragmites australis : A tool for alleviating Fe-deficiency in constructed wetlands 83
Phylogeography reveals a potential cryptic invasion in the Southern Hemisphere of Ceratophyllum demersum, New Zealand's worst invasive macrophyte 83
Invasion of old world phragmites australis in the new world : Precipitation and temperature patterns combined with human influences redesign the invasive niche 82
Do ploidy level and nuclear genome size and latitude of origin modify the expression of Phragmites australis traits and interactions with herbivores? 82
Clone-specific differences in Phragmites australis : Effects of ploidy level and geographic origin 81
Why are tall-statured energy grasses of polyploid species complexes potentially invasive? A review of their genetic variation patterns and evolutionary plasticity 79
Genetic diversity in three invasive clonal aquatic species in New Zealand 79
Growth and morphology in relation to temperature and light availability during the establishment of three invasive aquatic plant species 79
Phragmites australis: How do genotypes of different phylogeographic origins differ from their invasive genotypes in growth, nitrogen allocation and gas exchange? 76
Genetic relationships in Phragmites Adanson 74
Expression of major photosynthetic and salt-resistance genes in invasive reed lineages grown under elevated CO2 and temperature 72
Areas with Natural Constraints to Agriculture: Possibilities and Limitations for The Cultivation of Switchgrass (Panicum Virgatum L.) and Giant Reed (Arundo Donax L.) in Europe 72
The value of repetitive sequences in chloroplast DNA for phylogeographic inference : A comment on Vachon & Freeland 2011 71
Genetic structure of the submersed Ranunculus baudotii (sect. Batrachium) population in a lowland stream in Denmark 70
Heteroplasmy due to chloroplast paternal leakage: another insight into Phragmites haplotypic diversity in North America 69
Tracing the origin of Gulf Coast Phragmites (Poaceae): A story of long-distance dispersal and hybridization 67
The potential for biological control on cryptic plant invasions 66
Ammonium and nitrate are both suitable inorganic nitrogen forms for the highly productive wetland grass Arundo donax, a candidate species for wetland paludiculture 66
Herbarium specimens as a source of DNA for AFLP fingerprinting of Phragmites (Poaceae): Possibilities and limitations 65
Increased invasive potential of non-native Phragmites australis: Elevated CO2 and temperature alleviate salinity effects on photosynthesis and growth 65
A phylogeographic study of the cosmopolitan genus Phragmites (Poaceae) based on AFLPs 61
Phenotypic traits of the Mediterranean Phragmites australis M1 lineage : differences between the native and introduced ranges 60
Salinity effects on germination, seedlings and full-grown plants of upland and lowland switchgrass cultivars 56
Genomic analysis of botanical collections: opportunities and challenges 54
Intraspecific adaptation to bioclimatic origins: Intricate interplay of above‐ and below‐ground traits in a cosmopolitan grass species 51
Mowing regime has different effects on reed stands in relation to habitat 51
IAPT chromosome data 45 49
Utilizzo di informazioni vegetazionali per la datazione di eventi di debris flow 46
Environmental Filtering of Leaf Traits, Spectral and Genetic Variation in Phragmites australis: Responses and Spatial Patterns 23
Totale 7.688
Categoria #
all - tutte 28.704
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 28.704


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022573 0 0 0 0 0 67 14 88 58 81 33 232
2022/2023964 157 97 72 31 71 183 42 62 96 9 109 35
2023/2024573 28 43 21 40 157 12 40 27 14 25 77 89
2024/20251.750 69 182 44 126 204 156 62 159 112 162 137 337
2025/20263.349 274 218 339 304 258 188 387 207 360 264 274 276
2026/2027479 285 194 0 0 0 0 0 0 0 0 0 0
Totale 7.688