LAMBERTINI, CARLA
 Distribuzione geografica
Continente #
AS - Asia 2.472
NA - Nord America 2.008
EU - Europa 1.910
SA - Sud America 317
AF - Africa 79
OC - Oceania 27
Continente sconosciuto - Info sul continente non disponibili 1
Totale 6.814
Nazione #
US - Stati Uniti d'America 1.901
SG - Singapore 854
CN - Cina 683
IT - Italia 563
SE - Svezia 279
RU - Federazione Russa 275
HK - Hong Kong 269
BR - Brasile 250
DE - Germania 168
IN - India 136
FR - Francia 131
BD - Bangladesh 112
VN - Vietnam 103
IE - Irlanda 100
GB - Regno Unito 68
ID - Indonesia 68
NL - Olanda 66
CA - Canada 62
TR - Turchia 56
IQ - Iraq 37
FI - Finlandia 34
JP - Giappone 33
KR - Corea 32
ES - Italia 29
CZ - Repubblica Ceca 27
PL - Polonia 26
AR - Argentina 24
AU - Australia 24
RO - Romania 23
CI - Costa d'Avorio 22
MX - Messico 20
ZA - Sudafrica 20
PK - Pakistan 19
CO - Colombia 15
BE - Belgio 13
AT - Austria 12
EC - Ecuador 12
CH - Svizzera 11
MT - Malta 10
PH - Filippine 10
PT - Portogallo 10
UA - Ucraina 10
HU - Ungheria 8
NP - Nepal 8
EG - Egitto 7
IL - Israele 7
NG - Nigeria 7
DK - Danimarca 6
MY - Malesia 6
UZ - Uzbekistan 6
CR - Costa Rica 5
DZ - Algeria 5
LT - Lituania 5
SK - Slovacchia (Repubblica Slovacca) 5
TH - Thailandia 5
AE - Emirati Arabi Uniti 4
CL - Cile 4
GR - Grecia 4
HR - Croazia 4
JO - Giordania 4
LU - Lussemburgo 4
MA - Marocco 4
NI - Nicaragua 4
VE - Venezuela 4
BY - Bielorussia 3
DO - Repubblica Dominicana 3
EE - Estonia 3
ME - Montenegro 3
PE - Perù 3
SA - Arabia Saudita 3
TN - Tunisia 3
AZ - Azerbaigian 2
BA - Bosnia-Erzegovina 2
GT - Guatemala 2
HN - Honduras 2
NO - Norvegia 2
NZ - Nuova Zelanda 2
OM - Oman 2
PA - Panama 2
PR - Porto Rico 2
PY - Paraguay 2
SN - Senegal 2
SY - Repubblica araba siriana 2
TT - Trinidad e Tobago 2
TW - Taiwan 2
AO - Angola 1
BH - Bahrain 1
BO - Bolivia 1
BS - Bahamas 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
GY - Guiana 1
IM - Isola di Man 1
IR - Iran 1
Totale 6.797
Città #
Singapore 430
Ashburn 242
Hong Kong 240
San Jose 197
Milan 182
Chandler 171
Council Bluffs 119
Beijing 99
Dublin 99
Princeton 98
Dallas 91
Frankfurt am Main 84
Los Angeles 67
Lauterbourg 65
Jakarta 58
Santa Clara 57
Hefei 52
Buffalo 47
Bengaluru 45
Cambridge 44
Guangzhou 40
Rome 39
Istanbul 36
Boardman 34
Ho Chi Minh City 34
New York 32
Roxbury 32
Medford 30
Bologna 29
Berlin 28
Hanoi 27
Moscow 27
Cangzhou 24
São Paulo 24
Abidjan 22
Helsinki 21
Nuremberg 20
Turin 19
Naples 18
Shanghai 18
Tokyo 18
Kingston 17
Atlanta 16
Chicago 14
Fairfield 14
Montreal 14
Rio de Janeiro 14
Tianjin 13
Baghdad 12
Baton Rouge 12
Toronto 12
Shenzhen 11
Florence 10
Lappeenranta 10
Seoul 10
Basra 9
Belo Horizonte 9
Granada 9
Prague 8
San Diego 8
Seattle 8
Sydney 8
Warsaw 8
Bucharest 7
Kent 7
Lagos 7
Manaus 7
Qingdao 7
Thetford 7
Valencia 7
Vienna 7
Wakefield 7
Amsterdam 6
Brno 6
Brussels 6
Cesena 6
Chennai 6
Columbus 6
Da Nang 6
Des Moines 6
Duisburg 6
Durban 6
Fragagnano 6
Fuzhou 6
Hyderabad 6
Imsida 6
Kathmandu 6
Manila 6
Mexico City 6
Modena 6
Paris 6
Quito 6
Stockholm 6
Tashkent 6
Washington 6
Wuhan 6
Zhengzhou 6
Zurich 6
Bogotá 5
Boston 5
Totale 3.534
Nome #
Physiology of a plant invasion : Biomass production, growth and tissue chemistry of invasive and native Phragmites australis populations 501
Ecosistemi da progettare : Esercizi progettuali per la conservazione della biodiversità, il ripristino funzionale degli ecosistemi e l’accessibilità alle risorse naturali 322
La caratterizzazione genetica: La storia della domesticazione del pomodoro registrata nel genoma delle sue varietà 253
Physiological adaptation to water salinity in six wild halophytes suitable for mediterranean agriculture 208
Genetic diversity of common reed in the southern Baltic Sea region – Is there an influence of disturbance? 160
Climate and genome size shape the intraspecific variation in ecological adaptive strategies of a cosmopolitan grass species 159
Nutrient sequestration and biomass production by Phragmites australis and Typha latifolia in European rewetted peatlands 132
Rivisiting Phragmites australis variation in the Danube Delta with DNA molecular techniques 129
The c4 atriplex halimus vs. The c3 atriplex hortensis: Similarities and differences in the salinity stress response 125
Salt tolerance and Na allocation in sorghum bicolor under variable soil and water salinity 123
Small genome separates native and invasive populations in an ecologically important cosmopolitan grass 119
Extensive hybridization in Ranunculus section Batrachium (Ranunculaceae) in rivers of two postglacial landscapes of East Europe 118
Living in two worlds : Evolutionary mechanisms act differently in the native and introduced ranges of an invasive plant 115
Complex responses to climate warming of arctic‐alpine plant populations from different geographic provenance 114
Recovery from Salinity and Drought Stress in the Perennial Sarcocornia fruticosa vs. the Annual Salicornia europaea and S. veneta 114
La dimensione storica delle idrofite invasive: un database condiviso, potenzialità e studi fatti 112
Competition among native and invasive Phragmites australis populations : An experimental test of the effects of invasion status, genome size, and ploidy level 107
Exploring the borders of European Phragmites within a cosmopolitan genus 106
Interactive effects of elevated temperature and CO2 on two phylogeographically distinct clones of common reed (Phragmites australis) 105
Invasion trends of aquatic Ludwigia hexapetala and L. peploides subsp. montevidensis (Onagraceae) in Italy based on herbarium records and global datasets 104
Intraspecific variation in Phragmites australis : Clinal adaption of functional traits and phenotypic plasticity vary with latitude of origin 104
Cosmopolitan species as models for ecophysiological responses to global change: The common reed phragmites australis 101
Phylogenetic diversity shapes salt tolerance in Phragmites australis estuarine populations in East China 99
The invasion history of Elodea canadensis and E. nuttallii (Hydrocharitaceae) in Italy from herbarium accessions, field records and historical literature 97
Contributo alla conoscenza della flora vascolare del Parco Regionale dell’Abbazia di Monteveglio (Emilia-Romagna, provincia di Bologna) 96
Expansive reed populations-alien invasion or disturbed wetlands? 96
New highlights on Old World giant Phragmites (Poaceae) using leaf and floral bract microscopic characters 95
Genetic diversity patterns in Phragmites australis populations in straightened and in natural river sites in Lithuania 95
Assessing nutrient responses and biomass quality for selection of appropriate paludiculture crops 94
Caratterizzazione morfologica, genetica ed ecologica di popolamenti di Phragmites australis (Cav.) Trin ex Steudel in aree umide della pianura bolognese 90
Evidence does not support the targeting of cryptic invaders at the subspecies level using classical biological control : the example of Phragmites 89
Invasion strategies in clonal aquatic plants: Are phenotypic differences caused by phenotypic plasticity or local adaptation? 88
Genetic diversity patterns in Phragmites australis at the population, regional and continental scales 88
Assessment of Anthropogenic Impacts on the Genetic Diversity of Phragmites australis in Small-River Habitats 86
Gas exchange and growth responses to nutrient enrichment in invasive Glyceria maxima and native New Zealand Carex species 86
Some like it hot: small genomes may be more prevalent under climate extremes 83
Phenotypic traits of phragmites australis clones are not related to ploidy level and distribution range 83
Cryptic lineages and potential introgression in a mixed-ploidy species (Phragmites australis) across temperate China 83
Tall-statured grasses: a useful functional group for invasion science 83
Hybridization of common reed in North America? The answer is blowing in the wind 80
Genetic diversity patterns of rice (Oryza sativa L.) landraces after migration by Tai Lue and Akha between China and Thailand 80
Clone-specific differences in Phragmites australis : Effects of ploidy level and geographic origin 77
Preadaptation and post-introduction evolution facilitate the invasion of Phragmites australis in North America 77
Invasion of old world phragmites australis in the new world : Precipitation and temperature patterns combined with human influences redesign the invasive niche 76
Do ploidy level and nuclear genome size and latitude of origin modify the expression of Phragmites australis traits and interactions with herbivores? 76
Minimum Fe requirement and toxic tissue concentration of Fe in Phragmites australis : A tool for alleviating Fe-deficiency in constructed wetlands 75
Phylogeography reveals a potential cryptic invasion in the Southern Hemisphere of Ceratophyllum demersum, New Zealand's worst invasive macrophyte 75
Why are tall-statured energy grasses of polyploid species complexes potentially invasive? A review of their genetic variation patterns and evolutionary plasticity 74
Genetic diversity in three invasive clonal aquatic species in New Zealand 74
Growth and morphology in relation to temperature and light availability during the establishment of three invasive aquatic plant species 73
Global networks for invasion science: benefits, challenges and guidelines 72
Phragmites australis: How do genotypes of different phylogeographic origins differ from their invasive genotypes in growth, nitrogen allocation and gas exchange? 70
Photosynthesis of co-existing Phragmites haplotypes in their non-native range: are characteristics determined by adaptations derived from their native origin? 70
Expression of major photosynthetic and salt-resistance genes in invasive reed lineages grown under elevated CO2 and temperature 68
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 68
The value of repetitive sequences in chloroplast DNA for phylogeographic inference : A comment on Vachon & Freeland 2011 67
Genetic structure of the submersed Ranunculus baudotii (sect. Batrachium) population in a lowland stream in Denmark 67
Genetic relationships in Phragmites Adanson 67
The potential for biological control on cryptic plant invasions 65
Heteroplasmy due to chloroplast paternal leakage: another insight into Phragmites haplotypic diversity in North America 64
Ammonium and nitrate are both suitable inorganic nitrogen forms for the highly productive wetland grass Arundo donax, a candidate species for wetland paludiculture 64
Herbarium specimens as a source of DNA for AFLP fingerprinting of Phragmites (Poaceae): Possibilities and limitations 60
A phylogeographic study of the cosmopolitan genus Phragmites (Poaceae) based on AFLPs 57
Increased invasive potential of non-native Phragmites australis: Elevated CO2 and temperature alleviate salinity effects on photosynthesis and growth 57
Phenotypic traits of the Mediterranean Phragmites australis M1 lineage : differences between the native and introduced ranges 56
Tracing the origin of Gulf Coast Phragmites (Poaceae): A story of long-distance dispersal and hybridization 56
Salinity effects on germination, seedlings and full-grown plants of upland and lowland switchgrass cultivars 51
Mowing regime has different effects on reed stands in relation to habitat 45
IAPT chromosome data 45 42
Utilizzo di informazioni vegetazionali per la datazione di eventi di debris flow 42
Intraspecific adaptation to bioclimatic origins: Intricate interplay of above‐ and below‐ground traits in a cosmopolitan grass species 41
Genomic analysis of botanical collections: opportunities and challenges 22
Environmental Filtering of Leaf Traits, Spectral and Genetic Variation in Phragmites australis: Responses and Spatial Patterns 15
Totale 7.085
Categoria #
all - tutte 26.637
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 26.637


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
2025/20263.225 274 218 339 304 258 188 387 207 360 264 274 152
Totale 7.085