|
Impact ID |
Scientific Name
|
Impact Type
|
Study Type
|
Study Location
|
Impact Description
|
Geographic Location
|
Reference
|
3554
|
Proterorhinus semilunaris
|
Predation/Herbivory
|
Anecdotal
|
N/A
|
Minor impact (e.g. impacts 1 species, <20% population decline, limited host damage)
|
|
34187
|
3555
|
Proterorhinus semilunaris
|
Predation/Herbivory
|
Observational
|
Field
|
Can dominate the local fish assemblage when competing with only native species (not other gobiids).
|
|
34188
|
3557
|
Proterorhinus semilunaris
|
Predation/Herbivory
|
Observational
|
Field
|
Dipterans, small-bodied insects such as Caenis
and trichopterans (Cheumatopsyche), and crustaceans
(isopods and the amphipod Gammarus)
were common food of tubenose gobies
from May through late June and in December. Tubenose gobies also consumed numerous dipterans.
|
|
16594
|
3559
|
Proterorhinus semilunaris
|
Predation/Herbivory
|
Observational
|
Field
|
Three of nine tubenose gobies consumed round goby eggs (June, daytime)
|
|
16594
|
3596
|
Proterorhinus semilunaris
|
Predation/Herbivory
|
Anecdotal
|
N/A
|
Consumption of fish eggs and juveniles by invading gobies was very low.
|
Dyje River, Danube, central Europe
|
34199
|
3598
|
Proterorhinus semilunaris
|
Predation/Herbivory
|
Anecdotal
|
N/A
|
it is too small to efficiently feed on zebra mussels (French and Jude 2001). Ecological impacts, therefore, are expected to be minimal.
|
|
13825
|
3605
|
Proterorhinus semilunaris
|
Predation/Herbivory
|
Observational
|
Field
|
diet included chironomids (60% of diet by weight in 70% of fish), ostracods (0.5% of diet in 50% of fish), planktonic crustaceans (5% of diet in 21% of fish), Caddisfly larvae (Hydropsyche sp., Leptoceridae and Hydroptila sparsa) and
mayfly nympha (Siphlonurus aestivalis, Potamanthus luteus and Caenis sp.)
constituted 5.5% of diet in 36%
of the fish. Corophium curvispinum (1.75% of diet in 14% of fish
|
Slovak part of the Danube River
|
20836
|
3607
|
Proterorhinus semilunaris
|
Predation/Herbivory
|
Anecdotal
|
N/A
|
According to our preliminary results (PRÁS?EK and ADÁMEK, personal observations) chironomid larvae and pupae, isopod Asellus aquaticus and water bugs (Corixidae) were the dominant food items in the diet of the tubenose goby
|
|
20836
|
3623
|
Proterorhinus semilunaris
|
Predation/Herbivory
|
Anecdotal
|
Field
|
Since tubenose gobies tend to approximate rather than exceed the size of native sculpins, feed almost exclusively on benthos, and are infrequently found outside macrophyte beds, their population will probably not reach high abundances in the St. Clair River, and are thus not expected to have substantial effects on native fishes in that river.
|
|
22782
|
3639
|
Proterorhinus semilunaris
|
Predation/Herbivory
|
Anecdotal
|
Field
|
A strong dependence on specific
prey species, as indicated in the Tubenose Goby, could be a risk to food web stability following invasion, particularly in unstable food webs such as those that suffer perpetual invasions.
|
|
28019
|
3649
|
Proterorhinus semilunaris
|
Predation/Herbivory
|
Experimental
|
Laboratory
|
Tubenose goby are a Type 2 functional response predator (based on Cyprinus carpio larvae feeding experiments) and consequently, may have a destabilizing effect on population dynamics of cyprinids through high prey
exploitation at low prey densities
|
based on fish collected in Europe
|
32182
|
3650
|
Proterorhinus semilunaris
|
Predation/Herbivory
|
Anecdotal
|
Laboratory
|
Proterorhinus semilunaris reaches high densities in shallow
macrophyte-rich habitats (Kocovsky et al. 2011), where it can pose serious threat for phytophilic fauna, including cyprind larvae.
|
|
32182
|
3654
|
Proterorhinus semilunaris
|
Predation/Herbivory
|
Experimental
|
Laboratory
|
Despite a lack of difference in FR types among habitats, we
found differences in model parameters. Proterorhinus semilunaris
attack rate values significantly differed among habitats, with the highest value for substrate with artificial plants. Higher attack rate implies high efficiency at even low prey densities.
|
|
34254
|
3656
|
Proterorhinus semilunaris
|
Predation/Herbivory
|
Experimental
|
Laboratory
|
Proterorhinus semilunaris showed significantly lower handling time
in gravel habitat but no difference based on artificial plant cover.
|
|
34254
|
3658
|
Proterorhinus semilunaris
|
Predation/Herbivory
|
Experimental
|
Laboratory
|
we observed significant differences among habitat conditions, with highest weight specific maximum feeding rate on gravel substrate, followed by gravel with artificial plant and sand. reflects habitat preference and induced stress in non-sheltered habitats. forage efficiently in structured habitats that might otherwise serve as prey refugia
|
|
34254
|
3659
|
Proterorhinus semilunaris
|
Predation/Herbivory
|
Experimental
|
Laboratory
|
results confirm that Neogobius melanostomus and Proterorhinus
semilunaris can have a detrimental impact on fish larva populations
|
|
34254
|
3671
|
Proterorhinus semilunaris
|
Predation/Herbivory
|
Experimental
|
Laboratory
|
Considering large amount of fish larvae consumed by both fishes round and tubenose gobies) confirmed in our study, pelagic lifestyle of juveniles (Hensler and Jude, 2007) and their preference for soft-bodied prey (Ray and Corkum, 1997), the influence on fish populations by direct predation can be tremendous.
|
|
34286
|
3673
|
Proterorhinus semilunaris
|
Predation/Herbivory
|
Observational
|
Field
|
Overall, predators were estimated to have taken approximately 52 % of annual goby biomass (round and tubenose combined). Perch and catfish showed a strong selection for tubenose goby, pike and burbot showed no selectivity toward tubenose goby relative to native fish, while both sander species strongly preferred native prey.
|
River Dyje
|
34287
|
3680
|
Proterorhinus semilunaris
|
Predation/Herbivory
|
Observational
|
Field
|
Although cottids are presently believed to be most vulnerable to gobiid invasion, we observed no
negative trend in bullhead abundance over the 8-year dataset, the population remaining stable and at similar
abundances to gobiids.
|
|
34308
|
3682
|
Proterorhinus semilunaris
|
Predation/Herbivory
|
Observational
|
Field
|
Its diet was exclusively of animal origin with significant dominance of and preference for two food items – chironomid (Chironomidae) larvae and waterlouse (Asellus aquaticus),
|
Dyje River
|
34312
|
3689
|
Proterorhinus semilunaris
|
Predation/Herbivory
|
Observational
|
Field
|
tubenose gobies quickly became the dominant species along the reservoir bankside, making them an attractive prey for =1 + perch. There was a clear increasing trend in the numbers of larger perch caught along the rip-rap, with the largest fish clearly specialising on gobies.
|
Musov reservoir
|
34323
|
3690
|
Proterorhinus semilunaris
|
Predation/Herbivory
|
Observational
|
Field
|
tubenose gobies quickly became the dominant species along the reservoir bankside, making them an attractive prey for =1 + perch. There was a clear increasing trend in the numbers of larger perch caught along the rip-rap, with the largest fish clearly specialising on gobies.
|
Musov reservoir
|
34323
|
3691
|
Proterorhinus semilunaris
|
Predation/Herbivory
|
Observational
|
Field
|
tubenose gobies quickly became the dominant species along the reservoir bankside, making them an attractive prey for =1 + perch. There was a clear increasing trend in the numbers of larger perch caught along the rip-rap, with the largest fish clearly specialising on gobies.
|
Musov Reservoir
|
34323
|
3856
|
Proterorhinus semilunaris
|
Predation/Herbivory
|
Anecdotal
|
N/A
|
tubenose goby preys on zebra and quagga mussels
|
Great Lakes
|
13595
|
3874
|
Proterorhinus semilunaris
|
Predation/Herbivory
|
Anecdotal
|
N/A
|
interspecific predation of larvae
|
Great Lakes
|
13595
|
|