CRIS Current Research Information System

LAMBERTINI, CARLA
 Distribuzione geografica
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Continente #
NA - Nord America 3.260
AS - Asia 2.239
EU - Europa 1.671
SA - Sud America 153
AF - Africa 129
OC - Oceania 4
Totale 7.456
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Nazione #
US - Stati Uniti d'America 3.234
SG - Singapore 735
GB - Regno Unito 530
CN - Cina 513
VN - Vietnam 404
IT - Italia 259
DE - Germania 230
HK - Hong Kong 192
IN - India 139
FR - Francia 134
RU - Federazione Russa 115
BR - Brasile 113
SE - Svezia 93
JO - Giordania 57
IE - Irlanda 53
ZA - Sudafrica 52
CH - Svizzera 49
BD - Bangladesh 48
UA - Ucraina 45
EE - Estonia 43
FI - Finlandia 28
KR - Corea 28
CI - Costa d'Avorio 26
TG - Togo 26
NL - Olanda 25
ID - Indonesia 18
AR - Argentina 17
BG - Bulgaria 15
JP - Giappone 15
CA - Canada 14
IQ - Iraq 14
TH - Thailandia 13
BE - Belgio 12
PK - Pakistan 11
BW - Botswana 9
TW - Taiwan 9
EC - Ecuador 8
PH - Filippine 8
PL - Polonia 8
AT - Austria 7
TR - Turchia 7
CL - Cile 6
GR - Grecia 6
MX - Messico 6
ES - Italia 5
SA - Arabia Saudita 5
AE - Emirati Arabi Uniti 4
MY - Malesia 4
UZ - Uzbekistan 4
EG - Egitto 3
KZ - Kazakistan 3
LT - Lituania 3
MA - Marocco 3
NO - Norvegia 3
NP - Nepal 3
PY - Paraguay 3
SC - Seychelles 3
VE - Venezuela 3
AL - Albania 2
AU - Australia 2
CO - Colombia 2
CR - Costa Rica 2
LB - Libano 2
TN - Tunisia 2
AO - Angola 1
AZ - Azerbaigian 1
BY - Bielorussia 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
GP - Guadalupe 1
HN - Honduras 1
HR - Croazia 1
IL - Israele 1
JM - Giamaica 1
KE - Kenya 1
LS - Lesotho 1
NZ - Nuova Zelanda 1
PG - Papua Nuova Guinea 1
PT - Portogallo 1
RS - Serbia 1
SN - Senegal 1
SY - Repubblica araba siriana 1
UY - Uruguay 1
Totale 7.456
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Città #
Southend 476
Singapore 464
Fairfield 376
Ashburn 367
Santa Clara 251
Houston 200
Seattle 195
San Jose 191
Hong Kong 189
Woodbridge 168
Wilmington 162
Cambridge 158
Princeton 112
Ann Arbor 107
Chandler 91
Hanoi 82
Ho Chi Minh City 78
Boardman 71
Bologna 69
Lauterbourg 61
Amman 57
Beijing 54
Council Bluffs 52
Dublin 52
Nanjing 49
Bern 46
Westminster 46
Berlin 45
Jinan 40
Dong Ket 37
Padova 36
Buffalo 28
Los Angeles 27
Abidjan 26
Lomé 26
Dallas 25
San Diego 25
Changsha 24
Seoul 23
Shenyang 22
Frankfurt am Main 21
Redondo Beach 20
Saint Petersburg 20
Redmond 19
Hefei 17
Guangzhou 16
Da Nang 15
Lappeenranta 15
Milan 15
New York 15
Falls Church 14
Hebei 14
Nanchang 14
Sofia 14
Jakarta 13
Tianjin 13
Brussels 12
Haikou 12
Helsinki 11
Rome 11
São Paulo 11
Dearborn 10
Johannesburg 10
Phoenix 10
Tokyo 10
Turin 10
Des Moines 9
Gaborone 9
Hangzhou 9
Jiaxing 9
London 9
Medford 9
Haiphong 8
Hải Dương 8
Thái Nguyên 8
Atlanta 7
Norwalk 7
The Dalles 7
Thetford 7
Biên Hòa 6
Chicago 6
Jacksonville 6
Naples 6
Ningbo 6
Ninh Bình 6
Redwood City 6
Toronto 6
Bühl 5
Denver 5
Düsseldorf 5
Hyderabad 5
Lanzhou 5
Munich 5
Nuremberg 5
Shanghai 5
Warsaw 5
Wuhan 5
Zhengzhou 5
Baghdad 4
Cesena 4
Totale 5.187
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Nome #
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 218
Physiological Adaptation to Water Salinity in Six Wild Halophytes Suitable for Mediterranean Agriculture 208
Salinity effects on germination, seedlings and full-grown plants of upland and lowland switchgrass cultivars 192
Minimum Fe requirement and toxic tissue concentration of Fe in Phragmites australis : A tool for alleviating Fe-deficiency in constructed wetlands 189
Genetic relationships in Phragmites Adanson 182
Ecosistemi da progettare. Esercizi progettuali per la conservazione della biodiversità, il ripristino funzionale degli ecosistemi e l’accessibilità alle risorse naturali. 179
Expression of major photosynthetic and salt-resistance genes in invasive reed lineages grown under elevated CO2 and temperature 170
Expansive reed populations – alien invasion or disturbed wetlands? 169
Salt Tolerance and Na Allocation in Sorghum bicolor under Variable Soil and Water Salinity 160
Gas exchange and growth responses to nutrient enrichment in invasive Glyceria maxima and native New Zealand Carex species 159
Global networks for invasion science: benefits, challenges and guidelines 159
Assessing nutrient responses and biomass quality for selection of appropriate paludiculture crops 159
Genetic structure of the submersed Ranunculus baudotii (sect. Batrachium) population in a lowland stream in Denmark 158
Living in two worlds: Evolutionary mechanisms act differently in the native and introduced ranges of an invasive plant 158
Competition among native and invasive Phragmites australis populations: An experimental test of the effects of invasion status, genome size, and ploidy level 156
The c4 atriplex halimus vs. The c3 atriplex hortensis: Similarities and differences in the salinity stress response 151
Genetic diversity in three invasive clonal aquatic species in New Zealand 149
Genetic diversity patterns of rice (Oryza sativa L.) landraces after migration by Tai Lue and Akha between China and Thailand 146
Genetic diversity patterns in Phragmites australis at the population, regional and continental scales 145
Interactive effects of elevated temperature and CO2 on two phylogeographically distinct clones of common reed (Phragmites australis) 145
Do ploidy level and nuclear genome size and latitude of origin modify the expression of Phragmites australis traits and interactions with herbivores? 141
A phylogeographic study of the cosmopolitan genus Phragmites (Poaceae) based on AFLPs 140
Photosynthesis of co-existing Phragmites haplotypes in their non-native range: Are characteristics determined by adaptations derived from their native origin? 140
Tracing the origin of Gulf Coast Phragmites (Poaceae): A story of long-distance dispersal and hybridization 137
Growth and morphology in relation to temperature and light availability during the establishment of three invasive aquatic plant species 137
Ammonium and nitrate are both suitable inorganic nitrogen forms for the highly productive wetland grass Arundo donax, a candidate species for wetland paludiculture 137
Caratterizzazione morfologica, genetica ed ecologica di popolamenti di Phragmites australis (Cav.) Trin ex Steudel in aree umide della pianura bolognese. 136
Phenotypic traits of phragmites australis clones are not related to ploidy level and distribution range 136
Hybridization of common reed in North America? The answer is blowing in the wind 135
Mowing regime has different effects on reed stands in relation to habitat 135
Recovery from Salinity and Drought Stress in the Perennial Sarcocornia fruticosa vs. the Annual Salicornia europaea and S. veneta 135
Tall-statured grasses: a useful functional group for invasion science 130
Exploring the borders of European Phragmites within a cosmopolitan genus 130
Increased invasive potential of non-native Phragmites australis: Elevated CO2 and temperature alleviate salinity effects on photosynthesis and growth 125
Invasion strategies in clonal aquatic plants: Are phenotypic differences caused by phenotypic plasticity or local adaptation? 124
Utilizzo di informazioni vegetazionali per la datazione di eventi di debris flow 122
Invasion of old world phragmites australis in the new world: Precipitation and temperature patterns combined with human influences redesign the invasive niche 120
Phenotypic traits of the Mediterranean Phragmites australis M1 lineage: differences between the native and introduced ranges 119
Herbarium specimens as a source of DNA for AFLP fingerprinting of Phragmites (Poaceae): Possibilities and limitations 118
Heteroplasmy due to chloroplast paternal leakage: another insight into Phragmites haplotypic diversity in North America 116
Phragmites australis: How do genotypes of different phylogeographic origins differ from their invasive genotypes in growth, nitrogen allocation and gas exchange? 116
Cosmopolitan species as models for ecophysiological responses to global change: The common reed phragmites australis 116
The value of repetitive sequences in chloroplast DNA for phylogeographic inference: A comment on Vachon & Freeland 2011 113
Phylogeography reveals a potential cryptic invasion in the Southern Hemisphere of Ceratophyllum demersum, New Zealand's worst invasive macrophyte 113
Small genome separates native and invasive populations in an ecologically important cosmopolitan grass 112
Preadaptation and post-introduction evolution facilitate the invasion of Phragmites australis in North America 112
Phylogenetic diversity shapes salt tolerance in Phragmites australis estuarine populations in East China 109
Evidence does not support the targeting of cryptic invaders at the subspecies level using classical biological control: the example of Phragmites 108
Nutrient removal potential and biomass production by Phragmites australis and Typha latifolia on European rewetted peat and mineral soils 106
The potential for biological control on cryptic plant invasions 106
Cryptic lineages and potential introgression in a mixed-ploidy species (Phragmites australis) across temperate China 99
Intraspecific variation in Phragmites australis: Clinal adaption of functional traits and phenotypic plasticity vary with latitude of origin 96
Why are tall-statured energy grasses of polyploid species complexes potentially invasive? A review of their genetic variation patterns and evolutionary plasticity 95
Physiology of a plant invasion: Biomass production, growth and tissue chemistry of invasive and native Phragmites australis populations 95
null 86
Rivisiting Phragmites australis variation in the Danube Delta with DNA molecular techniques 70
Clone-specific differences in Phragmites australis: Effects of ploidy level and geographic origin 66
Totale 7.683
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Categoria #
all - tutte 21.944
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 21.944
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021144 0 0 0 0 0 0 0 0 0 0 0 144
2021/2022859 46 32 84 57 90 77 21 79 47 66 110 150
2022/2023726 77 97 44 84 45 35 34 23 168 13 24 82
2023/2024216 14 41 24 20 15 23 5 28 5 25 14 2
2024/20251.129 38 176 87 72 316 62 60 29 6 55 30 198
2025/20262.155 142 192 288 112 201 129 200 190 362 157 78 104
Totale 7.683