CRIS Current Research Information System

LAMBERTINI, CARLA
 Distribuzione geografica
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Continente #
NA - Nord America 2.882
AS - Asia 1.732
EU - Europa 1.547
SA - Sud America 127
AF - Africa 116
OC - Oceania 4
Totale 6.408
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Nazione #
US - Stati Uniti d'America 2.866
SG - Singapore 637
GB - Regno Unito 523
CN - Cina 436
IT - Italia 224
VN - Vietnam 224
DE - Germania 219
HK - Hong Kong 179
IN - India 121
RU - Federazione Russa 114
BR - Brasile 97
SE - Svezia 93
FR - Francia 74
JO - Giordania 56
IE - Irlanda 52
CH - Svizzera 49
ZA - Sudafrica 49
UA - Ucraina 44
EE - Estonia 43
CI - Costa d'Avorio 26
FI - Finlandia 26
TG - Togo 26
NL - Olanda 25
KR - Corea 23
ID - Indonesia 17
BG - Bulgaria 15
AR - Argentina 14
BE - Belgio 12
BW - Botswana 9
EC - Ecuador 8
AT - Austria 7
CA - Canada 7
PL - Polonia 7
MX - Messico 6
PK - Pakistan 6
GR - Grecia 5
JP - Giappone 5
CL - Cile 4
ES - Italia 4
AE - Emirati Arabi Uniti 3
IQ - Iraq 3
LT - Lituania 3
MY - Malesia 3
PY - Paraguay 3
SC - Seychelles 3
TR - Turchia 3
UZ - Uzbekistan 3
AU - Australia 2
BD - Bangladesh 2
EG - Egitto 2
KZ - Kazakistan 2
NO - Norvegia 2
SA - Arabia Saudita 2
TH - Thailandia 2
AL - Albania 1
AZ - Azerbaigian 1
BY - Bielorussia 1
CO - Colombia 1
CR - Costa Rica 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
HN - Honduras 1
HR - Croazia 1
IL - Israele 1
LB - Libano 1
MA - Marocco 1
NP - Nepal 1
NZ - Nuova Zelanda 1
PG - Papua Nuova Guinea 1
PT - Portogallo 1
RS - Serbia 1
TW - Taiwan 1
Totale 6.408
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Città #
Southend 476
Singapore 389
Fairfield 376
Ashburn 330
Santa Clara 240
Houston 199
Seattle 195
Hong Kong 179
Woodbridge 168
Wilmington 162
Cambridge 158
Princeton 112
Ann Arbor 107
Chandler 91
Boardman 71
Bologna 68
Amman 56
Dublin 51
Bern 46
Nanjing 46
Westminster 46
Berlin 45
Beijing 43
Ho Chi Minh City 42
Jinan 40
Hanoi 38
Dong Ket 37
Padova 36
San Jose 30
Abidjan 26
Buffalo 26
Lomé 26
Los Angeles 25
San Diego 25
Changsha 23
Seoul 23
Dallas 21
Shenyang 21
Redondo Beach 20
Saint Petersburg 20
Redmond 19
Hefei 17
Falls Church 14
Frankfurt am Main 14
Hebei 14
Lappeenranta 14
Nanchang 14
Sofia 14
Jakarta 13
Tianjin 13
Brussels 12
Guangzhou 12
Haikou 12
Milan 11
Dearborn 10
Helsinki 10
Phoenix 10
Des Moines 9
Gaborone 9
Hangzhou 9
London 9
Medford 9
Jiaxing 8
Turin 8
Da Nang 7
Johannesburg 7
Norwalk 7
Rome 7
São Paulo 7
Jacksonville 6
Ningbo 6
Redwood City 6
The Dalles 6
Thái Nguyên 6
Bühl 5
Chicago 5
Düsseldorf 5
Hyderabad 5
Lanzhou 5
Munich 5
New York 5
Tokyo 5
Warsaw 5
Wuhan 5
Zhengzhou 5
Cesena 4
Fuzhou 4
Haiphong 4
Handan 4
Ninh Bình 4
Nuremberg 4
Paris 4
Shanghai 4
Suzhou 4
Biên Hòa 3
Brooklyn 3
Charlotte 3
Chennai 3
Denver 3
Falkenstein 3
Totale 4.591
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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 196
Physiological Adaptation to Water Salinity in Six Wild Halophytes Suitable for Mediterranean Agriculture 175
Genetic relationships in Phragmites Adanson 174
Minimum Fe requirement and toxic tissue concentration of Fe in Phragmites australis : A tool for alleviating Fe-deficiency in constructed wetlands 174
Salinity effects on germination, seedlings and full-grown plants of upland and lowland switchgrass cultivars 168
Expression of major photosynthetic and salt-resistance genes in invasive reed lineages grown under elevated CO2 and temperature 155
Genetic structure of the submersed Ranunculus baudotii (sect. Batrachium) population in a lowland stream in Denmark 143
Expansive reed populations – alien invasion or disturbed wetlands? 142
Assessing nutrient responses and biomass quality for selection of appropriate paludiculture crops 141
Gas exchange and growth responses to nutrient enrichment in invasive Glyceria maxima and native New Zealand Carex species 140
Genetic diversity in three invasive clonal aquatic species in New Zealand 138
Global networks for invasion science: benefits, challenges and guidelines 135
Living in two worlds: Evolutionary mechanisms act differently in the native and introduced ranges of an invasive plant 134
Ecosistemi da progettare. Esercizi progettuali per la conservazione della biodiversità, il ripristino funzionale degli ecosistemi e l’accessibilità alle risorse naturali. 133
Do ploidy level and nuclear genome size and latitude of origin modify the expression of Phragmites australis traits and interactions with herbivores? 130
Caratterizzazione morfologica, genetica ed ecologica di popolamenti di Phragmites australis (Cav.) Trin ex Steudel in aree umide della pianura bolognese. 129
Interactive effects of elevated temperature and CO2 on two phylogeographically distinct clones of common reed (Phragmites australis) 129
Genetic diversity patterns of rice (Oryza sativa L.) landraces after migration by Tai Lue and Akha between China and Thailand 129
A phylogeographic study of the cosmopolitan genus Phragmites (Poaceae) based on AFLPs 128
Competition among native and invasive Phragmites australis populations: An experimental test of the effects of invasion status, genome size, and ploidy level 127
Genetic diversity patterns in Phragmites australis at the population, regional and continental scales 125
Photosynthesis of co-existing Phragmites haplotypes in their non-native range: Are characteristics determined by adaptations derived from their native origin? 125
Salt Tolerance and Na Allocation in Sorghum bicolor under Variable Soil and Water Salinity 125
Ammonium and nitrate are both suitable inorganic nitrogen forms for the highly productive wetland grass Arundo donax, a candidate species for wetland paludiculture 122
Tracing the origin of Gulf Coast Phragmites (Poaceae): A story of long-distance dispersal and hybridization 119
Growth and morphology in relation to temperature and light availability during the establishment of three invasive aquatic plant species 119
Exploring the borders of European Phragmites within a cosmopolitan genus 119
Hybridization of common reed in North America? The answer is blowing in the wind 118
The c4 atriplex halimus vs. The c3 atriplex hortensis: Similarities and differences in the salinity stress response 116
Phenotypic traits of phragmites australis clones are not related to ploidy level and distribution range 115
Tall-statured grasses: a useful functional group for invasion science 114
Invasion strategies in clonal aquatic plants: Are phenotypic differences caused by phenotypic plasticity or local adaptation? 112
Herbarium specimens as a source of DNA for AFLP fingerprinting of Phragmites (Poaceae): Possibilities and limitations 108
Mowing regime has different effects on reed stands in relation to habitat 108
Utilizzo di informazioni vegetazionali per la datazione di eventi di debris flow 107
Phenotypic traits of the Mediterranean Phragmites australis M1 lineage: differences between the native and introduced ranges 107
The value of repetitive sequences in chloroplast DNA for phylogeographic inference: A comment on Vachon & Freeland 2011 107
Increased invasive potential of non-native Phragmites australis: Elevated CO2 and temperature alleviate salinity effects on photosynthesis and growth 107
Cosmopolitan species as models for ecophysiological responses to global change: The common reed phragmites australis 107
Phylogeography reveals a potential cryptic invasion in the Southern Hemisphere of Ceratophyllum demersum, New Zealand's worst invasive macrophyte 106
Heteroplasmy due to chloroplast paternal leakage: another insight into Phragmites haplotypic diversity in North America 104
Invasion of old world phragmites australis in the new world: Precipitation and temperature patterns combined with human influences redesign the invasive niche 103
Phragmites australis: How do genotypes of different phylogeographic origins differ from their invasive genotypes in growth, nitrogen allocation and gas exchange? 102
Small genome separates native and invasive populations in an ecologically important cosmopolitan grass 93
Preadaptation and post-introduction evolution facilitate the invasion of Phragmites australis in North America 88
Recovery from Salinity and Drought Stress in the Perennial Sarcocornia fruticosa vs. the Annual Salicornia europaea and S. veneta 88
Evidence does not support the targeting of cryptic invaders at the subspecies level using classical biological control: the example of Phragmites 87
The potential for biological control on cryptic plant invasions 87
null 86
Phylogenetic diversity shapes salt tolerance in Phragmites australis estuarine populations in East China 84
Cryptic lineages and potential introgression in a mixed-ploidy species (Phragmites australis) across temperate China 81
Nutrient removal potential and biomass production by Phragmites australis and Typha latifolia on European rewetted peat and mineral soils 79
Why are tall-statured energy grasses of polyploid species complexes potentially invasive? A review of their genetic variation patterns and evolutionary plasticity 78
Physiology of a plant invasion: Biomass production, growth and tissue chemistry of invasive and native Phragmites australis populations 76
Intraspecific variation in Phragmites australis: Clinal adaption of functional traits and phenotypic plasticity vary with latitude of origin 72
Rivisiting Phragmites australis variation in the Danube Delta with DNA molecular techniques 64
Clone-specific differences in Phragmites australis: Effects of ploidy level and geographic origin 50
Totale 6.628
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Categoria #
all - tutte 19.444
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 19.444
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021479 0 0 0 0 0 0 20 69 153 64 29 144
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
2025/20261.100 142 192 288 112 201 129 36 0 0 0 0 0
Totale 6.628